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

Oxytocin and vasopressin in the human brain: social neuropeptides for translational medicine

(2011) Andreas Meyer-Lindenberg et al.   NATURE REVIEWS NEUROSCIENCE

The I4895T mutation in the type 1 ryanodine receptor induces fiber-type specific alterations in skeletal muscle that mimic premature aging

(2010) Simona Boncompagni et al.   AGING CELL

Neuronal Calcium Homeostasis and Dysregulation

(2010) Marc Gleichmann et al.   ANTIOXIDANTS & REDOX SIGNALING

Mechanistic models for muscle diseases and disorders originating in the sarcoplasmic reticulum

(2010) David H. MacLennan et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

de novo RYR1 heterozygous mutation (I4898T) causing lethal core–rod myopathy in twins

(2010) Aurelio Hernandez-Lain et al.   European Journal of Medical Genetics

Muscle weakness inRyr1I4895T/WTknock-in mice as a result of reduced ryanodine receptor Ca2+ion permeation and release from the sarcoplasmic reticulum

(2010) Ryan E. Loy et al.   JOURNAL OF GENERAL PHYSIOLOGY

Ryanodine Receptors: Structure, Expression, Molecular Details, and Function in Calcium Release

(2010) J. T. Lanner et al.   Cold Spring Harbor Perspectives in Biology

Congenital myopathies - a comprehensive update of recent advancements

(2009) M. C. Sharma et al.   ACTA NEUROLOGICA SCANDINAVICA

Homeostatic and stimulus-induced coupling of the L-type Ca2+ channel to the ryanodine receptor in the hippocampal neuron in slices

(2009) Jonathan Berrout et al.   CELL CALCIUM

Suppression of Ca2+syntillas increases spontaneous exocytosis in mouse adrenal chromaffin cells

(2009) Jason J. Lefkowitz et al.   JOURNAL OF GENERAL PHYSIOLOGY

Individual Calcium Syntillas Do Not Trigger Spontaneous Exocytosis from Nerve Terminals of the Neurohypophysis

(2009) J. M. McNally et al.   JOURNAL OF NEUROSCIENCE

Ionic conditions modulate stimulus-induced capacitance changes in isolated neurohypophysial terminals of the rat

(2009) Héctor G. Marrero et al.   JOURNAL OF PHYSIOLOGY-LONDON

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

(2009) E. Zvaritch et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

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

(2009) Srinivas Ramachandran et al.   PLoS Computational Biology

Calcium Sparks

(2008) Heping Cheng et al.   PHYSIOLOGICAL REVIEWS