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Ryanodine receptor 2
Unnatural Verticilide Enantiomer Inhibits Type 2 Ryanodine Receptor-Mediated Calcium Leak and Is Antiarrhythmic
Aquaporin Channels in the Heart—Physiology and Pathophysiology
Supplemental Material
Supplemental Data Supplemental Table 1. Technical Specifications of the Primers Used for Individual Genotyping
Ion Channels 3 1
Disease Mutations in the Ryanodine Receptor N-Terminal Region Couple to a Mobile Intersubunit Interface
Physiological and Pathophysiological Regulation of the Ryanodine Receptor in Skeletal Muscle
Spatial Distribution of Leading Pacemaker Sites in the Normal, Intact Rat Sinoa
RYR2 Gene Ryanodine Receptor 2
MALAT1 Knockdown Protects from Bronchial/Tracheal Smooth Muscle Cell Injury Via Regulation of Microrna-133A/Ryanodine Receptor 2 Axis
Supplementary Table 2
Original Article Unbalanced Upregulation of Ryanodine Receptor 2 Plays a Particular Role in Early Development of Daunorubicin Cardiomyopathy
Skeletal Muscle in Aged Mice Reveals Extensive Transformation of Muscle
Cysteine-Rich Secretory Protein 4 Is an Inhibitor of Transient Receptor Potential M8 with a Role in Establishing Sperm Function
Structure and Function of the Human Ryanodine Receptors and Their Association with Myopathies—Present State, Challenges, and Perspectives
Genetic Testing Medical Policy – Genetics
Is Ryanodine Receptor Phosphorylation Key to the Fight Or Flight Response and Heart Failure? Thomas Eschenhagen
Catecholaminergic Polymorphic Ventricular Tachycardia
Top View
Calcium Entry Through TRPV1: a Potential Target for the Regulation of Proliferation and Apoptosis in Cancerous and Healthy Cells
Tbx20 Regulates a Genetic Program Essential to Adult Mouse Cardiomyocyte Function
Ion Channels in the P14 Rat Brain
Leaky Ryr2 Channels Unleash a Brainstem Spreading Depolarization
Ca2+ Handling in a Mice Model of CPVT Yueyi Wang
Chemistry of Cation Hydration and Conduction in a Skeletal Muscle Ryanodine Receptor
Table S1. Primers and Probes Used in Qpcr Analysis
Phenytoin Reduces Activity of Cardiac Ryanodine Receptor 2; a Potential Mechanism for Its Cardioprotective Action S
De Novo Mutations in Moderate Or Severe Intellectual Disability
Arrhythmia Mutations in Calmodulin Cause Conformational Changes That Affect Interactions with the Cardiac Voltage-Gated Calcium Channel
Pediatric Catecholaminergic Polymorphic Ventricular Tachycardia: a Translational Perspective for the Clinician-Scientist
Somatic Mutations
Supplementary Material
Polycystin‐2 Plays an Essential Role in Glucose Starvation‐Induced
Mrna and Mirna Profiles in the Nucleus Accumbens Are Related To
Supplementary Table 1 Molecular and Genetic Characteristics of Inherited Cardiac Channelopathies
Aberrant Intracellular Calcium Cycling in the Heart
Genetics and Cardiac Channelopathies
CPG Islandtargetid Chr MAPINFO SYMBOL 29 TRUE Cg00027083
The Ryanodine Receptor As a Sensor for Cellular Environments in Muscles
UNIVERSITY of CALIFORNIA SAN DIEGO the KCNMA1 Drosophila
Official Symbol Accession Alias / Previous Symbol Official Full Name
Ncounter® Mouse Neuropathology Panel - Gene and Probe Details
RNA-Sequencing Identifies Dysregulation of the Human Pancreatic Islet Transcriptome
Molecular Basis for Allosteric Regulation of the Type 2 Ryanodine Receptor Channel Gating by Key Modulators
Functional Analysis of Ryanodine Receptor 2 Mutations in Induced Pluripotent Stem Cell- Derived Cardiomyocytes from CPVT Patients
Systems-Level Perspective of Sudden Infant Death Syndrome
Ryanodine Receptor 2 Mutation: Not Only Catecholaminergic Polymorphic Ventricular Tachycardia but Also Epileptiform Discharges in Electroencephalogram
The Role of Modified UNC-68 in Age-Related Caenorhabditis Elegans Muscle Function Loss
Molecular Basis for Gating and Regulation of Cardiac Ryanodine Receptor: Underlying Mechanisms for Gain- and Loss-Of Function Mutations
Cellular and Molecular Landscape of Mammalian Sinoatrial Node Revealed by Single-Cell RNA Sequencing
Supporting Information Materials and Methods
Download Author Version (PDF)
2008 Study Book: Part 2
Dellostritto Dissertation
The Molecular and Electrophysiological Characterisation of Catecholaminergic Polymorphic Ventricular Tachycardia
Ion Channels 3 1
Decreased Polycystin 2 Expression Alters Calcium-Contraction Coupling and Changes Β-Adrenergic Signaling Pathways
Permeation and Inhibition of Polycystin-L Channel by Monovalent Organic Cations ⁎ Xiao-Qing Dai, Edward Karpinski, Xing-Zhen Chen