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Blood Advances|October 6, 2019
High-level protein production in erythroid cells derived from in vivo transduced hematopoietic stem cellsHongjie Wang, Zhinan Liu, Chang Li, et al.
Molecular Therapy Oncolytics|July 17, 2020
Non-signaling Chimeric Antigen Receptors Enhance Antigen-Directed Killing by γδ T Cells in Contrast to αβ T CellsLauren C Fleischer, Scott A Becker, Rebecca E Ryan, et al.
Plos One|November 16, 2012
Development and characterization of recombinant ovine coagulation factor VIIIPhilip M Zakas, Bagirath Gangadharan, Graca Almeida-Porada, et al.
Molecular Therapy. Methods & Clinical Development|March 20, 2018
Target-Cell-Directed Bioengineering Approaches for Gene Therapy of Hemophilia AHarrison C Brown, Philip M Zakas, Stephan N George, et al.
Human Gene Therapy|April 8, 2020
Lentiviral Gene Therapy for Familial Hemophagocytic Lymphohistiocytosis Type 3, Caused by <i>UNC13D</i> Genetic DefectsSarah E Takushi, Na Yoon Paik, Andrew Fedanov, et al.
Journal of Thrombosis and Haemostasis : JTH|November 22, 2019
Unaccompanied mechanosensory domain mediates low expression of glycoprotein Ibα: implications for Bernard-Soulier syndromeYue Tao, Chi Gan, Xiaoqin Zhang, et al.
Human Gene Therapy|February 19, 2009
Comparison of factor VIII transgenes bioengineered for improved expression in gene therapy of hemophilia AKerry L Dooriss, Gabriela Denning, Bagirath Gangadharan, et al.
Nature Biotechnology|November 8, 2016
Enhancing the pharmaceutical properties of protein drugs by ancestral sequence reconstructionPhilip M Zakas, Harrison C Brown, Kristopher Knight, et al.
Molecular Therapy Oncolytics|December 10, 2016
Genetic engineering of chimeric antigen receptors using lamprey derived variable lymphocyte receptorsRobert Moot, Sunil S Raikar, Lauren Fleischer, et al.
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