Characterization of mouse and human GTP cyclohydrolase I genes. Mutations in patients with GTP cyclohydrolase I deficiency
about
GTP cyclohydrolase I mRNA: novel splice variants in the slime mould Physarum polycephalum and in human monocytes (THP-1) indicate conservation of mRNA processingTetrahydrobiopterin biosynthesis, regeneration and functionsCrystal structure of the stimulatory complex of GTP cyclohydrolase I and its feedback regulatory protein GFRP.Specificity and kinetic studies on the cleavage of various prohormone mono- and paired-basic residue sites by yeast aspartic protease 3.Clinical spectrum of dopa-responsive dystonia and related disordersThe role of cathepsin E in terminal differentiation of keratinocytes.Dopa-responsive dystonia: functional analysis of single nucleotide substitutions within the 5' untranslated GCH1 region.The catecholamine system in health and disease -Relation to tyrosine 3-monooxygenase and other catecholamine-synthesizing enzymes.GTP cyclohydrolase I mutations in patients with dystonia responsive to anticholinergic drugsClinical similarities of hereditary progressive/dopa responsive dystonia caused by different types of mutations in the GTP cyclohydrolase I gene.Effect of peripherally administered lipopolysaccharide (LPS) on GTP cyclohydrolase I, tetrahydrobiopterin and norepinephrine in the locus coeruleus in mice.Erythropoietin increases endothelial biosynthesis of tetrahydrobiopterin by activation of protein kinase B alpha/Akt1.Predisposition of genetic disease by modestly decreased expression of GCH1 mutant allele.The genetics of dystonia: new twists in an old tale.Utility of the Biosynthetic Folate Pathway for Targets in Antimicrobial Discovery.Interaction of human GTP cyclohydrolase I with its splice variants.Generation of human artificial chromosomes expressing naturally controlled guanosine triphosphate cyclohydrolase I gene.Molecular cloning of a cDNA coding for GTP cyclohydrolase I from Dictyostelium discoideum.A new selective substrate for cathepsin E based on the cleavage site sequence of alpha2-macroglobulin.Clinical and molecular genetic evaluation of patients with primary dystonia.Disruption of structural and functional integrity of alpha 2-macroglobulin by cathepsin E.Association of cathepsin E deficiency with the increased territorial aggressive response of mice.
P2860
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P2860
Characterization of mouse and human GTP cyclohydrolase I genes. Mutations in patients with GTP cyclohydrolase I deficiency
description
1995 nî lūn-bûn
@nan
1995 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1995年の論文
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1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Characterization of mouse and ...... TP cyclohydrolase I deficiency
@ast
Characterization of mouse and ...... TP cyclohydrolase I deficiency
@en
Characterization of mouse and ...... TP cyclohydrolase I deficiency
@en-gb
Characterization of mouse and ...... TP cyclohydrolase I deficiency
@nl
type
label
Characterization of mouse and ...... TP cyclohydrolase I deficiency
@ast
Characterization of mouse and ...... TP cyclohydrolase I deficiency
@en
Characterization of mouse and ...... TP cyclohydrolase I deficiency
@en-gb
Characterization of mouse and ...... TP cyclohydrolase I deficiency
@nl
prefLabel
Characterization of mouse and ...... TP cyclohydrolase I deficiency
@ast
Characterization of mouse and ...... TP cyclohydrolase I deficiency
@en
Characterization of mouse and ...... TP cyclohydrolase I deficiency
@en-gb
Characterization of mouse and ...... TP cyclohydrolase I deficiency
@nl
P2093
P2860
P356
P1476
Characterization of mouse and ...... TP cyclohydrolase I deficiency
@en
P2093
H Ichinose
P2860
P304
P356
10.1074/JBC.270.32.19135
P407
P577
1995-04-28T00:00:00Z