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Showing results (981-990 of 1,001) with videos related to

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Journal of Medical Genetics|July 13, 2013
Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencingXia Wang, Hui Wang, Vincent Sun, et al.
Ophthalmology|October 29, 2015
North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13Kent W Small, Adam P DeLuca, S Scott Whitmore, et al.
Investigative Ophthalmology & Visual Science|August 2, 2016
Residual Foveal Cone Structure in CNGB3-Associated AchromatopsiaChristopher S Langlo, Emily J Patterson, Brian P Higgins, et al.
Plos One|December 15, 2015
Safety and Proof-of-Concept Study of Oral QLT091001 in Retinitis Pigmentosa Due to Inherited Deficiencies of Retinal Pigment Epithelial 65 Protein (RPE65) or Lecithin:Retinol Acyltransferase (LRAT)Hendrik P N Scholl, Anthony T Moore, Robert K Koenekoop, et al.
Science Advances|June 5, 2020
Linking indirect effects of cytomegalovirus in transplantation to modulation of monocyte innate immune functionPritha Sen, Adrian R Wilkie, Fei Ji, et al.
Nature Medicine|December 28, 2004
Heart transplantation in baboons using alpha1,3-galactosyltransferase gene-knockout pigs as donors: initial experienceKenji Kuwaki, Yau-Lin Tseng, Frank J M F Dor, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 14, 2011
Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 yearsSamuel G Jacobson, Artur V Cideciyan, Ramakrishna Ratnakaram, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|March 21, 2024
Research opportunities and ethical considerations for heart and lung xenotransplantation research: A report from the National Heart, Lung, and Blood Institute workshopKiran K Khush, James L Bernat, Richard N Pierson, et al.
Investigative Ophthalmology & Visual Science|November 15, 2012
Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative diseaseKari Branham, Mohammad Othman, Matthew Brumm, et al.
Nature Genetics|July 31, 2012
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degenerationRobert K Koenekoop, Hui Wang, Jacek Majewski, et al.
Pageof 101

Showing results (981-990 of 1,001) with videos related to

Sort By:
Pageof 101
Journal of Medical Genetics|July 13, 2013
Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencingXia Wang, Hui Wang, Vincent Sun, et al.
Ophthalmology|October 29, 2015
North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13Kent W Small, Adam P DeLuca, S Scott Whitmore, et al.
Investigative Ophthalmology & Visual Science|August 2, 2016
Residual Foveal Cone Structure in CNGB3-Associated AchromatopsiaChristopher S Langlo, Emily J Patterson, Brian P Higgins, et al.
Plos One|December 15, 2015
Safety and Proof-of-Concept Study of Oral QLT091001 in Retinitis Pigmentosa Due to Inherited Deficiencies of Retinal Pigment Epithelial 65 Protein (RPE65) or Lecithin:Retinol Acyltransferase (LRAT)Hendrik P N Scholl, Anthony T Moore, Robert K Koenekoop, et al.
Science Advances|June 5, 2020
Linking indirect effects of cytomegalovirus in transplantation to modulation of monocyte innate immune functionPritha Sen, Adrian R Wilkie, Fei Ji, et al.
Nature Medicine|December 28, 2004
Heart transplantation in baboons using alpha1,3-galactosyltransferase gene-knockout pigs as donors: initial experienceKenji Kuwaki, Yau-Lin Tseng, Frank J M F Dor, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 14, 2011
Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 yearsSamuel G Jacobson, Artur V Cideciyan, Ramakrishna Ratnakaram, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|March 21, 2024
Research opportunities and ethical considerations for heart and lung xenotransplantation research: A report from the National Heart, Lung, and Blood Institute workshopKiran K Khush, James L Bernat, Richard N Pierson, et al.
Investigative Ophthalmology & Visual Science|November 15, 2012
Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative diseaseKari Branham, Mohammad Othman, Matthew Brumm, et al.
Nature Genetics|July 31, 2012
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degenerationRobert K Koenekoop, Hui Wang, Jacek Majewski, et al.
Pageof 101