Rezultaty - Nicolas Sévenet

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  1. 1
    Constitutional Mutations of the hSNF5/INI1 Gene Predispose to a Variety of Cancers

    Constitutional Mutations of the hSNF5/INI1 Gene Predispose to a Variety of Cancers od Nicolas Sévenet, Eammon Sheridan, Daniel Amram, Pascale Schneider, Rupert Handgretinger, Olivier Delattre

    Wydane 1999
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  2. 2
    INI1 mutations in meningiomas at a potential hotspot in exon 9

    INI1 mutations in meningiomas at a potential hotspot in exon 9 od Ulrike Schmitz, Wolf Mueller, Mathias Weber, Nicolas Sévenet, Olivier Delattre, Andreas von Deimling

    Wydane 2001
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  3. 3
    Expression of Gastrin-Releasing Peptide Receptor in Breast Cancer and Its Association with Pathologic, Biologic, and Clinical Parameters: A Study of 1,432 Primary Tumors

    Expression of Gastrin-Releasing Peptide Receptor in Breast Cancer and Its Association with Pathologic, Biologic, and Clinical Parameters: A Study of 1,432 Primary Tumors od Clément Morgat, Gaëtan MacGrogan, Véronique Brouste, Valérie Velasco, Nicolas Sévenet, Hervé Bonnefoi, Philippe Fernandez, Marc Debled, Elif Hindié

    Wydane 2017
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  4. 4
    Prostate cancer and PARP inhibitors: progress and challenges

    Prostate cancer and PARP inhibitors: progress and challenges od Diego Teyssonneau, Henri Margot, Mathilde Cabart, Mylène Anonnay, Paul Sargos, Nam‐Son Vuong, Isabelle Soubeyran, Nicolas Sévenet, Guilhem Roubaud

    Wydane 2021
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  5. 5
    Spectrum of hSNF5IINI1 Somatic Mutations in Human Cancer and Genotype-Phenotype Correlations

    Spectrum of hSNF5IINI1 Somatic Mutations in Human Cancer and Genotype-Phenotype Correlations od Nicolas Sévenet, Arielle Lellouch‐Tubiana, Deborah E. Schofield, Khê Hoang‐Xuan, Manfred Gessler, Daniel Birnbaum, Marc Jeanpierre, Anne Jouvet, Olivier Delattre

    Wydane 1999
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  6. 6
    Alterations of the p53 and PIK3CA/AKT/mTOR pathways in angiosarcomas

    Alterations of the p53 and PIK3CA/AKT/mTOR pathways in angiosarcomas od Antoîne Italiano, Chun‐Liang Chen, Rachael Thomas, Matthew Breen, Françoise Bonnet, Nicolas Sévenet, Michel Longy, Robert G. Maki, Jean‐Michel Coindre, Cristina R. Antonescu

    Wydane 2012
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  7. 7
    Comprehensive analysis of PTEN status in breast carcinomas

    Comprehensive analysis of PTEN status in breast carcinomas od Natalie Jones, Françoise Bonnet, Sana Sfar, M. Lafitte, D Lafon, Ghislaine Sierankowski, Véronique Brouste, Guillaume Banneau, C. Tunon de Lara, Marc Debled, Gaëtan MacGrogan, Michel Longy, Nicolas Sévenet

    Wydane 2013
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  8. 8
    Molecular apocrine differentiation is a common feature of breast cancer in patients with germline PTEN mutations

    Molecular apocrine differentiation is a common feature of breast cancer in patients with germline PTEN mutations od Guillaume Banneau, Mickaël Guedj, Gaëtan MacGrogan, Isabelle de Mascarel, Valérie Velasco, Renaud Schiappa, Valérie Bonadona, Albert David, Catherine Dugast, Brigitte Gilbert‐Dussardier, Olivier Ingster, P. Vabres, F. Caux, Aurélien de Reyniès, Richard Iggo, Nicolas Sévenet, Françoise Bonnet, Michel Longy

    Wydane 2010
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  9. 9
    Germline <i>SUFU</i> mutation carriers and medulloblastoma: clinical characteristics, cancer risk, and prognosis

    Germline <i>SUFU</i> mutation carriers and medulloblastoma: clinical characteristics, cancer risk, and prognosis od Léa Guerrini‐Rousseau, Christelle Dufour, Pascale Varlet, Julien Masliah‐Planchon, Franck Bourdeaut, Marine Guillaud-Bataille, Rachid Abbas, Anne-Isabelle Bertozzi, Fanny Fouyssac, Sophie Huybrechts, Stéphanie Puget, Brigitte Bressac–de Paillerets, Olivier Caron, Nicolas Sévenet, Marina Dimaria, Sophie Villebasse, Olivier Delattre, Dominique Valteau‐Couanet, Jacques Grill, Laurence Brugières

    Wydane 2017
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  10. 10
    The transfer of multigene panel testing for hereditary breast and ovarian cancer to healthcare: What are the implications for the management of patients and families?

    The transfer of multigene panel testing for hereditary breast and ovarian cancer to healthcare: What are the implications for the management of patients and families? od Marie Eliade, J. Skrzypski, Amandine Baurand, Caroline Jacquot, Geoffrey Bertolone, Catherine Loustalot, Charles Coutant, France Guy, P. Fumoleau, Yannis Duffourd, Laurent Arnould, Alexandra Delignette, Marie‐Martine Padeano, Côme Lepage, Géraldine Raichon-Patru, Axelle Boudrant, M.C. Böne-Lépinoy, Anne-Laure Villing, Aurélie Charpin, Karine Peignaux, Sandy Chevrier, Frédérique Végran, François Ghiringhelli, Romain Boidot, Nicolas Sévenet, Sarab Lizard, Laurence Faivre

    Wydane 2016
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  11. 11
    Assessment of branch point prediction tools to predict physiological branch points and their alteration by variants

    Assessment of branch point prediction tools to predict physiological branch points and their alteration by variants od Raphaël Leman, Hélène Tubeuf, Sabine Raad, Isabelle Tournier, Céline Derambure, Raphaël Lanos, Pascaline Gaildrat, G Castelain, Julie Hauchard, Audrey Killian, Stéphanie Baert‐Desurmont, Angélina Legros, Nicolas Goardon, Céline Quesnelle, Agathe Ricou, Laurent Castéra, Dominique Vaur, Gérald Le Gac, Chandran Ka, Yann Fichou, Françoise Bonnet‐Dorion, Nicolas Sévenet, Marine Guillaud-Bataille, Nadia Boutry‐Kryza, Inès Schultz, Virginie Caux‐Moncoutier, Maria Rossing, Logan C. Walker, Amanda B. Spurdle, Claude Houdayer, Alexandra Martins, Sophie Krieger

    Wydane 2020
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  12. 12
    Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort

    Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort od Raphaël Leman, Pascaline Gaildrat, Gérald Le Gac, Chandran Ka, Yann Fichou, Marie‐Pierre Audrézet, Virginie Caux‐Moncoutier, Sandrine M. Caputo, Nadia Boutry‐Kryza, Mélanie Léoné, Sylvie Mazoyer, Françoise Bonnet‐Dorion, Nicolas Sévenet, Marine Guillaud-Bataille, Étienne Rouleau, Brigitte Bressac–de Paillerets, Barbara Wappenschmidt, Maria Rossing, Danielle Muller, Violaine Bourdon, Françoise Révillon, Michael T. Parsons, Antoine Rousselin, Grégoire Davy, G Castelain, Laurent Castéra, Joanna Sokołowska, Florence Coulet, Capucine Delnatte, Claude Férec, Amanda B. Spurdle, Alexandra Martins, Sophie Krieger, Claude Houdayer

    Wydane 2018
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  13. 13
    BRCA Share: A Collection of Clinical BRCA Gene Variants

    BRCA Share: A Collection of Clinical BRCA Gene Variants od Christophe Béroud, Stanley Letovsky, Corey Braastad, Sandrine M. Caputo, Olivia Beaudoux, Yves Jean Bignon, Brigitte Bressac–de Paillerets, Myriam Bronner, Crystal M. Buell, Gwenaëlle Collod‐Béroud, Florence Coulet, Nicolas Derive, Christina DiVincenzo, Christopher Elzinga, Céline Garrec, Claude Houdayer, Izabela Karbassi, Sarab Lizard, Angela Love, Danièle Muller, Narasimhan Nagan, Camille Nery, Ghadi Raï, Françoise Révillion, David Salgado, Nicolas Sévenet, Olga M. Sinilnikova, Hagay Sobol, Dominique Stoppa‐Lyonnet, Christine Toulas, Edwin Trautman, Dominique Vaur, Paul Vilquin, Katelyn S. Weymouth, Alecia Willis, Marcia Eisenberg, Charles M. Strom

    Wydane 2016
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  14. 14
    Engineering Genetic Predisposition in Human Neuroepithelial Stem Cells Recapitulates Medulloblastoma Tumorigenesis

    Engineering Genetic Predisposition in Human Neuroepithelial Stem Cells Recapitulates Medulloblastoma Tumorigenesis od Miller Huang, Jignesh Tailor, Qiqi Zhen, Aaron H. Gillmor, Matthew L. Miller, Holger Weishaupt, Justin Chen, Tina Zheng, Emily K. Nash, Lauren McHenry, Zhenyi An, Fubaiyang Ye, Yasuhiro Takashima, James Clarke, Harold Ayetey, Florence M.G. Cavalli, Betty Luu, Branden S. Moriarity, Shirin Ilkhanizadeh, Lukas Chávez, Chun‐Ying Yu, Kathreena M. Kurian, Thierry Magnaldo, Nicolas Sévenet, Philipp Koch, Steven M. Pollard, Peter B. Dirks, M Snyder, David A. Largaespada, Yoon Jae Cho, Joanna J. Phillips, Fredrik J. Swartling, A. Sorana Morrissy, Marcel Kool, Stefan M. Pfister, Michael D. Taylor, Austin Smith, William A. Weiss

    Wydane 2019
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  15. 15
    Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus

    Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus od Kate Lawrenson, Siddhartha Kar, Karen McCue, Karoline B. Kuchenbaeker, Kyriaki Michailidou, Jonathan P. Tyrer, Jonathan Beesley, Susan J. Ramus, Qiyuan Li, Melissa K. Delgado, Janet M. Lee, Kristiina Aittomäki, Irene L. Andrulis, Hoda Anton‐Culver, Volker Arndt, Banu K. Arun, Brita Arver, Elisa V. Bandera, Monica Barile, Rósa B. Barkardóttir, Daniel Barrowdale, Matthias W. Beckmann, Javier Benı́tez, Andrew Berchuck, Maria Bisogna, Line Bjørge, Carl Blomqvist, William J. Blot, Natalia Bogdanova, Anders Bojesen, Stig E. Bojesen, Manjeet K. Bolla, Bernardo Bonanni, Anne‐Lise Børresen‐Dale, Hiltrud Brauch, Paul Brennan, Hermann Brenner, Fiona Bruinsma, Joan Brunet, Shaik Ahmad Buhari, Barbara Burwinkel, Ralf Bützow, Saundra S. Buys, Qiuyin Cai, Trinidad Caldés, Ian Campbell, Rikki Canniotto, Jenny Chang‐Claude, Jocelyne Chiquette, Ji‐Yeob Choi, Kathleen Claes, Marie- Agnès Collonge-Rame, Alexandre Damette, Emmanuelle Barouk-Simonet, Françoise Bonnet, Virginie Bubien, Nicolas Sévenet, Michel Longy, Pascaline Berthet, Dominique Vaur, Laurent Castéra, Sandra Fert Ferrer, Yves‐Jean Bignon, Nancy Uhrhammer, Fanny Coron, Laurence Faivre, Amandine Baurand, Caroline Jacquot, Geoffrey Bertolone, Sarab Lizard, Dominique Leroux, Hélène Dreyfus, Christine Rebischung, Magalie Peysselon, Jean‐Philippe Peyrat, Joëlle Fournier, Françoise Révillion, Claude Adenis, Laurence Venat‐Bouvet, Mélanie Léone, Nadia Boutry‐Kryza, Alain Calender, Sophie Giraud, Carole Verny-Pierre, Christine Lasset, Valérie Bonadona, Laure Barjhoux, Hagay Sobol, Violaine Bourdon, Tetsuro Noguchi, Audrey Remenieras, Isabelle Coupier, Pascal Pujol, Johanna Sokolowska, Myriam Bronner, Capucine Delnatte, Stéphane Bézieau, Véronique Mari, Marion Gauthier‐Villars, Bruno Buecher

    Wydane 2016
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  16. 16
    Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

    Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers od Antonis C. Antoniou, Olga M. Sinilnikova, Lesley McGuffog, Sue Healey, Heli Nevanlinna, Tuomas Heikkinen, Jacques Simard, Amanda B. Spurdle, Jonathan Beesley, Xiaohong Chen, Susan L. Neuhausen, Yuan Chun Ding, Fergus J. Couch, Xianshu Wang, Zachary Fredericksen, Paolo Peterlongo, Bernard Peissel, Bernardo Bonanni, Alessandra Viel, Loris Bernard, Paolo Radice, Csilla I. Szabo, Lenka Foretová, Michal Zikán, Kathleen Claes, Mark H. Greene, L. Phuong, Gad Rennert, Flavio Lejbkowicz, Irene L. Andrulis, Hilmi Özçelik, Gord Glendon, Anne‐Marie Gerdes, Mads Thomassen, Lone Sunde, Maria A. Caligo, Yael Laitman, Tair Kontorovich, Shimrit Cohen, Bella Kaufman, Efrat Dagan, Ruth Gershoni Baruch, Eitan Friedman, Katja Harbst, Gisela Barbany, Johanna Rantala, Hans Ehrencrona, Per Karlsson, Susan M. Domchek, Katherine L. Nathanson, Ana Osório, Ignacio Blanco, Adriana Lasa, Javier Benı́tez, Ute Hamann, Frans B.L. Hogervorst, Matti A. Rookus, J. Margriet Collée, Peter Devilee, Marjolijn J. L. Ligtenberg, Rob B. van der Luijt, Cora M. Aalfs, Quinten Waisfisz, Juul Wijnen, C. E. P. van Roozendaal, Susan Peock, Margaret Cook, Debra Frost, Clare Oliver, Radka Platte, D. Gareth Evans, Fiona Lalloo, Rosalind A. Eeles, Louise Izatt, Rosemarie Davidson, Carol Chu, Diana Eccles, Trevor Cole, Shirley Hodgson, Andrew K. Godwin, Dominique Stoppa‐Lyonnet, Bruno Buecher, Mélanie Léoné, Brigitte Bressac–de Paillerets, Audrey Remenieras, Olivier Caron, Gilbert Lenoir, Nicolas Sévenet, Michel Longy, Sandra Fert Ferrer, Fabienne Prieur, David E. Goldgar, Alexander Miron, Esther M. John, Saundra S. Buys, Mary B. Daly, John L. Hopper, Mary Beth Terry, Yosuf Yassin, Daphne Gschwantler‐Kaulich

    Wydane 2009
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