or crossed. Complementation will ordinarily occur if the mutations are in different genes (intergenic complementation). Complementation may also occur...

between two alleles leads to intragenic complementation while disruption of transvection disrupts the complementation. Transvection is believed to occur through...

property whereby double stranded nucleic acids pair with each other Complementation (genetics), a test to determine if independent recessive mutant phenotypes...

compared with others and is a standard technique used in forensics. Complementation (genetics) DNA damage (naturally occurring) DNA damage theory of aging Epigenetics...

wild-type alleles, as discussed in the articles Heterosis and Complementation (genetics), but there were also findings of overdominance, especially in...

cause epistasis. This is sometimes called allelic complementation, or interallelic complementation. It may be caused by several mechanisms, for example...

wild-type allele, this masking phenomenon is referred to as complementation (see complementation (genetics)). In general, sexual reproduction in eukaryotes has...

Competence factor Competent Complementarity genes Complementary DNA Complementation Complementation test Complete linkage Complex trait Component of fitness Composite...

Forward genetics is a molecular genetics approach of determining the genetic basis responsible for a phenotype. Forward genetics provides an unbiased approach...

Bimolecular fluorescence complementation (also known as BiFC) is a technology typically used to validate protein interactions. It is based on the association...

Fanconi anemia, complementation group E protein is a protein that in humans is encoded by the FANCE gene. The Fanconi anemia complementation group (FANC)...

that would otherwise be harmful to sexual spore formation (see Complementation (genetics)). Neurospora crassa is not only a model organism for the study...

would otherwise be deleterious to sexual spore formation (see Complementation (genetics)). Saccharomyces cerevisiae, brewer's and baker's yeast, is in...

Quantitative genetics is the study of quantitative traits, which are phenotypes that vary continuously—such as height or mass—as opposed to phenotypes...

infantile lethal cerebro-oculo-facio-skeletal syndrome. There are seven complementation groups, plus one variant form: There is no cure for the disorder; all...

(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...

9". Nature Genetics. 1 (3): 196–8. doi:10.1038/ng0692-196. PMID 1303234. S2CID 7341515. "Entrez Gene: FANCC Fanconi anemia, complementation group C". PMC...

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...

of complementation group D1, N, and S, are embryonically lethal in most cases, which might account for the rare observation of these complementation groups...

of progeny. The masking effect of outcrossing is known as genetic complementation, an effect also recognized as hybrid vigor or heterosis. Once outcrossing...

of gene clusters. His early work on intragenic complementation led to the insight that complementation between allelic mutants is of widespread occurrence...

are part of the population genetics discipline and are used to analyze the ancestry of Jewish populations, complementing research in other fields such...

phenomenon is referred to as intragenic complementation (also called inter-allelic complementation). Intragenic complementation has been demonstrated in many different...

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...

Transheterozygotes are useful in the study of genetic interactions and complementation testing. A transheterozygote is a diploid organism that is heterozygous...

anemia complementation group B". Nat Genet. 36 (11): 1219–24. doi:10.1038/ng1458. PMID 15502827. "Entrez Gene: FANCB Fanconi anemia, complementation group...

history of genetics, Hugo de Vries supposed these were caused by mutation. Genetic complementation is a hybridization test widely used in genetics to determine...

cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I". Proceedings...

contributions included the discovery of intracistronic or interallelic complementation with John Fincham, as well as developing our understanding of gene...

screening relies on the principle of α-complementation, where a fragment of the lacZ gene (lacZα) in the plasmid can complement another mutant lacZ gene (lacZΔM15)...