| 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 | 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] |
| 2005 | D Faust | J. Inherit. Metab. Dis. | Peroxisome biogenesis disorders: the role of peroxisomes and metabolic dysfunction in developing brain.[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] |
| 2004 | Kovacs Kovacs | Mol. Cell. Biol. | Disturbed cholesterol homeostasis in a peroxisome-deficient PEX2 knockout mouse model.[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] |
| 2003 | Faust Faust | J. Comp. Neurol. | Abnormal cerebellar histogenesis in PEX2 Zellweger mice reflects multiple neuronal defects induced by peroxisome deficiency.[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 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] |
| 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] |
| 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 | 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] |
| 1997 | K Okumoto | Exp. Cell Res. | Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III.[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] |