Published in Biochem Biophys Res Commun on January 24, 2003
Conserved function of pex11p and the novel pex25p and pex27p in peroxisome biogenesis. Mol Biol Cell (2003) 1.29
The peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathway. J Cell Biol (2008) 1.25
Pex11-related proteins in peroxisome dynamics: a role for the novel peroxin Pex27p in controlling peroxisome size and number in Saccharomyces cerevisiae. Mol Biol Cell (2003) 1.14
Tissue-selective, bidirectional regulation of PEX11 alpha and perilipin genes through a common peroxisome proliferator response element. Mol Cell Biol (2004) 1.04
Peroxisome biogenesis in mammalian cells. Front Physiol (2014) 0.98
A subtle interplay between three Pex11 proteins shapes de novo formation and fission of peroxisomes. Traffic (2011) 0.95
Membrane elongation factors in organelle maintenance: the case of peroxisome proliferation. Biomol Concepts (2011) 0.87
Self-interaction of human Pex11pβ during peroxisomal growth and division. PLoS One (2013) 0.83
Mff functions with Pex11pβ and DLP1 in peroxisomal fission. Biol Open (2013) 0.81
One of Three Pex11 Family Members Is Required for Peroxisomal Proliferation and Full Virulence of the Rice Blast Fungus Magnaporthe oryzae. PLoS One (2015) 0.77
Pex11mediates peroxisomal proliferation by promoting deformation of the lipid membrane. Biol Open (2015) 0.77
Peroxisome biogenesis and human peroxisome-deficiency disorders. Proc Jpn Acad Ser B Phys Biol Sci (2016) 0.75
Peroxisomal targeting signal receptor Pex5p interacts with cargoes and import machinery components in a spatiotemporally differentiated manner: conserved Pex5p WXXXF/Y motifs are critical for matrix protein import. Mol Cell Biol (2002) 1.42
Shuttling mechanism of peroxisome targeting signal type 1 receptor Pex5: ATP-independent import and ATP-dependent export. Mol Cell Biol (2005) 1.42
Fis1, DLP1, and Pex11p coordinately regulate peroxisome morphogenesis. Exp Cell Res (2007) 1.37
The peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathway. J Cell Biol (2008) 1.25
The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes. Nat Cell Biol (2003) 1.20
Sec16B is involved in the endoplasmic reticulum export of the peroxisomal membrane biogenesis factor peroxin 16 (Pex16) in mammalian cells. Proc Natl Acad Sci U S A (2011) 1.09
The peroxin Pex14p is involved in LC3-dependent degradation of mammalian peroxisomes. Exp Cell Res (2008) 1.08
Recruitment of the RNA helicase RHAU to stress granules via a unique RNA-binding domain. J Biol Chem (2008) 1.08
Cysteine ubiquitination of PTS1 receptor Pex5p regulates Pex5p recycling. Traffic (2011) 1.06
Functional domain mapping of peroxin Pex19p: interaction with Pex3p is essential for function and translocation. J Cell Sci (2006) 1.05
A novel fluorescent sensor protein for visualization of redox states in the cytoplasm and in peroxisomes. Mol Cell Biol (2010) 1.04
Functional domains and dynamic assembly of the peroxin Pex14p, the entry site of matrix proteins. J Biol Chem (2006) 1.03
Posttranslational regulation of fatty acyl-CoA reductase 1, Far1, controls ether glycerophospholipid synthesis. J Biol Chem (2010) 1.03
The membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assembly. J Biol Chem (2002) 1.00
Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells. J Biol Chem (2001) 1.00
Isolation and characterization of mutant animal cell line defective in alkyl-dihydroxyacetonephosphate synthase: localization and transport of plasmalogens to post-Golgi compartments. Biochim Biophys Acta (2008) 1.00
Peroxisome division is impaired in a CHO cell mutant with an inactivating point-mutation in dynamin-like protein 1 gene. Exp Cell Res (2006) 0.98
In vitro transport of membrane proteins to peroxisomes by shuttling receptor Pex19p. J Biol Chem (2005) 0.98
Ligand-dependent nucleo-cytoplasmic shuttling of peroxisome proliferator-activated receptors, PPARα and PPARγ. Genes Cells (2012) 0.97
Tail-anchored PEX26 targets peroxisomes via a PEX19-dependent and TRC40-independent class I pathway. J Cell Biol (2013) 0.97
Lessons from peroxisome-deficient Chinese hamster ovary (CHO) cell mutants. Biochim Biophys Acta (2006) 0.97
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation. Am J Hum Genet (2003) 0.91
Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p. J Biol Chem (2006) 0.90
AWP1/ZFAND6 functions in Pex5 export by interacting with cys-monoubiquitinated Pex5 and Pex6 AAA ATPase. Traffic (2011) 0.88
Two proteases, trypsin domain-containing 1 (Tysnd1) and peroxisomal lon protease (PsLon), cooperatively regulate fatty acid β-oxidation in peroxisomal matrix. J Biol Chem (2011) 0.87
New insights into dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p in shuttling of PTS1-receptor Pex5p during peroxisome biogenesis. Biochim Biophys Acta (2011) 0.86
Characterization of the interaction between recombinant human peroxin Pex3p and Pex19p: identification of TRP-104 IN Pex3p as a critical residue for the interaction. J Biol Chem (2008) 0.86
Molecular mechanisms of import of peroxisome-targeting signal type 2 (PTS2) proteins by PTS2 receptor Pex7p and PTS1 receptor Pex5pL. J Biol Chem (2006) 0.85
Crystal structure of the conserved N-terminal domain of the peroxisomal matrix protein import receptor, Pex14p. Proc Natl Acad Sci U S A (2009) 0.84
In vitro import of peroxisome-targeting signal type 2 (PTS2) receptor Pex7p into peroxisomes. Biochim Biophys Acta (2009) 0.84
Defective lipid remodeling of GPI anchors in peroxisomal disorders, Zellweger syndrome, and rhizomelic chondrodysplasia punctata. J Lipid Res (2012) 0.83
Topogenesis and homeostasis of fatty acyl-CoA reductase 1. J Biol Chem (2013) 0.83
Docosahexaenoic acid mediates peroxisomal elongation, a prerequisite for peroxisome division. J Cell Sci (2012) 0.83
Pex5p imports folded tetrameric catalase by interaction with Pex13p. Traffic (2012) 0.82
Mff functions with Pex11pβ and DLP1 in peroxisomal fission. Biol Open (2013) 0.81
Recruiting mechanism of the AAA peroxins, Pex1p and Pex6p, to Pex26p on the peroxisomal membrane. Traffic (2011) 0.81
Overexpression of human acyl-CoA thioesterase upregulates peroxisome biogenesis. Exp Cell Res (2004) 0.80
Interaction defect of the medium isoform of PTS1-receptor Pex5p with PTS2-receptor Pex7p abrogates the PTS2 protein import into peroxisomes in mammals. J Biochem (2010) 0.79
Mutations 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 complex. J Biol Chem (2005) 0.79
Pex5p stabilizes Pex14p: a study using a newly isolated pex5 CHO cell mutant, ZPEG101. Biochem J (2013) 0.79
Nuclear transport of peroxisome-proliferator activated receptor α. J Biochem (2010) 0.78
Isolation of Chinese hamster ovary cell pex mutants: two PEX7-defective mutants. Biochem Biophys Res Commun (2002) 0.78
Peroxin Pex14p is the key component for coordinated autophagic degradation of mammalian peroxisomes by direct binding to LC3-II. Genes Cells (2014) 0.78
CUL4A-DDB1-Rbx1 E3 ligase controls the quality of the PTS2 receptor Pex7p. Biochem J (2014) 0.77
Monomer-dimer transition of the conserved N-terminal domain of the mammalian peroxisomal matrix protein import receptor, Pex14p. Biochem Biophys Res Commun (2010) 0.76
System to quantify the import of peroxisomal matrix proteins by fluorescence intensity. Genes Cells (2013) 0.76
A novel pex2 mutant: catalase-deficient but temperature-sensitive PTS1 and PTS2 import. Biochem Biophys Res Commun (2002) 0.76
A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome. Biochem Biophys Res Commun (2002) 0.76
Molecular cloning of Chinese hamster ceramide glucosyltransferase and its enhanced expression in peroxisome-defective mutant Z65 cells. Arch Biochem Biophys (2002) 0.76
AAA+ proteins. Editorial. J Struct Biol (2012) 0.76
A temperature-sensitive CHO pex1 mutant with a novel mutation in the AAA Walker A1 motif. Biochem Biophys Res Commun (2006) 0.75
Alterations in the molecular species of plasmalogen phospholipids and glycolipids due to peroxisomal dysfunction in Chinese hamster ovary-mutant Z65 cells by FABMS method. J Chromatogr B Analyt Technol Biomed Life Sci (2007) 0.75
Mislocalization and inhibition of acetyl-CoA carboxylase 1 by a synthetic small molecule. Biochem J (2012) 0.75
Isolation and characterization of novel phenotype CHO cell mutants defective in peroxisome assembly, using ICR191 as a potent mutagenic agent. Cell Biochem Funct (2008) 0.75