Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders
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Peroxisome synthesis in the absence of preexisting peroxisomesHuman PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assemblyIdentification of peroxisomal acyl-CoA thioesterases in yeast and humansCharacterization of PECI, a novel monofunctional Delta(3), Delta(2)-enoyl-CoA isomerase of mammalian peroxisomesPEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein importPEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesisIdentification and characterization of HAOX1, HAOX2, and HAOX3, three human peroxisomal 2-hydroxy acid oxidasesMolecular anatomy of the peroxin Pex12p: ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type 1-receptor Pex5p and a ring peroxin, Pex10pMultiple distinct targeting signals in integral peroxisomal membrane proteinsIdentification of PEX5p-related novel peroxisome-targeting signal 1 (PTS1)-binding proteins in mammalsAlternative splicing suggests extended function of PEX26 in peroxisome biogenesis.Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disordersPEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.The peroxin pex3p initiates membrane assembly in peroxisome biogenesisPeroxisomes in brain development and functionThe peroxin Pex14p. cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysisDelineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closureDifferent functions of the C3HC4 zinc RING finger peroxins PEX10, PEX2, and PEX12 in peroxisome formation and matrix protein import.Adrenoleukodystrophy and related disorders.Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders.Peroxisomal remnant structures in Hansenula polymorpha Pex5 cells can develop into normal peroxisomes upon induction of the PTS2 protein amine oxidase.Genetic and dietary regulation of lipid droplet expansion in Caenorhabditis elegans.Peroxisome biogenesis and peroxisome biogenesis disorders.Therapeutic developments in peroxisome biogenesis disorders.How peroxisomes arise.Peripheral nervous system defects in a mouse model for peroxisomal biogenesis disorders.Genetic and molecular bases of peroxisome biogenesis disorders.AthPEX10, a nuclear gene essential for peroxisome and storage organelle formation during Arabidopsis embryogenesis.DCA1 Acts as a Transcriptional Co-activator of DST and Contributes to Drought and Salt Tolerance in RiceCharacterization of glycosomal RING finger proteins of trypanosomatids.PEX11 promotes peroxisome division independently of peroxisome metabolismInhibitors of COPI and COPII do not block PEX3-mediated peroxisome synthesis.Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay.Pex19p interacts with Pex3p and Pex10p and is essential for peroxisome biogenesis in Pichia pastoris.Peroxisome biogenesis and human peroxisome-deficiency disorders.Distinct modes of ubiquitination of peroxisome-targeting signal type 1 (PTS1) receptor Pex5p regulate PTS1 protein import.Deciphering Supramolecular Structures with Protein-Protein Interaction Network ModelingIdentification of a novel mutation in PEX10 in a patient with attenuated Zellweger spectrum disorder: a case report.Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels.The mouse gene PDCR encodes a peroxisomal delta(2), delta(4)-dienoyl-CoA reductase.
P2860
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P2860
Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders
description
1998 nî lūn-bûn
@nan
1998 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
name
Identification of PEX10, the g ...... eroxisome-biogenesis disorders
@ast
Identification of PEX10, the g ...... eroxisome-biogenesis disorders
@en
Identification of PEX10, the g ...... eroxisome-biogenesis disorders
@en-gb
Identification of PEX10, the g ...... eroxisome-biogenesis disorders
@nl
type
label
Identification of PEX10, the g ...... eroxisome-biogenesis disorders
@ast
Identification of PEX10, the g ...... eroxisome-biogenesis disorders
@en
Identification of PEX10, the g ...... eroxisome-biogenesis disorders
@en-gb
Identification of PEX10, the g ...... eroxisome-biogenesis disorders
@nl
prefLabel
Identification of PEX10, the g ...... eroxisome-biogenesis disorders
@ast
Identification of PEX10, the g ...... eroxisome-biogenesis disorders
@en
Identification of PEX10, the g ...... eroxisome-biogenesis disorders
@en-gb
Identification of PEX10, the g ...... eroxisome-biogenesis disorders
@nl
P2093
P2860
P356
P1476
Identification of PEX10, the g ...... eroxisome-biogenesis disorders
@en
P2093
P2860
P304
P356
10.1086/301963
P407
P577
1998-08-01T00:00:00Z