Browsing by Author Capellá, G. (Gabriel)

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Issue DateTitleAuthor(s)
13-Dec-2019Desarrollo de nuevas aproximaciones para el diagnóstico molecular de los síndromes de predisposición hereditaria al cáncer asociados a deficiencia del sistema de reparación de apareamientos erróneosGonzález Acosta, María Isabel
Feb-2012A DNA methylation fingerprint of 1628 human samplesFernández, Agustín F.; Martín-Subero, José Ignacio; Hidalgo, Manuel; Ferrer, Isidro (Ferrer Abizanda); Sánchez Céspedes, Montserrat; Villanueva Garatachea, Alberto; Carmona, F. Javier; Sanchez-Mut, Jose Vicente; Berdasco, María; Moreno Aguado, Víctor; Capellá, G. (Gabriel); Ballestar Tarín, Esteban; Pérez Jurado, Luis; Mora Graupera, Jaume; Puig i Sardà, Susana; Prat, Jaime; Badimón, Lina, 1953-; Esteller, Manel
22-Dec-2018Does multilocus inherited neoplasia alleles syndrome have severe clinical expression?Stradella, Agostina; Valle, Jesús del; Rofes, Paula; Feliubadaló i Elorza, Maria Lídia; Grau Garcés, Èlia; Velasco, Àngela; González, Sara; Vargas Parra, Gardenía María; Izquierdo, Ángel; Campos, Olga; Tornero, Eva; Navarro, Matilde; Balmaña, Judith; Capellá, G. (Gabriel); Pineda Riu, Marta; Brunet, Joan; Lázaro García, Conxi
1-Jun-2020Dominantly inherited hereditary nonpolyposis colorectal cancer not caused by MMR genesTerradas, Mariona; Capellá, G. (Gabriel); Valle, Laura
1-Feb-2021Duodenal adenomas and cancer in MUTYH-associated polyposis: an international cohort studyCollaborative Group on Duodenal Polyposis in MAP; Thomas, Laura E.; Hurley, Joanna J.; Alonso Sánchez, Ángel; Aznárez, M. Rosario; Backman, Ann Sofie; Bjork, Jan; Capellá, G. (Gabriel); Clark, Susan K.; Colas, Chrystelle; Dekker, Evelien; Dolwani, Sunil; Ghorbanoghli, Zeinab; Gonn, Mark; González Romero, S.; Hes, Frederik J.; Jundi, Hala; Kelland, Sarah; Latchford, Andrew R.; Leon Brito, Helena; Lynch, Patrick M.; Meuser, Elena; Mork, Maureen E.; Mort, Matthew; Navarro García, Matilde; Nielsen, Maartje; Parc, Yann; Ricci, Maria T.; Saurin, Jean Christophe; van der Tuin, Karin; Vasen, Hans; Vilar, Eduardo; Vinet, Olivier; Vitellaro, Marco; Walton, Sarah Jane; West, Hannah D.; Sampson, Julian R.
19-Feb-2016Elucidating the molecular basis of Lynch-Like syndromeVargas Parra, Gardenía María
19-Feb-2013Estudi de variants de significat desconegut en la síndrome de LynchBorràs Flores, Ester
1-Dec-2020Evaluation of CNV detection tools for NGS panel data in genetic diagnosticsMoreno Cabrera, José Marcos; Valle Domínguez, Jesús del; Castellanos, Elisabeth; Feliubadaló i Elorza, Maria Lídia; Pineda Riu, Marta; Brunet, Joan; Serra, Eduard; Capellá, G. (Gabriel); Lázaro García, Conxi; Gel, Bernat
20-Jun-2007Evidence for systems-level molecular mechanisms of tumorigenesisHernández, Pilar; Huerta Cepas, Jaime; Montaner, David; Al-Shahrour, Fatima; Valls i Marsal, Joan; Gómez Baldó, Laia; Capellá, G. (Gabriel); Dopazo, Joaquín; Pujana Genestar, M. Ángel
27-May-2021Exome sequencing of early-onset patients supports genetic heterogeneity in colorectal cancerFernández Rozadilla, C.; Álvarez Barona, M.; Quintana, Isabel; López Novo, Anael; Amigo, J.; Cameselle Teijeiro, J. M.; Roman, E.; González, D.; Llor, Xavier; Bujanda, L.; Bessa, X.; Jover, R.; Balaguer, F.; Castells, A.; Castellví Bel, Sergi; Capellá, G. (Gabriel); Carracedo Álvarez, Ángel; Valle, Laura; Ruiz Ponte, Clara
1-Apr-2020Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer PatientsValle, Jesús del; Rofes, Paula; Moreno Cabrera, José Marcos; López Dóriga Guerra, Adriana; Belhadj, Sami; Vargas Parra, Gardenía María; Teulé-Vega, Àlex; Cuesta, Raquel; Muñoz, Xavier; Campos, Olga; Salinas Masdeu, Mònica; Cid, Rafael de; Brunet, Joan; González, Sara; Capellá, G. (Gabriel); Pineda Riu, Marta; Feliubadaló i Elorza, Maria Lídia; Lázaro García, Conxi
6-Sep-2019Expression and Role of MicroRNAs from the miR-200 Family in the Tumor Formation and Metastatic Propensity of Pancreatic CancerDiaz Riascos, Zamira Vanessa; Ginestà, Mireia M.; Fabregat Prous, Joan; Serrano Piñol, M. Teresa; Busquets Barenys, Juli; Buscail, Louis; Cordelier, Pierre; Capellá, G. (Gabriel)
2-Apr-2010Filamin B plays a key role in VEGF-induced endothelial cell motility through its interaction with Rac-1 and Vav-2Del Valle-Pérez, Beatriz; Martinez, Vanesa Gabriela; Lacasa Salavert, Cristina; Figueras i Amat, Agnès; Shapiro, Sandor S.; Takafuta, Toshiro; Casanovas i Casanovas, Oriol; Capellá, G. (Gabriel); Ventura Pujol, Francesc; Viñals Canals, Francesc
17-Apr-2013Functional and Structural Analysis of C-Terminal BRCA1 Missense VariantsQuiles Vidal, Francisco de Asís; Fernández-Rodríguez, Juana; Mosca, Roberto; Feliubadaló i Elorza, Maria Lídia; Tornero, Eva; Brunet, Joan; Blanco Guillermo, Ignacio; Capellá, G. (Gabriel); Pujana Genestar, M. Ángel; Aloy, Patrick, 1972-; Monteiro, Alvaro N.; Lázaro García, Conxi
11-Jan-2008Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibilitySolé Acha, Xavier; Hernández, Pilar; López de Heredia, Miguel; Armengol, Lluís; Rodríguez Santiago, Benjamín; Gómez, Laia; Maxwell, Christopher A.; Aguiló Lúcia, Fernando; Condom i Mundó, Enric; Abril, Jesús; Pérez Jurado, Luis; Estivill, Xavier, 1955-; Nunes Martínez, Virginia; Capellá, G. (Gabriel); Gruber, Stephen B.; Moreno Aguado, Víctor; Pujana Genestar, M. Ángel
23-Jul-2021Genetic Screening for TLR7 Variants in Young and Previously Healthy Men With Severe COVID-19Solanich, Xavier; Vargas Parra, Gardenia; Van Der Made, Caspar I.; Simons, Annet; Schuurs Hoeijmakers, Janneke; Antolí, Arnau; Valle, Jesús del; Rocamora Blanch, Gemma; Setién, Fernando; Esteller, Manel; Van Reijmersdal, Simon V.; Riera Mestre, Antoni; Sabater Riera, Joan; Capellá, G. (Gabriel); Van De Veerdonk, Frank L.; Van Der Hoven, Ben; Corbella, Xavier; Hoischen, Alexander; Lázaro García, Conxi
Jul-2020Germline Mutations in FAF1 Are Associated With Hereditary Colorectal CancerBonjoch Gassol, Laia; Franch Expósito, Sebastià; Garre, Pilar; Belhadj, Sami; Muñoz, Jenifer; Arnau Collell, Coral; Díaz Gay, Marcos; Gratacós Mulleras, Anna; Raimondi, Giulia; Esteban Jurado, Clara; Soares de Lima, Yasmin; Herrera Pariente, Cristina; Cuatrecasas Freixas, Miriam; Ocaña, Teresa; Castells Garangou, Antoni; Fillat i Fonts, Cristina; Capellá, G. (Gabriel); Balaguer Prunés, Francesc; Caldés, Trinidad; Valle Velasco, Laura; Castellví Bel, Sergi
15-Feb-2018Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposisMur, Pilar; de Voer, Richarda M.; Olivera-Salguero, Rubén; Rodriguez Perales, Sandra; Pons, Tirso; Setién, Fernando; Aiza, Gemma; Valdés Mas, Rafael; Bertini, Angelo; Pineda Riu, Marta; Vreede, Lilian; Navarro, Matilde; Iglesias Casals, Sílvia; González, Sara; Brunet, Joan; Valencia, Alfonso; Esteller, Manel; Lázaro García, Conxi; Kops, Geert J. P. L.; Urioste, Miguel; Puente, Xose S.; Capellá, G. (Gabriel); Valle Velasco, Laura
2008Guidelines for the clinical management of familial adenomatous polyposis (FAP)Vasen, Hans F. A.; Möslein, Gabriela; Alonso, A.; Aretz, S.; Bernstein, Inge; Bertario, Lucio; Blanco Guillermo, Ignacio; Bülow, S.; Burn, John; Capellá, G. (Gabriel); Colas, Chrystelle; Engel, Christoph; Frayling, Ian M.; Friedl, W.; Hes, F. J.; Hodgson, Shirley; Järvinen, Heikki; Mecklin, Jukka-Pekka; Møller, Pål; Myrhoi, T.; Nagengast, F. M.; Parc, Yann; Phillips, R.; Clark, Susan K.; Ponz de Leon, Maurizio; Renkonen-Sinisalo, Laura; Sampson, J. R.; Stormorken, A.; Tejpar, Sabine; Thomas, H. J. W.; Wijnen, Juul
15-Apr-2017Helicobacter pylori infection, chronic corpus atrophic gastritis and pancreatic cancer risk in the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort: a nested case-control studyHuang, Jiaqi; Zagai, Ulrika; Hallmans, Göran; Nyrén, Olof; Engstrand, Lars; Stolzenberg-Solomon, Rachael Z.; Duell, Eric J.; Overvad, Kim; Katzke, Verena; Kaaks, Rudolf; Jenab, Mazda; Park, Jing Young; Murillo, Raul; Trichopoulou, Antonia; Lagiou, Pagona; Bamia, Christina; Bradbury, Kathryn E.; Riboli, Elio; Aune, Dagfinn; Tsilidis, Konstantinos K.; Capellá, G. (Gabriel); Agudo, Antonio; Krogh, Vittorio; Palli, Domenico; Panico, Salvatore; Weiderpass, Elisabete; Tjønneland, Anne; Olsen, Anja; Martínez, Begoña; Redondo Sánchez, Daniel; Chirlaque, María Dolores; Peeters, Petra H. M.; Regnér, Sara; Lindkvist, Björn; Naccarati, Alessio; Ardanaz, Eva; Dorronsoro, Miren; Larrañaga, Nerea; Rebours, Vinciane; Barré, Amélie