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The New England Journal of Medicine|October 16, 1975
Phenylketonuria due to a deficiency of dihydropteridine reductaseS Kaufman, N A Holtzman, S Milstien, et al.The Journal of Pediatrics|January 1, 1987
Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuriaF Güttler, F D Ledley, A S Lidsky, et al.Journal of Neurochemistry|October 1, 1980
Neopterin and biopterin levels in patients with atypical forms of phenylketonuriaJ C Nixon, C L Lee, S Milstien, et al.Journal of Neurochemistry|February 1, 1988
Biochemical defect of the hph-1 mouse mutant is a deficiency in GTP-cyclohydrolase activityJ D McDonald, R G Cotton, I Jennings, et al.Genomics|January 1, 1990
Complete cDNA sequence and chromosomal localization of mouse alpha 1-antitrypsinR N Sifers, F D Ledley, L Reed-Fourquet, et al.Somatic Cell and Molecular Genetics|September 1, 1987
Assignment of human tryptophan hydroxylase locus to chromosome 11: gene duplication and translocation in evolution of aromatic amino acid hydroxylasesF D Ledley, H E Grenett, D P Bartos, et al.Proceedings of the National Academy of Sciences of the United States of America|November 1, 1988
Retroviral-mediated gene transfer and expression of human phenylalanine hydroxylase in primary mouse hepatocytesH Peng, D Armentano, L MacKenzie-Graham, et al.The Journal of Pediatrics|September 1, 1988
Phenylalanine hydroxylase expression in liver of a fetus with phenylketonuriaF D Ledley, R Koch, K Jew, et al.American Journal of Human Genetics|January 1, 1993
Cloning of functional alpha propionyl CoA carboxylase and correction of enzyme deficiency in pccA fibroblastsJ Stankovics, F D LedleySomatic Cell and Molecular Genetics|November 1, 1992
Correction of methylmalonyl-CoA mutase deficiency in Mut0 fibroblasts and constitution of gene expression in primary human hepatocytes by retroviral-mediated gene transferT Sawada, F D LedleyPageof 245