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Takashi Osumi
Articles in Scholarly Journals [Incomplete List]
Metabolic pathway that produces essential fatty acids from polymethylene-interrupted polyunsaturated fatty acids in animal cells
FEBS Journal, vol. 274, no. 11, pp. 2728–2737, 2007
hDREF Regulates Cell Proliferation and Expression of Ribosomal Protein Genes
Molecular and Cellular Biology, vol. 27, no. 6, pp. 2003–2013, 2007
CGI-58 facilitates lipolysis on lipid droplets but is not involved in the vesiculation of lipid droplets caused by hormonal stimulation
The Journal of Lipid Research, vol. 48, no. 5, pp. 1078–1089, 2007
Peroxisome Proliferator-Activated Receptor Subtypes Differentially Cooperate with Other Transcription Factors in Selective Transactivation of the Perilipin/PEX11 Gene Pair
Journal of Biochemistry, vol. 139, no. 3, pp. 563–573, 2006
Orphan Nuclear Receptor Nur77 Accelerates the Initial Phase of Adipocyte Differentiation in 3T3-L1 Cells by Promoting Mitotic Clonal Expansion
Journal of Biochemistry, vol. 141, no. 2, pp. 181–192, 2006
MLDP, a Novel PAT Family Protein Localized to Lipid Droplets and Enriched in the Heart, Is Regulated by Peroxisome Proliferator-activated Receptor
Journal of Biological Chemistry, vol. 281, no. 20, pp. 14232–14240, 2006
Human DNA Replication-related Element Binding Factor (hDREF) Self-association via hATC Domain Is Necessary for Its Nuclear Accumulation and DNA Binding
Journal of Biological Chemistry, vol. 282, no. 10, pp. 7563–7575, 2006
Analysis of interaction partners for perilipin and ADRP on lipid droplets*
Molecular and Cellular Biochemistry, vol. 284, no. 1-2, pp. 167–173, 2006
Aspects of the regulatory mechanisms of PPAR functions: Analysis of a bidirectional response element and regulation by sumoylation
Molecular and Cellular Biochemistry, vol. 286, no. 1-2, pp. 33–42, 2006
Aberrant peroxisome morphology in peroxisomal beta-oxidation enzyme deficiencies
Brain and Development, vol. 28, no. 5, pp. 287–292, 2006
Identification of a Gene Sharing a Promoter and Peroxisome Proliferator-Response Elements With Acyl-CoA Oxidase Gene
PPAR Research, vol. 2006, Article ID 71916, 10 pages, 2006
Negative regulation of adipogenesis from human mesenchymal stem cells by Jun N-terminal kinase
Biochemical and Biophysical Research Communications, vol. 326, no. 2, pp. 499–504, 2005
Estrogen receptor-related receptor ? has an exceptionally broad specificity of DNA sequence recognition
Gene, vol. 340, no. 2, pp. 275–282, 2004
SKIP modifies gene expression by affecting both transcription and splicing
Biochemical and Biophysical Research Communications, vol. 316, no. 2, pp. 512–517, 2004
Identification of a new complementation group of the peroxisome biogenesis disorders andPEX14 as the mutated gene
Human Mutation, vol. 23, no. 6, pp. 552–558, 2004
CGI-58 Interacts with Perilipin and Is Localized to Lipid Droplets: POSSIBLE INVOLVEMENT OF CGI-58 MISLOCALIZATION IN CHANARIN-DORFMAN SYNDROME
Journal of Biological Chemistry, vol. 279, no. 29, pp. 30490–30497, 2004
The transactivating function of peroxisome proliferator-activated receptor gamma is negatively regulated by SUMO conjugation in the amino-terminal domain
Genes to Cells, vol. 9, no. 11, pp. 1017–1029, 2004
Tissue-Selective, Bidirectional Regulation of PEX11 and Perilipin Genes through a Common Peroxisome Proliferator Response Element
Molecular and Cellular Biology, vol. 24, no. 3, pp. 1313–1323, 2004
Functional characterization of a peroxisome proliferator response-element located in the intron 3 of rat peroxisomal thiolase B gene
Biochemical and Biophysical Research Communications, vol. 311, no. 1, pp. 149–155, 2003
Peroxisomes Are Formed from Complex Membrane Structures in PEX6-deficient CHO Cells upon Genetic Complementation
Molecular Biology of the Cell, vol. 13, no. 2, pp. 711–722, 2002
The Newly Identified Human Nuclear Protein NXP-2 Possesses Three Distinct Domains, the Nuclear Matrix-binding, RNA-binding, and Coiled-coil Domains
Journal of Biological Chemistry, vol. 277, no. 23, pp. 20611–20617, 2002
Carboxyl-terminal basic amino acids in the X domain are essential for the nuclear import of phospholipase C delta1
Genes to Cells, vol. 7, no. 9, pp. 985–996, 2002
Genetic and molecular bases of peroxisome biogenesis disorders
Genetics in Medicine, vol. 3, no. 5, pp. 372–376, 2001
Temperature sensitive acyl-CoA oxidase import in group A peroxisome biogenesis disorders
Journal of Medical Genetics, vol. 38, no. 12, pp. 871–874, 2001
Stabilization of Peroxisome Proliferator-Activated Receptor a by the Ligand
Biochemical and Biophysical Research Communications, vol. 288, no. 1, pp. 106–110, 2001
NXP-1, a Human Protein Related to Rad21/Scc1/Mcd1, Is a Component of the Nuclear Matrix
Biochemical and Biophysical Research Communications, vol. 267, no. 1, pp. 418–422, 2000
Molecular Mechanism of Detectable Catalase-Containing Particles, Peroxisomes, in Fibroblasts from a PEX2-Defective Patient
Biochemical and Biophysical Research Communications, vol. 268, no. 1, pp. 31–35, 2000
The Peroxisome Proliferator Response Element (PPRE) Present at Positions -681/-669 in the Rat Liver 3-Ketoacyl-CoA Thiolase B Gene Functionally Interacts Differently with PPARa and HNF-4
Biochemical and Biophysical Research Communications, vol. 269, no. 2, pp. 347–351, 2000
The 70-kDa Peroxisomal Membrane Protein (PMP70), an ATP-Binding Cassette Transporter
Cell Biochemistry and Biophysics, vol. 32, no. 1-3, pp. 131–138, 2000
Temperature Sensitivity in Peroxisome Assembly Processes Characterizes Milder Forms of Peroxisome Biogenesis Disorders
Cell Biochemistry and Biophysics, vol. 32, no. 1-3, pp. 165–170, 2000
Nuclear receptor binding factor-2 (NRBF-2), a possible gene activator protein interacting with nuclear hormone receptors
Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression, vol. 1490, no. 1-2, pp. 189–197, 2000
Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans
Brain and Development, vol. 22, no. 1, pp. 8–12, 2000
Catalase-less Peroxisomes. IMPLICATION IN THE MILDER FORMS OF PEROXISOME BIOGENESIS DISORDER
Journal of Biological Chemistry, vol. 275, no. 47, pp. 37271–37277, 2000
Characterization of the 70-kDa Peroxisomal Membrane Protein, an ATP Binding Cassette Transporter
Journal of Biological Chemistry, vol. 274, no. 17, pp. 11968–11976, 1999
Characterization of the Amino-terminal Activation Domain of Peroxisome Proliferator-activated Receptor alpha . IMPORTANCE OF alpha -HELICAL STRUCTURE IN THE TRANSACTIVATING FUNCTION
Journal of Biological Chemistry, vol. 274, no. 49, pp. 35152–35158, 1999
Formation of Peroxisomes from Peroxisomal Ghosts in a Peroxisome-deficient Mammalian Cell Mutant upon Complementation by Protein Microinjection
Journal of Biological Chemistry, vol. 274, no. 50, pp. 35293–35296, 1999
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders
Human Molecular Genetics, vol. 8, no. 6, pp. 1077–1083, 1999
Genomic structure and identification of 11 novel mutations of thePEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders
Human Mutation, vol. 13, no. 6, pp. 487–496, 1999
Functional Heterogeneity of C-Terminal Peroxisome Targeting Signal 1 in PEX5-Defective Patients
Biochemical and Biophysical Research Communications, vol. 262, no. 2, pp. 504–508, 1999
Peroxisome Biogenesis Disorders: Identification of a New Complementation Group Distinct from Peroxisome-Deficient CHO Mutants and Not Complemented by Human PEX 13
Biochemical and Biophysical Research Communications, vol. 243, no. 2, pp. 368–371, 1998
A Cytoplasmic AAA Family Peroxin, Pex1p, Interacts with Pex6p???
Biochemical and Biophysical Research Communications, vol. 245, no. 3, pp. 883–886, 1998
Genetic Basis of Peroxisome-Assembly Mutants of Humans, Chinese Hamster Ovary Cells, and Yeast: Identification of a New Complementation Group of Peroxisome-Biogenesis Disorders Apparently Lacking Peroxisomal-Membrane Ghosts
The American Journal of Human Genetics, vol. 63, no. 6, pp. 1898–1903, 1998
Nuclear receptor binding factor-1 (NRBF-1), a protein interacting with a wide spectrum of nuclear hormone receptors
Gene, vol. 221, no. 2, pp. 225–233, 1998
Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I
Proceedings of the National Academy of Sciences, vol. 95, no. 8, pp. 4350–4355, 1998
Isolation of a New Peroxisome-Deficient CHO Cell Mutant Defective in Peroxisome Targeting Signal-1 Receptor
Biochemical and Biophysical Research Communications, vol. 230, no. 2, pp. 402–406, 1997
Isolation and Characterization of Peroxisome-Deficient Chinese Hamster Ovary Cell Mutants Representing Human Complementation Group III
Experimental Cell Research, vol. 233, no. 1, pp. 11–20, 1997
An orphan nuclear receptor lacking a zinc-finger DNA-binding domain: interaction with several nuclear receptors
Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression, vol. 1350, no. 1, pp. 27–32, 1997
Insertion of the 70-kDa Peroxisomal Membrane Protein into Peroxisomal Membranes in Vivo and in Vitro
Journal of Biological Chemistry, vol. 271, no. 7, pp. 3706–3713, 1996
A unified nomenclature for peroxisome biogenesis factors
The Journal of Cell Biology, vol. 135, no. 1, pp. 1–3, 1996
Analysis of Peroxisome Proliferator?responsive Enhancer of the Rat Acyl-CoA Oxidase Gene
Annals of the New York Academy of Sciences, vol. 804, no. 1 Peroxisomes, pp. 202–213, 1996
Cloning of Peroxisome Assembly Factor-2
Annals of the New York Academy of Sciences, vol. 804, no. 1 Peroxisomes, pp. 656–657, 1996
Sorting of the 70-kDa Peroxisomal Membrane Protein into Rat Liver Peroxisomes in Vitro
Annals of the New York Academy of Sciences, vol. 804, no. 1 Peroxisomes, pp. 663–665, 1996
Analysis of the Essential Sequence Elements in the Peroxisome Proliferator-Responsive Enhancer of Rat Acyl-CoA Oxidase Gene
Annals of the New York Academy of Sciences, vol. 804, no. 1 Peroxisomes, pp. 706–708, 1996
Cloning, Expression, and Characterization of cDNAs Encoding Arabidopsis thaliana Squalene Synthase
Proceedings of the National Academy of Sciences, vol. 92, no. 6, pp. 2328–2332, 1995
Peroxisome assembly factor–2, a putative ATPase cloned by functional complementation on a peroxisome–deficient mammalian cell mutant
Nature Genetics, vol. 11, no. 4, Article ID ng1295-395, 6 pages, 1995
Identification of two splice isoforms of mRNA for mouse hepatocyte nuclear factor 4 (HNF-4)
Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression, vol. 1260, no. 1, pp. 55–61, 1995
Molecular cloning and functional expression of a cDNA for mouse squalene synthase
Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression, vol. 1260, no. 1, pp. 49–54, 1995
Nucleotide sequence of a cDNA for mouse squalene epoxidase
Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression, vol. 1260, no. 3, pp. 345–348, 1995
cDNA cloning of a putative G protein-coupled receptor from brain
Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression, vol. 1261, no. 1, pp. 121–125, 1995
Assignment of the Human Peroxisome Assembly Factor-1 Gene (PXMP3) Responsible for Zellweger Syndrome to Chromosome 8q21.1 by Fluorescence in Situ Hybridization
Genomics, vol. 20, no. 1, pp. 141–142, 1994
Structure and expression of the genes encoding peroxisomal ß-oxidation enzymes
Biochimie, vol. 75, no. 3-4, pp. 243–250, 1993
Molecular basis of 3-ketothiolase deficiency: Detection of gene mutations and expression of mutant cDNAs of mitochondrial acetoacetyl-CoA thiolase
Journal of Inherited Metabolic Disease, vol. 15, no. 5, pp. 815–820, 1992
Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting
Biochemical and Biophysical Research Communications, vol. 181, no. 3, pp. 947–954, 1991
Topogenesis of peroxisomal proteins
BioEssays, vol. 12, no. 5, pp. 217–222, 1990
Isolation and characterization of the rat catalase-encoding gene
Gene, vol. 79, no. 2, pp. 279–288, 1989
Molecular cloning and sequence analysis of the cDNA for rat mitochondrial enoyl-CoA hydratase. Structural and evolutionary relationships linked to the bifunctional enzyme of the peroxisomal beta-oxidation system
European Journal of Biochemistry, vol. 185, no. 1, pp. 73–78, 1989
Molecular cloning of cDNA for rat mitochondrial 3-oxoacyl-CoA thiolase
European Journal of Biochemistry, vol. 154, no. 2, pp. 479–484, 1986
The inducible fatty acid oxidation system in mammalian peroxisomes
Trends in Biochemical Sciences, vol. 9, no. 7, pp. 317–319, 1984
Molecular cloning of cDNA for rat liver catalase
Biochemical and Biophysical Research Communications, vol. 122, no. 2, pp. 831–837, 1984
Induction of peroxisomal ?-oxidation by the administration of acetylsalicylic acid*1
Toxicology and Applied Pharmacology, vol. 59, no. 1, pp. 8–14, 1981
Turnover of enzymes of peroxisomal ß-oxidation in rat liver
Biochimica et Biophysica Acta (BBA) - General Subjects, vol. 630, no. 3, pp. 367–374, 1980
Purification and properties of mitochondrial and peroxisomal 3-hydroxyacyl-CoA dehydrogenase from rat liver
Archives of Biochemistry and Biophysics, vol. 203, no. 1, pp. 372–383, 1980
The Presence of a New 3-Oxoacyl-CoA Thiolase in Rat Liver Peroxisomes
European Journal of Biochemistry, vol. 103, no. 3, pp. 589–596, 1980
Characterization of sterol-ester hydrolase in Saccharomyces cerevisiae
Biochimica et Biophysica Acta (BBA) - Enzymology, vol. 525, no. 1, pp. 87–92, 1978
Acyl-CoA oxidase of rat liver: A new enzyme for fatty acid oxidation
Biochemical and Biophysical Research Communications, vol. 83, no. 2, pp. 479–485, 1978
Effects of administration of di-(2-ethylhexyl)phthalate on rat liver mitochondria
Biochemical Pharmacology, vol. 27, no. 23, pp. 2683–2688, 1978