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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 of orthotopic implantat in digestive tumors in athymic mice


Selected papers (2009)

Del Valle J, Feliubadaló L, Nadal M, Teulé A, Miró R, Cuesta R, Tornero E, Menéndez M, Darder E, Brunet J, Capellà G, Blanco I, Lázaro C. Identification and comprehensive characterization of large genomic rearrangements in the BRCA1 and BRCA2 genes. Breast Cancer Res Treat. 2009 Nov 6.
 
Pros E, Fernández-Rodríguez J, Canet B, Benito L, Sánchez A, Benavides A, Ramos FJ, López-Ariztegui MA, Capellá G, Blanco I, Serra E, Lázaro C. Antisense Therapeutics for Neurofibromatosis Type 1 Caused by Deep Intronic Mutations. Human Mutation. 2009; 30(3):454-62.

Sumalla EC, Ochoa C, Blanco I. Posttraumatic growth in cancer: reality or illusion? Clin Psychol Rev. 2009 Feb;29(1):24-33
 
Mayor R, Casadome L, Azuara D, Moreno V, Clark SJ, Capella G, Peinado MA Long-range epigenetic silencing at 2q14.2 affects most human colorectal cancers and may have application as a non-invasive biomarker of disease. British Journal of Cancer. 2009;100(10):1534-9.
 
Pineda M, González S, Lázaro C, Blanco I, Capellá G. Detection of genetic alterations in hereditary colorectal cancer screening. Mutat Res. 2009 Nov 26 IF: 3,198

imatge personal
 

Group leader

Gabriel Capella
Telephone  
+34 932607461
E-mail  
gcapella@idibell.cat
 
© 2013 Institut d'Investigació Biomèdica de Bellvitge



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