133 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]