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Blood Advances|December 14, 2021
Investigational curative gene therapy approaches to sickle cell diseaseDavid A Williams, Erica EsrickCytotherapy|June 8, 2026
Curative treatment for severe sickle cell disease: allogeneic hematopoietic cell transplant or gene therapyMary Eapen, David A WilliamsJournal of Pharmaceutical and Biomedical Analysis|November 22, 2005
Determination of methenamine, methenamine mandelate and methenamine hippurate in pharmaceutical preparations using ion-exchange HPLCChiravi Pavitrapok, David A WilliamsMolecular Cell|October 21, 2004
Retroviral pseudotransduction for targeted cell manipulationMelanie Galla, Elke Will, Janine Kraunus, et al.Biochemical and Biophysical Research Communications|February 22, 2002
Role of the Multidrug Resistance Protein 1 in protection from heavy metal oxyanions: investigations in vitro and in MRP1-deficient miceAurelio Lorico, Antonella Bertola, Christopher Baum, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|April 5, 2007
Improving transcriptional termination of self-inactivating gamma-retroviral and lentiviral vectorsAxel Schambach, Melanie Galla, Tobias Maetzig, et al.Journal of Molecular Biology|July 24, 2010
Multiplexing RMCE: versatile extensions of the Flp-recombinase-mediated cassette-exchange technologySoeren Turan, Johannes Kuehle, Axel Schambach, et al.Human Gene Therapy|March 21, 2006
Mutagenesis and oncogenesis by chromosomal insertion of gene transfer vectorsChristopher Baum, Olga Kustikova, Ute Modlich, et al.Stem Cells and Development|May 25, 2007
CD34 modulates the trafficking behavior of hematopoietic cells in vivoClaudia Lange, Zhixiong Li, Lubin Fang, et al.Journal of Clinical Immunology|November 4, 2022
Lentiviral Gene Transfer Corrects Immune Abnormalities in XIAP DeficiencyJoseph Topal, Neelam Panchal, Amairelys Barroeta, et al.Pageof 94