PEX12 by Pubmed references

YEAR FIRST AUTHOR JOURNAL TITLE
2009 Singh Singh Plant J. Molecular components required for the targeting of PEX7 to peroxisomes in Arabidopsis thaliana.[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 Tracy Saveria Eukaryotic Cell Conservation of PEX19-binding motifs required for protein targeting to mammalian peroxisomal and trypanosome glycosomal membranes.[Pubmed]
2007 Tracy Saveria Exp. Parasitol. Characterization of glycosomal RING finger proteins of trypanosomatids.[Pubmed]
2007 Avraham Zeharia J. Hum. Genet. A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 degrees C.[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]
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 Jilian Fan Plant Physiol. The Arabidopsis PEX12 gene is required for peroxisome biogenesis and is essential for development.[Pubmed]
2004 Steven Steinberg Mol. Genet. Metab. The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.[Pubmed]
2004 Jeannette Gootjes Hum. Mutat. Identification of the molecular defect in patients with peroxisomal mosaicism using a novel method involving culturing of cells at 40 degrees C: implications for other inborn errors of metabolism.[Pubmed]
2004 J Gootjes Neurology Reinvestigation of trihydroxycholestanoic acidemia reveals a peroxisome biogenesis disorder.[Pubmed]
2004 Jeannette Gootjes Eur. J. Hum. Genet. Novel mutations in the PEX12 gene of patients with a peroxisome biogenesis disorder.[Pubmed]
2003 Harper Harper J. Biol. Chem. PEX5 binds the PTS1 independently of Hsp70 and the peroxin PEX12.[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]
2002 Masanori Honsho J. Biol. Chem. The membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assembly.[Pubmed]
2001 Y Suzuki J. Inherit. Metab. Dis. Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.[Pubmed]
2001 C Reguenga J. Biol. Chem. Characterization of the mammalian peroxisomal import machinery: Pex2p, Pex5p, Pex12p, and Pex14p are subunits of the same protein assembly.[Pubmed]
2001 M Fransen Mol. Cell. Biol. Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences.[Pubmed]
2001 M Albertini Eur. J. Cell Biol. Pex12p of Saccharomyces cerevisiae is a component of a multi-protein complex essential for peroxisomal matrix protein import.[Pubmed]
1999 K Ghaedi Exp. Cell Res. Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein.[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 K Okumoto Mol. Cell. Biol. PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p.[Pubmed]
1998 Chang Chang Am. J. Hum. Genet. Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders.[Pubmed]
1997 K Okumoto Nat. Genet. PEX12 encodes an integral membrane protein of peroxisomes.[Pubmed]
1996 G Dodt J. Cell Biol. Multiple PEX genes are required for proper subcellular distribution and stability of Pex5p, the PTS1 receptor: evidence that PTS1 protein import is mediated by a cycling receptor.[Pubmed]