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European Journal of Haematology|March 24, 2007
Murine leukemia following irradiation conditioning for transplantation of lentivirally-modified hematopoietic stem cellsElena K Siapati, Brian W Bigger, Karl Kashofer, et al.
Molecular Therapy. Methods & Clinical Development|March 23, 2023
An improved medium formulation for efficient ex vivo gene editing, expansion and engraftment of hematopoietic stem and progenitor cellsRajeev Rai, Asma Naseem, Winston Vetharoy, et al.
Stem Cells (Dayton, Ohio)|November 8, 2012
Brief report: self-organizing neuroepithelium from human pluripotent stem cells facilitates derivation of photoreceptorsCédric Boucherie, Sayandip Mukherjee, Els Henckaerts, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 5, 2008
Improvement of migratory defects in a murine model of Wiskott-Aldrich syndrome gene therapyMichael P Blundell, Gerben Bouma, Yolanda Calle, et al.
Best Practice & Research. Clinical Haematology|October 23, 2004
Safety and efficacy in retrovirally modified haematopoietic cell therapyZhixiong Li, Ute Modlich, Christopher Baum
Methods in Molecular Biology (Clifton, N.J.)|January 9, 2013
Retrovirus-based mRNA transfer for transient cell manipulationMelanie Galla, Axel Schambach, Christopher Baum
Seminars in Cancer Biology|July 6, 2010
The genomic risk of somatic gene therapyOlga Kustikova, Martijn Brugman, Christopher Baum
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