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The Journal of Clinical Investigation
|
June 10, 2025
Expression of full-length dystrophin reverses muscular dystrophy defects in young and old mdx4cv mice
Hichem Tasfaout, Timothy S McMillen, Theodore R Reyes, et al.
Human Gene Therapy
|
April 14, 2006
Prevalence of neutralizing antibodies against adeno-associated virus (AAV) types 2, 5, and 6 in cystic fibrosis and normal populations: Implications for gene therapy using AAV vectors
Christine L Halbert, A Dusty Miller, Sharon McNamara, et al.
Journal of Virology
|
May 20, 2011
Jaagsiekte sheep retrovirus and enzootic nasal tumor virus promoters drive gene expression in all airway epithelial cells of mice but only induce tumors in the alveolar region of the lungs
Darrick L Yu, Nicolle M Linnerth-Petrik, Christine L Halbert, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
April 8, 2010
Expression of human alpha1-antitrypsin in mice and dogs following AAV6 vector-mediated gene transfer to the lungs
Christine L Halbert, David K Madtes, Andrew E Vaughan, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 29, 2004
Efficient transduction of skeletal muscle using vectors based on adeno-associated virus serotype 6
Michael J Blankinship, Paul Gregorevic, James M Allen, et al.
Nature
|
July 17, 2024
Split intein-mediated protein trans-splicing to express large dystrophins
Hichem Tasfaout, Christine L Halbert, Timothy S McMillen, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 14, 2012
Successful regional delivery and long-term expression of a dystrophin gene in canine muscular dystrophy: a preclinical model for human therapies
Zejing Wang, Rainer Storb, Christine L Halbert, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 17 results.
The Journal of Clinical Investigation
|
June 10, 2025
Expression of full-length dystrophin reverses muscular dystrophy defects in young and old mdx4cv mice
Hichem Tasfaout, Timothy S McMillen, Theodore R Reyes, et al.
Human Gene Therapy
|
April 14, 2006
Prevalence of neutralizing antibodies against adeno-associated virus (AAV) types 2, 5, and 6 in cystic fibrosis and normal populations: Implications for gene therapy using AAV vectors
Christine L Halbert, A Dusty Miller, Sharon McNamara, et al.
Journal of Virology
|
May 20, 2011
Jaagsiekte sheep retrovirus and enzootic nasal tumor virus promoters drive gene expression in all airway epithelial cells of mice but only induce tumors in the alveolar region of the lungs
Darrick L Yu, Nicolle M Linnerth-Petrik, Christine L Halbert, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
April 8, 2010
Expression of human alpha1-antitrypsin in mice and dogs following AAV6 vector-mediated gene transfer to the lungs
Christine L Halbert, David K Madtes, Andrew E Vaughan, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 29, 2004
Efficient transduction of skeletal muscle using vectors based on adeno-associated virus serotype 6
Michael J Blankinship, Paul Gregorevic, James M Allen, et al.
Nature
|
July 17, 2024
Split intein-mediated protein trans-splicing to express large dystrophins
Hichem Tasfaout, Christine L Halbert, Timothy S McMillen, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 14, 2012
Successful regional delivery and long-term expression of a dystrophin gene in canine muscular dystrophy: a preclinical model for human therapies
Zejing Wang, Rainer Storb, Christine L Halbert, et al.
Page
of 2