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Hereditary cancer


Research lines

Study of colorectal cancer and hereditary breast cancer molecular basis


Molecular diagnosis of gastrointestinal tumors and breast cancer


Development of animal models after orthotopic implantation of tumors from patients with hereditary cancer in athymic mice


Clinical, genetic and molecular basis of Neurofibromatosis


Selected papers (2012)

 

Marín F, Bonet C, Muñoz X, García N, Pardo ML, Ruiz-Liso JM, Alonso P, Capellà G, Sanz- Anquela JM, González CA, Sala N.

Genetic variation in MUC1, MUC2 and MUC6 genes and evolution of gastric cancer precursor lesions in a long-term follow-up in a high-risk area in Spain

CARCINOGENESIS 2012 May; 33(5):1072-1080

 

Borràs E, Pineda M, Brieger A, Hinrichsen I, Gómez C, Navarro M, Balmaña J, Ramón y Cajal T, Torres A, Brunet J, Blanco I, Plotz G, Lázaro C, Capellá G.

Comprehensive functional assessment of MLH1 variants of unknown significance

HUMAN MUTATION Nov; 33(11):1576-88

 

Menéndez M, Castellsagué J, Mirete M, Pros E, Feliubadaló L, Osorio A, Calaf M, Tornero E, del Valle J, Fernández-Rodríguez J, Quiles F, Salinas M, Velasco A, Teulé A, Brunet J, Blanco I, Capellá G, Lázaro C.

Assessing the RNA effect of 26 DNA variants in the BRCA1 and BRCA2 genes

BREAST CANCER RESEARCH AND TREATMENT 2012 Apr; 132(3):979-92

 

Gausachs, Mireia; Mur, Pilar; Corral, Julieta; Pineda, Marta; Gonzalez, Sara; Benito, Llucia; Menendez, Mireia; Alfons Espinas, Josep; Brunet, Joan; Iniesta, Maria Dolores; Gruber, Stephen B.; Lazaro, Conxi; Blanco, Ignacio;

Capella, Gabriel.

MLH1 promoter hypermethylation in the analytical algorithm of Lynch syndrome: a cost-effectiveness study

LANCET ONCOLOGY 2012 Jan; 13(1): 100-110

imatge personal
 

Group leader

Gabriel Capella
Telephone  
+34 932607461
E-mail  
gcapella@idibell.cat
 
© 2014 Institut d'Investigació Biomèdica de Bellvitge



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