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Neil R Hackett

Showing results (51-60 of 90) with videos related to

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Cell|June 14, 2002
Recruitment of stem and progenitor cells from the bone marrow niche requires MMP-9 mediated release of kit-ligandBeate Heissig, Koichi Hattori, Sergio Dias, et al.
BMC Genomics|March 2, 2012
RNA-Seq quantification of the human small airway epithelium transcriptomeNeil R Hackett, Marcus W Butler, Renat Shaykhiev, et al.
The Journal of Clinical Investigation|April 21, 2005
Protection against P. aeruginosa with an adenovirus vector containing an OprF epitope in the capsidStefan Worgall, Anja Krause, Michael Rivara, et al.
Journal of Neurosurgery. Pediatrics|August 3, 2010
Gene therapy for late infantile neuronal ceroid lipofuscinosis: neurosurgical considerationsMark M Souweidane, Justin F Fraser, Lisa M Arkin, et al.
Plos One|August 11, 2011
Biologic phenotyping of the human small airway epithelial response to cigarette smokingAnn E Tilley, Timothy P O'Connor, Neil R Hackett, et al.
Human Gene Therapy|December 31, 2013
Partial correction of the CNS lysosomal storage defect in a mouse model of juvenile neuronal ceroid lipofuscinosis by neonatal CNS administration of an adeno-associated virus serotype rh.10 vector expressing the human CLN3 geneDolan Sondhi, Emma C Scott, Alvin Chen, et al.
Journal of Virology|February 14, 2004
Modification to the capsid of the adenovirus vector that enhances dendritic cell infection and transgene-specific cellular immune responsesStefan Worgall, Annette Busch, Michael Rivara, et al.
The Journal of Clinical Investigation|March 15, 2005
Neurotrophins promote revascularization by local recruitment of TrkB+ endothelial cells and systemic mobilization of hematopoietic progenitorsPouneh Kermani, Dahlia Rafii, David K Jin, et al.
Molecular Therapy. Methods & Clinical Development|December 13, 2023
Predicted deleterious variants in the human genome relevant to gene therapy with adeno-associated virus vectorsMahboubeh R Rostami, Philip L Leopold, Jenifer M Vasquez, et al.
Human Gene Therapy Methods|November 8, 2012
Long-term expression and safety of administration of AAVrh.10hCLN2 to the brain of rats and nonhuman primates for the treatment of late infantile neuronal ceroid lipofuscinosisDolan Sondhi, Linda Johnson, Keith Purpura, et al.
Pageof 9

Showing results (51-60 of 90) with videos related to

Sort By:
Pageof 9
Cell|June 14, 2002
Recruitment of stem and progenitor cells from the bone marrow niche requires MMP-9 mediated release of kit-ligandBeate Heissig, Koichi Hattori, Sergio Dias, et al.
BMC Genomics|March 2, 2012
RNA-Seq quantification of the human small airway epithelium transcriptomeNeil R Hackett, Marcus W Butler, Renat Shaykhiev, et al.
The Journal of Clinical Investigation|April 21, 2005
Protection against P. aeruginosa with an adenovirus vector containing an OprF epitope in the capsidStefan Worgall, Anja Krause, Michael Rivara, et al.
Journal of Neurosurgery. Pediatrics|August 3, 2010
Gene therapy for late infantile neuronal ceroid lipofuscinosis: neurosurgical considerationsMark M Souweidane, Justin F Fraser, Lisa M Arkin, et al.
Plos One|August 11, 2011
Biologic phenotyping of the human small airway epithelial response to cigarette smokingAnn E Tilley, Timothy P O'Connor, Neil R Hackett, et al.
Human Gene Therapy|December 31, 2013
Partial correction of the CNS lysosomal storage defect in a mouse model of juvenile neuronal ceroid lipofuscinosis by neonatal CNS administration of an adeno-associated virus serotype rh.10 vector expressing the human CLN3 geneDolan Sondhi, Emma C Scott, Alvin Chen, et al.
Journal of Virology|February 14, 2004
Modification to the capsid of the adenovirus vector that enhances dendritic cell infection and transgene-specific cellular immune responsesStefan Worgall, Annette Busch, Michael Rivara, et al.
The Journal of Clinical Investigation|March 15, 2005
Neurotrophins promote revascularization by local recruitment of TrkB+ endothelial cells and systemic mobilization of hematopoietic progenitorsPouneh Kermani, Dahlia Rafii, David K Jin, et al.
Molecular Therapy. Methods & Clinical Development|December 13, 2023
Predicted deleterious variants in the human genome relevant to gene therapy with adeno-associated virus vectorsMahboubeh R Rostami, Philip L Leopold, Jenifer M Vasquez, et al.
Human Gene Therapy Methods|November 8, 2012
Long-term expression and safety of administration of AAVrh.10hCLN2 to the brain of rats and nonhuman primates for the treatment of late infantile neuronal ceroid lipofuscinosisDolan Sondhi, Linda Johnson, Keith Purpura, et al.
Pageof 9