BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 6457913)

  • 1. Long-term intracellular retention of hexosaminidase A by Tay-Sachs disease brain and lung cells in vitro.
    Brooks SE; Hoffman LM; Amsterdam D; Adachi M; Schneck L
    J Neurosci Res; 1981; 6(3):381-8. PubMed ID: 6457913
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Tay-Sachs disease brain cells in culture: mobilization of stored GM2 after concanavalin A-mediated uptake of hexosaminidase A.
    Hoffman LM; Brooks SE; Amsterdam D; Oropello J; Schneck L
    J Neurosci Res; 1980; 5(5):413-7. PubMed ID: 7441795
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Unusual thermolability properties of beta-hexosaminidase: studies of enzyme from cultured cells and clinical implications.
    Prence EM; Zalewski I; Natowicz MR
    Am J Med Genet; 1996 Nov; 65(4):320-4. PubMed ID: 8923943
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Tay-Sachs disease and normal cerebellar cells in culture: elevated levels of lysosomal enzymes in Tay-Sachs disease cells.
    Hoffman LM; Brooks SE; Schneck L
    J Neurosci Res; 1982; 8(1):49-55. PubMed ID: 6816949
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Beta-hexosaminidase isozymes and replacement therapy in Gm2 gangliosidosis.
    Rattazzi MC
    Isozymes Curr Top Biol Med Res; 1983; 11():65-81. PubMed ID: 6227586
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A new form of residual hexosaminidase activity in infantile Tay Sachs disease fibroblasts.
    Hechtman P; Khoo K; Isaacs C
    Clin Genet; 1983 Sep; 24(3):206-15. PubMed ID: 6226462
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Restoration of hexosaminidase A activity in human Tay-Sachs fibroblasts via adenoviral vector-mediated gene transfer.
    Akli S; Guidotti JE; Vigne E; Perricaudet M; Sandhoff K; Kahn A; Poenaru L
    Gene Ther; 1996 Sep; 3(9):769-74. PubMed ID: 8875224
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Enzyme replacement treatment for Tay-Sachs disease brain cells in culture utilizing concanavalin A-mediated hexosaminidase A uptake: biochemical and morphological evidence of GM2 mobilization.
    Brooks SE; Hoffman LM; Adachi M; Amsterdam D; Schneck L
    Acta Neuropathol; 1980; 50(1):9-17. PubMed ID: 7376831
    [TBL] [Abstract][Full Text] [Related]  

  • 9. II. Characterization and development of the regional- and cellular-specific abnormalities in the epididymis of mice with beta-hexosaminidase A deficiency.
    Adamali HI; Somani IH; Huang JQ; Gravel RA; Trasler JM; Hermo L
    J Androl; 1999; 20(6):803-24. PubMed ID: 10591619
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular forms of beta-N-acetylhexosaminidase in Epstein-Barr virus-transformed lymphoid cell lines from normal subjects and patients with Tay-Sachs disease.
    Salvayre R; Maret A; Negre A; Lenoir G; Vuillaume M; Icart J; Didier J; Douste-Blazy L
    Eur J Biochem; 1983 Jul; 133(3):627-33. PubMed ID: 6305653
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Activity and appearance of isoenzyme spectrums of some lysosomal hydrolases in biopsy material of human chorion].
    Beĭer EM; Vidershaĭn GIa; Bakharev VA; Rozovskiĭ IS
    Vopr Med Khim; 1983; 29(2):130-3. PubMed ID: 6222539
    [TBL] [Abstract][Full Text] [Related]  

  • 12. beta-hexosaminidase in cultured normal and mutant human fibroblasts: an immunohistochemical and biochemical investigation.
    Elsafi ME; Elbashir MI; Hultberg B; Isaksson A; Hägerstrand I; Stenram U
    Scand J Clin Lab Invest; 1991 Dec; 51(8):711-4. PubMed ID: 1839650
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene.
    Myerowitz R
    Hum Mutat; 1997; 9(3):195-208. PubMed ID: 9090523
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Isoenzyme pattern and partial characterization of hexosaminidases in the membrane and cytosol of human erythrocytes.
    Massaccesi L; Lombardo A; Venerando B; Tettamanti G; Goi G
    Clin Biochem; 2007 Apr; 40(7):467-77. PubMed ID: 17321512
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Reconstruction of hexosaminidase isoenzymes during hybridization of fibroblasts from Tay-Sachs and Sandhoff diseases].
    Beĭer EM; Vidershaĭn GIa; Venert M
    Biull Eksp Biol Med; 1984 Jan; 97(1):83-6. PubMed ID: 6229294
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosis.
    Sango K; McDonald MP; Crawley JN; Mack ML; Tifft CJ; Skop E; Starr CM; Hoffmann A; Sandhoff K; Suzuki K; Proia RL
    Nat Genet; 1996 Nov; 14(3):348-52. PubMed ID: 8896570
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Beta-hexosaminidase isoenzyme profiles in serum, plasma, platelets and mononuclear, polymorphonuclear and unfractionated total leukocytes.
    Casal JA; Cano E; Tutor JC
    Clin Biochem; 2005 Oct; 38(10):938-42. PubMed ID: 16024010
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular basis of heat labile hexosaminidase B among Jews and Arabs.
    Narkis G; Adam A; Jaber L; Pennybacker M; Proia RL; Navon R
    Hum Mutat; 1997; 10(6):424-9. PubMed ID: 9401004
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary heat-labile hexosaminidase B: its implication for recognizing Tay-Sachs genotypes.
    Navon R; Nutman J; Kopel R; Gaber L; Gadoth N; Goldman B; Nitzan M
    Am J Hum Genet; 1981 Nov; 33(6):907-15. PubMed ID: 6459736
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis for Tay-Sachs disease using chorionic villus sampling.
    Grebner EE; Jackson LG
    Prenat Diagn; 1985; 5(5):313-20. PubMed ID: 2933645
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.