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.
2. Gaucher disease. III. Substrate specificity of glucocerebrosidase and the use of nonlabeled natural substrates for the investigation of patients. Choy FY; Davidson RG Am J Hum Genet; 1980 Sep; 32(5):670-80. PubMed ID: 6775530 [TBL] [Abstract][Full Text] [Related]
3. Electrophoresis of glucocerebrosidase from normal and Gaucher disease fibroblasts. Dale GL; Gudas J; Woloszyn W; Beutler E Am J Hum Genet; 1979 Jul; 31(4):518-21. PubMed ID: 484554 [TBL] [Abstract][Full Text] [Related]
4. The assay of glucocerebrosidase activity using the natural substrata. Strasberg PM; Lowden JA Clin Chim Acta; 1982 Jan; 118(1):9-20. PubMed ID: 7053909 [TBL] [Abstract][Full Text] [Related]
5. An immunoelectron microscopic study of glucocerebrosidase in type 1 Gaucher's disease spleen. Willemsen R; van Dongen JM; Aerts JM; Schram AW; Tager JM; Goudsmit R; Reuser AJ Ultrastruct Pathol; 1988; 12(5):471-8. PubMed ID: 3194992 [TBL] [Abstract][Full Text] [Related]
6. Diagnosis of adult Gaucher disease: use of a new chromogenic substrate, 2-hexadecanoylamino-4-nitrophenyl-beta-D-glucopyranoside, in cultured skin fibroblasts. Johnson WG; Gal AE; Miranda AF; Pentchev PG Clin Chim Acta; 1980 Mar; 102(1):91-7. PubMed ID: 7389109 [TBL] [Abstract][Full Text] [Related]
7. Differentiation of beta-glucocerebrosidase from beta-glucosidase in human tissues using sodium taurocholate. Peters SP; Coyle P; Glew RH Arch Biochem Biophys; 1976 Aug; 175(2):569-82. PubMed ID: 958319 [No Abstract] [Full Text] [Related]
8. An improved procedure for diagnosis of Gaucher disease using cultured skin fibroblasts and the chromogenic substrate, 2-hexadecanoylamino-4-nitrophenyl-beta-D-glucopyranoside. Barns RJ; Clague AE Clin Chim Acta; 1982 Mar; 120(1):57-63. PubMed ID: 7067140 [TBL] [Abstract][Full Text] [Related]
9. Heterogeneity in human acid beta-glucosidase revealed by cellulose-acetate electrophoresis. Sa Miranda MC; Aerts JM; Pinto RA; Magalhaes JA; Barranger JA; Tager JM; Schram AW Biochim Biophys Acta; 1988 May; 965(2-3):163-8. PubMed ID: 3130106 [TBL] [Abstract][Full Text] [Related]
11. Immunological and isoelectric focusing study of beta-glucocerebrosidase from normal and Gaucher disease. Hardy B; Hoffman J; Ossimi Z Biochem Biophys Res Commun; 1984 Apr; 120(2):325-32. PubMed ID: 6375656 [TBL] [Abstract][Full Text] [Related]
12. Inhibitors of beta-glucosidases of animal tissues. Radin NS Adv Exp Med Biol; 1978; 101():589-600. PubMed ID: 96666 [No Abstract] [Full Text] [Related]
14. Biochemical studies in a patient with subacute neuropathic Gaucher disease without visceral glucosylceramide storage. Wenger DA; Roth S; Kudoh T; Grover WD; Tucker SH; Kaye EM; Ullman MD Pediatr Res; 1983 May; 17(5):344-8. PubMed ID: 6856396 [TBL] [Abstract][Full Text] [Related]
15. Gaucher disease: isolation and comparison of normal and mutant glucocerebrosidase from human spleen tissue. Pentchev PG; Brady RO; Blair HE; Britton DE; Sorrell SH Proc Natl Acad Sci U S A; 1978 Aug; 75(8):3970-3. PubMed ID: 29293 [TBL] [Abstract][Full Text] [Related]
16. [Properties of the molecular forms of beta-glucosidase and beta-glucocerebrosidase from normal human and Gaucher disease spleen (author's transl)]. Maret A; Salvayre R; Negre A; Douste-Blazy L Eur J Biochem; 1981 Apr; 115(3):455-61. PubMed ID: 6786882 [No Abstract] [Full Text] [Related]
17. Assay of enzymes of lipid metabolism with colored and fluorescent derivatives of natural lipids. Gatt S; Barenholz Y; Goldberg R; Dinur T; Besley G; Leibovitz-Ben Gershon Z; Rosenthal J; Desnick RJ; Devine EA; Shafit-Zagardo B; Tsuruki F Methods Enzymol; 1981; 72():351-75. PubMed ID: 6273689 [No Abstract] [Full Text] [Related]
18. Comparison of synthetic and natural glucosylceramides as substrate for glucosylceramidase assay. Vaccaro AM; Kobayashi T; Suzuki K Clin Chim Acta; 1982 Jan; 118(1):1-7. PubMed ID: 7053901 [TBL] [Abstract][Full Text] [Related]
19. Gaucher type I (Ashkenazi) disease: a new method for heterozygote detection using a novel fluorescent natural substrate. Grabowski GA; Dinur T; Gatt S; Desnick RJ Clin Chim Acta; 1982 Sep; 124(1):123-35. PubMed ID: 6889929 [TBL] [Abstract][Full Text] [Related]
20. A kinetic study of the effects of galactocerebroside 3-sulphate on human spleen glucocerebrosidase. Evidence for two activator-binding sites. Prence EM; Garrett KO; Glew RH Biochem J; 1986 Aug; 237(3):655-62. PubMed ID: 3800908 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]