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La ricerca find articoli where soggetti phrase all words 'ZELLWEGER-SYNDROME' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 409 riferimenti
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    1. Matsumoto, N; Tamura, S; Moser, A; Moser, HW; Braverman, N; Suzuki, Y; Shimozawa, N; Kondo, N; Fujiki, Y
      The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6

      JOURNAL OF HUMAN GENETICS
    2. Vanhorebeek, I; Baes, M; Declercq, PE
      Isoprenoid biosynthesis is not compromised in a Zellweger syndrome mouse model

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    3. Yamaguchi, S; Iga, M; Kimura, M; Suzuki, Y; Shimozawa, N; Fukao, T; Kondo, N; Tazawa, Y; Orii, T
      Urinary organic acids in peroxisomal disorders: a simple screening method

      JOURNAL OF CHROMATOGRAPHY B
    4. Suzuki, Y; Shimozawa, N; Orii, T; Tsukamoto, T; Osumi, T; Fujiki, Y; Kondo, N
      Genetic and molecular bases of peroxisome biogenesis disorders

      GENETICS IN MEDICINE
    5. Gleeson, JG
      Neuronal migration disorders

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    6. Lambkin, GR; Rachubinski, RA
      Yarrowia lipolytica cells mutant for the peroxisomal peroxin Pex19p contain structures resembling wild-type peroxisomes

      MOLECULAR BIOLOGY OF THE CELL
    7. Titorenko, VI; Rachubinski, RA
      Dynamics of peroxisome assembly and function

      TRENDS IN CELL BIOLOGY
    8. Johnson, JM; Babul-Hirji, R; Chitayat, D
      First-trimester increased nuchal translucency and fetal hypokinesia associated with Zellweger syndrome

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    9. Tatsumi, K; Saito, M; Lin, B; Iwamori, M; Ichiseki, H; Shimozawa, N; Kamoshita, S; Igarashi, T; Sakakihara, Y
      Enhanced expression of a-series gangliosides in fibroblasts of patients with peroxisome biogenesis disorders

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    10. Farooqui, AA; Horrocks, LA
      Plasmalogens, phospholipase A(2), and docosahexaenoic acid turnover in brain tissue

      JOURNAL OF MOLECULAR NEUROSCIENCE
    11. Powers, JM
      Normal and defective neuronal membranes: Structure and function - Neuronallesions in peroxisomal disorders

      JOURNAL OF MOLECULAR NEUROSCIENCE
    12. Martinez, M
      Restoring the DHA levels in the brains of Zellweger patients

      JOURNAL OF MOLECULAR NEUROSCIENCE
    13. Gilgenkrantz, S
      The beginning of peroxisome biogenesis

      M S-MEDECINE SCIENCES
    14. Carver, JD; Benford, VJ; Han, B; Cantor, AB
      The relationship between age and the fatty acid composition of cerebral cortex and erythrocytes in human subjects

      BRAIN RESEARCH BULLETIN
    15. Moller, G; van Grunsven, EG; Wanders, RJA; Adamski, J
      Molecular basis of D-bifunctional protein deficiency

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    16. Breitling, R; Marijanovic, Z; Perovic, D; Adamski, J
      Evolution of 17 beta-HSD type 4, a multifunctional protein of beta-oxidation

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    17. Wanders, RJA; Vreken, P; Ferdinandusse, S; Jansen, GA; Waterham, HR; van Roermund, CWT; Van Grunsven, EG
      Peroxisomal fatty acid alpha- and beta-oxidation in humans: enzymology, peroxisomal metabolite transporters and peroxisomal diseases

      BIOCHEMICAL SOCIETY TRANSACTIONS
    18. Van Veldhoven, PP; Casteels, M; Mannaerts, GP; Baes, M
      Further insights into peroxisomal lipid breakdown via alpha- and beta-oxidation

      BIOCHEMICAL SOCIETY TRANSACTIONS
    19. Amery, L; Sano, H; Mannaerts, GP; Snider, J; Van Looy, J; Fransen, M; Van Veldhoven, PP
      Identification of PEX5p-related novel peroxisome-targeting signal 1 (PTS1)-binding proteins in mammals

      BIOCHEMICAL JOURNAL
    20. Tamura, S; Matsumoto, N; Imamura, A; Shimozawa, N; Suzuki, Y; Kondo, N; Fujiki, Y
      Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction

      BIOCHEMICAL JOURNAL
    21. Huyghe, S; Casteels, M; Janssen, A; Meulders, L; Mannaerts, GP; Declercq, PE; van Veldhoven, PP; Baes, M
      Prenatal and postnatal development of peroxisomal lipid-metabolizing pathways in the mouse

      BIOCHEMICAL JOURNAL
    22. Verhoeven, NM; Jakobs, C
      Human metabolism of phytanic acid and pristanic acid

      PROGRESS IN LIPID RESEARCH
    23. Suzuki, Y; Shimozawa, N; Imamura, A; Fukuda, S; Zhang, Z; Orii, T; Kondo, N
      Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders

      JOURNAL OF INHERITED METABOLIC DISEASE
    24. Barth, PG; Gootjes, J; Bode, H; Vreken, P; Majoie, CBLM; Wanders, RJA
      Late onset white matter disease in peroxisome biogenesis disorder

      NEUROLOGY
    25. Nissenkorn, A; Michelson, M; Ben-Zeev, B; Lerman-Sagie, T
      Inborn errors of metabolism - A cause of abnormal brain development

      NEUROLOGY
    26. Wanders, RJA; Jansen, GA; Skjeldal, OH
      Refsum disease, peroxisomes and phytanic acid oxidation: A review

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    27. Dodt, G; Warren, D; Becker, E; Rehling, P; Gould, SJ
      Domain mapping of human PEX5 reveals functional and structural similarities to Saccharomyces cerevisiae Pex18p and Pex21p

      JOURNAL OF BIOLOGICAL CHEMISTRY
    28. Otera, H; Nishimura, M; Setoguchi, K; Mori, T; Fujiki, Y
      Biogenesis of nonspecific lipid transfer protein and sterol carrier protein x - Studies using peroxisome assembly-defective pex cell mutants

      JOURNAL OF BIOLOGICAL CHEMISTRY
    29. 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
    30. Honsho, M; Fujiki, Y
      Topogenesis of peroxisomal membrane protein requires a short, positively charged intervening-loop sequence and flanking hydrophobic segments - Study using human membrane protein PMP34

      JOURNAL OF BIOLOGICAL CHEMISTRY
    31. Horiguchi, H; Yurimoto, H; Goh, TK; Nakagawa, T; Kato, N; Sakai, Y
      Peroxisomal. catalase in the methylotrophic yeast Candida boidinii: Transport efficiency and metabolic significance

      JOURNAL OF BACTERIOLOGY
    32. Holroyd, C; Erdmann, R
      Protein translocation machineries of peroxisomes

      FEBS LETTERS
    33. Van Veldhoven, PP; Meyhi, E; Squires, RH; Fransen, M; Fournier, B; Brys, V; Bennett, MJ; Mannaerts, GP
      Fibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiency

      EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
    34. Panjan, DP; Meglic, NP; Neubauer, D
      A case of Zellweger syndrome with extensive MRI abnormalities and unusual EEG findings

      CLINICAL ELECTROENCEPHALOGRAPHY
    35. Reisse, S; Rothardt, G; Volkl, A; Beier, K
      Peroxisomes and ether lipid biosynthesis in rat testis and epididymis

      BIOLOGY OF REPRODUCTION
    36. Jansen, GA; van den Brink, DM; Ofman, R; Draghici, O; Dacremont, G; Wanders, RJA
      Identification of pristanal dehydrogenase activity in peroxisomes: Conclusive evidence that the complete phytanic acid alpha-oxidation pathway is localized in peroxisomes

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    37. Konakova, M; Huynh, DP; Yong, W; Pulst, SM
      Cellular distribution of torsin A and torsin B in normal human brain

      ARCHIVES OF NEUROLOGY
    38. Walter, C; Gootjes, J; Mooijer, PA; Portsteffen, H; Klein, C; Waterham, HR; Barth, PG; Epplen, JT; Kunau, WH; Wanders, RJA; Dodt, G
      Disorders of peroxisome biogenesis due to mutations in PEX1: Phenotypes and PEX1 protein levels

      AMERICAN JOURNAL OF HUMAN GENETICS
    39. Muntau, AC; Mayerhofer, PU; Albet, S; Schmid, TE; Bugaut, M; Roscher, AA; Kammerer, S
      Genomic organization, expression analysis, and chromosomal localization ofthe mouse PEX3 gene encoding a peroxisomal assembly protein

      BIOLOGICAL CHEMISTRY
    40. Houten, SM; Wanders, RJA; Waterham, HR
      Biochemical and genetic aspects of mevalonate kinase and its deficiency

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    41. McGuinness, MC; Wei, HM; Smith, KD
      Therapeutic developments in peroxisome biogenesis disorders

      EXPERT OPINION ON INVESTIGATIONAL DRUGS
    42. Moser, HW
      Molecular genetics of peroxisomal disorders

      FRONTIERS IN BIOSCIENCE
    43. Warren, DS; Wolfe, BD; Gould, SJ
      Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients

      HUMAN MUTATION
    44. Ghaedi, K; Tamura, S; Okumoto, K; Matsuzono, Y; Fujiki, Y
      The peroxin Pex3p initiates membrane assembly in peroxisome biogenesis

      MOLECULAR BIOLOGY OF THE CELL
    45. Bottger, G; Barnett, P; Klein, ATJ; Kragt, A; Tabak, HF; Distel, B
      Saccharomyces cerevisiae PTS1 receptor Pex5p interacts with the SH3 domainof the peroxisomal membrane protein Pex13p in an unconventional, non-PXXP-related manner

      MOLECULAR BIOLOGY OF THE CELL
    46. Imamura, A; Shimozawa, N; Suzuki, Y; Zhang, ZY; Tsukamoto, T; Fujiki, Y; Orii, T; Osumi, T; Kondo, N
      Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans

      BRAIN & DEVELOPMENT
    47. Rizzo, WB
      Peroxisome 1, 2, 3 ...

      ANNALS OF NEUROLOGY
    48. Wei, HM; Kemp, S; McGuinness, MC; Moser, AB; Smith, KD
      Pharmacological induction of peroxisomes in peroxisome biogenesis disorders

      ANNALS OF NEUROLOGY
    49. Baumgartner, MR; Jansen, GA; Verhoeven, NM; Mooyer, PAW; Jakobs, C; Roels, F; Espeel, M; Fourmaintraux, A; Bellet, H; Wanders, RJA; Saudubray, JM
      Atypical Refsum disease with pipecolic acidemia and abnormal catalase distribution

      ANNALS OF NEUROLOGY
    50. Singh, I; Carillo, O; Namboodiri, A
      Isolation and biochemical characterization of peroxisomes from cultured rat glial cells

      NEUROCHEMICAL RESEARCH
    51. Gartner, J
      Organelle disease: peroxisomal disorders

      EUROPEAN JOURNAL OF PEDIATRICS
    52. Wanders, RJA; van Grunsven, EG; Jansen, GA
      Lipid metabolism in peroxisomes: enzymology, functions and dysfunctions ofthe fatty acid alpha- and beta-oxidation systems in humans

      BIOCHEMICAL SOCIETY TRANSACTIONS
    53. Collins, CS; Kalish, JE; Morrell, JC; McCaffery, JM; Gould, SJ
      The peroxisome biogenesis factors Pex4p, Pex22p, Pex1p, and Pex6p act in the terminal steps of peroxisomal matrix protein import

      MOLECULAR AND CELLULAR BIOLOGY
    54. Knott, TG; Birdsey, GM; Sinclair, KE; Gallagher, IM; Purdue, PE; Danpure, CJ
      The peroxisomal targeting sequence type 1 receptor, Pex5p, and the peroxisomal import efficiency of alanine : glyoxylate aminotransferase

      BIOCHEMICAL JOURNAL
    55. Szilard, RK; Rachubinski, RA
      Tetratricopeptide repeat domain of Yarrowia lipolytica Pex5p is essential for recognition of the type 1 peroxisomal targeting signal but does not confer full biological activity on Pex5p

      BIOCHEMICAL JOURNAL
    56. Dodt, G; Kim, DG; Reimann, SA; Reuber, BE; McCabe, K; Gould, SJ; Mihalik, SJ
      L-pipecolic acid oxidase, a human enzyme essential for the degradation of L-pipecolic acid, is most similar to the monomeric sarcosine oxidases

      BIOCHEMICAL JOURNAL
    57. Santos, MJ; Henderson, SC; Moser, AB; Moser, HW; Lazarow, PB
      Peroxisomal ghosts are intracellular structures distinct from lysosomal compartments in Zellweger Syndrome: A confocal laser scanning microscopy study

      BIOLOGY OF THE CELL
    58. Kiel, JAKW; Hilbrands, RE; Bovenberg, RAL; Veenhuis, M
      Isolation of Penicillium chrysogenum PEX1 and PEX6 encoding AAA proteins involved in peroxisome biogenesis

      APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
    59. Gould, SJ; Valle, D
      Peroxisome biogenesis disorders - genetics and cell biology

      TRENDS IN GENETICS
    60. Baerends, RJS; Faber, KN; Kiel, JAKW; van der Klei, IJ; Harder, W; Veenhuis, M
      Sorting and function of peroxisomal membrane proteins

      FEMS MICROBIOLOGY REVIEWS
    61. Bader, PI; Dougherty, S; Cangany, N; Raymond, G; Jackson, GE
      Infantile Refsum disease in four Amish sibs

      AMERICAN JOURNAL OF MEDICAL GENETICS
    62. Johnson, DW
      A rapid screening procedure for the diagnosis of peroxisomal disorders: Quantification of very long-chain fatty acids, as dimethylaminoethyl esters, in plasma and blood spots, by electrospray tandem mass spectrometry

      JOURNAL OF INHERITED METABOLIC DISEASE
    63. Korman, SH; Mandel, H; Gutman, A
      Characteristic urine organic acid profile in peroxisomal biogenesis disorders

      JOURNAL OF INHERITED METABOLIC DISEASE
    64. Gartner, J
      Disorders related to peroxisomal membranes

      JOURNAL OF INHERITED METABOLIC DISEASE
    65. Sacksteder, KA; Gould, SJ
      The genetics of peroxisome biogenesis

      ANNUAL REVIEW OF GENETICS
    66. Subramani, S; Koller, A; Snyder, WB
      Import of peroxisomal matrix and membrane proteins

      ANNUAL REVIEW OF BIOCHEMISTRY
    67. Solaas, K; Sletta, RJ; Soreide, O; Kase, BF
      Presence of choloyl- and chenodeoxycholoyl-coenzyme A thioesterase activity in human liver

      SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION
    68. Landrieu, P
      Progress in pediatric neurology.

      REVUE NEUROLOGIQUE
    69. Gressens, P
      Mechanisms and disturbances of neuronal migration

      PEDIATRIC RESEARCH
    70. Imamura, A; Shimozawa, N; Suzuki, Y; Zhang, ZY; Tsukamoto, T; Fujiki, Y; Orii, T; Osumi, T; Wanders, RJA; Kondo, N
      Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): Comparative study of PEX6 and PEX1

      PEDIATRIC RESEARCH
    71. Sandhir, R; Khan, M; Singh, I
      Identification of the pathway of alpha-oxidation of cerebronic acid in peroxisomes

      LIPIDS
    72. Janssen, A; Baes, M; Gressens, P; Mannaerts, GP; Declercq, P; Van Veldhoven, PP
      Docosahexaenoic acid deficit is not a major pathogenic factor in peroxisome-deficient mice

      LABORATORY INVESTIGATION
    73. Ferdinandusse, S; Denis, S; van Berkel, E; Dacremont, G; Wanders, RJA
      Peroxisomal fatty acid oxidation disorders and 58 kDa sterol carrier protein X (SCPx): activity measurements in liver and fibroblasts using a newly developed method

      JOURNAL OF LIPID RESEARCH
    74. 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
    75. South, ST; Sacksteder, KA; Li, XL; Liu, YF; Gould, SJ
      Inhibitors of COPI and COPII do not block PEX3-mediated peroxisome synthesis

      JOURNAL OF CELL BIOLOGY
    76. Sacksteder, KA; Jones, JM; South, ST; Li, XL; Liu, YF; Gould, SJ
      PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis

      JOURNAL OF CELL BIOLOGY
    77. Titorenko, VI; Chan, H; Rachubinski, RA
      Fusion of small peroxisomal vesicles in vitro reconstructs an early step in the in vivo multistep peroxisome assembly pathway of Yarrowia lipolytica

      JOURNAL OF CELL BIOLOGY
    78. Fujiwara, C; Imamura, A; Hashiguchi, N; Shimozawa, N; Suzuki, Y; Kondo, N; Imanaka, T; Tsukamoto, T; Osumi, T
      Catalase-less peroxisomes - Implication in the milder forms of peroxisome biogenesis disorder

      JOURNAL OF BIOLOGICAL CHEMISTRY
    79. Okumoto, K; Abe, I; Fujiki, Y
      Molecular anatomy of the peroxin Pex12p - Ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type1-receptor Pex5p and a ring peroxin, Pex10p

      JOURNAL OF BIOLOGICAL CHEMISTRY
    80. Otera, H; Harano, T; Honsho, M; Ghaedi, K; Mukai, S; Tanaka, A; Kawai, A; Shimizu, N; Fujiki, Y
      The mammalian peroxin Pex5pL, the longer isoform of the mobile peroxisome targeting signal (PTS) type 1 transporter, translocates the Pex7p center dot PTS2 protein complex into peroxisomes via its initial docking site, Pex14p

      JOURNAL OF BIOLOGICAL CHEMISTRY
    81. Matsumura, T; Otera, H; Fujiki, Y
      Disruption of the interaction of the longer isoform of Pex5p, Pex5pL, withPex7p abolishes peroxisome targeting signal type 2 - Study with a novel PEX5-impaired Chinese hamster ovary cell mutant

      JOURNAL OF BIOLOGICAL CHEMISTRY
    82. Baes, M; Huyghe, S; Carmeliet, P; Declercq, PE; Collen, D; Mannaerts, GP; Van Veldhoven, PP
      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

      JOURNAL OF BIOLOGICAL CHEMISTRY
    83. Jones, JM; Morrell, JC; Gould, SJ
      Identification and characterization of HAOX1, HAOX2, and HAOX3, three human peroxisomal 2-hydroxy acid oxidases

      JOURNAL OF BIOLOGICAL CHEMISTRY
    84. Hajra, AK; Larkins, LK; Das, AK; Hemati, N; Erickson, RL; MacDougald, OA
      Induction of the peroxisomal glycerolipid-synthesizing enzymes during differentiation of 3T3-L1 adipocytes - Role in triacylglycerol synthesis

      JOURNAL OF BIOLOGICAL CHEMISTRY
    85. Lee, JG; Cho, SP; Lee, HS; Lee, CH; Bae, KS; Maeng, PJ
      Identification of a cryptic N-terminal signal in Saccharomyces cerevisiae peroxisomal citrate synthase that functions in both peroxisomal and mitochondrial targeting

      JOURNAL OF BIOCHEMISTRY
    86. Fujiki, Y
      Peroxisome biogenesis and peroxisome biogenesis disorders

      FEBS LETTERS
    87. Smith, BT; Sengupta, TK; Singh, I
      Intraperoxisomal localization of very-long-chain fatty acyl-CoA synthetase: Implication in X-adrenoleukodystrophy

      EXPERIMENTAL CELL RESEARCH
    88. Zomer, AWM; Jansen, GA; van der Burg, B; Verhoeven, NM; Jakobs, C; van der Saag, PT; Wanders, RJA; Poll-The, T
      Phytanoyl-CoA hydroxylase activity is induced by phytanic acid

      EUROPEAN JOURNAL OF BIOCHEMISTRY
    89. Cerullo, A; Marini, C; Cevoli, S; Carelli, V; Montagna, P; Tinuper, P
      Colpocephaly in two siblings: further evidence of a genetic transmission

      DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
    90. Itoh, M; Suzuki, Y; Akaboshi, S; Zhang, ZY; Miyabara, S; Takashima, S
      Developmental and pathological expression of peroxisomal enzymes: their relationship of D-bifunctional protein deficiency and Zellweger syndrome

      BRAIN RESEARCH
    91. Biermanns, M; Gartner, J
      Genomic organization and characterization of human PEX2 encoding a 35-kDa peroxisomal membrane protein

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    92. IJlst, L; de Kromme, I; Oostheim, W; Wanders, RJA
      Molecular cloning and expression of human L-pipecolate oxidase

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    93. Muntau, AC; Holzinger, A; Mayerhofer, PU; Gartner, J; Roscher, AA; Kammerer, S
      The human PEX3 gene encoding a peroxisomal assembly protein: Genomic organization, positional mapping, and mutation analysis in candidate phenotypes

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    94. Shimozawa, N; Zhang, ZY; Imamura, A; Suzuki, Y; Fujiki, Y; Tsukamoto, T; Osumi, T; Aubourg, P; Wanders, RJA; Kondo, N
      Molecular mechanism of detectable catalase-containing particles, peroxisomes, in fibroblasts from a PEX2-defective patient

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    95. Martinez, M; Vazquez, E; Garcia-Silva, MT; Manzanares, J; Bertran, JM; Castello, F; Mougan, I
      Therapeutic effects of docosahexaenoic acid ethyl ester in patients with generalized peroxisomal disorders

      AMERICAN JOURNAL OF CLINICAL NUTRITION
    96. Qin, J; Mizuguchi, M; Itoh, M; Takashima, S
      A novel migration-related gene product, doublecortin, in neuronal migration disorder of fetuses and infants with Zellweger syndrome

      ACTA NEUROPATHOLOGICA
    97. Moser, HW
      Molecular genetics of peroxisomal disorders

      PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
    98. Jansen, GA; Verhoeven, NM; Denis, S; Romeijn, GJ; Jakobs, C; ten Brink, HJ; Wanders, RJA
      Phytanic acid alpha-oxidation: identification of 2-hydroxyphytanoyl-CoA lyase in rat liver and its localisation in peroxisomes

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    99. Saito, M; Iwamori, M; Lin, B; Oka, A; Fujiki, Y; Shimozawa, N; Kamoshita, S; Yanagisawa, M; Sakakihara, Y
      Accumulation of glycolipids in mutant Chinese hamster ovary cells (Z65) with defective peroxisomal assembly and comparison of the metabolic rate of glycosphingolipids between Z65 cells and wild-type CHO-K1 cells

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    100. Hussain-Yusuf, H; Onodera, R; Nasser, MEA; Sato, H
      Simple method for the simultaneous analysis of pipecolic acid and lysine by high-performance liquid chromatography and its application to rumen liquor and plasma of ruminants

      JOURNAL OF CHROMATOGRAPHY B


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Documento generato il 09/08/20 alle ore 05:30:35