Leaky RyR2 trigger ventricular arrhythmias in Duchenne muscular dystrophy.
Fauconnier, Jérémy; Thireau, Jérôme; Reiken, Steven; Cassan, Cécile; Richard, Sylvain; Matecki, Stefan; Marks, Andrew R; Lacampagne, Alain.
Proc Natl Acad Sci U S A
; 107(4): 1559-64, 2010 Jan 26.
Artigo em Inglês | MEDLINE | ID: mdl-20080623
Breath isoprene: muscle dystrophy patients support the concept of a pool of isoprene in the periphery of the human body.
Monitoring disease activity noninvasively in the <i>mdx</i> model of Duchenne muscular dystrophy.
What has the mdx mouse model of Duchenne muscular dystrophy contributed to our understanding of this disease?
Exon Skipping Therapy.
Ciliary Hedgehog Signaling Restricts Injury-Induced Adipogenesis.
Circ-ZNF609 Is a Circular RNA that Can Be Translated and Functions in Myogenesis.
Crosstalk between RyR2 oxidation and phosphorylation contributes to cardiac dysfunction in mice with Duchenne muscular dystrophy.
Enhanced currents through L-type calcium channels in cardiomyocytes disturb the electrophysiology of the dystrophic heart.
A long noncoding RNA controls muscle differentiation by functioning as a competing endogenous RNA.
RNA mis-splicing in disease.