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Journal Abstract Search

408 related items for PubMed ID: 1594045

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  • 4. Generation of a conditional knockout of murine glucocerebrosidase: utility for the study of Gaucher disease.
    Sinclair GB, Jevon G, Colobong KE, Randall DR, Choy FY, Clarke LA.
    Mol Genet Metab; 2007 Feb; 90(2):148-56. PubMed ID: 17079175
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  • 5. Impaired trafficking of mutants of lysosomal glucocerebrosidase in Gaucher's disease.
    Schmitz M, Alfalah M, Aerts JM, Naim HY, Zimmer KP.
    Int J Biochem Cell Biol; 2005 Nov; 37(11):2310-20. PubMed ID: 15982918
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  • 8. Gaucher disease in the neonate: a distinct Gaucher phenotype is analogous to a mouse model created by targeted disruption of the glucocerebrosidase gene.
    Sidransky E, Sherer DM, Ginns EI.
    Pediatr Res; 1992 Oct; 32(4):494-8. PubMed ID: 1437405
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  • 13. Gaucher's disease: the best laid schemes of mice and men.
    Sidransky E, Ginns EI.
    Baillieres Clin Haematol; 1997 Dec; 10(4):725-37. PubMed ID: 9497860
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  • 16. [Molecular diagnosis and gene therapy for Gaucher disease].
    Ohashi T.
    Nihon Rinsho; 1993 Sep; 51(9):2300-7. PubMed ID: 8411706
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  • 18. Bone-marrow transplantation in severe Gaucher's disease.
    Rappeport JM, Ginns EI.
    N Engl J Med; 1984 Jul 12; 311(2):84-8. PubMed ID: 6377066
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  • 19. Gene transfer and bone marrow transplantation with special reference to Gaucher's disease.
    Karlsson S, Correll PH, Xu L.
    Bone Marrow Transplant; 1993 Jul 12; 11 Suppl 1():124-7. PubMed ID: 8448536
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  • 20. [Gaucher's disease].
    Livandovskiĭ IuA, Kapustina ND, Beĭer EM.
    Klin Med (Mosk); 1991 Apr 12; 69(4):87-9. PubMed ID: 1865664
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