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Journal of Lipid Research
|
April 1, 2014
Gene therapy for the neurological manifestations in lysosomal storage disorders
Seng 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 diseases
Lamya S Shihabuddin, Seng H Cheng
Pediatric Endocrinology Reviews : PER
|
January 2, 2014
Gene therapy for lysosomal storage disorders
Nelson S Yew, Seng H Cheng
Current Gene Therapy
|
April 14, 2006
Cell and gene-based therapies for the lysosomal storage diseases
Bradley 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 therapy
Nelson S Yew, Seng H Cheng
Trends in Molecular Medicine
|
February 22, 2011
Prospects for the gene therapy of spinal muscular atrophy
Marco A Passini, Seng H Cheng
Current Gene Therapy
|
March 23, 2004
Fas ligand gene therapy for vascular intimal hyperplasia
Canwen 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) angle
S 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 Therapy
Frank 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 macrophages
Yunxiang Zhu, Xuemei Li, Edward H Schuchman, et al.
Page
of 16
Search research articles
Search
Showing results (1-10 of 157) with videos related to
Sort By:
Page
of 16
Journal of Lipid Research
|
April 1, 2014
Gene therapy for the neurological manifestations in lysosomal storage disorders
Seng 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 diseases
Lamya S Shihabuddin, Seng H Cheng
Pediatric Endocrinology Reviews : PER
|
January 2, 2014
Gene therapy for lysosomal storage disorders
Nelson S Yew, Seng H Cheng
Current Gene Therapy
|
April 14, 2006
Cell and gene-based therapies for the lysosomal storage diseases
Bradley 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 therapy
Nelson S Yew, Seng H Cheng
Trends in Molecular Medicine
|
February 22, 2011
Prospects for the gene therapy of spinal muscular atrophy
Marco A Passini, Seng H Cheng
Current Gene Therapy
|
March 23, 2004
Fas ligand gene therapy for vascular intimal hyperplasia
Canwen 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) angle
S 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 Therapy
Frank 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 macrophages
Yunxiang Zhu, Xuemei Li, Edward H Schuchman, et al.
Page
of 16