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Genetics: The MAPT locus-a genetic paradigm in disease susceptibility.
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Genetic characterization of the Dyscalc locus
Mammalian Genome, 2002Calcification occurs frequently in the development of atherosclerotic lesions, and studies in mice have indicated a genetic contribution. We now show that one genetic factor contributing to aortic calcification is the Dyscalc locus, previously shown to contribute to myocardial calcification. Thus, the Dyscalc locus, on proximal mouse Chromosome (Chr) 7,
Veronica V, Colinayo +5 more
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Journal of Experimental Zoology, 1987
AbstractTyrosinase activities and dopachrome conversion activity were evaluated in extracts made from skins of 6‐day‐old mice that were mutant at the agouti and albino loci. Dopa oxidase (DO) activity of tyrosinase in fully pigmented (C/C) mice is reduced in extracts made from skins of yellow 6‐day‐old mice as compared to those of black mice ...
M L, Lamoreux, P, Pendergast
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AbstractTyrosinase activities and dopachrome conversion activity were evaluated in extracts made from skins of 6‐day‐old mice that were mutant at the agouti and albino loci. Dopa oxidase (DO) activity of tyrosinase in fully pigmented (C/C) mice is reduced in extracts made from skins of yellow 6‐day‐old mice as compared to those of black mice ...
M L, Lamoreux, P, Pendergast
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Genetic linkage analysis places locus DXS250 between locus DXYS1 and locus DXS3 in Xq21.3
Cytogenetic and Genome Research, 1992The locus DXS250, which is linked to the Allan-Herndon type of X-linked mental retardation, maps between DXS3 and DXYS1 in a panel of 40 families established by the Centre d’Etude du Polymorphisme Humain, Paris.
S, Epting, C, Schwartz
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Genetical feedback repression I. Single locus models
Journal of Theoretical Biology, 1974Abstract The process of genetical feedback-repression analogous to the Jacob-Monod system has been simulated by digital computer modelling, allowing inclusion of stochastic variation of the components. In the absence of stochastic variability, the model shows a damped oscillation over a wide range of specifications.
J, Tiwari, A, Fraser, R, Beckman
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Human protoporphyria: genetic heterogeneity at the ferrochelatase locus
Photodermatology, Photoimmunology & Photomedicine, 1995Inherited deficiency of ferrochelatase results in erythropoietic protoporphyria (EPP). Genetic heterogeneity at the locus for human ferrochelatase was investigated. Analysis of genomic DNA of patients with EPP and of control subjects by restriction endonuclease techniques using ten different enzymes detected polymorphisms only at sites recognized by ...
L T, Ostasiewicz +4 more
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Genetics of Minute Locus in Drosophila Melanogaster
1980Minutes are a class of dominant mutants that are characterized by their recessive lethality, increased developmental time, smaller body with short fine bristles in the heterozygotes and with varying degrees of reduced survival and fertility (Lindsley et al., 1972).
A K, Duttagupta, D L, Shellenbarger
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Genetic mapping of a second myotonic dystrophy locus
Nature Genetics, 1998We report the mapping of a second myotonic dystrophy locus, myotonic dystrophy type 2 (DM2). Myotonic dystrophy (DM) is a multi-system disease and the most common form of muscular dystrophy in adults. In 1992, DM was shown to be caused by an expanded CTG repeat in the 3' untranslated region of the dystrophia myotonica-protein kinase gene (DMPK) on ...
L P, Ranum +4 more
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