Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells.
about
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humansPEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12pA close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression patternA PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parentsAbsence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndromeCorrection by gene expression of biochemical abnormalities in fibroblasts from Zellweger patientsPeroxisome assembly factor 1: nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysisPresence of cytoplasmic factors functional in peroxisomal protein import implicates organelle-associated defects in several human peroxisomal disorders.Therapeutic developments in peroxisome biogenesis disorders.Genetic and molecular bases of peroxisome biogenesis disorders.Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndromeNovel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis.Novel peroxisome clustering mutants and peroxisome biogenesis mutants of Saccharomyces cerevisiae.Targeting of human catalase to peroxisomes is dependent upon a novel COOH-terminal peroxisomal targeting sequence.Cloning and characterization of PAS5: a gene required for peroxisome biogenesis in the methylotrophic yeast Pichia pastorisPeroxisome biogenesis in the yeast Hansenula polymorpha is controlled by a complex set of interacting gene productsThe Yarrowia lipolytica gene PAY2 encodes a 42-kDa peroxisomal integral membrane protein essential for matrix protein import and peroxisome enlargement but not for peroxisome membrane proliferation.Oxidation of pristanic acid in fibroblasts and its application to the diagnosis of peroxisomal beta-oxidation defectsNewly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals.Multiplicity of antioxidant enzyme catalase in mouse liver cells.Peroxisomal disorders: overview.Approaches to studies on peroxisome biogenesis and human peroxisome-deficient disorders.Epilepsy in peroxisomal diseases.Biogenesis of peroxisomes in fetal liver.Differential protein import deficiencies in human peroxisome assembly disorders.Peroxisomal disorders: clinical aspects.Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect.PER3, a gene required for peroxisome biogenesis in Pichia pastoris, encodes a peroxisomal membrane protein involved in protein import.
P2860
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P2860
Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Complementation study of perox ...... aracterization of fused cells.
@en
type
label
Complementation study of perox ...... aracterization of fused cells.
@en
prefLabel
Complementation study of perox ...... aracterization of fused cells.
@en
P2093
P2860
P356
P1433
P1476
Complementation study of perox ...... aracterization of fused cells.
@en
P2093
N Shimozawa
S Yamaguchi
T Hashimoto
P2860
P2888
P304
P356
10.1007/BF00219334
P577
1992-03-01T00:00:00Z
P6179
1003521077