| YEAR | FIRST AUTHOR | JOURNAL | TITLE |
|---|---|---|---|
| 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] |
| 2009 | Pedro Brites | Brain | Plasmalogens participate in very-long-chain fatty acid-induced pathology.[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 | 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] |
| 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] |
| 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 | 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] |
| 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] |
| 2001 | Y Suzuki | J. Inherit. Metab. Dis. | Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.[Pubmed] |
| 2001 | G Dodt | J. Biol. Chem. | Domain mapping of human PEX5 reveals functional and structural similarities to Saccharomyces cerevisiae Pex18p and Pex21p.[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] |