Infante M - Search Results

1

Increased Co-Occurrence of Pathogenic Variants in Hereditary Breast and Ovarian Cancer and Lynch Syndromes: A Consequence of Multigene Panel Genetic Testing?

Infante M, Arranz-Ledo M, Lastra E, Abella LE, Ferreira R, Orozco M, Hernández L, Martínez N, Durán M. Infante M, et al. Int J Mol Sci. 2022 Sep 29;23(19):11499. doi: 10.3390/ijms231911499. Int J Mol Sci. 2022. PMID: 36232793 Free PMC article.

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

Heteroduplex analysis by capillary array electrophoresis for rapid mutation detection in large multiexon genes.

Velasco E, Infante M, Durán M, Pérez-Cabornero L, Sanz DJ, Esteban-Cardeñosa E, Miner C. Velasco E, et al. Among authors: infante m. Nat Protoc. 2007;2(1):237-46. doi: 10.1038/nprot.2006.482. Nat Protoc. 2007. PMID: 17401359

7

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

8

BRCA1 5272-1G>A and BRCA2 5374delTATG are founder mutations of high relevance for genetic counselling in breast/ovarian cancer families of Spanish origin.

Infante M, Durán M, Acedo A, Pérez-Cabornero L, Sanz DJ, García-González M, Beristain E, Esteban-Cardeñosa E, de la Hoya M, Teulé A, Vega A, Tejada MI, Lastra E, Miner C, Velasco EA. Infante M, et al. Clin Genet. 2010 Jan;77(1):60-9. doi: 10.1111/j.1399-0004.2009.01272.x. Epub 2009 Nov 2. Clin Genet. 2010. PMID: 19912264 Free article.

9

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. 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.

10

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.

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