Lázaro C - Search Results

1

Comprehensive establishment and characterization of orthoxenograft mouse models of malignant peripheral nerve sheath tumors for personalized medicine.

Castellsagué J, Gel B, Fernández-Rodríguez J, Llatjós R, Blanco I, Benavente Y, Pérez-Sidelnikova D, García-Del Muro J, Viñals JM, Vidal A, Valdés-Mas R, Terribas E, López-Doriga A, Pujana MA, Capellá G, Puente XS, Serra E, Villanueva A, Lázaro C. Castellsagué J, et al. Among authors: lazaro c. EMBO Mol Med. 2015 May;7(5):608-27. doi: 10.15252/emmm.201404430. EMBO Mol Med. 2015. PMID: 25810463 Free PMC article.

2

Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1.

Ars E, Serra E, García J, Kruyer H, Gaona A, Lázaro C, Estivill X. Ars E, et al. Among authors: lazaro c. Hum Mol Genet. 2000 Jan 22;9(2):237-47. doi: 10.1093/hmg/9.2.237. Hum Mol Genet. 2000. PMID: 10607834

3

Cold shock induces the insertion of a cryptic exon in the neurofibromatosis type 1 (NF1) mRNA.

Ars E, Serra E, de la Luna S, Estivill X, Lázaro C. Ars E, et al. Among authors: lazaro c. Nucleic Acids Res. 2000 Mar 15;28(6):1307-12. doi: 10.1093/nar/28.6.1307. Nucleic Acids Res. 2000. PMID: 10684924 Free PMC article.

4

Schwann cells harbor the somatic NF1 mutation in neurofibromas: evidence of two different Schwann cell subpopulations.

Serra E, Rosenbaum T, Winner U, Aledo R, Ars E, Estivill X, Lenard HG, Lázaro C. Serra E, et al. Among authors: lazaro c. Hum Mol Genet. 2000 Dec 12;9(20):3055-64. doi: 10.1093/hmg/9.20.3055. Hum Mol Genet. 2000. PMID: 11115850

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: lazaro c. Genes Chromosomes Cancer. 2007 Sep;46(9):820-7. doi: 10.1002/gcc.20468. Genes Chromosomes Cancer. 2007. PMID: 17563086

6

Nature and mRNA effect of 282 different NF1 point mutations: focus on splicing alterations.

Pros E, Gómez C, Martín T, Fábregas P, Serra E, Lázaro C. Pros E, et al. Among authors: lazaro c. Hum Mutat. 2008 Sep;29(9):E173-93. doi: 10.1002/humu.20826. Hum Mutat. 2008. PMID: 18546366

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: lazaro c. 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: lazaro c. 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: lazaro c. 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: lazaro c. 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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