Capella G - Search Results

1

Usefulness of epithelial cell adhesion molecule expression in the algorithmic approach to Lynch syndrome identification.

Musulen E, Blanco I, Carrato C, Fernandez-Figueras MT, Pineda M, Capella G, Ariza A. Musulen E, et al. Among authors: capella g. Hum Pathol. 2013 Mar;44(3):412-6. doi: 10.1016/j.humpath.2012.06.006. Epub 2012 Sep 29. Hum Pathol. 2013. PMID: 23026194

2

Intron splice acceptor site polymorphism in the hMSH2 gene in sporadic and familial colorectal cancer.

Palicio M, Blanco I, Tórtola S, González I, Marcuello E, Brunet J, Lluis F, González-Aguilera JJ, Peinado MA, Capella G. Palicio M, et al. Among authors: capella g. Br J Cancer. 2000 Feb;82(3):535-7. doi: 10.1054/bjoc.1999.0959. Br J Cancer. 2000. PMID: 10682661 Free PMC article.

3

DCC and SMAD4 alterations in human colorectal and pancreatic tumor dissemination.

Tarafa G, Villanueva A, Farré L, Rodríguez J, Musulén E, Reyes G, Seminago R, Olmedo E, Paules AB, Peinado MA, Bachs O, Capellá G. Tarafa G, et al. Among authors: capella g. Oncogene. 2000 Jan 27;19(4):546-55. doi: 10.1038/sj.onc.1203353. Oncogene. 2000. PMID: 10698524

4

Standardized approach for microsatellite instability detection in gastric carcinomas.

Musulén E, Moreno V, Reyes G, Sancho FJ, Peinado MA, Esteller M, Herman JG, Combalia N, Rey M, Capellá G. Musulén E, et al. Among authors: capella g. Hum Pathol. 2004 Mar;35(3):335-42. doi: 10.1016/j.humpath.2003.10.021. Hum Pathol. 2004. PMID: 15017590

5

Colorectal cancer risk and the APC D1822V variant.

Menéndez M, González S, Blanco I, Guinó E, Peris M, Peinado MA, Capellá G, Moreno V. Menéndez M, et al. Among authors: capella g. Int J Cancer. 2004 Oct 20;112(1):161-3. doi: 10.1002/ijc.20361. Int J Cancer. 2004. PMID: 15305389 No abstract available.

6

Low levels of microsatellite instability characterize MLH1 and MSH2 HNPCC carriers before tumor diagnosis.

Alazzouzi H, Domingo E, González S, Blanco I, Armengol M, Espín E, Plaja A, Schwartz S, Capella G, Schwartz S Jr. Alazzouzi H, et al. Among authors: capella g. Hum Mol Genet. 2005 Jan 15;14(2):235-9. doi: 10.1093/hmg/ddi021. Epub 2004 Nov 24. Hum Mol Genet. 2005. PMID: 15563510

7

Founder mutation in familial adenomatous polyposis (FAP) in the Balearic Islands.

González S, Blanco I, Campos O, Julià M, Reyes J, Llompart A, Cabeza E, Germà JR, Obrador A, Capellá G. González S, et al. Among authors: capella g. Cancer Genet Cytogenet. 2005 Apr 1;158(1):70-4. doi: 10.1016/j.cancergencyto.2004.07.003. Cancer Genet Cytogenet. 2005. PMID: 15771908

8

Polymorphisms in genes of nucleotide and base excision repair: risk and prognosis of colorectal cancer.

Moreno V, Gemignani F, Landi S, Gioia-Patricola L, Chabrier A, Blanco I, González S, Guino E, Capellà G, Canzian F. Moreno V, et al. Among authors: capella g. Clin Cancer Res. 2006 Apr 1;12(7 Pt 1):2101-8. doi: 10.1158/1078-0432.CCR-05-1363. Clin Cancer Res. 2006. PMID: 16609022

9

Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).

Vasen HF, Möslein G, Alonso A, Bernstein I, Bertario L, Blanco I, Burn J, Capella G, Engel C, Frayling I, Friedl W, Hes FJ, Hodgson S, Mecklin JP, Møller P, Nagengast F, Parc Y, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Wijnen J. Vasen HF, et al. Among authors: capella g. J Med Genet. 2007 Jun;44(6):353-62. doi: 10.1136/jmg.2007.048991. Epub 2007 Feb 27. J Med Genet. 2007. PMID: 17327285 Free PMC article. Review.

10

Tumor LOH analysis provides reliable linkage information for prenatal genetic testing of sporadic NF1 patients.

Serra E, Pros E, García C, López E, Gili ML, Gómez C, Ravella A, Capellá G, Blanco I, Lázaro C. Serra E, et al. Among authors: capella g. Genes Chromosomes Cancer. 2007 Sep;46(9):820-7. doi: 10.1002/gcc.20468. Genes Chromosomes Cancer. 2007. PMID: 17563086

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