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Enzyme|January 1, 1987
Genetic analysis of human hypoxanthine-guanine phosphoribosyltransferase deficiencyL J Silverman, W N Kelley, T D PalellaGene|August 15, 1988
Human hypoxanthine-guanine phosphoribosyltransferase: a single nucleotide substitution in cDNA clones isolated from a patient with Lesch-Nyhan syndrome (HPRTMidland)B L Davidson, T D Palella, W N KelleyThe 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.Advances 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|July 1, 1989
Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in ten subjects determined by direct sequencing of amplified transcriptsB L Davidson, S A Tarlé, T D Palella, et al.Human Genetics|May 1, 1988
Identification of a single nucleotide change in a mutant gene for hypoxanthine-guanine phosphoribosyltransferase (HPRT Ann Arbor)S Fujimori, Y Hidaka, B L Davidson, et al.The Journal of Clinical Investigation|November 1, 1987
Human adenine phosphoribosyltransferase. Identification of allelic mutations at the nucleotide level as a cause of complete deficiency of the enzymeY Hidaka, T D Palella, T E O'Toole, et al.Pageof 10