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Journal of Lipid Research
|
April 17, 2008
Wolman disease/cholesteryl ester storage disease: efficacy of plant-produced human lysosomal acid lipase in mice
Hong Du, Terri L Cameron, Stephen J Garger, et al.
The Journal of Biological Chemistry
|
March 13, 2009
Involvement of acid beta-glucosidase 1 in the salvage pathway of ceramide formation
Kazuyuki Kitatani, Kely Sheldon, Vinodh Rajagopalan, et al.
Cells
|
September 28, 2021
Substrate Reduction Therapy Reverses Mitochondrial, mTOR, and Autophagy Alterations in a Cell Model of Gaucher Disease
Yanyan Peng, Benjamin Liou, Yi Lin, et al.
Scientific Reports
|
April 5, 2019
Combination of acid β-glucosidase mutation and Saposin C deficiency in mice reveals Gba1 mutation dependent and tissue-specific disease phenotype
Benjamin Liou, Wujuan Zhang, Venette Fannin, et al.
The Journal of Gene Medicine
|
March 11, 2006
AAV8-mediated expression of glucocerebrosidase ameliorates the storage pathology in the visceral organs of a mouse model of Gaucher disease
Kerry Anne McEachern, Jennifer B Nietupski, Wei-Lien Chuang, et al.
Seminars in Hematology
|
October 7, 2004
Therapeutic goals in the treatment of Gaucher disease
Gregory M Pastores, Neal J Weinreb, Hans Aerts, et al.
Cell
|
June 25, 2011
Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathies
Joseph R Mazzulli, You-Hai Xu, Ying Sun, et al.
Journal of Lipid Research
|
December 3, 2013
Endogenous β-glucocerebrosidase activity in Abca12⁻/⁻epidermis elevates ceramide levels after topical lipid application but does not restore barrier function
Jorge F Haller, Paul Cavallaro, Nicholas J Hernandez, et al.
BMC Genomics
|
January 13, 2011
Global gene expression profile progression in Gaucher disease mouse models
You-Hai Xu, Li Jia, Brian Quinn, et al.
Molecular Genetics and Metabolism
|
May 20, 2014
Reversal of advanced disease in lysosomal acid lipase deficient mice: a model for lysosomal acid lipase deficiency disease
Ying Sun, You-Hai Xu, Hong Du, et al.
Page
of 13
Search research articles
Search
Showing results (81-90 of 128) with videos related to
Sort By:
Page
of 13
Journal of Lipid Research
|
April 17, 2008
Wolman disease/cholesteryl ester storage disease: efficacy of plant-produced human lysosomal acid lipase in mice
Hong Du, Terri L Cameron, Stephen J Garger, et al.
The Journal of Biological Chemistry
|
March 13, 2009
Involvement of acid beta-glucosidase 1 in the salvage pathway of ceramide formation
Kazuyuki Kitatani, Kely Sheldon, Vinodh Rajagopalan, et al.
Cells
|
September 28, 2021
Substrate Reduction Therapy Reverses Mitochondrial, mTOR, and Autophagy Alterations in a Cell Model of Gaucher Disease
Yanyan Peng, Benjamin Liou, Yi Lin, et al.
Scientific Reports
|
April 5, 2019
Combination of acid β-glucosidase mutation and Saposin C deficiency in mice reveals Gba1 mutation dependent and tissue-specific disease phenotype
Benjamin Liou, Wujuan Zhang, Venette Fannin, et al.
The Journal of Gene Medicine
|
March 11, 2006
AAV8-mediated expression of glucocerebrosidase ameliorates the storage pathology in the visceral organs of a mouse model of Gaucher disease
Kerry Anne McEachern, Jennifer B Nietupski, Wei-Lien Chuang, et al.
Seminars in Hematology
|
October 7, 2004
Therapeutic goals in the treatment of Gaucher disease
Gregory M Pastores, Neal J Weinreb, Hans Aerts, et al.
Cell
|
June 25, 2011
Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathies
Joseph R Mazzulli, You-Hai Xu, Ying Sun, et al.
Journal of Lipid Research
|
December 3, 2013
Endogenous β-glucocerebrosidase activity in Abca12⁻/⁻epidermis elevates ceramide levels after topical lipid application but does not restore barrier function
Jorge F Haller, Paul Cavallaro, Nicholas J Hernandez, et al.
BMC Genomics
|
January 13, 2011
Global gene expression profile progression in Gaucher disease mouse models
You-Hai Xu, Li Jia, Brian Quinn, et al.
Molecular Genetics and Metabolism
|
May 20, 2014
Reversal of advanced disease in lysosomal acid lipase deficient mice: a model for lysosomal acid lipase deficiency disease
Ying Sun, You-Hai Xu, Hong Du, et al.
Page
of 13