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A Grabowski

Showing results (131-140 of 259) with videos related to

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Arteriosclerosis, Thrombosis, and Vascular Biology|November 15, 2003
Reduction of atherosclerotic plaques by lysosomal acid lipase supplementationHong Du, Susan Schiavi, Nick Wan, et al.
Pharmacogenetics|April 1, 1997
Human Ah receptor (AHR) gene: localization to 7p15 and suggestive correlation of polymorphism with CYP1A1 inducibilityJ Micka, A Milatovich, A Menon, et al.
American Journal of Medical Genetics. Part A|December 12, 2002
Gaucher disease: in vivo evidence for allele dose leading to neuronopathic and nonneuronopathic phenotypesHuiquan Zhao, Laurie A Bailey, Louis J Elsas, et al.
American Journal of Human Genetics|December 1, 1986
Human acid beta-glucosidase: Northern blot and S1 nuclease analysis of mRNA from HeLa cells and normal and Gaucher disease fibroblastsP N Graves, G A Grabowski, M D Ludman, et al.
Metabolism: Clinical and Experimental|December 1, 1989
Resting energy expenditure in Gaucher's disease type 1: effect of Gaucher's cell burden on energy requirementsD J Barton, M D Ludman, K Benkov, et al.
American Journal of Human Genetics|May 1, 1985
Gaucher disease types 1, 2, and 3: differential mutations of the acid beta-glucosidase active site identified with conduritol B epoxide derivatives and sphingosineG A Grabowski, T Dinur, K M Osiecki, et al.
Molecular Genetics and Metabolism|July 20, 2002
Ex vivo localization of the mouse saposin C activation region for acid beta-glucosidaseXiaoyang Qi, Keiji Kondoh, Hulian Yin, et al.
Birth Defects Original Article Series|January 1, 1980
Enzyme therapy XVII: metabolic and immunologic evaluation of alpha- galactosidase A replacement in Fabry diseaseR J Desnick, K J Dean, G A Grabowski, et al.
Neurology|July 1, 1981
Chronic GM2 gangliosidosis masquerading as atypical Friedreich ataxia: clinical, morphologic, and biochemical studies of nine casesJ P Willner, G A Grabowski, R E Gordon, et al.
American Journal of Human Genetics|December 29, 2005
The role of mannosylated enzyme and the mannose receptor in enzyme replacement therapyHong Du, Mark Levine, Chandrashekar Ganesa, et al.
Pageof 26

Showing results (131-140 of 259) with videos related to

Sort By:
Pageof 26
Arteriosclerosis, Thrombosis, and Vascular Biology|November 15, 2003
Reduction of atherosclerotic plaques by lysosomal acid lipase supplementationHong Du, Susan Schiavi, Nick Wan, et al.
Pharmacogenetics|April 1, 1997
Human Ah receptor (AHR) gene: localization to 7p15 and suggestive correlation of polymorphism with CYP1A1 inducibilityJ Micka, A Milatovich, A Menon, et al.
American Journal of Medical Genetics. Part A|December 12, 2002
Gaucher disease: in vivo evidence for allele dose leading to neuronopathic and nonneuronopathic phenotypesHuiquan Zhao, Laurie A Bailey, Louis J Elsas, et al.
American Journal of Human Genetics|December 1, 1986
Human acid beta-glucosidase: Northern blot and S1 nuclease analysis of mRNA from HeLa cells and normal and Gaucher disease fibroblastsP N Graves, G A Grabowski, M D Ludman, et al.
Metabolism: Clinical and Experimental|December 1, 1989
Resting energy expenditure in Gaucher's disease type 1: effect of Gaucher's cell burden on energy requirementsD J Barton, M D Ludman, K Benkov, et al.
American Journal of Human Genetics|May 1, 1985
Gaucher disease types 1, 2, and 3: differential mutations of the acid beta-glucosidase active site identified with conduritol B epoxide derivatives and sphingosineG A Grabowski, T Dinur, K M Osiecki, et al.
Molecular Genetics and Metabolism|July 20, 2002
Ex vivo localization of the mouse saposin C activation region for acid beta-glucosidaseXiaoyang Qi, Keiji Kondoh, Hulian Yin, et al.
Birth Defects Original Article Series|January 1, 1980
Enzyme therapy XVII: metabolic and immunologic evaluation of alpha- galactosidase A replacement in Fabry diseaseR J Desnick, K J Dean, G A Grabowski, et al.
Neurology|July 1, 1981
Chronic GM2 gangliosidosis masquerading as atypical Friedreich ataxia: clinical, morphologic, and biochemical studies of nine casesJ P Willner, G A Grabowski, R E Gordon, et al.
American Journal of Human Genetics|December 29, 2005
The role of mannosylated enzyme and the mannose receptor in enzyme replacement therapyHong Du, Mark Levine, Chandrashekar Ganesa, et al.
Pageof 26