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Methods in Molecular Biology (Clifton, N.J.)|July 30, 2014
Second generation codon optimized minicircle (CoMiC) for nonviral reprogramming of human adult fibroblastsSebastian Diecke, Leszek Lisowski, Nigel G Kooreman, et al.Microbial Cell Factories|December 21, 2022
The future of recombinant host defense peptidesRamon Roca-Pinilla, Leszek Lisowski, Anna Arís, et al.Human Gene Therapy|March 17, 2022
AAV-p40 Bioengineering Platform for Variant Selection Based on Transgene ExpressionAdrian Westhaus, Marti Cabanes-Creus, Timo Jonker, et al.Research and Practice in Thrombosis and Haemostasis|September 6, 2021
The intersection of vector biology, gene therapy, and hemophiliaLeszek Lisowski, Janice M Staber, J Fraser Wright, et al.Experimental Hematology|August 20, 2013
Comparison of transduction efficiency among various lentiviruses containing GFP reporter in bone marrow hematopoietic stem cell transplantationNan Wang, Narendiran Rajasekaran, Tieying Hou, et al.Annals of the New York Academy of Sciences|December 13, 2005
Progress toward the genetic treatment of the beta-thalassemiasMichel Sadelain, Leszek Lisowski, Selda Samakoglu, et al.Nucleic Acids Research|February 12, 2013
The anti-genomic (negative) strand of Hepatitis C Virus is not targetable by shRNALeszek Lisowski, Menashe Elazar, Kirk Chu, et al.FEBS Open Bio|September 10, 2024
Identifying adeno-associated virus (AAV) vectors that efficiently target high grade glioma cells, for in vitro monitoring of temporal cell responsesFarhana A Sarker, Yuyan Chen, Adrian Westhaus, et al.The CRISPR Journal|July 26, 2022
Gene Editing and Rett Syndrome: Does It Make the Cut?Bronte Coorey, Florencia Haase, Carolyn Ellaway, et al.JACC. Cardiooncology|January 6, 2022
Potential Applications for Targeted Gene Therapy to Protect Against Anthracycline Cardiotoxicity: <i>JACC: CardioOncology</i> PrimerCindy Y Kok, Lauren M MacLean, Jett C Ho, et al.Pageof 9