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cancer breast brca 1 mutation carrier breast cancer risk university study genetic department rhamm research genetics service centre center hospital aurka institute figure analysis breast cancer depletion polarization result service association model netherland centrosome erasmus university rotterdam foundation acini expression oncology brca 1 depletion microtubule epithelial estimate medicine table mcf 10a cells grant tpx 2 differentiation 703-rhamm genet mutation carriers control tumor carcinogenesi protein evidence genotyping brca 2 activity brca 1 function 2 q 35 culture epithelial apicobasal polarization image family function italy experiment biology allele brca 2 carriers taqman modifier luminal consortium assay proteasome inhibition epithelial cells rhamm abundance disease apicobasal sample cimba representative bright-field images
3 Most Recent Publications
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Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer
(Article)
Maxwell, C.A. Benitez, J. Mohan, P. Buys, S.S. John, E.M. Miron, A. Southey, M.C. Daly, M. Schmutzler, R.K. Wappenschmidt, B. Meindl, A. Arnold, N. Deissler, H. Català, I. Varon-Mateeva, R. Sutter, C. Niederacher, D. Imyamitov, E. Sinilnikova, O. Stoppa-Lyonne, D. Mazoyer, S. Verny-Pierre, C. Castera, L. Pauw, A. de Petit, A. Bignon, Y.-J. Uhrhammer, N. Peyrat, J.-P. Vennin, P. Ferrer, S.F. Collonge-Rame, M.-A. Mortemousque, I. Spurdle, A.B. Beesley, J. Healey, S. Aguilar, H. Barcellos-Hoff, M.H. Vidal, M. Gruber, S.B. Lazaro, C. Capellá, G. McGuffog, L. Nathanson, K.L. Antoniou, A.C. Chenevix-Trench, G. Fleisch, M.C. Villanueva, A. Moreno, V. Pujana, M.A. Aytes, A. Serra-Musach, J. Rennert, G. Lejbkowicz, F. Peterlongo, P. Gómez-Baldó, L. Manoukian, S. Peissel, B. Ripamonti, C.B. Bonanni, B. Viel, A. Allavena, A. Bernard, L. Radice, P. Friedman, E. Kaufman, B. Osorio, A. Laitman, Y. Dubrovsky, M. Milgrom, R. Jakubowska, A. Cybulski, C. Górski, B. Jaworska, K. Durda, K. Sukiennicki, G. Lubinski, J. Bonifaci, N. Shugart, Y.Y. Domchek, S.M. Letrero, R. Weber, B.L. Hogervorst, F.B.L. Rookus, M.A. Collée, J.M. Devilee, P. Ligtenberg, M. Luijt, R.B. van der Fernández-Ramires, R. Aalfs, C. Waisfisz, Q. Wijnen, J.T. Roozendaal, C.E.P. van Easton, D.F. Peock, S. Cook, J. Oliver, C. Frost, D. Harrington, P. Costes, S.V. Lalloo, F. Eeles, R. Izatt, L. Chu, C. Eccles, D. Douglas, F. Brewer, C. Nevanlinna, H. Heikinen, T. Couch, F.J. Guinó, E. Lindor, N.M. Wang, X. Godwin, A.K. Caligo, M.A. Lombardi, G. Loman, N. Karlsson, P. Ehrencrona, H. Wachenfeldt, A. von Barkardottir, R.B. Chen, H. Hamann, U. Rashid, M.U. Lasa, A. Caldes, T. Andres, R. Schmitt, M. Assmann, V. Stevens, K. Offit, K. Curado, J. Evans, G.J.R. Tilgner, H. Guigó, R. Aiza, G. Brunet, J. Castellsagué, J. Martrat, G. Urruticoechea, A. Blanco, I. Tihomirova, L. Goldgar, D. |
2011-11-01
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Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2
(Article)
Osorio, A. Milne, R.L. Konstantopoulou, I. Hogervorst, F.B.L. Verhoef, S. Dooren, M.F. van Jager, A. Ausems, M.G.E.M. Aalfs, C. Asperen, C.J. van Vreeswijk, M.P. Waisfisz, Q. Pallás-Alonso, C.R. Roozendaal, C.E.P. van Ligtenberg, M. Easton, D.F. Peock, S. Cook, M.S. Oliver, C.T. Frost, D. Curzon, B. Evans, D.G. Lalloo, F. Pita, G. Eeles, R. Izatt, L. Davidson, R. Adlard, J.W. Eccles, D. Ong, K.R. Douglas, F. Downing, S. Brewer, C. Walker, L. Peterlongo, P. Nevanlinna, H. Aittomäki, K. Couch, F.J. Fredericksen, Z. Lindor, N.M. Godwin, A.K. Isaacs, C. Caligo, M.A. Loman, N. Jernström, H. Teulé, A. Barbany-Bustinza, G. Liljegren, A. Ehrencrona, H. Stenmark-Askmalm, M. Feliubadaló, L. Manoukian, S. Peissel, B. Zaffaroni, D. Bonanni, B. Fortuzzi, S. Nathanson, K.L. Johannsson, O.T. Chenevix-Trench, G. Chen, X.C. Beesley, J. Spurdle, A.B. Sinilnikova, O. Healey, S. McGuffog, L. Antoniou, A.C. Brunet, J. Domchek, S.M. Radice, P. Benítez, J. Rebbeck, T.R. Lasa, A. |
2011-05-01
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Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
(Article)
Antoniou, A.C. Sinilnikova, O. Neuhausen, S.L. Gschwantler-Kaulich, D. Staudigl, C. Hansen, T.V.O. Barkardottir, R.B. Kirchhoff, T. Pal, P. Kosarin, K. Offit, K. Piedmonte, M. Rodriguez, G.C. Ding, Y.C. Wakeley, K. Boggess, J.F. Basil, J. Schwartz, P.E. Blank, S.V. Toland, A.E. Montagna, M. Casella, C. Imyanitov, E.N. Allavena, A. Couch, F.J. Schmutzler, R.K. Versmold, B. Engel, C. Meindl, A. Ditsch, N. Arnold, N. Niederacher, D. Deissler, H. Fiebig, B. Suttner, C. Wang, X. Schönbuchner, I. Gadzicki, D. Caldes, T. Hoya, M. de La Pooley, K.A. Easton, D.F. Fredericksen, Z. Peterlongo, P. Peissel, B. Bonanni, B. Viel, A. Bernard, L. McGuffog, L. Radice, P. Szabo, C. Foretova, L. Zikan, M. Claes, K. Greene, M.H. Mai, P.L. Rennert, G. Lejbkowicz, F. Andrulis, I.L. Healey, S. Ozcelik, H. Glendon, G. Gerdes, A-M. Thomassen, M. Sunde, L. Caligo, M.A. Laitman, Y. Kontorovich, T. Cohen, S. Kaufman, B. Nevanlinna, H. Dagan, E. Baruch, R.G. Friedman, E. Harbst, K. Barbany-Bustinza, G. Rantala, J. Ehrencrona, H. Karlsson, P. Domchek, S.M. Nathanson, K.L. Heikinen, T. Osorio, A. Blanco, I. Lasa, A. Benitez, J. Hamann, U. Hogervorst, F.B.L. Rookus, M.A. Collee, J.M. Devilee, P. Ligtenberg, M. Simard, J. Luijt, R.B. van der Aalfs, C. Waisfisz, Q. Wijnen, J.T. Roozendaal, C.E.P. van Peock, S. Cook, J. Frost, D. Oliver, C. Platte, R. Spurdle, A.B. Evans, D.G. Lalloo, F. Eeles, R. Izatt, L. Davidson, R. Chu, C. Eccles, D. Cole, T.J. Hodgson, S.V. Godwin, A.K. Beesley, J. Stoppa-Lyonnet, D. Buecher, B. Léoné, M. Bressac-de Paillerets, B. Remenieras, A. Caron, O. Lenoir, G.M. Sevenet, N. Longy, M. Ferrer, S.F. Chenevix-Trench, G. Prieur, F. Goldgar, D. Miron, A. John, E.M. Buys, S.S. Daly, M. Hopper, J. Terry, M-B. Yassin, Y. Singer, C.F. |
2009-11-16
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