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Annals of the New York Academy of Sciences|March 31, 2007
Insertional mutagenesis by replication-deficient retroviral vectors encoding the large T oncogeneZhixiong Li, Olga S Kustikova, Kenji Kamino, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 28, 2010
Biochemical correction of X-CGD by a novel chimeric promoter regulating high levels of transgene expression in myeloid cellsGiorgia Santilli, Elena Almarza, Christian Brendel, et al.
Plos One|December 7, 2023
Correction: The Tight Junction Associated Signalling Proteins ZO-1 and ZONAB Regulate Retinal Pigment Epithelium Homeostasis in MiceAnastasios Georgiadis, Marion Tschernutter, James W B Bainbridge, et al.
Gene Therapy|June 14, 2020
Lentiviral gene therapy rescues p47phox chronic granulomatous disease and the ability to fight Salmonella infection in miceAndrea Schejtman, Walmir Cutrim Aragão-Filho, Simon Clare, et al.
Human Molecular Genetics|May 20, 2011
Functional human artificial chromosomes are generated and stably maintained in human embryonic stem cellsMohammad A Mandegar, Daniela Moralli, Suhail Khoja, et al.
Plos One|January 7, 2011
The tight junction associated signalling proteins ZO-1 and ZONAB regulate retinal pigment epithelium homeostasis in miceAnastasios Georgiadis, Marion Tschernutter, James W B Bainbridge, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 1, 2010
Lymphomagenesis in SCID-X1 mice following lentivirus-mediated phenotype correction independent of insertional mutagenesis and gammac overexpressionSamantha L Ginn, Sophia H Y Liao, Allison P Dane, et al.
Science Translational Medicine|August 26, 2011
Long-term persistence of a polyclonal T cell repertoire after gene therapy for X-linked severe combined immunodeficiencyH Bobby Gaspar, Samantha Cooray, Kimberly C Gilmour, et al.
Nature Communications|March 13, 2021
Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humansNatalia Izotova, Christine Rivat, Cristina Baricordi, et al.
Molecular Therapy. Methods & Clinical Development|October 10, 2022
Preclinical model for phenotypic correction of dystrophic epidermolysis bullosa by in vivo CRISPR-Cas9 delivery using adenoviral vectorsMarta García, Jose Bonafont, Jesús Martínez-Palacios, et al.
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