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T D Palella

Showing results (21-30 of 30) with videos related to

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Gene|January 30, 1993
Synthesis of normal and variant human hypoxanthine-guanine phosphoribosyltransferase in Escherichia coliB L Davidson, J E Brown, C H Weber, et al.
The Journal of Clinical Investigation|March 1, 1988
Human adenine phosphoribosyltransferase deficiency. Demonstration of a single mutant allele common to the JapaneseY Hidaka, S A Tarlé, S Fujimori, et al.
Gene|August 1, 1989
Expression of human HPRT mRNA in brains of mice infected with a recombinant herpes simplex virus-1 vectorT D Palella, Y Hidaka, L J Silverman, et al.
The Journal of Clinical Investigation|December 1, 1988
Hypoxanthine-guanine phosphoribosyltransferase. Genetic evidence for identical mutations in two partially deficient subjectsB L Davidson, S J Chin, J M Wilson, et al.
Molecular and Cellular Biology|January 1, 1988
Herpes simplex virus-mediated human hypoxanthine-guanine phosphoribosyltransferase gene transfer into neuronal cellsT D Palella, L J Silverman, C T Schroll, et al.
The New England Journal of Medicine|August 3, 1989
Cyclosporine-induced hyperuricemia and goutH Y Lin, L L Rocher, M A McQuillan, et al.
The Journal of Clinical Investigation|January 1, 1986
A molecular survey of hypoxanthine-guanine phosphoribosyltransferase deficiency in manJ M Wilson, J T Stout, T D Palella, et al.
American Journal of Human Genetics|May 1, 1991
Identification of 17 independent mutations responsible for human hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiencyB L Davidson, S A Tarlé, M Van Antwerp, et al.
The Journal of Biological Chemistry|December 15, 1993
Human X-linked phosphoribosylpyrophosphate synthetase superactivity is associated with distinct point mutations in the PRPS1 geneB J Roessler, J M Nosal, P R Smith, et al.
Genomics|June 1, 1991
Determination of the mutations responsible for the Lesch-Nyhan syndrome in 17 subjectsS A Tarlé, B L Davidson, V C Wu, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Gene|January 30, 1993
Synthesis of normal and variant human hypoxanthine-guanine phosphoribosyltransferase in Escherichia coliB L Davidson, J E Brown, C H Weber, et al.
The Journal of Clinical Investigation|March 1, 1988
Human adenine phosphoribosyltransferase deficiency. Demonstration of a single mutant allele common to the JapaneseY Hidaka, S A Tarlé, S Fujimori, et al.
Gene|August 1, 1989
Expression of human HPRT mRNA in brains of mice infected with a recombinant herpes simplex virus-1 vectorT D Palella, Y Hidaka, L J Silverman, et al.
The Journal of Clinical Investigation|December 1, 1988
Hypoxanthine-guanine phosphoribosyltransferase. Genetic evidence for identical mutations in two partially deficient subjectsB L Davidson, S J Chin, J M Wilson, et al.
Molecular and Cellular Biology|January 1, 1988
Herpes simplex virus-mediated human hypoxanthine-guanine phosphoribosyltransferase gene transfer into neuronal cellsT D Palella, L J Silverman, C T Schroll, et al.
The New England Journal of Medicine|August 3, 1989
Cyclosporine-induced hyperuricemia and goutH Y Lin, L L Rocher, M A McQuillan, et al.
The Journal of Clinical Investigation|January 1, 1986
A molecular survey of hypoxanthine-guanine phosphoribosyltransferase deficiency in manJ M Wilson, J T Stout, T D Palella, et al.
American Journal of Human Genetics|May 1, 1991
Identification of 17 independent mutations responsible for human hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiencyB L Davidson, S A Tarlé, M Van Antwerp, et al.
The Journal of Biological Chemistry|December 15, 1993
Human X-linked phosphoribosylpyrophosphate synthetase superactivity is associated with distinct point mutations in the PRPS1 geneB J Roessler, J M Nosal, P R Smith, et al.
Genomics|June 1, 1991
Determination of the mutations responsible for the Lesch-Nyhan syndrome in 17 subjectsS A Tarlé, B L Davidson, V C Wu, et al.
Pageof 3