YEAR |
FIRST AUTHOR |
JOURNAL |
TITLE |
2009 |
Melanie Lingard |
Proc. Natl. Acad. Sci. U.S.A. |
Peroxisome-associated matrix protein degradation in Arabidopsis.[Pubmed] |
2009 |
Cindy Krause |
Eur. J. Hum. Genet. |
Rational diagnostic strategy for Zellweger syndrome spectrum patients.[Pubmed] |
2009 |
Yik Yik |
Hum. Mutat. |
Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.[Pubmed] |
2008 |
Yukio Fujiki |
Biochem. Soc. Trans. |
Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p involved in shuttling of the PTS1 receptor Pex5p in peroxisome biogenesis.[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] |
2008 |
Helmut Jungwirth |
FEBS Lett. |
Loss of peroxisome function triggers necrosis.[Pubmed] |
2007 |
Carolin Delker |
Phytochemistry |
Jasmonate biosynthesis in Arabidopsis thaliana requires peroxisomal beta-oxidation enzymes--additional proof by properties of pex6 and aim1.[Pubmed] |
2007 |
Kazumasa Nito |
Plant Cell Physiol. |
Functional classification of Arabidopsis peroxisome biogenesis factors proposed from analyses of knockdown mutants.[Pubmed] |
2007 |
Alexander Idnurm |
Eukaryotic Cell |
Peroxisome function regulates growth on glucose in the basidiomycete fungus Cryptococcus neoformans.[Pubmed] |
2007 |
Jae-Gu Seo |
Aging Cell |
A novel role of peroxin PEX6: suppression of aging defects in mitochondria.[Pubmed] |
2006 |
Cindy Krause |
Hum. Mutat. |
Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients.[Pubmed] |
2006 |
Shigehiko Tamura |
J. Biol. Chem. |
Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p.[Pubmed] |
2006 |
Wei Fan |
Biochem. Biophys. Res. Commun. |
A temperature-sensitive CHO pex1 mutant with a novel mutation in the AAA Walker A1 motif.[Pubmed] |
2006 |
Satomi Furuki |
J. Biol. Chem. |
Mutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complex.[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 |
Katja Rosenkranz |
FEBS J. |
Functional association of the AAA complex and the peroxisomal importomer.[Pubmed] |
2005 |
Ingvild Birschmann |
FEBS J. |
Structural and functional analysis of the interaction of the AAA-peroxins Pex1p and Pex6p.[Pubmed] |
2005 |
Astrid Kragt |
J. Biol. Chem. |
The Saccharomyces cerevisiae peroxisomal import receptor Pex5p is monoubiquitinated in wild type cells.[Pubmed] |
2005 |
Sabine Weller |
Am. J. Hum. Genet. |
Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis.[Pubmed] |
2005 |
Tatiana Boukh-Viner |
J. Cell Biol. |
Dynamic ergosterol- and ceramide-rich domains in the peroxisomal membrane serve as an organizing platform for peroxisome fusion.[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 |
Silke Platta |
Nat. Cell Biol. |
Functional role of the AAA peroxins in dislocation of the cycling PTS1 receptor back to the cytosol.[Pubmed] |
2004 |
Bonnie Zolman |
Proc. Natl. Acad. Sci. U.S.A. |
An Arabidopsis indole-3-butyric acid-response mutant defective in PEROXIN6, an apparent ATPase implicated in peroxisomal function.[Pubmed] |
2004 |
Steven Steinberg |
Mol. Genet. Metab. |
The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.[Pubmed] |
2004 |
Kumiko Shiozawa |
Acta Crystallogr. D Biol. Crystallogr. |
Crystallographic characterization of the N-terminal domain of PEX1.[Pubmed] |
2004 |
Kumiko Shiozawa |
J. Biol. Chem. |
Structure of the N-terminal domain of PEX1 AAA-ATPase. Characterization of a putative adaptor-binding domain.[Pubmed] |
2004 |
Inderjit Singh |
Brain Res. |
Impaired peroxisomal function in the central nervous system with inflammatory disease of experimental autoimmune encephalomyelitis animals and protection by lovastatin treatment.[Pubmed] |
2003 |
Naomi Matsumoto |
Nat. Cell Biol. |
The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes.[Pubmed] |
2003 |
Ingvild Birschmann |
Mol. Biol. Cell |
Pex15p of Saccharomyces cerevisiae provides a molecular basis for recruitment of the AAA peroxin Pex6p to peroxisomal membranes.[Pubmed] |
2003 |
Frank Roels |
Adv. Exp. Med. Biol. |
Peroxisome mosaics.[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 |
Annick Raas-Rothschild |
Am. J. Hum. Genet. |
A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents.[Pubmed] |
2002 |
Noriyo Hashiguchi |
Mol. Biol. Cell |
Peroxisomes are formed from complex membrane structures in PEX6-deficient CHO cells upon genetic complementation.[Pubmed] |
2002 |
Gould Gould |
Nat. Rev. Mol. Cell Biol. |
Opinion: peroxisomal-protein import: is it really that complex?[Pubmed] |
2001 |
S Tamura |
Biochem. J. |
Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.[Pubmed] |
2001 |
N Matsumoto |
J. Hum. Genet. |
The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6.[Pubmed] |
2001 |
A Kaplan |
Biochim. Biophys. Acta |
Identification and characterisation of PEX6 orthologues from plants.[Pubmed] |
2001 |
Y Suzuki |
J. Inherit. Metab. Dis. |
Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.[Pubmed] |
2000 |
A Imamura |
Pediatr. Res. |
Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1.[Pubmed] |
2000 |
M Kiel |
Appl. Microbiol. Biotechnol. |
Isolation of Penicillium chrysogenum PEX1 and PEX6 encoding AAA proteins involved in peroxisome biogenesis.[Pubmed] |
2000 |
A Baker |
Biochem. Soc. Trans. |
Biochemical and molecular approaches to understanding protein import into peroxisomes.[Pubmed] |
2000 |
Titorenko Titorenko |
Cell Biochem. Biophys. |
Peroxisome biogenesis in the yeast Yarrowia lipolytica.[Pubmed] |
2000 |
Titorenko Titorenko |
J. Cell Biol. |
Peroxisomal membrane fusion requires two AAA family ATPases, Pex1p and Pex6p.[Pubmed] |
2000 |
H Titorenko |
J. Cell Biol. |
Fusion of small peroxisomal vesicles in vitro reconstructs an early step in the in vivo multistep peroxisome assembly pathway of Yarrowia lipolytica.[Pubmed] |
1999 |
Z Zhang |
Hum. Mutat. |
Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders.[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] |
1998 |
A Gurvitz |
Histochem. Cell Biol. |
Fate and role of peroxisomes during the life cycle of the yeast Saccharomyces cerevisiae: inheritance of peroxisomes during meiosis.[Pubmed] |
1998 |
N Kinoshita |
J. Biol. Chem. |
Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals.[Pubmed] |
1998 |
S Tamura |
Biochem. Biophys. Res. Commun. |
A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p.[Pubmed] |
1998 |
Titorenko Titorenko |
Mol. Cell. Biol. |
Mutants of the yeast Yarrowia lipolytica defective in protein exit from the endoplasmic reticulum are also defective in peroxisome biogenesis.[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 |
Titorenko Titorenko |
Mol. Cell. Biol. |
Four distinct secretory pathways serve protein secretion, cell surface growth, and peroxisome biogenesis in the yeast Yarrowia lipolytica.[Pubmed] |
1996 |
T Tsukamoto |
Ann. N. Y. Acad. Sci. |
Cloning of peroxisome assembly factor-2.[Pubmed] |
1994 |
M Nuttley |
J. Biol. Chem. |
PAY4, a gene required for peroxisome assembly in the yeast Yarrowia lipolytica, encodes a novel member of a family of putative ATPases.[Pubmed] |