PEX10 by Pubmed references

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 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]
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]
2006 Cindy Krause Hum. Mutat. Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients.[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]
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 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]
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]
2001 Y Suzuki J. Inherit. Metab. Dis. Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.[Pubmed]
2000 Warren Warren Hum. Mutat. Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients.[Pubmed]
2000 A Baker Biochem. Soc. Trans. Biochemical and molecular approaches to understanding protein import into peroxisomes.[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]
1999 S Chang J. Cell. Sci. Metabolic control of peroxisome abundance.[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]