RyR1-related myopathy mutations in ATP and calcium binding sites impair channel regulation (original) (raw)

Mapping domains and mutations on the skeletal muscle ryanodine receptor channel

Susan Treves

Trends in Molecular Medicine, 2012

View PDFchevron_right

Functional Effects of Central Core Disease Mutations in the Cytoplasmic Region of the Skeletal Muscle Ryanodine Receptor

Zhao Loke

Journal of General Physiology, 2001

View PDFchevron_right

Function of a mutant ryanodine receptor (T4709M) linked to congenital myopathy

János Almássy

Scientific Reports

View PDFchevron_right

Muscle weakness in Ryr1I4895T/WT knock-in mice as a result of reduced ryanodine receptor Ca2+ ion permeation and release from the sarcoplasmic reticulum

Ryan Loy

The Journal of General Physiology, 2010

View PDFchevron_right

Quantitative RyR1 reduction and loss of calcium sensitivity of RyR1Q1970fsX16+A4329D cause cores and loss of muscle strength

Jan Eckhardt

Human Molecular Genetics, 2019

View PDFchevron_right

Ryanodine receptor defects in muscle genetic diseases

Marisa Brini

Biochemical and Biophysical Research Communications, 2004

View PDFchevron_right

Congenital muscle disorders with cores: the ryanodine receptor calcium channel paradigm

Susan Treves

Current Opinion in Pharmacology, 2008

View PDFchevron_right

Hypernitrosylated ryanodine receptor calcium release channels are leaky in dystrophic muscle

Alain Lacampagne

Nature Medicine, 2009

View PDFchevron_right

RyR1-mediated Ca2+ Leak and Ca2+ Entry Determine Resting Intracellular Ca2+ in Skeletal Myotubes

Tadeusz Molinski

Journal of Biological Chemistry, 2010

View PDFchevron_right

A Structural Model of the Pore-Forming Region of the Skeletal Muscle Ryanodine Receptor (RyR1)

Nikolay Dokholyan

PLoS Computational Biology, 2009

View PDFchevron_right

RyR1 Deficiency in Congenital Myopathies Disrupts Excitation-Contraction Coupling

Michael Duchen

Human Mutation, 2013

View PDFchevron_right

Identification of four novel mutations in the C-terminal membrane spanning domain of the ryanodine receptor 1: association with central core disease and alteration of calcium homeostasis

Frank Lehmann-Horn

Human Molecular Genetics, 2001

View PDFchevron_right

Quantitative reduction of RyR1 protein caused by a single-allele frameshift mutation in RYR1 ex36 impairs the strength of adult skeletal muscle fibres

Jan Eckhardt

Human Molecular Genetics, 2019

View PDFchevron_right

Ca2+ dysregulation in Ryr1I4895T/wt mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods

Christine Seidman, E. Zvaritch

Proceedings of the National Academy of Sciences, 2009

View PDFchevron_right

Role of Ryanodine Receptors in the Assembly of Calcium Release Units in Skeletal Muscle

Clara Franzini-armstrong

The Journal of Cell Biology, 1998

View PDFchevron_right

Contractile impairment and structural alterations of skeletal muscles from knockout mice lacking type 1 and type 3 ryanodine receptors

Vincenzo Sorrentino

FEBS Letters, 1998

View PDFchevron_right

Evidence for a role of C-terminus in Ca2+ inactivation of skeletal muscle Ca2+ release channel (ryanodine receptor)

Daniel Pasek

FEBS Letters, 1999

View PDFchevron_right

Insights into channel modulation mechanism of RYR1 mutants using Ca2+ imaging and molecular dynamics

Masamitsu Iino

Journal of General Physiology, 2019

View PDFchevron_right

Type 1 ryanodine receptor knock-in mutation causing central core disease of skeletal muscle also displays a neuronal phenotype

E. Zvaritch

Proceedings of the National Academy of Sciences, 2012

View PDFchevron_right

Structural Determinants of Skeletal Muscle Ryanodine Receptor Gating

Nikolay Dokholyan

Journal of Biological Chemistry, 2013

View PDFchevron_right

Dampened activity of ryanodine receptor channels in mutant skeletal muscle lacking TRIC-A

Chris Lindsay

The Journal of physiology, 2017

View PDFchevron_right

Clinical and functional effects of a deletion in a COOH-terminal lumenal loop of the skeletal muscle ryanodine receptor

Susan Treves

Human Molecular Genetics, 2003

View PDFchevron_right

ATP-induced activation of expressed RyR3 at low free calcium

Maria D I Manunta, Maria Manunta

View PDFchevron_right

Differential distribution of ryanodine receptor type 3 (RyR3) gene product in mammalian skeletal muscles

Vincenzo Sorrentino

The Biochemical journal, 1996

View PDFchevron_right

In vivo RyR1 reduction in muscle triggers a core-like myopathy

Diane Giovannini

2020

View PDFchevron_right

Core skeletal muscle ryanodine receptor calcium release complex

Marco Casarotto

Clinical and Experimental Pharmacology and Physiology, 2016

View PDFchevron_right

Ryanodine Receptor Oxidation Causes Intracellular Calcium Leak and Muscle Weakness in Aging

Alain Lacampagne

Cell Metabolism, 2011

View PDFchevron_right

Ca2+ influx through 1S DHPR may play a role in regulating Ca2+ release from RyR1 in skeletal muscle

Cecilia Paolini

AJP: Cell Physiology, 2003

View PDFchevron_right