de la Hoya M - Search Results

1

Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families.

Osorio A, Endt D, Fernández F, Eirich K, de la Hoya M, Schmutzler R, Caldés T, Meindl A, Schindler D, Benitez J. Osorio A, et al. Among authors: de la hoya m. Hum Mol Genet. 2012 Jul 1;21(13):2889-98. doi: 10.1093/hmg/dds115. Epub 2012 Mar 26. Hum Mol Genet. 2012. PMID: 22451500

2

Denaturing gradient gel electrophoresis-based analysis of loss of heterozygosity distinguishes nonobvious, deleterious BRCA1 variants from nonpathogenic polymorphisms.

de La Hoya M, Díaz-Rubio E, Caldés T. de La Hoya M, et al. Clin Chem. 1999 Nov;45(11):2028-30. Clin Chem. 1999. PMID: 10545082 No abstract available.

3

Low frequency of microsatellite instability in sporadic breast cancer.

Caldes T, Perez-Segura P, Tosar A, De La Hoya M, Diaz-Rubio E. Caldes T, et al. Among authors: de la hoya m. Int J Oncol. 2000 Jun;16(6):1235-42. doi: 10.3892/ijo.16.6.1235. Int J Oncol. 2000. PMID: 10812001

4

Microsatellite instability correlates with negative expression of estrogen and progesterone receptors in sporadic breast cancer.

Caldés T, Perez-Segura P, Tosar A, de La Hoya M, Diaz-Rubio E. Caldés T, et al. Among authors: de la hoya m. Teratog Carcinog Mutagen. 2000;20(5):283-91. Teratog Carcinog Mutagen. 2000. PMID: 10992275

5

New mutation in the hMSH2 gene in a Spanish Muir-Torre syndrome.

Caldés T, Godino J, Perez-Segura P, de la Hoya M, Diaz-Rubio E, Benito M. Caldés T, et al. Among authors: de la hoya m. Am J Gastroenterol. 2000 Sep;95(9):2389-90. doi: 10.1111/j.1572-0241.2000.02344.x. Am J Gastroenterol. 2000. PMID: 11007253 No abstract available.

6

Spanish family study on hereditary breast and/or ovarian cancer: analysis of the BRCA1 gene.

de la Hoya M, Pérez-Segura P, Van Orsouw N, Díaz-Rubio E, Caldés T. de la Hoya M, et al. Int J Cancer. 2001 Jan 1;91(1):137-40. doi: 10.1002/1097-0215(20010101)91:1<137::aid-ijc1020>3.0.co;2-r. Int J Cancer. 2001. PMID: 11149413 No abstract available.

7

Eight novel germline MLH1 and MSH2 mutations in hereditary non-polyposis colorectal cancer families from Spain.

Godino J, de La Hoya M, Diaz-Rubio E, Benito M, Caldés T. Godino J, et al. Among authors: de la hoya m. Hum Mutat. 2001 Dec;18(6):549. doi: 10.1002/humu.1240. Hum Mutat. 2001. PMID: 11748856

8

Association between BRCA1 and BRCA2 mutations and cancer phenotype in Spanish breast/ovarian cancer families: implications for genetic testing.

de la Hoya M, Osorio A, Godino J, Sulleiro S, Tosar A, Perez-Segura P, Fernandez C, Rodríguez R, Díaz-Rubio E, Benítez J, Devilee P, Caldés T. de la Hoya M, et al. Int J Cancer. 2002 Feb 1;97(4):466-71. doi: 10.1002/ijc.1627. Int J Cancer. 2002. PMID: 11802208

9

Prevalence of germline mutations of MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer families from Spain.

Caldes T, Godino J, de la Hoya M, Garcia Carbonero I, Perez Segura P, Eng C, Benito M, Diaz-Rubio E. Caldes T, et al. Among authors: de la hoya m. Int J Cancer. 2002 Apr 10;98(5):774-9. doi: 10.1002/ijc.10240. Int J Cancer. 2002. PMID: 11920650

10

Loss of heterozygosity analysis at the BRCA loci in tumor samples from patients with familial breast cancer.

Osorio A, de la Hoya M, Rodríguez-López R, Martínez-Ramírez A, Cazorla A, Granizo JJ, Esteller M, Rivas C, Caldés T, Benítez J. Osorio A, et al. Among authors: de la hoya m. Int J Cancer. 2002 May 10;99(2):305-9. doi: 10.1002/ijc.10337. Int J Cancer. 2002. PMID: 11979449

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