PEX7 by Pubmed references

2009 Pedro Brites Brain Plasmalogens participate in very-long-chain fatty acid-induced pathology.[Pubmed]
2009 Silke Grunau Traffic Peroxisomal targeting of PTS2 pre-import complexes in the yeast Saccharomyces cerevisiae.[Pubmed]
2009 Singh Singh Plant J. Molecular components required for the targeting of PEX7 to peroxisomes in Arabidopsis thaliana.[Pubmed]
2008 Kamran Ghaedi Cell Biochem. Funct. Isolation and characterization of novel phenotype CHO cell mutants defective in peroxisome assembly, using ICR191 as a potent mutagenic agent.[Pubmed]
2008 Armando Pilar Mol. Biochem. Parasitol. Interaction of Leishmania PTS2 receptor peroxin 7 with the glycosomal protein import machinery.[Pubmed]
2007 Nathalie Galland Biochim. Biophys. Acta Characterization of the role of the receptors PEX5 and PEX7 in the import of proteins into glycosomes of Trypanosoma brucei.[Pubmed]
2007 Kazumasa Nito Plant Cell Physiol. Functional classification of Arabidopsis peroxisome biogenesis factors proposed from analyses of knockdown mutants.[Pubmed]
2006 Satoru Mukai J. Biol. Chem. Molecular mechanisms of import of peroxisome-targeting signal type 2 (PTS2) proteins by PTS2 receptor Pex7p and PTS1 receptor Pex5pL.[Pubmed]
2006 Gabriele Steinberg Biochim. Biophys. Acta Peroxisome biogenesis disorders.[Pubmed]
2006 Shoji Mano Plant J. The Arabidopsis pex12 and pex13 mutants are defective in both PTS1- and PTS2-dependent protein transport to peroxisomes.[Pubmed]
2005 Bonnie Woodward Mol. Biol. Cell The Arabidopsis peroxisomal targeting signal type 2 receptor PEX7 is necessary for peroxisome function and dependent on PEX5.[Pubmed]
2005 Non Miyata Mol. Cell. Biol. Shuttling mechanism of peroxisome targeting signal type 1 receptor Pex5: ATP-independent import and ATP-dependent export.[Pubmed]
2005 Karsten Niederhoff J. Biol. Chem. Yeast Pex14p possesses two functionally distinct Pex5p and one Pex7p binding sites.[Pubmed]
2005 Annette Schell-Steven Mol. Cell. Biol. Identification of a novel, intraperoxisomal pex14-binding site in pex13: association of pex13 with the docking complex is essential for peroxisomal matrix protein import.[Pubmed]
2005 Makoto Hayashi J. Biol. Chem. Differential contribution of two peroxisomal protein receptors to the maintenance of peroxisomal functions in Arabidopsis.[Pubmed]
2004 Miki Kikuchi J. Biol. Chem. Proteomic analysis of rat liver peroxisome: presence of peroxisome-specific isozyme of Lon protease.[Pubmed]
2004 Nair Nair J. Cell Biol. Pex7p translocates in and out of peroxisomes in Saccharomyces cerevisiae.[Pubmed]
2004 Jansen Jansen Hum. Mutat. Molecular basis of Refsum disease: sequence variations in phytanoyl-CoA hydroxylase (PHYH) and the PTS2 receptor (PEX7).[Pubmed]
2004 João Azevedo Cell Biochem. Biophys. Protein translocation across the peroxisomal membrane.[Pubmed]
2003 Pedro Brites Hum. Mol. Genet. Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata.[Pubmed]
2003 Jungwoo Choe Biochemistry Analysis of the sequence motifs responsible for the interactions of peroxins 14 and 5, which are involved in glycosome biogenesis in Trypanosoma brucei.[Pubmed]
2003 Nobuyuki Shimozawa Am. J. Med. Genet. A Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: evidence for a founder haplotype for the most common PEX10 gene mutation.[Pubmed]
2002 Satoru Mukai J. Biol. Chem. Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells.[Pubmed]
2002 Jukka Kallijärvi Am. J. Hum. Genet. The TRIM37 gene encodes a peroxisomal RING-B-box-coiled-coil protein: classification of mulibrey nanism as a new peroxisomal disorder.[Pubmed]
2002 Pedro Motley Am. J. Hum. Genet. Mutational spectrum in the PEX7 gene and functional analysis of mutant alleles in 78 patients with rhizomelic chondrodysplasia punctata type 1.[Pubmed]
2002 Eiko Yanago Biochem. Biophys. Res. Commun. Isolation of Chinese hamster ovary cell pex mutants: two PEX7-defective mutants.[Pubmed]
2002 Nancy Braverman Hum. Mutat. Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotype.[Pubmed]
2001 G Dodt J. Biol. Chem. Domain mapping of human PEX5 reveals functional and structural similarities to Saccharomyces cerevisiae Pex18p and Pex21p.[Pubmed]
2001 Y Suzuki J. Inherit. Metab. Dis. Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.[Pubmed]
2000 Lee Lee J. Biochem. Identification of a cryptic N-terminal signal in Saccharomyces cerevisiae peroxisomal citrate synthase that functions in both peroxisomal and mitochondrial targeting.[Pubmed]
2000 M Ito Biochim. Biophys. Acta Rapid isolation and characterization of CHO mutants deficient in peroxisome biogenesis using the peroxisomal forms of fluorescent proteins.[Pubmed]
2000 N Braverman Genomics PEX7 gene structure, alternative transcripts, and evidence for a founder haplotype for the frequent RCDP allele, L292ter.[Pubmed]
1999 Moser Moser Mol. Genet. Metab. Genotype-phenotype correlations in disorders of peroxisome biogenesis.[Pubmed]
1999 S Chang J. Cell. Sci. Metabolic control of peroxisome abundance.[Pubmed]
1999 N Shimozawa J. Hum. Genet. A novel nonsense mutation of the PEX7 gene in a patient with rhizomelic chondrodysplasia punctata.[Pubmed]
1998 A Gurvitz Histochem. Cell Biol. Fate and role of peroxisomes during the life cycle of the yeast Saccharomyces cerevisiae: inheritance of peroxisomes during meiosis.[Pubmed]
1998 Y Elgersma J. Cell Biol. A mobile PTS2 receptor for peroxisomal protein import in Pichia pastoris.[Pubmed]
1997 M Purdue Nat. Genet. Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor.[Pubmed]
1996 P Rehling Ann. N. Y. Acad. Sci. Protein import into peroxisomes: new developments.[Pubmed]
1996 X Lazarow Ann. N. Y. Acad. Sci. A branched pathway for peroxisomal protein import: S. cerevisiae ghosts and an intraperoxisomal PTS2 receptor.[Pubmed]
1996 S Terlecky Ann. N. Y. Acad. Sci. Signals, receptors, and cytosolic factors involved in peroxisomal protein import.[Pubmed]
1996 P Rehling EMBO J. The import receptor for the peroxisomal targeting signal 2 (PTS2) in Saccharomyces cerevisiae is encoded by the PAS7 gene.[Pubmed]
1996 Zhang Zhang J. Cell Biol. Peb1p (Pas7p) is an intraperoxisomal receptor for the NH2-terminal, type 2, peroxisomal targeting sequence of thiolase: Peb1p itself is targeted to peroxisomes by an NH2-terminal peptide.[Pubmed]
1995 Zhang Zhang J. Cell Biol. PEB1 (PAS7) in Saccharomyces cerevisiae encodes a hydrophilic, intra-peroxisomal protein that is a member of the WD repeat family and is essential for the import of thiolase into peroxisomes.[Pubmed]
1994 M Marzioch EMBO J. PAS7 encodes a novel yeast member of the WD-40 protein family essential for import of 3-oxoacyl-CoA thiolase, a PTS2-containing protein, into peroxisomes.[Pubmed]