Genetic Complementation Test
"Genetic Complementation Test" 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.
A test used to determine whether or not complementation (compensation in the form of dominance) will occur in a cell with a given mutant phenotype when another mutant genome, encoding the same mutant phenotype, is introduced into that cell.
Concept/Terms
Genetic Complementation Test- Genetic Complementation Test
- Complementation Test, Genetic
- Complementation Tests, Genetic
- Genetic Complementation Tests
- Trans Test
- Trans Tests
- Complementation Test
- Complementation Tests
- Allelism Test
- Allelism Tests
Below are MeSH descriptors whose meaning is more general than "Genetic Complementation Test".
Below are MeSH descriptors whose meaning is more specific than "Genetic Complementation Test".
This graph shows the total number of publications written about "Genetic Complementation Test" by people in Harvard Catalyst Profiles by year, and whether "Genetic Complementation Test" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1993 | 1 | 17 | 18 |
1994 | 2 | 18 | 20 |
1995 | 2 | 22 | 24 |
1996 | 0 | 23 | 23 |
1997 | 1 | 15 | 16 |
1998 | 1 | 13 | 14 |
1999 | 0 | 16 | 16 |
2000 | 1 | 19 | 20 |
2001 | 0 | 14 | 14 |
2002 | 0 | 17 | 17 |
2003 | 1 | 11 | 12 |
2004 | 0 | 9 | 9 |
2005 | 0 | 10 | 10 |
2006 | 0 | 9 | 9 |
2007 | 0 | 11 | 11 |
2008 | 0 | 16 | 16 |
2009 | 0 | 14 | 14 |
2010 | 0 | 15 | 15 |
2011 | 2 | 6 | 8 |
2012 | 0 | 11 | 11 |
2013 | 0 | 10 | 10 |
2014 | 0 | 4 | 4 |
2015 | 0 | 7 | 7 |
2016 | 1 | 8 | 9 |
2017 | 1 | 11 | 12 |
2018 | 0 | 4 | 4 |
2019 | 0 | 1 | 1 |
2020 | 1 | 2 | 3 |
2021 | 0 | 2 | 2 |
2022 | 0 | 1 | 1 |
Below are the most recent publications written about "Genetic Complementation Test" by people in Profiles.
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Recombinant Lloviu virus as a tool to study viral replication and host responses. PLoS Pathog. 2022 02; 18(2):e1010268.
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Wild-type FUS corrects ALS-like disease induced by cytoplasmic mutant FUS through autoregulation. Mol Neurodegener. 2021 09 06; 16(1):61.
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Mammalian cell proliferation requires noncatalytic functions of O-GlcNAc transferase. Proc Natl Acad Sci U S A. 2021 01 26; 118(4).
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A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizures. Neurogenetics. 2020 10; 21(4):259-267.
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Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic-dyskinetic encephalopathy. Hum Mutat. 2020 07; 41(7):1263-1279.
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A proactive genotype-to-patient-phenotype map for cystathionine beta-synthase. Genome Med. 2020 01 30; 12(1):13.
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Destruction complex dynamics: Wnt/ß-catenin signaling alters Axin-GSK3ß interactions in vivo. Development. 2019 07 02; 146(13).
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A single-cell platform for reconstituting and characterizing fatty acid elongase component enzymes. PLoS One. 2019; 14(3):e0213620.
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Neural blastocyst complementation enables mouse forebrain organogenesis. Nature. 2018 11; 563(7729):126-130.
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Genome-wide SWAp-Tag yeast libraries for proteome exploration. Nat Methods. 2018 08; 15(8):617-622.