| YEAR | FIRST AUTHOR | JOURNAL | TITLE |
|---|---|---|---|
| 2009 | A Steinberg | J. Inherit. Metab. Dis. | A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts.[Pubmed] |
| 2009 | Yik Yik | Hum. Mutat. | Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.[Pubmed] |
| 2007 | Tracy Saveria | Exp. Parasitol. | Characterization of glycosomal RING finger proteins of trypanosomatids.[Pubmed] |
| 2007 | Tracy Saveria | Eukaryotic Cell | Conservation of PEX19-binding motifs required for protein targeting to mammalian peroxisomal and trypanosome glycosomal membranes.[Pubmed] |
| 2007 | Kazumasa Nito | Plant Cell Physiol. | Functional classification of Arabidopsis peroxisome biogenesis factors proposed from analyses of knockdown mutants.[Pubmed] |
| 2007 | Turner Turner | Am. J. Med. Genet. A | Zellweger syndrome resulting from maternal isodisomy of chromosome 1.[Pubmed] |
| 2007 | Uwe Schumann | Proc. Natl. Acad. Sci. U.S.A. | Requirement of the C3HC4 zinc RING finger of the Arabidopsis PEX10 for photorespiration and leaf peroxisome contact with chloroplasts.[Pubmed] |
| 2006 | Hanane Krazy | Biochim. Biophys. Acta | Identification and characterization of three peroxins--PEX6, PEX10 and PEX12--involved in glycosome biogenesis in Trypanosoma brucei.[Pubmed] |
| 2006 | Cindy Krause | Hum. Mutat. | Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients.[Pubmed] |
| 2005 | Chris Sparkes | Plant Physiol. | AtPEX2 and AtPEX10 are targeted to peroxisomes independently of known endoplasmic reticulum trafficking routes.[Pubmed] |
| 2004 | Steven Steinberg | Mol. Genet. Metab. | The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.[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] |
| 2003 | Nils Eckert | J. Cell. Sci. | Pex10p links the ubiquitin conjugating enzyme Pex4p to the protein import machinery of the peroxisome.[Pubmed] |
| 2003 | Birgit Agne | Mol. Cell | Pex8p: an intraperoxisomal organizer of the peroxisomal import machinery.[Pubmed] |
| 2003 | Nobuyuki Shimozawa | Adv. Exp. Med. Biol. | Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene.[Pubmed] |
| 2003 | Federica Sparkes | Plant Physiol. | An Arabidopsis pex10 null mutant is embryo lethal, implicating peroxisomes in an essential role during plant embryogenesis.[Pubmed] |
| 2003 | Uwe Schumann | Proc. Natl. Acad. Sci. U.S.A. | AthPEX10, a nuclear gene essential for peroxisome and storage organelle formation during Arabidopsis embryogenesis.[Pubmed] |
| 2001 | Y Suzuki | J. Inherit. Metab. Dis. | Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.[Pubmed] |
| 2000 | A Baker | Biochem. Soc. Trans. | Biochemical and molecular approaches to understanding protein import into peroxisomes.[Pubmed] |
| 2000 | Warren Warren | Hum. Mutat. | Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients.[Pubmed] |
| 1999 | S Chang | J. Cell. Sci. | Metabolic control of peroxisome abundance.[Pubmed] |
| 1999 | A Snyder | Mol. Biol. Cell | Pex19p interacts with Pex3p and Pex10p and is essential for peroxisome biogenesis in Pichia pastoris.[Pubmed] |
| 1999 | Chang Chang | J. Cell Biol. | PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import.[Pubmed] |
| 1998 | D Warren | Am. J. Hum. Genet. | Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.[Pubmed] |
| 0 | Mol. Membr. Biol. | Arabidopsis PEX19 is a dimeric protein that binds the peroxin PEX10.[Pubmed] |