Infante M - Search Results

1

GALNT12 is not a major contributor of familial colorectal cancer type X.

Seguí N, Pineda M, Navarro M, Lázaro C, Brunet J, Infante M, Durán M, Soto JL, Blanco I, Capellá G, Valle L. Seguí N, et al. Among authors: infante m. Hum Mutat. 2014 Jan;35(1):50-2. doi: 10.1002/humu.22454. Epub 2013 Oct 17. Hum Mutat. 2014. PMID: 24115450

2

Mutational analysis of BRCA2 in Spanish breast cancer patients from Castilla-Leon: identification of four novel truncating mutations.

Duran M, Esteban-Cardeñosa E, Velasco E, Infante M, Miner C. Duran M, et al. Among authors: infante m. Hum Mutat. 2003 Apr;21(4):448. doi: 10.1002/humu.9126. Hum Mutat. 2003. PMID: 12655567

3

High-throughput mutation detection method to scan BRCA1 and BRCA2 based on heteroduplex analysis by capillary array electrophoresis.

Esteban-Cardeñosa E, Duran M, Infante M, Velasco E, Miner C. Esteban-Cardeñosa E, et al. Among authors: infante m. Clin Chem. 2004 Feb;50(2):313-20. doi: 10.1373/clinchem.2003.023614. Epub 2003 Dec 18. Clin Chem. 2004. PMID: 14684619 Free article.

4

Rapid mutation detection in complex genes by heteroduplex analysis with capillary array electrophoresis.

Velasco E, Infante M, Durán M, Esteban-Cardeñosa E, Lastra E, García-Girón C, Miner C. Velasco E, et al. Among authors: infante m. Electrophoresis. 2005 Jun;26(13):2539-52. doi: 10.1002/elps.200410425. Electrophoresis. 2005. PMID: 15937982

5

High proportion of novel mutations of BRCA1 and BRCA2 in breast/ovarian cancer patients from Castilla-León (central Spain).

Infante M, Durán M, Esteban-Cardeñosa E, Miner C, Velasco E. Infante M, et al. J Hum Genet. 2006;51(7):611-7. doi: 10.1007/s10038-006-0404-7. Epub 2006 Jun 7. J Hum Genet. 2006. PMID: 16758124 Free article.

6

A new strategy to screen MMR genes in Lynch Syndrome: HA-CAE, MLPA and RT-PCR.

Perez-Cabornero L, Velasco E, Infante M, Sanz D, Lastra E, Hernández L, Miner C, Duran M. Perez-Cabornero L, et al. Among authors: infante m. Eur J Cancer. 2009 May;45(8):1485-93. doi: 10.1016/j.ejca.2009.01.030. Epub 2009 Feb 26. Eur J Cancer. 2009. PMID: 19250818

7

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: infante m. 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.

8

Detection of a large rearrangement in PALB2 in Spanish breast cancer families with male breast cancer.

Blanco A, de la Hoya M, Balmaña J, Ramón y Cajal T, Teulé A, Miramar MD, Esteban E, Infante M, Benítez J, Torres A, Tejada MI, Brunet J, Graña B, Balbín M, Pérez-Segura P, Osorio A, Velasco EA, Chirivella I, Calvo MT, Feliubadaló L, Lasa A, Díez O, Carracedo A, Caldés T, Vega A. Blanco A, et al. Among authors: infante m. Breast Cancer Res Treat. 2012 Feb;132(1):307-15. doi: 10.1007/s10549-011-1842-2. Epub 2011 Nov 4. Breast Cancer Res Treat. 2012. PMID: 22052327 Free article.

9

Incidence of -93 MLH1 promoter polymorphism in familial and sporadic colorectal cancer.

Martínez-Urueña N, Macías L, Pérez-Cabornero L, Infante M, Lastra E, Cruz JJ, Miner C, González R, Durán M. Martínez-Urueña N, et al. Among authors: infante m. Colorectal Dis. 2013 Mar;15(3):e118-23. doi: 10.1111/codi.12112. Colorectal Dis. 2013. PMID: 23374646

10

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: infante m. 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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