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American Journal of Human Genetics|December 29, 2005
The role of mannosylated enzyme and the mannose receptor in enzyme replacement therapyHong Du, Mark Levine, Chandrashekar Ganesa, et al.Blood|July 10, 2009
Characterization of Gaucher disease bone marrow mesenchymal stromal cells reveals an altered inflammatory secretomePhilippe M Campeau, Moutih Rafei, Marie-Noëlle Boivin, et al.Plant Cell Reports|September 5, 2014
Membrane anchors effectively traffic recombinant human glucocerebrosidase to the protein storage vacuole of Arabidopsis seeds but do not adequately control N-glycan maturationXu He, Jason D Galpin, Yansong Miao, 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.Current Opinion in Pediatrics|November 21, 2007
Enzyme reconstitution/replacement therapy for lysosomal storage diseasesT Andrew Burrow, Robert J Hopkin, Nancy D Leslie, et al.Plos One|June 15, 2016
Effect of Recurrent Selection on Drought Tolerance and Related Morpho-Physiological Traits in Bread WheatRamya P, Gyanendra Pratap Singh, Neelu Jain, et al.Plos One|October 15, 2013
Gaucher disease: transcriptome analyses using microarray or mRNA sequencing in a Gba1 mutant mouse model treated with velaglucerase alfa or imigluceraseNupur Dasgupta, You-Hai Xu, Sunghee Oh, et al.Molecular Genetics and Metabolism|September 5, 2002
Prosaposin: threshold rescue and analysis of the "neuritogenic" region in transgenic miceYing Sun, Xiaoyang Qi, David P Witte, et al.Physical Chemistry Chemical Physics : PCCP|January 23, 2019
Understanding charge carrier dynamics in a P3HT:FLR blendJessica Patel, Abhishek Sharma, Mihirsinh Chauhan, et al.Biochimica Et Biophysica Acta|August 25, 2009
Chemical screen to reduce sterol accumulation in Niemann-Pick C disease cells identifies novel lysosomal acid lipase inhibitorsAnton I Rosenbaum, Madalina Rujoi, Amy Y Huang, et al.Pageof 20