PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.
about
Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interactionMutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complexThe membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assemblyMutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlationPeroxisome biogenesis in mammalian cellsYeast peroxisomes multiply by growth and division.Glycosome biogenesis in trypanosomes and the de novo dilemma.Pex11mediates peroxisomal proliferation by promoting deformation of the lipid membrane.Activation of Type I and III Interferon Response by Mitochondrial and Peroxisomal MAVS and Inhibition by Hepatitis C Virus.Zellweger syndrome with unusual findings: non-immune hydrops fetalis, dermal erythropoiesis and hypoplastic toe nails.Peroxisome biogenesis and human peroxisome-deficiency disorders.The role of conserved PEX3 regions in PEX19-binding and peroxisome biogenesis.Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells.Novel PEX3 Gene Mutations Resulting in a Moderate Zellweger Spectrum Disorder.New insights into the distribution, protein abundance and subcellular localisation of the endogenous peroxisomal biogenesis proteins PEX3 and PEX19 in different organs and cell types of the adult mouse.Dysregulation of Plasmalogen Homeostasis Impairs Cholesterol Biosynthesis.Recruiting mechanism of the AAA peroxins, Pex1p and Pex6p, to Pex26p on the peroxisomal membrane.Peroxisome biogenesis disorders.
P2860
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P2860
PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.
description
2000 nî lūn-bûn
@nan
2000 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի օգոստոսին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年论文
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name
PEX3 is the causal gene respon ...... ome of complementation group G
@nl
PEX3 is the causal gene respon ...... me of complementation group G.
@ast
PEX3 is the causal gene respon ...... me of complementation group G.
@en
type
label
PEX3 is the causal gene respon ...... ome of complementation group G
@nl
PEX3 is the causal gene respon ...... me of complementation group G.
@ast
PEX3 is the causal gene respon ...... me of complementation group G.
@en
prefLabel
PEX3 is the causal gene respon ...... ome of complementation group G
@nl
PEX3 is the causal gene respon ...... me of complementation group G.
@ast
PEX3 is the causal gene respon ...... me of complementation group G.
@en
P2093
P2860
P356
P1476
PEX3 is the causal gene respon ...... me of complementation group G.
@en
P2093
P2860
P304
P356
10.1086/303086
P407
P577
2000-08-31T00:00:00Z