"Genes, 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.
Genes that are located on the MITOCHONDRIAL DNA. Mitochondrial inheritance is often referred to as maternal inheritance but should be differentiated from maternal inheritance that is transmitted chromosomally.
| Descriptor ID |
D050259
|
| MeSH Number(s) |
G05.360.340.024.340.365 G05.420.275.500
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Genes, Mitochondrial".
Below are MeSH descriptors whose meaning is more specific than "Genes, Mitochondrial".
This graph shows the total number of publications written about "Genes, Mitochondrial" by people in this website by year, and whether "Genes, 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 |
|---|
| 2009 | 0 | 1 | 1 |
| 2010 | 0 | 1 | 1 |
| 2011 | 1 | 1 | 2 |
| 2014 | 2 | 0 | 2 |
| 2015 | 2 | 1 | 3 |
| 2016 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2019 | 1 | 1 | 2 |
| 2021 | 1 | 0 | 1 |
| 2023 | 1 | 2 | 3 |
| 2024 | 1 | 1 | 2 |
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Below are the most recent publications written about "Genes, Mitochondrial" by people in Profiles.
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Rapid evolution of mitochondrion-related genes in haplodiploid arthropods. BMC Biol. 2024 Oct 10; 22(1):229.
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Deregulation of mitochondrial gene expression in cancer: mechanisms and therapeutic opportunities. Br J Cancer. 2024 Nov; 131(9):1415-1424.
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Mitochondrial Gene Abnormality Complicated by Perinatal-Onset Depression. Prim Care Companion CNS Disord. 2023 09 07; 25(5).
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Core mitochondrial genes are down-regulated during SARS-CoV-2 infection of rodent and human hosts. Sci Transl Med. 2023 08 09; 15(708):eabq1533.
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New Dielis species and structural dichotomy of the mitochondrial cox2 gene in Scoliidae wasps. Sci Rep. 2023 02 02; 13(1):1950.
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Loss of coordinated expression between ribosomal and mitochondrial genes revealed by comprehensive characterization of a large family with a rare Mendelian disorder. Genomics. 2021 07; 113(4):1895-1905.
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Validation of a mitochondrial RNA therapeutic strategy using fibroblasts from a Leigh syndrome patient with a mutation in the mitochondrial ND3 gene. Sci Rep. 2020 05 05; 10(1):7511.
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Application of metagenomic shotgun sequencing to detect vector-borne pathogens in clinical blood samples. PLoS One. 2019; 14(10):e0222915.
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Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3'-end processing. Hum Mutat. 2019 10; 40(10):1731-1748.
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Reply to Lutz-Bonengel et al.: Biparental mtDNA transmission is unlikely to be the result of nuclear mitochondrial DNA segments. Proc Natl Acad Sci U S A. 2019 02 05; 116(6):1823-1824.