Published in Biochim Biophys Acta on March 02, 2009
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Interdependence of the peroxisome-targeting receptors in Arabidopsis thaliana: PEX7 facilitates PEX5 accumulation and import of PTS1 cargo into peroxisomes. Mol Biol Cell (2010) 0.96
Matrix proteins are inefficiently imported into Arabidopsis peroxisomes lacking the receptor-docking peroxin PEX14. Plant Mol Biol (2011) 0.91
Mapping the cargo protein membrane translocation step into the PEX5 cycling pathway. J Biol Chem (2009) 0.90
Import of proteins into the peroxisomal matrix. Front Physiol (2013) 0.90
PEX5 and ubiquitin dynamics on mammalian peroxisome membranes. PLoS Comput Biol (2014) 0.82
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The putative Saccharomyces cerevisiae hydrolase Ldh1p is localized to lipid droplets. Eukaryot Cell (2011) 0.80
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Fis1, DLP1, and Pex11p coordinately regulate peroxisome morphogenesis. Exp Cell Res (2007) 1.37
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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
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
Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells. J Biol Chem (2001) 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
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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
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
cDNA cloning and characterization of the third isoform of human peroxin Pex11p. Biochem Biophys Res Commun (2003) 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
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
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
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Recruiting mechanism of the AAA peroxins, Pex1p and Pex6p, to Pex26p on the peroxisomal membrane. Traffic (2011) 0.81
Mff functions with Pex11pβ and DLP1 in peroxisomal fission. Biol Open (2013) 0.81
Overexpression of human acyl-CoA thioesterase upregulates peroxisome biogenesis. Exp Cell Res (2004) 0.80
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
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
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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
The protective effects of lafutidine for bortezomib induced peripheral neuropathy. J Blood Med (2013) 0.77
CUL4A-DDB1-Rbx1 E3 ligase controls the quality of the PTS2 receptor Pex7p. Biochem J (2014) 0.77
Extramedullary plasmacytoma of the dura mimicking meningioma. Int J Hematol (2010) 0.77
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
A novel pex2 mutant: catalase-deficient but temperature-sensitive PTS1 and PTS2 import. Biochem Biophys Res Commun (2002) 0.76
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
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A Rare t(9;22;16)(q34;q11;q24) Translocation in Chronic Myeloid Leukemia for Which Imatinib Mesylate Was Effective: A Case Report. Leuk Res Treatment (2011) 0.75
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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
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A temperature-sensitive CHO pex1 mutant with a novel mutation in the AAA Walker A1 motif. Biochem Biophys Res Commun (2006) 0.75
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Diffuse large B-cell lymphoma with hemolytic crisis developed twenty years after the onset of Evans syndrome. Rinsho Ketsueki (2014) 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