Respiratory chain dysfunction in perifascicular muscle fibres in patients with dermatomyositis is associated with mitochondrial DNA depletion
出版年份 2022 全文链接
标题
Respiratory chain dysfunction in perifascicular muscle fibres in patients with dermatomyositis is associated with mitochondrial DNA depletion
作者
关键词
-
出版物
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
Volume -, Issue -, Pages -
出版商
Wiley
发表日期
2022-07-27
DOI
10.1111/nan.12841
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients with mitochondrial myopathy associated with the homoplasmic m.14674T>C variant
- (2021) Sara Roos et al. BRAIN PATHOLOGY
- Co-expression network analysis reveals the pivotal role of mitochondrial dysfunction and interferon signature in juvenile dermatomyositis
- (2020) Danli Zhong et al. PeerJ
- Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencing
- (2020) Carola Hedberg‐Oldfors et al. BRAIN PATHOLOGY
- Accurate mapping of mitochondrial DNA deletions and duplications using deep sequencing
- (2020) Swaraj Basu et al. PLoS Genetics
- 239th ENMC International Workshop: Classification of dermatomyositis, Amsterdam, the Netherlands, 14–16 December 2018
- (2019) Andrew L. Mammen et al. NEUROMUSCULAR DISORDERS
- Classification of myositis
- (2018) Ingrid E. Lundberg et al. Nature Reviews Rheumatology
- Development of a New Classification System for Idiopathic Inflammatory Myopathies Based on Clinical Manifestations and Myositis-Specific Autoantibodies
- (2018) Kubéraka Mariampillai et al. JAMA Neurology
- Microvascular alterations and the role of complement in dermatomyositis
- (2016) Rajat Lahoria et al. BRAIN
- The genetics and pathology of mitochondrial disease
- (2016) Charlotte L Alston et al. JOURNAL OF PATHOLOGY
- Inflammatory Muscle Diseases
- (2015) Marinos C. Dalakas NEW ENGLAND JOURNAL OF MEDICINE
- A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis
- (2015) Mariana C. Rocha et al. Scientific Reports
- Assessing Mitochondrial DNA Variation and Copy Number in Lymphocytes of ~2,000 Sardinians Using Tailored Sequencing Analysis Tools
- (2015) Jun Ding et al. PLoS Genetics
- Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations
- (2014) S. Roos et al. NEUROMUSCULAR DISORDERS
- Subnormal levels of POLγA cause inefficient initiation of light-strand DNA synthesis and lead to mitochondrial DNA deletions and autosomal dominant progressive external ophthalmoplegia
- (2013) Sara Roos et al. HUMAN MOLECULAR GENETICS
- Human mitochondrial DNA: roles of inherited and somatic mutations
- (2012) Eric A. Schon et al. NATURE REVIEWS GENETICS
- Diagnosis and treatment of mitochondrial myopathies
- (2011) Gerald Pfeffer et al. ANNALS OF MEDICINE
- Mitochondrial pathology in immune and inflammatory myopathies
- (2010) Arun S Varadhachary et al. CURRENT OPINION IN RHEUMATOLOGY
- Mitochondrial DNA depletion syndromes – Many genes, common mechanisms
- (2010) Anu Suomalainen et al. NEUROMUSCULAR DISORDERS
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