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Page 1
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects.
Simon AJ, Lev A, Zhang Y, Weiss B, Rylova A, Eyal E, Kol N, Barel O, Cesarkas K, Soudack M, Greenberg-Kushnir N, Rhodes M, Wiest DL, Schiby G, Barshack I, Katz S, Pras E, Poran H, Reznik-Wolf H, Ribakovsky E, Simon C, Hazou W, Sidi Y, Lahad A, Katzir H, Sagie S, Aqeilan HA, Glousker G, Amariglio N, Tzfati Y, Selig S, Rechavi G, Somech R. Simon AJ, et al. Among authors: rechavi g. J Exp Med. 2016 Jul 25;213(8):1429-40. doi: 10.1084/jem.20151618. Epub 2016 Jul 18. J Exp Med. 2016. PMID: 27432940 Free PMC article.
GLI3 is not mutated commonly in sporadic medulloblastomas.
Erez A, Ilan T, Amariglio N, Muler I, Brok-Simoni F, Rechavi G, Izraeli S. Erez A, et al. Among authors: rechavi g. Cancer. 2002 Jul 1;95(1):28-31. doi: 10.1002/cncr.10642. Cancer. 2002. PMID: 12115313 Free article.
Determination of chromosome 13 status in bone marrow cells of patients with multiple myeloma using combined morphologic and fluorescence in situ hybridization analysis.
Hardan I, Rothman R, Gelibter A, Cohen N, Shimoni A, Sokolovsky M, Reichart M, Ishoev G, Amariglio N, Rechavi G, Nagler A, Trakhtenbrot L. Hardan I, et al. Among authors: rechavi g. Exp Hematol. 2004 Mar;32(3):254-60. doi: 10.1016/j.exphem.2003.12.001. Exp Hematol. 2004. PMID: 15003310 Free article.
501 results