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Journal Abstract Search

112 related items for PubMed ID: 7730322

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  • 4. Microheterogeneity of arylsulfatase A from human tissues.
    Stevens RL, Fluharty AL, Killgrove AR, Kihara H.
    Biochim Biophys Acta; 1976 Oct 11; 445(3):661-71. PubMed ID: 9992
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  • 5. Assay for cerebroside sulfate (sulfatide) sulfatase in cultured skin fibroblasts with the natural activator protein.
    Lee-Vaupel M, Conzelmann E.
    Clin Chim Acta; 1987 Sep 15; 168(1):55-68. PubMed ID: 2889546
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  • 6. 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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  • 7. Metachromatic leukodystrophy without arylsulfatase A deficiency.
    Shapiro LJ, Aleck KA, Kaback MM, Itabashi H, Desnick RJ, Brand N, Stevens RL, Fluharty AL, Kihara H.
    Pediatr Res; 1979 Oct 31; 13(10):1179-81. PubMed ID: 41211
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  • 8. P-Nitrocatechol sulfate for arylsulfatase assay: detection of metachromatic leukodystrophy variants.
    Dubois G, Turpin J, Baumann N.
    Adv Exp Med Biol; 1976 Oct 31; 68():233-7. PubMed ID: 7104
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  • 9. Partial characterization of steroid sulfohydrolase and steroid sulfotransferase activities in purified porcine Leydig cells.
    Hobkirk R, Renaud R, Raeside JI.
    J Steroid Biochem; 1989 Mar 31; 32(3):387-92. PubMed ID: 2523010
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  • 10. 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 Mar 31; 68():239-51. PubMed ID: 7105
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  • 11. Galactosylceramide sulfotransferase, arylsulfatase A and cerebroside sulfatase activity in different regions of developing rat brain.
    van der Pal RH, Klein W, van Golde LM, Lopes-Cardozo M.
    Biochim Biophys Acta; 1990 Mar 12; 1043(1):91-6. PubMed ID: 1968763
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  • 12. Determination of galactose and galactocerebroside using a galactose oxidase column and electrochemical detector.
    Stoecker PW, Manowitz P, Harvey R, Yacynych AM.
    Anal Biochem; 1998 Apr 10; 258(1):103-8. PubMed ID: 9527855
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  • 13. Metachromatic leukodystrophy: subtype genotype/phenotype correlations and identification of novel missense mutations (P148L and P191T) causing the juvenile-onset disease.
    Qu Y, Shapira E, Desnick RJ.
    Mol Genet Metab; 1999 Jul 10; 67(3):206-12. PubMed ID: 10381328
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  • 14. Characterization of iodothyronine sulfatase activities in human and rat liver and placenta.
    Kester MH, Kaptein E, Van Dijk CH, Roest TJ, Tibboel D, Coughtrie MW, Visser TJ.
    Endocrinology; 2002 Mar 10; 143(3):814-9. PubMed ID: 11861502
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  • 15. Prevalence of partial cerebroside sulfate sulfatase (arylsulfatase A) defect in adult psychiatric patients.
    Shah SN, Johnson RC, Stone RK, Mahon-Haft H.
    Biol Psychiatry; 1985 Jan 10; 20(1):50-7. PubMed ID: 2856894
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  • 16. Sulfatide excreting heterozygous carrier of juvenile metachromatic leukodystrophy or asymptomatic patient of adult metachromatic leukodystrophy.
    Harzer K, Recke AS.
    Humangenetik; 1975 Oct 07; 29(4):299-307. PubMed ID: 1176145
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  • 17. Enzymes from human articular cartilage: isolation of arylsulfatase B and its comparison with arylsulfatase A.
    Gold EW, Gussler D, Schwartz ER.
    Connect Tissue Res; 1976 Oct 07; 4(4):237-45. PubMed ID: 11079
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  • 18. Purification and characterization of (Ca2+-Mg2+)-ATPase in rat liver lysosomal membranes.
    Ezaki J, Himeno M, Kato K.
    J Biochem; 1992 Jul 07; 112(1):33-9. PubMed ID: 1331035
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  • 19. Regulation of sulfotransferase activity by vitamin K in mouse brain.
    Sundaram KS, Lev M.
    Arch Biochem Biophys; 1990 Feb 15; 277(1):109-13. PubMed ID: 1968327
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  • 20. Purification of heparan sulfate D-glucosaminyl 3-O-sulfotransferase.
    Liu J, Shworak NW, Fritze LM, Edelberg JM, Rosenberg RD.
    J Biol Chem; 1996 Oct 25; 271(43):27072-82. PubMed ID: 8900198
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