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Philippe Moullier

Showing results (31-40 of 92) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|October 16, 2002
Five recombinant simian immunodeficiency virus pseudotypes lead to exclusive transduction of retinal pigmented epithelium in ratGhislaine Duisit, Hervé Conrath, Sylvie Saleun, et al.
Journal of Virology|May 28, 2004
Early detection of a two-long-terminal-repeat junction molecule in the cytoplasm of recombinant murine leukemia virus-infected cellsFatima Serhan, Magalie Penaud, Caroline Petit, et al.
Journal of Virological Methods|May 19, 2009
Adeno-associated virus capsid serotype identification: Analytical methods development and applicationKim Van Vliet, Yasmin Mohiuddin, Scott McClung, et al.
Human Gene Therapy|September 9, 2022
Cellular and Structural Characterization of VP1 and VP2 Knockout Mutants of AAV3B Serotype and Implications for AAV ManufacturingIker Arriaga, Aitor Navarro, Amaia Etxabe, et al.
Human Gene Therapy|October 22, 2014
Early interaction of adeno-associated virus serotype 8 vector with the host immune system following intramuscular delivery results in weak but detectable lymphocyte and dendritic cell transductionGwladys Gernoux, Mickaël Guilbaud, Laurence Dubreil, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 10, 2004
Optimal design of a single recombinant adeno-associated virus derived from serotypes 1 and 2 to achieve more tightly regulated transgene expression from nonhuman primate musclePierre Chenuaud, Thibaut Larcher, Joseph E Rabinowitz, et al.
Plos One|June 21, 2011
Adeno-associated viral vector-mediated transgene expression is independent of DNA methylation in primate liver and skeletal muscleAdrien Léger, Caroline Le Guiner, Michael L Nickerson, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 6, 2003
Recombinant adeno-associated virus serotype 4 mediates unique and exclusive long-term transduction of retinal pigmented epithelium in rat, dog, and nonhuman primate after subretinal deliveryMichel Weber, Joseph Rabinowitz, Nathalie Provost, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 16, 2009
Intravenous administration of self-complementary AAV9 enables transgene delivery to adult motor neuronsSandra Duque, Béatrice Joussemet, Christel Riviere, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 29, 2012
Integration frequency and intermolecular recombination of rAAV vectors in non-human primate skeletal muscle and liverAli Nowrouzi, Magalie Penaud-Budloo, Christine Kaeppel, et al.
Pageof 10

Showing results (31-40 of 92) with videos related to

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Pageof 10
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 16, 2002
Five recombinant simian immunodeficiency virus pseudotypes lead to exclusive transduction of retinal pigmented epithelium in ratGhislaine Duisit, Hervé Conrath, Sylvie Saleun, et al.
Journal of Virology|May 28, 2004
Early detection of a two-long-terminal-repeat junction molecule in the cytoplasm of recombinant murine leukemia virus-infected cellsFatima Serhan, Magalie Penaud, Caroline Petit, et al.
Journal of Virological Methods|May 19, 2009
Adeno-associated virus capsid serotype identification: Analytical methods development and applicationKim Van Vliet, Yasmin Mohiuddin, Scott McClung, et al.
Human Gene Therapy|September 9, 2022
Cellular and Structural Characterization of VP1 and VP2 Knockout Mutants of AAV3B Serotype and Implications for AAV ManufacturingIker Arriaga, Aitor Navarro, Amaia Etxabe, et al.
Human Gene Therapy|October 22, 2014
Early interaction of adeno-associated virus serotype 8 vector with the host immune system following intramuscular delivery results in weak but detectable lymphocyte and dendritic cell transductionGwladys Gernoux, Mickaël Guilbaud, Laurence Dubreil, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 10, 2004
Optimal design of a single recombinant adeno-associated virus derived from serotypes 1 and 2 to achieve more tightly regulated transgene expression from nonhuman primate musclePierre Chenuaud, Thibaut Larcher, Joseph E Rabinowitz, et al.
Plos One|June 21, 2011
Adeno-associated viral vector-mediated transgene expression is independent of DNA methylation in primate liver and skeletal muscleAdrien Léger, Caroline Le Guiner, Michael L Nickerson, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 6, 2003
Recombinant adeno-associated virus serotype 4 mediates unique and exclusive long-term transduction of retinal pigmented epithelium in rat, dog, and nonhuman primate after subretinal deliveryMichel Weber, Joseph Rabinowitz, Nathalie Provost, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 16, 2009
Intravenous administration of self-complementary AAV9 enables transgene delivery to adult motor neuronsSandra Duque, Béatrice Joussemet, Christel Riviere, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 29, 2012
Integration frequency and intermolecular recombination of rAAV vectors in non-human primate skeletal muscle and liverAli Nowrouzi, Magalie Penaud-Budloo, Christine Kaeppel, et al.
Pageof 10