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Journal Abstract Search


240 related items for PubMed ID: 3519003

  • 21. Peroxisomal localization of the immunoreactive beta-oxidation enzymes in a neonate with a beta-oxidation defect. Pathological observations in liver, adrenal cortex and kidney.
    Espeel M, Roels F, Van Maldergem L, De Craemer D, Dacremont G, Wanders RJ, Hashimoto T.
    Virchows Arch A Pathol Anat Histopathol; 1991; 419(4):301-8. PubMed ID: 1949612
    [Abstract] [Full Text] [Related]

  • 22. Peroxisomal beta-oxidation: enzymology and molecular biology.
    Hashimoto T.
    Ann N Y Acad Sci; 1996 Dec 27; 804():86-98. PubMed ID: 8993538
    [No Abstract] [Full Text] [Related]

  • 23. Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme.
    Heikoop JC, van Roermund CW, Just WW, Ofman R, Schutgens RB, Heymans HS, Wanders RJ, Tager JM.
    J Clin Invest; 1990 Jul 27; 86(1):126-30. PubMed ID: 2365812
    [Abstract] [Full Text] [Related]

  • 24. Participation of peroxisomes in the metabolism of xenobiotic acyl compounds: comparison between peroxisomal and mitochondrial beta-oxidation of omega-phenyl fatty acids in rat liver.
    Yamada J, Ogawa S, Horie S, Watanabe T, Suga T.
    Biochim Biophys Acta; 1987 Sep 25; 921(2):292-301. PubMed ID: 3651489
    [Abstract] [Full Text] [Related]

  • 25. Biosynthesis and intracellular transport of enzymes of peroxisomal beta-oxidation.
    Miura S, Mori M, Takiguchi M, Tatibana M, Furuta S, Miyazawa S, Hashimoto T.
    J Biol Chem; 1984 May 25; 259(10):6397-402. PubMed ID: 6725256
    [Abstract] [Full Text] [Related]

  • 26. Complementation analysis of patients with intact peroxisomes and impaired peroxisomal beta-oxidation.
    McGuinness MC, Moser AB, Poll-The BT, Watkins PA.
    Biochem Med Metab Biol; 1993 Apr 25; 49(2):228-42. PubMed ID: 8484962
    [Abstract] [Full Text] [Related]

  • 27. Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease.
    Schram AW, Strijland A, Hashimoto T, Wanders RJ, Schutgens RB, van den Bosch H, Tager JM.
    Proc Natl Acad Sci U S A; 1986 Aug 25; 83(16):6156-8. PubMed ID: 2426710
    [Abstract] [Full Text] [Related]

  • 28. [Genes of peroxisomal enzymes].
    Osumi T, Hashimoto T.
    Tanpakushitsu Kakusan Koso; 1990 Jun 25; 35(8):1439-46. PubMed ID: 2374815
    [No Abstract] [Full Text] [Related]

  • 29. Reinvestigation of peroxisomal 3-ketoacyl-CoA thiolase deficiency: identification of the true defect at the level of d-bifunctional protein.
    Ferdinandusse S, van Grunsven EG, Oostheim W, Denis S, Hogenhout EM, IJlst L, van Roermund CW, Waterham HR, Goldfischer S, Wanders RJ.
    Am J Hum Genet; 2002 Jun 25; 70(6):1589-93. PubMed ID: 11992265
    [Abstract] [Full Text] [Related]

  • 30. Bile acid profiles in peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.
    Clayton PT, Patel E, Lawson AM, Carruthers RA, Collins J.
    J Clin Invest; 1990 Apr 25; 85(4):1267-73. PubMed ID: 2318981
    [Abstract] [Full Text] [Related]

  • 31. On the mechanism of stimulation of peroxisomal beta-oxidation in rat heart by partially hydrogenated fish oil.
    Kvannes J, Eikhom TS, Flatmark T.
    Biochim Biophys Acta; 1995 Mar 02; 1255(1):39-49. PubMed ID: 7893736
    [Abstract] [Full Text] [Related]

  • 32. X-linked adrenoleukodystrophy: defective peroxisomal oxidation of very long chain fatty acids but not of very long chain fatty acyl-CoA esters.
    Wanders RJ, van Roermund CW, van Wijland MJ, Nijenhuis AA, Tromp A, Schutgens RB, Brouwer-Kelder EM, Schram AW, Tager JM, van den Bosch H.
    Clin Chim Acta; 1987 Jun 15; 165(2-3):321-9. PubMed ID: 3652454
    [Abstract] [Full Text] [Related]

  • 33. Induction of peroxisomal beta-oxidation enzymes in primary cultured rat hepatocytes by clofibric acid.
    Ozasa H, Miyazawa S, Furuta S, Osumi T, Hashimoto T.
    J Biochem; 1985 May 15; 97(5):1273-8. PubMed ID: 4030722
    [Abstract] [Full Text] [Related]

  • 34.
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  • 35. Peroxisomal disorders: overview.
    Moser HW, Moser AB.
    Ann N Y Acad Sci; 1996 Dec 27; 804():427-41. PubMed ID: 8993562
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
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  • 37. Peroxisomal disorders in children: immunohistochemistry and neuropathology.
    Kamei A, Houdou S, Takashima S, Suzuki Y, Becker LE, Armstrong DL.
    J Pediatr; 1993 Apr 27; 122(4):573-9. PubMed ID: 8463903
    [Abstract] [Full Text] [Related]

  • 38. Biochemical and immunocytochemical properties of peroxisomes and mitochondria in bovine chromaffin cells.
    Suzuki Y, Lee K, Shimozawa N, Orii T, Kondo N.
    Cell Struct Funct; 1997 Dec 27; 22(6):615-9. PubMed ID: 9591053
    [Abstract] [Full Text] [Related]

  • 39. Immunochemical identity of peroxisomal enoyl-CoA hydratase with the peroxisome-proliferation-associated 80,000 mol wt polypeptide in rat liver.
    Reddy MK, Qureshi SA, Hollenberg PF, Reddy JK.
    J Cell Biol; 1981 Jun 27; 89(3):406-17. PubMed ID: 6788778
    [Abstract] [Full Text] [Related]

  • 40. Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctata.
    Balfe A, Hoefler G, Chen WW, Watkins PA.
    Pediatr Res; 1990 Mar 27; 27(3):304-10. PubMed ID: 2181395
    [Abstract] [Full Text] [Related]


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