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Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 27, 2007
The enhancing effects of the light chain on heavy chain secretion in split delivery of factor VIII gene
Lingxia Chen, Fuxiang Zhu, Juan Li, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 8, 2008
Safety and efficacy of regional intravenous (r.i.) versus intramuscular (i.m.) delivery of rAAV1 and rAAV8 to nonhuman primate skeletal muscle
Alice Toromanoff, Yan Chérel, Mickaël Guilbaud, et al.
Blood
|
March 26, 2010
Peripheral transvenular delivery of adeno-associated viral vectors to skeletal muscle as a novel therapy for hemophilia B
Valder R Arruda, Hansell H Stedman, Virginia Haurigot, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
January 23, 2008
Reversal of blindness in animal models of leber congenital amaurosis using optimized AAV2-mediated gene transfer
Jeannette Bennicelli, John Fraser Wright, Andras Komaromy, et al.
Blood
|
January 8, 2003
AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B
Catherine S Manno, Amy J Chew, Sylvia Hutchison, et al.
Nature Medicine
|
February 14, 2006
Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response
Catherine S Manno, Glenn F Pierce, Valder R Arruda, et al.
The New England Journal of Medicine
|
December 7, 2017
Hemophilia B Gene Therapy with a High-Specific-Activity Factor IX Variant
Lindsey A George, Spencer K Sullivan, Adam Giermasz, et al.
The New England Journal of Medicine
|
April 29, 2008
Safety and efficacy of gene transfer for Leber's congenital amaurosis
Albert M Maguire, Francesca Simonelli, Eric A Pierce, et al.
Page
of 9
Search research articles
Search
Showing results (81-90 of 88) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 88 results.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 27, 2007
The enhancing effects of the light chain on heavy chain secretion in split delivery of factor VIII gene
Lingxia Chen, Fuxiang Zhu, Juan Li, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 8, 2008
Safety and efficacy of regional intravenous (r.i.) versus intramuscular (i.m.) delivery of rAAV1 and rAAV8 to nonhuman primate skeletal muscle
Alice Toromanoff, Yan Chérel, Mickaël Guilbaud, et al.
Blood
|
March 26, 2010
Peripheral transvenular delivery of adeno-associated viral vectors to skeletal muscle as a novel therapy for hemophilia B
Valder R Arruda, Hansell H Stedman, Virginia Haurigot, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
January 23, 2008
Reversal of blindness in animal models of leber congenital amaurosis using optimized AAV2-mediated gene transfer
Jeannette Bennicelli, John Fraser Wright, Andras Komaromy, et al.
Blood
|
January 8, 2003
AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B
Catherine S Manno, Amy J Chew, Sylvia Hutchison, et al.
Nature Medicine
|
February 14, 2006
Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response
Catherine S Manno, Glenn F Pierce, Valder R Arruda, et al.
The New England Journal of Medicine
|
December 7, 2017
Hemophilia B Gene Therapy with a High-Specific-Activity Factor IX Variant
Lindsey A George, Spencer K Sullivan, Adam Giermasz, et al.
The New England Journal of Medicine
|
April 29, 2008
Safety and efficacy of gene transfer for Leber's congenital amaurosis
Albert M Maguire, Francesca Simonelli, Eric A Pierce, et al.
Page
of 9