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Journal of Protein Chemistry|April 1, 1995
Position of the sulfhydryl group and the disulfide bonds of human glucocerebrosidaseY Lee, H Kinoshita, G Radke, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 24, 1998
Long-term expression and secretion of human glucocerebrosidase by primary murine and human myoblasts and differentiated myotubesC Liu, A B Bahnson, J T Dunigan, et al.
Biochemical Medicine|February 1, 1984
Molecular weight characterization of beta-D-glucocerebrosidase in mononuclear white blood cells in Gaucher's diseaseS Pirruccello, J A Barranger, N W Barton, et al.
Radiology|September 1, 1986
Gaucher disease: sonographic appearance of the spleenS C Hill, J W Reinig, J A Barranger, et al.
Birth Defects Original Article Series|January 1, 1980
Status of enzyme replacement therapy for Gaucher diseaseR O Brady, J A Barranger, A E Gal, et al.
Annals of Neurology|October 1, 1980
Lafora disease: diagnosis by liver biopsyR N Nishimura, K G Ishak, R Reddick, et al.
Biochemical Medicine|February 1, 1985
Lectin-specific targeting of beta-glucocerebrosidase to different liver cells via glycosylated liposomesP K Das, G J Murray, G C Zirzow, et al.
Acta Paediatrica Japonica : Overseas Edition|April 1, 1996
Gene therapy for metachromatic leukodystrophyT Ohashi, K Watabe, Y Sato, et al.
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