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Page 1
Ataxia-telangiectasia: founder effect among north African Jews.
Gilad S, Bar-Shira A, Harnik R, Shkedy D, Ziv Y, Khosravi R, Brown K, Vanagaite L, Xu G, Frydman M, Lavin MF, Hill D, Tagle DA, Shiloh Y. Gilad S, et al. Among authors: shkedy d. Hum Mol Genet. 1996 Dec;5(12):2033-7. doi: 10.1093/hmg/5.12.2033. Hum Mol Genet. 1996. PMID: 8968760
Predominance of null mutations in ataxia-telangiectasia.
Gilad S, Khosravi R, Shkedy D, Uziel T, Ziv Y, Savitsky K, Rotman G, Smith S, Chessa L, Jorgensen TJ, Harnik R, Frydman M, Sanal O, Portnoi S, Goldwicz Z, Jaspers NG, Gatti RA, Lenoir G, Lavin MF, Tatsumi K, Wegner RD, Shiloh Y, Bar-Shira A. Gilad S, et al. Among authors: shkedy d. Hum Mol Genet. 1996 Apr;5(4):433-9. doi: 10.1093/hmg/5.4.433. Hum Mol Genet. 1996. PMID: 8845835 Free article.
Identification of ATM mutations using extended RT-PCR and restriction endonuclease fingerprinting, and elucidation of the repertoire of A-T mutations in Israel.
Gilad S, Khosravi R, Harnik R, Ziv Y, Shkedy D, Galanty Y, Frydman M, Levi J, Sanal O, Chessa L, Smeets D, Shiloh Y, Bar-Shira A. Gilad S, et al. Among authors: shkedy d. Hum Mutat. 1998;11(1):69-75. doi: 10.1002/(SICI)1098-1004(1998)11:1<69::AID-HUMU11>3.0.CO;2-X. Hum Mutat. 1998. PMID: 9450906
Requirement of ATM-dependent monoubiquitylation of histone H2B for timely repair of DNA double-strand breaks.
Moyal L, Lerenthal Y, Gana-Weisz M, Mass G, So S, Wang SY, Eppink B, Chung YM, Shalev G, Shema E, Shkedy D, Smorodinsky NI, van Vliet N, Kuster B, Mann M, Ciechanover A, Dahm-Daphi J, Kanaar R, Hu MC, Chen DJ, Oren M, Shiloh Y. Moyal L, et al. Among authors: shkedy d. Mol Cell. 2011 Mar 4;41(5):529-42. doi: 10.1016/j.molcel.2011.02.015. Mol Cell. 2011. PMID: 21362549 Free PMC article.
Regulation of Elg1 activity by phosphorylation.
Shkedy D, Singh N, Shemesh K, Amir A, Geiger T, Liefshitz B, Harari Y, Kupiec M. Shkedy D, et al. Cell Cycle. 2015;14(23):3689-97. doi: 10.1080/15384101.2015.1068475. Cell Cycle. 2015. PMID: 26177013 Free PMC article.
17 results