145 related articles for article (PubMed ID: 7268761)
21. 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]
22. 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]
23. Characterization of unusual hexosaminidase A (HEX A) deficient human mutants.
O'Brien JS; Tennant L; Veath ML; Scott CR; Bucknall WE
Am J Hum Genet; 1978 Nov; 30(6):602-8. PubMed ID: 747188
[TBL] [Abstract][Full Text] [Related]
24. Prenatal Diagnosis of Tay-Sachs Disease.
Zhang J; Chen H; Kornreich R; Yu C
Methods Mol Biol; 2019; 1885():233-250. PubMed ID: 30506202
[TBL] [Abstract][Full Text] [Related]
25. Human hexosaminidase isozymes. IV. Effects of oral contraceptive steroids on serum hexosaminidase activity.
Nitowsky HM; Davis J; Nakagawa S; Fox D
Am J Obstet Gynecol; 1979 Jul; 134(6):642-7. PubMed ID: 463955
[TBL] [Abstract][Full Text] [Related]
26. Prenatal diagnosis of Tay-Sachs disease with heat-labile beta-hexosaminidase B.
Momoi T; Kikuchi K; Shigematsu Y; Sudo M; Tanioka K
Clin Chim Acta; 1983 Oct; 133(3):331-4. PubMed ID: 6226459
[TBL] [Abstract][Full Text] [Related]
27. Juvenile GM2 gangliosidosis (AMB variant): inability to activate hexosaminidase A by activator protein.
Inui K; Grebner EE; Jackson LG; Wenger DA
Am J Hum Genet; 1983 Jul; 35(4):551-64. PubMed ID: 6224417
[TBL] [Abstract][Full Text] [Related]
28. Two abnormalities of hexosaminidase A in clinically normal individuals.
Grebner EE; Mansfield DA; Raghavan SS; Kolodny EH; d'Azzo A; Neufeld EF; Jackson LG
Am J Hum Genet; 1986 Apr; 38(4):505-14. PubMed ID: 2939713
[TBL] [Abstract][Full Text] [Related]
29. Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs disease.
Korneluk RG; Mahuran DJ; Neote K; Klavins MH; O'Dowd BF; Tropak M; Willard HF; Anderson MJ; Lowden JA; Gravel RA
J Biol Chem; 1986 Jun; 261(18):8407-13. PubMed ID: 3013851
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Rapid detection of fetal Mendelian disorders: Tay-Sachs disease.
Guetta E; Peleg L
Methods Mol Biol; 2008; 444():147-59. PubMed ID: 18425478
[TBL] [Abstract][Full Text] [Related]
32. Tay-Sachs disease in Jacob sheep.
Torres PA; Zeng BJ; Porter BF; Alroy J; Horak F; Horak J; Kolodny EH
Mol Genet Metab; 2010 Dec; 101(4):357-63. PubMed ID: 20817517
[TBL] [Abstract][Full Text] [Related]
33. First-trimester prenatal diagnosis of Tay-Sachs disease.
Grabowski GA; Kruse JR; Goldberg JD; Chockkalingam K; Gordon RE; Blakemore KJ; Mahoney MJ; Desnick RJ
Am J Hum Genet; 1984 Nov; 36(6):1369-78. PubMed ID: 6240199
[TBL] [Abstract][Full Text] [Related]
34. Radioimmunoassay and heat denaturation enzyme assay for the detection of Tay-sachs heterozygotes during pregnancy.
Nguyen C; Gold RJ; Mahuran D; Lowden JA
Clin Chim Acta; 1981 Jun; 113(1):13-25. PubMed ID: 6453673
[TBL] [Abstract][Full Text] [Related]
35. The metabolism of Tay-Sachs ganglioside: catabolic studies with lysosomal enzymes from normal and Tay-Sachs brain tissue.
Tallman JF; Johnson WG; Brady RO
J Clin Invest; 1972 Sep; 51(9):2339-45. PubMed ID: 4639018
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. Characterization of polypeptides serologically and structurally related to hexosaminidase in cultured fibroblasts.
Tsui F; Mahuran DJ; Lowden JA; Mosmann T; Gravel RA
J Clin Invest; 1983 Apr; 71(4):965-73. PubMed ID: 6833496
[TBL] [Abstract][Full Text] [Related]
39. [Detection of homozygotes and heterozygote carriers of GM2-gangliosidosis].
Aronovich EL; Krasnopol'skaia KD; Kukharenko VI; Pichugina EM
Genetika; 1986 Aug; 22(8):2179-85. PubMed ID: 3770476
[TBL] [Abstract][Full Text] [Related]
40. Ganglioside GM2 N-acetyl-beta-D-galactosaminidase activity in cultured fibroblasts of late-infantile and adult GM2 gangliosidosis patients and of healthy probands with low hexosaminidase level.
Conzelmann E; Kytzia HJ; Navon R; Sandhoff K
Am J Hum Genet; 1983 Sep; 35(5):900-13. PubMed ID: 6614006
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]