ExLibris header image
SFX Logo
Title: Efficient routing of glucocerebrosidase to lysosomes requires complex oligosaccharide chain formation
Source:

Biochemical and Biophysical Research Communications [0006-291X] Aerts, J.M.F.G. yr:1986


Collapse list of basic services Basic
Full text
Full text available via EZB-NALI5-00465 Elsevier Archive NL
GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. Weely, S. "Function of oligosaccharide modification in glucocerebrosidase, a membrane-associated lysosomal hydrolase." European journal of biochemistry 191.3 (1990): 669-677. Link to Full Text for this item Link to SFX for this item
2. GINNS, E. "MUTATIONS OF GLUCOCEREBROSIDASE - DISCRIMINATION OF NEUROLOGIC AND NON-NEUROLOGIC PHENOTYPES OF GAUCHER DISEASE." Proceedings of the National Academy of Sciences of the United States of America 79.18 (1982): 5607-5610. Link to Full Text for this item Link to SFX for this item
3. CHOUDARY, P. "GENE-MAPPING AND LEADER POLYPEPTIDE SEQUENCE OF HUMAN GLUCOCEREBROSIDASE - IMPLICATIONS FOR GAUCHER DISEASE." Proceedings of the National Academy of Sciences of the United States of America 82.20 (1985): 7101-7105. Link to Full Text for this item Link to SFX for this item
4. DONKERKOOPMAN, W. "A PROCEDURE FOR THE RAPID PURIFICATION IN HIGH-YIELD OF HUMAN GLUCOCEREBROSIDASE USING IMMUNOAFFINITY CHROMATOGRAPHY WITH MONOCLONAL-ANTIBODIES." Analytical biochemistry 154.2 (1986): 655-663. Link to Full Text for this item Link to SFX for this item
5. Hollak, C. "Glucocerebrosidase genotype of Gaucher patients in The Netherlands: Limitations in prognostic value." Human Mutation 10.5 (1997): 348-358. Link to Full Text for this item Link to SFX for this item
6. BEUTLER, E. "GAUCHER DISEASE - GENE-FREQUENCIES IN THE ASHKENAZI JEWISH POPULATION." American journal of human genetics 52.1 (1993): 85-88. Link to Full Text for this item Link to SFX for this item
7. Filocamo, M. "Analysis of the glucocerebrosidase gene and mutation profile in 144 Italian gaucher patients." Human mutation 20.3 (2002): 234-5. Link to Full Text for this item Link to SFX for this item
8. Erickson, A H. "Biosynthesis of the lysosomal enzyme glucocerebrosidase." Journal of biological chemistry (1985): 14319-14324. Link to SFX for this item
9. Tsuji, S. "Genetic heterogeneity in type 1 Gaucher disease: multiple genotypes in Ashkenazic and non-Ashkenazic individuals." Proceedings of the National Academy of Sciences of the United States of America 85.7 (1988): 2349-52. Link to Full Text for this item Link to SFX for this item
10. Abrahamov, A. "Gaucher's disease variant characterised by progressive calcification of heart valves and unique genotype." The lancet 346.8981 (1995): 1000-3. Link to SFX for this item
11. Weinreb, Neal J. "Life expectancy in Gaucher disease type 1." American journal of hematology 83.12 (2008): 896-900. Link to Full Text for this item Link to SFX for this item
12. BRADY, R. "GAUCHER DISEASE - ISOLATION AND COMPARISON OF NORMAL AND MUTANT GLUCOCEREBROSIDASE FROM HUMAN SPLEEN TISSUE." Proceedings of the National Academy of Sciences of the United States of America 75.8 (1978): 3970-3973. Link to Full Text for this item Link to SFX for this item
13. Boivin, J. "Part I. Reduction of S-alkyl-thionocarbonates and related compounds in the presence of trialkylboranes/air." Beilstein journal of organic chemistry 3 (2007): 45-. Link to Full Text for this item Link to SFX for this item
14. Fairley, C. "Phenotypic heterogeneity of N370S homozygotes with type I Gaucher disease: an analysis of 798 patients from the ICGG Gaucher Registry." Journal of inherited metabolic disease 31.6 (2009): 738-44. Link to Full Text for this item Link to SFX for this item
15. Puffenberger, E G G. "Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22." Human Molecular Genetics 3.8 (1994): 1217-25. Link to Full Text for this item Link to SFX for this item
16. le Coutre, P. "Molecular analysis of Gaucher disease: distribution of eight mutations and the complete gene deletion in 27 patients from Germany." Human genetics (1997): 816-21. Link to Full Text for this item Link to SFX for this item
17. Pietrangelo, A. "Hereditary hemochromatosis--a new look at an old disease." The New England journal of medicine 350.23 (2004): 2383-97. Link to SFX for this item
18. Aerts, J M M. "Pathogenesis of lysosomal storage disorders as illustrated by Gaucher disease." Journal of inherited metabolic disease 16.2 (1993): 288-91. Link to Full Text for this item Link to SFX for this item
19. Aerts, J M M. "Plasma and metabolic abnormalities in Gaucher's disease." Bailliè€re's clinical haematology 10.4 (1998): 691-709. Link to Full Text for this item Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced
A service provided by the Library of the Wissenschaftspark Albert Einstein, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.