"Suppression, Genetic" 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.
Mutation process that restores the wild-type PHENOTYPE in an organism possessing a mutationally altered GENOTYPE. The second "suppressor" mutation may be on a different gene, on the same gene but located at a distance from the site of the primary mutation, or in extrachromosomal genes (EXTRACHROMOSOMAL INHERITANCE).
Descriptor ID |
D013489
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MeSH Number(s) |
G05.365.590.835 G05.558.835
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Concept/Terms |
Suppression, Genetic- Suppression, Genetic
- Genetic Suppression
- Genetic Suppressions
- Suppressions, Genetic
Suppressor Mutation- Suppressor Mutation
- Mutation, Suppressor
- Mutations, Suppressor
- Suppressor Mutations
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Below are MeSH descriptors whose meaning is more general than "Suppression, Genetic".
Below are MeSH descriptors whose meaning is more specific than "Suppression, Genetic".
This graph shows the total number of publications written about "Suppression, Genetic" by people in this website by year, and whether "Suppression, Genetic" 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 |
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1995 | 1 | 0 | 1 |
1999 | 0 | 1 | 1 |
2006 | 1 | 0 | 1 |
2008 | 1 | 0 | 1 |
2009 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Suppression, Genetic" by people in Profiles.
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Natori Y, Tagami K, Murakami K, Yoshida S, Tanigawa O, Moh Y, Masuda K, Wada T, Suzuki S, Nanamiya H, Tozawa Y, Kawamura F. Transcription activity of individual rrn operons in Bacillus subtilis mutants deficient in (p)ppGpp synthetase genes, relA, yjbM, and ywaC. J Bacteriol. 2009 Jul; 191(14):4555-61.
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Park H, Davidson E, King MP. Overexpressed mitochondrial leucyl-tRNA synthetase suppresses the A3243G mutation in the mitochondrial tRNA(Leu(UUR)) gene. RNA. 2008 Nov; 14(11):2407-16.
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Kirino Y, Yasukawa T, Marjavaara SK, Jacobs HT, Holt IJ, Watanabe K, Suzuki T. Acquisition of the wobble modification in mitochondrial tRNALeu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect. Hum Mol Genet. 2006 Mar 15; 15(6):897-904.
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Matsumura I, Kitamura T, Wakao H, Tanaka H, Hashimoto K, Albanese C, Downward J, Pestell RG, Kanakura Y. Transcriptional regulation of the cyclin D1 promoter by STAT5: its involvement in cytokine-dependent growth of hematopoietic cells. EMBO J. 1999 Mar 1; 18(5):1367-77.
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Bailis AM, Maines S, Negritto MT. The essential helicase gene RAD3 suppresses short-sequence recombination in Saccharomyces cerevisiae. Mol Cell Biol. 1995 Aug; 15(8):3998-4008.
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Boettiger D, Menko AS. Effect of oncogenes on chondrogenesis. Pathol Immunopathol Res. 1988; 7(1-2):32-7.