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Methods in Enzymology|February 28, 2012
Retrovirus and lentivirus vector design and methods of cell conditioningSamantha Cooray, Steven J Howe, Adrian J ThrasherExpert Opinion on Biological Therapy|January 16, 2008
Development of lentiviral gene therapy for Wiskott Aldrich syndromeAnne Galy, Maria-Grazia Roncarolo, Adrian J ThrasherBritish Journal of Haematology|April 14, 2006
Autoimmune lymphoproliferative syndrome: molecular basis of disease and clinical phenotypeAusten Worth, Adrian J Thrasher, H Bobby GasparTrends in Molecular Medicine|March 20, 2016
Treating Immunodeficiency through HSC Gene TherapyClaire Booth, H Bobby Gaspar, Adrian J ThrasherBritish Journal of Haematology|June 6, 2015
Gene therapy for monogenic disorders of the bone marrowSujal Ghosh, Adrian J Thrasher, H Bobby GasparArchives of Disease in Childhood|October 24, 2007
Update on clinical gene therapy in childhoodWaseem Qasim, H Bobby Gaspar, Adrian J ThrasherCurrent Opinion in Pharmacology|September 13, 2015
Lentivirus technologies for modulation of the immune systemBenjamin C Houghton, Claire Booth, Adrian J ThrasherMolecular Therapy : the Journal of the American Society of Gene Therapy|October 18, 2005
Equal potency of gammaretroviral and lentiviral SIN vectors for expression of O6-methylguanine-DNA methyltransferase in hematopoietic cellsAxel Schambach, Jens Bohne, Saurabh Chandra, et al.Immunobiology|July 25, 2009
Wiskott-Aldrich Syndrome: Immunodeficiency resulting from defective cell migration and impaired immunostimulatory activationGerben Bouma, Siobhan O Burns, Adrian J ThrasherGenes & Diseases|March 18, 2020
Gene therapy and genome editing for primary immunodeficiency diseasesZhi-Yong Zhang, Adrian J Thrasher, Fang ZhangPageof 94