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PEX3 gene

Known as: peroxisomal biogenesis factor 3, PEROXIN 3, PEX3 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Distinct requirements for intra-ER sorting and budding of peroxisomal membrane proteins from the ER
An intra-ER sorting process regulates segregation, packaging, and budding of peroxisomal importomer subcomplexes, thereby… 
2015
2015
Mechanisms of Selective Autophagy of Peroxisomes
Author(s): Burnett, Sarah Frances | Abstract: The study of pexophagy (selective peroxisome degradation by autophagy) is relevant… 
2014
2014
Association between the Intrinsically Disordered Protein PEX19 and PEX3
In peroxisomes, peroxins (PEXs) 3 and 19 are the principal protein components of the machinery required for early peroxisomal… 
Highly Cited
2012
Highly Cited
2012
Peroxisome Formation Requires the Endoplasmic Reticulum Channel Protein Sec61
In peroxisome formation, models of near‐autonomous peroxisome biogenesis with membrane protein integration directly from the… 
2008
2008
Isolation and characterization of novel phenotype CHO cell mutants defective in peroxisome assembly, using ICR191 as a potent mutagenic agent
To elucidate molecular and cellular mechanisms of peroxisome biogenesis, we have isolated Chinese hamster ovary (CHO) cell… 
Review
2006
Review
2006
Peroxisome biogenesis: where Arf and coatomer might be involved.
Highly Cited
2003
Highly Cited
2003
The interaction between human PEX3 and PEX19 characterized by fluorescence resonance energy transfer (FRET) analysis.
The process of peroxisome biogenesis involves several PEX genes that encode the machinery required to assemble the organelle… 
2003
2003
Interaction of PEX3 and PEX19 visualized by fluorescence resonance energy transfer (FRET).
The process of peroxisome biogenesis involves several PEX genes that encode the machinery required to assemble the organelle… 
Review
2001
Review
2001
Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders
Peroxisome biogenesis disorders (PBDs) are severe autosomal recessive neurological diseases caused by a defect of peroxisomal… 
2000
2000
The human PEX3 gene encoding a peroxisomal assembly protein: genomic organization, positional mapping, and mutation analysis in candidate phenotypes.
In yeasts, the peroxin Pex3p was identified as a peroxisomal integral membrane protein that presumably plays a role in the early… 
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