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Dominance (genetics) - Wikipedia, the free encyclopedia
In genetics, dominance describes a relationship between different forms (alleles) of a gene at a particular physical location (locus) on a chromosome. Typical plants and animals have two sets of chr...
en.wikipedia.org/wiki/Dominance_(genetics) |
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We have shown that tumor-derived IDH1 mutations impair the enzyme's affinity for its substrate and dominantly inhibit wild-type IDH1 activity through the formation of catalytically inactive heterodimers.
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Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyo...Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.
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Inheriting a disease, condition, or trait depends on the type of chromosome affected (autosomal or sex ... A single, abnormal gene on one of the first 22 nonsex chromosomes from either parent can cause an autosomal disorder. ... Dominant inheritance means an abnormal gene from one parent is capable of causing disease,
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Welcome to the website of the Dominantly Inherited Alzheimer Network (DIAN). DIAN is an international research partnership of leading scientists determined to understand a rare form of Alzheimer’s disease that is caused by a gene mutation.
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We describe a pedigree of Anglo-Celtic origin with a phenotypically unique form of dominantly inherited spinocerebellar ataxia (SCA) in 14 personally examined affected members. A remarkable observation is dentate nucleus calcification, producing a low signal on MRI sequences.
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This article has been cited by other articles: ... * Division of Vaccine Research, Institute of Human Virology, University of Maryland Biotechnology Institute, and Departments of; Microbiology and Immunology and; Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore ... Correspondence: George K.
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PT and AT dominantly inhibit IL-12 and TNF- production by LPS-activated MDDC; Previously, it was shown that CT inhibits the production of inflammatory cytokines and chemokines by LPS-stimulated MDDC [37 ], and we showed that LT, d-cAMP, and Forskolin mimic this effect (in press).
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In a symptom-free individual at risk for a dominantly inherited disease, an abnormal DNA result generally indicates the development of the disease at some point in later life [4], but neither age of onset, nor overall severity can be predicted.
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However, the mutations identified to date do not seem to account for the dominantly inherited form of the disease. We have examined a German family in which the father and all 4 children were affected with hypophosphatasia, whereas the mother was healthy.
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