Dissecting the mechanisms underlying the accumulation of mitochondrial DNA deletions in human skeletal muscle-Reference-Cited by-同舟云学术

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Dissecting the mechanisms underlying the accumulation of mitochondrial DNA deletions in human skeletal muscle

Published:2014-04-15 Issue:17 Volume:23 Page:4612-4620
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Campbell G.,Krishnan K. J.,Deschauer M.,Taylor R. W.,Turnbull D. M.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/23/17/4612/2212866/ddu176.pdf

Reference33 articles.

1. Prevalence of mitochondrial DNA disease in adults

2. Somatic Mitochondrial DNA Mutations in Mammalian Aging

3. Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons

4. High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

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1. Dissecting the sequential evolution of a selfish mitochondrial genome in Caenorhabditis elegans;Heredity;2024-07-05

2. Nanobiopsy investigation of the subcellular mtDNA heteroplasmy in human tissues;Scientific Reports;2024-06-14

3. Mechanisms and pathologies of human mitochondrial DNA replication and deletion formation;Biochemical Journal;2024-05-28

4. Myopathy and Ophthalmologic Abnormalities in Association With Multiple Skeletal Muscle Mitochondrial DNA Deletions;Journal of Neuro-Ophthalmology;2023-09-04

5. Nanobiopsy investigation of the subcellular mtDNA heteroplasmy in human tissues;2023-07-20

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