Mitochondrial Mutation Accumulation
Mitochondrial Mutation Accumulation is a biological phenomenon characterized by the progressive retention and increase of deleterious genetic alterations in mitochondrial DNA over time, distinguished from nuclear mutation accumulation by its maternal inheritance pattern, high mutation rate, and limited repair mechanisms in the mitochondrial genome.
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19.5K
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1.1K
Authors
392
Institutions
Publications per year
2017–2026
41
Parents
226
Mitochondrial DNA mutations in human colonic crypt stem cells
Robert W. Taylor, Martin Barron, Gillian M. Borthwick et al. · Journal of Clinical Investigation · 2003 · 520 citations · Full text
Life Sciences, Biology, Genetics +17
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392

Newcastle University
Newcastle upon Tyne, United Kingdom
17 h-index
75 publications
7.4K citations

Monash University
Melbourne, Australia
14 h-index
39 publications
3.4K citations
University of Washington
Seattle, United States
12 h-index
60 publications
5.4K citations
University College London
London, United Kingdom
9 h-index
17 publications
762 citations
Wellcome Centre for Mitochondrial Research
Newcastle upon Tyne, United Kingdom
8 h-index
36 publications
2.4K citations

National Yang Ming Chiao Tung University
Hsinchu, Taiwan
7 h-index
24 publications
2K citations
Newcastle Hospitals - Campus for Ageing and Vitality
Newcastle upon Tyne, United Kingdom
7 h-index
18 publications
921 citations
University of Wisconsin–Madison
Madison, United States
6 h-index
18 publications
4.5K citations
1–8 of 392
PNAS · 12 publications · 2.1K citations
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Repository · 10 publications · 979 citations
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MBE · 9 publications · 1.1K citations
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8 publications · 389 citations
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7 publications · 408 citations
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