These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 4367631)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Different gene mutations in variants of GM1- and GM2-gangliosidosis demonstrated by enzyme analysis of (single) somatic hybrid cells.
    Galjaard H; Hoogeveen A; Keijzer W; de Wit-Verbeek HA; Reuser AJ
    Cytogenet Cell Genet; 1975; 14(3-6):320-6. PubMed ID: 1192809
    [No Abstract]   [Full Text] [Related]  

  • 9. [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]  

  • 10. 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]  

  • 11. [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]  

  • 12. Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosis.
    Rattazzi MC; Brown JA; Davidson RG; Shows TB
    Am J Hum Genet; 1976 Mar; 28(2):143-54. PubMed ID: 817596
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A study of hexosaminadases in interspecific hybrids and in GM2 gangliosidosis with a discussion on their genetic control.
    Van Cong N; Weil D; Rebourcet R; Frézal J; Richard-Mollard AM
    Ann Hum Genet; 1975 Jul; 39(1):111-23. PubMed ID: 810068
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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; 278(13):1761-4. PubMed ID: 4368227
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. Hexosaminidase C in Tay-Sachs and Sandhoff disease.
    Penton E; Poenaru L; Dreyfus JC
    Biochim Biophys Acta; 1975 May; 391(1):162-9. PubMed ID: 237554
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Tay-Sachs disease--the use of tears for the detection of heterozygotes.
    Carmody PJ; Rattazzi MC; Davidson RG
    N Engl J Med; 1973 Nov; 289(20):1072-4. PubMed ID: 4742222
    [No Abstract]   [Full Text] [Related]  

  • 19. Separation of N-acetyl- -D-hexosaminamidase-isoenzymes from human brain and leukocytes by cellulose acetate paper electrophoresis: a simple procedure for the diagnosis of Tay-Sachs disease.
    Klibansky C
    Isr J Med Sci; 1971 Sep; 7(9):1086-9. PubMed ID: 5151274
    [No Abstract]   [Full Text] [Related]  

  • 20. Segregation within a family of two mutant alleles for hexosaminidase A.
    Kelly TE; Reynolds LW; O'Brien JS
    Clin Genet; 1976 May; 9(5):540-3. PubMed ID: 1269177
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.