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Journal of Hematotherapy & Stem Cell Research|June 14, 2003
Homocysteine and prothrombin fragment 1+2 levels in patients with veno-occlusive disease after stem cell transplantationJohn Gerecitano, Clarissa Mathias, Rosemarie Mick, et al.
Blood|July 5, 2007
Modulation of tolerance to the transgene product in a nonhuman primate model of AAV-mediated gene transfer to liverFederico Mingozzi, Nicole C Hasbrouck, Etiena Basner-Tschakarjan, et al.
Molecular Therapy. Methods & Clinical Development|July 9, 2020
Experimental Variables that Affect Human Hepatocyte AAV Transduction in Liver Chimeric MiceChenhui Zou, Koen O A Vercauteren, Eleftherios Michailidis, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 30, 2016
Superior In vivo Transduction of Human Hepatocytes Using Engineered AAV3 CapsidKoen Vercauteren, Brad E Hoffman, Irene Zolotukhin, et al.
Blood|October 3, 2013
Robust ZFN-mediated genome editing in adult hemophilic miceXavier M Anguela, Rajiv Sharma, Yannick Doyon, et al.
Blood|January 18, 2013
Engineered AAV vector minimizes in vivo targeting of transduced hepatocytes by capsid-specific CD8+ T cellsAshley T Martino, Etiena Basner-Tschakarjan, David M Markusic, et al.
EMBO Molecular Medicine|June 23, 2018
Hepato-entrained B220<sup>+</sup>CD11c<sup>+</sup>NK1.1<sup>+</sup> cells regulate pre-metastatic niche formation in the lungSachie Hiratsuka, Takeshi Tomita, Taishi Mishima, et al.
Journal of Virological Methods|January 2, 2007
Separation of adeno-associated virus type 2 empty particles from genome containing vectors by anion-exchange column chromatographyGuang Qu, Jennifer Bahr-Davidson, Joseph Prado, et al.
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