114 related articles for article (PubMed ID: 1192834)
21. Immunochemical characterization of human beta-D-N-acetyl hexosaminidase from normal individuals and patients with Tay-Sachs disease. I. Antigenic differences between hexosaminidase A and hexosaminidase B.
Bartholomew WR; Rattazzi MC
Int Arch Allergy Appl Immunol; 1974; 46(4):512-24. PubMed ID: 4132060
[No Abstract] [Full Text] [Related]
22. The expression of hex A and hex B isozymes of hexosaminidase in parental and experimental human fibroblast cells and their components.
Bladon MT
Biochem Genet; 1981 Oct; 19(9-10):971-86. PubMed ID: 7332532
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Hydrolysis of Tay-Sachs ganglioside by beta-hexosaminidase A of human liver and urine.
Li YT; Mazzotta MY; Wan CC; Orth R; Li SC
J Biol Chem; 1973 Nov; 248(21):7512-5. PubMed ID: 4745777
[No Abstract] [Full Text] [Related]
25. Studies in Tay-Sachs and Sandhoff's diseases. Immunologic and structural properties of hexosaminidase A and hexosaminidase B.
Beutler E; Srivastava SK
Isr J Med Sci; 1973; 9(9):1335-7. PubMed ID: 4798071
[No Abstract] [Full Text] [Related]
26. [Biosynthesis and biodegradation of GM2 ganglioside].
Hirabayashi Y; Kasakura H; Matsumoto M
Tanpakushitsu Kakusan Koso; 1984 Sep; 29(9):708-22. PubMed ID: 6240072
[No Abstract] [Full Text] [Related]
27. Hexosaminidase A analysis of various biological fluids by pH inactivation for the identification of Tay-Sachs disease genotypes.
Saifer A; Perle G
Prog Clin Biol Res; 1977; 18():227-38. PubMed ID: 23555
[No Abstract] [Full Text] [Related]
28. Tay-Sachs disease in Quebec: evidence for a geographic aggregate in the French-Canadian population and identification of a new retardation syndrome with possible linkage to the Tay-Sachs gene.
Andermann E; Andermann F; Patry G; Lafontaine R; Geoffroy G; Scriver CR; Wolfe L
Trans Am Neurol Assoc; 1973; 98():20-4. PubMed ID: 4784938
[No Abstract] [Full Text] [Related]
29. Identification of Tay-Sachs by hexosaminidase analysis of urine and tear samples.
Saifer A; Amoroso J; Perle G
Adv Exp Med Biol; 1976; 68():339-66. PubMed ID: 7107
[TBL] [Abstract][Full Text] [Related]
30. Tay-Sachs carrier detection by mechanized serum hexosaminidase assay.
Rosenberg D; Cutler R
Clin Chim Acta; 1974 Jun; 53(2):247-53. PubMed ID: 4841990
[No Abstract] [Full Text] [Related]
31. N-acetyl-beta-hexosaminidase: role in the degradation of glycosaminoglycans.
Thompson JN; Stoolmiller AC; Matalon R; Dorfman A
Science; 1973 Aug; 181(4102):866-7. PubMed ID: 4269276
[TBL] [Abstract][Full Text] [Related]
32. Tay-Sachs disease: a pilot screening program for the detection of the heterozygote in the Charleston Jewish community.
Rogers JF; Hogan EL; Jorgenson RJ
South Med J; 1976 Nov; 69(11):1453-5. PubMed ID: 1019641
[TBL] [Abstract][Full Text] [Related]
33. Automated determination of serum hexosaminidase A by pH inactivation for detection of Tay-Sachs disease heterozygotes.
Saifer A; Perle G
Clin Chem; 1974 May; 20(5):538-43. PubMed ID: 4826945
[No Abstract] [Full Text] [Related]
34. Tay-Sachs disease: interrelation of hexosaminidases A and B.
Robinson D; Carroll M
Lancet; 1972 Feb; 1(7745):322-3. PubMed ID: 4109961
[No Abstract] [Full Text] [Related]
35. Gangliosidosis with total hexosaminidase deficiency: clinical, biochemical and ultrastructural studies and comparison with conventional cases of Tay-Sachs disease.
Fontaine G; Résibois A; Tondeur M; Jonniaux G; Farriaux JP; Voet W; Maillard E; Loeb H
Acta Neuropathol; 1973 Jan; 23(2):118-32. PubMed ID: 4349527
[No Abstract] [Full Text] [Related]
36. 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]
37. Hexosaminidase-A and hexosaminidase-B: studies in Tay-Sachs' and Sandhoff's disease.
Srivastava SK; Beutler E
Nature; 1973 Feb; 241(5390):463. PubMed ID: 4122341
[No Abstract] [Full Text] [Related]
38. NN'-diacetylchitobiase activity in Tay-Sachs disease and Sandhoff's disease.
Stirling JL
Biochem J; 1974 Aug; 141(2):597-9. PubMed ID: 4455225
[TBL] [Abstract][Full Text] [Related]
39. Subcellular fractions from Tay-Sachs brains: ganglioside, lipid, and protein composition and hexosaminidase activities.
Kornguth S; Wannamaker B; Kolodny E; Geison R; Scott G; O'Brien JF
J Neurol Sci; 1974 Jul; 22(3):383-406. PubMed ID: 4857837
[No Abstract] [Full Text] [Related]
40. Newer aspects of some interesting lipid storage diseases: Tay-Sachs and Gaucher's diseases.
Beutler E
West J Med; 1977 Jan; 126(1):46-54. PubMed ID: 831367
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
