116 related articles for article (PubMed ID: 810068)
1. 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]
2. [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]
3. 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]
4. Hexosaminidase isozyme in type O Gm2 gangliosidosis (Sandhoff-Jatzkewitz disease).
Beutler E; Kuhl W; Comings D
Am J Hum Genet; 1975 Sep; 27(5):628-38. PubMed ID: 808963
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Synthesis of 4-methylumbelliferyl-beta-D-N-acetylglucosamine-6-sulfate and its use in classification of GM2 gangliosidosis genotypes.
Bayleran J; Hechtman P; Saray W
Clin Chim Acta; 1984 Nov; 143(2):73-89. PubMed ID: 6239713
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Characterization of Hex S, the major residual beta hexosaminidase activity in type O Gm2 gangliosidosis (Sandhoff-Jatzkewitz disease).
Ikonne JU; Rattazzi MC; Desnick RJ
Am J Hum Genet; 1975 Sep; 27(5):639-50. PubMed ID: 240271
[TBL] [Abstract][Full Text] [Related]
10. Genetic complementation in somatic cell hybrids of four variants of infantile GM2 gangliosidosis.
Sonderfeld S; Brendler S; Sandhoff K; Galjaard H; Hoogeveen AT
Hum Genet; 1985; 71(3):196-200. PubMed ID: 2933318
[TBL] [Abstract][Full Text] [Related]
11. Human recombinant lysosomal β-Hexosaminidases produced in Pichia pastoris efficiently reduced lipid accumulation in Tay-Sachs fibroblasts.
Espejo-Mojica AJ; Rodríguez-López A; Li R; Zheng W; Alméciga-Díaz CJ; Dulcey-Sepúlveda C; Combariza G; Barrera LA
Am J Med Genet C Semin Med Genet; 2020 Dec; 184(4):885-895. PubMed ID: 33111489
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Characterization of beta-D-N-acetylhexosaminidase isoenzymes in man-Chinese hamster somatic cell hybrids.
Hoeksema HL; Reuser AJ; Hoogeveen A; Westerveld A; Braidman I; Robinson D
Am J Hum Genet; 1977 Jan; 29(1):14-23. PubMed ID: 835571
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Characterization of residual hexosaminidase activity in Sandhoff's disease using man-Chinese hamster cell hybrids.
Hoeksema HL; Reuser AJ; Hoogeveen AT; Westerveld A; Galjaard H
Hum Genet; 1977 Dec; 39(3):315-9. PubMed ID: 413781
[TBL] [Abstract][Full Text] [Related]
16. Apoptotic cell death in mouse models of GM2 gangliosidosis and observations on human Tay-Sachs and Sandhoff diseases.
Huang JQ; Trasler JM; Igdoura S; Michaud J; Hanal N; Gravel RA
Hum Mol Genet; 1997 Oct; 6(11):1879-85. PubMed ID: 9302266
[TBL] [Abstract][Full Text] [Related]
17. Characterization and tissue distribution of N-acetyl hexosaminidase C: suggestive evidence for a separate hexosaminidase locus.
Swallow DM; Evans L; Saha N; Harris H
Ann Hum Genet; 1976 Jul; 40(1):55-66. PubMed ID: 9025
[TBL] [Abstract][Full Text] [Related]
18. [Molecular pathogenesis and therapeutic approach of GM2 gangliosidosis].
Tsuji D
Yakugaku Zasshi; 2013; 133(2):269-74. PubMed ID: 23370522
[TBL] [Abstract][Full Text] [Related]
19. 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
Birth Defects Orig Artic Ser; 1975; 11(3):150-6. PubMed ID: 812565
[No Abstract] [Full Text] [Related]
20. The biochemical genetics of the hexosaminidase system in man.
Beutler E
Am J Hum Genet; 1979 Mar; 31(2):95-105. PubMed ID: 377957
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
