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Alexander J Smith

Showing results (81-90 of 113) with videos related to

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Human Gene Therapy|September 14, 2013
Successful gene therapy in older Rpe65-deficient dogs following subretinal injection of an adeno-associated vector expressing RPE65Matthew J Annear, Freya M Mowat, Joshua T Bartoe, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 27, 2005
Local administration of an adeno-associated viral vector expressing IL-10 reduces monocyte infiltration and subsequent photoreceptor damage during experimental autoimmune uveitisCathryn A Broderick, Alexander J Smith, Kam S Balaggan, et al.
Nature Communications|January 24, 2015
Gene therapy restores vision in rd1 mice after removal of a confounding mutation in Gpr179Koji M Nishiguchi, Livia S Carvalho, Matteo Rizzi, et al.
Stem Cell Research & Therapy|June 14, 2018
Use of bioreactors for culturing human retinal organoids improves photoreceptor yieldsPatrick Ovando-Roche, Emma L West, Matthew J Branch, et al.
Bulletin Et Memoires De L'Academie Royale De Medecine De Belgique|May 17, 2007
Gene therapeutic prospects in early onset of severe retinal dystrophy: restoration of vision in RPE65 Briard dogs using an AAV serotype 4 vector that specifically targets the retinal pigmented epitheliumF Rolling, Guylène Le Meur, Knut Stieger, et al.
The Journal of Cell Biology|September 19, 2022
Spatiotemporal control of actomyosin contractility by MRCKβ signaling drives phagocytosisCeniz Zihni, Anastasios Georgiadis, Conor M Ramsden, et al.
The Journal of Biological Chemistry|April 21, 2022
mTORC1 regulates high levels of protein synthesis in retinal ganglion cells of adult micePatrice E Fort, Mandy K Losiewicz, Lynda Elghazi, et al.
Journal of Vision|November 26, 2015
Spectral sensitivity measurements reveal partial success in restoring missing rod function with gene therapyCaterina Ripamonti, G Bruce Henning, Scott J Robbie, et al.
Human Molecular Genetics|August 23, 2014
The severity of retinal pathology in homozygous Crb1rd8/rd8 mice is dependent on additional genetic factorsUlrich F O Luhmann, Livia S Carvalho, Sophia-Martha Kleine Holthaus, et al.
Angiogenesis|October 5, 2019
Stabilization of myeloid-derived HIFs promotes vascular regeneration in retinal ischemiaPilar Villacampa, Sidath E Liyanage, Izabela P Klaska, et al.
Pageof 12

Showing results (81-90 of 113) with videos related to

Sort By:
Pageof 12
Human Gene Therapy|September 14, 2013
Successful gene therapy in older Rpe65-deficient dogs following subretinal injection of an adeno-associated vector expressing RPE65Matthew J Annear, Freya M Mowat, Joshua T Bartoe, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 27, 2005
Local administration of an adeno-associated viral vector expressing IL-10 reduces monocyte infiltration and subsequent photoreceptor damage during experimental autoimmune uveitisCathryn A Broderick, Alexander J Smith, Kam S Balaggan, et al.
Nature Communications|January 24, 2015
Gene therapy restores vision in rd1 mice after removal of a confounding mutation in Gpr179Koji M Nishiguchi, Livia S Carvalho, Matteo Rizzi, et al.
Stem Cell Research & Therapy|June 14, 2018
Use of bioreactors for culturing human retinal organoids improves photoreceptor yieldsPatrick Ovando-Roche, Emma L West, Matthew J Branch, et al.
Bulletin Et Memoires De L'Academie Royale De Medecine De Belgique|May 17, 2007
Gene therapeutic prospects in early onset of severe retinal dystrophy: restoration of vision in RPE65 Briard dogs using an AAV serotype 4 vector that specifically targets the retinal pigmented epitheliumF Rolling, Guylène Le Meur, Knut Stieger, et al.
The Journal of Cell Biology|September 19, 2022
Spatiotemporal control of actomyosin contractility by MRCKβ signaling drives phagocytosisCeniz Zihni, Anastasios Georgiadis, Conor M Ramsden, et al.
The Journal of Biological Chemistry|April 21, 2022
mTORC1 regulates high levels of protein synthesis in retinal ganglion cells of adult micePatrice E Fort, Mandy K Losiewicz, Lynda Elghazi, et al.
Journal of Vision|November 26, 2015
Spectral sensitivity measurements reveal partial success in restoring missing rod function with gene therapyCaterina Ripamonti, G Bruce Henning, Scott J Robbie, et al.
Human Molecular Genetics|August 23, 2014
The severity of retinal pathology in homozygous Crb1rd8/rd8 mice is dependent on additional genetic factorsUlrich F O Luhmann, Livia S Carvalho, Sophia-Martha Kleine Holthaus, et al.
Angiogenesis|October 5, 2019
Stabilization of myeloid-derived HIFs promotes vascular regeneration in retinal ischemiaPilar Villacampa, Sidath E Liyanage, Izabela P Klaska, et al.
Pageof 12