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T D Palella

Showing results (11-20 of 30) with videos related to

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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|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.
The Journal of Laboratory and Clinical Medicine|August 1, 1982
S-Adenosylhomocysteine accumulation and selective cytotoxicity in cultured T- and B-lymphocytesT D Palella, R A Schatz, T E Wilens, 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.
American Journal of Human Genetics|August 1, 1989
Detection of an amino acid substitution in the mutant enzyme for a special type of adenine phosphoribosyltransferase (APRT) deficiency by sequence-specific protein cleavageN Kamatani, S Kuroshima, C Terai, 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 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
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|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.
The Journal of Laboratory and Clinical Medicine|August 1, 1982
S-Adenosylhomocysteine accumulation and selective cytotoxicity in cultured T- and B-lymphocytesT D Palella, R A Schatz, T E Wilens, 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.
American Journal of Human Genetics|August 1, 1989
Detection of an amino acid substitution in the mutant enzyme for a special type of adenine phosphoribosyltransferase (APRT) deficiency by sequence-specific protein cleavageN Kamatani, S Kuroshima, C Terai, 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 3