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Publications

Filtros: Autor es González, S  [Restablecer todos los filtros]
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Obrador-Hevia A, Chin SF, González S, Rees J, Vilardell F, Greenson JK, et al. Oncogenic KRAS is not necessary for Wnt signalling activation in APC-associated FAP adenomas. The Journal of pathology. 2010;221(1):57-67. Abstract
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Feliubadaló L, Lopez-Doriga A, Castellsagué E, Del Valle J, Menéndez M, Tornero E, et al. Next-generation sequencing meets genetic diagnostics: development of a comprehensive workflow for the analysis of BRCA1 and BRCA2 genes. European journal of human genetics : EJHG. 2012. Abstract
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Borràs E, Pineda M, Blanco I, Jewett EM, Wang F, Teulé A, et al. MLH1 founder mutations with moderate penetrance in Spanish Lynch syndrome families. Cancer research. 2010;70(19):7379-91. Abstract
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Menéndez M, González S, Obrador-Hevia A, Domínguez A, Pujol MJ, Valls J, et al. Functional characterization of the novel APC N1026S variant associated with attenuated familial adenomatous polyposis. Gastroenterology. 2008;134(1):56-64.
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Castellsagué E, González S, Nadal M, Campos O, Guinó E, Urioste M, et al. Detection of APC gene deletions using quantitative multiplex PCR of short fluorescent fragments. Clinical chemistry. 2008;54(7):1132-40. Abstract
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Castellsagué E, González S, Guinó E, Stevens KN, Borràs E, Raymond VM, et al. Allele-specific expression of APC in adenomatous polyposis families. Gastroenterology. 2010;139(2):439-7, 447.e1. Abstract