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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 GrabowskiMolecular Genetics and Metabolism|December 5, 2003
Cell cycle dependent intracellular distribution of two spliced isoforms of TCP/ILF3 proteinsYou Hai Xu, Tatyana Leonova, Gregory A GrabowskiZhongguo Shi Yan Xue Ye Xue Za Zhi|April 19, 2018
[Imatinib as Second-Line Treatment Drug for CML Patients Intolerant to Nilotinib]Jing Qi, You-Hai Xu, He-Sheng HeZhongguo Shi Yan Xue Ye Xue Za Zhi|July 4, 2025
[Clinical Characteristic of Castleman Disease with Renal and Orbit Involvement]Yin-Qian Liu, You-Hai Xu, He-Sheng HeJournal of Lipid Research|March 10, 2010
Multi-system disorders of glycosphingolipid and ganglioside metabolismYou-Hai Xu, Sonya Barnes, Ying Sun, et al.The American Journal of Pathology|October 28, 2003
Viable mouse models of acid beta-glucosidase deficiency: the defect in Gaucher diseaseYou-Hai Xu, Brian Quinn, David Witte, et al.Plos One|May 28, 2010
Comparative therapeutic effects of velaglucerase alfa and imiglucerase in a Gaucher disease mouse modelYou-Hai Xu, Ying Sun, Sonya Barnes, 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 modelsYing Sun, Benjamin Liou, Brian Quinn, 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 levelsYou-Hai Xu, Rachel Reboulet, Brian Quinn, et al.Journal of Lipid Research|July 25, 2006
Conditional expression of human acid beta-glucosidase improves the visceral phenotype in a Gaucher disease mouse modelYing Sun, Brian Quinn, You-Hai Xu, et al.Pageof 3