Aberrant transcription caused by an intronic non-canonical CDH1 variant.

Autor: Bouras, Ahmed, Grand-Masson, Chloé, Lefol, Cedrick, Ruano, Eric, Prieur, Fabienne, Wang, Qing

Publikováno v: Familial Cancer; Nov2024, Vol. 23 Issue 4, p671-673, 3p

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Combining Homologous Recombination and Phosphopeptide-binding Data to Predict the Impact of BRCA1 BRCT Variants on Cancer Risk

Autor: Petitalot, Ambre, Dardillac, Elodie, Jacquet, Eric, Nhiri, Naima, Guirouilh-Barbat, Josee, Julien, Patrick, Bouazzaoui, Isslam, Bonte, Dorine, Feunteun, Jean, Schnell, Jeff A., Lafitte, Philippe, Aude, Jean-Christophe, Nogues, Catherine, Rouleau, Etienne, Lidereau, Rosette, Lopez, Bernard S., Zinn-Justin, Sophie, Caputo, Sandrine M., Bonnet, Francoise, Jones, Natalie, Bubien, Virginie, Longy, Michel, Sevenet, Nicolas, Krieger, Sophie, Casters, Laurent, Vaur, Dominique, Uhrhammer, Nancy, Bignon, Yves Jean, Lizard, Sarab, Dumont, Aurelie, Revillion, Francoise, Leone, Melanie, Boutry-Kryza, Nadia, Sinilnikova, Olga, Remenieras, Audrey, Bourdon, Violaine, Noguchi, Tetsuro, Sobol, Hagay, Harmand, Pierre-Olivier, Vilquin, Paul, Pujol, Pascal, Jonveaux, Philippe, Bronner, Myriam, Sokolowska, Joanna, Delnatte, Capucine, Guibert, Virginie, Garrec, Celine, Bezieau, Stephan, Soubrier, Florent, Guillerm, Erell, Coulet, Florence, Lefol, Cedrick, Caux-Moncoutier, Virginie, Golmard, Lisa, Houdayer, Claude, Stoppa-Lyonnet, Dominique, Delvincoun, Chantal, Beaudoux, Olivia, Muller, Daniele, Toulas, Christine, Guillaud-Bataille, Marine, Bressac-De Paillerets, Brigitte

Publikováno v: Molecular Cancer Research
Molecular Cancer Research, American Association for Cancer Research, 2019, 17 (1), pp.54--69. ⟨10.1158/1541-7786.MCR-17-0357⟩
Molecular Cancer Research, American Association for Cancer Research, 2019, 17 (1), pp.54-69. ⟨10.1158/1541-7786.MCR-17-0357⟩
Molecular Cancer Research, 2019, 17 (1), pp.54--69. ⟨10.1158/1541-7786.MCR-17-0357⟩

BRCA1 mutations have been identified that increase the risk of developing hereditary breast and ovarian cancers. Genetic screening is now offered to patients with a family history of cancer, to adapt their treatment and the management of their relati

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::456920938871e1394b4edab0f553fdaa
https://hal.archives-ouvertes.fr/hal-02173633