Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase.
about
Structure and expression of human dihydropteridine reductaseCloning and characterization of human and rat liver cDNAs coding for a gap junction proteinCloning and substrate specificity of a human phenol UDP-glucuronosyltransferase expressed in COS-7 cellsCloning and characterization of the cDNA encoding human adenylosuccinate synthetaseHuman microsomal epoxide hydrolase: genetic polymorphism and functional expression in vitro of amino acid variantsExpression of recombinant human phenylalanine hydroxylase as fusion protein in Escherichia coli circumvents proteolytic degradation by host cell proteases. Isolation and characterization of the wild-type enzymeCloning of a human liver microsomal UDP-glucuronosyltransferase cDNASerum vitamin D-binding protein is a third member of the albumin and alpha fetoprotein gene familyFull-length cDNA for rabbit tryptophan hydroxylase: functional domains and evolution of aromatic amino acid hydroxylasesAlternative splicing in the human cytochrome P450IIB6 gene generates a high level of aberrant messagesIsolation of human cDNA clones of myb-related genes, A-myb and B-mybIsolation of human cDNA clones of ski and the ski-related gene, snoClose linkage of the human cytochrome P450IIA and P450IIB gene subfamilies: implications for the assignment of substrate specificityMolecular cloning of cDNA coding for brain-specific 14-3-3 protein, a protein kinase-dependent activator of tyrosine and tryptophan hydroxylasesMolecular cloning of L-methylmalonyl-CoA mutase: gene transfer and analysis of mut cell linesCloning and cDNA sequence of the dihydrolipoamide dehydrogenase component human alpha-ketoacid dehydrogenase complexesCloning and expression of the cDNA encoding human fumarylacetoacetate hydrolase, the enzyme deficient in hereditary tyrosinemia: assignment of the gene to chromosome 15Phenylketonuria: translating research into novel therapiesMolecular cloning and chromosomal localization of human 4-beta-galactosyltransferaseBeta-subunits of the human liver Gs/Gi signal-transducing proteins and those of bovine retinal rod cell transducin are identicalCharacterization of a cDNA coding for human factor VIIPhenylketonuria in U.S. blacks: molecular analysis of the phenylalanine hydroxylase geneThe accessibility of iron at the active site of recombinant human phenylalanine hydroxylase to water as studied by 1H NMR paramagnetic relaxation. Effect of L-Phe and comparison with the rat enzyme.Deamidations in recombinant human phenylalanine hydroxylase. Identification of labile asparagine residues and functional characterization of Asn --> Asp mutant forms.BmPAH catalyzes the initial melanin biosynthetic step in Bombyx mori.A comparison of kinetic and regulatory properties of the tetrameric and dimeric forms of wild-type and Thr427-->Pro mutant human phenylalanine hydroxylase: contribution of the flexible hinge region Asp425-Gln429 to the tetramerization and cooperativPhenylketonuria: old disease, new approach to treatment.Identification of the haplotype pattern associated with the mutant PKU allele in the Gypsy population of WalesRapid and efficient PCR/StyI test for identification of common mutation R408W in phenylketonuria patients.Genetic analysis of treated and untreated phenylketonuria in one family.Retroviral-mediated gene transfer and expression of human phenylalanine hydroxylase in primary mouse hepatocytesThree prevalent mutations in a patient with phenylalanine hydroxylase deficiency: implications for diagnosis and genetic counselling.Complete amino acid sequence of human vitronectin deduced from cDNA. Similarity of cell attachment sites in vitronectin and fibronectin.Mouse models of human phenylketonuria.Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations.The gene for the alpha polypeptide of pyruvate dehydrogenase is X-linked in humansLinking genotypes database with locus-specific database and genotype-phenotype correlation in phenylketonuriaCloning of functional alpha propionyl CoA carboxylase and correction of enzyme deficiency in pccA fibroblastsMolecular basis for the polymorphic forms of human serum paraoxonase/arylesterase: glutamine or arginine at position 191, for the respective A or B allozymes.Mutation detection in phenylketonuria by using chemical cleavage of mismatch: importance of using probes from both normal and patient samples.
P2860
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P2860
Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase.
description
1985 nî lūn-bûn
@nan
1985年の論文
@ja
1985年学术文章
@wuu
1985年学术文章
@zh-cn
1985年学术文章
@zh-hans
1985年学术文章
@zh-my
1985年学术文章
@zh-sg
1985年學術文章
@yue
1985年學術文章
@zh
1985年學術文章
@zh-hant
name
Nucleotide sequence of a full- ...... man phenylalanine hydroxylase.
@ast
Nucleotide sequence of a full- ...... man phenylalanine hydroxylase.
@en
type
label
Nucleotide sequence of a full- ...... man phenylalanine hydroxylase.
@ast
Nucleotide sequence of a full- ...... man phenylalanine hydroxylase.
@en
prefLabel
Nucleotide sequence of a full- ...... man phenylalanine hydroxylase.
@ast
Nucleotide sequence of a full- ...... man phenylalanine hydroxylase.
@en
P2093
P356
P1433
P1476
Nucleotide sequence of a full- ...... man phenylalanine hydroxylase.
@en
P2093
P304
P356
10.1021/BI00324A002
P407
P577
1985-01-01T00:00:00Z