نتایج جستجو برای: heterozygotes
تعداد نتایج: 4125 فیلتر نتایج به سال:
Viability relative to Cy/Pm as a standard was studied in Drosophila melanogaster. One experiment, E1, consisted of progeny from eleven distinct 7 x 7 factorial mating designs with reciprocals for second chromosomes extracted from a natural population. The other experiment, E2, consisted of two distinct sets of heterozygotes with reciprocals and corresponding homozygotes. It was established from...
Background:Prostate cancer is increasing among Iranian men and gene polymorphisms may play a role in the development of prostate cancer. Insulin-like growth factor 1 (IGF1) gene polymorphisms have been deeply explored in different malignancies. In this study, we aimed to explore the association of IGF1 CA repeat length polymorphism with the risk of prostate cancer development i...
Using plasma isotope-kinetic methods, we measured the absorption and turnover rates of cholesterol and sitosterol (24-ethylcholesterol) in two obligate heterozygotes (parents) and their homozygous daughter with sitosterolemia with xanthomatosis. Diets contained approximately 500 mg/day cholesterol and 100 mg/day sitosterol. In the homozygote, plasma cholesterol and apolipoprotein B concentratio...
Fabry disease (FD) is an X-linked lysosomal storage disorder resulting from deficiency of α-galactosidase A (GLA). Traditionally, heterozygotes were considered asymptomatic carriers of FD, but it is now apparent that the asymptomatic female carrier is the exception and most heterozygotes suffer significant multisystemic disease. To determine why the process of cross-correction does not occur ef...
HE recombinant off spring of Drosophila melanogaster females having free X T chromosomnls heterozygous for a long inversion are limited to even multiple crossover types. But from inversion heterozygotes in which the two X chromosomes are attached at their centromeric ends (= tandem metacentric compound X chromosome), single crossovers are frequently recovered. The synaptic configurations of the...
The genetic control of pigmentation was analyzed using five unlinked mutants, namely, c, pk, Bl, ev and l. Each mutant blocks or reduces pigmentation. Chick melanocyte cultures of each mutant type were fused to produce all ten possible pair combinations of nondividing heterokaryons. Heterokaryons were identified autoradiographically (One partner in each pair was labeled with 3H-thymidine.) Cros...
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