Capella G - Search Results

1

Constitutional MLH1 Methylation Is a Major Contributor to Mismatch Repair-Deficient, MLH1-Methylated Colorectal Cancer in Patients Aged 55 Years and Younger.

Hitchins MP, Dámaso E, Alvarez R, Zhou L, Hu Y, Diniz MA, Pineda M, Capella G, Pearlman R, Hampel H. Hitchins MP, et al. Among authors: capella g. J Natl Compr Canc Netw. 2023 Jul;21(7):743-752.e11. doi: 10.6004/jnccn.2023.7020. J Natl Compr Canc Netw. 2023. PMID: 37433431

2

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

3

EPHB4 and survival of colorectal cancer patients.

Davalos V, Dopeso H, Castaño J, Wilson AJ, Vilardell F, Romero-Gimenez J, Espín E, Armengol M, Capella G, Mariadason JM, Aaltonen LA, Schwartz S Jr, Arango D. Davalos V, et al. Among authors: capella g. Cancer Res. 2006 Sep 15;66(18):8943-8. doi: 10.1158/0008-5472.CAN-05-4640. Cancer Res. 2006. PMID: 16982731

4

Non-Hodgkin lymphoma related to hereditary nonpolyposis colorectal cancer in a patient with a novel heterozygous complex deletion in the MSH2 gene.

Pineda M, Castellsagué E, Musulén E, Llort G, Frebourg T, Baert-Desurmont S, González S, Capellá G, Blanco I. Pineda M, et al. Among authors: capella g. Genes Chromosomes Cancer. 2008 Apr;47(4):326-32. doi: 10.1002/gcc.20536. Genes Chromosomes Cancer. 2008. PMID: 18181177

5

Detection of genetic alterations in hereditary colorectal cancer screening.

Pineda M, González S, Lázaro C, Blanco I, Capellá G. Pineda M, et al. Among authors: capella g. Mutat Res. 2010 Nov 10;693(1-2):19-31. doi: 10.1016/j.mrfmmm.2009.11.002. Epub 2009 Nov 27. Mutat Res. 2010. PMID: 19931546 Review.

6

Founder effect of a pathogenic MSH2 mutation identified in Spanish families with Lynch syndrome.

Menéndez M, Castellví-Bel S, Pineda M, de Cid R, Muñoz J, González S, Teulé A, Balaguer F, Ramón y Cajal T, Reñé JM, Blanco I, Castells A, Capellà G. Menéndez M, et al. Among authors: capella g. Clin Genet. 2010 Aug;78(2):186-90. doi: 10.1111/j.1399-0004.2009.01346.x. Epub 2010 Jan 20. Clin Genet. 2010. PMID: 20095990

7

MLH1 founder mutations with moderate penetrance in Spanish Lynch syndrome families.

Borràs E, Pineda M, Blanco I, Jewett EM, Wang F, Teulé A, Caldés T, Urioste M, Martínez-Bouzas C, Brunet J, Balmaña J, Torres A, Ramón y Cajal T, Sanz J, Pérez-Cabornero L, Castellví-Bel S, Alonso A, Lanas A, González S, Moreno V, Gruber SB, Rosenberg NA, Mukherjee B, Lázaro C, Capellá G. Borràs E, et al. Among authors: capella g. Cancer Res. 2010 Oct 1;70(19):7379-91. doi: 10.1158/0008-5472.CAN-10-0570. Epub 2010 Sep 21. Cancer Res. 2010. PMID: 20858721 Free article.

8

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

Gausachs M, Mur P, Corral J, Pineda M, González S, Benito L, Menéndez M, Espinàs JA, Brunet J, Iniesta MD, Gruber SB, Lázaro C, Blanco I, Capellá G. Gausachs M, et al. Among authors: capella g. Eur J Hum Genet. 2012 Jul;20(7):762-8. doi: 10.1038/ejhg.2011.277. Epub 2012 Jan 25. Eur J Hum Genet. 2012. PMID: 22274583 Free PMC article.

9

Comprehensive functional assessment of MLH1 variants of unknown significance.

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. Borràs E, et al. Among authors: capella g. Hum Mutat. 2012 Nov;33(11):1576-88. doi: 10.1002/humu.22142. Epub 2012 Jul 12. Hum Mutat. 2012. PMID: 22736432

10

MLH1 methylation screening is effective in identifying epimutation carriers.

Pineda M, Mur P, Iniesta MD, Borràs E, Campos O, Vargas G, Iglesias S, Fernández A, Gruber SB, Lázaro C, Brunet J, Navarro M, Blanco I, Capellá G. Pineda M, et al. Among authors: capella g. Eur J Hum Genet. 2012 Dec;20(12):1256-64. doi: 10.1038/ejhg.2012.136. Epub 2012 Jul 4. Eur J Hum Genet. 2012. PMID: 22763379 Free PMC article.

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