PEX2 by Pubmed references

YEAR FIRST AUTHOR JOURNAL TITLE
2009 Kovacs Kovacs J. Biol. Chem. Peroxisome deficiency causes a complex phenotype because of hepatic SREBP/Insig dysregulation associated with endoplasmic reticulum stress.[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]
2007 Kazumasa Nito Plant Cell Physiol. Functional classification of Arabidopsis peroxisome biogenesis factors proposed from analyses of knockdown mutants.[Pubmed]
2007 Henk Keane Hepatology Bile acid treatment alters hepatic disease and bile acid transport in peroxisome-deficient PEX2 Zellweger mice.[Pubmed]
2007 Tracy Saveria Exp. Parasitol. Characterization of glycosomal RING finger proteins of trypanosomatids.[Pubmed]
2006 Cindy Krause Hum. Mutat. Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients.[Pubmed]
2005 D Faust J. Inherit. Metab. Dis. Peroxisome biogenesis disorders: the role of peroxisomes and metabolic dysfunction in developing brain.[Pubmed]
2005 Tracy Banerjee Mol. Biochem. Parasitol. Identification of trypanosomatid PEX19: functional characterization reveals impact on cell growth and glycosome size and number.[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]
2004 Kovacs Kovacs Mol. Cell. Biol. Disturbed cholesterol homeostasis in a peroxisome-deficient PEX2 knockout mouse model.[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 Pediatr. Res. Novel mutations in the PEX2 gene of four unrelated patients with a peroxisome biogenesis disorder.[Pubmed]
2003 Faust Faust J. Comp. Neurol. Abnormal cerebellar histogenesis in PEX2 Zellweger mice reflects multiple neuronal defects induced by peroxisome deficiency.[Pubmed]
2003 Stéphanie Boisnard Mol. Microbiol. Overexpression of a human and a fungal ABC transporter similarly suppresses the differentiation defects of a fungal peroxisomal mutant but introduces pleiotropic cellular effects.[Pubmed]
2003 Martina Biermanns Eur. J. Cell Biol. The peroxisomal membrane targeting elements of human peroxin 2 (PEX2).[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 Xiaoling Li Mol. Cell. Biol. PEX11 beta deficiency is lethal and impairs neuronal migration but does not abrogate peroxisome function.[Pubmed]
2002 Cristina Guerra-Giraldez J. Cell. Sci. Compartmentation of enzymes in a microbody, the glycosome, is essential in Trypanosoma brucei.[Pubmed]
2002 Noriko Akiyama Biochem. Biophys. Res. Commun. A novel pex2 mutant: catalase-deficient but temperature-sensitive PTS1 and PTS2 import.[Pubmed]
2002 Yuan Huang Biochim. Biophys. Acta Different accumulations of 3-ketoacyl-CoA thiolase precursor in peroxisomes of Chinese hamster ovary cells harboring a dysfunction in the PEX2 protein.[Pubmed]
2001 Y Suzuki J. Inherit. Metab. Dis. Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.[Pubmed]
2001 Infante Infante Mol. Genet. Metab. Zellweger syndrome knockout mouse models challenge putative peroxisomal beta-oxidation involvement in docosahexaenoic acid (22:6n-3) biosynthesis.[Pubmed]
2000 T Matsumura J. Biol. Chem. Disruption of the interaction of the longer isoform of Pex5p, Pex5pL, with Pex7p abolishes peroxisome targeting signal type 2 protein import in mammals. Study with a novel Pex5-impaired Chinese hamster ovary cell mutant.[Pubmed]
2000 N Shimozawa Biochem. Biophys. Res. Commun. Molecular mechanism of detectable catalase-containing particles, peroxisomes, in fibroblasts from a PEX2-defective patient.[Pubmed]
2000 T Osumi Cell Biochem. Biophys. Temperature sensitivity in peroxisome assembly processes characterizes milder forms of peroxisome biogenesis disorders.[Pubmed]
2000 C Fujiwara J. Biol. Chem. Catalase-less peroxisomes. Implication in the milder forms of peroxisome biogenesis disorder.[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]
1999 N Aboushadi J. Histochem. Cytochem. Role of peroxisomes in isoprenoid biosynthesis.[Pubmed]
1999 N Shimozawa J. Med. Genet. Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders.[Pubmed]
1999 R Toyama Hum. Mol. Genet. Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants.[Pubmed]
1999 S Chang J. Cell. Sci. Metabolic control of peroxisome abundance.[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 K Ghaedi Exp. Cell Res. Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals.[Pubmed]
1998 J Gärtner Eur. J. Cell Biol. Restoration of PEX2 peroxisome assembly defects by overexpression of PMP70.[Pubmed]
1997 K Okumoto Exp. Cell Res. Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III.[Pubmed]
1997 T Tsukamoto Biochem. Biophys. Res. Commun. Isolation of a new peroxisome-deficient CHO cell mutant defective in peroxisome targeting signal-1 receptor.[Pubmed]
1997 Titorenko Titorenko Mol. Cell. Biol. Four distinct secretory pathways serve protein secretion, cell surface growth, and peroxisome biogenesis in the yeast Yarrowia lipolytica.[Pubmed]
1997 Faust Faust J. Cell Biol. Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder.[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]
0 J. Mol. Neurosci. The peroxisome deficient PEX2 Zellweger mouse: pathologic and biochemical correlates of lipid dysfunction.[Pubmed]