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Duchenne's muscular dystrophy involves a defective transsulfuration pathway activity

  • Published:2021-09 Issue: Volume:45 Page:102040
  • ISSN:2213-2317
  • Container-title:Redox Biology
  • language:en
  • Short-container-title:Redox Biology

Author:

Panza E.,Vellecco V.,Iannotti F.A.,Paris D.,Manzo O.L.,Smimmo M.,Mitilini N.,Boscaino A.,de Dominicis G.,Bucci M.,Di Lorenzo A.,Cirino G.

Funder

Duchenne Parent Project

Ministero dell’Istruzione, dell’Università e della Ricerca

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,Clinical Biochemistry

Reference68 articles.

1. Determinants of the incidence of Duchenne muscular dystrophy;Stark;Ann. Transl. Med.,2015

2. Dystrophin protects the sarcolemma from stresses developed during muscle contraction;Petrof;Proc. Natl. Acad. Sci. Unit. States Am.,1993

3. The dystrophin-associated protein complex;Ehmsen;J. Cell Sci.,2002

4. Short telomeres and stem cell exhaustion model Duchenne muscular dystrophy in mdx/mTR mice;Sacco;Cell,2010

5. Anti-inflammatory drugs for Duchenne muscular dystrophy: focus on skeletal muscle-releasing factors;Miyatake;Drug Des. Dev. Ther.,2016
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