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Methods in Molecular Biology (Clifton, N.J.)|October 29, 2011
Design and construction of functional AAV vectorsJohn T Gray, Serge Zolotukhin
The Application of Clinical Genetics|October 26, 2013
Developments in the treatment of hemophilia B: focus on emerging gene therapyMaria I Cancio, Ulrike M Reiss, Amit C Nathwani, et al.
Blood Cells, Molecules & Diseases|July 3, 2007
A chromatin insulator blocks interactions between globin regulatory elements and cellular promoters in erythroid cellsByoung Y Ryu, Derek A Persons, Marguerite V Evans-Galea, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 1, 2005
Efficiency of transduction of highly purified murine hematopoietic stem cells by lentiviral and oncoretroviral vectors under conditions of minimal in vitro manipulationGustavo Mostoslavsky, Darrell N Kotton, Attila J Fabian, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 4, 2008
Correction of murine sickle cell disease using gamma-globin lentiviral vectors to mediate high-level expression of fetal hemoglobinTamara I Pestina, Phillip W Hargrove, Dennis Jay, et al.
Blood|November 10, 2007
An experimental system for the evaluation of retroviral vector design to diminish the risk for proto-oncogene activationByoung Y Ryu, Marguerite V Evans-Galea, John T Gray, et al.
Human Gene Therapy Methods|October 19, 2012
Transduction of human CD34+ repopulating cells with a self-inactivating lentiviral vector for SCID-X1 produced at clinical scale by a stable cell lineMichael R Greene, Timothy Lockey, Perdeep K Mehta, et al.
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