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384 related items for PubMed ID: 1687673

  • 1. Arylsulfatases A and B in EBV-transformed lymphoid cell lines: studies on their molecular forms in cells from patients with inborn sulfatase deficiencies. Comparative diagnostic value of enzymatic assays.
    Tempesta MC, Levade T, Salvayre R.
    Clin Chim Acta; 1991 Oct 31; 202(3):149-65. PubMed ID: 1687673
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  • 2. Arylsulfatases A and B in metachromatic leukodystrophy and Maroteaux-Lamy syndrome: studies with 4-methylumelliferyl sulfate.
    Kolodny EH, Mumford RA.
    Adv Exp Med Biol; 1976 Oct 31; 68():239-51. PubMed ID: 7105
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  • 7. Multiple deficiency of mucopolysaccharide sulfatases in mucosulfatidosis.
    Basner R, von Figura K, Glössl J, Klein U, Kresse H, Mlekusch W.
    Pediatr Res; 1979 Dec 31; 13(12):1316-8. PubMed ID: 523191
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  • 10. Multiple molecular forms of arylsulfatase A in different forms of metachromatic leukodystrophy (MLD).
    Farrell DF, MacMartin MP, Clark AF.
    Neurology; 1979 Jan 31; 29(1):16-20. PubMed ID: 34126
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  • 11. An improved method for heterozygote identification in feline and human mucopolysaccharidosis VI, arylsulfatase-B deficiency.
    McGovern MM, Vine DT, Haskins ME, Desnick RJ.
    Enzyme; 1981 Jan 31; 26(4):206-10. PubMed ID: 6113958
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  • 13. Impaired cerebroside sulfate hydrolysis in fibroblasts of sibs with "pseudo" arylsulfatase A deficiency without metachromatic leukodystrophy.
    Hreidarsson SJ, Thomas GH, Kihara H, Fluharty AL, Kolodny EH, Moser HW, Reynolds LW.
    Pediatr Res; 1983 Sep 31; 17(9):701-4. PubMed ID: 6137805
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  • 15. Synthesis of pyrene derivatives of cerebroside sulfate and their use for determining arylsulfatase A activity.
    Marchesini S, Viani P, Cestaro B, Gatt S.
    Biochim Biophys Acta; 1989 Mar 14; 1002(1):14-9. PubMed ID: 2564282
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  • 16. Measurement of recombinant human arylsulfatase A and leukocyte sulfatase activities by analytical isotachophoresis.
    Pajarola S, Weißenberg C, Baysal F, Bruchelt G, Krägeloh-Mann I, Böhringer J.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2019 Aug 15; 1124():109-113. PubMed ID: 31195190
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  • 17. Multiple sulfatase deficiency: degradation of arylsulfatase A and B after endocytosis in fibroblasts.
    Steckel F, Hasilik A, von Figura K.
    Eur J Biochem; 1985 Aug 15; 151(1):147-52. PubMed ID: 2863139
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  • 18. Metachromatic leukodystrophy caused by a partial cerebroside sulfatase.
    Kihara H, Fluharty AL, O'Brien JS, Fish CH.
    Clin Genet; 1982 Apr 15; 21(4):253-61. PubMed ID: 6125284
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  • 19. Lysosomal arylsulfatase deficiencies in humans: chromosome assignments for arylsulfatase A and B.
    DeLuca C, Brown JA, Shows TB.
    Proc Natl Acad Sci U S A; 1979 Apr 15; 76(4):1957-61. PubMed ID: 36611
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  • 20. Pseudo arylsulfatase-A deficiency in healthy individuals: genetic and biochemical relationship to metachromatic leukodystrophy.
    Chang PL, Davidson RG.
    Proc Natl Acad Sci U S A; 1983 Dec 15; 80(23):7323-7. PubMed ID: 6580647
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