From worms to fish to mice

Identification of drug modifiers for RYR1-related myopathy using a multi-species discovery pipeline

(2020) Jonathan R Volpatti et al.   eLife

Mouse model of severe recessive RYR1-related myopathy

(2019) Stephanie Brennan et al.   HUMAN MOLECULAR GENETICS

Congenital myopathies: disorders of excitation–contraction coupling and muscle contraction

(2018) Heinz Jungbluth et al.   Nature Reviews Neurology

Malignant hyperthermia, environmental heat stress, and intracellular calcium dysregulation in a mouse model expressing the p.G2435R variant of RYR1

(2018) J.R. Lopez et al.   BRITISH JOURNAL OF ANAESTHESIA

P38α MAPK underlies muscular dystrophy and myofiber death through a Bax-dependent mechanism

(2014) Erin R. Wissing et al.   HUMAN MOLECULAR GENETICS

CeleST: Computer Vision Software for Quantitative Analysis of C. elegans Swim Behavior Reveals Novel Features of Locomotion

(2014) Christophe Restif et al.   PLoS Computational Biology