"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.
| Descriptor ID |
D005816
|
| MeSH Number(s) |
E05.393.281.526
|
| 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 this website by year, and whether "Genetic Complementation Test" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2010 | 0 | 1 | 1 |
| 2012 | 0 | 3 | 3 |
| 2016 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Genetic Complementation Test" by people in Profiles.
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Stability of Single-Parent Gene Expression Complementation in Maize Hybrids upon Water Deficit Stress. Plant Physiol. 2017 02; 173(2):1247-1257.
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Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH. Hum Mol Genet. 2012 Sep 15; 21(18):3969-83.
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Molecular interactions of ROOTLESS CONCERNING CROWN AND SEMINAL ROOTS, a LOB domain protein regulating shoot-borne root initiation in maize (Zea mays L.). Philos Trans R Soc Lond B Biol Sci. 2012 Jun 05; 367(1595):1542-51.
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Molecular signatures of the three stem cell lineages in hydra and the emergence of stem cell function at the base of multicellularity. Mol Biol Evol. 2012 Nov; 29(11):3267-80.
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Arabidopsis thaliana transcription factors bZIP19 and bZIP23 regulate the adaptation to zinc deficiency. Proc Natl Acad Sci U S A. 2010 Jun 01; 107(22):10296-301.
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IFAP syndrome is caused by deficiency in MBTPS2, an intramembrane zinc metalloprotease essential for cholesterol homeostasis and ER stress response. Am J Hum Genet. 2009 Apr; 84(4):459-67.
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Foot differentiation and genomic plasticity in Hydra: lessons from the PPOD gene family. Dev Genes Evol. 2006 Feb; 216(2):57-68.
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Mammalian cells express two VPS4 proteins both of which are involved in intracellular protein trafficking. J Mol Biol. 2001 Sep 21; 312(3):469-80.
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The VPS4 gene is involved in protein transport out of a yeast pre-vacuolar endosome-like compartment. Curr Genet. 1997 Jun; 31(6):469-80.
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Domain 5 interacts with domain 6 and influences the second transesterification reaction of group II intron self-splicing. Nucleic Acids Res. 1993 Apr 25; 21(8):1797-804.
MeSH information
