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J Roman

Showing results (1111-1120 of 1,201) with videos related to

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International Journal of Cardiology|July 23, 2013
Genome-wide linkage analysis of carotid artery lumen diameter: the strong heart family studyJonathan N Bella, Shelley A Cole, Sandy Laston, et al.
European Journal of Echocardiography : the Journal of the Working Group on Echocardiography of the European Society of Cardiology|February 7, 2006
Recommendations for chamber quantificationRoberto M Lang, Michelle Bierig, Richard B Devereux, et al.
Investigative Ophthalmology & Visual Science|January 27, 2005
Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotypeSharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
The Journal of Biological Chemistry|December 31, 1997
An autoinhibitory control element defines calcium-regulated isoforms of nitric oxide synthaseJ C Salerno, D E Harris, K Irizarry, et al.
Nano Letters|March 29, 2023
Plasmonic Response of Complex Nanoparticle AssembliesZachary M Sherman, Kihoon Kim, Jiho Kang, et al.
Frontiers in Epidemiology|October 23, 2025
Carotid artery atherosclerosis, MRI-defined structural brain abnormalities, and cognitive performance in elderly American Indians: The Strong Heart StudyTauqeer Ali, Dedra Buchwald, Dean Shibata, et al.
Investigative Ophthalmology & Visual Science|December 22, 2023
Treatment Strategy With Gene Editing for Late-Onset Retinal Degeneration Caused by a Founder Variant in C1QTNF5Randa T H Li, Alejandro J Roman, Alexander Sumaroka, et al.
Plos Medicine|June 28, 2007
Canine and human visual cortex intact and responsive despite early retinal blindness from RPE65 mutationGeoffrey K Aguirre, András M Komáromy, Artur V Cideciyan, et al.
Human Molecular Genetics|October 5, 2012
Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutantsSamuel G Jacobson, Artur V Cideciyan, Igor V Peshenko, et al.
Human Gene Therapy|July 9, 2009
Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 yearArtur V Cideciyan, William W Hauswirth, Tomas S Aleman, et al.
Pageof 121

Showing results (1111-1120 of 1,201) with videos related to

Sort By:
Pageof 121
International Journal of Cardiology|July 23, 2013
Genome-wide linkage analysis of carotid artery lumen diameter: the strong heart family studyJonathan N Bella, Shelley A Cole, Sandy Laston, et al.
European Journal of Echocardiography : the Journal of the Working Group on Echocardiography of the European Society of Cardiology|February 7, 2006
Recommendations for chamber quantificationRoberto M Lang, Michelle Bierig, Richard B Devereux, et al.
Investigative Ophthalmology & Visual Science|January 27, 2005
Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotypeSharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
The Journal of Biological Chemistry|December 31, 1997
An autoinhibitory control element defines calcium-regulated isoforms of nitric oxide synthaseJ C Salerno, D E Harris, K Irizarry, et al.
Nano Letters|March 29, 2023
Plasmonic Response of Complex Nanoparticle AssembliesZachary M Sherman, Kihoon Kim, Jiho Kang, et al.
Frontiers in Epidemiology|October 23, 2025
Carotid artery atherosclerosis, MRI-defined structural brain abnormalities, and cognitive performance in elderly American Indians: The Strong Heart StudyTauqeer Ali, Dedra Buchwald, Dean Shibata, et al.
Investigative Ophthalmology & Visual Science|December 22, 2023
Treatment Strategy With Gene Editing for Late-Onset Retinal Degeneration Caused by a Founder Variant in C1QTNF5Randa T H Li, Alejandro J Roman, Alexander Sumaroka, et al.
Plos Medicine|June 28, 2007
Canine and human visual cortex intact and responsive despite early retinal blindness from RPE65 mutationGeoffrey K Aguirre, András M Komáromy, Artur V Cideciyan, et al.
Human Molecular Genetics|October 5, 2012
Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutantsSamuel G Jacobson, Artur V Cideciyan, Igor V Peshenko, et al.
Human Gene Therapy|July 9, 2009
Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 yearArtur V Cideciyan, William W Hauswirth, Tomas S Aleman, et al.
Pageof 121