287 related articles for article (PubMed ID: 6229294)
1. [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]
2. 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]
3. Late-onset hexosaminidase A and hexosaminidase A and B deficiency: family study and review.
Adams C; Green S
Dev Med Child Neurol; 1986 Apr; 28(2):236-43. PubMed ID: 2940136
[TBL] [Abstract][Full Text] [Related]
4. GM2 gangliosidoses in Spain: analysis of the HEXA and HEXB genes in 34 Tay-Sachs and 14 Sandhoff patients.
Gort L; de Olano N; Macías-Vidal J; Coll MA;
Gene; 2012 Sep; 506(1):25-30. PubMed ID: 22789865
[TBL] [Abstract][Full Text] [Related]
5. [Study of the genetic heterogeneity of gangliosidoses in humans].
Akhunov VS; Aronovich EL; Krasnopol'skaia KD; Mirenburg TV
Genetika; 1989 Oct; 25(10):1861-71. PubMed ID: 2533574
[TBL] [Abstract][Full Text] [Related]
6. A new form of residual hexosaminidase activity in infantile Tay Sachs disease fibroblasts.
Hechtman P; Khoo K; Isaacs C
Clin Genet; 1983 Sep; 24(3):206-15. PubMed ID: 6226462
[TBL] [Abstract][Full Text] [Related]
7. Mouse models of Tay-Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolism.
Sango K; Yamanaka S; Hoffmann A; Okuda Y; Grinberg A; Westphal H; McDonald MP; Crawley JN; Sandhoff K; Suzuki K; Proia RL
Nat Genet; 1995 Oct; 11(2):170-6. PubMed ID: 7550345
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. [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]
10. [Beta-N-acetyl-hexosaminidase--the enzyme of Tay-Sachs and Sandhoff diseases].
Zwierz K; Juszkiewicz J; Arciuch L; Gindzieński A
Postepy Biochem; 1992; 38(3):127-32. PubMed ID: 1461844
[No Abstract] [Full Text] [Related]
11. [Genetic deficiencies of beta-N-acetylhexosaminidase A and B: Tay-Sachs and Sandhoff diseases (GM2-gangliosidosis)].
Suzuki K
Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):721-7. PubMed ID: 2978703
[No Abstract] [Full Text] [Related]
12. 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]
13. 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]
14. Heterozygosity for Tay-Sachs and Sandhoff diseases among Massachusetts residents with French Canadian background.
Prence EM; Jerome CA; Triggs-Raine BL; Natowicz MR
J Med Screen; 1997; 4(3):133-6. PubMed ID: 9368869
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Isoenzymes of N-acetyl-beta-hexosaminidase.
Zwierz K; Zalewska A; Zoch-Zwierz A
Acta Biochim Pol; 1999; 46(3):739-51. PubMed ID: 10698282
[TBL] [Abstract][Full Text] [Related]
17. Chromatofocusing coupled with automated assay for beta-hexosaminidase isoenzymes in GM2 gangliosidosis.
Orlacchio A; Maffei C; Emiliani C; Coppa GV; Felici L
Experientia; 1985 Apr; 41(4):525-7. PubMed ID: 3157597
[TBL] [Abstract][Full Text] [Related]
18. Heterozygosity for Tay-Sachs and Sandhoff diseases in non-Jewish Americans with ancestry from Ireland, Great Britain, or Italy.
Branda KJ; Tomczak J; Natowicz MR
Genet Test; 2004; 8(2):174-80. PubMed ID: 15345116
[TBL] [Abstract][Full Text] [Related]
19. Hexosaminidase A deficiency in adults.
Navon R; Argov Z; Frisch A
Am J Med Genet; 1986 May; 24(1):179-96. PubMed ID: 2939718
[TBL] [Abstract][Full Text] [Related]
20. Adult-onset GM2 gangliosidosis diagnosed in a fetus.
Navon R; Sandbank U; Frisch A; Baram D; Adam A
Prenat Diagn; 1986; 6(3):169-76. PubMed ID: 2941730
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]