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The Journal of Biological Chemistry
|
September 10, 2014
The LIMP-2/SCARB2 binding motif on acid β-glucosidase: basic and applied implications for Gaucher disease and associated neurodegenerative diseases
Benjamin Liou, Wendy D Haffey, Kenneth D Greis, et al.
American Journal of Hematology
|
March 20, 2009
Gaucher disease: resetting the clinical and scientific agenda
Pramod K Mistry, Neal J Weinreb, Roscoe O Brady, et al.
Annals of the New York Academy of Sciences
|
September 24, 2005
Saposin C: neuronal effect and CNS delivery by liposomes
Zhengtao Chu, Ying Sun, Chia Yi Kuan, et al.
Molecular Genetics and Metabolism
|
May 19, 2012
Immunological cell type characterization and Th1-Th17 cytokine production in a mouse model of Gaucher disease
Manoj Kumar Pandey, Reena Rani, Wujuan Zhang, et al.
Human Gene Therapy
|
August 7, 2002
Lysosomal acid lipase deficiency: correction of lipid storage by adenovirus-mediated gene transfer in mice
Hong Du, Martin Heur, David P Witte, et al.
Molecular Genetics and Metabolism
|
January 9, 2021
Gaucher disease: Basic and translational science needs for more complete therapy and management
Gregory A Grabowski, Armand H M Antommaria, Edwin H Kolodny, et al.
Molecular Genetics and Metabolism
|
March 19, 2008
Dependence of reversibility and progression of mouse neuronopathic Gaucher disease on acid beta-glucosidase residual activity levels
You-Hai Xu, Rachel Reboulet, Brian Quinn, et al.
Plos One
|
October 8, 2009
In vivo and ex vivo evaluation of L-type calcium channel blockers on acid beta-glucosidase in Gaucher disease mouse models
Ying Sun, Benjamin Liou, Brian Quinn, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
November 15, 2003
Reduction of atherosclerotic plaques by lysosomal acid lipase supplementation
Hong Du, Susan Schiavi, Nick Wan, 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 phenotypes
Huiquan Zhao, Laurie A Bailey, Louis J Elsas, et al.
Page
of 13
Search research articles
Search
Showing results (41-50 of 128) with videos related to
Sort By:
Page
of 13
The Journal of Biological Chemistry
|
September 10, 2014
The LIMP-2/SCARB2 binding motif on acid β-glucosidase: basic and applied implications for Gaucher disease and associated neurodegenerative diseases
Benjamin Liou, Wendy D Haffey, Kenneth D Greis, et al.
American Journal of Hematology
|
March 20, 2009
Gaucher disease: resetting the clinical and scientific agenda
Pramod K Mistry, Neal J Weinreb, Roscoe O Brady, et al.
Annals of the New York Academy of Sciences
|
September 24, 2005
Saposin C: neuronal effect and CNS delivery by liposomes
Zhengtao Chu, Ying Sun, Chia Yi Kuan, et al.
Molecular Genetics and Metabolism
|
May 19, 2012
Immunological cell type characterization and Th1-Th17 cytokine production in a mouse model of Gaucher disease
Manoj Kumar Pandey, Reena Rani, Wujuan Zhang, et al.
Human Gene Therapy
|
August 7, 2002
Lysosomal acid lipase deficiency: correction of lipid storage by adenovirus-mediated gene transfer in mice
Hong Du, Martin Heur, David P Witte, et al.
Molecular Genetics and Metabolism
|
January 9, 2021
Gaucher disease: Basic and translational science needs for more complete therapy and management
Gregory A Grabowski, Armand H M Antommaria, Edwin H Kolodny, et al.
Molecular Genetics and Metabolism
|
March 19, 2008
Dependence of reversibility and progression of mouse neuronopathic Gaucher disease on acid beta-glucosidase residual activity levels
You-Hai Xu, Rachel Reboulet, Brian Quinn, et al.
Plos One
|
October 8, 2009
In vivo and ex vivo evaluation of L-type calcium channel blockers on acid beta-glucosidase in Gaucher disease mouse models
Ying Sun, Benjamin Liou, Brian Quinn, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
November 15, 2003
Reduction of atherosclerotic plaques by lysosomal acid lipase supplementation
Hong Du, Susan Schiavi, Nick Wan, 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 phenotypes
Huiquan Zhao, Laurie A Bailey, Louis J Elsas, et al.
Page
of 13