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KCNV2-associated retinopathy: genotype-phenotype correlations - KCNV2 study group report 3.
de Guimaraes TAC, Georgiou M, Robson AG, Fujinami K, Vincent A, Nasser F, Khateb S, Mahroo OA, Pontikos N, Vargas ME, Thiadens AAHJ, Carvalho ER, Nguyen XT, Arno G, Fujinami-Yokokawa Y, Liu X, Tsunoda K, Hayashi T, Jiménez-Rolando B, Martin-Merida MI, Avila-Fernandez A, Salas EC, Garcia-Sandoval B, Ayuso C, Sharon D, Kohl S, Huckfeldt RM, Banin E, Pennesi ME, Khan AO, Wissinger B, Webster AR, Heon E, Boon CJF, Zrenner E, Michaelides M. de Guimaraes TAC, et al. Among authors: khateb s. Br J Ophthalmol. 2024 Jul 23;108(8):1137-1144. doi: 10.1136/bjo-2023-323640. Br J Ophthalmol. 2024. PMID: 37852740 Free PMC article.
Visualizing Vitreous Traction by Biomicroscopy versus OCT.
Vofo BN, Yosef YB, Tiosano L, Levy J, Khateb S, Chowers I. Vofo BN, et al. Among authors: khateb s. Ophthalmol Retina. 2023 Dec;7(12):1116-1117. doi: 10.1016/j.oret.2023.08.020. Epub 2023 Sep 9. Ophthalmol Retina. 2023. PMID: 37673398 No abstract available.
Docking interactions of the JNK scaffold protein WDR62.
Cohen-Katsenelson K, Wasserman T, Khateb S, Whitmarsh AJ, Aronheim A. Cohen-Katsenelson K, et al. Among authors: khateb s. Biochem J. 2011 Nov 1;439(3):381-90. doi: 10.1042/BJ20110284. Biochem J. 2011. PMID: 21749326 Free PMC article.
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss.
Namburi P, Ratnapriya R, Khateb S, Lazar CH, Kinarty Y, Obolensky A, Erdinest I, Marks-Ohana D, Pras E, Ben-Yosef T, Newman H, Gross M, Swaroop A, Banin E, Sharon D. Namburi P, et al. Among authors: khateb s. Am J Hum Genet. 2016 Sep 1;99(3):777-784. doi: 10.1016/j.ajhg.2016.07.010. Am J Hum Genet. 2016. PMID: 27588452 Free PMC article.
55 results