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3,619 results

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Multiexon deletion alleles of ATF6 linked to achromatopsia.
Lee EJ, Chiang WJ, Kroeger H, Bi CX, Chao DL, Skowronska-Krawczyk D, Mastey RR, Tsang SH, Chea L, Kim K, Lambert SR, Grandjean JM, Baumann B, Audo I, Kohl S, Moore AT, Wiseman RL, Carroll J, Lin JH. Lee EJ, et al. Among authors: carroll j. JCI Insight. 2020 Apr 9;5(7):e136041. doi: 10.1172/jci.insight.136041. JCI Insight. 2020. PMID: 32271167 Free PMC article. Clinical Trial.
Integrity of the cone photoreceptor mosaic in oligocone trichromacy.
Michaelides M, Rha J, Dees EW, Baraas RC, Wagner-Schuman ML, Mollon JD, Dubis AM, Andersen MK, Rosenberg T, Larsen M, Moore AT, Carroll J. Michaelides M, et al. Among authors: carroll j. Invest Ophthalmol Vis Sci. 2011 Jul 1;52(7):4757-64. doi: 10.1167/iovs.10-6659. Invest Ophthalmol Vis Sci. 2011. PMID: 21436275 Free PMC article.
Photoreceptor structure and function in patients with congenital achromatopsia.
Genead MA, Fishman GA, Rha J, Dubis AM, Bonci DM, Dubra A, Stone EM, Neitz M, Carroll J. Genead MA, et al. Among authors: carroll j. Invest Ophthalmol Vis Sci. 2011 Sep 21;52(10):7298-308. doi: 10.1167/iovs.11-7762. Invest Ophthalmol Vis Sci. 2011. PMID: 21778272 Free PMC article.
Assessing retinal structure in complete congenital stationary night blindness and Oguchi disease.
Godara P, Cooper RF, Sergouniotis PI, Diederichs MA, Streb MR, Genead MA, McAnany JJ, Webster AR, Moore AT, Dubis AM, Neitz M, Dubra A, Stone EM, Fishman GA, Han DP, Michaelides M, Carroll J. Godara P, et al. Among authors: carroll j. Am J Ophthalmol. 2012 Dec;154(6):987-1001.e1. doi: 10.1016/j.ajo.2012.06.003. Epub 2012 Sep 7. Am J Ophthalmol. 2012. PMID: 22959359 Free PMC article.
The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic.
Carroll J, Dubra A, Gardner JC, Mizrahi-Meissonnier L, Cooper RF, Dubis AM, Nordgren R, Genead M, Connor TB Jr, Stepien KE, Sharon D, Hunt DM, Banin E, Hardcastle AJ, Moore AT, Williams DR, Fishman G, Neitz J, Neitz M, Michaelides M. Carroll J, et al. Invest Ophthalmol Vis Sci. 2012 Dec 5;53(13):8006-15. doi: 10.1167/iovs.12-11087. Invest Ophthalmol Vis Sci. 2012. PMID: 23139274 Free PMC article.
Human cone visual pigment deletions spare sufficient photoreceptors to warrant gene therapy.
Cideciyan AV, Hufnagel RB, Carroll J, Sumaroka A, Luo X, Schwartz SB, Dubra A, Land M, Michaelides M, Gardner JC, Hardcastle AJ, Moore AT, Sisk RA, Ahmed ZM, Kohl S, Wissinger B, Jacobson SG. Cideciyan AV, et al. Among authors: carroll j. Hum Gene Ther. 2013 Dec;24(12):993-1006. doi: 10.1089/hum.2013.153. Epub 2013 Oct 30. Hum Gene Ther. 2013. PMID: 24067079 Free PMC article.
Retinal structure and function in achromatopsia: implications for gene therapy.
Sundaram V, Wilde C, Aboshiha J, Cowing J, Han C, Langlo CS, Chana R, Davidson AE, Sergouniotis PI, Bainbridge JW, Ali RR, Dubra A, Rubin G, Webster AR, Moore AT, Nardini M, Carroll J, Michaelides M. Sundaram V, et al. Among authors: carroll j. Ophthalmology. 2014 Jan;121(1):234-245. doi: 10.1016/j.ophtha.2013.08.017. Epub 2013 Oct 20. Ophthalmology. 2014. PMID: 24148654 Free PMC article.
A prospective longitudinal study of retinal structure and function in achromatopsia.
Aboshiha J, Dubis AM, Cowing J, Fahy RT, Sundaram V, Bainbridge JW, Ali RR, Dubra A, Nardini M, Webster AR, Moore AT, Rubin G, Carroll J, Michaelides M. Aboshiha J, et al. Among authors: carroll j. Invest Ophthalmol Vis Sci. 2014 Aug 7;55(9):5733-43. doi: 10.1167/iovs.14-14937. Invest Ophthalmol Vis Sci. 2014. PMID: 25103266 Free PMC article.
3,619 results