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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 Nov 3;99(5):1222-1223. doi: 10.1016/j.ajhg.2016.09.012. Am J Hum Genet. 2016. PMID: 27814526 Free PMC article. 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.
Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies.
Beryozkin A, Shevah E, Kimchi A, Mizrahi-Meissonnier L, Khateb S, Ratnapriya R, Lazar CH, Blumenfeld A, Ben-Yosef T, Hemo Y, Pe'er J, Averbuch E, Sagi M, Boleda A, Gieser L, Zlotogorski A, Falik-Zaccai T, Alimi-Kasem O, Jacobson SG, Chowers I, Swaroop A, Banin E, Sharon D. Beryozkin A, et al. Among authors: khateb s. Sci Rep. 2015 Aug 26;5:13187. doi: 10.1038/srep13187. Sci Rep. 2015. PMID: 26306921 Free PMC article.
The Genetics of Usher Syndrome in the Israeli and Palestinian Populations.
Khalaileh A, Abu-Diab A, Ben-Yosef T, Raas-Rothschild A, Lerer I, Alswaiti Y, Chowers I, Banin E, Sharon D, Khateb S. Khalaileh A, et al. Among authors: khateb s. Invest Ophthalmol Vis Sci. 2018 Feb 1;59(2):1095-1104. doi: 10.1167/iovs.17-22817. Invest Ophthalmol Vis Sci. 2018. PMID: 29490346
55 results