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Seng H Cheng

Showing results (1-10 of 157) with videos related to

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Journal of Lipid Research|April 1, 2014
Gene therapy for the neurological manifestations in lysosomal storage disordersSeng H Cheng
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|September 10, 2011
Neural stem cell transplantation as a therapeutic approach for treating lysosomal storage diseasesLamya S Shihabuddin, Seng H Cheng
Pediatric Endocrinology Reviews : PER|January 2, 2014
Gene therapy for lysosomal storage disordersNelson S Yew, Seng H Cheng
Current Gene Therapy|April 14, 2006
Cell and gene-based therapies for the lysosomal storage diseasesBradley L Hodges, Seng H Cheng
Expert Opinion on Drug Delivery|November 22, 2005
Reducing the immunostimulatory activity of CpG-containing plasmid DNA vectors for non-viral gene therapyNelson S Yew, Seng H Cheng
Trends in Molecular Medicine|February 22, 2011
Prospects for the gene therapy of spinal muscular atrophyMarco A Passini, Seng H Cheng
Current Gene Therapy|March 23, 2004
Fas ligand gene therapy for vascular intimal hyperplasiaCanwen Jiang, Yi-Feng Yang, Seng H Cheng
Progress in Neurobiology|January 10, 2015
Gaucher-related synucleinopathies: the examination of sporadic neurodegeneration from a rare (disease) angleS Pablo Sardi, Seng H Cheng, Lamya S Shihabuddin
DNA and Cell Biology Reports|September 19, 2025
Correction of Disease Phenotype in Pompe Disease Knockout Mice Following Cationic Lipid-GL-67-Mediated Gene TherapyFrank Martiniuk, Justin Martiniuk, Adra Mack, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 12, 2003
Dexamethasone-mediated up-regulation of the mannose receptor improves the delivery of recombinant glucocerebrosidase to Gaucher macrophagesYunxiang Zhu, Xuemei Li, Edward H Schuchman, et al.
Pageof 16

Showing results (1-10 of 157) with videos related to

Sort By:
Pageof 16
Journal of Lipid Research|April 1, 2014
Gene therapy for the neurological manifestations in lysosomal storage disordersSeng H Cheng
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|September 10, 2011
Neural stem cell transplantation as a therapeutic approach for treating lysosomal storage diseasesLamya S Shihabuddin, Seng H Cheng
Pediatric Endocrinology Reviews : PER|January 2, 2014
Gene therapy for lysosomal storage disordersNelson S Yew, Seng H Cheng
Current Gene Therapy|April 14, 2006
Cell and gene-based therapies for the lysosomal storage diseasesBradley L Hodges, Seng H Cheng
Expert Opinion on Drug Delivery|November 22, 2005
Reducing the immunostimulatory activity of CpG-containing plasmid DNA vectors for non-viral gene therapyNelson S Yew, Seng H Cheng
Trends in Molecular Medicine|February 22, 2011
Prospects for the gene therapy of spinal muscular atrophyMarco A Passini, Seng H Cheng
Current Gene Therapy|March 23, 2004
Fas ligand gene therapy for vascular intimal hyperplasiaCanwen Jiang, Yi-Feng Yang, Seng H Cheng
Progress in Neurobiology|January 10, 2015
Gaucher-related synucleinopathies: the examination of sporadic neurodegeneration from a rare (disease) angleS Pablo Sardi, Seng H Cheng, Lamya S Shihabuddin
DNA and Cell Biology Reports|September 19, 2025
Correction of Disease Phenotype in Pompe Disease Knockout Mice Following Cationic Lipid-GL-67-Mediated Gene TherapyFrank Martiniuk, Justin Martiniuk, Adra Mack, et al.
The Journal of Pharmacology and Experimental Therapeutics|November 12, 2003
Dexamethasone-mediated up-regulation of the mannose receptor improves the delivery of recombinant glucocerebrosidase to Gaucher macrophagesYunxiang Zhu, Xuemei Li, Edward H Schuchman, et al.
Pageof 16