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G Jacobson

Showing results (521-530 of 677) with videos related to

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Human Molecular Genetics|April 18, 2003
Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal laminationSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|October 3, 2009
Normal central retinal function and structure preserved in retinitis pigmentosaSamuel G Jacobson, Alejandro J Roman, Tomas S Aleman, et al.
Experimental Eye Research|February 5, 2003
In vivo micropathology of Best macular dystrophy with optical coherence tomographyMichael J Pianta, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|January 2, 2007
RDH12 and RPE65, visual cycle genes causing leber congenital amaurosis, differ in disease expressionSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Nature Genetics|April 16, 1998
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosisC L Freund, Q L Wang, S Chen, et al.
Investigative Ophthalmology & Visual Science|November 6, 1998
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) geneS G Jacobson, A V Cideciyan, Y Huang, et al.
Investigative Ophthalmology & Visual Science|July 31, 2014
TULP1 mutations causing early-onset retinal degeneration: preserved but insensitive macular conesSamuel G Jacobson, Artur V Cideciyan, Wei Chieh Huang, et al.
Clinical Genetics|March 13, 2003
USH1C: a rare cause of USH1 in a non-Acadian population and a founder effect of the Acadian alleleX M Ouyang, J F Hejtmancik, S G Jacobson, et al.
Investigative Ophthalmology & Visual Science|December 13, 2022
Photoreceptor Function and Structure in Autosomal Dominant Vitelliform Macular Dystrophy Caused by BEST1 MutationsArtur V Cideciyan, Samuel G Jacobson, Malgorzata Swider, et al.
The New England Journal of Medicine|October 9, 1986
Cardiac allotransplantation in newborns as therapy for hypoplastic left heart syndromeL L Bailey, S L Nehlsen-Cannarella, R W Doroshow, et al.
Pageof 68

Showing results (521-530 of 677) with videos related to

Sort By:
Pageof 68
Human Molecular Genetics|April 18, 2003
Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal laminationSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|October 3, 2009
Normal central retinal function and structure preserved in retinitis pigmentosaSamuel G Jacobson, Alejandro J Roman, Tomas S Aleman, et al.
Experimental Eye Research|February 5, 2003
In vivo micropathology of Best macular dystrophy with optical coherence tomographyMichael J Pianta, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|January 2, 2007
RDH12 and RPE65, visual cycle genes causing leber congenital amaurosis, differ in disease expressionSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Nature Genetics|April 16, 1998
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosisC L Freund, Q L Wang, S Chen, et al.
Investigative Ophthalmology & Visual Science|November 6, 1998
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) geneS G Jacobson, A V Cideciyan, Y Huang, et al.
Investigative Ophthalmology & Visual Science|July 31, 2014
TULP1 mutations causing early-onset retinal degeneration: preserved but insensitive macular conesSamuel G Jacobson, Artur V Cideciyan, Wei Chieh Huang, et al.
Clinical Genetics|March 13, 2003
USH1C: a rare cause of USH1 in a non-Acadian population and a founder effect of the Acadian alleleX M Ouyang, J F Hejtmancik, S G Jacobson, et al.
Investigative Ophthalmology & Visual Science|December 13, 2022
Photoreceptor Function and Structure in Autosomal Dominant Vitelliform Macular Dystrophy Caused by BEST1 MutationsArtur V Cideciyan, Samuel G Jacobson, Malgorzata Swider, et al.
The New England Journal of Medicine|October 9, 1986
Cardiac allotransplantation in newborns as therapy for hypoplastic left heart syndromeL L Bailey, S L Nehlsen-Cannarella, R W Doroshow, et al.
Pageof 68