Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Evelyn P. Semenov"'
Autor:
Alejandro J. Roman, Rebecca Sheplock, Alexandra V. Garafalo, Evelyn P. Semenov, Alexander Sumaroka, Samuel G. Jacobson, Arun kumar Krishnan, Artur V. Cideciyan
Publikováno v:
Investigative Ophthalmology & Visual Science
Purpose To use supervised machine learning to predict visual function from retinal structure in retinitis pigmentosa (RP) and apply these estimates to CEP290- and NPHP5-associated Leber congenital amaurosis (LCA) to determine the potential for functi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4774928bf9d0ffed4ec04851772a1d3
https://pubmed.ncbi.nlm.nih.gov/31212307
https://pubmed.ncbi.nlm.nih.gov/31212307
Autor:
Alejandro J, Roman, Christian A, Powers, Evelyn P, Semenov, Rebecca, Sheplock, Valeryia, Aksianiuk, Robert C, Russell, Alexander, Sumaroka, Alexandra V, Garafalo, Artur V, Cideciyan, Samuel G, Jacobson
Publikováno v:
International Journal of Molecular Sciences
Recessively-inherited NR2E3 gene mutations cause an unusual retinopathy with abnormally-increased short-wavelength sensitive cone (S-cone) function, in addition to reduced rod and long/middle-wavelength sensitive cone (L/M-cone) function. Progress to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::77dc7f86d2811e5c9bf53c1a2aeeab3b
https://pubmed.ncbi.nlm.nih.gov/31117170
https://pubmed.ncbi.nlm.nih.gov/31117170
Autor:
Alejandro J. Roman, Rebecca Sheplock, Evelyn P. Semenov, Artur V. Cideciyan, David B. McGuigan, Samuel G. Jacobson, Malgorzata Swider
Publikováno v:
Translational Vision Science & Technology
Purpose Blue cone monochromacy (BCM), a congenital X-linked retinal disease caused by mutations in the OPN1LW/OPN1MW gene cluster, is under consideration for intravitreal gene therapy. Difficulties with near vision tasks experienced by these patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af79ef8a546755373704447339c10458
https://doi.org/10.1167/tvst.9.13.13
https://doi.org/10.1167/tvst.9.13.13
Autor:
Alexandra V. Garafalo, Alexander Sumaroka, Christian A. Powers, Samuel G. Jacobson, Alejandro J. Roman, Evelyn P. Semenov, Artur V. Cideciyan, Robert C. Russell, Rebecca Sheplock, Valeryia Aksianiuk
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 10, p 2497 (2019)
Recessively-inherited NR2E3 gene mutations cause an unusual retinopathy with abnormally-increased short-wavelength sensitive cone (S-cone) function, in addition to reduced rod and long/middle-wavelength sensitive cone (L/M-cone) function. Progress to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15097d8cd7e299868ce434b07497c4a1
https://doi.org/10.3390/ijms20102497
https://doi.org/10.3390/ijms20102497
Autor:
Roman, Alejandro J.1 aroman@pennmedicine.upenn.edu, Powers, Christian A.1, Semenov, Evelyn P.1, Sheplock, Rebecca1, Aksianiuk, Valeryia1, Russell, Robert C.1, Sumaroka, Alexander1, Garafalo, Alexandra V.1, Cideciyan, Artur V.1, Jacobson, Samuel G.1 jacobsos@pennmedicine.upenn.edu
Publikováno v:
International Journal of Molecular Sciences. May2019, Vol. 20 Issue 10, p2497. 1p. 1 Diagram, 3 Graphs.