299 related articles for article (PubMed ID: 6816949)
1. Tay-Sachs disease and normal cerebellar cells in culture: elevated levels of lysosomal enzymes in Tay-Sachs disease cells.
Hoffman LM; Brooks SE; Schneck L
J Neurosci Res; 1982; 8(1):49-55. PubMed ID: 6816949
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. [Activity and appearance of isoenzyme spectrums of some lysosomal hydrolases in biopsy material of human chorion].
Beĭer EM; Vidershaĭn GIa; Bakharev VA; Rozovskiĭ IS
Vopr Med Khim; 1983; 29(2):130-3. PubMed ID: 6222539
[TBL] [Abstract][Full Text] [Related]
5. Changes of serum hexosaminidase for the presumptive diagnosis of type I Gaucher disease in Tay-Sachs carrier screening.
Nakagawa S; Kumin S; Sachs G; Nitowsky HM
Am J Med Genet; 1983 Mar; 14(3):525-32. PubMed ID: 6859103
[TBL] [Abstract][Full Text] [Related]
6. Use of microtechniques for the detection of lysosomal enzyme disorders: Tay-Sachs disease, Gm1-gangliosidosis and Fabry disease.
Bladon MT; Milunsky A
Clin Genet; 1978 Dec; 14(6):359-66. PubMed ID: 215359
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Beta-hexosaminidase isozymes and replacement therapy in Gm2 gangliosidosis.
Rattazzi MC
Isozymes Curr Top Biol Med Res; 1983; 11():65-81. PubMed ID: 6227586
[TBL] [Abstract][Full Text] [Related]
9. Cultured skin fibroblasts in lipidoses. Enzymatic, histochemical, and ultrastructural relationship in Fabry's Tay-Sachs, and Sandhoff's diseases.
Yuasa T; Fukuma M; Takashima S; Takaki R
Arch Pathol Lab Med; 1980 Jun; 104(6):321-7. PubMed ID: 6246846
[TBL] [Abstract][Full Text] [Related]
10. The lysosomal hexosaminidase isozymes.
Mahuran D; Novak A; Lowden JA
Isozymes Curr Top Biol Med Res; 1985; 12():229-88. PubMed ID: 3886595
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [Tay-Sachs disease: a case report. Interest of ultrastructural studies of cultured skin fibroblasts (author's transl)].
Charbonne F; Rousseau P; Malpuech G; Geneix A
Arch Fr Pediatr; 1980 Jan; 37(1):51-3. PubMed ID: 7469686
[TBL] [Abstract][Full Text] [Related]
13. [Prenatal diagnosis of hereditary lysosomal diseases].
Mirenburg TV; Aronovich EL; Lebedeva TV; Akhunov VS; Krasnopol'skaia KD
Vopr Med Khim; 1988; 34(4):41-6. PubMed ID: 3143186
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene.
Myerowitz R
Hum Mutat; 1997; 9(3):195-208. PubMed ID: 9090523
[TBL] [Abstract][Full Text] [Related]
16. Comparison of the measurement of lysosomal hydrolase activity in mycoplasma-contaminated and non-contaminated human fibroblast cultures treated with mycoplasma removal agent.
Souza FT; Souza Sostruznik L; Casagrande Scolari R; Maciel de Castro KJ; Giugliani R; Coelho JC
Clin Biochem; 2007 May; 40(8):521-5. PubMed ID: 17367773
[TBL] [Abstract][Full Text] [Related]
17. Isoenzyme pattern and partial characterization of hexosaminidases in the membrane and cytosol of human erythrocytes.
Massaccesi L; Lombardo A; Venerando B; Tettamanti G; Goi G
Clin Biochem; 2007 Apr; 40(7):467-77. PubMed ID: 17321512
[TBL] [Abstract][Full Text] [Related]
18. Lysosomal acid hydrolases in established lymphoblastoid cell lines, transformed by Epstein-Barr virus, from patients with genetic lysosomal storage diseases.
Minami R; Watanabe Y; Kudoh T; Suzuki M; Oyanagi K; Orii T; Nakao T
Hum Genet; 1978 Oct; 44(1):79-87. PubMed ID: 213379
[TBL] [Abstract][Full Text] [Related]
19. [Activity of glycosidases in amniotic fluid cell cultures].
Tsvetkova IV; Zolotukhina TV; Rozenfel'd EL; Rozovskiĭ IS
Vopr Med Khim; 1979; 25(2):214-8. PubMed ID: 442593
[TBL] [Abstract][Full Text] [Related]
20. Tay-Sachs and Sandhoff diseases: enzymatic diagnosis in dried blood spots on filter paper: retrospective diagnoses in newborn-screening cards.
Chamoles NA; Blanco M; Gaggioli D; Casentini C
Clin Chim Acta; 2002 Apr; 318(1-2):133-7. PubMed ID: 11880123
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
