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Alexander J Smith

Showing results (71-80 of 113) with videos related to

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Human Gene Therapy|June 26, 2019
Development of a Gene Therapy Vector for <i>RDH12</i>-Associated Retinal DystrophyKecia L Feathers, Lin Jia, Nirosha Dayanthi Perera, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 24, 2004
Dysregulated FcepsilonRI signaling and altered Fyn and SHIP activities in Lyn-deficient mast cellsValerie Hernandez-Hansen, Alexander J Smith, Zurab Surviladze, et al.
Plos One|June 19, 2010
HIF-1alpha and HIF-2alpha are differentially activated in distinct cell populations in retinal ischaemiaFreya M Mowat, Ulrich F O Luhmann, Alexander J Smith, et al.
Human Molecular Genetics|March 21, 2009
Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectorsMei Hong Tan, Alexander J Smith, Basil Pawlyk, et al.
Glia|May 24, 2021
RNAi-mediated suppression of vimentin or glial fibrillary acidic protein prevents the establishment of Müller glial cell hypertrophy in progressive retinal degenerationClaire Hippert, Anna B Graca, Mark Basche, et al.
Stem Cells (Dayton, Ohio)|September 22, 2010
Long-term survival of photoreceptors transplanted into the adult murine neural retina requires immune modulationEmma L West, Rachael A Pearson, Susie E Barker, et al.
The Journal of Gene Medicine|April 3, 2009
Subretinal delivery of adeno-associated virus serotype 2 results in minimal immune responses that allow repeat vector administration in immunocompetent miceSusie E Barker, Cathryn A Broderick, Scott J Robbie, et al.
Disease Models & Mechanisms|January 23, 2016
Multimodal analysis of ocular inflammation using the endotoxin-induced uveitis mouse modelColin J Chu, Peter J Gardner, David A Copland, et al.
The Lancet. Neurology|November 25, 2018
Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosisSara E Mole, Glenn Anderson, Heather A Band, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 12, 2017
Corrigendum to "Local Administration of an Adeno-Associated Viral Vector Expressing IL-10 Reduces Monocyte Infiltration and Subsequent Photoreceptor Damage During Experimental Autoimmune Uveitis"Cathryn A Broderick, Alexander J Smith, Kam S Balaggan, et al.
Pageof 12

Showing results (71-80 of 113) with videos related to

Sort By:
Pageof 12
Human Gene Therapy|June 26, 2019
Development of a Gene Therapy Vector for <i>RDH12</i>-Associated Retinal DystrophyKecia L Feathers, Lin Jia, Nirosha Dayanthi Perera, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 24, 2004
Dysregulated FcepsilonRI signaling and altered Fyn and SHIP activities in Lyn-deficient mast cellsValerie Hernandez-Hansen, Alexander J Smith, Zurab Surviladze, et al.
Plos One|June 19, 2010
HIF-1alpha and HIF-2alpha are differentially activated in distinct cell populations in retinal ischaemiaFreya M Mowat, Ulrich F O Luhmann, Alexander J Smith, et al.
Human Molecular Genetics|March 21, 2009
Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectorsMei Hong Tan, Alexander J Smith, Basil Pawlyk, et al.
Glia|May 24, 2021
RNAi-mediated suppression of vimentin or glial fibrillary acidic protein prevents the establishment of Müller glial cell hypertrophy in progressive retinal degenerationClaire Hippert, Anna B Graca, Mark Basche, et al.
Stem Cells (Dayton, Ohio)|September 22, 2010
Long-term survival of photoreceptors transplanted into the adult murine neural retina requires immune modulationEmma L West, Rachael A Pearson, Susie E Barker, et al.
The Journal of Gene Medicine|April 3, 2009
Subretinal delivery of adeno-associated virus serotype 2 results in minimal immune responses that allow repeat vector administration in immunocompetent miceSusie E Barker, Cathryn A Broderick, Scott J Robbie, et al.
Disease Models & Mechanisms|January 23, 2016
Multimodal analysis of ocular inflammation using the endotoxin-induced uveitis mouse modelColin J Chu, Peter J Gardner, David A Copland, et al.
The Lancet. Neurology|November 25, 2018
Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosisSara E Mole, Glenn Anderson, Heather A Band, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 12, 2017
Corrigendum to "Local Administration of an Adeno-Associated Viral Vector Expressing IL-10 Reduces Monocyte Infiltration and Subsequent Photoreceptor Damage During Experimental Autoimmune Uveitis"Cathryn A Broderick, Alexander J Smith, Kam S Balaggan, et al.
Pageof 12