Results 281 to 290 of about 253,035 (314)
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Genetics of IgCH (allotype) locus in the mouse
Springer Seminars in Immunopathology, 1978The mouse is particularly useful in studies of the immunogenetics of immunoglobulins because of the availability of (1) many inbred strains [60], (2) many allotype congenic strains that genetically resemble the parental strains except for selected allotype genes [40], (3) strains in which genes regulating VH structural expression have been identified ...
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Population genetics of the hypervariable locus D12S391 in Koreans
International Journal of Legal Medicine, 2000The hypervariable short tandem repeat (STR) locus D12S391 was investigated in a Korean population and 34 fragments were sequenced to confirm the structure of alleles. From these sequenced fragments an allelic ladder containing 13 sequenced alleles was constructed.
Hye-Seung Lee +6 more
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Genetic complexity of a minute locus in drosophila
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 1978Abstract Minute loci in Drosophila melanogaster are an unusual class of genes in that mutations express a syndrome of dominant defects including short, thin bristles, slow development, small body size, and varying degress of reduced survival and fertility. This set of defects is similar to that observed for mutations known to affect protein synthesis.
D.L. Shellenbarger, A.K. Duttagupta
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Evidence for a second genetic locus in Carney complex
British Journal of Dermatology, 1998Carney complex (MIM no. 160980) is an autosomal dominant condition of lentiginosis, cutaneous and cardiac myxomas and multiple endocrine neoplasia. A locus for Carney complex has recently been mapped to chromosome 2p16. We have studied two Northern Irish families with this disorder.
Hughes +5 more
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The locus coeruleus: a quantitative and genetic study in mice
Brain Research, 1982A fluorescence histochemical study of the pontine catecholaminergic (CA) neurons of two inbred strains of mice, BALB/c (C) and C57BL/6 (B6) and their F1 hybrids revealed that the total number of the fluorescent cells in the C strain was 38% lower than that of the B6 strain. In F1 hybrids, the total number of neurons was not statistically different from
Touret, M, Valatx, J, Jouvet, M
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Genetic Diversity at the FMR1 Locus in Mexican Population
Archives of Medical Research, 2005Fragile X syndrome is the most frequent cause of inherited mental retardation; it is caused by expansion of CGG repeats in the first exon of the FMR1 gene. Number of CGG repeats varies between 6 and 50 triplets in normal individuals and the most common alleles have 29 or 30 repeats.
Claudina Medina +4 more
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Developmental Genetics of Specific Locus Mutations [PDF]
, 1983 The remarkable complexities of eukaryotic gene organization and gene expression have received much emphasis in recent years. Whereas the organizational characteristics of polycistronic operons in E. coli are fairly well understood and appear quite straight forward, those of eukaryotes are considerably more complex as exemplified particularly by the ...
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Sam Karlin and multi-locus population genetics
Theoretical Population Biology, 2009Between 1967 and 1982, Sam Karlin made fundamental contributions to many areas of deterministic population genetic theory. This remembrance focuses on his work in multi-locus population genetics, primarily on the interaction between genotypic selection and the rate of recombination.
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Genetic Studies of a STR at the UGB Locus
1996The so called Short Tandem Repeats (STR) constitute nowadays one of the most interesting sources of information in human genetic studies. This paper deals with the analysis of a tetranucleotide repeat in the Uteroglobin Gene (UGB) (Stohr & Weber 1994), localised in chromosome 11q (Wolf et al. 1992). Thus, an initial survey in a sample of the population
P. Leyenda, B. Caeiro
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Genetic Analysis of the R Locus in Mormoniella
Journal of Heredity, 1969Kenneth J. Roozen, George W. Conner
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