 DNA, Mitochondrial
"DNA, Mitochondrial" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Double-stranded DNA of MITOCHONDRIA. In eukaryotes, the mitochondrial GENOME is circular and codes for ribosomal RNAs, transfer RNAs, and about 10 proteins.
| Descriptor ID |
D004272
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| MeSH Number(s) |
D13.444.308.283.225
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "DNA, Mitochondrial".
Below are MeSH descriptors whose meaning is more specific than "DNA, Mitochondrial".
This graph shows the total number of publications written about "DNA, Mitochondrial" by people in this website by year, and whether "DNA, Mitochondrial" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 0 | 1 | 1 | | 1996 | 0 | 1 | 1 | | 1997 | 1 | 1 | 2 | | 1998 | 1 | 1 | 2 | | 1999 | 1 | 0 | 1 | | 2000 | 1 | 0 | 1 | | 2001 | 2 | 0 | 2 | | 2002 | 1 | 1 | 2 | | 2003 | 3 | 2 | 5 | | 2004 | 3 | 4 | 7 | | 2005 | 6 | 4 | 10 | | 2006 | 4 | 3 | 7 | | 2007 | 3 | 2 | 5 | | 2008 | 2 | 3 | 5 | | 2009 | 3 | 2 | 5 | | 2010 | 0 | 8 | 8 | | 2011 | 3 | 9 | 12 | | 2012 | 2 | 2 | 4 | | 2013 | 3 | 7 | 10 | | 2014 | 2 | 2 | 4 | | 2015 | 4 | 3 | 7 | | 2016 | 4 | 1 | 5 | | 2017 | 4 | 2 | 6 | | 2018 | 4 | 4 | 8 | | 2019 | 3 | 2 | 5 | | 2020 | 4 | 2 | 6 | | 2021 | 5 | 5 | 10 | | 2022 | 0 | 1 | 1 | | 2023 | 1 | 4 | 5 | | 2024 | 1 | 4 | 5 |
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Below are the most recent publications written about "DNA, Mitochondrial" by people in Profiles.
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Fern?ndez AC, Estrella J, Oglesbee D, Larson AA, Van Hove JLK. The clinical utility in hospital-wide use of growth differentiation factor 15 as a biomarker for mitochondrial DNA-related disorders. J Inherit Metab Dis. 2025 01; 48(1):e12821.
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Karaa A, Bertini E, Carelli V, Cohen B, Ennes GM, Falk MJ, Goldstein A, Gorman G, Haas R, Hirano M, Klopstock T, Koenig MK, Kornblum C, Lamperti C, Lehman A, Longo N, Molnar MJ, Parikh S, Phan H, Pitceathly RDS, Saneto R, Scaglia F, Servidei S, Tarnopolsky M, Toscano A, Van Hove JLK, Vissing J, Vockley J, Finman JS, Abbruscato A, Brown DA, Sullivan A, Shiffer JA, Mancuso M. Genotype-specific effects of elamipretide in patients with primary mitochondrial myopathy: a post hoc analysis of the MMPOWER-3 trial. Orphanet J Rare Dis. 2024 Nov 21; 19(1):431.
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Kelly C, Trumpff C, Acosta C, Assuras S, Baker J, Basarrate S, Behnke A, Bo K, Bobba-Alves N, Champagne FA, Conklin Q, Cross M, De Jager P, Engelstad K, Epel E, Franklin SG, Hirano M, Huang Q, Junker A, Juster RP, Kapri D, Kirschbaum C, Kurade M, Lauriola V, Li S, Liu CC, Liu G, McEwen B, McGill MA, McIntyre K, Monzel AS, Michelson J, Prather AA, Puterman E, Rosales XQ, Shapiro PA, Shire D, Slavich GM, Sloan RP, Smith JLM, Spann M, Spicer J, Sturm G, Tepler S, de Schotten MT, Wager TD, Picard M. A platform to map the mind-mitochondria connection and the hallmarks of psychobiology: the MiSBIE study. Trends Endocrinol Metab. 2024 Oct; 35(10):884-901.
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Garcia EL, Cushing PE. Historical biogeography and the evolution of habitat preference in the North American camel spider family, Eremobatidae (Arachnida:Solifugae). Mol Phylogenet Evol. 2024 Dec; 201:108193.
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O'Halloran K, Hakimjavadi H, Bootwalla M, Ostrow D, Kerawala R, Cotter JA, Yellapantula V, Kaneva K, Wadhwani NR, Treece A, Foreman NK, Alexandrescu S, Velazquez Vega J, Biegel JA, Gai X. Pediatric Chordoma: A Tale of Two Genomes. Mol Cancer Res. 2024 08 02; 22(8):721-729.
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Lynch MT, Taub MA, Farfel JM, Yang J, Abadir P, De Jager PL, Grodstein F, Bennett DA, Mathias RA. Evaluating genomic signatures of aging in brain tissue as it relates to Alzheimer's disease. Sci Rep. 2023 09 07; 13(1):14747.
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Zhang H, Zhu Y, Suehiro Y, Mitani S, Xue D. AMPK-FOXO-IP3R signaling pathway mediates neurological and developmental defects caused by mitochondrial DNA mutations. Proc Natl Acad Sci U S A. 2023 09 05; 120(36):e2302490120.
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Squires JE, Miethke AG, Valencia CA, Hawthorne K, Henn L, Van Hove JLK, Squires RH, Bove K, Horslen S, Kohli R, Molleston JP, Romero R, Alonso EM, Bezerra JA, Guthery SL, Hsu E, Karpen SJ, Loomes KM, Ng VL, Rosenthal P, Mysore K, Wang KS, Friederich MW, Magee JC, Sokol RJ. Clinical spectrum and genetic causes of mitochondrial hepatopathy phenotype in children. Hepatol Commun. 2023 06 01; 7(6).
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Newman NJ, Yu-Wai-Man P, Subramanian PS, Moster ML, Wang AG, Donahue SP, Leroy BP, Carelli V, Biousse V, Vignal-Clermont C, Sergott RC, Sadun AA, Rebolleda Fern?ndez G, Chwalisz BK, Banik R, Bazin F, Roux M, Cox ED, Taiel M, Sahel JA. Randomized trial of bilateral gene therapy injection for m.11778G>A MT-ND4 Leber optic neuropathy. Brain. 2023 04 19; 146(4):1328-1341.
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Dimasuay KG, Berg B, Schaunaman N, Chu HW. Role of Myeloid Cell-Specific TLR9 in Mitochondrial DNA-Induced Lung Inflammation in Mice. Int J Mol Sci. 2023 Jan 04; 24(2).
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