Capellá G - Search Results

1

Highly sensitive MLH1 methylation analysis in blood identifies a cancer patient with low-level mosaic MLH1 epimutation.

Dámaso E, Canet-Hermida J, Vargas-Parra G, Velasco À, Marín F, Darder E, Del Valle J, Fernández A, Izquierdo À, Mateu G, Oliveras G, Escribano C, Piñol V, Uchima HI, Soto JL, Hitchins M, Farrés R, Lázaro C, Queralt B, Brunet J, Capellá G, Pineda M. Dámaso E, et al. Among authors: capella g. Clin Epigenetics. 2019 Nov 28;11(1):171. doi: 10.1186/s13148-019-0762-6. Clin Epigenetics. 2019. PMID: 31779681 Free PMC article.

2

[Ganglionic metastasis in the laryngeal cancer].

Capellá G, Izquierdo A. Capellá G, et al. Acta Otorinolaryngol Iber Am. 1967;18(1):23-34. Acta Otorinolaryngol Iber Am. 1967. PMID: 5598162 Spanish. No abstract available.

3

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.

4

Hypermethylation of the prostacyclin synthase (PTGIS) promoter is a frequent event in colorectal cancer and associated with aneuploidy.

Frigola J, Muñoz M, Clark SJ, Moreno V, Capellà G, Peinado MA. Frigola J, et al. Among authors: capella g. Oncogene. 2005 Nov 10;24(49):7320-6. doi: 10.1038/sj.onc.1208883. Oncogene. 2005. PMID: 16007128

5

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

6

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

7

Antisense therapeutics for neurofibromatosis type 1 caused by deep intronic mutations.

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. Pros E, et al. Among authors: capella g. Hum Mutat. 2009 Mar;30(3):454-62. doi: 10.1002/humu.20933. Hum Mutat. 2009. PMID: 19241459

8

Identification and comprehensive characterization of large genomic rearrangements in the BRCA1 and BRCA2 genes.

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. del Valle J, et al. Among authors: capella g. Breast Cancer Res Treat. 2010 Aug;122(3):733-43. doi: 10.1007/s10549-009-0613-9. Epub 2009 Nov 6. Breast Cancer Res Treat. 2010. PMID: 19894111

9

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.

10

Modulation of aberrant NF1 pre-mRNA splicing by kinetin treatment.

Pros E, Fernández-Rodríguez J, Benito L, Ravella A, Capellá G, Blanco I, Serra E, Lázaro C. Pros E, et al. Among authors: capella g. Eur J Hum Genet. 2010 May;18(5):614-7. doi: 10.1038/ejhg.2009.212. Epub 2009 Nov 25. Eur J Hum Genet. 2010. PMID: 19935827 Free PMC article.

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