Secondary mitochondrial dysfunction across the spectrum of hereditary and acquired muscle disorders-Reference-Cited by-同舟云学术

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Secondary mitochondrial dysfunction across the spectrum of hereditary and acquired muscle disorders

Published:2024-09 Issue: Volume:78 Page:101945
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Mak Gloria^ORCID,Tarnopolsky Mark^ORCID,Lu Jian-Qiang

Publisher

Elsevier BV

Reference133 articles.

1. Limb immobilization induces a coordinate down-regulation of mitochondrial and other metabolic pathways in men and women;Abadi;PLoS One,2009

2. Mitochondrial abnormalities in dermatomyositis: Characteristic pattern of neuropathology;Alhatou;J. Mol. Histol.,2004

3. Immune-mediated necrotizing myopathy: Clinical features and pathogenesis;Allenbach;Nat. Rev. Rheumatol.,2020

4. Dynamic transcriptomic analysis reveals suppression of PGC1alpha/ERRalpha drives perturbed myogenesis in facioscapulohumeral muscular dystrophy;Banerji;Hum. Mol. Genet.,2019

5. Loss of dysferlin or myoferlin results in differential defects in excitation-contraction coupling in mouse skeletal muscle;Barefield;Sci. Rep.,2021

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