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Journal Abstract Search

107 related items for PubMed ID: 4743635

  • 1. Identification of a possible subunit of hexosaminidase A and B.
    Robinson D, Carrol M, Stirling JL.
    Nature; 1973 Jun 15; 243(5407):415-6. PubMed ID: 4743635
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  • 2. Studies in Tay-Sachs and Sandhoff's diseases. Immunologic and structural properties of hexosaminidase A and hexosaminidase B.
    Beutler E, Srivastava SK.
    Isr J Med Sci; 1973 Jun 15; 9(9):1335-7. PubMed ID: 4798071
    [No Abstract] [Full Text] [Related]

  • 3. An enzymological approach to the lipidoses.
    Tallman JF, Pentchev PG, Brady RO.
    Enzyme; 1974 Jun 15; 18(1):136-49. PubMed ID: 4211795
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  • 4. Hexosaminidase-A and hexosaminidase-B: studies in Tay-Sachs' and Sandhoff's disease.
    Srivastava SK, Beutler E.
    Nature; 1973 Feb 16; 241(5390):463. PubMed ID: 4122341
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  • 7. Multiple forms of glycosidases in the normal and pathological states.
    Robinson D.
    Enzyme; 1974 Feb 16; 18(1):114-35. PubMed ID: 4277585
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  • 12. Ganglioside storage diseases.
    O'Brien JS.
    Adv Hum Genet; 1972 Feb 16; 3():39-98. PubMed ID: 4268938
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  • 13. Probable existence of hexosaminidase C locus located on chromosome 7 in man.
    Van Cong N, Rebourcet R, Weil D, Billardon C, Blanchard MG, Finaz C, Frézal J.
    C R Acad Hebd Seances Acad Sci D; 1974 Mar 25; 278(13):1761-4. PubMed ID: 4368227
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  • 14. Characterization and tissue distribution of N-acetyl hexosaminidase C: suggestive evidence for a separate hexosaminidase locus.
    Swallow DM, Evans L, Saha N, Harris H.
    Ann Hum Genet; 1976 Jul 25; 40(1):55-66. PubMed ID: 9025
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  • 15. Tay-Sachs and other lipid storage diseases.
    Friedman B.
    HSMHA Health Rep; 1971 Sep 25; 86(9):769-74. PubMed ID: 4331588
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  • 18. Apparent deficiency of hexosaminidase A in healthy members of a family with Tay-Sachs disease.
    Navon R, Padeh B, Adam A.
    Am J Hum Genet; 1973 May 25; 25(3):287-93. PubMed ID: 4704860
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