Further studies on the activity and subcellular distribution of alanine:glyoxylate aminotransferase in the livers of patients with primary hyperoxaluria type 1
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Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1Human wild-type alanine:glyoxylate aminotransferase and its naturally occurring G82E variant: functional properties and physiological implicationsHuman peroxisomal L-alanine: glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codonMistargeting of peroxisomal L-alanine:glyoxylate aminotransferase to mitochondria in primary hyperoxaluria patients depends upon activation of a cryptic mitochondrial targeting sequence by a point mutationFunctional synergism between the most common polymorphism in human alanine:glyoxylate aminotransferase and four of the most common disease-causing mutationsAn enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria.ATP-dependent degradation of a mutant serine: pyruvate/alanine:glyoxylate aminotransferase in a primary hyperoxaluria type 1 caseRecent advances in the understanding, diagnosis and treatment of primary hyperoxaluria type 1.Evolution of alanine:glyoxylate aminotransferase intracellular targeting: structural and functional analysis of the guinea pig gene.Idiopathic calcium oxalate urolithiasis and endogenous oxalate production.Molecular Insight into the Synergism between the Minor Allele of Human Liver Peroxisomal Alanine:Glyoxylate Aminotransferase and the F152I MutationMolecular evolution of alanine/glyoxylate aminotransferase 1 intracellular targeting. Analysis of the marmoset and rabbit genes.Molecular evolution of alanine/glyoxylate aminotransferase 1 intracellular targeting. Analysis of the feline gene.Fetal liver alanine: glyoxylate aminotransferase and the prenatal diagnosis of primary hyperoxaluria type 1.Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase gene.glyoxylate + alanine => glycine + pyruvateTwo-step transplantation for primary hyperoxaluria: a winning strategy to prevent progression of systemic oxalosis in early onset renal insufficiency cases.An institutional experience of pre-emptive liver transplantation for pediatric primary hyperoxaluria type 1.Recurrent primary hyperoxaluria type 2 leads to early post-transplant renal function loss: A case report.
P2860
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P2860
Further studies on the activity and subcellular distribution of alanine:glyoxylate aminotransferase in the livers of patients with primary hyperoxaluria type 1
description
1988 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1988
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im September 1988 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
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vedecký článok (publikovaný 1988/09/01)
@sk
vědecký článek publikovaný v roce 1988
@cs
wetenschappelijk artikel (gepubliceerd op 1988/09/01)
@nl
наукова стаття, опублікована у вересні 1988
@uk
مقالة علمية (نشرت في سبتمبر 1988)
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name
Further studies on the activit ...... h primary hyperoxaluria type 1
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Further studies on the activit ...... h primary hyperoxaluria type 1
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Further studies on the activit ...... h primary hyperoxaluria type 1
@nl
type
label
Further studies on the activit ...... h primary hyperoxaluria type 1
@ast
Further studies on the activit ...... h primary hyperoxaluria type 1
@en
Further studies on the activit ...... h primary hyperoxaluria type 1
@nl
prefLabel
Further studies on the activit ...... h primary hyperoxaluria type 1
@ast
Further studies on the activit ...... h primary hyperoxaluria type 1
@en
Further studies on the activit ...... h primary hyperoxaluria type 1
@nl
P356
P1433
P1476
Further studies on the activit ...... h primary hyperoxaluria type 1
@en
P2093
C. J. Danpure
P. R. Jennings
P304
P356
10.1042/CS0750315
P407
P577
1988-09-01T00:00:00Z