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Journal Abstract Search

230 related items for PubMed ID: 1373633

  • 41. Transformation and characterization of mutant human fibroblasts defective in peroxisome assembly.
    Okamoto H, Suzuki Y, Shimozawa N, Yajima S, Masuno M, Orii T.
    Exp Cell Res; 1992 Aug; 201(2):307-12. PubMed ID: 1639130
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  • 43. Complementation in Zellweger syndrome: biochemical analysis of newly generated peroxisomes.
    Stanczak H, Kremser K, Singh AK, Ashcraft J, Stanley W, Singh I.
    Hum Hered; 1992 Aug; 42(3):172-8. PubMed ID: 1511996
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  • 46. Peroxisomal disorders: a review.
    Wanders RJ, Schutgens RB, Barth PG.
    J Neuropathol Exp Neurol; 1995 Sep; 54(5):726-39. PubMed ID: 7545216
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  • 47. Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders.
    Wanders RJ, van Roermund CW, van Wijland MJ, Schutgens RB, Heikoop J, van den Bosch H, Schram AW, Tager JM.
    J Clin Invest; 1987 Dec; 80(6):1778-83. PubMed ID: 3680527
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  • 49. Peroxisomal disorders in neurology.
    Wanders RJ, Heymans HS, Schutgens RB, Barth PG, van den Bosch H, Tager JM.
    J Neurol Sci; 1988 Dec; 88(1-3):1-39. PubMed ID: 3066850
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  • 52. [Peroxisomes and peroxisomal diseases].
    Petelenz M, Gonciarz Z, Grzybek H, Panz B.
    Postepy Hig Med Dosw; 1991 Dec; 45(1-2):77-99. PubMed ID: 1717967
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  • 53. [Function and diseases of peroxisomes].
    Wehr H, Zaremba J.
    Neurol Neurochir Pol; 1991 Dec; 25(6):769-74. PubMed ID: 1725818
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  • 54. [Peroxisomal disorders].
    Stradomska TJ.
    Postepy Biochem; 2018 Dec 29; 64(4):359-367. PubMed ID: 30656921
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  • 55. Phenotypic and genotypic variability of generalized peroxisomal disorders.
    Naidu S, Moser AE, Moser HW.
    Pediatr Neurol; 1988 Dec 29; 4(1):5-12. PubMed ID: 3069099
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  • 56. Molecular genetics of peroxisomal disorders.
    Moser HW.
    Front Biosci; 2000 Mar 01; 5():D298-306. PubMed ID: 10704429
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  • 57. A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).
    Poll-The BT, Roels F, Ogier H, Scotto J, Vamecq J, Schutgens RB, Wanders RJ, van Roermund CW, van Wijland MJ, Schram AW.
    Am J Hum Genet; 1988 Mar 01; 42(3):422-34. PubMed ID: 2894756
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  • 58. Peroxisomal L-pipecolic acid oxidation is deficient in liver from Zellweger syndrome patients.
    Mihalik SJ, Moser HW, Watkins PA, Danks DM, Poulos A, Rhead WJ.
    Pediatr Res; 1989 May 01; 25(5):548-52. PubMed ID: 2717271
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  • 59. Biochemical features of a patient with Zellweger-like syndrome with normal PTS-1 and PTS-2 peroxisomal protein import systems: a new peroxisomal disease.
    Singh I, Voigt RG, Sheikh FG, Kremser K, Brown FR.
    Biochem Mol Med; 1997 Aug 01; 61(2):198-207. PubMed ID: 9259985
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  • 60. Neonatal adrenoleukodystrophy. Impaired plasmalogen biosynthesis and peroxisomal beta-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fibroblasts.
    Wanders RJ, Schutgens RB, Schrakamp G, Tager JM, Van den Bosch H, Moser AB, Moser HW.
    J Neurol Sci; 1987 Feb 01; 77(2-3):331-40. PubMed ID: 3819771
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