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Advances in Experimental Medicine and Biology|January 1, 1991
Expression of normal and variant human hypoxanthine-guanine phosphoribosyltransferase in E. coliB L Davidson, B J Roessler, T D PalellaEnzyme|January 1, 1987
Genetic analysis of human hypoxanthine-guanine phosphoribosyltransferase deficiencyL J Silverman, W N Kelley, T D PalellaCancer Research|August 1, 1990
Mutations induced at the hypoxanthine-guanine phosphoribosyltransferase locus of human T-lymphoblasts by perturbations of purine deoxyribonucleoside triphosphate poolsS S Mattano, T D Palella, B S MitchellThe Journal of Laboratory and Clinical Medicine|August 1, 1985
Adenosine triphosphate degradation in specific diseaseI H FoxMetabolism: Clinical and Experimental|June 1, 1981
Metabolic basis for disorders of purine nucleotide degradationI H FoxAdvances in Experimental Medicine and Biology|January 1, 1989
Lesch-Nyhan syndrome due to a single nucleotide change in the hypoxanthine-guanine phosphoribosyltransferase gene (HPRTYale)S Fujimori, B L Davidson, W N Kelley, et al.The Journal of Clinical Investigation|January 1, 1989
Identification of a single nucleotide change in the hypoxanthine-guanine phosphoribosyltransferase gene (HPRTYale) responsible for Lesch-Nyhan syndromeS Fujimori, B L Davidson, W N Kelley, et al.Gene|March 31, 1988
Genetic basis of hypoxanthine guanine phosphoribosyltransferase deficiency in a patient with the Lesch-Nyhan syndrome (HPRTFlint)B L Davidson, M Pashmforoush, W N Kelley, et al.The Journal of Biological Chemistry|January 5, 1989
Human hypoxanthine-guanine phosphoribosyltransferase deficiency. The molecular defect in a patient with gout (HPRTAshville)B L Davidson, M Pashmforoush, W N Kelley, et al.Human Genetics|October 1, 1990
Crossovers within a short DNA sequence indicate a long evolutionary history of the APRT*J mutationN Kamatani, S Kuroshima, M Hakoda, et al.Pageof 13