Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G
about
Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interactionCharacterization of the interaction between recombinant human peroxin Pex3p and Pex19p: identification of TRP-104 IN Pex3p as a critical residue for the interactionThe membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assemblyStructural basis for docking of peroxisomal membrane protein carrier Pex19p onto its receptor Pex3pThe peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathwayPeroxisomes in brain development and functionThe different facets of organelle interplay-an overview of organelle interactionsPeroxisome biogenesis in mammalian cellsInsights into Peroxisome Function from the Structure of PEX3 in Complex with a Soluble Fragment of PEX19Yeast peroxisomes multiply by growth and division.The peroxisome: still a mysterious organelleGlycosome biogenesis in trypanosomes and the de novo dilemma.Newly born peroxisomes are a hybrid of mitochondrial and ER-derived pre-peroxisomes.The evolutionary origin of peroxisomes: an ER-peroxisome connection.Peroxisome biogenesis and function.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 membrane proteins: multiple trafficking routes and multiple functions?Multiple pathways for protein transport to peroxisomes.The role of conserved PEX3 regions in PEX19-binding and peroxisome biogenesis.Trypanosoma brucei glycosomal ABC transporters: identification and membrane targeting.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.Human Peroxin PEX3 Is Co-translationally Integrated into the ER and Exits the ER in Budding Vesicles.The making of a mammalian peroxisome, version 2.0: mitochondria get into the mix.Pexophagy: Molecular Mechanisms and Implications for Health and Diseases.Hydrophobic regions adjacent to transmembrane domains 1 and 5 are important for the targeting of the 70-kDa peroxisomal membrane protein.The import competence of a peroxisomal membrane protein is determined by Pex19p before the docking step.Endoplasmic reticulum-directed Pex3p routes to peroxisomes and restores peroxisome formation in a Saccharomyces cerevisiae pex3Delta strain.
P2860
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P2860
Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G
description
2000 nî lūn-bûn
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2000 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
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2000 թվականի օգոստոսին հրատարակված գիտական հոդված
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2000年の論文
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Defective peroxisome membrane ...... drome, complementation group G
@ast
Defective peroxisome membrane ...... drome, complementation group G
@en
Defective peroxisome membrane ...... drome, complementation group G
@en-gb
Defective peroxisome membrane ...... drome, complementation group G
@nl
type
label
Defective peroxisome membrane ...... drome, complementation group G
@ast
Defective peroxisome membrane ...... drome, complementation group G
@en
Defective peroxisome membrane ...... drome, complementation group G
@en-gb
Defective peroxisome membrane ...... drome, complementation group G
@nl
prefLabel
Defective peroxisome membrane ...... drome, complementation group G
@ast
Defective peroxisome membrane ...... drome, complementation group G
@en
Defective peroxisome membrane ...... drome, complementation group G
@en-gb
Defective peroxisome membrane ...... drome, complementation group G
@nl
P2093
P2860
P356
P1476
Defective peroxisome membrane ...... drome, complementation group G
@en
P2093
A A Roscher
A C Muntau
P U Mayerhofer
S Kammerer
P2860
P304
P356
10.1086/303071
P407
P577
2000-08-24T00:00:00Z