Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B
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Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assemblyPEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein importMolecular 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, Pex10pThe TRIM37 gene encodes a peroxisomal RING-B-box-coiled-coil protein: classification of mulibrey nanism as a new peroxisomal disorderThe membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assemblyPEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.Ariadne-1: a vital Drosophila gene is required in development and defines a new conserved family of ring-finger proteinsThe peroxin pex3p initiates membrane assembly in peroxisome biogenesisPeroxisomal membrane proteins insert into the endoplasmic reticulum.A systematic search for endoplasmic reticulum (ER) membrane-associated RING finger proteins identifies Nixin/ZNRF4 as a regulator of calnexin stability and ER homeostasisThe peroxin Pex14p. cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysisNovel mutations in the PEX12 gene of patients with a peroxisome biogenesis disorderAtPEX2 and AtPEX10 are targeted to peroxisomes independently of known endoplasmic reticulum trafficking routes.Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders.Genetic and dietary regulation of lipid droplet expansion in Caenorhabditis elegans.Peroxisome biogenesis and peroxisome biogenesis disorders.Genetic and molecular bases of peroxisome biogenesis disorders.AthPEX10, a nuclear gene essential for peroxisome and storage organelle formation during Arabidopsis embryogenesis.Conservation of PEX19-binding motifs required for protein targeting to mammalian peroxisomal and trypanosome glycosomal membranesCharacterization of glycosomal RING finger proteins of trypanosomatids.Endoplasmic reticulum degradation requires lumen to cytosol signaling. Transmembrane control of Hrd1p by Hrd3p.Peroxisome biogenesis and human peroxisome-deficiency disorders.Novel mutations in the PEX2 gene of four unrelated patients with a peroxisome biogenesis disorder.Distinct modes of ubiquitination of peroxisome-targeting signal type 1 (PTS1) receptor Pex5p regulate PTS1 protein import.Stress induces peroxisome biogenesis genes.Dysregulation of Plasmalogen Homeostasis Impairs Cholesterol Biosynthesis.Trichomonas vaginalis Hmp35, a putative pore-forming hydrogenosomal membrane protein, can form a complex in yeast mitochondria.An Arabidopsis pex10 null mutant is embryo lethal, implicating peroxisomes in an essential role during plant embryogenesis.A novel method to determine the topology of peroxisomal membrane proteins in vivo using the tobacco etch virus protease.Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia.System to quantify the import of peroxisomal matrix proteins by fluorescence intensity.Peroxisome biogenesis: a novel inducible PEX19 splicing variant is involved in early stages of peroxisome proliferation.Deficiency of a Retinal Dystrophy Protein, Acyl-CoA Binding Domain-containing 5 (ACBD5), Impairs Peroxisomal β-Oxidation of Very-long-chain Fatty Acids.
P2860
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P2860
Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B
description
1998 nî lūn-bûn
@nan
1998 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Mutations in PEX10 is the caus ...... ome of complementation group B
@ast
Mutations in PEX10 is the caus ...... ome of complementation group B
@en
Mutations in PEX10 is the caus ...... ome of complementation group B
@en-gb
Mutations in PEX10 is the caus ...... ome of complementation group B
@nl
type
label
Mutations in PEX10 is the caus ...... ome of complementation group B
@ast
Mutations in PEX10 is the caus ...... ome of complementation group B
@en
Mutations in PEX10 is the caus ...... ome of complementation group B
@en-gb
Mutations in PEX10 is the caus ...... ome of complementation group B
@nl
prefLabel
Mutations in PEX10 is the caus ...... ome of complementation group B
@ast
Mutations in PEX10 is the caus ...... ome of complementation group B
@en
Mutations in PEX10 is the caus ...... ome of complementation group B
@en-gb
Mutations in PEX10 is the caus ...... ome of complementation group B
@nl
P2093
P356
P1476
Mutations in PEX10 is the caus ...... ome of complementation group B
@en
P2093
N Shimozawa
P304
P356
10.1093/HMG/7.9.1399
P407
P577
1998-09-01T00:00:00Z