Breast cancer risk in BRCA1 and BRCA2 mutation carriers and polyglutamine repeat length in the AIB1 gene by Hughes, David J., Ginolhac, Sophie M., Coupier, Isabelle, Barjhoux, Laure, Gaborieau, Valérie, Bressac‐de‐Paillerets, Brigitte, Chompret, Agnès, Bignon, Yves‐Jean, Uhrhammer, Nancy, Lasset, Christine, Giraud, Sophie, Sobol, Hagay, Hardouin, Agnès, Berthet, Pascaline, Peyrat, Jean‐Philippe, Fournier, Joelle, Nogues, Catherine, Lidereau, Rosette, Muller, Danièle, Fricker, Jean‐Pierre, Longy, Michel, Toulas, Christine, Guimbaud, Rosine, Yannoukakos, Drakoulis, Mazoyer, Sylvie, Lynch, Henry T., Lenoir, Gilbert M., Goldgar, David E., Stoppa‐Lyonnet, Dominique, Sinilnikova, Olga M.

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Genomic Structure and Promoter Characterization of the Human ACTH Receptor Gene by Naville, Danielle, Jaillard, Christine, Barjhoux, Laure, Durand, Philippe, Bégeot, Martine

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Demonstration by transfection studies that mutations in the adrenocorticotropin receptor gene are one cause of the hereditary syndrome of glucocorticoid deficiency by NAVILLE, D, BARJHOUX, L, JAILLARD, C, FAURY, D, DESPERT, F, ESTEVA, B, DURAND, P, SAEZ, J. M, BEGEOT, M

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Estimation of the RNU2 macrosatellite mutation rate by BRCA1 mutation tracing by Tessereau, Chloé, Lesecque, Yann, Monnet, Nastasia, Buisson, Monique, Barjhoux, Laure, Léoné, Mélanie, Feng, Bingjian, Goldgar, David E, Sinilnikova, Olga M, Mousset, Sylvain, Duret, Laurent, Mazoyer, Sylvie

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Mutation analysis of PALB2 gene in French breast cancer families by Damiola, Francesca, Schultz, Inès, Barjhoux, Laure, Sornin, Valérie, Dondon, Marie-Gabrielle, Eon-Marchais, Séverine, Marcou, Morgane, Caron, Olivier, Gauthier-Villars, Marion, de Pauw, Antoine, Luporsi, Elisabeth, Berthet, Pascaline, Delnatte, Capucine, Bonadona, Valérie, Maugard, Christine, Pujol, Pascal, Lasset, Christine, Longy, Michel, Bignon, Yves-Jean, Fricker, Jean-Pierre, Andrieu, Nadine, Sinilnikova, Olga M., Stoppa-Lyonnet, Dominique, Mazoyer, Sylvie, Muller, Danièle

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Stable expression of normal and mutant human ACTH receptor: Study of ACTH binding and coupling to adenylate cyclase by Naville, Danielle, Barjhoux, Laure, Jaillard, Christine, Saez, José M, Durand, Philippe, Bégeot, Martine

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Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study by Jakubowska, A, Rozkrut, D, Hamann, U, Scott, R J, McGuffog, L, Healy, S, Sinilnikova, O M, Rennert, G, Lejbkowicz, F, Flugelman, A, Andrulis, I L, Glendon, G, Ozcelik, H, Thomassen, M, Paligo, M, Kantala, J, Aroer, B, von Wachenfeldt, A, Loman, N, Herbst, K, Kristoffersson, U, Rosenquist, R, Karlsson, P, Stenmark-Askmalm, M, Melin, B, Nathanson, K L, Domchek, S M, Byrski, T, Huzarski, T, Gronwald, J, Menkiszak, J, Cybulski, C, Serrano, P, Cajal, T R, Tsitlaidou, M, Benítez, J, Rookus, M, Kluijt, I, Boessenkool-Pape, J L, Meijers-Heijboer, H E J, Oosterwijk, J C, van Asperen, C J, Nelen, M R, van den Ouweland, A M W, Seynaeve, C, Easton, D F, Frost, D, Platte, R, Ellis, S D, Fineberg, E, Evans, D G, Lalloo, F, Eeles, R, Jacobs, C, Adlard, J, Davidson, R, Eccles, D, Cole, T, Cook, J, Godwin, A, Bove, B, Stoppa-Lyonnet, D, Caux-Moncoutier, V, Belotti, M, Tirapo, C, Barjhoux, L, Pujol, P, Coupier, I, Peyrat, J-P, Vennin, P, Fricker, J-P, Venat-Bouvet, L, Johannsson, O Th, Isaacs, C, Schmutzler, R, Wappenschmidt, B, Meindl, A, Arnold, N, Varon-Mateeva, R, Niederacher, D, Sutter, C, Deissler, H, Preisler-Adams, S, Simard, J, Durocher, F, Beesley, J, Chen, X, Rebbeck, T, Couch, F, Wang, X, Lindor, N, Fredericksen, Z, Pankratz, V S, Peterlongo, P, Bonanni, B, Fortuzzi, S, Peissel, B, Szabo, C, Mai, P L, Loud, J T

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Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers by Cox, David G., Simard, Jacques, Hamdi, Yosr, Soucy, Penny, Ouimet, Manon, Barjhoux, Laure, Verny-Pierre, Carole, McGuffog, Lesley, Healey, Sue, Greene, Mark H., Mai, Phuong L., Thomassen, Mads, Gerdes, Anne-Marie, Caligo, Maria A., Friedman, Eitan, Laitman, Yael, Kaufman, Bella, Paluch, Shani S., Borg, Åke, Karlsson, Per, Stenmark Askmalm, Marie, Barbany Bustinza, Gisela, Nathanson, Katherine L., Domchek, Susan M., Rebbeck, Timothy R., Benítez, Javier, Hamann, Ute, Rookus, Matti A., van den Ouweland, Ans M.W., Ausems, Margreet G.E.M., Aalfs, Cora M., van Asperen, Christi J., Devilee, Peter, Gille, Hans J.J.P., Peock, Susan, Frost, Debra, Evans, D. Gareth, Eeles, Ros, Izatt, Louise, Adlard, Julian, Paterson, Joan, Eason, Jacqueline, Godwin, Andrew K., Moncoutier, Virginie, Gauthier-Villars, Marion, Lasset, Christine, Giraud, Sophie, Hardouin, Agnès, Berthet, Pascaline, Sobol, Hagay, Eisinger, François, Bressac de Paillerets, Brigitte, Caron, Olivier, Delnatte, Capucine, Goldgar, David, Ozcelik, Hilmi, Buys, Saundra, Southey, Melissa C., Terry, Mary Beth, Singer, Christian F., Dressler, Anne-Catharina, Tea, Muy-Kheng, Hansen, Thomas V.O., Johannsson, Oskar, Piedmonte, Marion, Rodriguez, Gustavo C., Basil, Jack B., Blank, Stephanie, Toland, Amanda E., Montagna, Marco, Isaacs, Claudine, Blanco, Ignacio, Gayther, Simon A., Moysich, Kirsten B., Schmutzler, Rita K., Wappenschmidt, Barbara, Engel, Christoph, Meindl, Alfons, Ditsch, Nina, Arnold, Norbert, Niederacher, Dieter, Sutter, Christian, Gadzicki, Dorothea, Caldes, Trinidad, Laframboise, Rachel, Nevanlinna, Heli, Chen, Xiaoqing, Beesley, Jonathan, Neuhausen, Susan L., Ding, Yuan C., Couch, Fergus J., Wang, Xianshu, Peterlongo, Paolo, Manoukian, Siranoush, Bernard, Loris, Easton, Douglas F., Antoniou, Antonis C., Stoppa-Lyonnet, Dominique, Mazoyer, Sylvie, Sinilnikova, Olga M.

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Association of the Variants CASP8 D302H and CASP10 V410I with Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers by ENGEL, Christoph, VERSMOLD, Beatrix, GARETH EVANS, D, EELES, Rosalind, PATERSON, Joan, BREWER, Carole, MCGUFFOG, Lesley, ANTONIOU, Antonis C, STOPPA-LYONNET, Dominique, SINILNIKOVA, Olga M, BARJHOUX, Laure, FRENAY, Marc, WAPPENSCHMIDT, Barbara, MICHEL, Cécile, LEROUX, Dominique, DREYFUS, Helene, TOULAS, Christine, GLADIEFF, Laurence, UHRHAMMER, Nancy, BIGNON, Yves-Jean, MEINDL, Alfons, ARNOLD, Norbert, VARON-MATEEVA, Raymonda, SIMARD, Jacques, NIEDERACHER, Dieter, PREISLER-ADAMS, Sabine, KAST, Karin, DEISSLER, Helmut, SUTTER, Christian, GADZICKI, Dorothea, CHENEVIX-TRENCH, Georgia, SPURDLE, Amanda B, XIAOQING CHEN, BEESLEY, Jonathan, EASTON, Douglas F, OLSSON, Håkan, KRISTOFFERSSON, Ulf, EHRENCRONA, Hans, LILJEGREN, Annelie, VAN DER LUIJT, Rob B, VAN OS, Theo A, VAN LEEUWEN, Flora E, DOMCHEK, Susan M, REBBECK, Timothy R, NATHANSON, Katherine L, PEOCK, Susan, OSORIO, Ana, RAMON Y CAJAL, Teresa, KONSTANTOPOULOU, Irene, BENITEZ, Javier, FRIEDMAN, Eitan, KAUFMAN, Bella, LAITMAN, Yael, MAI, Phuong L, GREENE, Mark H, NEVANLINNA, Heli, COOK, Margaret, OLIVER, Clare, FROST, Debra, MAYES, Rebecca

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Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers by SPURDLE, Amanda B, MARQUART, Louise, GSCHWANTLER-KAULICH, Daphne, BLUM, Joanne L, TUNG, Nadine, WEITZEL, Jeff, LYNCH, Henry, GARBER, Judy, EASTON, Douglas F, PEOCK, Susan, COOK, Margaret, OLIVER, Clare T, MCGUFFOG, Lesley, FROST, Debra, CONROY, Don, GARETH EVANS, D, LALLOO, Fiona, EELES, Ros, IZATT, Louise, DAVIDSON, Rosemarie, CHU, Carol, ECCLES, Diana, SELKIRK, Christina G, HEALEY, Sue, DALY, Mary, ISAACS, Claudine, STOPPA-LYONNET, Dominique, SINILNIKOVA, Olga M, BUECHER, Bruno, BELOTTI, Muriel, MAZOYER, Sylvie, BARJHOUX, Laure, VERNY-PIERRE, Carole, LASSET, Christine, SINILNIKOVA, Olga, DREYFUS, Hélène, PUJOL, Pascal, COLLONGE-RAME, Marie-Agnès, ROOKUS, Matti A, VERHOEF, Senno, KRIEGE, Mieke, HOOGERBRUGGE, Nicoline, AUSEMS, Margreet G. E. M, VAN OS, Theo A, WIJNEN, Juul, FEI WAN, DEVILEE, Peter, MEIJERS-HEIJBOER, Hanne E. J, BLOK, Marinus J, HEIKKINEN, Tuomas, NEVANLINNA, Heli, JAKUBOWSKA, Anna, LUBINSKI, Jan, HUZARSKI, Tomasz, BYRSKI, Tomasz, DUROCHER, Francine, XIAOQING CHEN, BEESLEY, Jonathan, SINGER, Christian F, DRESSLER, Anne-Catharine

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Association of PHB 1630 C > T and MTHFR 677 C > T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study by Jakubowska, A., Rozkrut, D., Antoniou, A., Hamann, U., Scott, R. J., McGuffog, L., Sinilnikova, O. M., Rennert, G., Lejbkowicz, F., Flugelman, A., Andrulis, I. L., Glendon, G., Ozcelik, H., Thomassen, M., Kantala, J., Aroer, B., Von Wachenfeldt, A., Liljegren, A., Loman, N., Kristoffersson, U., Rosenquist, R., Karlsson, P., Stenmark-Askmalm, M., Nathanson, K. L., Domchek, S. M., Byrski, T., Gronwald, J., Cybulski, C., Serrano, P., Osorio, A., Cajal, T. R., Tsitlaidou, M., Benitez, J., Gilbert, M., Rookus, M., Aalfs, C. M., Kluijt, I., Boessenkool-Pape, J. L., Oosterwijk, J. C., van Asperen, C. J., Blok, M. J., Nelen, M. R., van den Ouweland, A. M. W., van der Luijt, R. B., Devilee, P., Easton, D. F., Peock, S., Frost, D., Platte, R., Ellis, S. D., Fineberg, E., Evans, D. G., Lalloo, F., Eeles, R., Jacobs, C., Cole, T., Cook, J., Godwin, A., Bove, B., Stoppa-Lyonnet, D., Caux-Moncoutier, V., Belotti, M., Tirapo, C., Mazoyer, S., Barjhoux, L., Boutry-Kryza, N., Pujol, P., Vennin, P., Muller, D., Fricker, J-P, Venat-Bouvet, L., Johannsson, OTh, Isaacs, C., Schmutzler, R., Wappenschmidt, B., Meindl, A., Arnold, N., Varon-Mateeva, R., Niederacher, D., Sutter, C., Deissler, H., Preisler-Adams, S., Simard, J., Soucy, P., Durocher, F., Chenevix-Trench, G., Beesley, J., Chen, X., Rebbeck, T., Couch, F., Wang, X., Lindor, N., Pankratz, V. S., Peterlongo, P., Bonanni, B., Fortuzzi, S., Peissel, B., Mai, P. L., Loud, J. T., Lubinski, J.

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Association of PHB 1630 C andgt; T and MTHFR 677 C andgt; T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study by Jakubowska, A, Rozkrut, D, Antoniou, A, McGuffog, L, Healy, S, Sinilnikova, O M, Rennert, G, Lejbkowicz, F, Flugelman, A, Andrulis, I L, Glendon, G, Ozcelik, H, Thomassen, M, Paligo, M, Aretini, P, Kantala, J, Aroer, B, Von Wachenfeldt, A, Liljegren, A, Loman, N, Herbst, K, Kristoffersson, U, Rosenquist, R, Karlsson, P, Stenmark-Askmalm, Marie, Melin, B, Nathanson, K L, Domchek, S M, Byrski, T, Gronwald, J, Menkiszak, J, Serrano, P, Osorio, A, Cajal, T R, Tsitlaidou, M, Benitez, J, Gilbert, M, Rookus, M, Kluijt, I, Boessenkool-Pape, J L, Meijers-Heijboer, H E J, C Oosterwijk, J, J van Asperen, C, J Blok, M, R Nelen, M, M W van den Ouweland, A, Seynaeve, C, B van der Luijt, R, Devilee, P, F Easton, D, Peock, S, Frost, D, D Ellis, S, Fineberg, E, G Evans, D, Eeles, R, Jacobs, C, Adlard, J, Davidson, R, Eccles, D, Cole, T, Cook, J, Godwin, A, Bove, B, Stoppa-Lyonnet, D, Belotti, M, Mazoyer, S, Barjhoux, L, Boutry-Kryza, N, Pujol, P, Peyrat, J-P, Vennin, P, Muller, D, Fricker, J-P, Venat-Bouvet, L, Johannsson, OTh, Isaacs, C, Schmutzler, R, Wappenschmidt, B, Arnold, N, Varon-Mateeva, R, Niederacher, D, Sutter, C, Preisler-Adams, S, Simard, J, Soucy, P, Durocher, F, Beesley, J, Chen, X, Couch, F, Wang, X, Fredericksen, Z, S Pankratz, V, Peterlongo, P, Bonanni, B, Fortuzzi, S, Peissel, B, Szabo, C, L Mai, P, T Loud, J

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Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers o... by Osorio, A, Milne, R L, Simard, J, Chenevix-Trench, G, Spurdle, A B, Beesley, J, Chen, X, Neuhausen, S L, Ding, Y C, Lindor, N, Manoukian, S, Barile, M, Tizzoni, L, Szabo, C I, Foretova, L, Claes, K, Greene, M H, Mai, P, Lejbkowicz, F, Andrulis, I L, Gerdes, A-M, Cruger, D G, Caligo, M A, Kaufman, B, Cohen, S, Gershoni-Baruch, R, Dagan, E, Jernström, H, Askmalm, M S, Arver, B, Malmer, B, Domchek, S M, Nathanson, K L, Brunet, J, Ramón y Cajal, T, Yannoukakos, D, Hamann, U, Verhoef, S, García, EB Gómez, Wijnen, J T, van den Ouweland, A, Easton, D F, Peock, S, Cook, M, Frost, D, Luccarini, C, Evans, D G, Lalloo, F, Eeles, R, Pichert, G, Cook, J, Hodgson, S, Morrison, P J, Douglas, F, Sinilnikova, O M, Barjhoux, L, Cassini, C, Révillion, F, Peyrat, J-P, Muller, D, Fricker, J-P, Lynch, H T, John, E M, Buys, S, Daly, M, Hopper, J L, Terry, M B, Goldgar, D, Singer, C F, Pfeiler, G, Hansen, Thomas v O, Johannsson, O T, Kirchhoff, T, Offit, K, Kosarin, K, Piedmonte, M, Wakeley, K, Boggess, J F, Basil, J, Blank, S V, Toland, A E, Imyanitov, E N, Schmutzler, R K, Engel, C, Meindl, A, Ditsch, N, Arnold, N, Niederacher, D, Deißler, H, Fiebig, B, Varon-Mateeva, R, Schaefer, D, Froster, U G, Caldes, T, de la Hoya, M, McGuffog, L, Antoniou, A C, Nevanlinna, H, Radice, P, Benítez, J

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The DNA sequence coding for the 5' untranslated region of herpes simplex virus type 1 ICP22 mRNA mediates a high level of gene expression by Greco, Anna, Simonin, Denis, Diaz, Jean-Jacques, Barjhoux, Laure, Kindbeiter, Karine, Madjar, Jean-Jacques, Masse, Thierry

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RAD51 135G arrow right C Modifies Breast Cancer Risk among BRCA2 Mutation Carriers: Results from a Combined Analysis of 19 Studies by Antoniou, A C, Siniinikova, OM, Simard, J, Leone, M, Dumont, M, Neuhausen, S L, Struewing, J P, Stoppa-Lyonnet, D, Barjhoux, L, Hughes, D J, Coupler, I, Belotti, M, Lasset, C, Bonadona, V

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Demonstration by transfection studies that mutations in the adrenocorticotropin receptor gene are one cause of the hereditary syndrome of glucocorticoid deficiency by Naville, D, Barjhoux, L, Jaillard, C, Faury, D, Despert, F, Esteva, B, Durand, P, Saez, J M, Begeot, M

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Latest Developments of OLYMPE Platform for Optimizing Design of Fusion Cryomagnetic Systems by Lacroix, B., Le Coz, Q., Louzguiti, A., Nicollet, S., Torre, A., Zani, L., Barjhoux, P., Bonne, F., Nunio, F.

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Efficacy of perindopril in reduction of cardiovascular events among patients with stable coronary artery disease: randomised, double-blind, placebo-controlled, multicentre trial (t... by Fox, K M

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Goiter in a newborn exposed to lithium in utero by Frassetto, F, Tourneur Martel, F, Barjhoux, CE, Villier, C, Bot, BL, Vincent, F

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Chemical submission: results of 4-year French inquiry by Djezzar, S., Questel, F., Burin, E., Dally, S.

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