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    1. McGuinness, MC; Zhang, HP; Smith, KD
      Evaluation of pharmacological induction of fatty acid beta-oxidation in X-linked adrenoleukodystrophy

      MOLECULAR GENETICS AND METABOLISM
    2. Silva, MFB; Jakobs, C; Duran, M; de Almeida, IT; Wanders, RJA
      Valproate induces in vitro accumulation of long-chain fatty acylcarnitines

      MOLECULAR GENETICS AND METABOLISM
    3. Yang, BZ; Mallory, JM; Roe, DS; Brivet, M; Strobel, GD; Jones, KM; Ding, JH; Roe, CR
      Carnitine/acylcarnitine translocase deficiency (neonatal phenotype): Successful prenatal and postmortem diagnosis associated with a novel mutation ina single family

      MOLECULAR GENETICS AND METABOLISM
    4. Rylott, EL; Hooks, MA; Graham, IA
      Co-ordinate regulation of genes involved in storage lipid mobilization in Arabidopsis thaliana

      BIOCHEMICAL SOCIETY TRANSACTIONS
    5. Reddy, JK
      Nonalcoholic steatosis and steatohepatitis - III. Peroxisomal beta-oxidation, PPAR alpha, and steatohepatitis

      AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY
    6. Hayashi, Y; Hayashi, M; Hayashi, H; Hara-Nishimura, I; Nishimura, M
      Direct interaction between glyoxysomes and lipid bodies in cotyledons of the Arabidopsis thaliana ped1 mutant

      PROTOPLASMA
    7. Johnson, TL; Olsen, LJ
      Building new models for peroxisome biogenesis

      PLANT PHYSIOLOGY
    8. Fukao, Y; Hayashi, Y; Mano, S; Hayashi, M; Nishimura, M
      Developmental analysis of a putative ATP/ADP carrier protein localized on glyoxysomal membranes during the peroxisome transition in pumpkin cotyledons

      PLANT AND CELL PHYSIOLOGY
    9. Miyajima, H; Ouchi, Y; Sakamoto, M; Takahashi, Y; Kono, S; Suzuki, H
      Increased anaerobic glycolysis in mitochondrial trifunctional protein-deficient brain

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    10. Ibdah, JA; Zhao, YW; Viola, J; Gibson, B; Bennett, MJ; Strauss, AW
      Molecular prenatal diagnosis in families with fetal mitochondrial trifunctional protein mutations

      JOURNAL OF PEDIATRICS
    11. Yu, ST; Cao, WQ; Kashireddy, P; Meyer, K; Jia, YZ; Hughes, DE; Tan, YJ; Feng, JC; Yeldandi, AV; Rao, MS; Costa, RH; Gonzalez, FJ; Reddy, JK
      Human peroxisome proliferator-activated receptor alpha (PPAR alpha) supports the induction of peroxisome proliferation in PPAR alpha-deficient mouse liver

      JOURNAL OF BIOLOGICAL CHEMISTRY
    12. Vaz, FM; Ofman, R; Westinga, K; Back, JW; Wanders, RJA
      Molecular and biochemical characterization of rat epsilon-N-Trimethyllysine hydroxylase, the first enzyme of carnitine biosynthesis

      JOURNAL OF BIOLOGICAL CHEMISTRY
    13. Kessler, B; Ren, Q; de Roo, G; Prieto, MA; Witholt, B
      Engineering of biological systems for the synthesis of tailor-made polyhydroxyalkanoates, a class of versatile polymers

      CHIMIA
    14. Silva, MFB; Ruiter, JPN; IJlst, L; Jakobs, C; Duran, M; de Almeida, IT; Wanders, RJA
      Differential effect of valproate and its Delta(2)- and Delta(4)-unsaturated metabolites, on the beta-oxidation rate of long-chain and medium-chain fatty acids

      CHEMICO-BIOLOGICAL INTERACTIONS
    15. Chace, DH
      Mass spectrometry in the clinical laboratory

      CHEMICAL REVIEWS
    16. Ijlst, L; van Roermund, CWT; Iacobazzi, V; Oostheim, W; Ruiter, JPN; Williams, JC; Palmieri, F; Wanders, RJA
      Functional analysis of mutant human carnitine acylcarnitine translocases in yeast

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    17. Watanabe, H; Orii, KE; Fukao, T; Song, XQ; Aoyama, T; Ijlst, L; Ruiter, J; Wanders, RJA; Kondo, N
      Molecular basis of very long chain acyl-CoA dehydrogenase deficiency in three Israeli patients: Identification of a complex mutant allele with P65L and K247Q mutations, the former being an exonic mutation causing exon 3 skipping

      HUMAN MUTATION
    18. Hayashi, M
      Plant peroxisomes: Molecular basis of the regulation of their functions

      JOURNAL OF PLANT RESEARCH
    19. Antonio, RV; Steinbuchel, A; Rehm, BHA
      Analysis of in vivo substrate specificity of the PHA synthase from Ralstonia eutropha: formation of novel copolyesters in recombinant Escherichia coli

      FEMS MICROBIOLOGY LETTERS
    20. Singh, I; Carillo, O; Namboodiri, A
      Isolation and biochemical characterization of peroxisomes from cultured rat glial cells

      NEUROCHEMICAL RESEARCH
    21. Das, AM; Fingerhut, R; Wanders, RJA; Ullrich, K
      Secondary respiratory chain defect in a boy with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: possible diagnostic pitfalls

      EUROPEAN JOURNAL OF PEDIATRICS
    22. Van Maldergem, L; Tuerlinckx, D; Wanders, RJ; Vianey-Saban, C; Van Hoof, F; Martin, JJ; Fourneau, C; Gillerot, Y; Bachy, A
      Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and early-onset liver cirrhosis in two siblings

      EUROPEAN JOURNAL OF PEDIATRICS
    23. Bongcam, V; Petetot, JMC; Mittendorf, V; Robertson, EJ; Leech, RM; Qin, YM; Hiltunen, JK; Poirier, Y
      Importance of sequences adjacent to the terminal tripeptide in the import of a peroxisomal Candida tropicalis protein in plant peroxisomes

      PLANTA
    24. Den Boer, MEJ; Ijlst, L; Wijburg, FA; Oostheim, W; Van Werkhoven, MA; Van Pampus, MG; Heymans, HSA; Wanders, RJA
      Heterozygosity for the common LCHAD mutation (1528G > C) is not a major cause of HELLP syndrome and the prevalence of the mutation in the Dutch population is low

      PEDIATRIC RESEARCH
    25. Ferdinandusse, S; Denis, S; Ijlst, L; Dacremont, G; Waterham, HR; Wanders, RJA
      Subcellular localization and physiological role of alpha-methylacyl-CoA racemase

      JOURNAL OF LIPID RESEARCH
    26. Smith, BT; Sengupta, TK; Singh, I
      Intraperoxisomal localization of very-long-chain fatty acyl-CoA synthetase: Implication in X-adrenoleukodystrophy

      EXPERIMENTAL CELL RESEARCH
    27. Glasgow, JFT; Middleton, B; Moore, R; Gray, A; Hill, J
      The mechanism of inhibition of beta-oxidation by aspirin metabolites in skin fibroblasts from Reye's syndrome patients and controls

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    28. Koller, A; Spong, AP; Luers, GH; Subramani, S
      Analysis of the peroxisomal acyl-CoA oxidase gene product from Pichia pastoris and determination of its targeting signal

      YEAST
    29. Ikegwuonu, FI; Jefcoate, CR
      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)

      MOLECULAR AND CELLULAR BIOCHEMISTRY
    30. Chevet, E; Lemaitre, G; Cailleret, K; Dahan, S; Bergeron, JJM; Katinka, MD
      Identification and characterization of an intracellular protein complex that binds fibroblast growth factor-2 in bovine brain

      BIOCHEMICAL JOURNAL
    31. van Roermund, CWT; Hettema, EH; van den Berg, M; Tabak, HF; Wanders, RJA
      Molecular characterization of carnitine-dependent transport of acetyl-CoA from peroxisomes to mitochondria in Saccharomyces cerevisiae and identification of a plasma membrane carnitine transporter, Agp2p

      EMBO JOURNAL
    32. Otto, LR; Boriack, RL; Marsh, DJ; Kum, JB; Eng, C; Burlina, AB; Bennett, MJ
      Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (ERRS)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    33. Strauss, AW; Bennett, MJ; Rinaldo, P; Sims, HF; O'Brien, LK; Zhao, YW; Gibson, B; Ibdah, J
      Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications

      SEMINARS IN PERINATOLOGY
    34. Ventura, FV; Costa, CG; Struys, EA; Ruiter, J; Allers, P; Ijlst, L; de Almeida, T; Duran, M; Jakobs, C; Wanders, RJA
      Quantitative acylcarnitine profiling in fibroblasts using [U-C-13] palmitic acid: an improved tool for the diagnosis of fatty acid oxidation defects

      CLINICA CHIMICA ACTA
    35. van Grunsven, EG; van Berkel, E; Mooijer, PAW; Watkins, PA; Moser, HW; Suzuki, Y; Jiang, LL; Hashimoto, T; Hoefler, G; Adamski, J; Wanders, RJA
      Peroxisomal bifunctional protein deficiency revisited: Resolution of its true enzymatic and molecular basis

      AMERICAN JOURNAL OF HUMAN GENETICS
    36. SACK MN; KELLY DP
      THE ENERGY SUBSTRATE SWITCH DURING DEVELOPMENT OF HEART-FAILURE - GENE REGULATORY MECHANISMS (REVIEW)

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    37. KEMP S; WEI HM; LU JF; BRAITERMAN LT; MCGUINNESS MC; MOSER AB; WATKINS PA; SMITH KD
      GENE REDUNDANCY AND PHARMACOLOGICAL GENE-THERAPY - IMPLICATIONS FOR X-LINKED ADRENOLEUKODYSTROPHY

      Nature medicine
    38. WATAYA K; AKANUMA J; CAVADINI P; AOKI Y; KURE S; INVERNIZZI F; YOSHIDA I; KIRA J; TARONI F; MATSUBARA Y; NARISAWA K
      2 CPT2 MUTATIONS IN 3 JAPANESE PATIENTS WITH CARNITINE PALMITOYLTRANSFERASE-II DEFICIENCY - FUNCTIONAL-ANALYSIS AND ASSOCIATION WITH POLYMORPHIC HAPLOTYPES AND 2 CLINICAL PHENOTYPES

      Human mutation
    39. KAWASHIMA H; KUGE Y; YAJIMA K; MIYAKE Y; HASHIMOTO N
      DEVELOPMENT OF STEP-SPECIFIC PET TRACERS FOR STUDYING FATTY-ACID BETA-OXIDATION - BIODISTRIBUTION OF [1-C-11] OCTANOATE ANALOGS IN RATS ANDA CAT

      Nuclear medicine and biology
    40. MINETTI C; GARAVAGLIA B; BADO M; INVERNIZZI F; BRUNO C; RIMOLDI M; PONS R; TARONI F; CORDONE G
      VERY-LONG-CHAIN ACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY IN A CHILD WITH RECURRENT MYOGLOBINURIA

      Neuromuscular disorders
    41. NISHIMURA M; HAYASHI M; TORIYAMA K; KATO A; MANO S; YAMAGUCHI K; KONDO M; HAYASHI H
      MICROBODY DEFECTIVE-MUTANTS OF ARABIDOPSIS

      Journal of plant research
    42. QI QS; STEINBUCHEL A; REHM BHA
      METABOLIC ROUTING TOWARDS POLYHYDROXYALKANOIC ACID SYNTHESIS IN RECOMBINANT ESCHERICHIA-COLI (FADR) - INHIBITION OF FATTY-ACID BETA-OXIDATION BY ACRYLIC-ACID

      FEMS microbiology letters
    43. TYNI T; KIVELA T; LAPPI M; SUMMANEN P; NIKOSKELAINEN E; PIHKO H
      OPHTHALMOLOGIC FINDINGS IN LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY CAUSED BY THE G1528C MUTATION - A NEW-TYPE OF HEREDITARY METABOLIC CHORIORETINOPATHY

      Ophthalmology
    44. CROCKER JFS; DIGOUT SC; LEE SH; ROZEE KR; RENTON K; FIELD CA; ACOTT P; MURPHY MG
      EFFECTS OF ANTIPYRETICS ON MORTALITY DUE TO INFLUENZA-B VIRUS IN A MOUSE MODEL OF REYES-SYNDROME

      Clinical and investigative medicine
    45. BROUQUISSE R; GAUDILLERE JP; RAYMOND P
      INDUCTION OF A CARBON-STARVATION-RELATED PROTEOLYSIS IN WHOLE MAIZE PLANTS SUBMITTED TO LIGHT DARK CYCLES AND TO EXTENDED DARKNESS/

      Plant physiology
    46. PUST B; BERGER A; LEHNERT W; WANDERS RJA
      EARLY MANIFESTATION OF VERY-LONG-CHAIN AC YL-COA DEHYDROGENASE-DEFICIENCY (VLCADD) WITH A FATAL COMPLICATION

      Monatsschrift fur Kinderheilkunde
    47. IBDAH JA; TEIN I; DIONISIVICI C; BENNETT MJ; IJLST L; GIBSON B; WANDERS RJA; STRAUSS AW
      MILD TRIFUNCTIONAL PROTEIN-DEFICIENCY IS ASSOCIATED WITH PROGRESSIVE NEUROPATHY AND MYOPATHY AND SUGGESTS A NOVEL GENOTYPE-PHENOTYPE CORRELATION

      The Journal of clinical investigation
    48. KANAYAMA N; UEDA M; ATOMI H; TANAKA A
      GENETIC EVALUATION OF PHYSIOLOGICAL FUNCTIONS OF THIOLASE ISOZYMES INTHE N-ALKANE-ASSIMILATING YEAST CANDIDA-TROPICALIS

      Journal of bacteriology
    49. ESCHER CL; WIDMER F
      LIPID MOBILIZATION AND GLUCONEOGENESIS IN PLANTS - DO GLYOXYLATE CYCLE ENZYME-ACTIVITIES CONSTITUTE A REAL CYCLE - A HYPOTHESIS

      Biological chemistry
    50. FORSSPETTER S; WERNER H; BERGER J; LASSMANN H; MOLZER B; SCHWAB MH; BERNHEIMER H; ZIMMERMANN F; NAVE KA
      TARGETED INACTIVATION OF THE X-LINKED ADRENOLEUKODYSTROPHY GENE IN MICE

      Journal of neuroscience research
    51. HOFSTRA AH; KING LM; WALKER RM
      EARLY EFFECTS OF CI-924 ON HEPATIC PEROXISOME PROLIFERATION, MICROSOMAL-ENZYME INDUCTION, PCNA, AND APOPTOSIS IN B6C3F1 MICE AND WISTAR RATS

      Archives of toxicology
    52. ORELLANA M; VALDES E; DELVILLAR E
      MICROSOMAL AND PEROXISOMAL FATTY-ACID OXIDATION IN STREPTOZOTOCIN-DIABETIC RAT-LIVER

      General pharmacology
    53. SINGH I
      BIOCHEMISTRY OF PEROXISOMES IN HEALTH AND DISEASE

      Molecular and cellular biochemistry
    54. ISMAIL I; DEBELLIS L; ALPI A; SMITH SM
      EXPRESSION OF GLYOXYLATE CYCLE GENES IN CUCUMBER ROOTS RESPONDS TO SUGAR SUPPLY AND CAN BE ACTIVATED BY SHADING OR DEFOLIATION OF THE SHOOT

      Plant molecular biology
    55. AOYAGI T; SUGIURA S; ETO Y; YONEKURA K; MATSUMOTO A; YOKOYAMA I; KOBAYAKAWA N; OMATA M; KIRIMOTO T; HAYASHI Y; MOMOMURA S
      INHIBITION OF CARNITINE SYNTHESIS PROTECTS AGAINST LEFT-VENTRICULAR DYSFUNCTION IN RATS WITH MYOCARDIAL-ISCHEMIA

      Journal of cardiovascular pharmacology
    56. DIEUAIDENOUBHANI M; CANIONI P; RAYMOND P
      SUGAR-STARVATION-INDUCED CHANGES OF CARBON METABOLISM IN EXCISED MAIZE ROOT-TIPS

      Plant physiology
    57. MIYAJIMA H; ORII KE; SHINDO Y; HASHIMOTO T; SHINKA T; KUHARA T; MATSUMOTO I; SHIMIZU H; KANEKO E
      MITOCHONDRIAL TRIFUNCTIONAL PROTEIN-DEFICIENCY ASSOCIATED WITH RECURRENT MYOGLOBINURIA IN ADOLESCENCE

      Neurology
    58. SACK MN; DISCH DL; ROCKMAN HA; KELLY DP
      A ROLE FOR SP AND NUCLEAR RECEPTOR TRANSCRIPTION FACTORS IN A CARDIACHYPERTROPHIC GROWTH PROGRAM

      Proceedings of the National Academy of Sciences of the United Statesof America
    59. TYNI T; PALOTIE A; VIINIKKA L; VALANNE L; SALO MK; VONDOBELN U; JACKSON S; WANDERS R; VENIZELOS N; PIHKO H
      LONG-CHAIN 3-HYDROXYACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY WITH THEG1528C MUTATION - CLINICAL PRESENTATION OF 13 PATIENTS

      The Journal of pediatrics
    60. KANAYAMA N; HIMEDA Y; ATOMI H; UEDA M; TANAKA A
      EXPRESSION OF ACETOACETYL-COA THIOLASE ISOZYME GENES OF N-ALKANE-ASSIMILATING YEAST, CANDIDA-TROPICALIS - ISOZYMES IN 2 INTRACELLULAR COMPARTMENTS ARE DERIVED FROM THE SAME GENES

      Journal of Biochemistry
    61. NAKAGAWA J; MORONI C
      A 20-AMINO-ACID AUTONOMOUS RNA-BINDING DOMAIN CONTAINED IN AN ENOYL-COA HYDRATASE

      European journal of biochemistry
    62. SCHRIJVERWIELING I; VANRENS GHMB; WITTEBOLPOST D; SMEITINK JAM; DEJAGER JP; DEKLERK HBC; VANLITH GHM
      RETINAL DYSTROPHY IN LONG-CHAIN 3-HYDROXY-ACYL-COA DEHYDROGENASE-DEFICIENCY

      British journal of ophthalmology
    63. WU WJ; ANDERSON VE; RALEIGH DP; TONGE PJ
      STRUCTURE OF HEXADIENOYL-COA BOUND TO ENOYL-COA HYDRATASE DETERMINED BY TRANSFERRED NUCLEAR OVERHAUSER EFFECT MEASUREMENTS - MECHANISTIC PREDICTIONS BASED ON THE X-RAY STRUCTURE OF 4-(CHLOROBENZOYL)-COA DEHALOGENASE

      Biochemistry
    64. MURPHY VJ; MANTAMADIOTIS T; BALDWIN GS
      GASTRIN AND GASTRIN RECEPTOR ANTAGONISTS BIND TO BOTH N-TERMINAL AND C-TERMINAL HALVES OF THE 78KDA GASTRIN-BINDING PROTEIN

      International journal of biochemistry & cell biology
    65. STRAUSS AW
      DEFECTS OF MITOCHONDRIAL PROTEINS AND PEDIATRIC HEART-DISEASE

      Progress in pediatric cardiology
    66. TYNI T; MAJANDER A; KALIMO H; RAPOLA J; PIHKO H
      PATHOLOGY OF SKELETAL-MUSCLE AND IMPAIRED RESPIRATORY-CHAIN FUNCTION IN LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY WITH THE G1528C MUTATION

      Neuromuscular disorders
    67. CHEVALIER C; BOURGEOIS E; JUST D; RAYMOND P
      METABOLIC-REGULATION OF ASPARAGINE SYNTHETASE GENE-EXPRESSION IN MAIZE (ZEA-MAYS L) ROOT-TIPS

      Plant journal
    68. MURPHY MG; CROCKER JFS; HER H
      ABNORMALITIES IN HEPATIC FATTY-ACID METABOLISM IN A SURFACTANT INFLUENZA-B VIRUS MOUSE MODEL FOR ACUTE ENCEPHALOPATHY

      Biochimica et biophysica acta. Molecular basis of disease
    69. PONS R; ROIG M; RIUDOR E; RIBES A; BRIONES P; ORTIGOSA L; BALDELLOU A; GILGIBERNAU J; OLESTI M; NAVARRO C; WANDERS RJA
      THE CLINICAL SPECTRUM OF LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY

      Pediatric neurology
    70. KAMASAWA N; OHTSUKA I; KAMADA Y; UEDA M; TANAKA A; OSUMI M
      IMMUNOELECTRON MICROSCOPIC OBSERVATION OF THE BEHAVIORS OF PEROXISOMAL ENZYMES INDUCIBLY SYNTHESIZED IN AN N-ALKANE-UTILIZABLE YEAST-CELL, CANDIDA-TROPICALIS

      Cell structure and function
    71. THERON JJ; VANPAPENDORP DH
      PEROXISOMAL DISEASES - OVERVIEW

      South African medical journal
    72. WIEMER EAC; IJLST L; VANROY J; WANDERS RJA; OPPERDOES FR
      IDENTIFICATION OF 2-ENOYL COENZYME-A HYDRATASE AND NADP(-DEPENDENT 3-HYDROXYACYL-COA DEHYDROGENASE-ACTIVITY IN GLYCOSOMES OF PROCYCLIC TRYPANOSOMA-BRUCEI())

      Molecular and biochemical parasitology
    73. UCHIYAMA A; AOYAMA T; KAMIJO K; UCHIDA Y; KONDO N; ORII T; HASHIMOTO T
      MOLECULAR-CLONING OF CDNA-ENCODING RAT VERY LONG-CHAIN ACYL-COA SYNTHETASE

      The Journal of biological chemistry
    74. KAWACHI H; ATOMI H; UEDA M; TANAKA A
      PEROXISOMAL AND MITOCHONDRIAL CARNITINE ACETYLTRANSFERASES OF THE N-ALKANE-ASSIMILATING YEAST CANDIDA-TROPICALIS - ANALYSIS OF GENE STRUCTURE AND TRANSLATION PRODUCTS

      European journal of biochemistry
    75. HOFSTRA AH; KING LM; WALKER RM
      PEROXISOME PROLIFERATION AND MICROSOMAL-ENZYME INDUCTION BY THE HYPOLIPIDEMIC CI-924 IN RATS AND MICE - RELATIONSHIP TO TUMORGENICITY

      Fundamental and applied toxicology
    76. VANROERMUND CWT; ELGERSMA Y; SINGH N; WANDERS RJA; TABAK HF
      THE MEMBRANE OF PEROXISOMES IN SACCHAROMYCES-CEREVISIAE IS IMPERMEABLE TO NAD(H) AND ACETYL-COA UNDER IN-VIVO CONDITIONS

      EMBO journal
    77. IJLST L; USKIKUBO S; KAMIJO T; HASHIMOTO T; RUITER JPN; DEKLERK JBC; WANDERS RJA
      LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY - HIGH-FREQUENCY OF THE G1528C MUTATION WITH NO APPARENT CORRELATION WITH THE CLINICAL PHENOTYPE

      Journal of inherited metabolic disease
    78. HOOKS MA; BODE K; COUEE I
      REGULATION OF ACYL-COA OXIDASES IN MAIZE SEEDLINGS

      Phytochemistry
    79. ZHU YJ; KORENBERG JR; CHEN XN; NOYA D; RAO MS; REDDY JK
      STRUCTURAL ORGANIZATION OF MOUSE PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR-GAMMA (MPPAR-GAMMA) GENE - ALTERNATIVE PROMOTER USE AND DIFFERENT SPLICING YIELD 2 MPPAR-GAMMA ISOFORMS

      Proceedings of the National Academy of Sciences of the United Statesof America
    80. CHU S; HUANG Q; ALVARES K; YELDANDI AV; RAO MS; REDDY JK
      TRANSFORMATION OF MAMMALIAN-CELLS BY OVEREXPRESSING H2O2-GENERATING PEROXISOMAL FATTY ACYL-COA OXIDASE

      Proceedings of the National Academy of Sciences of the United Statesof America
    81. VISENTIN M; BELLASIO R; TACCONI MT
      REYE SYNDROME MODEL IN RATS - PROTECTION AGAINST LIVER ABNORMALITIES BY L-CARNITINE AND ACETYL-L-CARNITINE

      The Journal of pharmacology and experimental therapeutics
    82. MOORE SA; HURT E; YODER E; SPRECHER H; SPECTOR AA
      DOCOSAHEXAENOIC ACID SYNTHESIS IN HUMAN SKIN FIBROBLASTS INVOLVES PEROXISOMAL RETROCONVERSION OF TETRACOSAHEXAENOIC ACID

      Journal of lipid research
    83. AOYAMA T; SOURI M; USHIKUBO S; KAMIJO T; YAMAGUCHI S; KELLEY RI; RHEAD WJ; UETAKE K; TANAKA K; HASHIMOTO T
      PURIFICATION OF HUMAN VERY-LONG-CHAIN ACYL-COENZYME-A DEHYDROGENASE AND CHARACTERIZATION OF ITS DEFICIENCY IN 7 PATIENTS

      The Journal of clinical investigation
    84. DIEUAIDENOUBHANI M; RAFFARD G; CANIONI P; PRADET A; RAYMOND P
      QUANTIFICATION OF COMPARTMENTED METABOLIC FLUXES IN MAIZE ROOT-TIPS USING ISOTOPE DISTRIBUTION FROM C-13-LABELED OR C-14-LABELED GLUCOSE

      The Journal of biological chemistry
    85. FURUTA S; HASHIMOTO T
      PURIFICATION AND PROPERTIES OF 3-HYDROXYACYL COENZYME-A DEHYDROGENASE-BINDING PROTEIN FROM RAT-LIVER MITOCHONDRIA

      Journal of Biochemistry
    86. MULLERNEWEN G; JANSSEN U; STOFFEL W
      ENOYL-COA HYDRATASE AND ISOMERASE FORM A SUPERFAMILY WITH A COMMON ACTIVE-SITE GLUTAMATE RESIDUE

      European journal of biochemistry
    87. HASHIMOTO F; ISHIKAWA T; HAMADA S; HAYASHI H
      EFFECT OF GEMFIBROZIL ON LIPID BIOSYNTHESIS FROM ACETYL-COA DERIVED FROM PEROXISOMAL BETA-OXIDATION

      Biochemical pharmacology
    88. LUO MJ; MAO LF; SCHULZ H
      SHORT-CHAIN 3-HYDROXY-2-METHYLACYL-COA DEHYDROGENASE FROM RAT-LIVER -PURIFICATION AND CHARACTERIZATION OF A NOVEL ENZYME OF ISOLEUCINE METABOLISM

      Archives of biochemistry and biophysics
    89. CARTIER N; LEPETIT N; ROCCHICCIOLI F; BOUGNERES PF
      USE OF SOME MOLECULAR-BIOLOGY TO EXAMINE CASES OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY

      Archives de pediatrie
    90. KANAYAMA N; UEDA M; ATOMI H; KURIHARA T; KONDO J; TERANISHI Y; TANAKA A
      COMPARISON OF MOLECULAR-STRUCTURES AND REGULATION OF BIOSYNTHESIS OF UNIQUE THIOLASE ISOZYMES LOCALIZED ONLY IN PEROXISOMES OF N-ALKANE-UTILIZABLE YEAST, CANDIDA-TROPICALIS

      Journal of fermentation and bioengineering
    91. UEDA M
      MOLECULAR PHYSIOLOGY OF YEAST PEROXISOMES AND ITS DEVELOPMENT

      Seibutsu kogaku kaishi
    92. SUNDBERG C; WACHTMEISTER CA; LUNDGREN B; DEPIERRE JW
      COMPARISON OF THE POTENCIES OF (-2-ETHYLHEXANOIC AND (-)-2-ETHYLHEXANOIC ACID IN CAUSING PEROXISOME PROLIFERATION AND RELATED BIOLOGICAL EFFECTS IN MOUSE-LIVER())

      Chirality
    93. TAKAHASHI Y; HIRATA Y; BURSTEIN Y; LISTOWSKY I
      DELTA(3),DELTA(2)-ENOYL-COA ISOMERASE IS THE PROTEIN THAT COPURIFIES WITH HUMAN GLUTATHIONE S-TRANSFERASES FROM S-HEXYLGLUTATHIONE AFFINITYMATRICES

      Biochemical journal
    94. FERNANDEZMORENO MA; MARTINEZ E; CABALLERO JL; ICHINOSE K; HOPWOOD DA; MALPARTIDA F
      DNA-SEQUENCE AND FUNCTIONS OF THE ACTVI REGION OF THE ACTINORHODIN BIOSYNTHETIC GENE-CLUSTER OF STREPTOMYCES-COELICOLOR A3(2)

      The Journal of biological chemistry
    95. CAI YO; SOHLENIUS AK; ANDERSSON K; SUNDBERG C; DEPIERRE JW
      EFFECTS OF ACETYLSALICYLIC-ACID ON PARAMETERS RELATED TO PEROXISOME PROLIFERATION IN MOUSE-LIVER

      Biochemical pharmacology
    96. SONG XQ; FUKAO T; YAMAGUCHI S; MIYAZAWA S; HASHIMOTO T; ORII T
      MOLECULAR-CLONING AND NUCLEOTIDE-SEQUENCE OF COMPLEMENTARY-DNA FOR HUMAN HEPATIC CYTOSOLIC ACETOACETYL-COENZYME-A THIOLASE

      Biochemical and biophysical research communications
    97. IJLST L; WANDERS RJA; USHIKUBO S; KAMIJO T; HASHIMOTO T
      MOLECULAR-BASIS OF LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY - IDENTIFICATION OF THE MAJOR DISEASE-CAUSING MUTATION IN THE ALPHA-SUBUNIT OF THE MITOCHONDRIAL TRIFUNCTIONAL PROTEIN

      Biochimica et biophysica acta, L. Lipids and lipid metabolism
    98. CABLE S; KEDINGER M; DAUCA M
      PEROXISOMES AND PEROXISOMAL ENZYMES ALONG THE CRYPT-VILLUS AXIS OF THE RAT INTESTINE

      Differentiation
    99. KAWAI Y; TAKAHASHI S; SATOH A; KATO N
      DECREASED ACTIVITY OF XANTHINE DEHYDROGENASE AND SERUM URIC-ACID IN RATS FED PARTIALLY HYDROGENATED FISH-OIL

      Nutrition research
    100. CAUSERET C; BENTEJAC M; BUGAUT M
      PROTEINS AND ENZYMES OF THE PEROXISOMAL MEMBRANE IN MAMMALS

      Biology of the cell


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 24/10/20 alle ore 21:10:16