BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

169 related articles for article (PubMed ID: 851488)

  • 1. Human hexosaminidase isozymes: chromatographic separation as an aid to heterozygote identification.
    Nakagawa S; Kumin S; Nitowsky HM
    Clin Chim Acta; 1977 Mar; 75(2):181-91. PubMed ID: 851488
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Human hexosaminidase isozymes. Assay of platelet activity for heterozygote identification during pregnancy.
    Nakagawa S; Kumin S; Chandra P; Nitowsky HM
    Clin Chim Acta; 1978 Sep; 88(2):249-56. PubMed ID: 699320
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Automated differentiation and measurement of hexosaminidase isoenzymes in biological fluids and its application to pre- and postnatal detection of Tay-Sachs disease.
    Saifer A; Parkhurst GW; Amoroso J
    Clin Chem; 1975 Mar; 21(3):334-42. PubMed ID: 1112042
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Human hexosaminidase isozymes. III. Distribution and activity of isozymes in peripheral blood leukocytes and platelets.
    Nakagawa S; Kumin S; Fox D; Nitowsky HM
    J Lab Clin Med; 1978 Jun; 91(6):922-8. PubMed ID: 650058
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Isoenzymes of serum N-acetyl-beta-D-glucosaminidase in the I cell disease heterozygote.
    Van Elsen AF; Leroy JG; VanneuvilleFJ ; Vercruyssen AL
    Hum Genet; 1976 Jan; 31(1):75-81. PubMed ID: 174996
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Human hexosaminidase isozymes. IV. Effects of oral contraceptive steroids on serum hexosaminidase activity.
    Nitowsky HM; Davis J; Nakagawa S; Fox D
    Am J Obstet Gynecol; 1979 Jul; 134(6):642-7. PubMed ID: 463955
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detection of GM2-gangliosidosis (Tay-Sachs and Sandhoff disease) gene carriers by serum hexosaminidase assay.
    Molzer B; Bernheimer H
    Clin Chim Acta; 1976 Nov; 73(1):163-9. PubMed ID: 826357
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of Tay-Sachs by hexosaminidase analysis of urine and tear samples.
    Saifer A; Amoroso J; Perle G
    Adv Exp Med Biol; 1976; 68():339-66. PubMed ID: 7107
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The prenatal diagnosis of Tay-Sachs disease.
    Lane AB; Skikne MI; Jenkins T
    S Afr Med J; 1976 Sep; 50(40):1553-5. PubMed ID: 982208
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Serum beta-hexosaminidases in pregnancy.
    Lowden JA
    Clin Chim Acta; 1979 May; 93(3):409-17. PubMed ID: 445857
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Serum hexosaminidase activity in I-cell disease carriers.
    Vidgoff J; Buist NR
    Hum Genet; 1977 May; 36(3):307-16. PubMed ID: 852874
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hexosaminidase A in amniotic fluid of Tay-Sachs fetuses.
    Geiger B; Navon R; Arnon R
    Clin Chem; 1978 Jul; 24(7):1131-3. PubMed ID: 657491
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Detection of Tay-Sachs disease carriers among individuals with thermolabile hexosaminidase B.
    Peleg L; Goldman B
    Eur J Clin Chem Clin Biochem; 1994 Feb; 32(2):65-9. PubMed ID: 8003579
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A rapid and simple microfractionation method for the analysis of hexosaminidase A and B activities in small numbers of cultured (amniotic fluid) cells.
    D'Azzo A; Hoogeveen A; De Wit-Verbeek HA
    Clin Chim Acta; 1978 Aug; 88(1):1-7. PubMed ID: 679481
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [GM2 gangliosidosis diagnosis and carriers detection by fractionation of N-acetyl-beta-D-hexosaminidase by electrophoresis on cellulose acetate gel (author's transl)].
    Pampols T; Girós ML; González Sastre F; Sabater J
    An Esp Pediatr; 1977 Oct; 10(10):695-704. PubMed ID: 607830
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Changes of serum hexosaminidase for the presumptive diagnosis of type I Gaucher disease in Tay-Sachs carrier screening.
    Nakagawa S; Kumin S; Sachs G; Nitowsky HM
    Am J Med Genet; 1983 Mar; 14(3):525-32. PubMed ID: 6859103
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Tay-Sachs disease: an improved, fully-automated method for heterozygote identification by tear beta-hexosaminidase assay.
    Goldberg JD; Truex JH; Desnick RJ
    Clin Chim Acta; 1977 May; 77(1):43-52. PubMed ID: 872421
    [No Abstract]   [Full Text] [Related]  

  • 18. Prenatal diagnosis of Tay-Sachs disease with heat-labile beta-hexosaminidase B.
    Momoi T; Kikuchi K; Shigematsu Y; Sudo M; Tanioka K
    Clin Chim Acta; 1983 Oct; 133(3):331-4. PubMed ID: 6226459
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis and fetal pathology of Tay-Sachs disease.
    Higami S; Nishizawa K; Omura K; Sugimoto K; Isshiki G
    Tohoku J Exp Med; 1976 Apr; 118(4):323-30. PubMed ID: 936207
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Maternal serum hexosaminidase A in pregnancy: effects of gestational age and fetal genotype.
    Ben-Yoseph Y; Pack BA; Thomas PM; Nadler HL; Kaback MM
    Am J Med Genet; 1988 Apr; 29(4):891-9. PubMed ID: 2969680
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.