Browsing BIO Faculty Scholarship by Subject "Alleles"
Now showing items 1-4 of 4
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Characterization of the mouse phenylalanine hydroxylase mutation Pah(enu3)
(Academic Press, 2001-01)Phenylketonuria (PKU) is an inborn error of metabolism that is inherited in an autosomal recessive manner. It arises from a deficiency of phenylalanine hydroxylase, which is responsible for converting phenylalanine to ... -
Linkage analysis of the hph-1 mutation and the GTP cyclohydrolase I structural gene
(Academic Press, 1999-09)Our research establishes genetic linkage between the hph-1 mutation and the GTP-CH I structural gene. Our results indicate that these two loci are within an 8 cM region with 95% confidence. This finding lends additional ... -
Production of mouse models for the study of human inborn errors of metabolism
(Academic Press, 2000-09) -
Response of genotypes of Hyalella azteca to zinc toxicity
(Springer New York, 1999-07)Toxicity tests are most frequently conducted on organisms derived from laboratory cultures that have been reared for many generations following standardized protocols. The restricted density of laboratory populations and ...