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102 results

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Page 1
Prevalence of Lynch syndrome among patients with newly diagnosed endometrial cancers.
Egoavil C, Alenda C, Castillejo A, Paya A, Peiro G, Sánchez-Heras AB, Castillejo MI, Rojas E, Barberá VM, Cigüenza S, Lopez JA, Piñero O, Román MJ, Martínez-Escoriza JC, Guarinos C, Perez-Carbonell L, Aranda FI, Soto JL. Egoavil C, et al. Among authors: soto jl. PLoS One. 2013 Nov 7;8(11):e79737. doi: 10.1371/journal.pone.0079737. eCollection 2013. PLoS One. 2013. PMID: 24244552 Free PMC article.
Molecular biology of exocrine pancreatic cancer.
Soto JL, Barbera VM, Saceda M, Carrato A. Soto JL, et al. Clin Transl Oncol. 2006 May;8(5):306-12. doi: 10.1007/s12094-006-0175-9. Clin Transl Oncol. 2006. PMID: 16760004 Review.
Utility of p16 immunohistochemistry for the identification of Lynch syndrome.
Payá A, Alenda C, Pérez-Carbonell L, Rojas E, Soto JL, Guillén C, Castillejo A, Barberá VM, Carrato A, Castells A, Llor X, Andreu M, Koh J, Enders GH, Benlloch S, Jover R. Payá A, et al. Among authors: soto jl. Clin Cancer Res. 2009 May 1;15(9):3156-62. doi: 10.1158/1078-0432.CCR-08-3116. Epub 2009 Apr 21. Clin Cancer Res. 2009. PMID: 19383812 Free PMC article.
The Int7G24A variant of transforming growth factor-beta receptor type I is a risk factor for colorectal cancer in the male Spanish population: a case-control study.
Castillejo A, Mata-Balaguer T, Guarinos C, Castillejo MI, Martínez-Cantó A, Barberá VM, Montenegro P, Ochoa E, Lázaro R, Guillén-Ponce C, Carrato A, Soto JL. Castillejo A, et al. Among authors: soto jl. BMC Cancer. 2009 Nov 20;9:406. doi: 10.1186/1471-2407-9-406. BMC Cancer. 2009. PMID: 19930569 Free PMC article.
Biallelic MYH germline mutations as cause of Muir-Torre syndrome.
Guillén-Ponce C, Castillejo A, Barberá VM, Pascual-Ramírez JC, Andrada E, Castillejo MI, Guarinós C, Molina-Garrido MJ, Carrato A, Soto JL. Guillén-Ponce C, et al. Among authors: soto jl. Fam Cancer. 2010 Jun;9(2):151-4. doi: 10.1007/s10689-009-9309-x. Fam Cancer. 2010. PMID: 19998059
Methylation analysis of MLH1 improves the selection of patients for genetic testing in Lynch syndrome.
Pérez-Carbonell L, Alenda C, Payá A, Castillejo A, Barberá VM, Guillén C, Rojas E, Acame N, Gutiérrez-Aviñó FJ, Castells A, Llor X, Andreu M, Soto JL, Jover R. Pérez-Carbonell L, et al. Among authors: soto jl. J Mol Diagn. 2010 Jul;12(4):498-504. doi: 10.2353/jmoldx.2010.090212. Epub 2010 May 20. J Mol Diagn. 2010. PMID: 20489114 Free PMC article.
EPCAM germ line deletions as causes of Lynch syndrome in Spanish patients.
Guarinos C, Castillejo A, Barberá VM, Pérez-Carbonell L, Sánchez-Heras AB, Segura A, Guillén-Ponce C, Martínez-Cantó A, Castillejo MI, Egoavil CM, Jover R, Payá A, Alenda C, Soto JL. Guarinos C, et al. Among authors: soto jl. J Mol Diagn. 2010 Nov;12(6):765-70. doi: 10.2353/jmoldx.2010.100039. Epub 2010 Sep 23. J Mol Diagn. 2010. PMID: 20864635 Free PMC article.
Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome.
Castillejo A, Guarinos C, Martinez-Canto A, Barbera VM, Egoavil C, Castillejo MI, Perez-Carbonell L, Sanchez-Heras AB, Segura A, Ochoa E, Lazaro R, Ruiz-Ponte C, Bujanda L, Andreu M, Castells A, Carracedo A, Llor X, Clofent J, Alenda C, Paya A, Jover R, Soto JL. Castillejo A, et al. Among authors: soto jl. BMC Med Genet. 2011 Jan 19;12:12. doi: 10.1186/1471-2350-12-12. BMC Med Genet. 2011. PMID: 21247423 Free PMC article.
102 results