Gyrate atrophy of the choroid and retina: deficiency of ornithine aminotransferase in transformed lymphocytes.
about
Molecular cloning of human ornithine aminotransferase mRNALinkage analysis of Norrie disease with X-chromosomal ornithine aminotransferaseMolecular genetics of retinitis pigmentosaMolecular basis of ornithine aminotransferase deficiency in B-6-responsive and -nonresponsive forms of gyrate atrophy.Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.Hyperprolinaemia and gyrate atrophy of the choroid and retina in members of the same familyAt least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.Clinical research methodology in ophthalmologyA sensitive assay for ornithine amino transferase in rat brain mitochondria by ninhydrin methodGyrate atrophy of the choroid and retina with hyperornithinemia: biochemical and histologic studies and response to vitamin B6The ornithine aminotransferase (OAT) locus: analysis of RFLPs in gyrate atrophy.Inheritance of ornithine aminotransferase gene, mRNA, and enzyme defect in a family with gyrate atrophy of the choroid and retina.Gyrate atrophy of the choroid and retina: assignment of the ornithine aminotransferase structural gene to human chromosome 10 and mouse chromosome 7.Ornithine-δ-Aminotransferase Inhibits Neurogenesis During Xenopus Embryonic Development.Effect of pH on spectral characteristics of P5C-ninhydrin derivative: Application in the assay of ornithine amino transferase activity from tissue lysate.Gyrate atrophy of the choroid and retina with hyperornithinemia: characterization of mutant liver L-ornithine:2-oxoacid aminotransferase kinetics.Gyrate atrophy of the choroid and retina: amino acid metabolism and correction of hyperornithinemia with an arginine-deficient dietGyrate atrophy of the choroid and retina with hyperornithinemia. Deficient formation of guanidinoacetic acid from arginineSplice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutationNonsense-codon mutations of the ornithine aminotransferase gene with decreased levels of mutant mRNA in gyrate atrophy.Treatment of gyrate atrophy of the choroid and retina with low arginine diet."Basolateral" and mitochondrial membrane transport defect in the hepatocytes in lysinuric protein intolerance.Catalysts of the urea cycle.Special Issue Introduction: Inherited Retinal Disease: Novel Candidate Genes, Genotype-Phenotype Correlations, and Inheritance Models.
P2860
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P2860
Gyrate atrophy of the choroid and retina: deficiency of ornithine aminotransferase in transformed lymphocytes.
description
1977 nî lūn-bûn
@nan
1977 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1977 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1977年の論文
@ja
1977年論文
@yue
1977年論文
@zh-hant
1977年論文
@zh-hk
1977年論文
@zh-mo
1977年論文
@zh-tw
1977年论文
@wuu
name
Gyrate atrophy of the choroid ...... se in transformed lymphocytes.
@ast
Gyrate atrophy of the choroid ...... se in transformed lymphocytes.
@en
type
label
Gyrate atrophy of the choroid ...... se in transformed lymphocytes.
@ast
Gyrate atrophy of the choroid ...... se in transformed lymphocytes.
@en
prefLabel
Gyrate atrophy of the choroid ...... se in transformed lymphocytes.
@ast
Gyrate atrophy of the choroid ...... se in transformed lymphocytes.
@en
P2093
P2860
P356
P1476
Gyrate atrophy of the choroid ...... se in transformed lymphocytes.
@en
P2093
Del Valle LA
Kaiser-Kupfer MI
P2860
P304
P356
10.1073/PNAS.74.11.5159
P407
P577
1977-11-01T00:00:00Z