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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2005 1
2009 2
2010 3
2011 2
2013 3
2015 1
2018 3
2019 2
2020 2
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16 results
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Page 1
A PALB2 truncating mutation: Implication in cancer prevention and therapy of Hereditary Breast and Ovarian Cancer.
Velázquez C, Esteban-Cardeñosa EM, Lastra E, Abella LE, de la Cruz V, Lobatón CD, Durán M, Infante M. Velázquez C, et al. Among authors: lastra e. Breast. 2019 Feb;43:91-96. doi: 10.1016/j.breast.2018.11.010. Epub 2018 Nov 29. Breast. 2019. PMID: 30521987
A high proportion of DNA variants of BRCA1 and BRCA2 is associated with aberrant splicing in breast/ovarian cancer patients.
Sanz DJ, Acedo A, Infante M, Durán M, Pérez-Cabornero L, Esteban-Cardeñosa E, Lastra E, Pagani F, Miner C, Velasco EA. Sanz DJ, et al. Among authors: lastra e. Clin Cancer Res. 2010 Mar 15;16(6):1957-67. doi: 10.1158/1078-0432.CCR-09-2564. Epub 2010 Mar 9. Clin Cancer Res. 2010. PMID: 20215541 Free article.
Genetic dissection of the BRCA2 promoter and transcriptional impact of DNA variants.
Fraile-Bethencourt E, Valenzuela-Palomo A, Díez-Gómez B, Infante M, Durán M, Marcos G, Lastra E, Gómez-Barrero S, Velasco EA. Fraile-Bethencourt E, et al. Among authors: lastra e. Breast Cancer Res Treat. 2018 Aug;171(1):53-63. doi: 10.1007/s10549-018-4826-7. Epub 2018 May 15. Breast Cancer Res Treat. 2018. PMID: 29766361
Unraveling the molecular effect of a rare missense mutation in BRIP1 associated with inherited breast cancer.
Velázquez C, Esteban-Cardeñosa EM, Lastra E, Abella LE, de la Cruz V, Lobatón CD, Durán M, Infante M. Velázquez C, et al. Among authors: lastra e. Mol Carcinog. 2019 Jan;58(1):156-160. doi: 10.1002/mc.22910. Epub 2018 Sep 22. Mol Carcinog. 2019. PMID: 30230034
SEOM clinical guidelines for hereditary cancer.
Graña B, Lastra E, Llort G, Brunet J, Isla D. Graña B, et al. Among authors: lastra e. Clin Transl Oncol. 2011 Aug;13(8):580-6. doi: 10.1007/s12094-011-0701-2. Clin Transl Oncol. 2011. PMID: 21821494
Genotype-phenotype correlation in MMR mutation-positive families with Lynch syndrome.
Pérez-Cabornero L, Infante M, Velasco E, Lastra E, Miner C, Durán M. Pérez-Cabornero L, et al. Among authors: lastra e. Int J Colorectal Dis. 2013 Sep;28(9):1195-201. doi: 10.1007/s00384-013-1685-x. Epub 2013 Apr 16. Int J Colorectal Dis. 2013. PMID: 23588873
Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair.
Seguí N, Mina LB, Lázaro C, Sanz-Pamplona R, Pons T, Navarro M, Bellido F, López-Doriga A, Valdés-Mas R, Pineda M, Guinó E, Vidal A, Soto JL, Caldés T, Durán M, Urioste M, Rueda D, Brunet J, Balbín M, Blay P, Iglesias S, Garré P, Lastra E, Sánchez-Heras AB, Valencia A, Moreno V, Pujana MÁ, Villanueva A, Blanco I, Capellá G, Surrallés J, Puente XS, Valle L. Seguí N, et al. Among authors: lastra e. Gastroenterology. 2015 Sep;149(3):563-6. doi: 10.1053/j.gastro.2015.05.056. Epub 2015 Jun 5. Gastroenterology. 2015. PMID: 26052075 Free article.
Two founder BRCA2 mutations predispose to breast cancer in young women.
Infante M, Durán M, Lasa A, Acedo A, de la Hoya M, Esteban-Cardeñosa E, Sanz DJ, Pérez-Cabornero L, Lastra E, Miner C, Velasco EA. Infante M, et al. Among authors: lastra e. Breast Cancer Res Treat. 2010 Jul;122(2):567-71. doi: 10.1007/s10549-009-0661-1. Epub 2009 Dec 1. Breast Cancer Res Treat. 2010. PMID: 19949853 Free article.
The highly prevalent BRCA2 mutation c.2808_2811del (3036delACAA) is located in a mutational hotspot and has multiple origins.
Infante M, Durán M, Acedo A, Sánchez-Tapia EM, Díez-Gómez B, Barroso A, García-González M, Feliubadaló L, Lasa A, de la Hoya M, Esteban-Cardeñosa E, Díez O, Martínez-Bouzas C, Godino J, Teulé A, Osorio A, Lastra E, González-Sarmiento R, Miner C, Velasco EA. Infante M, et al. Among authors: lastra e. Carcinogenesis. 2013 Nov;34(11):2505-11. doi: 10.1093/carcin/bgt272. Epub 2013 Aug 8. Carcinogenesis. 2013. PMID: 23929434 Free article.
Evaluating the effect of unclassified variants identified in MMR genes using phenotypic features, bioinformatics prediction, and RNA assays.
Pérez-Cabornero L, Infante M, Velasco E, Lastra E, Miner C, Durán M. Pérez-Cabornero L, et al. Among authors: lastra e. J Mol Diagn. 2013 May;15(3):380-90. doi: 10.1016/j.jmoldx.2013.02.003. Epub 2013 Mar 20. J Mol Diagn. 2013. PMID: 23523604 Free article.
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