Rowlan JS - Search Results

1

A novel form of progressive retinal atrophy in Swedish vallhund dogs.

Cooper AE, Ahonen S, Rowlan JS, Duncan A, Seppälä EH, Vanhapelto P, Lohi H, Komáromy AM. Cooper AE, et al. Among authors: rowlan js. PLoS One. 2014 Sep 8;9(9):e106610. doi: 10.1371/journal.pone.0106610. eCollection 2014. PLoS One. 2014. PMID: 25198798 Free PMC article.

2

Gene therapy rescues cone function in congenital achromatopsia.

Komáromy AM, Alexander JJ, Rowlan JS, Garcia MM, Chiodo VA, Kaya A, Tanaka JC, Acland GM, Hauswirth WW, Aguirre GD. Komáromy AM, et al. Among authors: rowlan js. Hum Mol Genet. 2010 Jul 1;19(13):2581-93. doi: 10.1093/hmg/ddq136. Epub 2010 Apr 8. Hum Mol Genet. 2010. PMID: 20378608 Free PMC article.

3

Equine Multiple Congenital Ocular Anomalies (MCOA) syndrome in PMEL17 (Silver) mutant ponies: five cases.

Komáromy AM, Rowlan JS, La Croix NC, Mangan BG. Komáromy AM, et al. Among authors: rowlan js. Vet Ophthalmol. 2011 Sep;14(5):313-20. doi: 10.1111/j.1463-5224.2011.00878.x. Epub 2011 Apr 18. Vet Ophthalmol. 2011. PMID: 21929608 Free PMC article.

4

Transient photoreceptor deconstruction by CNTF enhances rAAV-mediated cone functional rescue in late stage CNGB3-achromatopsia.

Komáromy AM, Rowlan JS, Corr AT, Reinstein SL, Boye SL, Cooper AE, Gonzalez A, Levy B, Wen R, Hauswirth WW, Beltran WA, Aguirre GD. Komáromy AM, et al. Among authors: rowlan js. Mol Ther. 2013 Jun;21(6):1131-41. doi: 10.1038/mt.2013.50. Epub 2013 Apr 9. Mol Ther. 2013. PMID: 23568263 Free PMC article.

5

Role of a Dual Splicing and Amino Acid Code in Myopia, Cone Dysfunction and Cone Dystrophy Associated with L/M Opsin Interchange Mutations.

Greenwald SH, Kuchenbecker JA, Rowlan JS, Neitz J, Neitz M. Greenwald SH, et al. Among authors: rowlan js. Transl Vis Sci Technol. 2017 May 10;6(3):2. doi: 10.1167/tvst.6.3.2. eCollection 2017 May. Transl Vis Sci Technol. 2017. PMID: 28516000 Free PMC article.

6

CFH Haploinsufficiency and Complement Alterations in Early-Onset Macular Degeneration.

Lim RR, Shirali S, Rowlan J, Engel AL, Nazario M Jr, Gonzalez K, Tong A, Neitz J, Neitz M, Chao JR. Lim RR, et al. Invest Ophthalmol Vis Sci. 2024 Apr 1;65(4):43. doi: 10.1167/iovs.65.4.43. Invest Ophthalmol Vis Sci. 2024. PMID: 38683564 Free PMC article.

7

[No title available]

[No authors listed] [No authors listed] PMID: 38109582

8

Tritan color vision deficiency may be associated with an OPN1SW splicing defect and haploinsufficiency.

Neitz M, Krekling ED, Hagen LA, Pedersen HR, Rowlan J, Barborek R, Neitz J, Crain A, Baraas RC. Neitz M, et al. J Opt Soc Am A Opt Image Sci Vis. 2020 Apr 1;37(4):A26-A34. doi: 10.1364/JOSAA.381919. J Opt Soc Am A Opt Image Sci Vis. 2020. PMID: 32400513 Free PMC article.

9

Insight from OPN1LW Gene Haplotypes into the Cause and Prevention of Myopia.

Neitz M, Wagner-Schuman M, Rowlan JS, Kuchenbecker JA, Neitz J. Neitz M, et al. Among authors: rowlan js. Genes (Basel). 2022 May 25;13(6):942. doi: 10.3390/genes13060942. Genes (Basel). 2022. PMID: 35741704 Free PMC article.

10

Effects of color-enhancing glasses on color vision in congenital red-green color deficiencies.

Patterson EJ, Mastey RR, Kuchenbecker JA, Rowlan J, Neitz J, Neitz M, Carroll J. Patterson EJ, et al. Opt Express. 2022 Aug 15;30(17):31182-31194. doi: 10.1364/OE.451295. Opt Express. 2022. PMID: 36242206 Free PMC article.

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