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Cytogenetics and Cell Genetics|January 1, 1988
Localization of mouse phenylalanine hydroxylase locus on chromosome 10F D Ledley, S A Ledbetter, D H Ledbetter, et al.Proceedings of the National Academy of Sciences of the United States of America|January 1, 1986
Retroviral-mediated gene transfer of human phenylalanine hydroxylase into NIH 3T3 and hepatoma cellsF D Ledley, H E Grenett, M McGinnis-Shelnutt, et al.The Biochemical Journal|April 15, 1990
Mouse phenylalanine hydroxylase. Homology and divergence from human phenylalanine hydroxylaseF D Ledley, H E Grenett, B S Dunbar, et al.European Journal of Pediatrics|September 8, 1978
Hyperphenylalaninaemia due to dihydropteridine reductase deficiencyH Gröbe, K Bartholome, S Milstien, et al.Proceedings of the National Academy of Sciences of the United States of America|August 1, 1987
Full-length cDNA for rabbit tryptophan hydroxylase: functional domains and evolution of aromatic amino acid hydroxylasesH E Grenett, F D Ledley, L L Reed, et al.The Journal of Biological Chemistry|September 10, 1976
In vitro activation of rat liver phenylalanine hydroxylase by phosphorylationJ P Abita, S Milstien, N Chang, et al.Proceedings of the National Academy of Sciences of the United States of America|May 1, 1976
Hepatic phenylalanine 4-monooxygenase is a phosphoproteinS Milstien, J P Abita, N Chang, et al.Journal of Neurochemistry|April 1, 1990
Immunological evidence for the requirement of sepiapterin reductase for tetrahydrobiopterin biosynthesis in brainR A Levine, G Kapatos, S Kaufman, et al.AIDS (London, England)|May 1, 1991
Cerebrospinal fluid and serum neopterin and biopterin in D-retrovirus-infected rhesus macaques (Macaca mulatta): relationship to clinical and viral statusM P Heyes, A Lackner, S Kaufman, et al.Pediatrics|May 1, 1977
Atypical phenylketonuria with normal phenylalanine hydroxylase and dihydropteridine reductase activity in vitroK Bartholomé, D J Byrd, S Kaufman, et al.Pageof 245