These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
94 related articles for article (PubMed ID: 6274059)
21. Carrier detection of sialidosis with partial beta-galactosidase deficiency by the assay of lysosomal sialidase in lymphocytes. Tsuji S; Yamada T; Ariga T; Toyoshima I; Yamaguchi H; Kitahara Y; Miyatake T; Yamakawa T Ann Neurol; 1984 Feb; 15(2):181-3. PubMed ID: 6703657 [TBL] [Abstract][Full Text] [Related]
22. A lymphoblastoid cell line from an adenosine deaminase deficient patient established by Epstein-Barr virus. Tsuchiya S; Narisawa K; Konno T; Tada K Tohoku J Exp Med; 1979 Oct; 129(2):105-10. PubMed ID: 227140 [TBL] [Abstract][Full Text] [Related]
23. Biochemical diagnosis of Hunter syndrome on Epstein-Barr virus-transformed lymphoblastoid cell lines. Morabito E; Giambarrasi I; Rocchi M; Di Natale P Clin Chim Acta; 1989 May; 181(2):125-33. PubMed ID: 2567642 [TBL] [Abstract][Full Text] [Related]
24. Marked variation in blood beta-hexosaminidase in Gaucher disease. Natowicz MR; Prence EM; Cajolet A Clin Chim Acta; 1991 Nov; 203(1):17-22. PubMed ID: 1837502 [TBL] [Abstract][Full Text] [Related]
25. Significance of glycosidase patterns in lymphoid cells. Bjare U; Lundblad G; Räbb I Int J Biochem; 1985; 17(1):67-72. PubMed ID: 2987056 [TBL] [Abstract][Full Text] [Related]
27. Carrier screening techniques for Tay-Sachs and other lysosomal storage diseases. Kolodny EH Prog Clin Biol Res; 1977; 18():213-9. PubMed ID: 601077 [No Abstract] [Full Text] [Related]
28. Isoenzymes of serum N-acetyl-beta-D-glucosaminidase in the I cell disease heterozygote. Van Elsen AF; Leroy JG; VanneuvilleFJ ; Vercruyssen AL Hum Genet; 1976 Jan; 31(1):75-81. PubMed ID: 174996 [TBL] [Abstract][Full Text] [Related]
29. Inborn errors of lysosomal catabolism--principles of heterozygote detection. Jolly RD; Desnick RJ Am J Med Genet; 1979; 4(3):293-307. PubMed ID: 117711 [TBL] [Abstract][Full Text] [Related]
30. A case of GM1-gangliosidosis type I: glycosphingolipid profiles of urine and transformed lymphocytes and beta-D-galactosidase activities in peripheral lymphocytes, cultured skin fibroblasts and transformed lymphocytes. Asano K; Shindo N; Nakasuji M; Inamori K; Ohta M; Matsushita T; Yamaguchi M; Oshima M Jpn J Exp Med; 1990 Apr; 60(2):73-9. PubMed ID: 2117086 [TBL] [Abstract][Full Text] [Related]
31. High sensitivity but normal DNA-repair activity after UV irradiation in Epstein--Barr virus-transformed lymphoblastoid cell lines from Chediak--Higashi syndrome. Tanaka H; Orii T Mutat Res; 1980 Aug; 72(1):143-50. PubMed ID: 6255323 [TBL] [Abstract][Full Text] [Related]
32. [Total activity and distribution of multiple forms of lysosomal glycosidases in subfractions of human leukocytes]. Kuz'micheva NA; Vidershaĭn GIa Vopr Med Khim; 1984; 30(5):76-81. PubMed ID: 6241372 [TBL] [Abstract][Full Text] [Related]
33. The separation and characterization of marmoset kidney beta-D-galactosidase and beta-D-glucosidase. Pierce RJ; Price RG Biochem J; 1977 Dec; 167(3):765-73. PubMed ID: 23762 [TBL] [Abstract][Full Text] [Related]
35. 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]
36. Enzyme replacement for GM1-gangliosidosis: Uptake, lysosomal activation, and cellular disease correction using a novel β-galactosidase:RTB lectin fusion. Condori J; Acosta W; Ayala J; Katta V; Flory A; Martin R; Radin J; Cramer CL; Radin DN Mol Genet Metab; 2016 Feb; 117(2):199-209. PubMed ID: 26766614 [TBL] [Abstract][Full Text] [Related]
37. Thermodynamic determination of plasma and leukocyte beta-hexosaminidase isoenzymes in homozygote and heterozygote carriers for the GM2 gangliosidosis B1 variant. Casal JA; Pérez LF; Tutor JC Am J Clin Pathol; 2003 May; 119(5):684-8. PubMed ID: 12760286 [TBL] [Abstract][Full Text] [Related]
38. Tay-Sachs disease with altered beta-hexosaminidase B: a new variant? Momoi T; Sudo M; Tanioka K; Nakao Y Pediatr Res; 1978 Feb; 12(2):77-81. PubMed ID: 25409 [No Abstract] [Full Text] [Related]
39. Acid hydrolases in leukocytes and platelets of normal subjects and in patients with Gaucher's and Fabry's disease. Beutler E; Kuhl W; Matsumoto F; Pangalis G J Exp Med; 1976 Apr; 143(4):975-80. PubMed ID: 3620 [TBL] [Abstract][Full Text] [Related]
40. Hexosaminidase C in brain affected by Tay-Sachs Disease. Minami R; Nakamura F; Oyanagi K; Nakao T Tohoku J Exp Med; 1981 Feb; 133(2):175-85. PubMed ID: 7268761 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]