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Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopia.
Erjavec E, Angée C, Hadjadj D, Passet B, David P, Kostic C, Dodé E, Zanlonghi X, Cagnard N, Nedelec B, Crippa SV, Bole-Feysot C, Zarhrate M, Creuzet S, Castille J, Vilotte JL, Calvas P, Plaisancié J, Chassaing N, Kaplan J, Rozet JM, Taie LF. Erjavec E, et al. Among authors: kostic c. Am J Hum Genet. 2024 Oct 3;111(10):2265-2282. doi: 10.1016/j.ajhg.2024.08.019. Epub 2024 Sep 17. Am J Hum Genet. 2024. PMID: 39293448
Remaining rod activity mediates visual behavior in adult Rpe65-/- mice.
Cachafeiro M, Bemelmans AP, Canola K, Pignat V, Crippa SV, Kostic C, Arsenijevic Y. Cachafeiro M, et al. Among authors: kostic c. Invest Ophthalmol Vis Sci. 2010 Dec;51(12):6835-42. doi: 10.1167/iovs.09-3870. Epub 2010 Aug 11. Invest Ophthalmol Vis Sci. 2010. PMID: 20702833 Free article.
Lentiviral vectors containing a retinal pigment epithelium specific promoter for leber congenital amaurosis gene therapy. Lentiviral gene therapy for LCA.
Bemelmans AP, Kostic C, Hornfeld D, Jaquet M, Crippa SV, Hauswirth WW, Lem J, Wang Z, Schorderet DE, Munier FL, Wenzel A, Arsenijevic Y. Bemelmans AP, et al. Among authors: kostic c. Adv Exp Med Biol. 2006;572:247-53. doi: 10.1007/0-387-32442-9_35. Adv Exp Med Biol. 2006. PMID: 17249581 No abstract available.
43 results