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Human Gene Therapy|November 1, 1994
Trans complementation of an E1A-deleted adenovirus with codelivered E1A sequences to make recombinant adenoviral producer cellsK T Goldsmith, D T Curiel, J A Engler, et al.Human Gene Therapy|February 1, 1995
Replication-deficient adenovirus induces expression of interleukin-8 by airway epithelial cells in vitroR Amin, R Wilmott, Y Schwarz, et al.Human Gene Therapy|July 13, 2019
Gene Therapy for Pompe Disease: The Time is nowPasqualina Colella, Federico MingozziHuman Gene Therapy|February 19, 2010
Cytotoxicity associated with artemis overexpression after lentiviral vector-mediated gene transferMegan Multhaup, Andrea D Karlen, Debra L Swanson, et al.Human Gene Therapy|October 24, 2009
Efficient inhibition of hepatitis B virus replication in vivo, using polyethylene glycol-modified adenovirus vectorsCarol Crowther, Abdullah Ely, Judith Hornby, et al.Human Gene Therapy|March 6, 2010
TK.007: A novel, codon-optimized HSVtk(A168H) mutant for suicide gene therapyEllen Preuss, Alexandra Treschow, Sebastian Newrzela, et al.Human Gene Therapy|January 15, 2010
Functional differentiation between Rep-mediated site-specific integration and transcriptional repression of the adeno-associated viral p5 promoterYang-bo Yue, Yuan-yuan Xue, Ling Tian, et al.Human Gene Therapy|January 16, 2010
Optimization of adeno-associated viral vector-mediated gene delivery to the hypothalamusMarijke W A de Backer, Maike A D Brans, Mieneke C Luijendijk, et al.Human Gene Therapy|March 12, 2010
Fusion of the Human Cytomegalovirus pp65 antigen with both ubiquitin and ornithine decarboxylase additively enhances antigen presentation to CD8(+) T cells in human dendritic cellsMin-Ji Park, Eun-Kyung Kim, Ji-Young Han, et al.Human Gene Therapy|July 1, 1997
A simple and reliable method for screening retroviral producer clones without selectable markersM Onodera, A Yachie, D M Nelson, et al.Pageof 413