PUBLICACIÓN

Inhibition by 4-hydroxynonenal (HNE) of Ca 2+ transport by SERCA1a: Low concentrations of HNE open protein-mediated leaks in the membrane

ACCEDER A LA PUBLICACIÓN: Scopus

Hortigon-Vinagre M.P., Chardonnet S., Montigny C., Gutierrez-Martin Y., Champeil P., Henao F.

2011 FREE RADICAL BIOLOGY AND MEDICINE

Biochemistry (Q1), Physiology (medical) (Q1)

JCR: 5.423

SJR: 2.198

CITAS

2

DOI

10.1016/j.freeradbiomed.2011.01.030

EID

2-s2.0-79955583081

ISSN

0891-5849

AUTORES DE LA UEX

María Pura Hortigón Vinagre

OTRAS PUBLICACIONES DE INTERÉS

Inhibition Of The Sarcoplasmic Reticulum (Ca2+ + Mg2+-Atpase By Zn(Ii)
Metformin Reduces Potassium Currents And Prolongs Repolarization In Non-Diabetic Heart
A Bioprinted Heart-On-A-Chip With Human Pluripotent Stem Cell-Derived Cardiomyocytes For Drug Evaluation
Metformin Reduces Potassium Currents And Prolongs Repolarization In Non-Diabetic Heart
A Bioprinted Heart-On-A-Chip With Human Pluripotent Stem Cell-Derived Cardiomyocytes For Drug Evaluation
The Use Of Voltage Sensitive Dye Di-4-Anepps And Video-Based Contractility Measurements To Assess Drug Effects On Excitation-Contraction Coupling In Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes
A Bioprinted Heart-On-A-Chip With Human Pluripotent Stem Cell-Derived Cardiomyocytes For Drug Evaluation
The Use Of Voltage Sensitive Dye Di-4-Anepps And Video-Based Contractility Measurements To Assess Drug Effects On Excitation-Contraction Coupling In Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes
Electrophysiology Of Hipsc-Cardiomyocytes Co-Cultured With Hek Cells Expressing The Inward Rectifier Channel
The Use Of Voltage Sensitive Dye Di-4-Anepps And Video-Based Contractility Measurements To Assess Drug Effects On Excitation-Contraction Coupling In Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes
Electrophysiology Of Hipsc-Cardiomyocytes Co-Cultured With Hek Cells Expressing The Inward Rectifier Channel
Adult And Developing Zebrafish As Suitable Models For Cardiac Electrophysiology And Pathology In Research And Industry
Electrophysiology Of Hipsc-Cardiomyocytes Co-Cultured With Hek Cells Expressing The Inward Rectifier Channel
Adult And Developing Zebrafish As Suitable Models For Cardiac Electrophysiology And Pathology In Research And Industry
Searching For Scientific Explanations For The Uses Of Spanish Folk Medicine: A Review On The Case Of Mullein (Verbascum, Scrophulariaceae)
Adult And Developing Zebrafish As Suitable Models For Cardiac Electrophysiology And Pathology In Research And Industry
Searching For Scientific Explanations For The Uses Of Spanish Folk Medicine: A Review On The Case Of Mullein (Verbascum, Scrophulariaceae)
Exercise Training Reveals Micro-Rnas Associated With Improved Cardiac Function And Electrophysiology In Rats With Heart Failure After Myocardial Infarction
Searching For Scientific Explanations For The Uses Of Spanish Folk Medicine: A Review On The Case Of Mullein (Verbascum, Scrophulariaceae)
Exercise Training Reveals Micro-Rnas Associated With Improved Cardiac Function And Electrophysiology In Rats With Heart Failure After Myocardial Infarction
The Use Of Voltage Sensitive Dye Di-4-Anepps And Video-Based Contractility Measurements To Assess Drug Effects On Excitation-Contraction Coupling In Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
Exercise Training Reveals Micro-Rnas Associated With Improved Cardiac Function And Electrophysiology In Rats With Heart Failure After Myocardial Infarction
The Use Of Voltage Sensitive Dye Di-4-Anepps And Video-Based Contractility Measurements To Assess Drug Effects On Excitation-Contraction Coupling In Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
Adult And Developing Zebrafish As Suitable Models For Cardiac Electrophysiology And Pathology In Research And Industry.
The Use Of Voltage Sensitive Dye Di-4-Anepps And Video-Based Contractility Measurements To Assess Drug Effects On Excitation-Contraction Coupling In Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
Adult And Developing Zebrafish As Suitable Models For Cardiac Electrophysiology And Pathology In Research And Industry.
Electrophysiological Characterization Of Drug Response In Hsc-Derived Cardiomyocytes Using Voltage-Sensitive Optical Platforms
Adult And Developing Zebrafish As Suitable Models For Cardiac Electrophysiology And Pathology In Research And Industry.
Electrophysiological Characterization Of Drug Response In Hsc-Derived Cardiomyocytes Using Voltage-Sensitive Optical Platforms
Bioactive Phytochemicals From Mercurialis Spp. Used In Traditional Spanish Medicine
Electrophysiological Characterization Of Drug Response In Hsc-Derived Cardiomyocytes Using Voltage-Sensitive Optical Platforms
Bioactive Phytochemicals From Mercurialis Spp. Used In Traditional Spanish Medicine
Tailoring Mathematical Models To Stem-Cell Derived Cardiomyocyte Lines Can Improve Predictions Of Drug-Induced Changes To Their Electrophysiology
Bioactive Phytochemicals From Mercurialis Spp. Used In Traditional Spanish Medicine
Tailoring Mathematical Models To Stem-Cell Derived Cardiomyocyte Lines Can Improve Predictions Of Drug-Induced Changes To Their Electrophysiology
Application Of Optical Action Potentials In Human Induced Pluripotent Stem Cells-Derived Cardiomyocytes To Predict Drug-Induced Cardiac Arrhythmias
Tailoring Mathematical Models To Stem-Cell Derived Cardiomyocyte Lines Can Improve Predictions Of Drug-Induced Changes To Their Electrophysiology
Application Of Optical Action Potentials In Human Induced Pluripotent Stem Cells-Derived Cardiomyocytes To Predict Drug-Induced Cardiac Arrhythmias
Deconvoluting Kinase Inhibitor Induced Cardiotoxicity
Application Of Optical Action Potentials In Human Induced Pluripotent Stem Cells-Derived Cardiomyocytes To Predict Drug-Induced Cardiac Arrhythmias
Deconvoluting Kinase Inhibitor Induced Cardiotoxicity
Comprehensive Translational Assessment Of Human- Induced Pluripotent Stem Cell Derived Cardiomyocytes For Evaluating Drug-Induced Arrhythmias
Deconvoluting Kinase Inhibitor Induced Cardiotoxicity
Comprehensive Translational Assessment Of Human- Induced Pluripotent Stem Cell Derived Cardiomyocytes For Evaluating Drug-Induced Arrhythmias
Correlation Between Human Ether-A-Go-Go-Related Gene Channel Inhibition And Action Potential Prolongation
Comprehensive Translational Assessment Of Human- Induced Pluripotent Stem Cell Derived Cardiomyocytes For Evaluating Drug-Induced Arrhythmias
Correlation Between Human Ether-A-Go-Go-Related Gene Channel Inhibition And Action Potential Prolongation
Gene Therapy With Angiotensin-(1-9) Preserves Left Ventricular Systolic Function After Myocardial Infarction
Correlation Between Human Ether-A-Go-Go-Related Gene Channel Inhibition And Action Potential Prolongation
Gene Therapy With Angiotensin-(1-9) Preserves Left Ventricular Systolic Function After Myocardial Infarction
Enhanced Human-Induced Pluripotent Stem Cell Derived Cardiomyocyte Maturation Using A Dual Microgradient Substrate
Gene Therapy With Angiotensin-(1-9) Preserves Left Ventricular Systolic Function After Myocardial Infarction
Enhanced Human-Induced Pluripotent Stem Cell Derived Cardiomyocyte Maturation Using A Dual Microgradient Substrate
The Use Of Ratiometric Fluorescence Measurements Of The Voltage Sensitive Dye Di-4-Anepps To Examine Action Potential Characteristics And Drug Effects On Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
Enhanced Human-Induced Pluripotent Stem Cell Derived Cardiomyocyte Maturation Using A Dual Microgradient Substrate
The Use Of Ratiometric Fluorescence Measurements Of The Voltage Sensitive Dye Di-4-Anepps To Examine Action Potential Characteristics And Drug Effects On Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
Comprehensive Translational Assessment Of Human-Induced Pluripotent Stem Cell Derived Cardiomyocytes For Evaluating Drug-Induced Arrhythmias.
The Use Of Ratiometric Fluorescence Measurements Of The Voltage Sensitive Dye Di-4-Anepps To Examine Action Potential Characteristics And Drug Effects On Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
Comprehensive Translational Assessment Of Human-Induced Pluripotent Stem Cell Derived Cardiomyocytes For Evaluating Drug-Induced Arrhythmias.
Thymbra Capitata Essential Oil Prevents Cell Death Induced By 4-Hydroxy-2-Nonenal In Neonatal Rat Cardiac Myocytes
Comprehensive Translational Assessment Of Human-Induced Pluripotent Stem Cell Derived Cardiomyocytes For Evaluating Drug-Induced Arrhythmias.
Thymbra Capitata Essential Oil Prevents Cell Death Induced By 4-Hydroxy-2-Nonenal In Neonatal Rat Cardiac Myocytes
Targeted Disruption Of The Heat Shock Protein 20-Phosphodiesterase 4d (Pde4d) Interaction Protects Against Pathological Cardiac Remodelling In A Mouse Model Of Hypertrophy
Thymbra Capitata Essential Oil Prevents Cell Death Induced By 4-Hydroxy-2-Nonenal In Neonatal Rat Cardiac Myocytes
Targeted Disruption Of The Heat Shock Protein 20-Phosphodiesterase 4d (Pde4d) Interaction Protects Against Pathological Cardiac Remodelling In A Mouse Model Of Hypertrophy
Apoptotic Cell Death In Cultured Cardiomyocytes Following Exposure To Low Concentrations Of 4-Hydroxy-2-Nonenal
Targeted Disruption Of The Heat Shock Protein 20-Phosphodiesterase 4d (Pde4d) Interaction Protects Against Pathological Cardiac Remodelling In A Mouse Model Of Hypertrophy
Apoptotic Cell Death In Cultured Cardiomyocytes Following Exposure To Low Concentrations Of 4-Hydroxy-2-Nonenal
2,3,7,8-Tetrachlorodibenzo-P-Dioxin Induces Apoptosis By Disruption Of Intracellular Calcium Homeostasis In Human Neuronal Cell Line Shsy5y
Apoptotic Cell Death In Cultured Cardiomyocytes Following Exposure To Low Concentrations Of 4-Hydroxy-2-Nonenal
2,3,7,8-Tetrachlorodibenzo-P-Dioxin Induces Apoptosis By Disruption Of Intracellular Calcium Homeostasis In Human Neuronal Cell Line Shsy5y
Inhibition By 4-Hydroxynonenal (Hne) Of Ca2+ Transport By Serca1a: Low Concentrations Of Hne Open Protein-Mediated Leaks In The Membrane
2,3,7,8-Tetrachlorodibenzo-P-Dioxin Induces Apoptosis By Disruption Of Intracellular Calcium Homeostasis In Human Neuronal Cell Line Shsy5y
Inhibition By 4-Hydroxynonenal (Hne) Of Ca2+ Transport By Serca1a: Low Concentrations Of Hne Open Protein-Mediated Leaks In The Membrane
Erratum: Inhibition By 4-Hydroxynonenal (Hne) Of Ca2+ Transport By Serca1a: Low Concentrations Of Hne Open Protein-Mediated Leaks In The Membrane (Free Radical Biology & Medicine (2011) 50 (323-336))
Inhibition By 4-Hydroxynonenal (Hne) Of Ca2+ Transport By Serca1a: Low Concentrations Of Hne Open Protein-Mediated Leaks In The Membrane
Erratum: Inhibition By 4-Hydroxynonenal (Hne) Of Ca2+ Transport By Serca1a: Low Concentrations Of Hne Open Protein-Mediated Leaks In The Membrane (Free Radical Biology & Medicine (2011) 50 (323-336))
Inhibition By 4-Hydroxynonenal (Hne) Of Ca 2+ Transport By Serca1a: Low Concentrations Of Hne Open Protein-Mediated Leaks In The Membrane
Erratum: Inhibition By 4-Hydroxynonenal (Hne) Of Ca2+ Transport By Serca1a: Low Concentrations Of Hne Open Protein-Mediated Leaks In The Membrane (Free Radical Biology & Medicine (2011) 50 (323-336))
Inhibition By 4-Hydroxynonenal (Hne) Of Ca 2+ Transport By Serca1a: Low Concentrations Of Hne Open Protein-Mediated Leaks In The Membrane
Role Of Transforming Growth Factor Β In Cancer Microenvironment
Inhibition By 4-Hydroxynonenal (Hne) Of Ca 2+ Transport By Serca1a: Low Concentrations Of Hne Open Protein-Mediated Leaks In The Membrane
Role Of Transforming Growth Factor Β In Cancer Microenvironment
Sarcoplasmic Reticulum Calcium Atpase Is Inhibited By Organic Vanadium Coordination Compounds: Pyridine-2,6-Dicarboxylatodioxovanadium(V), Bmov, And An Amavadine Analogue
Role Of Transforming Growth Factor Β In Cancer Microenvironment
Sarcoplasmic Reticulum Calcium Atpase Is Inhibited By Organic Vanadium Coordination Compounds: Pyridine-2,6-Dicarboxylatodioxovanadium(V), Bmov, And An Amavadine Analogue
Vanadate Induces Necrotic Death In Neonatal Rat Cardiomyocytes Through Mitochondrial Membrane Depolarization
Sarcoplasmic Reticulum Calcium Atpase Is Inhibited By Organic Vanadium Coordination Compounds: Pyridine-2,6-Dicarboxylatodioxovanadium(V), Bmov, And An Amavadine Analogue
Vanadate Induces Necrotic Death In Neonatal Rat Cardiomyocytes Through Mitochondrial Membrane Depolarization
Store-Operated Calcium Entry In Differentiated C2c12 Skeletal Muscle Cells
Vanadate Induces Necrotic Death In Neonatal Rat Cardiomyocytes Through Mitochondrial Membrane Depolarization
Store-Operated Calcium Entry In Differentiated C2c12 Skeletal Muscle Cells
Alteration Of Cytosolic Free Calcium Homeostasis By Sin-1: High Sensitivity Of L-Type Ca2+ Channels To Extracellular Oxidative/nitrosative Stress In Cerebellar Granule Cells
Store-Operated Calcium Entry In Differentiated C2c12 Skeletal Muscle Cells
Alteration Of Cytosolic Free Calcium Homeostasis By Sin-1: High Sensitivity Of L-Type Ca2+ Channels To Extracellular Oxidative/nitrosative Stress In Cerebellar Granule Cells
Modulation Of Sarcoplasmic Reticulum Ca2+-Atpase By Chronic And Acute Exposure To Peroxynitrite
Alteration Of Cytosolic Free Calcium Homeostasis By Sin-1: High Sensitivity Of L-Type Ca2+ Channels To Extracellular Oxidative/nitrosative Stress In Cerebellar Granule Cells
Modulation Of Sarcoplasmic Reticulum Ca2+-Atpase By Chronic And Acute Exposure To Peroxynitrite
Fluorescence Measurements Of Steady State Peroxynitrite Production Upon Sin-1 Decomposition: Nadh Versus Dihydrodichlorofluorescein And Dihydrorhodamine 123
Modulation Of Sarcoplasmic Reticulum Ca2+-Atpase By Chronic And Acute Exposure To Peroxynitrite
Fluorescence Measurements Of Steady State Peroxynitrite Production Upon Sin-1 Decomposition: Nadh Versus Dihydrodichlorofluorescein And Dihydrorhodamine 123
Inhibition Of Mouth Skeletal Muscle Relaxation By Flavonoids Of Cistus Ladanifer L.: A Plant Defense Mechanism Against Herbivores
Fluorescence Measurements Of Steady State Peroxynitrite Production Upon Sin-1 Decomposition: Nadh Versus Dihydrodichlorofluorescein And Dihydrorhodamine 123
Inhibition Of Mouth Skeletal Muscle Relaxation By Flavonoids Of Cistus Ladanifer L.: A Plant Defense Mechanism Against Herbivores
Projection Map Of Covalently Phosphorylated Ca-Atpase From Tubular Crystals
Inhibition Of Mouth Skeletal Muscle Relaxation By Flavonoids Of Cistus Ladanifer L.: A Plant Defense Mechanism Against Herbivores
Projection Map Of Covalently Phosphorylated Ca-Atpase From Tubular Crystals
The Nadh Oxidase Activity Of The Plasma Membrane Of Synaptosomes Is A Major Source Of Superoxide Anion And Is Inhibited By Peroxynitrite
Projection Map Of Covalently Phosphorylated Ca-Atpase From Tubular Crystals
The Nadh Oxidase Activity Of The Plasma Membrane Of Synaptosomes Is A Major Source Of Superoxide Anion And Is Inhibited By Peroxynitrite
Synaptosomal Plasma Membrane Ca2+ Pump Activity Inhibition By Repetitive Micromolar Onoo- Pulses
The Nadh Oxidase Activity Of The Plasma Membrane Of Synaptosomes Is A Major Source Of Superoxide Anion And Is Inhibited By Peroxynitrite
Synaptosomal Plasma Membrane Ca2+ Pump Activity Inhibition By Repetitive Micromolar Onoo- Pulses
The Content Of Glycogen Phosphorylase And Glycogen In Preparations Of Sarcoplasmic Reticulum - Glycogenolytic Complex Is Enhanced In Diabetic Rat Skeletal Muscle
Synaptosomal Plasma Membrane Ca2+ Pump Activity Inhibition By Repetitive Micromolar Onoo- Pulses
The Content Of Glycogen Phosphorylase And Glycogen In Preparations Of Sarcoplasmic Reticulum - Glycogenolytic Complex Is Enhanced In Diabetic Rat Skeletal Muscle
Phosphorylated Ca2+-Atpase Stable Enough For Structural Studies
The Content Of Glycogen Phosphorylase And Glycogen In Preparations Of Sarcoplasmic Reticulum - Glycogenolytic Complex Is Enhanced In Diabetic Rat Skeletal Muscle
Phosphorylated Ca2+-Atpase Stable Enough For Structural Studies
A Remarkably Stable Phosphorylated Form Of Ca2+-Atpase Prepared From Ca2+-Loaded And Fluorescein Isothiocyanate-Labeled Sarcoplasmic Reticulum Vesicles
Phosphorylated Ca2+-Atpase Stable Enough For Structural Studies
A Remarkably Stable Phosphorylated Form Of Ca2+-Atpase Prepared From Ca2+-Loaded And Fluorescein Isothiocyanate-Labeled Sarcoplasmic Reticulum Vesicles
Plausible Stoichiometry Of The Interacting Nucleotide-Binding Sites In The Ca2+-Atpase From Sarcoplasmic Reticulum Membranes
A Remarkably Stable Phosphorylated Form Of Ca2+-Atpase Prepared From Ca2+-Loaded And Fluorescein Isothiocyanate-Labeled Sarcoplasmic Reticulum Vesicles
Plausible Stoichiometry Of The Interacting Nucleotide-Binding Sites In The Ca2+-Atpase From Sarcoplasmic Reticulum Membranes
Characterization Of A Protease-Resistant Domain Of The Cytosolic Portion Of Sarcoplasmic Reticulum Ca2+-Atpase. Nucleotide- And Metal-Binding Sites
Plausible Stoichiometry Of The Interacting Nucleotide-Binding Sites In The Ca2+-Atpase From Sarcoplasmic Reticulum Membranes
Characterization Of A Protease-Resistant Domain Of The Cytosolic Portion Of Sarcoplasmic Reticulum Ca2+-Atpase. Nucleotide- And Metal-Binding Sites
Dissociation Of Ca2+ From Sarcoplasmic Reticulum Ca2+-Atpase And Changes In Fluorescence Of Optically Selected Trp Residues. Effects Of Kcl And Nacl And Implications For Substeps In Ca2+ Dissociation
Characterization Of A Protease-Resistant Domain Of The Cytosolic Portion Of Sarcoplasmic Reticulum Ca2+-Atpase. Nucleotide- And Metal-Binding Sites
Dissociation Of Ca2+ From Sarcoplasmic Reticulum Ca2+-Atpase And Changes In Fluorescence Of Optically Selected Trp Residues. Effects Of Kcl And Nacl And Implications For Substeps In Ca2+ Dissociation
Structural Changes Of The Sarcoplasmic Reticulum Ca(Ii)-Atpase Nucleotide Binding Domain By Ph And La(Iii)
Dissociation Of Ca2+ From Sarcoplasmic Reticulum Ca2+-Atpase And Changes In Fluorescence Of Optically Selected Trp Residues. Effects Of Kcl And Nacl And Implications For Substeps In Ca2+ Dissociation
Structural Changes Of The Sarcoplasmic Reticulum Ca(Ii)-Atpase Nucleotide Binding Domain By Ph And La(Iii)
Ca2+ Uptake Coupled To Glycogen Phosphorolysis In The Glycogenolytic-Sarcoplasmic Reticulum Complex From Rat Skeletal Muscle
Structural Changes Of The Sarcoplasmic Reticulum Ca(Ii)-Atpase Nucleotide Binding Domain By Ph And La(Iii)
Ca2+ Uptake Coupled To Glycogen Phosphorolysis In The Glycogenolytic-Sarcoplasmic Reticulum Complex From Rat Skeletal Muscle
Fluorescnece Anisotropy Of Fluorescein Phosphatidylethanolthiocarbamide In Lipid Bilayers And In Ca2+-Atpase/lipid Reconstituted Systems
Ca2+ Uptake Coupled To Glycogen Phosphorolysis In The Glycogenolytic-Sarcoplasmic Reticulum Complex From Rat Skeletal Muscle
Fluorescnece Anisotropy Of Fluorescein Phosphatidylethanolthiocarbamide In Lipid Bilayers And In Ca2+-Atpase/lipid Reconstituted Systems
Interaction Between Glycogen Phosphorylase And Sarcoplasmic Reticulum Membranes And Its Functional Implications
Fluorescnece Anisotropy Of Fluorescein Phosphatidylethanolthiocarbamide In Lipid Bilayers And In Ca2+-Atpase/lipid Reconstituted Systems
Interaction Between Glycogen Phosphorylase And Sarcoplasmic Reticulum Membranes And Its Functional Implications
Quantification And Removal Of Glycogen Phosphorylase And Other Enzymes Associated With Sarcoplasmic Reticulum Membrane Preparations
Interaction Between Glycogen Phosphorylase And Sarcoplasmic Reticulum Membranes And Its Functional Implications
Quantification And Removal Of Glycogen Phosphorylase And Other Enzymes Associated With Sarcoplasmic Reticulum Membrane Preparations
Cancellation Of The Cooperativity Of Ca2+ Binding To Sarcoplasmic Reticulum Ca2+‐atpase By The Non‐ionic Detergent Dodecylmaltoside
Quantification And Removal Of Glycogen Phosphorylase And Other Enzymes Associated With Sarcoplasmic Reticulum Membrane Preparations
Cancellation Of The Cooperativity Of Ca2+ Binding To Sarcoplasmic Reticulum Ca2+‐atpase By The Non‐ionic Detergent Dodecylmaltoside
The Metal Sites On Sarcoplasmic Reticulum Membranes That Bind Lanthanide Ions With The Highest Affinity Are Not The Atpase Ca2+ Transport Sites
Cancellation Of The Cooperativity Of Ca2+ Binding To Sarcoplasmic Reticulum Ca2+‐atpase By The Non‐ionic Detergent Dodecylmaltoside
The Metal Sites On Sarcoplasmic Reticulum Membranes That Bind Lanthanide Ions With The Highest Affinity Are Not The Atpase Ca2+ Transport Sites
Binding Of Gadolinium Ions To Sarcoplasmic Reticulum Membranes
The Metal Sites On Sarcoplasmic Reticulum Membranes That Bind Lanthanide Ions With The Highest Affinity Are Not The Atpase Ca2+ Transport Sites
Binding Of Gadolinium Ions To Sarcoplasmic Reticulum Membranes
Kinetic Characterization Of The Perturbation By Dodecylmaltoside Of Sarcoplasmic Reticulum Ca2+ ‐atpase
Binding Of Gadolinium Ions To Sarcoplasmic Reticulum Membranes
Kinetic Characterization Of The Perturbation By Dodecylmaltoside Of Sarcoplasmic Reticulum Ca2+ ‐atpase
Kinetic Characterization Of The Normal And Procaine‐perturbed Reaction Cycles Of The Sarcoplasmic Reticulum Calcium Pump
Kinetic Characterization Of The Perturbation By Dodecylmaltoside Of Sarcoplasmic Reticulum Ca2+ ‐atpase
Kinetic Characterization Of The Normal And Procaine‐perturbed Reaction Cycles Of The Sarcoplasmic Reticulum Calcium Pump
Modulation Of The Sarcoplasmic Reticulum (Ca2+ + Mg2+)-Atpase By Pentobarbital
Kinetic Characterization Of The Normal And Procaine‐perturbed Reaction Cycles Of The Sarcoplasmic Reticulum Calcium Pump
Modulation Of The Sarcoplasmic Reticulum (Ca2+ + Mg2+)-Atpase By Pentobarbital
Distances Between Functional Sites Of The Ca2++ Mg2+‐atpase From Sarcoplasmic Reticulum Using Co2+ As A Spectroscopic Ruler
Modulation Of The Sarcoplasmic Reticulum (Ca2+ + Mg2+)-Atpase By Pentobarbital
Distances Between Functional Sites Of The Ca2++ Mg2+‐atpase From Sarcoplasmic Reticulum Using Co2+ As A Spectroscopic Ruler
Inhibition Of The Sarcoplasmic Reticulum (Ca2+ + Mg2+-Atpase By Zn(Ii)
Distances Between Functional Sites Of The Ca2++ Mg2+‐atpase From Sarcoplasmic Reticulum Using Co2+ As A Spectroscopic Ruler
Inhibition Of The Sarcoplasmic Reticulum (Ca2+ + Mg2+-Atpase By Zn(Ii)
Metformin Reduces Potassium Currents And Prolongs Repolarization In Non-Diabetic Heart
WEB ACCESIBLE