BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 803466)

  • 1. Complementation after fusion of Sandhoff- and Tay-Sachs fibroblasts.
    Ropers HH; Grzeschik KH; Bühler E
    Humangenetik; 1975; 26(2):117-21. PubMed ID: 803466
    [No Abstract]   [Full Text] [Related]  

  • 2. Juvenile Sandhoff Disease: complementation tests with Sandhoff and Tay-Sachs disease using polyethylene glycol-induced cell fusion.
    Wood S
    Hum Genet; 1978 Apr; 41(3):325-9. PubMed ID: 417993
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic complementation after fusion of Tay-Sachs and Sandhoff cells.
    Thomas GH; Taylor HA; Miller CS; Axelman J; Migeon BR
    Nature; 1974 Aug; 250(467):580-2. PubMed ID: 4367631
    [No Abstract]   [Full Text] [Related]  

  • 4. [Genetic study of GM2 gangliosidosis (Tay-Sachs and Sandhoff) by the study of the hexosaminidases of the Sandhoff-rodents hybrids (mouse and hamster)].
    Weil D; Van Cong N; Rebourcet R; Frézal J
    Ann Genet; 1975 Sep; 18(3):163-8. PubMed ID: 810067
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Steroid hexosaminidase activity in Tay-Sachs and Sandhoff-Jatzkewitz diseases.
    Tomasi LG; Fukushima DK; Kolodny EH
    Neurology; 1974 Dec; 24(12):1158-65. PubMed ID: 4280528
    [No Abstract]   [Full Text] [Related]  

  • 6. Study of the beta-bexosyminidase separation by electrophoresis in homozygote and heterozygote Tay-Sachs cultured fibroblasts.
    Liebaers I; Vamos E; Mandelbaum IM
    Acta Clin Belg; 1974; 29(2):94-7. PubMed ID: 4839716
    [No Abstract]   [Full Text] [Related]  

  • 7. Tay-Sachs and Sandhoff-Jatzkewitz diseases: complementation of hexosaminidase A deficiency by somatic cell hybridization.
    Rattazzi MC; Brown JA; Davidson RG; Shows TB
    Birth Defects Orig Artic Ser; 1975; 11(3):232-5. PubMed ID: 812568
    [No Abstract]   [Full Text] [Related]  

  • 8. Sandhoff disease: impaired catabolism of sulfated glycosaminoglycans in cultured fibroblasts.
    Cantz M; O'Brien JF; Kresse H
    Birth Defects Orig Artic Ser; 1975; 11(6):261-7. PubMed ID: 127630
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Tay-Sachs and Sandhoff's disease: intergenic complementation after somatic cell hybridization.
    Galjaard H; Hoogeveen A; de Wit-Verbeek HA; Reuser AJ; Keijzer W; Westerveld A; Bootsma D
    Exp Cell Res; 1974 Aug; 87(2):444-8. PubMed ID: 4416048
    [No Abstract]   [Full Text] [Related]  

  • 10. Tay-Sachs and Sandhoff diseases: an hypothesis about the primary lesion based on hexosaminidase patterns in interspecific hybrids.
    Cong NV; Weil D; Rebourcet R; Pangalos C; Frézal J
    Cytogenet Cell Genet; 1975; 14(3-6):442-5. PubMed ID: 1192834
    [No Abstract]   [Full Text] [Related]  

  • 11. Cultured skin fibroblasts in lipidoses. Enzymatic, histochemical, and ultrastructural relationship in Fabry's Tay-Sachs, and Sandhoff's diseases.
    Yuasa T; Fukuma M; Takashima S; Takaki R
    Arch Pathol Lab Med; 1980 Jun; 104(6):321-7. PubMed ID: 6246846
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Enzyme diagnostics in lysosomal diseases with emphasis on sphingolipidoses].
    Dreyfus JC; Poenaru L
    Arch Fr Pediatr; 1975; 32(6):503-14. PubMed ID: 810108
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Tay-Sachs disease: ultrastructural studies on cultured fibroblasts.
    Wyatt PR; Cox DM; Hoogstraten J
    Pediatr Res; 1978 Apr; 12(4 Pt 1):310-3. PubMed ID: 652414
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. Tay-Sachs and Sandhoff diseases: an hypothesis about the primary lesion based on hexosaminidase patterns in interspecific hybrids.
    Van Cong N; Weil D; Rebourcet R; Pangalos C; Frézal J
    Birth Defects Orig Artic Ser; 1975; 11(3):272-5. PubMed ID: 812570
    [No Abstract]   [Full Text] [Related]  

  • 16. The Tay-Sachs disease fibroblast model: failure to respond to exogenous hexosaminidase A.
    Schneck L; Amsterdam D; Brooks SE; Rosenthal AL; Volk BW
    Pediatrics; 1973 Aug; 52(2):221-6. PubMed ID: 4721444
    [No Abstract]   [Full Text] [Related]  

  • 17. Characterization of beta-D-N-acetylhexosaminidases C and S in fibroplasts from control individuals and patients with Tay-Sachs disease.
    Reuser AJ; Galjaard H
    FEBS Lett; 1976 Nov; 72(1):1-5. PubMed ID: 11130
    [No Abstract]   [Full Text] [Related]  

  • 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(3):287-93. PubMed ID: 4704860
    [No Abstract]   [Full Text] [Related]  

  • 19. Tay-Sachs and Sandhoff-Jatzkewitz diseases: complementation of hexosaminidase A deficiency by somatic cell hybridization.
    Rattazzi MC; Brown JA; Davidson RG; Shows TB
    Cytogenet Cell Genet; 1975; 14(3-6):402-5. PubMed ID: 1192826
    [No Abstract]   [Full Text] [Related]  

  • 20. An autopsy case of Tay-Sachs' disease.
    Yutani C; Miyaji T
    Acta Pathol Jpn; 1974 May; 24(3):393-404. PubMed ID: 4408157
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.