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DNA Repair|May 8, 2007
Live and let die: in vivo selection of gene-modified hematopoietic stem cells via MGMT-mediated chemoprotectionMichael D Milsom, David A WilliamsTopics in Companion Animal Medicine|November 15, 2012
Pancreatitis in catsP Jane Armstrong, David A WilliamsMolecular Therapy : the Journal of the American Society of Gene Therapy|August 16, 2005
Comparison of HIV- and EIAV-based vectors on their efficiency in transducing murine and human hematopoietic repopulating cellsElena K Siapati, Brian W Bigger, James Miskin, et al.Nature Materials|January 8, 2013
The cytoplasm of living cells behaves as a poroelastic materialEmad Moeendarbary, Léo Valon, Marco Fritzsche, et al.Journal of Virology|April 23, 2010
Self-inactivating alpharetroviral vectors with a split-packaging designJulia D Suerth, Tobias Maetzig, Melanie Galla, et al.Human Gene Therapy|February 5, 2008
Hematopoietic-specific lentiviral vectors circumvent cellular toxicity due to ectopic expression of Wiskott-Aldrich syndrome proteinMiguel G Toscano, Cecilia Frecha, Karim Benabdellah, et al.European Journal of Immunology|June 20, 2014
Exacerbated experimental arthritis in Wiskott-Aldrich syndrome protein deficiency: modulatory role of regulatory B cellsGerben Bouma, Natalie A Carter, Mike Recher, et al.Journal of Virology|December 12, 2001
In vivo analysis of retroviral enhancer mutations in hematopoietic cells: SP1/EGR1 and ETS/GATA motifs contribute to long terminal repeat specificityAnke Wahlers, Peter F Zipfel, Maike Schwieger, et al.Therapeutic Delivery|July 27, 2012
17th Annual Meeting of the German Society for Gene TherapyHildegard Büning, Christopher Baum, Anja Ehrhardt, et al.Pageof 94