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A Grabowski

Showing results (51-60 of 295) with videos related to

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Developmental Disabilities Research Reviews|June 26, 2013
Neuronopathic lysosomal storage diseases: clinical and pathologic findingsCarlos E Prada, Gregory A Grabowski
Journal of Clinical Lipidology|September 29, 2016
Response to "Letter to the Editor by Drs Block and Razani"Gregory A Grabowski, Robert J Desnick
Molecular Genetics and Metabolism|August 15, 1998
Translational inefficiency of acid beta-glucosidase mRNA in transgenic mammalian cellsY H Xu, G A Grabowski
Plant Disease|January 4, 2019
Characterization of the Response of Ornamental Graminoids to Attempted Infection by Sclerotinia sclerotiorumMichelle A Grabowski, Dean K Malvick
Methods in Cell Biology|January 1, 1982
Prenatal diagnosis of inherited metabolic diseases; principles, pitfalls, and prospectsG A Grabowski, R J Desnick
Clinical Investigation|September 20, 2011
Velaglucerase alfa in the treatment of Gaucher disease type 1Thomas A Burrow, Gregory A Grabowski
Molecular Genetics and Metabolism|February 8, 2005
Translation modulation of acid beta-glucosidase in HepG2 cells: participation of the PKC pathwayYou-Hai Xu, Gregory A Grabowski
Critical Reviews in Oncogenesis|March 21, 2013
Immunological cells and functions in Gaucher diseaseManoj Kumar Pandey, Gregory A Grabowski
American Journal of Human Genetics|May 1, 1989
Posttranslational processing of human lysosomal acid beta-glucosidase: a continuum of defects in Gaucher disease type 1 and type 2 fibroblastsJ E Bergmann, G A Grabowski
American Journal of Hematology|June 23, 2015
Gaucher disease types 1 and 3: Phenotypic characterization of large populations from the ICGG Gaucher RegistryGregory A Grabowski, Ari Zimran, Hiroyuki Ida
Pageof 30

Showing results (51-60 of 295) with videos related to

Sort By:
Pageof 30
Developmental Disabilities Research Reviews|June 26, 2013
Neuronopathic lysosomal storage diseases: clinical and pathologic findingsCarlos E Prada, Gregory A Grabowski
Journal of Clinical Lipidology|September 29, 2016
Response to "Letter to the Editor by Drs Block and Razani"Gregory A Grabowski, Robert J Desnick
Molecular Genetics and Metabolism|August 15, 1998
Translational inefficiency of acid beta-glucosidase mRNA in transgenic mammalian cellsY H Xu, G A Grabowski
Plant Disease|January 4, 2019
Characterization of the Response of Ornamental Graminoids to Attempted Infection by Sclerotinia sclerotiorumMichelle A Grabowski, Dean K Malvick
Methods in Cell Biology|January 1, 1982
Prenatal diagnosis of inherited metabolic diseases; principles, pitfalls, and prospectsG A Grabowski, R J Desnick
Clinical Investigation|September 20, 2011
Velaglucerase alfa in the treatment of Gaucher disease type 1Thomas A Burrow, Gregory A Grabowski
Molecular Genetics and Metabolism|February 8, 2005
Translation modulation of acid beta-glucosidase in HepG2 cells: participation of the PKC pathwayYou-Hai Xu, Gregory A Grabowski
Critical Reviews in Oncogenesis|March 21, 2013
Immunological cells and functions in Gaucher diseaseManoj Kumar Pandey, Gregory A Grabowski
American Journal of Human Genetics|May 1, 1989
Posttranslational processing of human lysosomal acid beta-glucosidase: a continuum of defects in Gaucher disease type 1 and type 2 fibroblastsJ E Bergmann, G A Grabowski
American Journal of Hematology|June 23, 2015
Gaucher disease types 1 and 3: Phenotypic characterization of large populations from the ICGG Gaucher RegistryGregory A Grabowski, Ari Zimran, Hiroyuki Ida
Pageof 30