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] |
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] |
2009 |
Singh Singh |
Plant J. |
Molecular components required for the targeting of PEX7 to peroxisomes in Arabidopsis thaliana.[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 |
Henk Keane |
Hepatology |
Bile acid treatment alters hepatic disease and bile acid transport in peroxisome-deficient PEX2 Zellweger mice.[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 |
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] |
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 |
Shoji Mano |
Plant J. |
The Arabidopsis pex12 and pex13 mutants are defective in both PTS1- and PTS2-dependent protein transport to peroxisomes.[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 |
Jilian Fan |
Plant Physiol. |
The Arabidopsis PEX12 gene is required for peroxisome biogenesis and is essential for development.[Pubmed] |
2005 |
D Faust |
J. Inherit. Metab. Dis. |
Peroxisome biogenesis disorders: the role of peroxisomes and metabolic dysfunction in developing brain.[Pubmed] |
2005 |
Chris Sparkes |
Plant Physiol. |
AtPEX2 and AtPEX10 are targeted to peroxisomes independently of known endoplasmic reticulum trafficking routes.[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 |
Tracy Banerjee |
Mol. Biochem. Parasitol. |
Identification of trypanosomatid PEX19: functional characterization reveals impact on cell growth and glycosome size and number.[Pubmed] |
2004 |
Kovacs Kovacs |
Mol. Cell. Biol. |
Disturbed cholesterol homeostasis in a peroxisome-deficient PEX2 knockout mouse model.[Pubmed] |
2004 |
Jeannette Gootjes |
Pediatr. Res. |
Novel mutations in the PEX2 gene of four unrelated patients with a peroxisome biogenesis disorder.[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 |
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 |
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 |
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 |
Harper Harper |
J. Biol. Chem. |
PEX5 binds the PTS1 independently of Hsp70 and the peroxin PEX12.[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 |
Noriko Akiyama |
Biochem. Biophys. Res. Commun. |
A novel pex2 mutant: catalase-deficient but temperature-sensitive PTS1 and PTS2 import.[Pubmed] |
2002 |
Masanori Honsho |
J. Biol. Chem. |
The membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assembly.[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] |
2002 |
Cristina Guerra-Giraldez |
J. Cell. Sci. |
Compartmentation of enzymes in a microbody, the glycosome, is essential in Trypanosoma brucei.[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 Albertini |
Eur. J. Cell Biol. |
Pex12p of Saccharomyces cerevisiae is a component of a multi-protein complex essential for peroxisomal matrix protein import.[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] |
2001 |
Y Suzuki |
J. Inherit. Metab. Dis. |
Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.[Pubmed] |
2001 |
M Fransen |
Mol. Cell. Biol. |
Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences.[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 |
Warren Warren |
Hum. Mutat. |
Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients.[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 |
A Baker |
Biochem. Soc. Trans. |
Biochemical and molecular approaches to understanding protein import into peroxisomes.[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] |
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] |
1999 |
A Snyder |
Mol. Biol. Cell |
Pex19p interacts with Pex3p and Pex10p and is essential for peroxisome biogenesis in Pichia pastoris.[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 |
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 |
S Chang |
J. Cell. Sci. |
Metabolic control of peroxisome abundance.[Pubmed] |
1999 |
N Aboushadi |
J. Histochem. Cytochem. |
Role of peroxisomes in isoprenoid biosynthesis.[Pubmed] |
1999 |
R Toyama |
Hum. Mol. Genet. |
Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants.[Pubmed] |
1998 |
D Warren |
Am. J. Hum. Genet. |
Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.[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 |
J Gärtner |
Eur. J. Cell Biol. |
Restoration of PEX2 peroxisome assembly defects by overexpression of PMP70.[Pubmed] |
1998 |
Chang Chang |
Am. J. Hum. Genet. |
Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders.[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 |
K Okumoto |
Nat. Genet. |
PEX12 encodes an integral membrane protein of peroxisomes.[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] |
0 |
|
Mol. Membr. Biol. |
Arabidopsis PEX19 is a dimeric protein that binds the peroxin PEX10.[Pubmed] |