PXMP4 by Pubmed references

YEAR FIRST AUTHOR JOURNAL TITLE
2009 Aare Rokka PLoS ONE Pxmp2 is a channel-forming protein in Mammalian peroxisomal membrane.[Pubmed]
2009 Sadaki Yokota Histochem. Cell Biol. Degradation of excess peroxisomes in mammalian liver cells by autophagy and other mechanisms.[Pubmed]
2009 Daniela Dietrich Mol. Biol. Cell Mutations in the Arabidopsis peroxisomal ABC transporter COMATOSE allow differentiation between multiple functions in planta: insights from an allelic series.[Pubmed]
2009 Srikanth Karnati Histochem. Cell Biol. Peroxisomes in airway epithelia and future prospects of these organelles for pulmonary cell biology.[Pubmed]
2009 Sabine Angermüller Histochem. Cell Biol. Peroxisomes and reactive oxygen species, a lasting challenge.[Pubmed]
2009 Silke Grunau Traffic Peroxisomal targeting of PTS2 pre-import complexes in the yeast Saccharomyces cerevisiae.[Pubmed]
2009 Yik Yik Hum. Mutat. Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.[Pubmed]
2008 Holger Eubel Plant Physiol. Novel proteins, putative membrane transporters, and an integrated metabolic network are revealed by quantitative proteomic analysis of Arabidopsis cell culture peroxisomes.[Pubmed]
2008 Hunt Hunt Prog. Lipid Res. Novel functions of acyl-CoA thioesterases and acyltransferases as auxiliary enzymes in peroxisomal lipid metabolism.[Pubmed]
2008 Michael Schrader Histochem. Cell Biol. The peroxisome: still a mysterious organelle.[Pubmed]
2008 Katarzyna Piekarska Microbiology (Reading, Engl.) The activity of the glyoxylate cycle in peroxisomes of Candida albicans depends on a functional beta-oxidation pathway: evidence for reduced metabolite transport across the peroxisomal membrane.[Pubmed]
2008 Koepke Koepke Toxicol. Appl. Pharmacol. Progeric effects of catalase inactivation in human cells.[Pubmed]
2008 Zsuzsanna Pathak Virology The host Pex19p plays a role in peroxisomal localization of tombusvirus replication proteins.[Pubmed]
2008 M Morita J. Inherit. Metab. Dis. Baicalein 5,6,7-trimethyl ether activates peroxisomal but not mitochondrial fatty acid beta-oxidation.[Pubmed]
2008 Paolo Lasorsa J. Biol. Chem. Peroxisomes as novel players in cell calcium homeostasis.[Pubmed]
2008 Mitsunori Ikeda Biol. Pharm. Bull. Characterization of peroxisomal targeting signals on alanine: glyoxylate aminotransferase.[Pubmed]
2008 Yasuhiko Sato J. Biol. Chem. Characterization of the interaction between recombinant human peroxin Pex3p and Pex19p: identification of TRP-104 IN Pex3p as a critical residue for the interaction.[Pubmed]
2008 Parthasarathy Sampathkumar J. Mol. Biol. Structural insights into the recognition of peroxisomal targeting signal 1 by Trypanosoma brucei peroxin 5.[Pubmed]
2007 Kazumasa Nito Plant Cell Physiol. Functional classification of Arabidopsis peroxisome biogenesis factors proposed from analyses of knockdown mutants.[Pubmed]
2007 Eastmond Eastmond Plant Cell MONODEHYROASCORBATE REDUCTASE4 is required for seed storage oil hydrolysis and postgerminative growth in Arabidopsis.[Pubmed]
2007 Zhenzhen Jia J. Biol. Chem. Fatty acid transport protein 4 is the principal very long chain fatty acyl-CoA synthetase in skin fibroblasts.[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 Henk Keane Hepatology Bile acid treatment alters hepatic disease and bile acid transport in peroxisome-deficient PEX2 Zellweger mice.[Pubmed]
2007 Stephan Kemp Mol. Genet. Metab. X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism, ABC half-transporters and the complicated route to treatment.[Pubmed]
2007 Luigi Ko J. Biol. Chem. The sterol carrier protein SCP-x/pro-SCP-2 gene has transcriptional activity and regulates the Alzheimer disease gamma-secretase.[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 Johannes Berger Biochim. Biophys. Acta X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.[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 Bikramjit Raychaudhury Biochim. Biophys. Acta Peroxisome is a reservoir of intracellular calcium.[Pubmed]
2006 João Carvalho J. Mol. Biol. The N-terminal half of the peroxisomal cycling receptor Pex5p is a natively unfolded domain.[Pubmed]
2005 Nobuyuki Shimozawa J. Child Neurol. Molecular and neurologic findings of peroxisome biogenesis disorders.[Pubmed]
2005 L Moser J. Inherit. Metab. Dis. Orthotopic liver transplantation from a living-related donor in an infant with a peroxisome biogenesis defect of the infantile Refsum disease type.[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 Karnik Karnik Plant Physiol. Arabidopsis peroxin 16 coexists at steady state in peroxisomes and endoplasmic reticulum.[Pubmed]
2005 Anne-Marie Lamhonwah Biochem. Biophys. Res. Commun. OCTN3 is a mammalian peroxisomal membrane carnitine transporter.[Pubmed]
2005 Monica Fagarasanu J. Cell Biol. Inp1p is a peroxisomal membrane protein required for peroxisome inheritance in Saccharomyces cerevisiae.[Pubmed]
2004 Wanders Wanders Am. J. Med. Genet. A Metabolic and molecular basis of peroxisomal disorders: a review.[Pubmed]
2004 Jeannette Poll-The Am. J. Med. Genet. A Peroxisome biogenesis disorders with prolonged survival: phenotypic expression in a cohort of 31 patients.[Pubmed]
2004 Jeannette Gootjes Pediatr. Res. Novel mutations in the PEX2 gene of four unrelated patients with a peroxisome biogenesis disorder.[Pubmed]
2004 Martin Fulda Plant Cell Peroxisomal Acyl-CoA synthetase activity is essential for seedling development in Arabidopsis thaliana.[Pubmed]
2004 Rainer Breitling Pathogenesis of peroxisomal deficiency disorders (Zellweger syndrome) may be mediated by misregulation of the GABAergic system via the diazepam binding inhibitor.[Pubmed]
2004 Tomoko Nagase Biochim. Biophys. Acta Peroxisomal localization in the developing mouse cerebellum: implications for neuronal abnormalities related to deficiencies in peroxisomes.[Pubmed]
2004 Xiaodong Wang Mol. Biol. Cell Multiple targeting modules on peroxisomal proteins are not redundant: discrete functions of targeting signals within Pmp47 and Pex8p.[Pubmed]
2003 Savita McClelland Biochem. Biophys. Res. Commun. Peroxisomal membrane monocarboxylate transporters: evidence for a redox shuttle system?[Pubmed]
2003 Yuang Huang Biochem. Biophys. Res. Commun. Altered antigenic disposition of peroxisomal urate oxidase in PEX5-defective Chinese hamster ovary cells.[Pubmed]
2003 R Wightman Hum. Mutat. MLYCD mutation analysis: evidence for protein mistargeting as a cause of MLYCD deficiency.[Pubmed]
2003 Martina Biermanns Eur. J. Cell Biol. The peroxisomal membrane targeting elements of human peroxin 2 (PEX2).[Pubmed]
2003 Johnson Johnson Plant Physiol. Import of the peroxisomal targeting signal type 2 protein 3-ketoacyl-coenzyme a thiolase into glyoxysomes.[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 Johannes Berger Adv. Exp. Med. Biol. Lessons from knockout mice II: Mouse models for peroxisomal disorders with single protein deficiency.[Pubmed]
2003 Christian Dammann Plant Physiol. Subcellular targeting of nine calcium-dependent protein kinase isoforms from Arabidopsis.[Pubmed]
2003 Isao Ilieva Neurol. Res. Age-related changes in peroxisomal membrane protein 70 and superoxide dismutase 1 in transgenic G93A mice.[Pubmed]
2003 Ineke Tabak Traffic Peroxisomes start their life in the endoplasmic reticulum.[Pubmed]
2002 Petriv Petriv Physiol. Genomics RNA interference of peroxisome-related genes in C. elegans: a new model for human peroxisomal disorders.[Pubmed]
2002 M Depreter J. Endocrinol. Modulation of the peroxisomal gene expression pattern by dehydroepiandrosterone and vitamin D: therapeutic implications.[Pubmed]
2002 J Gärtner Endocr. Res. Functional characterization of the adrenoleukodystrophy protein (ALDP) and disease pathogenesis.[Pubmed]
2002 Ida Veenhuis Curr. Opin. Cell Biol. Peroxisomes: flexible and dynamic organelles.[Pubmed]
2002 Tanja Mayerhofer Biochem. Biophys. Res. Commun. Two splice variants of human PEX19 exhibit distinct functions in peroxisomal assembly.[Pubmed]
2002 Hidenori Otera Mol. Cell. Biol. Peroxisomal targeting signal receptor Pex5p interacts with cargoes and import machinery components in a spatiotemporally differentiated manner: conserved Pex5p WXXXF/Y motifs are critical for matrix protein import.[Pubmed]
2002 Xiaoling Li J. Cell Biol. PEX11 promotes peroxisome division independently of peroxisome metabolism.[Pubmed]
2002 Kazumasa Nito Plant Cell Physiol. Direct interaction and determination of binding domains among peroxisomal import factors in Arabidopsis thaliana.[Pubmed]
2001 Hagerman Hagerman Mol. Cell Biol. Res. Commun. A mutation in the yeast mitochondrial ribosomal protein Rml2p is associated with a defect in catalase gene expression.[Pubmed]
2001 M Honsho J. Biol. Chem. Topogenesis of peroxisomal membrane protein requires a short, positively charged intervening-loop sequence and flanking hydrophobic segments. study using human membrane protein PMP34.[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 W Kovacs Histochem. Cell Biol. Localization of mRNAs encoding peroxisomal proteins in cell culture by non-radioactive in situ hybridization. Comparison of rat and human hepatoma cells and their responses to two divergent hypolipidemic drugs.[Pubmed]
2001 S Yokota J. Histochem. Cytochem. The role of 15-lipoxygenase in disruption of the peroxisomal membrane and in programmed degradation of peroxisomes in normal rat liver.[Pubmed]
2001 R Pap Exp. Cell Res. Peptide-based targeting of fluorophores to organelles in living cells.[Pubmed]
2001 Dansen Dansen Histochem. J. Targeted fluorescent probes in peroxisome function.[Pubmed]
2001 L Amery Comb. Chem. High Throughput Screen. Identification of a novel human peroxisomal 2,4-dienoyl-CoA reductase related protein using the M13 phage protein VI phage display technology.[Pubmed]
2001 E Baumgart Am. J. Pathol. Mitochondrial alterations caused by defective peroxisomal biogenesis in a mouse model for Zellweger syndrome (PEX5 knockout mouse).[Pubmed]
2001 L Palmieri EMBO J. Identification and functional reconstitution of the yeast peroxisomal adenine nucleotide transporter.[Pubmed]
2000 S Muntau Biol. Chem. Genomic organization, expression analysis, and chromosomal localization of the mouse PEX3 gene encoding a peroxisomal assembly protein.[Pubmed]
2000 A Muntau Biochem. Biophys. Res. Commun. The human PEX3 gene encoding a peroxisomal assembly protein: genomic organization, positional mapping, and mutation analysis in candidate phenotypes.[Pubmed]
2000 Titorenko Titorenko J. Cell Biol. Peroxisomal membrane fusion requires two AAA family ATPases, Pex1p and Pex6p.[Pubmed]
2000 M Chikayama Histochem. Cell Biol. Enzyme cytochemical localization of sarcosine oxidase activity in the liver and kidney of several mammals.[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 G Jedd Nat. Cell Biol. A new self-assembled peroxisomal vesicle required for efficient resealing of the plasma membrane.[Pubmed]
2000 G Unterrainer Hum. Mol. Genet. Co-expression of mutated and normal adrenoleukodystrophy protein reduces protein function: implications for gene therapy of X-linked adrenoleukodystrophy.[Pubmed]
2000 K Ghaedi Am. J. Hum. Genet. PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.[Pubmed]
2000 S Muntau Am. J. Hum. Genet. Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G.[Pubmed]
2000 M Hayashi EMBO J. AtPex14p maintains peroxisomal functions by determining protein targeting to three kinds of plant peroxisomes.[Pubmed]
1999 J Berger Eur. J. Biochem. The four murine peroxisomal ABC-transporter genes differ in constitutive, inducible and developmental expression.[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]
1998 Wanders Wanders Mol. Aspects Med. Lipid metabolism in peroxisomes in relation to human disease.[Pubmed]
1998 S Kemp Nat. Med. Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophy.[Pubmed]
1998 J Gärtner Eur. J. Cell Biol. Restoration of PEX2 peroxisome assembly defects by overexpression of PMP70.[Pubmed]
1998 B Henke J. Biol. Chem. IDP3 encodes a peroxisomal NADP-dependent isocitrate dehydrogenase required for the beta-oxidation of unsaturated fatty acids.[Pubmed]
1998 Titorenko Titorenko J. Cell Biol. Pex20p of the yeast Yarrowia lipolytica is required for the oligomerization of thiolase in the cytosol and for its targeting to the peroxisome.[Pubmed]
1998 M Depreter Biol. Cell Maturation of the liver-specific peroxisome versus laminin, collagen IV and integrin expression.[Pubmed]
1998 C Piot Comp. Biochem. Physiol. B, Biochem. Mol. Biol. Contribution of mitochondria and peroxisomes to palmitate oxidation in rat and bovine tissues.[Pubmed]
1997 Magalhães Magalhães Microsc. Res. Tech. Peroxisomes in adrenal steroidogenesis.[Pubmed]
1997 Infante Infante Mol. Cell. Biochem. On the molecular etiology of decreased arachidonic (20:4n-6), docosapentaenoic (22:5n-6) and docosahexaenoic (22:6n-3) acids in Zellweger syndrome and other peroxisomal disorders.[Pubmed]
1997 H Portsteffen Nat. Genet. Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders.[Pubmed]
1996 S Subramani Curr. Opin. Cell Biol. Convergence of model systems for peroxisome biogenesis.[Pubmed]
1996 Titorenko Titorenko J. Biol. Chem. Mutations in the PAY5 gene of the yeast Yarrowia lipolytica cause the accumulation of multiple subpopulations of peroxisomes.[Pubmed]
1996 Purdue Purdue J. Cell Biol. Targeting of human catalase to peroxisomes is dependent upon a novel COOH-terminal peroxisomal targeting sequence.[Pubmed]
1996 J Swartzman J. Cell Biol. The PAL1 gene product is a peroxisomal ATP-binding cassette transporter in the yeast Saccharomyces cerevisiae.[Pubmed]
1996 Zhang Zhang J. Cell Biol. Peb1p (Pas7p) is an intraperoxisomal receptor for the NH2-terminal, type 2, peroxisomal targeting sequence of thiolase: Peb1p itself is targeted to peroxisomes by an NH2-terminal peptide.[Pubmed]
1996 T Imanaka J. Biol. Chem. Insertion of the 70-kDa peroxisomal membrane protein into peroxisomal membranes in vivo and in vitro.[Pubmed]
1995 M Espeel Eur. J. Cell Biol. Immunolocalization of a 43 kDa peroxisomal membrane protein in the liver of patients with generalized peroxisomal disorders.[Pubmed]
1995 Zhang Zhang J. Cell Biol. PEB1 (PAS7) in Saccharomyces cerevisiae encodes a hydrophilic, intra-peroxisomal protein that is a member of the WD repeat family and is essential for the import of thiolase into peroxisomes.[Pubmed]
1995 R Erdmann J. Cell Biol. Giant peroxisomes in oleic acid-induced Saccharomyces cerevisiae lacking the peroxisomal membrane protein Pmp27p.[Pubmed]
1994 P Aubourg Curr. Opin. Genet. Dev. Adrenoleukodystrophy and other peroxisomal diseases.[Pubmed]
1994 F Authier J. Biol. Chem. Endosomal proteolysis of insulin by an acidic thiol metalloprotease unrelated to insulin degrading enzyme.[Pubmed]
1993 J Gärtner Semin. Cell Biol. The 70 kDa peroxisomal membrane protein: an ATP-binding cassette transporter protein involved in peroxisome biogenesis.[Pubmed]
1993 N Shimozawa Am. J. Hum. Genet. Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect.[Pubmed]
1993 C Zhang Mol. Biol. Cell Three peroxisome protein packaging pathways suggested by selective permeabilization of yeast mutants defective in peroxisome biogenesis.[Pubmed]
1992 J Ericsson J. Biol. Chem. Isoprenoid biosynthesis in rat liver peroxisomes. Characterization of cis-prenyltransferase and squalene synthetase.[Pubmed]
1992 I Singh J. Biol. Chem. Transport of fatty acids into human and rat peroxisomes. Differential transport of palmitic and lignoceric acids and its implication to X-adrenoleukodystrophy.[Pubmed]
1991 K Zaar J. Histochem. Cytochem. Immunoelectron microscopic localization of the isozymes of L-alpha-hydroxyacid oxidase in renal peroxisomes of beef and sheep: evidence of distinct intraorganellar subcompartmentation.[Pubmed]
1991 W Lageweg Biochem. J. Topography of very-long-chain-fatty-acid-activating activity in peroxisomes from rat liver.[Pubmed]
1989 R Reiter Biochem. J. Subcellular distribution of selenium in deficient mouse liver.[Pubmed]
1989 K Just Hepatology Biochemical effects and zonal heterogeneity of peroxisome proliferation induced by perfluorocarboxylic acids in rat liver.[Pubmed]
1989 O Poll-The Hum. Genet. Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders.[Pubmed]
1988 T Santos J. Biol. Chem. Peroxisomal integral membrane proteins in control and Zellweger fibroblasts.[Pubmed]
1987 M Douma Arch. Microbiol. A proton-translocating adenosine triphosphatase is associated with the peroxisomal membrane of yeasts.[Pubmed]
1986 P Labarca J. Membr. Biol. Large cation-selective pores from rat liver peroxisomal membranes incorporated to planar lipid bilayers.[Pubmed]
1986 P Borst Biochim. Biophys. Acta How proteins get into microbodies (peroxisomes, glyoxysomes, glycosomes).[Pubmed]
1984 S Miura J. Biol. Chem. Biosynthesis and intracellular transport of enzymes of peroxisomal beta-oxidation.[Pubmed]
1983 J Bremer Physiol. Rev. Carnitine--metabolism and functions.[Pubmed]
1982 P Mannaerts Biochem. J. Evidence that peroxisomal acyl-CoA synthetase is located at the cytoplasmic side of the peroxisomal membrane.[Pubmed]
0 Histochem. J. Hepatocyte polarity and the peroxisomal compartment: a comparative study.[Pubmed]
0 Mol. Membr. Biol. Arabidopsis PEX19 is a dimeric protein that binds the peroxin PEX10.[Pubmed]
0 J. Cell. Mol. Med. Peroxisome biogenesis and the role of protein import.[Pubmed]
0 Histochem. Cell Biol. Detection of mRNAs encoding peroxisomal proteins by non-radioactive in situ hybridization with digoxigenin-labelled cRNAs.[Pubmed]