Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis
about
Requirement for microtubules and dynein motors in the earliest stages of peroxisome biogenesisNDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiencyPhenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disordersIsolation of peroxisome-deficient mutants of Saccharomyces cerevisiae.Novel mutations in the PEX12 gene of patients with a peroxisome biogenesis disorderHuman PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disordersPeroxisome assembly factor 1: nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysisTherapeutic developments in peroxisome biogenesis disorders.Photosensitized killing of cultured fibroblasts from patients with peroxisomal disorders due to pyrene fatty acid-mediated ultraviolet damage.Genetic and molecular bases of peroxisome biogenesis disorders.Import of stably folded proteins into peroxisomes.Mucolipidosis IV consists of one complementation groupAnimal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndromeGenetic heterogeneity in Niemann-Pick C disease: a study using somatic cell hybridization and linkage analysis.Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes.Targeting of human catalase to peroxisomes is dependent upon a novel COOH-terminal peroxisomal targeting sequence.Oxidation of pristanic acid in fibroblasts and its application to the diagnosis of peroxisomal beta-oxidation defectsNovel mutations in the PEX2 gene of four unrelated patients with a peroxisome biogenesis disorder.An efficient screen for peroxisome-deficient mutants of Pichia pastoris.Transport of microinjected proteins into peroxisomes of mammalian cells: inability of Zellweger cell lines to import proteins with the SKL tripeptide peroxisomal targeting signal.Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals.Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells.Components involved in peroxisome import, biogenesis, proliferation, turnover, and movement.Differential protein import deficiencies in human peroxisome assembly disorders.Mammalian alanine/glyoxylate aminotransferase 1 is imported into peroxisomes via the PTS1 translocation pathway. Increased degeneracy and context specificity of the mammalian PTS1 motif and implications for the peroxisome-to-mitochondrion mistargetiStandardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect.Does aminotriazole inhibit import of catalase into peroxisomes by retarding unfolding?Pex5p imports folded tetrameric catalase by interaction with Pex13p.
P2860
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P2860
Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis
description
1988 nî lūn-bûn
@nan
1988 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Genetic heterogeneity in the c ...... using complementation analysis
@ast
Genetic heterogeneity in the c ...... using complementation analysis
@en
Genetic heterogeneity in the c ...... using complementation analysis
@nl
type
label
Genetic heterogeneity in the c ...... using complementation analysis
@ast
Genetic heterogeneity in the c ...... using complementation analysis
@en
Genetic heterogeneity in the c ...... using complementation analysis
@nl
prefLabel
Genetic heterogeneity in the c ...... using complementation analysis
@ast
Genetic heterogeneity in the c ...... using complementation analysis
@en
Genetic heterogeneity in the c ...... using complementation analysis
@nl
P2093
P2860
P356
P1476
Genetic heterogeneity in the c ...... using complementation analysis
@en
P2093
A Strijland
A W Schram
A Westerveld
H S Heymans
H van den Bosch
R B Schutgens
R J Wanders
P2860
P304
P356
10.1172/JCI113510
P407
P577
1988-06-01T00:00:00Z