ER stress disturbs SR/ER-mitochondria Ca<sup>2+</sup> transfer: Implications in Duchenne muscular dystrophy.
Pauly, Marion; Angebault-Prouteau, Claire; Dridi, Haikel; Notarnicola, Cécile; Scheuermann, Valérie; Lacampagne, Alain; Matecki, Stefan; Fauconnier, Jérémy.
Biochim Biophys Acta Mol Basis Dis
; 1863(9): 2229-2239, 2017 09.
Artigo em Inglês | MEDLINE | ID: mdl-28625916
Exon Skipping Therapy.
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?
Ciliary Hedgehog Signaling Restricts Injury-Induced Adipogenesis.
Circ-ZNF609 Is a Circular RNA that Can Be Translated and Functions in Myogenesis.
Breath isoprene: muscle dystrophy patients support the concept of a pool of isoprene in the periphery of the human body.
A long noncoding RNA controls muscle differentiation by functioning as a competing endogenous RNA.
The role of Notch signaling in muscle progenitor cell depletion and the rapid onset of histopathology in muscular dystrophy.
What can Duchenne Connect teach us about treating Duchenne muscular dystrophy?
The importance of genetic diagnosis for Duchenne muscular dystrophy.