Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene.
about
Gene sharing by delta-crystallin and argininosuccinate lyaseIsolation and characterization of cDNA clones for rat ribophorin I: complete coding sequence and in vitro synthesis and insertion of the encoded product into endoplasmic reticulum membranesProtein stability and in vivo concentration of missense mutations in phenylalanine hydroxylase.Phenylketonuria in U.S. blacks: molecular analysis of the phenylalanine hydroxylase geneIdentification of the haplotype pattern associated with the mutant PKU allele in the Gypsy population of WalesMolecular analysis of contiguous exons of the phenylalanine hydroxylase gene: identification of a new PKU mutation.Genetic analysis of treated and untreated phenylketonuria in one family.A novel system for the production of fully deleted adenovirus vectors that does not require helper adenovirus.hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesisPhenylalanine hydroxylase deficiency.COUP-TF gene: a structure unique for the steroid/thyroid receptor superfamilyHaplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations.Screening for mutations in the phenylalanine hydroxylase gene from Italian patients with phenylketonuria by using the chemical cleavage method: a new splice mutationPolymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in European families with phenylketonuria (PKU)Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU).Missense mutations associated with RFLP haplotypes 1 and 4 of the human phenylalanine hydroxylase gene.Recurrent mutation in the human phenylalanine hydroxylase geneA termination mutant prevalent in Norwegian haplotype 7 phenylketonuria genesMolecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency.Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1.A genome-wide approach to identify genetic loci with a signature of natural selection in the Irish population.Single-dose, subcutaneous recombinant phenylalanine ammonia lyase conjugated with polyethylene glycol in adult patients with phenylketonuria: an open-label, multicentre, phase 1 dose-escalation trialHuman tyrosine hydroxylase and insulin genes are contiguous on chromosome 11Tissue specific expression of the human alpha-1-antitrypsin gene in transgenic mice.Nutrigenomics: A controversy.The activity of the highly inducible mouse phenylalanine hydroxylase gene promoter is dependent upon a tissue-specific, hormone-inducible enhancerMaternal hyperphenylalaninemia: rapid achievement of metabolic control predicts overall control throughout pregnancyClinical genomic database.Heat-transfer-based detection of SNPs in the PAH gene of PKU patients.Mechanisms of Inflammation-Associated Depression: Immune Influences on Tryptophan and Phenylalanine Metabolisms.PAH Mutation Analysis Consortium Database: a database for disease-producing and other allelic variation at the human PAH locus.The PAH mutation analysis consortium database: update 1996.Structure and function of the aromatic amino acid hydroxylases.GT to AT transition at a splice donor site causes skipping of the preceding exon in phenylketonuria.The 5' splice site: phylogenetic evolution and variable geometry of association with U1RNA.Clinical utility gene card for: Phenylketonuria.Associations between mutations and a VNTR in the human phenylalanine hydroxylase gene.Time and space clusters of the French-Canadian M1V phenylketonuria mutation in France.Molecular genetics of phenylketonuria in Orientals: linkage disequilibrium between a termination mutation and haplotype 4 of the phenylalanine hydroxylase gene.Novel PKU mutation on haplotype 2 in French-Canadians.
P2860
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P2860
Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene.
description
1986 nî lūn-bûn
@nan
1986 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1986 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
name
Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene.
@ast
Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene.
@en
Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene.
@nl
type
label
Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene.
@ast
Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene.
@en
Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene.
@nl
prefLabel
Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene.
@ast
Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene.
@en
Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene.
@nl
P2093
P356
P1433
P1476
Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene.
@en
P2093
P304
P356
10.1021/BI00352A001
P407
P577
1986-02-01T00:00:00Z