or crossed. Complementation will ordinarily occur if the mutations are in different genes (intergenic complementation). Complementation may also occur...
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property whereby double stranded nucleic acids pair with each other Complementation (genetics), a test to determine if independent recessive mutant phenotypes...
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Heterozygote advantage (category Population genetics)
wild-type alleles, as discussed in the articles Heterosis and Complementation (genetics), but there were also findings of overdominance, especially in...
24 KB (3,026 words) - 08:37, 23 June 2025
compared with others and is a standard technique used in forensics. Complementation (genetics) DNA damage (naturally occurring) DNA damage theory of aging Epigenetics...
31 KB (3,815 words) - 04:28, 26 May 2025
Inbreeding depression (category Population genetics)
wild-type allele, this masking phenomenon is referred to as complementation (see complementation (genetics)). In general, sexual reproduction in eukaryotes has...
26 KB (2,922 words) - 19:43, 22 May 2025
between two alleles leads to intragenic complementation while disruption of transvection disrupts the complementation. Transvection is believed to occur through...
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Genetic studies of Jews (redirect from Jewish genetics)
are part of the population genetics discipline and are used to analyze the ancestry of Jewish populations, complementing research in other fields such...
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Competence factor Competent Complementarity genes Complementary DNA Complementation Complementation test Complete linkage Complex trait Component of fitness Composite...
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would otherwise be deleterious to sexual spore formation (see Complementation (genetics)). Saccharomyces cerevisiae, brewer's and baker's yeast, is in...
36 KB (4,688 words) - 10:30, 21 April 2025
Bimolecular fluorescence complementation (also known as BiFC) is a technology typically used to validate protein interactions. It is based on the association...
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Epistasis (redirect from Intragenic complementation)
cause epistasis. This is sometimes called allelic complementation, or interallelic complementation. It may be caused by several mechanisms, for example...
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(1983-07-01). "46,XX/46,XY chimerism in a phenotypically normal man" (PDF). Human Genetics. 64 (1): 86–89. doi:10.1007/BF00289485. ISSN 1432-1203. PMID 6575956. S2CID 25946104...
56 KB (6,402 words) - 06:55, 20 June 2025
Neurospora crassa (category Fungus genetics)
that would otherwise be harmful to sexual spore formation (see Complementation (genetics)). Neurospora crassa is not only a model organism for the study...
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FANCE (redirect from Fanconi anemia, complementation group e)
Fanconi anemia, complementation group E protein is a protein that in humans is encoded by the FANCE gene. The Fanconi anemia complementation group (FANC)...
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Xeroderma pigmentosum (redirect from Xeroderma pigmentosum, complementation group G)
infantile lethal cerebro-oculo-facio-skeletal syndrome. There are seven complementation groups, plus one variant form: There is no cure for the disorder; all...
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of gene clusters. His early work on intragenic complementation led to the insight that complementation between allelic mutants is of widespread occurrence...
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Quantitative genetics is the study of quantitative traits, which are phenotypes that vary continuously—such as height or mass—as opposed to phenotypes...
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ENU (section Non-complementation screens)
pathways are lost, then this leads to non-allelic non-complementation. In a non-complementation screen, an ENU-induced male is crossed with a female carrying...
22 KB (2,548 words) - 02:20, 7 September 2024
Ehlers–Danlos syndrome (section Genetics)
of Medical Genetics. Part C, Seminars in Medical Genetics. 175 (1): 8–26. doi:10.1002/ajmg.c.31552. PMID 28306229. S2CID 4440499. "Genetics and Inheritance...
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Hybrid (biology) (category Population genetics)
history of genetics, Hugo de Vries supposed these were caused by mutation. Genetic complementation is a hybridization test widely used in genetics to determine...
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Claude Shannon (redirect from An Algebra for Theoretical Genetics)
graduated from MIT in 1940 with a PhD in mathematics; his thesis focusing on genetics contained important results, while initially going unpublished. Shannon...
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Forward genetics is a molecular genetics approach of determining the genetic basis responsible for a phenotype. Forward genetics provides an unbiased approach...
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alone. In such a case, the phenomenon is referred to as intragenic complementation. PCC is a heteropolymer composed of α and β subunits in a α6β6 structure...
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of progeny. The masking effect of outcrossing is known as genetic complementation, an effect also recognized as hybrid vigor or heterosis. Once outcrossing...
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Protein complex (section Intragenic complementation)
phenomenon is referred to as intragenic complementation (also called inter-allelic complementation). Intragenic complementation has been demonstrated in many different...
25 KB (2,847 words) - 05:35, 2 June 2025
Cistron (category Genetics stubs)
to emphasize that molecular genes exhibit a specific behavior in a complementation test (cis-trans test); distinct positions (or loci) within a genome...
5 KB (648 words) - 06:08, 2 August 2024
Mendelian inheritance (redirect from Mendelian genetics)
inheritance by Thomas Hunt Morgan in 1915, they became the core of classical genetics. Ronald Fisher combined these ideas with the theory of natural selection...
38 KB (4,045 words) - 18:23, 23 May 2025
Blue–white screen (category Genetics techniques)
method is based on the principle of α-complementation of the β-galactosidase gene. This phenomenon of α-complementation was first demonstrated in work done...
13 KB (1,821 words) - 00:36, 3 December 2023
phenomenon is referred to as intragenic complementation (also called inter-allelic complementation). Intragenic complementation appears to be common and has been...
21 KB (2,342 words) - 16:59, 19 May 2024
The cause of complement deficiency is genetics (though cases of an acquired nature do exist post infection). The majority of complement deficiencies are...
15 KB (1,248 words) - 18:12, 28 January 2025