5 results for author:"Brok-Simoni F." in Literature citations
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| Coinheritance of BRCA1 and BRCA2 mutations with Fanconi anemia and Bloom syndrome mutations in Ashkenazi Jewish population: possible role in risk modification for cancer development. Koren-Michowitz M., Friedman E., Gershoni-Baruch R., Brok-Simoni F., Patael Y., Rechavi G., Amariglio N. Am. J. Hematol. 78:203-206(2005) · Mapped (26) |
| MYH9 spectrum of autosomal-dominant giant platelet syndromes: unexpected association with fibulin-1 variant-D inactivation. Toren A., Rozenfeld-Granot G., Heath K.E., Amariglio N., Rocca B., Crosson J., Epstein C.J., Laghi F., Landolfi R., Carlsson L.E. et al. Am. J. Hematol. 74:254-262(2003) · Mapped (12) |
| MAP kinase activation by mu opioid receptor in cord blood CD34(+)CD38(-) cells. Rozenfeld-Granot G., Toren A., Amariglio N., Nagler A., Rosenthal E., Biniaminov M., Brok-Simoni F., Rechavi G. Exp. Hematol. 30:473-480(2002) · Mapped (10) |
| Nuclear membrane protein LAP2beta mediates transcriptional repression alone and together with its binding partner GCL (germ-cell-less). Nili E., Cojocaru G.S., Kalma Y., Ginsberg D., Copeland N.G., Gilbert D.J., Jenkins N.A., Berger R., Shaklai S., Amariglio N. et al. J. Cell Sci. 114:3297-3307(2001) · UniProtKB (2) · Mapped (42) |
| The characterization and localization of the mouse thymopoietin/lamina-associated polypeptide 2 gene and its alternatively spliced products. Berger R., Theodor L., Shoham J., Gokkel E., Brok-Simoni F., Avraham K.B., Copeland N.G., Jenkins N.A., Rechavi G., Simon A.J. |