PUBLICACIÓN

Detection of Genomic Variations in BRCA1 and BRCA2 Genes by Long-Range PCR and Next-Generation Sequencing

ACCEDER A LA PUBLICACIÓN: Orcid Dialnet

Hernan I; Borràs E; de Sousa Dias M; Gamundi MJ; Mañé B; Llort G; Agúndez JA; Blanca M; Carballo M

2012 JOURNAL OF MOLECULAR DIAGNOSTICS

Molecular Medicine (Q1), Pathology and Forensic Medicine (Q1)

JCR: 3.952

SJR: 1.728

DOI

10.1016/j.jmoldx.2012.01.013

ISSN

1525-1578

AUTORES DE LA UEX

José Augusto García-Agúndez Pérez-Coca

OTRAS PUBLICACIONES DE INTERÉS

Aminopyrine N-Demethylase Activity In Human Liver Microsomes.
Oxidative Stress In Huntington’s Disease
Essential Tremor - Drug Treatments Present And Future
Oxidative Stress In Huntington’s Disease
Essential Tremor - Drug Treatments Present And Future
Mdga1 Gene Variants And Risk For Restless Legs Syndrome
Essential Tremor - Drug Treatments Present And Future
Mdga1 Gene Variants And Risk For Restless Legs Syndrome
Editorial: Editor’s Feature: Negative Findings In Pharmacogenetics And Pharmacogenomics Volume Ii
Mdga1 Gene Variants And Risk For Restless Legs Syndrome
Editorial: Editor’s Feature: Negative Findings In Pharmacogenetics And Pharmacogenomics Volume Ii
Oxidative Stress And Antioxidant Therapies In Friedreich’s Ataxia
Editorial: Editor’s Feature: Negative Findings In Pharmacogenetics And Pharmacogenomics Volume Ii
Oxidative Stress And Antioxidant Therapies In Friedreich’s Ataxia
Clinical Pharmacogenetics Implementation Consortium Guideline For Nat2 Genotype And Hydralazine Therapy
Oxidative Stress And Antioxidant Therapies In Friedreich’s Ataxia
Clinical Pharmacogenetics Implementation Consortium Guideline For Nat2 Genotype And Hydralazine Therapy
Genetic And Serum Biomarkers Of Nsaid Hypersensitivity Reactions
Clinical Pharmacogenetics Implementation Consortium Guideline For Nat2 Genotype And Hydralazine Therapy
Genetic And Serum Biomarkers Of Nsaid Hypersensitivity Reactions
Oxidative Stress And Migraine
Genetic And Serum Biomarkers Of Nsaid Hypersensitivity Reactions
Oxidative Stress And Migraine
Ibuprofen And Other Arylpropionics: The Relevance In Immediate Hypersensitivity Drug Reactions
Oxidative Stress And Migraine
Ibuprofen And Other Arylpropionics: The Relevance In Immediate Hypersensitivity Drug Reactions
Oxidative Stress Markers In Multiple Sclerosis
Ibuprofen And Other Arylpropionics: The Relevance In Immediate Hypersensitivity Drug Reactions
Oxidative Stress Markers In Multiple Sclerosis
Clinical Pharmacogenetics Implementation Consortium Guideline (Cpic) For Cyp2d6, Adrb1, Adrb2, Adra2c, Grk4, And Grk5 Genotypes And Beta-Blocker Therapy
Oxidative Stress Markers In Multiple Sclerosis
Clinical Pharmacogenetics Implementation Consortium Guideline (Cpic) For Cyp2d6, Adrb1, Adrb2, Adra2c, Grk4, And Grk5 Genotypes And Beta-Blocker Therapy
Antioxidant Therapies In The Treatment Of Multiple Sclerosis
Clinical Pharmacogenetics Implementation Consortium Guideline (Cpic) For Cyp2d6, Adrb1, Adrb2, Adra2c, Grk4, And Grk5 Genotypes And Beta-Blocker Therapy
Antioxidant Therapies In The Treatment Of Multiple Sclerosis
Association Between Common Variants In The Lag3/cd4 Genes And Risk For Essential Tremor
Antioxidant Therapies In The Treatment Of Multiple Sclerosis
Association Between Common Variants In The Lag3/cd4 Genes And Risk For Essential Tremor
Editorial: Insights In Pharmacogenetics And Pharmacogenomics: 2023
Association Between Common Variants In The Lag3/cd4 Genes And Risk For Essential Tremor
Editorial: Insights In Pharmacogenetics And Pharmacogenomics: 2023
Developments In Pharmacogenetics, Pharmacogenomics, And Personalized Medicine
Editorial: Insights In Pharmacogenetics And Pharmacogenomics: 2023
Developments In Pharmacogenetics, Pharmacogenomics, And Personalized Medicine
Clinical Pharmacogenomics In Asthma Therapy
Developments In Pharmacogenetics, Pharmacogenomics, And Personalized Medicine
Clinical Pharmacogenomics In Asthma Therapy
Sleep Disorders In Patients With Choreic Syndromes
Clinical Pharmacogenomics In Asthma Therapy
Sleep Disorders In Patients With Choreic Syndromes
Vitamin D Receptor And Binding Protein Genes Variants In Patients With Migraine
Sleep Disorders In Patients With Choreic Syndromes
Vitamin D Receptor And Binding Protein Genes Variants In Patients With Migraine
Alpha-Synuclein In Peripheral Tissues As A Possible Marker For Neurological Diseases And Other Medical Conditions
Vitamin D Receptor And Binding Protein Genes Variants In Patients With Migraine
Alpha-Synuclein In Peripheral Tissues As A Possible Marker For Neurological Diseases And Other Medical Conditions
Editorial: Editor’s Feature: Negative Findings In Pharmacogenetics And Pharmacogenomics
Alpha-Synuclein In Peripheral Tissues As A Possible Marker For Neurological Diseases And Other Medical Conditions
Editorial: Editor’s Feature: Negative Findings In Pharmacogenetics And Pharmacogenomics
An Update On The Pharmacogenetic Considerations When Prescribing Dopamine Receptor Agonists For Parkinson’s Disease
Editorial: Editor’s Feature: Negative Findings In Pharmacogenetics And Pharmacogenomics
An Update On The Pharmacogenetic Considerations When Prescribing Dopamine Receptor Agonists For Parkinson’s Disease
Pharmvar Tutorial On Cyp2d6 Structural Variation Testing And Recommendations On Reporting
An Update On The Pharmacogenetic Considerations When Prescribing Dopamine Receptor Agonists For Parkinson’s Disease
Pharmvar Tutorial On Cyp2d6 Structural Variation Testing And Recommendations On Reporting
Inflammatory Factors And Restless Legs Syndrome: A Systematic Review And Meta-Analysis
Pharmvar Tutorial On Cyp2d6 Structural Variation Testing And Recommendations On Reporting
Inflammatory Factors And Restless Legs Syndrome: A Systematic Review And Meta-Analysis
Lack Of Association Between Common Lag3/cd4 Variants And Risk Of Migraine
Inflammatory Factors And Restless Legs Syndrome: A Systematic Review And Meta-Analysis
Lack Of Association Between Common Lag3/cd4 Variants And Risk Of Migraine
Coenzyme Q10 And Dementia: A Systematic Review
Lack Of Association Between Common Lag3/cd4 Variants And Risk Of Migraine
Coenzyme Q10 And Dementia: A Systematic Review
Fármacos Antineoplásicos
Coenzyme Q10 And Dementia: A Systematic Review
Fármacos Antineoplásicos
Inflammatory Factors And Restless Legs Syndrome: A Systematic Review And Meta-Analysis.
Fármacos Antineoplásicos
Inflammatory Factors And Restless Legs Syndrome: A Systematic Review And Meta-Analysis.
Association Between Lag3/cd4 Genes Variants And Risk For Multiple Sclerosis
Inflammatory Factors And Restless Legs Syndrome: A Systematic Review And Meta-Analysis.
Association Between Lag3/cd4 Genes Variants And Risk For Multiple Sclerosis
Lag3/cd4 Genes Variants And The Risk For Restless Legs Syndrome
Association Between Lag3/cd4 Genes Variants And Risk For Multiple Sclerosis
Lag3/cd4 Genes Variants And The Risk For Restless Legs Syndrome
Association Between Lag3/cd4 Gene Variants And Risk Of Parkinson's Disease
Lag3/cd4 Genes Variants And The Risk For Restless Legs Syndrome
Association Between Lag3/cd4 Gene Variants And Risk Of Parkinson's Disease
Coenzyme Q10 And Parkinsonian Syndromes: A Systematic Review
Association Between Lag3/cd4 Gene Variants And Risk Of Parkinson's Disease
Coenzyme Q10 And Parkinsonian Syndromes: A Systematic Review
Vitamin D Receptor And Binding Protein Gene Variants In Patients With Essential Tremor
Coenzyme Q10 And Parkinsonian Syndromes: A Systematic Review
Vitamin D Receptor And Binding Protein Gene Variants In Patients With Essential Tremor
Increased Serum Diamine Oxidase Activity In Nonallergic Patients With Migraine
Vitamin D Receptor And Binding Protein Gene Variants In Patients With Essential Tremor
Increased Serum Diamine Oxidase Activity In Nonallergic Patients With Migraine
Common Ugt1a6 Variant Alleles Determine Acetaminophen Pharmacokinetics In Man
Increased Serum Diamine Oxidase Activity In Nonallergic Patients With Migraine
Common Ugt1a6 Variant Alleles Determine Acetaminophen Pharmacokinetics In Man
Editorial: Insights In Pharmacogenetics And Pharmacogenomics: 2021
Common Ugt1a6 Variant Alleles Determine Acetaminophen Pharmacokinetics In Man
Editorial: Insights In Pharmacogenetics And Pharmacogenomics: 2021
Serum Trace Elements Concentrations In Patients With Restless Legs Syndrome
Editorial: Insights In Pharmacogenetics And Pharmacogenomics: 2021
Serum Trace Elements Concentrations In Patients With Restless Legs Syndrome
Association Of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study And Meta-Analysis
Serum Trace Elements Concentrations In Patients With Restless Legs Syndrome
Association Of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study And Meta-Analysis
Sleep Disorders And Sleep Problems In Patients With Tourette Syndrome And Other Tic Disorders: Current Perspectives
Association Of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study And Meta-Analysis
Sleep Disorders And Sleep Problems In Patients With Tourette Syndrome And Other Tic Disorders: Current Perspectives
Molecular Monitoring Of Patient Response To Painkiller Drugs
Sleep Disorders And Sleep Problems In Patients With Tourette Syndrome And Other Tic Disorders: Current Perspectives
Molecular Monitoring Of Patient Response To Painkiller Drugs
Pharmvar Genefocus: Cyp2c9
Molecular Monitoring Of Patient Response To Painkiller Drugs
Pharmvar Genefocus: Cyp2c9
Impact Of Gastrointestinal Tract Variability On Oral Drug Absorption And Pharmacokinetics: An Ungap Review
Pharmvar Genefocus: Cyp2c9
Impact Of Gastrointestinal Tract Variability On Oral Drug Absorption And Pharmacokinetics: An Ungap Review
Genetic Variants In Cytosolic Phospholipase A2 Associated With Nonsteroidal Anti-Inflammatory Drug–induced Acute Urticaria/angioedema
Impact Of Gastrointestinal Tract Variability On Oral Drug Absorption And Pharmacokinetics: An Ungap Review
Genetic Variants In Cytosolic Phospholipase A2 Associated With Nonsteroidal Anti-Inflammatory Drug–induced Acute Urticaria/angioedema
Pharmvar Genefocus: Cyp2c19
Genetic Variants In Cytosolic Phospholipase A2 Associated With Nonsteroidal Anti-Inflammatory Drug–induced Acute Urticaria/angioedema
Pharmvar Genefocus: Cyp2c19
Aradyal: The Spanish Multidisciplinary Research Network For Allergic Diseases
Pharmvar Genefocus: Cyp2c19
Aradyal: The Spanish Multidisciplinary Research Network For Allergic Diseases
Editorial: Nsaids Pharmacogenomics
Aradyal: The Spanish Multidisciplinary Research Network For Allergic Diseases
Editorial: Nsaids Pharmacogenomics
Current Treatment Options For Rem Sleep Behaviour Disorder
Editorial: Nsaids Pharmacogenomics
Current Treatment Options For Rem Sleep Behaviour Disorder
Lack Of Major Involvement Of Common Cyp2c Gene Polymorphisms In The Risk Of Developing Cross-Hypersensitivity To Nsaids
Current Treatment Options For Rem Sleep Behaviour Disorder
Lack Of Major Involvement Of Common Cyp2c Gene Polymorphisms In The Risk Of Developing Cross-Hypersensitivity To Nsaids
Neurochemical Features Of Rem Sleep Behaviour Disorder
Lack Of Major Involvement Of Common Cyp2c Gene Polymorphisms In The Risk Of Developing Cross-Hypersensitivity To Nsaids
Neurochemical Features Of Rem Sleep Behaviour Disorder
Association Between Restless Legs Syndrome And Peripheral Neuropathy: A Systematic Review And Meta-Analysis
Neurochemical Features Of Rem Sleep Behaviour Disorder
Association Between Restless Legs Syndrome And Peripheral Neuropathy: A Systematic Review And Meta-Analysis
Genetic Variants Of Alcohol Metabolizing Enzymes And Alcohol-Related Liver Cirrhosis Risk
Association Between Restless Legs Syndrome And Peripheral Neuropathy: A Systematic Review And Meta-Analysis
Genetic Variants Of Alcohol Metabolizing Enzymes And Alcohol-Related Liver Cirrhosis Risk
Sleep Disorders In Patients With Essential Tremor
Genetic Variants Of Alcohol Metabolizing Enzymes And Alcohol-Related Liver Cirrhosis Risk
Sleep Disorders In Patients With Essential Tremor
Correction To: Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome (Journal Of Neurology, (2021), 268, 4, (1461-1472), 10.1007/s00415-020-10312-9)
Sleep Disorders In Patients With Essential Tremor
Correction To: Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome (Journal Of Neurology, (2021), 268, 4, (1461-1472), 10.1007/s00415-020-10312-9)
Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome
Correction To: Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome (Journal Of Neurology, (2021), 268, 4, (1461-1472), 10.1007/s00415-020-10312-9)
Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome
Deep Sequencing Of Prostaglandin-Endoperoxide Synthase (Ptge) Genes Reveals Genetic Susceptibility For Cross-Reactive Hypersensitivity To Nsaid
Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome
Deep Sequencing Of Prostaglandin-Endoperoxide Synthase (Ptge) Genes Reveals Genetic Susceptibility For Cross-Reactive Hypersensitivity To Nsaid
Biological Fluid Levels Of Iron And Iron-Related Proteins In Parkinson’s Disease: Review And Meta-Analysis
Deep Sequencing Of Prostaglandin-Endoperoxide Synthase (Ptge) Genes Reveals Genetic Susceptibility For Cross-Reactive Hypersensitivity To Nsaid
Biological Fluid Levels Of Iron And Iron-Related Proteins In Parkinson’s Disease: Review And Meta-Analysis
Common Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphisms Are Not Related With The Risk For Restless Legs Syndrome
Biological Fluid Levels Of Iron And Iron-Related Proteins In Parkinson’s Disease: Review And Meta-Analysis
Common Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphisms Are Not Related With The Risk For Restless Legs Syndrome
Variability Of The Genes Involved In The Cellular Redox Status And Their Implication In Drug Hypersensitivity Reactions
Common Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphisms Are Not Related With The Risk For Restless Legs Syndrome
Variability Of The Genes Involved In The Cellular Redox Status And Their Implication In Drug Hypersensitivity Reactions
Cerebrospinal And Blood Levels Of Amino Acids As Potential Biomarkers For Parkinson's Disease: Review And Meta-Analysis. Response To Letter To The Editor By Zheng Et Al.
Variability Of The Genes Involved In The Cellular Redox Status And Their Implication In Drug Hypersensitivity Reactions
Cerebrospinal And Blood Levels Of Amino Acids As Potential Biomarkers For Parkinson's Disease: Review And Meta-Analysis. Response To Letter To The Editor By Zheng Et Al.
Genomic Markers For Essential Tremor
Cerebrospinal And Blood Levels Of Amino Acids As Potential Biomarkers For Parkinson's Disease: Review And Meta-Analysis. Response To Letter To The Editor By Zheng Et Al.
Genomic Markers For Essential Tremor
Exome-Wide Rare Variant Analysis In Familial Essential Tremor
Genomic Markers For Essential Tremor
Exome-Wide Rare Variant Analysis In Familial Essential Tremor
Clinical Pharmacogenetics Implementation Consortium Guideline (Cpic) For Cyp2c9 And Nonsteroidal Anti-Inflammatory Drugs
Exome-Wide Rare Variant Analysis In Familial Essential Tremor
Clinical Pharmacogenetics Implementation Consortium Guideline (Cpic) For Cyp2c9 And Nonsteroidal Anti-Inflammatory Drugs
Pharmvar Genefocus: Cyp2d6
Clinical Pharmacogenetics Implementation Consortium Guideline (Cpic) For Cyp2c9 And Nonsteroidal Anti-Inflammatory Drugs
Pharmvar Genefocus: Cyp2d6
Biological Fluid Levels Of Iron And Iron-Related Proteins In Parkinson's Disease: Review And Meta-Analysis.
Pharmvar Genefocus: Cyp2d6
Biological Fluid Levels Of Iron And Iron-Related Proteins In Parkinson's Disease: Review And Meta-Analysis.
Exome-Wide Rare Variant Analysis In Familial Essential Tremor.
Biological Fluid Levels Of Iron And Iron-Related Proteins In Parkinson's Disease: Review And Meta-Analysis.
Exome-Wide Rare Variant Analysis In Familial Essential Tremor.
Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome.
Exome-Wide Rare Variant Analysis In Familial Essential Tremor.
Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome.
Pharmvar Genefocus: Cyp2c19.
Serum Vitamin D, Vitamin D Receptor And Binding Protein Genes Polymorphisms In Restless Legs Syndrome.
Pharmvar Genefocus: Cyp2c19.
The Spanish Multidisciplinary Research Network For Allergic Diseases.
Pharmvar Genefocus: Cyp2c19.
The Spanish Multidisciplinary Research Network For Allergic Diseases.
Modulation Of Cyp2c9 Activity And Hydrogen Peroxide Production By Cytochrome B 5
The Spanish Multidisciplinary Research Network For Allergic Diseases.
Modulation Of Cyp2c9 Activity And Hydrogen Peroxide Production By Cytochrome B 5
Photomutagenicity Of Chlorpromazine And Its N-Demethylated Metabolites Assessed By Ngs
Modulation Of Cyp2c9 Activity And Hydrogen Peroxide Production By Cytochrome B 5
Photomutagenicity Of Chlorpromazine And Its N-Demethylated Metabolites Assessed By Ngs
Anti-Inflammatory Effects Of Amantadine And Memantine: Possible Therapeutics For The Treatment Of Covid-19?
Photomutagenicity Of Chlorpromazine And Its N-Demethylated Metabolites Assessed By Ngs
Anti-Inflammatory Effects Of Amantadine And Memantine: Possible Therapeutics For The Treatment Of Covid-19?
Cerebrospinal And Blood Levels Of Amino Acids As Potential Biomarkers For Parkinson’s Disease: Review And Meta-Analysis
Anti-Inflammatory Effects Of Amantadine And Memantine: Possible Therapeutics For The Treatment Of Covid-19?
Cerebrospinal And Blood Levels Of Amino Acids As Potential Biomarkers For Parkinson’s Disease: Review And Meta-Analysis
Sleep Disorders In Tourette Syndrome
Cerebrospinal And Blood Levels Of Amino Acids As Potential Biomarkers For Parkinson’s Disease: Review And Meta-Analysis
Sleep Disorders In Tourette Syndrome
Outcomes And Laboratory And Clinical Findings Of Asthma And Allergic Patients Admitted With Covid-19 In A Spanish University Hospital
Sleep Disorders In Tourette Syndrome
Outcomes And Laboratory And Clinical Findings Of Asthma And Allergic Patients Admitted With Covid-19 In A Spanish University Hospital
Sleep Disorders In Essential Tremor: Systematic Review And Meta-Analysis
Outcomes And Laboratory And Clinical Findings Of Asthma And Allergic Patients Admitted With Covid-19 In A Spanish University Hospital
Sleep Disorders In Essential Tremor: Systematic Review And Meta-Analysis
Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 Polymorphism And Risk For Multiple Sclerosis
Sleep Disorders In Essential Tremor: Systematic Review And Meta-Analysis
Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 Polymorphism And Risk For Multiple Sclerosis
Association Between Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 And The Risk For Migraine
Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 Polymorphism And Risk For Multiple Sclerosis
Association Between Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 And The Risk For Migraine
An Update On The Pharmacogenomics Of Nsaid Metabolism And The Risk Of Gastrointestinal Bleeding
Association Between Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 And The Risk For Migraine
An Update On The Pharmacogenomics Of Nsaid Metabolism And The Risk Of Gastrointestinal Bleeding
Current And Future Neuropharmacological Options For The Treatment Of Essential Tremor
An Update On The Pharmacogenomics Of Nsaid Metabolism And The Risk Of Gastrointestinal Bleeding
Current And Future Neuropharmacological Options For The Treatment Of Essential Tremor
An Update On The Neurochemistry Of Essential Tremor
Current And Future Neuropharmacological Options For The Treatment Of Essential Tremor
An Update On The Neurochemistry Of Essential Tremor
Pharmvar Genefocus: Cyp2d6.
An Update On The Neurochemistry Of Essential Tremor
Pharmvar Genefocus: Cyp2d6.
Association Between Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 And The Risk For Migraine.
Pharmvar Genefocus: Cyp2d6.
Association Between Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 And The Risk For Migraine.
Association Study Among Candidate Genetic Polymorphisms And Chemotherapy-Related Severe Toxicity In Testicular Cancer Patients
Association Between Endothelial Nitric Oxide Synthase (Nos3) Rs2070744 And The Risk For Migraine.
Association Study Among Candidate Genetic Polymorphisms And Chemotherapy-Related Severe Toxicity In Testicular Cancer Patients
Next-Generation Sequencing Of Ptgs Genes Reveals An Increased Frequency Of Non-Synonymous Variants Among Patients With Nsaid-Induced Liver Injury
Association Study Among Candidate Genetic Polymorphisms And Chemotherapy-Related Severe Toxicity In Testicular Cancer Patients
Next-Generation Sequencing Of Ptgs Genes Reveals An Increased Frequency Of Non-Synonymous Variants Among Patients With Nsaid-Induced Liver Injury
The Role Of Phase I And Ii Genetic Polymorphisms, Smoking, Alcohol And Cancer Family History, In The Risk Of Developing Testicular Cancer
Next-Generation Sequencing Of Ptgs Genes Reveals An Increased Frequency Of Non-Synonymous Variants Among Patients With Nsaid-Induced Liver Injury
The Role Of Phase I And Ii Genetic Polymorphisms, Smoking, Alcohol And Cancer Family History, In The Risk Of Developing Testicular Cancer
Alcohol Consumption And Risk For Parkinson’s Disease: A Systematic Review And Meta-Analysis
The Role Of Phase I And Ii Genetic Polymorphisms, Smoking, Alcohol And Cancer Family History, In The Risk Of Developing Testicular Cancer
Alcohol Consumption And Risk For Parkinson’s Disease: A Systematic Review And Meta-Analysis
Neurochemical Features Of Idiopathic Restless Legs Syndrome
Alcohol Consumption And Risk For Parkinson’s Disease: A Systematic Review And Meta-Analysis
Neurochemical Features Of Idiopathic Restless Legs Syndrome
Association Between Restless Legs Syndrome And Other Movement Disorders
Neurochemical Features Of Idiopathic Restless Legs Syndrome
Association Between Restless Legs Syndrome And Other Movement Disorders
Association Between The Missense Alcohol Dehydrogenase Rs1229984t Variant With The Risk For Parkinson’s Disease In Women
Association Between Restless Legs Syndrome And Other Movement Disorders
Association Between The Missense Alcohol Dehydrogenase Rs1229984t Variant With The Risk For Parkinson’s Disease In Women
Identification Of Novel Biomarkers For Drug Hypersensitivity After Sequencing Of The Promoter Area In 16 Genes Of The Vitamin D Pathway And The High-Affinity Ige Receptor
Association Between The Missense Alcohol Dehydrogenase Rs1229984t Variant With The Risk For Parkinson’s Disease In Women
Identification Of Novel Biomarkers For Drug Hypersensitivity After Sequencing Of The Promoter Area In 16 Genes Of The Vitamin D Pathway And The High-Affinity Ige Receptor
Pharmacogenetic Factors Affecting Asthma Treatment Response. Potential Implications For Drug Therapy
Identification Of Novel Biomarkers For Drug Hypersensitivity After Sequencing Of The Promoter Area In 16 Genes Of The Vitamin D Pathway And The High-Affinity Ige Receptor
Pharmacogenetic Factors Affecting Asthma Treatment Response. Potential Implications For Drug Therapy
An Update On The Neurochemistry Of Essential Tremor.
Pharmacogenetic Factors Affecting Asthma Treatment Response. Potential Implications For Drug Therapy
An Update On The Neurochemistry Of Essential Tremor.
Alcohol Consumption And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis.
An Update On The Neurochemistry Of Essential Tremor.
Alcohol Consumption And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis.
Nsaids-Hypersensitivity Often Induces A Blended Reaction Pattern Involving Multiple Organs
Alcohol Consumption And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis.
Nsaids-Hypersensitivity Often Induces A Blended Reaction Pattern Involving Multiple Organs
The Potential Role Of Pharmacogenomics And Biotransformation In Hypersensitivity Reactions To Paracetamol
Nsaids-Hypersensitivity Often Induces A Blended Reaction Pattern Involving Multiple Organs
The Potential Role Of Pharmacogenomics And Biotransformation In Hypersensitivity Reactions To Paracetamol
Asthma And Allergic Rhinitis Associate With The Rs2229542 Variant That Induces A P.lys90glu Mutation And Compromises Akr1b1 Protein Levels
The Potential Role Of Pharmacogenomics And Biotransformation In Hypersensitivity Reactions To Paracetamol
Asthma And Allergic Rhinitis Associate With The Rs2229542 Variant That Induces A P.lys90glu Mutation And Compromises Akr1b1 Protein Levels
Gamma-Aminobutyric Acid (Gaba) Receptors Genes Polymorphisms And Risk For Restless Legs Syndrome
Asthma And Allergic Rhinitis Associate With The Rs2229542 Variant That Induces A P.lys90glu Mutation And Compromises Akr1b1 Protein Levels
Gamma-Aminobutyric Acid (Gaba) Receptors Genes Polymorphisms And Risk For Restless Legs Syndrome
Genetics Of Restless Legs Syndrome: An Update
Gamma-Aminobutyric Acid (Gaba) Receptors Genes Polymorphisms And Risk For Restless Legs Syndrome
Genetics Of Restless Legs Syndrome: An Update
Gamma-Aminobutyric Acid (Gaba) Receptors Gabra4, Gabre, And Gabrq Gene Polymorphisms And Risk For Migraine
Genetics Of Restless Legs Syndrome: An Update
Gamma-Aminobutyric Acid (Gaba) Receptors Gabra4, Gabre, And Gabrq Gene Polymorphisms And Risk For Migraine
Missense Gamma-Aminobutyric Acid Receptor Polymorphisms Are Associated With Reaction Time, Motor Time, And Ethanol Effects In Vivo
Gamma-Aminobutyric Acid (Gaba) Receptors Gabra4, Gabre, And Gabrq Gene Polymorphisms And Risk For Migraine
Missense Gamma-Aminobutyric Acid Receptor Polymorphisms Are Associated With Reaction Time, Motor Time, And Ethanol Effects In Vivo
Human Arylamine N-Acetyltransferase Type 2: Phenotypic Correlation With Genotype-A Clinical Perspective
Missense Gamma-Aminobutyric Acid Receptor Polymorphisms Are Associated With Reaction Time, Motor Time, And Ethanol Effects In Vivo
Human Arylamine N-Acetyltransferase Type 2: Phenotypic Correlation With Genotype-A Clinical Perspective
Hypersensitivity Reactions To Nonsteroidal Anti-Inflammatory Drugs: An Update On Pharmacogenetics Studies
Human Arylamine N-Acetyltransferase Type 2: Phenotypic Correlation With Genotype-A Clinical Perspective
Hypersensitivity Reactions To Nonsteroidal Anti-Inflammatory Drugs: An Update On Pharmacogenetics Studies
Foreword
Hypersensitivity Reactions To Nonsteroidal Anti-Inflammatory Drugs: An Update On Pharmacogenetics Studies
Foreword
Genetics Of Restless Legs Syndrome: An Update.
Foreword
Genetics Of Restless Legs Syndrome: An Update.
Association Between The Rs1229984 Polymorphism In The Alcohol Dehydrogenase 1b Gene And Risk For Restless Legs Syndrome
Genetics Of Restless Legs Syndrome: An Update.
Association Between The Rs1229984 Polymorphism In The Alcohol Dehydrogenase 1b Gene And Risk For Restless Legs Syndrome
Gamma-Aminobutyric Acid (Gaba) Receptors Rho (Gabrr) Gene Polymorphisms And Risk For Migraine
Association Between The Rs1229984 Polymorphism In The Alcohol Dehydrogenase 1b Gene And Risk For Restless Legs Syndrome
Gamma-Aminobutyric Acid (Gaba) Receptors Rho (Gabrr) Gene Polymorphisms And Risk For Migraine
Editorial: Biomarkers In Drug Hypersensitivity
Gamma-Aminobutyric Acid (Gaba) Receptors Rho (Gabrr) Gene Polymorphisms And Risk For Migraine
Editorial: Biomarkers In Drug Hypersensitivity
Delta-Amino-Levulinic Acid Dehydratase Gene And Essential Tremor
Editorial: Biomarkers In Drug Hypersensitivity
Delta-Amino-Levulinic Acid Dehydratase Gene And Essential Tremor
Thr105ile (Rs11558538) Polymorphism In The Histamine-1-Methyl-Transferase (Hnmt) Gene And Risk For Restless Legs Syndrome
Delta-Amino-Levulinic Acid Dehydratase Gene And Essential Tremor
Thr105ile (Rs11558538) Polymorphism In The Histamine-1-Methyl-Transferase (Hnmt) Gene And Risk For Restless Legs Syndrome
Clinical Pharmacogenetics Implementation Consortium (Cpic) Guideline For Cyp2d6 Genotype And Use Of Ondansetron And Tropisetron
Thr105ile (Rs11558538) Polymorphism In The Histamine-1-Methyl-Transferase (Hnmt) Gene And Risk For Restless Legs Syndrome
Clinical Pharmacogenetics Implementation Consortium (Cpic) Guideline For Cyp2d6 Genotype And Use Of Ondansetron And Tropisetron
Clinical Pharmacogenetics Implementation Consortium (Cpic) Guidelines For Cyp2c19 And Voriconazole Therapy
Clinical Pharmacogenetics Implementation Consortium (Cpic) Guideline For Cyp2d6 Genotype And Use Of Ondansetron And Tropisetron
Clinical Pharmacogenetics Implementation Consortium (Cpic) Guidelines For Cyp2c19 And Voriconazole Therapy
Immediate Reactions To More Than 1 Nsaid Must Not Be Considered Cross-Hypersensitivity Unless Tolerance To Asa Is Verified
Clinical Pharmacogenetics Implementation Consortium (Cpic) Guidelines For Cyp2c19 And Voriconazole Therapy
Immediate Reactions To More Than 1 Nsaid Must Not Be Considered Cross-Hypersensitivity Unless Tolerance To Asa Is Verified
7th Drug Hypersensitivity Meeting: Part One
Immediate Reactions To More Than 1 Nsaid Must Not Be Considered Cross-Hypersensitivity Unless Tolerance To Asa Is Verified
7th Drug Hypersensitivity Meeting: Part One
An Update On The Role Of Nitric Oxide In The Neurodegenerative Processes Of Parkinson's Disease.
7th Drug Hypersensitivity Meeting: Part One
An Update On The Role Of Nitric Oxide In The Neurodegenerative Processes Of Parkinson's Disease.
Clinical Pharmacogenetics Implementation Consortium (Cpic®) Guideline For Cyp2c19 And Voriconazole Therapy.
An Update On The Role Of Nitric Oxide In The Neurodegenerative Processes Of Parkinson's Disease.
Clinical Pharmacogenetics Implementation Consortium (Cpic®) Guideline For Cyp2c19 And Voriconazole Therapy.
A Family Study Of Drd3 Rs6280, Slc1a2 Rs3794087 And Mapt Rs1052553 Variants In Essential Tremor
Clinical Pharmacogenetics Implementation Consortium (Cpic®) Guideline For Cyp2c19 And Voriconazole Therapy.
A Family Study Of Drd3 Rs6280, Slc1a2 Rs3794087 And Mapt Rs1052553 Variants In Essential Tremor
Fceri And Histamine Metabolism Gene Variability In Selective Responders To Nsaids
A Family Study Of Drd3 Rs6280, Slc1a2 Rs3794087 And Mapt Rs1052553 Variants In Essential Tremor
Fceri And Histamine Metabolism Gene Variability In Selective Responders To Nsaids
Pharmacogenomics Of Prostaglandin And Leukotriene Receptors
Fceri And Histamine Metabolism Gene Variability In Selective Responders To Nsaids
Pharmacogenomics Of Prostaglandin And Leukotriene Receptors
Detoxifying Enzymes At The Cross-Roads Of Inflammation, Oxidative Stress, And Drug Hypersensitivity: Role Of Glutathione Transferase P1-1 And Aldose Reductase
Pharmacogenomics Of Prostaglandin And Leukotriene Receptors
Detoxifying Enzymes At The Cross-Roads Of Inflammation, Oxidative Stress, And Drug Hypersensitivity: Role Of Glutathione Transferase P1-1 And Aldose Reductase
Nat2 Polymorphisms And Risk For Parkinson’s Disease: A Systematic Review And Meta-Analysis
Detoxifying Enzymes At The Cross-Roads Of Inflammation, Oxidative Stress, And Drug Hypersensitivity: Role Of Glutathione Transferase P1-1 And Aldose Reductase
Nat2 Polymorphisms And Risk For Parkinson’s Disease: A Systematic Review And Meta-Analysis
Asthma And Rhinitis Induced By Selective Immediate Reactions To Paracetamol And Non-Steroidal Anti-Inflammatory Drugs In Aspirin Tolerant Subjects
Nat2 Polymorphisms And Risk For Parkinson’s Disease: A Systematic Review And Meta-Analysis
Asthma And Rhinitis Induced By Selective Immediate Reactions To Paracetamol And Non-Steroidal Anti-Inflammatory Drugs In Aspirin Tolerant Subjects
An Update On The Role Of Nitric Oxide In The Neurodegenerative Processes Of Parkinson's Disease
Asthma And Rhinitis Induced By Selective Immediate Reactions To Paracetamol And Non-Steroidal Anti-Inflammatory Drugs In Aspirin Tolerant Subjects
An Update On The Role Of Nitric Oxide In The Neurodegenerative Processes Of Parkinson's Disease
Thr105ile (Rs11558538) Polymorphism In The Histamine N -Methyltransferase (Hnmt) Gene And Risk For Parkinson Disease
An Update On The Role Of Nitric Oxide In The Neurodegenerative Processes Of Parkinson's Disease
Thr105ile (Rs11558538) Polymorphism In The Histamine N -Methyltransferase (Hnmt) Gene And Risk For Parkinson Disease
Immediate Hypersensitivity Reactions To Ibuprofen And Other Arylpropionic Acid Derivatives
Thr105ile (Rs11558538) Polymorphism In The Histamine N -Methyltransferase (Hnmt) Gene And Risk For Parkinson Disease
Immediate Hypersensitivity Reactions To Ibuprofen And Other Arylpropionic Acid Derivatives
Allergic Reactions To Metamizole: Immediate And Delayed Responses
Immediate Hypersensitivity Reactions To Ibuprofen And Other Arylpropionic Acid Derivatives
Allergic Reactions To Metamizole: Immediate And Delayed Responses
Advances In Understanding Genomic Markers And Pharmacogenetics Of Parkinsons Disease
Allergic Reactions To Metamizole: Immediate And Delayed Responses
Advances In Understanding Genomic Markers And Pharmacogenetics Of Parkinsons Disease
Pyrazolones Metabolites Are Relevant For Identifying Selective Anaphylaxis To Metamizole
Advances In Understanding Genomic Markers And Pharmacogenetics Of Parkinsons Disease
Pyrazolones Metabolites Are Relevant For Identifying Selective Anaphylaxis To Metamizole
Gc Gene Polymorphism And Unbound Serum Retinol-Binding Protein 4 Are Related To The Risk Of Insulin Resistance In Patients With Chronic Hepatitis C: A Prospective Cross-Sectional Study
Pyrazolones Metabolites Are Relevant For Identifying Selective Anaphylaxis To Metamizole
Gc Gene Polymorphism And Unbound Serum Retinol-Binding Protein 4 Are Related To The Risk Of Insulin Resistance In Patients With Chronic Hepatitis C: A Prospective Cross-Sectional Study
Heme Oxygenase-1 And 2 Common Genetic Variants And Risk For Multiple Sclerosis
Gc Gene Polymorphism And Unbound Serum Retinol-Binding Protein 4 Are Related To The Risk Of Insulin Resistance In Patients With Chronic Hepatitis C: A Prospective Cross-Sectional Study
Heme Oxygenase-1 And 2 Common Genetic Variants And Risk For Multiple Sclerosis
A Nonsynonymous Fcer1b Snp Is Associated With Risk Of Developing Allergic Rhinitis And With Ige Levels
Heme Oxygenase-1 And 2 Common Genetic Variants And Risk For Multiple Sclerosis
A Nonsynonymous Fcer1b Snp Is Associated With Risk Of Developing Allergic Rhinitis And With Ige Levels
The Genetics Of Drug Hypersensitivity Reactions
A Nonsynonymous Fcer1b Snp Is Associated With Risk Of Developing Allergic Rhinitis And With Ige Levels
The Genetics Of Drug Hypersensitivity Reactions
Copy Number Variation In Alox5 And Ptger1 Is Associated With Nsaids-Induced Urticaria And/or Angioedema
The Genetics Of Drug Hypersensitivity Reactions
Copy Number Variation In Alox5 And Ptger1 Is Associated With Nsaids-Induced Urticaria And/or Angioedema
Molecular Interactions And Implications Of Aldose Reductase Inhibition By Pga1 And Clinically Used Prostaglandins
Copy Number Variation In Alox5 And Ptger1 Is Associated With Nsaids-Induced Urticaria And/or Angioedema
Molecular Interactions And Implications Of Aldose Reductase Inhibition By Pga1 And Clinically Used Prostaglandins
New Advances In The Study Of Ige Drug Recognition
Molecular Interactions And Implications Of Aldose Reductase Inhibition By Pga1 And Clinically Used Prostaglandins
New Advances In The Study Of Ige Drug Recognition
Pharmacogenetic Allele Nomenclature: International Workgroup Recommendations For Test Result Reporting
New Advances In The Study Of Ige Drug Recognition
Pharmacogenetic Allele Nomenclature: International Workgroup Recommendations For Test Result Reporting
Pharmacogenomics Testing For Type B Adverse Drug Reactions To Anti-Infective Drugs: The Example Of Hypersensitivity To Abacavir
Pharmacogenetic Allele Nomenclature: International Workgroup Recommendations For Test Result Reporting
Pharmacogenomics Testing For Type B Adverse Drug Reactions To Anti-Infective Drugs: The Example Of Hypersensitivity To Abacavir
Pharmacogenomics Testing For Type B Adverse Drug Reactions To Anti-Infective Drugs: The Example Of Hypersensitivity To Abacavir
Pharmacogenomics Testing For Type B Adverse Drug Reactions To Anti-Infective Drugs: The Example Of Hypersensitivity To Abacavir
Pharmacogenomics Testing For Type B Adverse Drug Reactions To Anti-Infective Drugs: The Example Of Hypersensitivity To Abacavir
Slc1a2 Rs3794087 Variant And Risk For Essential Tremor: A Systematic Review And Meta-Analysis
Pharmacogenomics Testing For Type B Adverse Drug Reactions To Anti-Infective Drugs: The Example Of Hypersensitivity To Abacavir
Slc1a2 Rs3794087 Variant And Risk For Essential Tremor: A Systematic Review And Meta-Analysis
Association Between Vitamin D Receptor Rs731236 (Taq1) Polymorphism And Risk For Restless Legs Syndrome In The Spanish Caucasian Population
Slc1a2 Rs3794087 Variant And Risk For Essential Tremor: A Systematic Review And Meta-Analysis
Association Between Vitamin D Receptor Rs731236 (Taq1) Polymorphism And Risk For Restless Legs Syndrome In The Spanish Caucasian Population
The Gstp1 Gene Variant Rs1695 Is Not Associated With An Increased Risk Of Multiple Sclerosis
Association Between Vitamin D Receptor Rs731236 (Taq1) Polymorphism And Risk For Restless Legs Syndrome In The Spanish Caucasian Population
The Gstp1 Gene Variant Rs1695 Is Not Associated With An Increased Risk Of Multiple Sclerosis
Neuronal Nitric Oxide Synthase (Nnos, Nos1) Rs693534 And Rs7977109 Variants And Risk For Migraine
The Gstp1 Gene Variant Rs1695 Is Not Associated With An Increased Risk Of Multiple Sclerosis
Neuronal Nitric Oxide Synthase (Nnos, Nos1) Rs693534 And Rs7977109 Variants And Risk For Migraine
Drug Metabolism And Hypersensitivity Reactions To Drugs
Neuronal Nitric Oxide Synthase (Nnos, Nos1) Rs693534 And Rs7977109 Variants And Risk For Migraine
Drug Metabolism And Hypersensitivity Reactions To Drugs
Genetic Determinants Of Metamizole Metabolism Modify The Risk Of Developing Anaphylaxis
Drug Metabolism And Hypersensitivity Reactions To Drugs
Genetic Determinants Of Metamizole Metabolism Modify The Risk Of Developing Anaphylaxis
Heme Oxygenase-1 And 2 Common Genetic Variants And Risk For Restless Legs Syndrome
Genetic Determinants Of Metamizole Metabolism Modify The Risk Of Developing Anaphylaxis
Heme Oxygenase-1 And 2 Common Genetic Variants And Risk For Restless Legs Syndrome
The Potential Of Lingo-1 As A Therapeutic Target For Essential Tremor
Heme Oxygenase-1 And 2 Common Genetic Variants And Risk For Restless Legs Syndrome
The Potential Of Lingo-1 As A Therapeutic Target For Essential Tremor
Missense Mutations In Tenm4, A Regulator Of Axon Guidance And Central Myelination, Cause Essential Tremor
The Potential Of Lingo-1 As A Therapeutic Target For Essential Tremor
Missense Mutations In Tenm4, A Regulator Of Axon Guidance And Central Myelination, Cause Essential Tremor
Heme Oxygenase 1 And 2 Common Genetic Variants And Risk For Essential Tremor
Missense Mutations In Tenm4, A Regulator Of Axon Guidance And Central Myelination, Cause Essential Tremor
Heme Oxygenase 1 And 2 Common Genetic Variants And Risk For Essential Tremor
Neuronal Nitric Oxide Synthase (Nnos, Nos1) Rs693534 And Rs7977109 Variants And Risk For Restless Legs Syndrome
Heme Oxygenase 1 And 2 Common Genetic Variants And Risk For Essential Tremor
Neuronal Nitric Oxide Synthase (Nnos, Nos1) Rs693534 And Rs7977109 Variants And Risk For Restless Legs Syndrome
Treatment Options For Idiopathic Restless Legs Syndrome
Neuronal Nitric Oxide Synthase (Nnos, Nos1) Rs693534 And Rs7977109 Variants And Risk For Restless Legs Syndrome
Treatment Options For Idiopathic Restless Legs Syndrome
Neurochemistry Of Idiopathic Restless Legs Syndrome
Treatment Options For Idiopathic Restless Legs Syndrome
Neurochemistry Of Idiopathic Restless Legs Syndrome
Pharmacogenomics Of Cyclooxygenases
Neurochemistry Of Idiopathic Restless Legs Syndrome
Pharmacogenomics Of Cyclooxygenases
Editorial On Cerebral Endothelial And Glial Cells Are More Than Bricks In The Great Wall Of The Brain: Insights Into The Way The Blood-Brain Barrier Actually Works (Celebrating The Centenary Of Goldman’s Experiments)
Pharmacogenomics Of Cyclooxygenases
Editorial On Cerebral Endothelial And Glial Cells Are More Than Bricks In The Great Wall Of The Brain: Insights Into The Way The Blood-Brain Barrier Actually Works (Celebrating The Centenary Of Goldman’s Experiments)
Trem2 R47h Variant And Risk Of Essential Tremor: A Cross-Sectional International Multicenter Study
Editorial On Cerebral Endothelial And Glial Cells Are More Than Bricks In The Great Wall Of The Brain: Insights Into The Way The Blood-Brain Barrier Actually Works (Celebrating The Centenary Of Goldman’s Experiments)
Trem2 R47h Variant And Risk Of Essential Tremor: A Cross-Sectional International Multicenter Study
Diamine Oxidase Rs10156191 And Rs2052129 Variants Are Associated With The Risk For Migraine
Trem2 R47h Variant And Risk Of Essential Tremor: A Cross-Sectional International Multicenter Study
Diamine Oxidase Rs10156191 And Rs2052129 Variants Are Associated With The Risk For Migraine
Evaluation Of Immediate Allergic Reactions To Dipyrone Using Dipyrone Metabolites In Basophil Activation Test.
Diamine Oxidase Rs10156191 And Rs2052129 Variants Are Associated With The Risk For Migraine
Evaluation Of Immediate Allergic Reactions To Dipyrone Using Dipyrone Metabolites In Basophil Activation Test.
Gene Variants And Haplotypes Modifying Transcription Factor Binding Sites In The Human Cyclooxygenase 1 And 2 (Ptgs1 And Ptgs2) Genes
Evaluation Of Immediate Allergic Reactions To Dipyrone Using Dipyrone Metabolites In Basophil Activation Test.
Gene Variants And Haplotypes Modifying Transcription Factor Binding Sites In The Human Cyclooxygenase 1 And 2 (Ptgs1 And Ptgs2) Genes
Gender And Functional Cyp2c And Nat2 Polymorphisms Determine The Metabolic Profile Of Metamizole
Gene Variants And Haplotypes Modifying Transcription Factor Binding Sites In The Human Cyclooxygenase 1 And 2 (Ptgs1 And Ptgs2) Genes
Gender And Functional Cyp2c And Nat2 Polymorphisms Determine The Metabolic Profile Of Metamizole
Cerebrospinal Fluid Biochemical Studies In Patients With Parkinson's Disease: Toward A Potential Search For Biomarkers For This Disease
Gender And Functional Cyp2c And Nat2 Polymorphisms Determine The Metabolic Profile Of Metamizole
Cerebrospinal Fluid Biochemical Studies In Patients With Parkinson's Disease: Toward A Potential Search For Biomarkers For This Disease
Drug And Xenobiotic Biotransformation In The Blood–brain Barrier: A Neglected Issue
Cerebrospinal Fluid Biochemical Studies In Patients With Parkinson's Disease: Toward A Potential Search For Biomarkers For This Disease
Drug And Xenobiotic Biotransformation In The Blood–brain Barrier: A Neglected Issue
Nqo1 Gene Rs1800566 Variant Is Not Associated With Risk For Multiple Sclerosis
Drug And Xenobiotic Biotransformation In The Blood–brain Barrier: A Neglected Issue
Nqo1 Gene Rs1800566 Variant Is Not Associated With Risk For Multiple Sclerosis
Slc1a2 Rs3794087 Variant And Risk For Migraine
Nqo1 Gene Rs1800566 Variant Is Not Associated With Risk For Multiple Sclerosis
Slc1a2 Rs3794087 Variant And Risk For Migraine
Variants Of Cep68 Gene Are Associated With Acute Urticaria/angioedema Induced By Multiple Non-Steroidal Anti-Inflammatory Drugs
Slc1a2 Rs3794087 Variant And Risk For Migraine
Variants Of Cep68 Gene Are Associated With Acute Urticaria/angioedema Induced By Multiple Non-Steroidal Anti-Inflammatory Drugs
Pitx3 And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis
Variants Of Cep68 Gene Are Associated With Acute Urticaria/angioedema Induced By Multiple Non-Steroidal Anti-Inflammatory Drugs
Pitx3 And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis
Importance Of Cyp2d6 Genotype/activity Testing And Applications
Pitx3 And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis
Importance Of Cyp2d6 Genotype/activity Testing And Applications
The Solute Carrier Family 1 (Glial High Affinity Glutamate Transporter), Member 2 Gene, Slc1a2, Rs3794087 Variant And Assessment Risk For Restless Legs Syndrome
Importance Of Cyp2d6 Genotype/activity Testing And Applications
The Solute Carrier Family 1 (Glial High Affinity Glutamate Transporter), Member 2 Gene, Slc1a2, Rs3794087 Variant And Assessment Risk For Restless Legs Syndrome
An Association Study Between Heme Oxygenase-1 Genetic Variants And Parkinson’s Disease
The Solute Carrier Family 1 (Glial High Affinity Glutamate Transporter), Member 2 Gene, Slc1a2, Rs3794087 Variant And Assessment Risk For Restless Legs Syndrome
An Association Study Between Heme Oxygenase-1 Genetic Variants And Parkinson’s Disease
Clinical Practice Guidelines For Translating Pharmacogenomic Knowledge To Bedside. Focus On Anticancer Drugs
An Association Study Between Heme Oxygenase-1 Genetic Variants And Parkinson’s Disease
Clinical Practice Guidelines For Translating Pharmacogenomic Knowledge To Bedside. Focus On Anticancer Drugs
Comt Gene And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis
Clinical Practice Guidelines For Translating Pharmacogenomic Knowledge To Bedside. Focus On Anticancer Drugs
Comt Gene And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis
Perception Of The Usefulness Of Drug/gene Pairs And Barriers For Pharmacogenomics In Latin America
Comt Gene And Risk For Parkinson's Disease: A Systematic Review And Meta-Analysis
Perception Of The Usefulness Of Drug/gene Pairs And Barriers For Pharmacogenomics In Latin America
Genomic And Pharmacogenomic Biomarkers Of Parkinson's Disease
Perception Of The Usefulness Of Drug/gene Pairs And Barriers For Pharmacogenomics In Latin America
Genomic And Pharmacogenomic Biomarkers Of Parkinson's Disease
Interview: Perspective On The Use Of Genomic Biomarkers In The Clinical Setting
Genomic And Pharmacogenomic Biomarkers Of Parkinson's Disease
Interview: Perspective On The Use Of Genomic Biomarkers In The Clinical Setting
Clinical Use Of Biomarkers In Drug Metabolism And Adverse Drug Reactions
Interview: Perspective On The Use Of Genomic Biomarkers In The Clinical Setting
Clinical Use Of Biomarkers In Drug Metabolism And Adverse Drug Reactions
Incorporation Of Pharmacogenomics Into Routine Clinical Practice: The Clinical Pharmacogenetics Implementation Consortium (Cpic) Guideline Development Process
Clinical Use Of Biomarkers In Drug Metabolism And Adverse Drug Reactions
Incorporation Of Pharmacogenomics Into Routine Clinical Practice: The Clinical Pharmacogenetics Implementation Consortium (Cpic) Guideline Development Process
Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia.
Incorporation Of Pharmacogenomics Into Routine Clinical Practice: The Clinical Pharmacogenetics Implementation Consortium (Cpic) Guideline Development Process
Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia.
Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia
Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia.
Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia
Fus: A Putative Biomarker For Essential Tremor Raised By Whole-Exome Sequencing Analyses.
Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia
Fus: A Putative Biomarker For Essential Tremor Raised By Whole-Exome Sequencing Analyses.
Genetic Biomarkers Of Essential Tremor: Time To Think Outside Of The Box.
Fus: A Putative Biomarker For Essential Tremor Raised By Whole-Exome Sequencing Analyses.
Genetic Biomarkers Of Essential Tremor: Time To Think Outside Of The Box.
Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia
Genetic Biomarkers Of Essential Tremor: Time To Think Outside Of The Box.
Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia
Metabolic Considerations Of Drugs In The Treatment Of Allergic Diseases
Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia
Metabolic Considerations Of Drugs In The Treatment Of Allergic Diseases
Influence Of Vitamin D-Related Gene Polymorphisms (Cyp27b And Vdr) On The Response To Interferon/ribavirin Therapy In Chronic Hepatitis C
Metabolic Considerations Of Drugs In The Treatment Of Allergic Diseases
Influence Of Vitamin D-Related Gene Polymorphisms (Cyp27b And Vdr) On The Response To Interferon/ribavirin Therapy In Chronic Hepatitis C
Anti-Parkinson's Disease Drugs And Pharmacogenetic Considerations
Influence Of Vitamin D-Related Gene Polymorphisms (Cyp27b And Vdr) On The Response To Interferon/ribavirin Therapy In Chronic Hepatitis C
Anti-Parkinson's Disease Drugs And Pharmacogenetic Considerations
Vitamin D3 Receptor (Vdr) Gene Rs2228570 (Fok1) And Rs731236 (Taq1) Variants Are Not Associated With The Risk For Multiple Sclerosis: Results Of A New Study And A Meta-Analysis
Anti-Parkinson's Disease Drugs And Pharmacogenetic Considerations
Vitamin D3 Receptor (Vdr) Gene Rs2228570 (Fok1) And Rs731236 (Taq1) Variants Are Not Associated With The Risk For Multiple Sclerosis: Results Of A New Study And A Meta-Analysis
Lingo1 Rs9652490 And Rs11856808 Polymorphisms Are Not Associated With Risk For Multiple Sclerosis
Vitamin D3 Receptor (Vdr) Gene Rs2228570 (Fok1) And Rs731236 (Taq1) Variants Are Not Associated With The Risk For Multiple Sclerosis: Results Of A New Study And A Meta-Analysis
Lingo1 Rs9652490 And Rs11856808 Polymorphisms Are Not Associated With Risk For Multiple Sclerosis
Dopamine Receptor D3 (Drd3) Gene Rs6280 Variant And Risk For Restless Legs Syndrome
Lingo1 Rs9652490 And Rs11856808 Polymorphisms Are Not Associated With Risk For Multiple Sclerosis
Dopamine Receptor D3 (Drd3) Gene Rs6280 Variant And Risk For Restless Legs Syndrome
Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia
Dopamine Receptor D3 (Drd3) Gene Rs6280 Variant And Risk For Restless Legs Syndrome
Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia
Genome-Wide Association Study Raised Biomarker Slc1a2 Rs3794087 And Essential Tremor: Is It Too Early To Say?
Hereditary Coproporphyria Associated With The Q306x Mutation In The Coproporphyrin Oxidase Gene Presenting With Acute Ataxia
Genome-Wide Association Study Raised Biomarker Slc1a2 Rs3794087 And Essential Tremor: Is It Too Early To Say?
Latest Perspectives In Genetic Risk Factors For Restless Legs Syndrome
Genome-Wide Association Study Raised Biomarker Slc1a2 Rs3794087 And Essential Tremor: Is It Too Early To Say?
Latest Perspectives In Genetic Risk Factors For Restless Legs Syndrome
No Association Of The Slc1a2 Rs3794087 Allele With Risk For Essential Tremor In The Spanish Population
Latest Perspectives In Genetic Risk Factors For Restless Legs Syndrome
No Association Of The Slc1a2 Rs3794087 Allele With Risk For Essential Tremor In The Spanish Population
Clarifying Haplotype Ambiguity Of Nat2 In Multi-National Cohorts
No Association Of The Slc1a2 Rs3794087 Allele With Risk For Essential Tremor In The Spanish Population
Clarifying Haplotype Ambiguity Of Nat2 In Multi-National Cohorts
Fused In Sarcoma (Fus) Gene Mutations Are Not A Frequent Cause Of Essential Tremor In Europeans
Clarifying Haplotype Ambiguity Of Nat2 In Multi-National Cohorts
Fused In Sarcoma (Fus) Gene Mutations Are Not A Frequent Cause Of Essential Tremor In Europeans
Mapt1 Gene Rs1052553 Variant Is Unrelated With The Risk For Restless Legs Syndrome
Fused In Sarcoma (Fus) Gene Mutations Are Not A Frequent Cause Of Essential Tremor In Europeans
Mapt1 Gene Rs1052553 Variant Is Unrelated With The Risk For Restless Legs Syndrome
Update On Genetics Of Essential Tremor
Mapt1 Gene Rs1052553 Variant Is Unrelated With The Risk For Restless Legs Syndrome
Update On Genetics Of Essential Tremor
Mapt Gene Rs1052553 Variant Is Not Associated With The Risk For Multiple Sclerosis
Update On Genetics Of Essential Tremor
Mapt Gene Rs1052553 Variant Is Not Associated With The Risk For Multiple Sclerosis
Variability In Histamine Receptor Genes Hrh1, Hrh2 And Hrh4 In Patients With Hypersensitivity To Nsaids
Mapt Gene Rs1052553 Variant Is Not Associated With The Risk For Multiple Sclerosis
Variability In Histamine Receptor Genes Hrh1, Hrh2 And Hrh4 In Patients With Hypersensitivity To Nsaids
Functional Polymorphisms Of Xenobiotics Metabolizing Enzymes-A Research Topic
Variability In Histamine Receptor Genes Hrh1, Hrh2 And Hrh4 In Patients With Hypersensitivity To Nsaids
Functional Polymorphisms Of Xenobiotics Metabolizing Enzymes-A Research Topic
High-Resolution Melting Analysis Of The Common C.1905+1g>a Mutation Causing Dihydropyrimidine Dehydrogenase Deficiency And Lethal 5-Fluorouracil Toxicity
Functional Polymorphisms Of Xenobiotics Metabolizing Enzymes-A Research Topic
High-Resolution Melting Analysis Of The Common C.1905+1g>a Mutation Causing Dihydropyrimidine Dehydrogenase Deficiency And Lethal 5-Fluorouracil Toxicity
Modulation Of Gstp1-1 Oligomerization By Electrophilic Inflammatory Mediators And Reactive Drugs.
High-Resolution Melting Analysis Of The Common C.1905+1g>a Mutation Causing Dihydropyrimidine Dehydrogenase Deficiency And Lethal 5-Fluorouracil Toxicity
Modulation Of Gstp1-1 Oligomerization By Electrophilic Inflammatory Mediators And Reactive Drugs.
Vitamin D Deficiency And Vitamin D Therapy In Chronic Hepatitis C
Modulation Of Gstp1-1 Oligomerization By Electrophilic Inflammatory Mediators And Reactive Drugs.
Vitamin D Deficiency And Vitamin D Therapy In Chronic Hepatitis C
Toward A Clinical Practice Guide In Pharmacogenomics Testing For Functional Polymorphisms Of Drug-Metabolizing Enzymes. Gene/drug Pairs And Barriers Perceived In Spain
Vitamin D Deficiency And Vitamin D Therapy In Chronic Hepatitis C
Toward A Clinical Practice Guide In Pharmacogenomics Testing For Functional Polymorphisms Of Drug-Metabolizing Enzymes. Gene/drug Pairs And Barriers Perceived In Spain
The Relationship Between Parkinson's Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor
Toward A Clinical Practice Guide In Pharmacogenomics Testing For Functional Polymorphisms Of Drug-Metabolizing Enzymes. Gene/drug Pairs And Barriers Perceived In Spain
The Relationship Between Parkinson's Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor
Frequencies Of 23 Functionally Significant Variant Alleles Related With Metabolism Of Antineoplastic Drugs In The Chilean Population: Comparison With Caucasian And Asian Populations
The Relationship Between Parkinson's Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor
Frequencies Of 23 Functionally Significant Variant Alleles Related With Metabolism Of Antineoplastic Drugs In The Chilean Population: Comparison With Caucasian And Asian Populations
Analysis Of The Functional Polymorphism In The Cytochrome P450 Cyp2c8 Gene Rs11572080 With Regard To Colorectal Cancer Risk
Frequencies Of 23 Functionally Significant Variant Alleles Related With Metabolism Of Antineoplastic Drugs In The Chilean Population: Comparison With Caucasian And Asian Populations
Analysis Of The Functional Polymorphism In The Cytochrome P450 Cyp2c8 Gene Rs11572080 With Regard To Colorectal Cancer Risk
Genetic Variants Of The Arachidonic Acid Pathway In Non-Steroidal Anti-Inflammatory Drug-Induced Acute Urticaria
Analysis Of The Functional Polymorphism In The Cytochrome P450 Cyp2c8 Gene Rs11572080 With Regard To Colorectal Cancer Risk
Genetic Variants Of The Arachidonic Acid Pathway In Non-Steroidal Anti-Inflammatory Drug-Induced Acute Urticaria
The Diamine Oxidase Gene Is Associated With Hypersensitivity Response To Non-Steroidal Anti-Inflammatory Drugs
Genetic Variants Of The Arachidonic Acid Pathway In Non-Steroidal Anti-Inflammatory Drug-Induced Acute Urticaria
The Diamine Oxidase Gene Is Associated With Hypersensitivity Response To Non-Steroidal Anti-Inflammatory Drugs
Trends In Qualifying Biomarkers In Drug Safety. Consensus Of The 2011 Meeting Of The Spanish Society Of Clinical Pharmacology
The Diamine Oxidase Gene Is Associated With Hypersensitivity Response To Non-Steroidal Anti-Inflammatory Drugs
Trends In Qualifying Biomarkers In Drug Safety. Consensus Of The 2011 Meeting Of The Spanish Society Of Clinical Pharmacology
The Differential Effect Of Nat2 Variant Alleles Permits Refinement In Phenotype Inference And Identifies A Very Slow Acetylation Genotype
Trends In Qualifying Biomarkers In Drug Safety. Consensus Of The 2011 Meeting Of The Spanish Society Of Clinical Pharmacology
The Differential Effect Of Nat2 Variant Alleles Permits Refinement In Phenotype Inference And Identifies A Very Slow Acetylation Genotype
H1-Mapt And The Risk For Familial Essential Tremor
The Differential Effect Of Nat2 Variant Alleles Permits Refinement In Phenotype Inference And Identifies A Very Slow Acetylation Genotype
H1-Mapt And The Risk For Familial Essential Tremor
Lingo1 And Risk For Essential Tremor: Results Of A Meta-Analysis Of Rs9652490 And Rs11856808
H1-Mapt And The Risk For Familial Essential Tremor
Lingo1 And Risk For Essential Tremor: Results Of A Meta-Analysis Of Rs9652490 And Rs11856808
Lingo1 Rs9652490 And Rs11856808 Are Not Associated With The Risk Of Parkinson's Disease: Results Of A Meta-Analysis
Lingo1 And Risk For Essential Tremor: Results Of A Meta-Analysis Of Rs9652490 And Rs11856808
Lingo1 Rs9652490 And Rs11856808 Are Not Associated With The Risk Of Parkinson's Disease: Results Of A Meta-Analysis
Relation Of Il28b Gene Polymorphism With Biochemical And Histological Features In Hepatitis C Virus-Induced Liver Disease
Lingo1 Rs9652490 And Rs11856808 Are Not Associated With The Risk Of Parkinson's Disease: Results Of A Meta-Analysis
Relation Of Il28b Gene Polymorphism With Biochemical And Histological Features In Hepatitis C Virus-Induced Liver Disease
Polymorphism Of The Tlr4 Gene Reduces The Risk Of Hepatitis C Virus-Induced Hepatocellular Carcinoma
Relation Of Il28b Gene Polymorphism With Biochemical And Histological Features In Hepatitis C Virus-Induced Liver Disease
Polymorphism Of The Tlr4 Gene Reduces The Risk Of Hepatitis C Virus-Induced Hepatocellular Carcinoma
The Relationship Between Parkinson’s Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor
Polymorphism Of The Tlr4 Gene Reduces The Risk Of Hepatitis C Virus-Induced Hepatocellular Carcinoma
The Relationship Between Parkinson’s Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor
Predicting Response To Therapy In Chronic Hepatitis C: An Approach Combining Interleukin-28b Gene Polymorphisms And Clinical Data
The Relationship Between Parkinson’s Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor
Predicting Response To Therapy In Chronic Hepatitis C: An Approach Combining Interleukin-28b Gene Polymorphisms And Clinical Data
Arylamine N-Acetyltransferase 2 Genotypes In A Mexican Population
Predicting Response To Therapy In Chronic Hepatitis C: An Approach Combining Interleukin-28b Gene Polymorphisms And Clinical Data
Arylamine N-Acetyltransferase 2 Genotypes In A Mexican Population
The Relationship Between Parkinson's Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor.
Arylamine N-Acetyltransferase 2 Genotypes In A Mexican Population
The Relationship Between Parkinson's Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor.
Detection Of Genomic Variations In Brca1 And Brca2 Genes By Long-Range Pcr And Next-Generation Sequencing
The Relationship Between Parkinson's Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, And Data On The Presence Of Cardinal Signs Of Parkinsonism In Essential Tremor.
Detection Of Genomic Variations In Brca1 And Brca2 Genes By Long-Range Pcr And Next-Generation Sequencing
The Relationship Between Parkinson’s Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, . . .
Detection Of Genomic Variations In Brca1 And Brca2 Genes By Long-Range Pcr And Next-Generation Sequencing
The Relationship Between Parkinson’s Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, . . .
Lack Of Association Of Lingo1 Rs9652490 And Rs11856808 Snps With Familial Essential Tremor
The Relationship Between Parkinson’s Disease And Essential Tremor: Review Of Clinical, Epidemiologic, Genetic, Neuroimaging And Neuropathological Data, . . .
Lack Of Association Of Lingo1 Rs9652490 And Rs11856808 Snps With Familial Essential Tremor
Assessment Of Nonsteroidal Anti-Inflammatory Drug-Induced Hepatotoxicity
Lack Of Association Of Lingo1 Rs9652490 And Rs11856808 Snps With Familial Essential Tremor
Assessment Of Nonsteroidal Anti-Inflammatory Drug-Induced Hepatotoxicity
Influence Of Age And Gender In Motor Performance In Healthy Subjects
Assessment Of Nonsteroidal Anti-Inflammatory Drug-Induced Hepatotoxicity
Influence Of Age And Gender In Motor Performance In Healthy Subjects
Lingo1 Gene Analysis In Parkinson's Disease Phenotypes
Influence Of Age And Gender In Motor Performance In Healthy Subjects
Lingo1 Gene Analysis In Parkinson's Disease Phenotypes
Cytochrome P450 Cyp2b6 Genotypes And Haplotypes In A Colombian Population: Identification Of Novel Variant Cyp2b6 Alleles
Lingo1 Gene Analysis In Parkinson's Disease Phenotypes
Cytochrome P450 Cyp2b6 Genotypes And Haplotypes In A Colombian Population: Identification Of Novel Variant Cyp2b6 Alleles
A Polymorphism Located At An Atg Transcription Start Site Of The Heme Oxygenase-2 Gene Is Associated With Classical Parkinson's Disease
Cytochrome P450 Cyp2b6 Genotypes And Haplotypes In A Colombian Population: Identification Of Novel Variant Cyp2b6 Alleles
A Polymorphism Located At An Atg Transcription Start Site Of The Heme Oxygenase-2 Gene Is Associated With Classical Parkinson's Disease
Gamma-Aminobutyric Acid Gabra4, Gabre, And Gabrq Receptor Polymorphisms And Risk For Essential Tremor
A Polymorphism Located At An Atg Transcription Start Site Of The Heme Oxygenase-2 Gene Is Associated With Classical Parkinson's Disease
Gamma-Aminobutyric Acid Gabra4, Gabre, And Gabrq Receptor Polymorphisms And Risk For Essential Tremor
Gamma-Aminobutyric Acid (Gaba) Receptor Rho (Gabrr) Polymorphisms And Risk For Essential Tremor
Gamma-Aminobutyric Acid Gabra4, Gabre, And Gabrq Receptor Polymorphisms And Risk For Essential Tremor
Gamma-Aminobutyric Acid (Gaba) Receptor Rho (Gabrr) Polymorphisms And Risk For Essential Tremor
N-Acetyltransferase 2 Polymorphisms And Risk Of Anti-Tuberculosis Drug-Induced Hepatotoxicity In Caucasians
Gamma-Aminobutyric Acid (Gaba) Receptor Rho (Gabrr) Polymorphisms And Risk For Essential Tremor
N-Acetyltransferase 2 Polymorphisms And Risk Of Anti-Tuberculosis Drug-Induced Hepatotoxicity In Caucasians
Clinical Pharmacogenomic Testing Of Kras, Braf And Egfr Mutations By High Resolution Melting Analysis And Ultra-Deep Pyrosequencing
N-Acetyltransferase 2 Polymorphisms And Risk Of Anti-Tuberculosis Drug-Induced Hepatotoxicity In Caucasians
Clinical Pharmacogenomic Testing Of Kras, Braf And Egfr Mutations By High Resolution Melting Analysis And Ultra-Deep Pyrosequencing
Acetylator Status And N-Acetyltransferase 2 Gene Polymorphisms; Phenotype-Genotype Correlation With The Sulfamethazine Test
Clinical Pharmacogenomic Testing Of Kras, Braf And Egfr Mutations By High Resolution Melting Analysis And Ultra-Deep Pyrosequencing
Acetylator Status And N-Acetyltransferase 2 Gene Polymorphisms; Phenotype-Genotype Correlation With The Sulfamethazine Test
Characteristics Of Subjects Experiencing Hypersensitivity To Non-Steroidal Anti-Inflammatory Drugs: Patterns Of Response
Acetylator Status And N-Acetyltransferase 2 Gene Polymorphisms; Phenotype-Genotype Correlation With The Sulfamethazine Test
Characteristics Of Subjects Experiencing Hypersensitivity To Non-Steroidal Anti-Inflammatory Drugs: Patterns Of Response
Variability Of The L-Histidine Decarboxylase Gene In Allergic Rhinitis
Characteristics Of Subjects Experiencing Hypersensitivity To Non-Steroidal Anti-Inflammatory Drugs: Patterns Of Response
Variability Of The L-Histidine Decarboxylase Gene In Allergic Rhinitis
Cyp2w1 Variant Alleles In Caucasians And Association Of The Cyp2w1 G541a (Ala181thr) Polymorphism With Increased Colorectal Cancer Risk
Variability Of The L-Histidine Decarboxylase Gene In Allergic Rhinitis
Cyp2w1 Variant Alleles In Caucasians And Association Of The Cyp2w1 G541a (Ala181thr) Polymorphism With Increased Colorectal Cancer Risk
Polimorfismos Genéticos Y Su Influencia En La Efectividad Del Tratamiento Quimioterapéutico De Pacientes Leucémicos
Cyp2w1 Variant Alleles In Caucasians And Association Of The Cyp2w1 G541a (Ala181thr) Polymorphism With Increased Colorectal Cancer Risk
Polimorfismos Genéticos Y Su Influencia En La Efectividad Del Tratamiento Quimioterapéutico De Pacientes Leucémicos
Paraoxonase 1 Polymorphisms Are Not Related With The Risk For Multiple Sclerosis
Polimorfismos Genéticos Y Su Influencia En La Efectividad Del Tratamiento Quimioterapéutico De Pacientes Leucémicos
Paraoxonase 1 Polymorphisms Are Not Related With The Risk For Multiple Sclerosis
Paraoxonase 1 (Pon1) Polymorphisms And Risk For Migraine
Paraoxonase 1 Polymorphisms Are Not Related With The Risk For Multiple Sclerosis
Paraoxonase 1 (Pon1) Polymorphisms And Risk For Migraine
Dopamine Receptor 3(Drd3) Polymorphism And Risk For Migraine
Paraoxonase 1 (Pon1) Polymorphisms And Risk For Migraine
Dopamine Receptor 3(Drd3) Polymorphism And Risk For Migraine
Two Common Nonsynonymous Paraoxonase 1 (Pon1) Gene Polymorphisms And Brain Astrocytoma And Meningioma
Dopamine Receptor 3(Drd3) Polymorphism And Risk For Migraine
Two Common Nonsynonymous Paraoxonase 1 (Pon1) Gene Polymorphisms And Brain Astrocytoma And Meningioma
Mitochondrial Superoxide Dismutase And Glutathione Peroxidase In Idiosyncratic Drug-Induced Liver Injury
Two Common Nonsynonymous Paraoxonase 1 (Pon1) Gene Polymorphisms And Brain Astrocytoma And Meningioma
Mitochondrial Superoxide Dismutase And Glutathione Peroxidase In Idiosyncratic Drug-Induced Liver Injury
Variability In Ethanol Biodisposition In Whites Is Modulated By Polymorphisms In The Adh1b And Adh1c Genes
Mitochondrial Superoxide Dismutase And Glutathione Peroxidase In Idiosyncratic Drug-Induced Liver Injury
Variability In Ethanol Biodisposition In Whites Is Modulated By Polymorphisms In The Adh1b And Adh1c Genes
Histamine-N-Methyl Transferase Polymorphism And Risk For Multiple Sclerosis
Variability In Ethanol Biodisposition In Whites Is Modulated By Polymorphisms In The Adh1b And Adh1c Genes
Histamine-N-Methyl Transferase Polymorphism And Risk For Multiple Sclerosis
Paraoxonase 1 (Pon1) Polymorphisms And Risk For Essential Tremor
Histamine-N-Methyl Transferase Polymorphism And Risk For Multiple Sclerosis
Paraoxonase 1 (Pon1) Polymorphisms And Risk For Essential Tremor
Alcohol Dehydrogenase 2 Genotype And Risk For Migraine
Paraoxonase 1 (Pon1) Polymorphisms And Risk For Essential Tremor
Alcohol Dehydrogenase 2 Genotype And Risk For Migraine
Oxidative Stress In Skin Fibroblasts Cultures From Patients With Parkinson's Disease
Alcohol Dehydrogenase 2 Genotype And Risk For Migraine
Oxidative Stress In Skin Fibroblasts Cultures From Patients With Parkinson's Disease
Loss-Of-Function Mutations In Hpse2 Cause The Autosomal Recessive Urofacial Syndrome
Oxidative Stress In Skin Fibroblasts Cultures From Patients With Parkinson's Disease
Loss-Of-Function Mutations In Hpse2 Cause The Autosomal Recessive Urofacial Syndrome
Erratum: Loss-Of-Function Mutations In Hpse2 Cause The Autosomal Recessive Urofacial Syndrome (The American Journal Of Human Genetics (2010) 86 (957-962))
Loss-Of-Function Mutations In Hpse2 Cause The Autosomal Recessive Urofacial Syndrome
Erratum: Loss-Of-Function Mutations In Hpse2 Cause The Autosomal Recessive Urofacial Syndrome (The American Journal Of Human Genetics (2010) 86 (957-962))
Impairment Of Rapid Repetitive Finger Movements And Visual Reaction Time In Patients With Essential Tremor
Erratum: Loss-Of-Function Mutations In Hpse2 Cause The Autosomal Recessive Urofacial Syndrome (The American Journal Of Human Genetics (2010) 86 (957-962))
Impairment Of Rapid Repetitive Finger Movements And Visual Reaction Time In Patients With Essential Tremor
Assessment Of Cumulative Evidence For The Association Between Glutathione S-Transferase Polymorphisms And Lung Cancer: Application Of The Venice Interim Guidelines.
Impairment Of Rapid Repetitive Finger Movements And Visual Reaction Time In Patients With Essential Tremor
Assessment Of Cumulative Evidence For The Association Between Glutathione S-Transferase Polymorphisms And Lung Cancer: Application Of The Venice Interim Guidelines.
Analysis Of A Non-Synonymous Single Nucleotide Polymorphism Of The Human Diamine Oxidase Gene (Ref. Snp Id: Rs1049793) In Patients With Crohn's Disease
Assessment Of Cumulative Evidence For The Association Between Glutathione S-Transferase Polymorphisms And Lung Cancer: Application Of The Venice Interim Guidelines.
Analysis Of A Non-Synonymous Single Nucleotide Polymorphism Of The Human Diamine Oxidase Gene (Ref. Snp Id: Rs1049793) In Patients With Crohn's Disease
Pharmacogenomics In Drug Induced Liver Injury
Analysis Of A Non-Synonymous Single Nucleotide Polymorphism Of The Human Diamine Oxidase Gene (Ref. Snp Id: Rs1049793) In Patients With Crohn's Disease
Pharmacogenomics In Drug Induced Liver Injury
Pharmacogenomics In Aspirin Intolerance
Pharmacogenomics In Drug Induced Liver Injury
Pharmacogenomics In Aspirin Intolerance
Dopamine Receptor D3 (Drd3) Genotype And Allelic Variants And Risk For Essential Tremor
Pharmacogenomics In Aspirin Intolerance
Dopamine Receptor D3 (Drd3) Genotype And Allelic Variants And Risk For Essential Tremor
Histamine Pharmacogenomics
Dopamine Receptor D3 (Drd3) Genotype And Allelic Variants And Risk For Essential Tremor
Histamine Pharmacogenomics
Genetically Based Impairment In Cyp2c8- And Cyp2c9-Dependent Nsaid Metabolism As A Risk Factor For Gastrointestinal Bleeding: Is A Combination Of Pharmacogenomics And Metabolomics Required To Improve Personalized Medicine?
Histamine Pharmacogenomics
Genetically Based Impairment In Cyp2c8- And Cyp2c9-Dependent Nsaid Metabolism As A Risk Factor For Gastrointestinal Bleeding: Is A Combination Of Pharmacogenomics And Metabolomics Required To Improve Personalized Medicine?
Polymorphic Drug Metabolism In Anaesthesia
Genetically Based Impairment In Cyp2c8- And Cyp2c9-Dependent Nsaid Metabolism As A Risk Factor For Gastrointestinal Bleeding: Is A Combination Of Pharmacogenomics And Metabolomics Required To Improve Personalized Medicine?
Polymorphic Drug Metabolism In Anaesthesia
Reply
Polymorphic Drug Metabolism In Anaesthesia
Reply
Current Drug Metabolism: Editorial
Reply
Current Drug Metabolism: Editorial
Hypersensitivity Reactions To Non-Steroidal Anti-Inflammatory Drugs
Current Drug Metabolism: Editorial
Hypersensitivity Reactions To Non-Steroidal Anti-Inflammatory Drugs
Motor Performance In Patients With Restless Legs Syndrome
Hypersensitivity Reactions To Non-Steroidal Anti-Inflammatory Drugs
Motor Performance In Patients With Restless Legs Syndrome
Recent Advances In Drug Intolerance.
Motor Performance In Patients With Restless Legs Syndrome
Recent Advances In Drug Intolerance.
The Nonsynonymous Thr105ile Polymorphism Of The Histamine N-Methyltransferase Is Associated To The Risk Of Developing Essential Tremor
Recent Advances In Drug Intolerance.
The Nonsynonymous Thr105ile Polymorphism Of The Histamine N-Methyltransferase Is Associated To The Risk Of Developing Essential Tremor
Response To The Letter To The Editor Regarding Improved Analytical Sensitivity Reveals The Occurrence Of Gender-Related Variability In Diamine Oxidase Enzyme Activity In Healthy Individuals
The Nonsynonymous Thr105ile Polymorphism Of The Histamine N-Methyltransferase Is Associated To The Risk Of Developing Essential Tremor
Response To The Letter To The Editor Regarding Improved Analytical Sensitivity Reveals The Occurrence Of Gender-Related Variability In Diamine Oxidase Enzyme Activity In Healthy Individuals
Histamine-N-Methyl Transferase Polymorphism And Risk For Migraine: Research Submission
Response To The Letter To The Editor Regarding Improved Analytical Sensitivity Reveals The Occurrence Of Gender-Related Variability In Diamine Oxidase Enzyme Activity In Healthy Individuals
Histamine-N-Methyl Transferase Polymorphism And Risk For Migraine: Research Submission
Glutathione S-Transferase M1 And T1 Null Genotypes Increase Susceptibility To Idiosyncratic Drug-Induced Liver Injury
Histamine-N-Methyl Transferase Polymorphism And Risk For Migraine: Research Submission
Glutathione S-Transferase M1 And T1 Null Genotypes Increase Susceptibility To Idiosyncratic Drug-Induced Liver Injury
Unraveling Ambiguous Nat2 Genotyping Data
Glutathione S-Transferase M1 And T1 Null Genotypes Increase Susceptibility To Idiosyncratic Drug-Induced Liver Injury
Unraveling Ambiguous Nat2 Genotyping Data
Genetic Variability Of Histamine Receptors In Patients With Parkinson's Disease
Unraveling Ambiguous Nat2 Genotyping Data
Genetic Variability Of Histamine Receptors In Patients With Parkinson's Disease
Nonsynonymous Polymorphisms Of Histamine-Metabolising Enzymes In Patients With Parkinson's Disease
Genetic Variability Of Histamine Receptors In Patients With Parkinson's Disease
Nonsynonymous Polymorphisms Of Histamine-Metabolising Enzymes In Patients With Parkinson's Disease
Glutathione-S-Transferase P1 Polymorphism And Risk For Essential Tremor
Nonsynonymous Polymorphisms Of Histamine-Metabolising Enzymes In Patients With Parkinson's Disease
Glutathione-S-Transferase P1 Polymorphism And Risk For Essential Tremor
Interaction Of Cyp2c8 And Cyp2c9 Genotypes Modifies The Risk For Nonsteroidal Anti-Inflammatory Drugs-Related Acute Gastrointestinal Bleeding
Glutathione-S-Transferase P1 Polymorphism And Risk For Essential Tremor
Interaction Of Cyp2c8 And Cyp2c9 Genotypes Modifies The Risk For Nonsteroidal Anti-Inflammatory Drugs-Related Acute Gastrointestinal Bleeding
Refinement Of The Basis And Impact Of Common 11q23.1 Variation To The Risk Of Developing Colorectal Cancer
Interaction Of Cyp2c8 And Cyp2c9 Genotypes Modifies The Risk For Nonsteroidal Anti-Inflammatory Drugs-Related Acute Gastrointestinal Bleeding
Refinement Of The Basis And Impact Of Common 11q23.1 Variation To The Risk Of Developing Colorectal Cancer
Editorial: N-Acetyltransferases: Lessons Learned From Eighty Years Of Research
Refinement Of The Basis And Impact Of Common 11q23.1 Variation To The Risk Of Developing Colorectal Cancer
Editorial: N-Acetyltransferases: Lessons Learned From Eighty Years Of Research
Polymorphisms Of Human N-Acetyltransferases And Cancer Risk
Editorial: N-Acetyltransferases: Lessons Learned From Eighty Years Of Research
Polymorphisms Of Human N-Acetyltransferases And Cancer Risk
A Genome-Wide Association Study Identifies Colorectal Cancer Susceptibility Loci On Chromosomes 10p14 And 8q23.3
Polymorphisms Of Human N-Acetyltransferases And Cancer Risk
A Genome-Wide Association Study Identifies Colorectal Cancer Susceptibility Loci On Chromosomes 10p14 And 8q23.3
Glutathione S-Transferase Gstt1 And Gstm1 Allozymes: Beyond Null Alleles
A Genome-Wide Association Study Identifies Colorectal Cancer Susceptibility Loci On Chromosomes 10p14 And 8q23.3
Glutathione S-Transferase Gstt1 And Gstm1 Allozymes: Beyond Null Alleles
Genetic Variability In Cyp3a4 And Cyp3a5 In Primary Liver, Gastric And Colorectal Cancer Patients
Glutathione S-Transferase Gstt1 And Gstm1 Allozymes: Beyond Null Alleles
Genetic Variability In Cyp3a4 And Cyp3a5 In Primary Liver, Gastric And Colorectal Cancer Patients
Effect Of Neurotransmitters On Nadph-Cytochrome P450 Reductase In Vitro Activity.
Genetic Variability In Cyp3a4 And Cyp3a5 In Primary Liver, Gastric And Colorectal Cancer Patients
Effect Of Neurotransmitters On Nadph-Cytochrome P450 Reductase In Vitro Activity.
Effect Of Common Nat2 Variant Alleles In The Acetylation Of The Major Clonazepam Metabolite, 7-Aminoclonazepam.
Effect Of Neurotransmitters On Nadph-Cytochrome P450 Reductase In Vitro Activity.
Effect Of Common Nat2 Variant Alleles In The Acetylation Of The Major Clonazepam Metabolite, 7-Aminoclonazepam.
Improved Analytical Sensitivity Reveals The Occurrence Of Gender-Related Variability In Diamine Oxidase Enzyme Activity In Healthy Individuals
Effect Of Common Nat2 Variant Alleles In The Acetylation Of The Major Clonazepam Metabolite, 7-Aminoclonazepam.
Improved Analytical Sensitivity Reveals The Occurrence Of Gender-Related Variability In Diamine Oxidase Enzyme Activity In Healthy Individuals
Genetic Variability Of Human Diamine Oxidase: Occurrence Of Three Nonsynonymous Polymorphisms And Study Of Their Effect On Serum Enzyme Activity
Improved Analytical Sensitivity Reveals The Occurrence Of Gender-Related Variability In Diamine Oxidase Enzyme Activity In Healthy Individuals
Genetic Variability Of Human Diamine Oxidase: Occurrence Of Three Nonsynonymous Polymorphisms And Study Of Their Effect On Serum Enzyme Activity
Glutathione S-Transferases Π1, Α1 And Μ3 Genetic Polymorphisms And The Risk Of Hepatocellular Carcinoma In Humans
Genetic Variability Of Human Diamine Oxidase: Occurrence Of Three Nonsynonymous Polymorphisms And Study Of Their Effect On Serum Enzyme Activity
Glutathione S-Transferases Π1, Α1 And Μ3 Genetic Polymorphisms And The Risk Of Hepatocellular Carcinoma In Humans
Polymorphisms Of Histamine-Metabolizing Enzymes And Clinical Manifestations Of Asthma And Allergic Rhinitis
Glutathione S-Transferases Π1, Α1 And Μ3 Genetic Polymorphisms And The Risk Of Hepatocellular Carcinoma In Humans
Polymorphisms Of Histamine-Metabolizing Enzymes And Clinical Manifestations Of Asthma And Allergic Rhinitis
Alcohol Dehydrogenase 2 Genotype And Allelic Variants Are Not Associated With The Risk For Essential Tremor
Polymorphisms Of Histamine-Metabolizing Enzymes And Clinical Manifestations Of Asthma And Allergic Rhinitis
Alcohol Dehydrogenase 2 Genotype And Allelic Variants Are Not Associated With The Risk For Essential Tremor
Gstt1 And Gstm1 Null Genotypes May Facilitate Hepatitis C Virus Infection Becoming Chronic
Alcohol Dehydrogenase 2 Genotype And Allelic Variants Are Not Associated With The Risk For Essential Tremor
Gstt1 And Gstm1 Null Genotypes May Facilitate Hepatitis C Virus Infection Becoming Chronic
Cytochrome P450 Cyp2c9 Polymorphism And Nsaid-Related Acute Gastrointestinal Bleeding
Gstt1 And Gstm1 Null Genotypes May Facilitate Hepatitis C Virus Infection Becoming Chronic
Cytochrome P450 Cyp2c9 Polymorphism And Nsaid-Related Acute Gastrointestinal Bleeding
Changes At The Cyp2c Locus And Disruption Of Cyp2c8/9 Linkage Disequilibrium In Patients With Essential Tremor
Cytochrome P450 Cyp2c9 Polymorphism And Nsaid-Related Acute Gastrointestinal Bleeding
Changes At The Cyp2c Locus And Disruption Of Cyp2c8/9 Linkage Disequilibrium In Patients With Essential Tremor
[The H63d Mutation In The Hfe Gene Is Related To The Risk Of Hepatocellular Carcinoma]
Changes At The Cyp2c Locus And Disruption Of Cyp2c8/9 Linkage Disequilibrium In Patients With Essential Tremor
[The H63d Mutation In The Hfe Gene Is Related To The Risk Of Hepatocellular Carcinoma]
The H63d Mutation Of The Hfe Gene Is Related To The Risk Of Hepatocellular Carcinoma
[The H63d Mutation In The Hfe Gene Is Related To The Risk Of Hepatocellular Carcinoma]
The H63d Mutation Of The Hfe Gene Is Related To The Risk Of Hepatocellular Carcinoma
Cyp2d6 Gene Amplification And The Risk Of Acute Myeloblast Leukemia
The H63d Mutation Of The Hfe Gene Is Related To The Risk Of Hepatocellular Carcinoma
Cyp2d6 Gene Amplification And The Risk Of Acute Myeloblast Leukemia
Increased Frequency Of Rapid Acetylator Genotypes In Patients With Brain Astrocytoma And Meningioma
Cyp2d6 Gene Amplification And The Risk Of Acute Myeloblast Leukemia
Increased Frequency Of Rapid Acetylator Genotypes In Patients With Brain Astrocytoma And Meningioma
Severity Of Ulcerative Colitis Is Associated With A Polymorphism At Diamine Oxidase Gene But Not At Histamine N-Methyltransferase Gene
Increased Frequency Of Rapid Acetylator Genotypes In Patients With Brain Astrocytoma And Meningioma
Severity Of Ulcerative Colitis Is Associated With A Polymorphism At Diamine Oxidase Gene But Not At Histamine N-Methyltransferase Gene
Clinical Pharmacogenomics For Cyp2c8 And Cyp2c9: General Concepts And Application To The Use Of Nsaids
Severity Of Ulcerative Colitis Is Associated With A Polymorphism At Diamine Oxidase Gene But Not At Histamine N-Methyltransferase Gene
Clinical Pharmacogenomics For Cyp2c8 And Cyp2c9: General Concepts And Application To The Use Of Nsaids
Cyp2c19 Polymorphism And Risk For Essential Tremor
Clinical Pharmacogenomics For Cyp2c8 And Cyp2c9: General Concepts And Application To The Use Of Nsaids
Cyp2c19 Polymorphism And Risk For Essential Tremor
Interethnic And Intraethnic Variability Of Cyp2c8 And Cyp2c9 Polymorphisms In Healthy Individuals
Cyp2c19 Polymorphism And Risk For Essential Tremor
Interethnic And Intraethnic Variability Of Cyp2c8 And Cyp2c9 Polymorphisms In Healthy Individuals
Glutathione S-Transferase M1 And T1 Genetic Polymorphisms Are Not Related To The Risk Of Hepatocellular Carcinoma: A Study In The Spanish Population
Interethnic And Intraethnic Variability Of Cyp2c8 And Cyp2c9 Polymorphisms In Healthy Individuals
Glutathione S-Transferase M1 And T1 Genetic Polymorphisms Are Not Related To The Risk Of Hepatocellular Carcinoma: A Study In The Spanish Population
Glutathione S-Transferases Μ1, Θ1, Π1 Α1 And Μ3 Genetic Polymorphisms And The Risk Of Colorectal And Gastric Cancers In Humans
Glutathione S-Transferase M1 And T1 Genetic Polymorphisms Are Not Related To The Risk Of Hepatocellular Carcinoma: A Study In The Spanish Population
Glutathione S-Transferases Μ1, Θ1, Π1 Α1 And Μ3 Genetic Polymorphisms And The Risk Of Colorectal And Gastric Cancers In Humans
Acquired Resistance To The Anticancer Drug Paclitaxel Is Associated With Induction Of Cytochrome P450 2c8
Glutathione S-Transferases Μ1, Θ1, Π1 Α1 And Μ3 Genetic Polymorphisms And The Risk Of Colorectal And Gastric Cancers In Humans
Acquired Resistance To The Anticancer Drug Paclitaxel Is Associated With Induction Of Cytochrome P450 2c8
The Role Of Cyp2c19 Polymorphism In The Development Of Adverse Effects To Drugs And The Risk For Diseases
Acquired Resistance To The Anticancer Drug Paclitaxel Is Associated With Induction Of Cytochrome P450 2c8
The Role Of Cyp2c19 Polymorphism In The Development Of Adverse Effects To Drugs And The Risk For Diseases
Identification Of Subtypes Of Cyp2d Gene Rearrangements Among Carriers Of Cyp2d6 Gene Deletion And Duplication
The Role Of Cyp2c19 Polymorphism In The Development Of Adverse Effects To Drugs And The Risk For Diseases
Identification Of Subtypes Of Cyp2d Gene Rearrangements Among Carriers Of Cyp2d6 Gene Deletion And Duplication
Cytochrome P450 Gene Polymorphisms And Variability In Response To Nsaids
Identification Of Subtypes Of Cyp2d Gene Rearrangements Among Carriers Of Cyp2d6 Gene Deletion And Duplication
Cytochrome P450 Gene Polymorphisms And Variability In Response To Nsaids
Polymorphisms Of The Glutathione S-Transferases Mu-1 (Gstm1) And Theta-1 (Gstt1) And The Risk Of Advanced Alcoholic Liver Disease
Cytochrome P450 Gene Polymorphisms And Variability In Response To Nsaids
Polymorphisms Of The Glutathione S-Transferases Mu-1 (Gstm1) And Theta-1 (Gstt1) And The Risk Of Advanced Alcoholic Liver Disease
The Effect Of The Cytochrome P450 Cyp2c8 Polymorphism On The Disposition Of (R)-Ibuprofen Enantiomer In Healthy Subjects
Polymorphisms Of The Glutathione S-Transferases Mu-1 (Gstm1) And Theta-1 (Gstt1) And The Risk Of Advanced Alcoholic Liver Disease
The Effect Of The Cytochrome P450 Cyp2c8 Polymorphism On The Disposition Of (R)-Ibuprofen Enantiomer In Healthy Subjects
Polymorhisms In The Transforming Growth Factor-Β1 Gene (Tgf-Β1) And The Risk Of Advanced Alcoholic Liver Disease
The Effect Of The Cytochrome P450 Cyp2c8 Polymorphism On The Disposition Of (R)-Ibuprofen Enantiomer In Healthy Subjects
Polymorhisms In The Transforming Growth Factor-Β1 Gene (Tgf-Β1) And The Risk Of Advanced Alcoholic Liver Disease
Interindividual Variability In Ibuprofen Pharmacokinetics Is Related To Interaction Of Cytochrome P450 2c8 And 2c9 Amino Acid Polymorphisms
Polymorhisms In The Transforming Growth Factor-Β1 Gene (Tgf-Β1) And The Risk Of Advanced Alcoholic Liver Disease
Interindividual Variability In Ibuprofen Pharmacokinetics Is Related To Interaction Of Cytochrome P450 2c8 And 2c9 Amino Acid Polymorphisms
Genetic Predisposition To Acute Gastrointestinal Bleeding After Nsaids Use
Interindividual Variability In Ibuprofen Pharmacokinetics Is Related To Interaction Of Cytochrome P450 2c8 And 2c9 Amino Acid Polymorphisms
Genetic Predisposition To Acute Gastrointestinal Bleeding After Nsaids Use
Cytochrome P450 Gene Polymorphism And Cancer
Genetic Predisposition To Acute Gastrointestinal Bleeding After Nsaids Use
Cytochrome P450 Gene Polymorphism And Cancer
Leflunomide-Induced Acute Hepatitis
Cytochrome P450 Gene Polymorphism And Cancer
Leflunomide-Induced Acute Hepatitis
High Resolution Mapping And Mutation Analyses Of Candidate Genes In The Urofacial Syndrome (Ufs) Critical Region
Leflunomide-Induced Acute Hepatitis
High Resolution Mapping And Mutation Analyses Of Candidate Genes In The Urofacial Syndrome (Ufs) Critical Region
Nat2 Genotyping: Equilibrium Between Accuracy And Feasibility In Routine Analyses
High Resolution Mapping And Mutation Analyses Of Candidate Genes In The Urofacial Syndrome (Ufs) Critical Region
Nat2 Genotyping: Equilibrium Between Accuracy And Feasibility In Routine Analyses
Influence Of Cytochrome P450 Cyp2c9 Genotypes In Lung Cancer Risk
Nat2 Genotyping: Equilibrium Between Accuracy And Feasibility In Routine Analyses
Influence Of Cytochrome P450 Cyp2c9 Genotypes In Lung Cancer Risk
Cyp3a4 Variant Alleles In White Individuals With Low Cyp3a4 Enzyme Activity
Influence Of Cytochrome P450 Cyp2c9 Genotypes In Lung Cancer Risk
Cyp3a4 Variant Alleles In White Individuals With Low Cyp3a4 Enzyme Activity
Expression Of Paclitaxel-Inactivating Cyp3a Activity In Human Colorectal Cancer: Implications For Drug Therapy
Cyp3a4 Variant Alleles In White Individuals With Low Cyp3a4 Enzyme Activity
Expression Of Paclitaxel-Inactivating Cyp3a Activity In Human Colorectal Cancer: Implications For Drug Therapy
Single Nucleotide Polymorphisms And Microsatellite Alleles Of Tumor Necrosis Factor Alpha And Interleukin-10 Genes And The Risk Of Advanced Chronic Alcoholic Liver Disease
Expression Of Paclitaxel-Inactivating Cyp3a Activity In Human Colorectal Cancer: Implications For Drug Therapy
Single Nucleotide Polymorphisms And Microsatellite Alleles Of Tumor Necrosis Factor Alpha And Interleukin-10 Genes And The Risk Of Advanced Chronic Alcoholic Liver Disease
N-Acetyltransferase 2 Polymorphism Is Not Related To The Risk Of Advanced Alcoholic Liver Disease
Single Nucleotide Polymorphisms And Microsatellite Alleles Of Tumor Necrosis Factor Alpha And Interleukin-10 Genes And The Risk Of Advanced Chronic Alcoholic Liver Disease
N-Acetyltransferase 2 Polymorphism Is Not Related To The Risk Of Advanced Alcoholic Liver Disease
N-Acetyltransferase 2 Single-Nucleotide Polymorphisms And Risk Of Gastric Carcinoma
N-Acetyltransferase 2 Polymorphism Is Not Related To The Risk Of Advanced Alcoholic Liver Disease
N-Acetyltransferase 2 Single-Nucleotide Polymorphisms And Risk Of Gastric Carcinoma
N-Acetyltransferase 2 Single-Nucleotide Polymorphisms And Risk Of Gastric Carcinoma
N-Acetyltransferase 2 Single-Nucleotide Polymorphisms And Risk Of Gastric Carcinoma
N-Acetyltransferase 2 Single-Nucleotide Polymorphisms And Risk Of Gastric Carcinoma
High Frequency Of Mutations Related To Impaired Cyp2c9 Metabolism In A Caucasian Population
N-Acetyltransferase 2 Single-Nucleotide Polymorphisms And Risk Of Gastric Carcinoma
High Frequency Of Mutations Related To Impaired Cyp2c9 Metabolism In A Caucasian Population
Association Of Cyp2c9 Genotypes Leading To High Enzyme Activity And Colorectal Cancer Risk
High Frequency Of Mutations Related To Impaired Cyp2c9 Metabolism In A Caucasian Population
Association Of Cyp2c9 Genotypes Leading To High Enzyme Activity And Colorectal Cancer Risk
Mutaciones C282y Y H63d Del Gen Hfe En Pacientes Con Hepatopatía Alcohólica Avanzada
Association Of Cyp2c9 Genotypes Leading To High Enzyme Activity And Colorectal Cancer Risk
Mutaciones C282y Y H63d Del Gen Hfe En Pacientes Con Hepatopatía Alcohólica Avanzada
C282y And H63d Mutations Of Hfe Gene In Patients With Advanced Alcoholic Liver Disease
Mutaciones C282y Y H63d Del Gen Hfe En Pacientes Con Hepatopatía Alcohólica Avanzada
C282y And H63d Mutations Of Hfe Gene In Patients With Advanced Alcoholic Liver Disease
Inhibition Of Cytochrome P450 2c9 Activity In Vitro By 5-Hydroxytryptamine And Adrenaline
C282y And H63d Mutations Of Hfe Gene In Patients With Advanced Alcoholic Liver Disease
Inhibition Of Cytochrome P450 2c9 Activity In Vitro By 5-Hydroxytryptamine And Adrenaline
Functionally Active Duplications Of The Cyp2d6 Gene Are More Prevalent Among Larynx And Lung Cancer Patients
Inhibition Of Cytochrome P450 2c9 Activity In Vitro By 5-Hydroxytryptamine And Adrenaline
Functionally Active Duplications Of The Cyp2d6 Gene Are More Prevalent Among Larynx And Lung Cancer Patients
N-Acetyltransferase 2 (Nat2) Genotype And Colorectal Carcinoma: Risk Variability According To Tumour Site?
Functionally Active Duplications Of The Cyp2d6 Gene Are More Prevalent Among Larynx And Lung Cancer Patients
N-Acetyltransferase 2 (Nat2) Genotype And Colorectal Carcinoma: Risk Variability According To Tumour Site?
Modulation Of Midazolam 1-Hydroxylation Activity In Vitro By Neurotransmitters And Precursors
N-Acetyltransferase 2 (Nat2) Genotype And Colorectal Carcinoma: Risk Variability According To Tumour Site?
Modulation Of Midazolam 1-Hydroxylation Activity In Vitro By Neurotransmitters And Precursors
Pharmacokinetic Interaction Of Fluvoxamine And Thioridazine In Schizophrenic Patients
Modulation Of Midazolam 1-Hydroxylation Activity In Vitro By Neurotransmitters And Precursors
Pharmacokinetic Interaction Of Fluvoxamine And Thioridazine In Schizophrenic Patients
Comparative In Vitro And In Vivo Inhibition Of Cytochrome P450 Cyp1a2, Cyp2d6, And Cyp3a By H2-Receptor Antagonists
Pharmacokinetic Interaction Of Fluvoxamine And Thioridazine In Schizophrenic Patients
Comparative In Vitro And In Vivo Inhibition Of Cytochrome P450 Cyp1a2, Cyp2d6, And Cyp3a By H2-Receptor Antagonists
Identification And Characterisation Of Novel Polymorphisms In The Cyp2a Locus: Implications For Nicotine Metabolism
Comparative In Vitro And In Vivo Inhibition Of Cytochrome P450 Cyp1a2, Cyp2d6, And Cyp3a By H2-Receptor Antagonists
Identification And Characterisation Of Novel Polymorphisms In The Cyp2a Locus: Implications For Nicotine Metabolism
Enzymatic Polymorphisms And Pulmonary Cancer | Polimorfismos Enzimáticos Y Cáncer De Pulmón.
Identification And Characterisation Of Novel Polymorphisms In The Cyp2a Locus: Implications For Nicotine Metabolism
Enzymatic Polymorphisms And Pulmonary Cancer | Polimorfismos Enzimáticos Y Cáncer De Pulmón.
Analysis Of Midazolam And Metabolites In Plasma By High-Performance Liquid Chromatography: Probe Of Cyp3a
Enzymatic Polymorphisms And Pulmonary Cancer | Polimorfismos Enzimáticos Y Cáncer De Pulmón.
Analysis Of Midazolam And Metabolites In Plasma By High-Performance Liquid Chromatography: Probe Of Cyp3a
Influence Of Genetic Admixture On Polymorphisms Of Drug-Metabolizing Enzymes: Analyses Of Mutations On Nat2 And Cyp2e1 Genes In A Mixed Hispanic Population
Analysis Of Midazolam And Metabolites In Plasma By High-Performance Liquid Chromatography: Probe Of Cyp3a
Influence Of Genetic Admixture On Polymorphisms Of Drug-Metabolizing Enzymes: Analyses Of Mutations On Nat2 And Cyp2e1 Genes In A Mixed Hispanic Population
Slow Allotypic Variants Of The Nat2 Gene And Susceptibility To Early- Onset Parkinson's Disease
Influence Of Genetic Admixture On Polymorphisms Of Drug-Metabolizing Enzymes: Analyses Of Mutations On Nat2 And Cyp2e1 Genes In A Mixed Hispanic Population
Slow Allotypic Variants Of The Nat2 Gene And Susceptibility To Early- Onset Parkinson's Disease
Expression In Human Prostate Of Drug- And Carcinogen-Metabolizing Enzymes: Association With Prostate Cancer Risk
Slow Allotypic Variants Of The Nat2 Gene And Susceptibility To Early- Onset Parkinson's Disease
Expression In Human Prostate Of Drug- And Carcinogen-Metabolizing Enzymes: Association With Prostate Cancer Risk
Modulation Of Cyp1a2 Enzyme Activity By Indoleamines: Inhibition By Serotonin And Tryptamine
Expression In Human Prostate Of Drug- And Carcinogen-Metabolizing Enzymes: Association With Prostate Cancer Risk
Modulation Of Cyp1a2 Enzyme Activity By Indoleamines: Inhibition By Serotonin And Tryptamine
Polimorfismos Enzimáticos Y Cáncer De Pulmón
Modulation Of Cyp1a2 Enzyme Activity By Indoleamines: Inhibition By Serotonin And Tryptamine
Polimorfismos Enzimáticos Y Cáncer De Pulmón
Urinary Bladder Cancer In A Girl With A Slow-Acetylator Genotype And Treated With Sulphasalazine (Multiple Letters) [2]
Polimorfismos Enzimáticos Y Cáncer De Pulmón
Urinary Bladder Cancer In A Girl With A Slow-Acetylator Genotype And Treated With Sulphasalazine (Multiple Letters) [2]
Molecular Heterogeneity At The Cyp2d Gene Locus In Nicaraguans: Impact Of Gene-Flow From Europe
Urinary Bladder Cancer In A Girl With A Slow-Acetylator Genotype And Treated With Sulphasalazine (Multiple Letters) [2]
Molecular Heterogeneity At The Cyp2d Gene Locus In Nicaraguans: Impact Of Gene-Flow From Europe
Cyp2d6, Nat2 And Cyp2e1 Genetic Polymorphisms In Nonagenarians
Molecular Heterogeneity At The Cyp2d Gene Locus In Nicaraguans: Impact Of Gene-Flow From Europe
Cyp2d6, Nat2 And Cyp2e1 Genetic Polymorphisms In Nonagenarians
Hallevorden-Spatz Disease
Cyp2d6, Nat2 And Cyp2e1 Genetic Polymorphisms In Nonagenarians
Hallevorden-Spatz Disease
Tryptamine: A Possible Endogenous Substrate For Cyp2d6
Hallevorden-Spatz Disease
Tryptamine: A Possible Endogenous Substrate For Cyp2d6
Urinary Bladder Cancer In A Girl With A Slow-Acetylator Genotype And Treated With Sulphasalazine
Tryptamine: A Possible Endogenous Substrate For Cyp2d6
Urinary Bladder Cancer In A Girl With A Slow-Acetylator Genotype And Treated With Sulphasalazine
Polymorphism Is Not Associated With Essential Tremor
Urinary Bladder Cancer In A Girl With A Slow-Acetylator Genotype And Treated With Sulphasalazine
Polymorphism Is Not Associated With Essential Tremor
Cyp2a6 Gene Polymorphism And Risk Of Liver Cancer And Cirrhosis
Polymorphism Is Not Associated With Essential Tremor
Cyp2a6 Gene Polymorphism And Risk Of Liver Cancer And Cirrhosis
Genetic Analysis Of The Nat2 And Cyp2d6 Polymorphisms In White Patients With Non-Insulin-Dependent Diabetes Mellitus
Cyp2a6 Gene Polymorphism And Risk Of Liver Cancer And Cirrhosis
Genetic Analysis Of The Nat2 And Cyp2d6 Polymorphisms In White Patients With Non-Insulin-Dependent Diabetes Mellitus
Identification And Prevalence Study Of 17 Allelic Variants Of The Human Nat2 Gene In A White Population
Genetic Analysis Of The Nat2 And Cyp2d6 Polymorphisms In White Patients With Non-Insulin-Dependent Diabetes Mellitus
Identification And Prevalence Study Of 17 Allelic Variants Of The Human Nat2 Gene In A White Population
Determination Of Aminopyrine And Dipyrone Metabolites In Urine [2]
Identification And Prevalence Study Of 17 Allelic Variants Of The Human Nat2 Gene In A White Population
Determination Of Aminopyrine And Dipyrone Metabolites In Urine [2]
Cyp2d6 Genotypes In Spanish Women With Breast Cancer
Determination Of Aminopyrine And Dipyrone Metabolites In Urine [2]
Cyp2d6 Genotypes In Spanish Women With Breast Cancer
Changes Induced By Ovariectomy On The Acute Effects Of 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine In A Model Of Rat Poor Metabolizer Of Debrisoquine
Cyp2d6 Genotypes In Spanish Women With Breast Cancer
Changes Induced By Ovariectomy On The Acute Effects Of 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine In A Model Of Rat Poor Metabolizer Of Debrisoquine
Rsa I Polymorphism At The Cytochrome P4502e1 Locus Is Not Related To The Risk Of Alcohol-Related Severe Liver Disease
Changes Induced By Ovariectomy On The Acute Effects Of 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine In A Model Of Rat Poor Metabolizer Of Debrisoquine
Rsa I Polymorphism At The Cytochrome P4502e1 Locus Is Not Related To The Risk Of Alcohol-Related Severe Liver Disease
Rsai Polymorphism At The Cytochrome P4502e1 Locus And Risk Of Hepatocellular Carcinoma
Rsa I Polymorphism At The Cytochrome P4502e1 Locus Is Not Related To The Risk Of Alcohol-Related Severe Liver Disease
Rsai Polymorphism At The Cytochrome P4502e1 Locus And Risk Of Hepatocellular Carcinoma
Increased Risk For Hepatocellular Carcinoma In Nat2-Slow Acetylators And Cyp2d6-Rapid Metabolizers
Rsai Polymorphism At The Cytochrome P4502e1 Locus And Risk Of Hepatocellular Carcinoma
Increased Risk For Hepatocellular Carcinoma In Nat2-Slow Acetylators And Cyp2d6-Rapid Metabolizers
Aminopyrine Metabolism In Man: The Acetylation Of Aminoantipyrine Cosegregates With Acetylation Of Caffeine
Increased Risk For Hepatocellular Carcinoma In Nat2-Slow Acetylators And Cyp2d6-Rapid Metabolizers
Aminopyrine Metabolism In Man: The Acetylation Of Aminoantipyrine Cosegregates With Acetylation Of Caffeine
Cyp2d6 Genes And Risk Of Liver Cancer
Aminopyrine Metabolism In Man: The Acetylation Of Aminoantipyrine Cosegregates With Acetylation Of Caffeine
Cyp2d6 Genes And Risk Of Liver Cancer
Lung Cancer And Mutations At The Polymorphic Nat2 Gene Locus
Cyp2d6 Genes And Risk Of Liver Cancer
Lung Cancer And Mutations At The Polymorphic Nat2 Gene Locus
Metabolism Of Aminopyrine And Derivatives In Man: In Vivo Study Of Monomorphic And Polymorphic Metabolic Pathways
Lung Cancer And Mutations At The Polymorphic Nat2 Gene Locus
Metabolism Of Aminopyrine And Derivatives In Man: In Vivo Study Of Monomorphic And Polymorphic Metabolic Pathways
Association Between The Oxidative Polymorphism And Early Onset Of Parkinson's Disease
Metabolism Of Aminopyrine And Derivatives In Man: In Vivo Study Of Monomorphic And Polymorphic Metabolic Pathways
Association Between The Oxidative Polymorphism And Early Onset Of Parkinson's Disease
Genetic Analysis Of The Arylamine N-Acetyltransferase Polymorphism In Breast Cancer Patients
Association Between The Oxidative Polymorphism And Early Onset Of Parkinson's Disease
Genetic Analysis Of The Arylamine N-Acetyltransferase Polymorphism In Breast Cancer Patients
Prevalence Of Cyp2d6 Gene Duplication And Its Repercussion On The Oxidative Phenotype In A White Population
Genetic Analysis Of The Arylamine N-Acetyltransferase Polymorphism In Breast Cancer Patients
Prevalence Of Cyp2d6 Gene Duplication And Its Repercussion On The Oxidative Phenotype In A White Population
Frequency Of Cyp2d6 Allelic Variants In Multiple Sclerosis
Prevalence Of Cyp2d6 Gene Duplication And Its Repercussion On The Oxidative Phenotype In A White Population
Frequency Of Cyp2d6 Allelic Variants In Multiple Sclerosis
Possible Implications Of Doxycycline-Rifampin Interaction For Treatment Of Brucellosis
Frequency Of Cyp2d6 Allelic Variants In Multiple Sclerosis
Possible Implications Of Doxycycline-Rifampin Interaction For Treatment Of Brucellosis
Determination Of Aminopyrine, Dipyrone And Its Metabolites In Urine By High-Performance Liquid Chromatography
Possible Implications Of Doxycycline-Rifampin Interaction For Treatment Of Brucellosis
Determination Of Aminopyrine, Dipyrone And Its Metabolites In Urine By High-Performance Liquid Chromatography
Genetic Basis For Differences In Debrisoquin Polymorphism Between A Spanish And Other White Populations
Determination Of Aminopyrine, Dipyrone And Its Metabolites In Urine By High-Performance Liquid Chromatography
Genetic Basis For Differences In Debrisoquin Polymorphism Between A Spanish And Other White Populations
Debrisoquin Oxidation Genotype And Susceptibility To Lung Cancer
Genetic Basis For Differences In Debrisoquin Polymorphism Between A Spanish And Other White Populations
Debrisoquin Oxidation Genotype And Susceptibility To Lung Cancer
Molecular Analysis Of The Arylamine N-Acetyltransferase Polymorphism In A Spanish Population
Debrisoquin Oxidation Genotype And Susceptibility To Lung Cancer
Molecular Analysis Of The Arylamine N-Acetyltransferase Polymorphism In A Spanish Population
Debrisoquin Oxidation Genotype And Susceptibility To Lung Cancer.
Molecular Analysis Of The Arylamine N-Acetyltransferase Polymorphism In A Spanish Population
Debrisoquin Oxidation Genotype And Susceptibility To Lung Cancer.
Genetic Basis For Differences In Debrisoquin Polymorphism Between A Spanish And Other White Populations.
Debrisoquin Oxidation Genotype And Susceptibility To Lung Cancer.
Genetic Basis For Differences In Debrisoquin Polymorphism Between A Spanish And Other White Populations.
Molecular Analysis Of The Arylamine N-Acetyltransferase Polymorphism In A Spanish Population.
Genetic Basis For Differences In Debrisoquin Polymorphism Between A Spanish And Other White Populations.
Molecular Analysis Of The Arylamine N-Acetyltransferase Polymorphism In A Spanish Population.
Debrisoquine Polymorphism: Mechanism For Very Rapid Oxidative Phenotype
Molecular Analysis Of The Arylamine N-Acetyltransferase Polymorphism In A Spanish Population.
Debrisoquine Polymorphism: Mechanism For Very Rapid Oxidative Phenotype
Caffeine Demethylase Activity In Human And Dark Agouti Rat Liver Microsomes: Comparison With Aminopyrine N-Demethylase Activity
Debrisoquine Polymorphism: Mechanism For Very Rapid Oxidative Phenotype
Caffeine Demethylase Activity In Human And Dark Agouti Rat Liver Microsomes: Comparison With Aminopyrine N-Demethylase Activity
Dinucleoside Tetraphosphatase From Human Blood Cells. Purification And Characterization As A High Specific Activity Enzyme Recognized By An Anti-Rat Tetraphosphatase Antibody
Caffeine Demethylase Activity In Human And Dark Agouti Rat Liver Microsomes: Comparison With Aminopyrine N-Demethylase Activity
Dinucleoside Tetraphosphatase From Human Blood Cells. Purification And Characterization As A High Specific Activity Enzyme Recognized By An Anti-Rat Tetraphosphatase Antibody
Particulate Diadenosine 5′,5‴-P1,p3-Triphosphate Hydrolases In Rat Brain: Two Specific Dinucleoside Triphosphatases And Two Phosphodiesterase I-Like Hydrolases
Dinucleoside Tetraphosphatase From Human Blood Cells. Purification And Characterization As A High Specific Activity Enzyme Recognized By An Anti-Rat Tetraphosphatase Antibody
Particulate Diadenosine 5′,5‴-P1,p3-Triphosphate Hydrolases In Rat Brain: Two Specific Dinucleoside Triphosphatases And Two Phosphodiesterase I-Like Hydrolases
Acute Effects Of 1‐methyl‐4‐phenyl‐1, 2, 3, 6‐tetrahydropyridine In A Model Of Rat Designated A Poor Metabolizer Of Debrisoquine
Particulate Diadenosine 5′,5‴-P1,p3-Triphosphate Hydrolases In Rat Brain: Two Specific Dinucleoside Triphosphatases And Two Phosphodiesterase I-Like Hydrolases
Acute Effects Of 1‐methyl‐4‐phenyl‐1, 2, 3, 6‐tetrahydropyridine In A Model Of Rat Designated A Poor Metabolizer Of Debrisoquine
Sex And Age-Related Differences In Aminopyrine N-Demethylase Activity In Da- And Wistar-Strain Rat Liver Microsomes. Effect Of Ovariectomy
Acute Effects Of 1‐methyl‐4‐phenyl‐1, 2, 3, 6‐tetrahydropyridine In A Model Of Rat Designated A Poor Metabolizer Of Debrisoquine
Sex And Age-Related Differences In Aminopyrine N-Demethylase Activity In Da- And Wistar-Strain Rat Liver Microsomes. Effect Of Ovariectomy
Purification To Homogeneity Of Rat Liver Dinucleoside Tetraphosphatase By Affinity Elution With Adenosine 5′-Tetraphosphate
Sex And Age-Related Differences In Aminopyrine N-Demethylase Activity In Da- And Wistar-Strain Rat Liver Microsomes. Effect Of Ovariectomy
Purification To Homogeneity Of Rat Liver Dinucleoside Tetraphosphatase By Affinity Elution With Adenosine 5′-Tetraphosphate
Aminopyrine N-Demethylase Activity In Human Liver Microsomes
Purification To Homogeneity Of Rat Liver Dinucleoside Tetraphosphatase By Affinity Elution With Adenosine 5′-Tetraphosphate
Aminopyrine N-Demethylase Activity In Human Liver Microsomes
Aminopyrine N-Demethylase Activity In Human Liver Microsomes.
Aminopyrine N-Demethylase Activity In Human Liver Microsomes
Aminopyrine N-Demethylase Activity In Human Liver Microsomes.
Oxidative Stress In Huntington’s Disease
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