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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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 Cis Test Cis Test Cis Tests Cis-Trans Test Cis-Trans Test Cis Trans Test Cis-Trans Tests

Below are MeSH descriptors whose meaning is more general than "Genetic Complementation Test".

Analytical, Diagnostic and Therapeutic Techniques and Equipment [E]
Investigative Techniques [E05]
Genetic Techniques [E05.393]
Crosses, Genetic [E05.393.281]
Genetic Complementation Test [E05.393.281.526]

Below are MeSH descriptors whose meaning is related to "Genetic Complementation Test".

Below are MeSH descriptors whose meaning is more specific than "Genetic Complementation Test".

publications

Timeline | Most Recent

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.

Bar chart showing 43 publications over 21 distinct years, with a maximum of 5 publications in 2003

To see the data from this visualization as text, click here.

Year	Minor Topic	Total
1994	1	1
1995	1	1
1996	2	2
1997	2	2
1998	1	1
2000	2	2
2001	2	2
2002	3	3
2003	5	5
2004	2	2
2005	4	4
2006	1	1
2007	2	2
2008	4	4
2009	1	1
2010	3	3
2011	2	2
2012	1	1
2013	1	1
2015	2	2
2016	1	1

Below are the most recent publications written about "Genetic Complementation Test" by people in Profiles.

Zhang Q, Wang D, Jiang G, Liu W, Deng Q, Li X, Qian W, Ouellet H, Sun J. EsxA membrane-permeabilizing activity plays a key role in mycobacterial cytosolic translocation and virulence: effects of single-residue mutations at glutamine 5. Sci Rep. 2016 09 07; 6:32618.

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Lin CJ, Smibert P, Zhao X, Hu JF, Ramroop J, Kellner SM, Benton MA, Govind S, Dedon PC, Sternglanz R, Lai EC. An extensive allelic series of Drosophila kae1 mutants reveals diverse and tissue-specific requirements for t6A biogenesis. RNA. 2015 Dec; 21(12):2103-18.

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Weems E, Singha UK, Hamilton V, Smith JT, Waegemann K, Mokranjac D, Chaudhuri M. Functional complementation analyses reveal that the single PRAT family protein of trypanosoma brucei is a divergent homolog of Tim17 in saccharomyces cerevisiae. Eukaryot Cell. 2015 Mar; 14(3):286-96.

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Sha J, Rosenzweig JA, Kozlova EV, Wang S, Erova TE, Kirtley ML, van Lier CJ, Chopra AK. Evaluation of the roles played by Hcp and VgrG type 6 secretion system effectors in Aeromonas hydrophila SSU pathogenesis. Microbiology (Reading). 2013 Jun; 159(Pt 6):1120-1135.

View in: PubMed
Sarovich DS, Price EP, Von Schulze AT, Cook JM, Mayo M, Watson LM, Richardson L, Seymour ML, Tuanyok A, Engelthaler DM, Pearson T, Peacock SJ, Currie BJ, Keim P, Wagner DM. Characterization of ceftazidime resistance mechanisms in clinical isolates of Burkholderia pseudomallei from Australia. PLoS One. 2012; 7(2):e30789.

View in: PubMed
Raju BV, Esteve-Gassent MD, Karna SL, Miller CL, Van Laar TA, Seshu J. Oligopeptide permease A5 modulates vertebrate host-specific adaptation of Borrelia burgdorferi. Infect Immun. 2011 Aug; 79(8):3407-20.

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Nallaparaju KC, Yu JJ, Rodriguez SA, Zogaj X, Manam S, Guentzel MN, Seshu J, Murthy AK, Chambers JP, Klose KE, Arulanandam BP. Evasion of IFN-? signaling by Francisella novicida is dependent upon Francisella outer membrane protein C. PLoS One. 2011 Mar 31; 6(3):e18201.

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Johnston JB, Ouellet H, Ortiz de Montellano PR. Functional redundancy of steroid C26-monooxygenase activity in Mycobacterium tuberculosis revealed by biochemical and genetic analyses. J Biol Chem. 2010 Nov 19; 285(47):36352-60.

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Heard M, Maina CV, Morehead BE, Hoener MC, Nguyen TQ, Williams CC, Rowan BG, Gissendanner CR. A functional NR4A nuclear receptor DNA-binding domain is required for organ development in Caenorhabditis elegans. Genesis. 2010 Aug; 48(8):485-91.

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Garcia AF, Abe LM, Erdem G, Cortez CL, Kurahara D, Yamaga K. An insert in the covS gene distinguishes a pharyngeal and a blood isolate of Streptococcus pyogenes found in the same individual. Microbiology (Reading). 2010 Oct; 156(Pt 10):3085-3095.

View in: PubMed

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