Mus musculus by Pubmed references

YEAR FIRST AUTHOR JOURNAL TITLE
2009 Stéphane Fourcade Am. J. Physiol. Endocrinol. Metab. A key role for the peroxisomal ABCD2 transporter in fatty acid homeostasis.[Pubmed]
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 Yoshinori Kashiwayama Exp. Cell Res. 70-kDa peroxisomal membrane protein related protein (P70R/ABCD4) localizes to endoplasmic reticulum not peroxisomes, and NH2-terminal hydrophobic property determines the subcellular localization of ABC subfamily D proteins.[Pubmed]
2009 Pedro Brites Brain Plasmalogens participate in very-long-chain fatty acid-induced pathology.[Pubmed]
2009 Liu Liu J. Lipid Res. ABCD2 is abundant in adipose tissue and opposes the accumulation of dietary erucic acid (C22:1) in fat.[Pubmed]
2009 Jaspreet Singh J. Lipid Res. Silencing of Abcd1 and Abcd2 genes sensitizes astrocytes for inflammation: implication for X-adrenoleukodystrophy.[Pubmed]
2009 Srikanth Karnati Histochem. Cell Biol. Peroxisomes in airway epithelia and future prospects of these organelles for pulmonary cell biology.[Pubmed]
2009 Aare Rokka PLoS ONE Pxmp2 is a channel-forming protein in Mammalian peroxisomal membrane.[Pubmed]
2009 K Kaczmarek Cytogenet. Genome Res. Ccdc33, a predominantly testis-expressed gene, encodes a putative peroxisomal protein.[Pubmed]
2009 Sadaki Yokota Histochem. Cell Biol. Degradation of excess peroxisomes in mammalian liver cells by autophagy and other mechanisms.[Pubmed]
2008 Ehtishamul Contreras Arch. Biochem. Biophys. Psychosine-induced alterations in peroxisomes of twitcher mouse liver.[Pubmed]
2008 Leen Hulshagen J. Neurosci. Absence of functional peroxisomes from mouse CNS causes dysmyelination and axon degeneration.[Pubmed]
2008 Sarah Jansen Biol. Reprod. Characterization and regulation of monocarboxylate cotransporters Slc16a7 and Slc16a3 in preimplantation mouse embryos.[Pubmed]
2008 Stéphane Fourcade Hum. Mol. Genet. Early oxidative damage underlying neurodegeneration in X-adrenoleukodystrophy.[Pubmed]
2008 Westin Westin Cell. Mol. Life Sci. Short- and medium-chain carnitine acyltransferases and acyl-CoA thioesterases in mouse provide complementary systems for transport of beta-oxidation products out of 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 Konstantinos Fletcher J. Immunol. Congenic analysis of the NKT cell control gene Nkt2 implicates the peroxisomal protein Pxmp4.[Pubmed]
2007 Jyh-Feng Lu Lab. Invest. The role of peroxisomal ABC transporters in the mouse adrenal gland: the loss of Abcd2 (ALDR), Not Abcd1 (ALD), causes oxidative damage.[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 Kun Du Biochem. Cell Biol. A 27.368 kDa retinal reductase in New Zealand white rabbit liver cytosol encoded by the peroxisomal retinol dehydrogenase-reductase cDNA: purification and characterization of the enzyme.[Pubmed]
2007 Henk Keane Hepatology Bile acid treatment alters hepatic disease and bile acid transport in peroxisome-deficient PEX2 Zellweger mice.[Pubmed]
2007 Stephan Wanders Pflugers Arch. The peroxisomal ABC transporter family.[Pubmed]
2007 Anca Nenicu Biol. Reprod. Peroxisomes in human and mouse testis: differential expression of peroxisomal proteins in germ cells and distinct somatic cell types of the testis.[Pubmed]
2007 Corinna Kassmann Nat. Genet. Axonal loss and neuroinflammation caused by peroxisome-deficient oligodendrocytes.[Pubmed]
2007 Barbara Ahlemeyer J. Comp. Neurol. Differential expression of peroxisomal matrix and membrane proteins during postnatal development of mouse brain.[Pubmed]
2007 Olga Krysko J. Neurosci. Res. Neocortical and cerebellar developmental abnormalities in conditions of selective elimination of peroxisomes from brain or from liver.[Pubmed]
2007 Sebastian Wiese Mol. Cell Proteomics Proteomics characterization of mouse kidney peroxisomes by tandem mass spectrometry and protein correlation profiling.[Pubmed]
2007 Noriko Shinjyo Biochem. Biophys. Res. Commun. Relationship between reactive oxygen species and heme metabolism during the differentiation of Neuro2a cells.[Pubmed]
2007 P Grzmil Cytogenet. Genome Res. The putative peroxisomal gene Pxt1 is exclusively expressed in the testis.[Pubmed]
2007 Bonini Bonini Free Radic. Biol. Med. Immunolocalization of hypochlorite-induced, catalase-bound free radical formation in mouse hepatocytes.[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 Jun Ren Mech. Ageing Dev. Cardiac overexpression of antioxidant catalase attenuates aging-induced cardiomyocyte relaxation dysfunction.[Pubmed]
2006 Lola MacLennan Hum. Mol. Genet. Targeted disruption of glycerol kinase gene in mice: expression analysis in liver shows alterations in network partners related to glycerol kinase activity.[Pubmed]
2006 Yang Salido Proc. Natl. Acad. Sci. U.S.A. Alanine-glyoxylate aminotransferase-deficient mice, a model for primary hyperoxaluria that responds to adenoviral gene transfer.[Pubmed]
2006 Tam Nguyen J. Cell. Sci. Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundance.[Pubmed]
2006 Johannes Berger Biochim. Biophys. Acta X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.[Pubmed]
2006 Reiko Iida Biochem. Biophys. Res. Commun. Human Mpv17-like protein is localized in peroxisomes and regulates expression of antioxidant enzymes.[Pubmed]
2006 Steven Huyghe Am. J. Pathol. Peroxisomal multifunctional protein-2 deficiency causes motor deficits and glial lesions in the adult central nervous system.[Pubmed]
2006 Yoko Huong Activity and mRNA levels of enzymes involved in hepatic fatty acid oxidation in mice fed citrus flavonoids.[Pubmed]
2006 Ryota Itoh J. Biol. Chem. Functional domains and dynamic assembly of the peroxin Pex14p, the entry site of matrix proteins.[Pubmed]
2005 Anne-Marie Lamhonwah Biochem. Biophys. Res. Commun. OCTN3 is a mammalian peroxisomal membrane carnitine transporter.[Pubmed]
2005 Reiko Iida Exp. Cell Res. A novel alternative spliced Mpv17-like protein isoform localizes in cytosol and is expressed in a kidney- and adult-specific manner.[Pubmed]
2005 Yoshinori Kashiwayama Biochim. Biophys. Acta Role of Pex19p in the targeting of PMP70 to peroxisome.[Pubmed]
2005 Piper Schriner Science Extension of murine life span by overexpression of catalase targeted to mitochondria.[Pubmed]
2005 K Dunster Clin. Exp. Immunol. Limkain b1, a novel human autoantigen localized to a subset of ABCD3 and PXF marked peroxisomes.[Pubmed]
2005 Isidre Ferrer Hum. Mol. Genet. Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage.[Pubmed]
2005 D Faust J. Inherit. Metab. Dis. Peroxisome biogenesis disorders: the role of peroxisomes and metabolic dysfunction in developing brain.[Pubmed]
2005 Catherine Gondcaille J. Cell Biol. Phenylbutyrate up-regulates the adrenoleukodystrophy-related gene as a nonclassical peroxisome proliferator.[Pubmed]
2005 Aud Eliassen Activity of peroxisomal enzymes, and levels of polyamines in LPA-transgenic mice on two different diets.[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 Mitsuru Ishizuka Exp. Cell Res. Overexpression of human acyl-CoA thioesterase upregulates peroxisome biogenesis.[Pubmed]
2004 Pedro Guimarães Biochim. Biophys. Acta Mouse liver PMP70 and ALDP: homomeric interactions prevail in vivo.[Pubmed]
2004 Kovacs Kovacs Mol. Cell. Biol. Disturbed cholesterol homeostasis in a peroxisome-deficient PEX2 knockout mouse model.[Pubmed]
2004 Xinlian Chen Arch. Biochem. Biophys. Catalase transgenic mice: characterization and sensitivity to oxidative stress.[Pubmed]
2004 Annett Koch J. Cell. Sci. Peroxisome elongation and constriction but not fission can occur independently of dynamin-like protein 1.[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 Myriam Pettus Rapid Commun. Mass Spectrom. Mass spectrometric analysis of ceramide perturbations in brain and fibroblasts of mice and human patients with peroxisomal disorders.[Pubmed]
2004 Grégory Chevillard Biochimie Targeted disruption of the peroxisomal thiolase B gene in mouse: a new model to study disorders related to peroxisomal lipid metabolism.[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 Xiong Su Biochemistry Sequential ordered fatty acid alpha oxidation and Delta9 desaturation are major determinants of lipid storage and utilization in differentiating adipocytes.[Pubmed]
2004 Cheng Cheng J. Biol. Chem. Mammalian wax biosynthesis. I. Identification of two fatty acyl-Coenzyme A reductases with different substrate specificities and tissue distributions.[Pubmed]
2004 Aurora Pujol Hum. Mol. Genet. Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-adrenoleukodystrophy.[Pubmed]
2003 Johannes Berger Adv. Exp. Med. Biol. Lessons from knockout mice II: Mouse models for peroxisomal disorders with single protein deficiency.[Pubmed]
2003 Reiko Iida J. Biol. Chem. M-LP, Mpv17-like protein, has a peroxisomal membrane targeting signal comprising a transmembrane domain and a positively charged loop and up-regulates expression of the manganese superoxide dismutase gene.[Pubmed]
2003 Sacha Ferdinandusse J. Lipid Res. Studies on the metabolic fate of n-3 polyunsaturated fatty acids.[Pubmed]
2003 Claus Rodemer Adv. Exp. Med. Biol. Targeted disruption of ether lipid synthesis in mice.[Pubmed]
2003 Ben Geuze Mol. Biol. Cell Involvement of the endoplasmic reticulum in peroxisome formation.[Pubmed]
2003 Naomi Matsumoto Am. J. Hum. Genet. Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.[Pubmed]
2003 Faust Faust J. Comp. Neurol. Abnormal cerebellar histogenesis in PEX2 Zellweger mice reflects multiple neuronal defects induced by peroxisome deficiency.[Pubmed]
2003 Xiaochun Zhang J. Mol. Cell. Cardiol. Cardiac-specific overexpression of catalase rescues ventricular myocytes from ethanol-induced cardiac contractile defect.[Pubmed]
2003 Xinhe Wang Gene Expr. Rapid hepatocyte nuclear translocation of the Forkhead Box M1B (FoxM1B) transcription factor caused a transient increase in size of regenerating transgenic hepatocytes.[Pubmed]
2003 Pedro Brites Hum. Mol. Genet. Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata.[Pubmed]
2003 Sonia Benhamida Mol. Ther. Transduced CD34+ cells from adrenoleukodystrophy patients with HIV-derived vector mediate long-term engraftment of NOD/SCID mice.[Pubmed]
2003 J-F McGuinness Mol. Cell. Biol. Role of ALDP (ABCD1) and mitochondria in X-linked adrenoleukodystrophy.[Pubmed]
2003 Megan Maxwell Mol. Cell. Biol. Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype.[Pubmed]
2003 Anneleen Janssen J. Neurosci. Neuronal migration depends on intact peroxisomal function in brain and in extraneuronal tissues.[Pubmed]
2003 Eveline Baumgart Microsc. Res. Tech. A review of morphological techniques for detection of peroxisomal (and mitochondrial) proteins and their corresponding mRNAs during ontogenesis in mice: application to the PEX5-knockout mouse with Zellweger syndrome.[Pubmed]
2003 Georg Neuberger J. Mol. Biol. Prediction of peroxisomal targeting signal 1 containing proteins from amino acid sequence.[Pubmed]
2003 Isao Ilieva Neurol. Res. Age-related changes in peroxisomal membrane protein 70 and superoxide dismutase 1 in transgenic G93A mice.[Pubmed]
2003 A Lüers Cytogenet. Genome Res. Expression of peroxisomal proteins provides clear evidence for the presence of peroxisomes in the male germ cell line GC1spg.[Pubmed]
2003 Ineke Tabak Traffic Peroxisomes start their life in the endoplasmic reticulum.[Pubmed]
2002 Kouichi Tanaka J. Biol. Chem. ATP binding/hydrolysis by and phosphorylation of peroxisomal ATP-binding cassette proteins PMP70 (ABCD3) and adrenoleukodystrophy protein (ABCD1).[Pubmed]
2002 Sietske Hogenboom J. Lipid Res. Absence of functional peroxisomes does not lead to deficiency of enzymes involved in cholesterol biosynthesis.[Pubmed]
2002 Hong Ruan Diabetes Tumor necrosis factor-alpha suppresses adipocyte-specific genes and activates expression of preadipocyte genes in 3T3-L1 adipocytes: nuclear factor-kappaB activation by TNF-alpha is obligatory.[Pubmed]
2002 Marek Malecki Proc. Natl. Acad. Sci. U.S.A. Molecular immunolabeling with recombinant single-chain variable fragment (scFv) antibodies designed with metal-binding domains.[Pubmed]
2002 Xiaoling Li Mol. Cell. Biol. PEX11 beta deficiency is lethal and impairs neuronal migration but does not abrogate peroxisome function.[Pubmed]
2002 Isabelle Weinhofer Hum. Mol. Genet. Cholesterol regulates ABCD2 expression: implications for the therapy of X-linked adrenoleukodystrophy.[Pubmed]
2002 Jonas Bjorkman Genesis Conditional inactivation of the peroxisome biogenesis Pex13 gene by Cre-loxP excision.[Pubmed]
2002 Jonas Björkman Genomics Pex13, the mouse ortholog of the human peroxisome biogenesis disorder PEX13 gene: gene structure, tissue expression, and localization of the protein to peroxisomes.[Pubmed]
2002 M Baes J. Neuropathol. Exp. Neurol. The neuronal migration defect in mice with Zellweger syndrome (Pex5 knockout) is not caused by the inactivity of peroxisomal beta-oxidation.[Pubmed]
2002 M Baes Genesis Generation of Pex5-loxP mice allowing the conditional elimination of peroxisomes.[Pubmed]
2002 Aurora Pujol Hum. Mol. Genet. Late onset neurological phenotype of the X-ALD gene inactivation in mice: a mouse model for adrenomyeloneuropathy.[Pubmed]
2001 C Thai Hum. Mol. Genet. Impaired membrane traffic in defective ether lipid biosynthesis.[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 I Vanhorebeek Biochim. Biophys. Acta Isoprenoid biosynthesis is not compromised in a Zellweger syndrome mouse model.[Pubmed]
2001 R Iida Biochem. Biophys. Res. Commun. Cloning, mapping, genomic organization, and expression of mouse M-LP, a new member of the peroxisomal membrane protein Mpv17 domain family.[Pubmed]
2001 M Casteels Biochem. Soc. Trans. Further insights into peroxisomal lipid breakdown via alpha- and beta-oxidation.[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 S Huyghe Biochem. J. Prenatal and postnatal development of peroxisomal lipid-metabolizing pathways in the mouse.[Pubmed]
2001 Y Suzuki J. Inherit. Metab. Dis. Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.[Pubmed]
2001 M Grabenbauer J. Histochem. Cytochem. Detection of peroxisomal proteins and their mRNAs in serial sections of fetal and newborn mouse organs.[Pubmed]
2001 S Recalcati J. Cell. Sci. Peroxisomal targeting of mammalian hydroxyacid oxidase 1 requires the C-terminal tripeptide SKI.[Pubmed]
2001 M Sadusky Genomics Identification of Serhl, a new member of the serine hydrolase family induced by passive stretch of skeletal muscle in vivo.[Pubmed]
2001 S Ferdinandusse J. Lipid Res. Identification of the peroxisomal beta-oxidation enzymes involved in the biosynthesis of docosahexaenoic acid.[Pubmed]
2001 Kovacs Kovacs Eur. J. Biochem. Purification of brain peroxisomes and localization of 3-hydroxy-3-methylglutaryl coenzyme A reductase.[Pubmed]
2000 A Janssen Lab. Invest. Docosahexaenoic acid deficit is not a major pathogenic factor in peroxisome-deficient mice.[Pubmed]
2000 P Borst Biochim. Biophys. Acta ABC transporters in lipid transport.[Pubmed]
2000 B Qu FEBS Lett. Caloric restriction prevents oxidative damage induced by the carcinogen clofibrate in mouse liver.[Pubmed]
2000 N Braverman Genomics PEX7 gene structure, alternative transcripts, and evidence for a founder haplotype for the frequent RCDP allele, L292ter.[Pubmed]
2000 A Knoll Neurosci. Lett. Peroxisomal beta-oxidation enzyme gene expression in the developing mouse brain.[Pubmed]
2000 S Watanabe J. Nutr. Sci. Vitaminol. Suppressive effect of curcumin on trichloroethylene-induced oxidative stress.[Pubmed]
2000 J Schriner Free Radic. Biol. Med. Levels of DNA damage are unaltered in mice overexpressing human catalase in nuclei.[Pubmed]
2000 Z Zhou J. Histochem. Cytochem. Cellular and subcellular localization of catalase in the heart of transgenic mice.[Pubmed]
2000 M Baes J. Biol. Chem. Inactivation of the peroxisomal multifunctional protein-2 in mice impedes the degradation of not only 2-methyl-branched fatty acids and bile acid intermediates but also of very long chain fatty acids.[Pubmed]
2000 N Hajra J. Biol. Chem. Induction of the peroxisomal glycerolipid-synthesizing enzymes during differentiation of 3T3-L1 adipocytes. Role in triacylglycerol synthesis.[Pubmed]
2000 P Aubourg Glia X-linked adrenoleukodystrophy enigma: how does the ALD peroxisomal transporter mutation affect CNS glia?[Pubmed]
2000 Sohlenius-Sternbeck Sohlenius-Sternbeck Biochem. Pharmacol. Effects of vitamin A deficiency on selected xenobiotic-metabolizing enzymes and defenses against oxidative stress in mouse liver.[Pubmed]
2000 T Yamada Cell Biochem. Biophys. Very-long-chain fatty acid metabolism in adrenoleukodystrophy protein-deficient mice.[Pubmed]
1999 C Thai FEBS Lett. Synthesis of plasmalogens in eye lens epithelial cells.[Pubmed]
1999 X Geisbrecht J. Biol. Chem. The mouse gene PDCR encodes a peroxisomal delta(2), delta(4)-dienoyl-CoA reductase.[Pubmed]
1999 J Berger Eur. J. Biochem. The four murine peroxisomal ABC-transporter genes differ in constitutive, inducible and developmental expression.[Pubmed]
1999 Ikegwuonu Ikegwuonu Mol. Cell. Biochem. Evidence for the involvement of the fatty acid and peroxisomal beta-oxidation pathways in the inhibition by dehydroepiandrosterone (DHEA) and induction by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and benz(a)anthracene (BA) of cytochrome P4501B1 (CYP1B1) in mouse embryo fibroblasts (C3H10T1/2 cells).[Pubmed]
1998 S Kemp Nat. Med. Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophy.[Pubmed]
1998 L Amery Biochem. J. C-terminal tripeptide Ser-Asn-Leu (SNL) of human D-aspartate oxidase is a functional peroxisome-targeting signal.[Pubmed]
1998 A Holzinger FEBS Lett. The mouse gene encoding the peroxisomal membrane protein 1-like protein (PXMP1-L): cDNA cloning, genomic organization and comparative expression studies.[Pubmed]
1998 T Shintaku Hepatic histopathology of a vitamin A overdose in mouse liver.[Pubmed]
1998 J Björkman Genomics Genomic structure of PEX13, a candidate peroxisome biogenesis disorder gene.[Pubmed]
1997 M Baes Nat. Genet. A mouse model for Zellweger syndrome.[Pubmed]
1997 S Schedin J. Biol. Chem. Peroxisomal impairment in Niemann-Pick type C disease.[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 E Tiidus Biochem. Mol. Biol. Int. Elevated catalase activity in red and white muscles of MyoD gene-inactivated mice.[Pubmed]
1996 G Lombard-Platet Proc. Natl. Acad. Sci. U.S.A. A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression pattern.[Pubmed]
1996 R Périchon Mech. Ageing Dev. Aging-related decrease in liver peroxisomal fatty acid oxidation in control and clofibrate-treated mice. A biochemical study and mechanistic approach.[Pubmed]
1996 M Sohlenius Biochem. Pharmacol. Hepatic peroxisome proliferation in vitamin A-deficient mice without a simultaneous increase in peroxisomal acyl-CoA oxidase activity.[Pubmed]
1996 A Kennedy Genomics Structure and location of the murine adrenoleukodystrophy gene.[Pubmed]
1996 DeLamatre DeLamatre Hepatology Influence of dietary fat on the effect of endotoxin on murine hepatic peroxisomes.[Pubmed]
1995 Austin Austin Toxicology Modification of lipoperoxidative effects of dichloroacetate and trichloroacetate is associated with peroxisome proliferation.[Pubmed]
1995 Z Pardo Proc. Natl. Acad. Sci. U.S.A. Superoxide dismutase is an abundant component in cell bodies, dendrites, and axons of motor neurons and in a subset of other neurons.[Pubmed]
1995 S Levak-Frank J. Clin. Invest. Muscle-specific overexpression of lipoprotein lipase causes a severe myopathy characterized by proliferation of mitochondria and peroxisomes in transgenic mice.[Pubmed]
1995 B Litwin Folia Histochem. Cytobiol. Morphological heterogeneity of peroxisomes in cultured mouse Leydig cells.[Pubmed]
1995 R Périchon Biochem. Mol. Biol. Int. Liver peroxisomal fatty acid oxidizing system during aging in control and clofibrate-treated mice.[Pubmed]
1995 B Bilińska Eur J Histochem Immunocytochemical demonstration of peroxisomes in cultured Leydig cells: a decrease in testosterone secretion precedes reduction of peroxisomes.[Pubmed]
1995 Y Vodovotz J. Immunol. Vesicle membrane association of nitric oxide synthase in primary mouse macrophages.[Pubmed]
1994 A Zwacka EMBO J. The glomerulosclerosis gene Mpv17 encodes a peroxisomal protein producing reactive oxygen species.[Pubmed]
1994 Y Cai Biochem. Pharmacol. Effects of acetylsalicylic acid on parameters related to peroxisome proliferation in mouse liver.[Pubmed]
1994 S Emami Arch Dermatol X-linked dominant ichthyosis with peroxisomal deficiency. An ultrastructural and ultracytochemical study of the Conradi-Hünermann syndrome and its murine homologue, the bare patches mouse.[Pubmed]
1994 C Sundberg Comparison of the potencies of (+)- and (-)-2-ethylhexanoic acid in causing peroxisome proliferation and related biological effects in mouse liver.[Pubmed]
1994 N Ashmarina J. Biol. Chem. 3-Hydroxy-3-methylglutaryl-CoA lyase is present in mouse and human liver peroxisomes.[Pubmed]
1993 J Meijer Eur. J. Cell Biol. Effects of clofibrate withdrawal on peroxisomes in mouse hepatocytes.[Pubmed]
1993 D Pauwels Virchows Arch., B, Cell Pathol. Peroxisomes in liver, kidney and duodenum of nude mice bearing xenografts of human pancreatic adenocarcinomas.[Pubmed]
1992 S Zoeller J. Biol. Chem. Mutants in a macrophage-like cell line are defective in plasmalogen biosynthesis, but contain functional peroxisomes.[Pubmed]
1992 A Demoz Lipids Eicosapentaenoic acid at hypotriglyceridemic dose enhances the hepatic antioxidant defense in mice.[Pubmed]
1992 B Sohlenius J. Biochem. Toxicol. Perfluorooctanoic acid has persistent effects on peroxisome proliferation and related parameters in mouse liver.[Pubmed]
1992 A Mann Comp. Biochem. Physiol., B Association of monoamine oxidase and malate dehydrogenase with liver peroxisomes of genetically obese (ob/ob and db/db) mice.[Pubmed]
1991 B Eriksson Eur. J. Biochem. Studies on the intracellular distributions of soluble epoxide hydrolase and of catalase by digitonin-permeabilization of hepatocytes isolated from control and clofibrate-treated mice.[Pubmed]
1991 C Chang Arch. Biochem. Biophys. Purification and characterization of an epoxide hydrolase from the peroxisomal fraction of mouse liver.[Pubmed]
1991 T Nishimaki-Mogami Biochem. Pharmacol. Effect of sorbic acid feeding on peroxisomes and sorboyl-CoA metabolizing enzymes in mouse liver. Selective induction of 2,4-dienoyl-CoA hydratase.[Pubmed]
1991 Moody Moody Toxicol. Lett. The effect of structurally divergent herbicides on mouse liver xenobiotic-metabolizing enzymes (P-450-dependent mono-oxygenases, epoxide hydrolases and glutathione S-transferases) and carnitine acetyltransferase.[Pubmed]
1991 R Konno Int. J. Biochem. Presence of D-amino-acid oxidase protein in mutant mice lacking D-amino-acid oxidase activity.[Pubmed]
1990 Stevens Stevens J. Biol. Chem. Class F Thy-1-negative murine lymphoma cells are deficient in ether lipid biosynthesis.[Pubmed]
1989 R Reiter Biochem. J. Subcellular distribution of selenium in deficient mouse liver.[Pubmed]
1989 V Joste FEBS Lett. In vitro translation of cytosolic and peroxisomal epoxide hydrolase and catalase on liver polyribosomes from untreated and clofibrate-treated C57B1/6 mice.[Pubmed]
1987 Patel Patel Biochem. J. Peroxisomal localization of glucose-6-phosphate dehydrogenase and pyrophosphate-stimulated dihydroxyacetone-phosphate acyltransferase in mouse kidney.[Pubmed]
1986 C Vamecq Pediatr. Res. Phytol and peroxisome proliferation.[Pubmed]
1986 S Kaur Biochem. Pharmacol. Distribution and nature of epoxide hydrolase activity in subcellular organelles of mouse liver.[Pubmed]
1986 V Patel Biochem. Pharmacol. Subcellular localization of epoxide hydrolase in mouse liver and kidney.[Pubmed]
1985 Mackness Mackness Comp. Biochem. Physiol., B Predominant localization of dihydroxyacetone-phosphate acyltransferase activity in renal peroxisomes of male and female mice.[Pubmed]
1983 D Crane Int. J. Biochem. On the synthesis and incorporation of catalase and urate oxidase into the peroxisomes of mouse liver.[Pubmed]
1983 F Waechter FEBS Lett. Epoxide hydrolase activity in isolated peroxisomes of mouse liver.[Pubmed]
1983 Farrell Farrell Arch. Biochem. Biophys. Carnitine octanoyltransferase of mouse liver peroxisomes: properties and effect of hypolipidemic drugs.[Pubmed]
1983 A Silcox Biochem. Int. Reduced levels of peroxisomal enzymes in the kidney of the genetically obese (ob/ob) mouse. Contrast with liver.[Pubmed]
1983 K Small Biochem. Int. Localization of carnitine acyltransferases and acyl-CoA beta-oxidation enzymes in small intestinal microperoxisomes (peroxisomes) of normal and clofibrate treated mice.[Pubmed]
1983 Connock Connock Biochem. Int. Detection of acyl-CoA beta-oxidation enzymes in peroxisomes (microperoxisomes) of mouse heart.[Pubmed]
1983 Titus Titus Plant Physiol. Purification and Characterization of Hydroxypyruvate Reductase from Cucumber Cotyledons.[Pubmed]
1978 Moody Moody Am. J. Pathol. The hepatic effects of hypolipidemic drugs (clofibrate, nafenopin, tibric acid, and Wy-14,643) on hepatic peroxisomes and peroxisome-associated enzymes.[Pubmed]
1977 Reddy Reddy Hepatic effects of some [4-chloro-6-(2,3-xylidino)-2-pyrimidinylthio] acetic acid (WY-14,643) analogs in the mouse.[Pubmed]
1975 Goeckermann Goeckermann J. Histochem. Cytochem. Peroxisome development in the metanephric kidney of mouse.[Pubmed]
1975 Brandt Brandt J. Cell Biol. Defective lysosomal enzyme secretion in kidneys of Chediak-Higashi (beige) mice.[Pubmed]
1974 Thomson Thomson Proc. Soc. Exp. Biol. Med. Preparation of peroxisomes from mouse liver by rate-zonal centrifugation.[Pubmed]
1974 S Brown J. Radiat. Res. Effect of x-irradiation on the permeability of L-alpha hydroxy acid oxidase from mouse liver peroxisomes.[Pubmed]
1972 Levy Levy Arch. Biochem. Biophys. Regulation of isocitrate metabolism in peroxisomes in Tetrahymena pyriformis.[Pubmed]
0 Toxicol Pathol Hepatotumorigenicity and peroxisome proliferation induced by the hypolipidemic CI-924 in a two-year study in male and female B6C3F1 mice.[Pubmed]
0 J. Am. Soc. Nephrol. Course of renal injury in the Mpv17-deficient transgenic mouse.[Pubmed]
0 J. Mol. Neurosci. The peroxisome deficient PEX2 Zellweger mouse: pathologic and biochemical correlates of lipid dysfunction.[Pubmed]
0 Drug Metab. Dispos. Characterization of the induction of cytosolic and microsomal epoxide hydrolases by 2-ethylhexanoic acid in mouse liver.[Pubmed]
0 Mol. Genet. Metab. X-linked adrenoleukodystrophy: role of very long-chain acyl-CoA synthetases.[Pubmed]