Permeabilised skeletal muscle reveals mitochondrial deficiency in malignant hyperthermia-susceptible individuals

Author:

Chang Leon,Daly Catherine,Miller Dorota M.,Allen Paul D.,Boyle John P.,Hopkins Philip M.,Shaw Marie-Anne

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

Anesthesiology and Pain Medicine

Reference40 articles.

1. Malignant hyperthermia – pharmacology of triggering;Hopkins;Br J Anaesth,2011

2. Malignant hyperthermia: advances in clinical management and diagnosis;Hopkins;Br J Anaesth,2000

3. Molecular cloning of cDNA encoding human and rabbit forms of the Ca2+ release channel (ryanodine receptor) of skeletal muscle sarcoplasmic reticulum;Zorzato;J Biol Chem,1990

4. Functional analysis of the R1086H malignant hyperthermia mutation in the DHPR reveals an unexpected influence of the III-IV loop on skeletal muscle EC coupling;Weiss;Am J Physiol Cell Physiol,2004

5. Malignant hyperthermia susceptibility arising from altered resting coupling between the skeletal muscle L-type Ca2+ channel and the type 1 ryanodine receptor;Eltit;Proc Natl Acad Sci USA,2012

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