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A Grabowski

Showing results (171-180 of 259) with videos related to

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Molecular Genetics and Metabolism|October 2, 2013
Gaucher disease: chemotactic factors and immunological cell invasion in a mouse modelManoj Kumar Pandey, Nicholas A Jabre, You-Hai Xu, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 17, 2003
Lysosomal enzymes are released from cultured human macrophages, hydrolyze LDL in vitro, and are present extracellularly in human atherosclerotic lesionsJukka K Hakala, Riina Oksjoki, Petri Laine, et al.
Pediatric Research|May 1, 1992
Enzyme augmentation in moderate to life-threatening Gaucher diseaseS Fallet, M E Grace, A Sibille, et al.
Clinical Genetics|August 1, 1984
Reduced plasma concentrations of total, low density lipoprotein and high density lipoprotein cholesterol in patients with Gaucher type I diseaseH Ginsberg, G A Grabowski, J C Gibson, et al.
Journal of Pediatric Surgery|June 1, 1989
Gaucher disease: fate of the splenic remnant after partial splenectomy--a case of rapid enlargementP R Fleshner, D J Astion, M D Ludman, et al.
ACS Macro Letters|June 2, 2022
Stability of Polymer Grafted Nanoparticle Monolayers: Impact of Architecture and Polymer-Substrate Interactions on DewettingJustin Che, Ali Jawaid, Christopher A Grabowski, et al.
Plos One|September 7, 2016
Progression of Behavioral and CNS Deficits in a Viable Murine Model of Chronic Neuronopathic Gaucher DiseaseMei Dai, Benjamin Liou, Brittany Swope, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 31, 2018
LAL (Lysosomal Acid Lipase) Promotes Reverse Cholesterol Transport In Vitro and In VivoKristin L Bowden, Joshua A Dubland, Teddy Chan, et al.
Muscle & Nerve|March 1, 1988
Hexosaminidase A activity and amyotrophic lateral sclerosisM Gudesblatt, M D Ludman, J A Cohen, et al.
Clinical Chemistry|February 5, 2000
Saposins A, B, C, and D in plasma of patients with lysosomal storage disordersM H Chang, C A Bindloss, G A Grabowski, et al.
Pageof 26

Showing results (171-180 of 259) with videos related to

Sort By:
Pageof 26
Molecular Genetics and Metabolism|October 2, 2013
Gaucher disease: chemotactic factors and immunological cell invasion in a mouse modelManoj Kumar Pandey, Nicholas A Jabre, You-Hai Xu, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 17, 2003
Lysosomal enzymes are released from cultured human macrophages, hydrolyze LDL in vitro, and are present extracellularly in human atherosclerotic lesionsJukka K Hakala, Riina Oksjoki, Petri Laine, et al.
Pediatric Research|May 1, 1992
Enzyme augmentation in moderate to life-threatening Gaucher diseaseS Fallet, M E Grace, A Sibille, et al.
Clinical Genetics|August 1, 1984
Reduced plasma concentrations of total, low density lipoprotein and high density lipoprotein cholesterol in patients with Gaucher type I diseaseH Ginsberg, G A Grabowski, J C Gibson, et al.
Journal of Pediatric Surgery|June 1, 1989
Gaucher disease: fate of the splenic remnant after partial splenectomy--a case of rapid enlargementP R Fleshner, D J Astion, M D Ludman, et al.
ACS Macro Letters|June 2, 2022
Stability of Polymer Grafted Nanoparticle Monolayers: Impact of Architecture and Polymer-Substrate Interactions on DewettingJustin Che, Ali Jawaid, Christopher A Grabowski, et al.
Plos One|September 7, 2016
Progression of Behavioral and CNS Deficits in a Viable Murine Model of Chronic Neuronopathic Gaucher DiseaseMei Dai, Benjamin Liou, Brittany Swope, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 31, 2018
LAL (Lysosomal Acid Lipase) Promotes Reverse Cholesterol Transport In Vitro and In VivoKristin L Bowden, Joshua A Dubland, Teddy Chan, et al.
Muscle & Nerve|March 1, 1988
Hexosaminidase A activity and amyotrophic lateral sclerosisM Gudesblatt, M D Ludman, J A Cohen, et al.
Clinical Chemistry|February 5, 2000
Saposins A, B, C, and D in plasma of patients with lysosomal storage disordersM H Chang, C A Bindloss, G A Grabowski, et al.
Pageof 26