Benítez J - Search Results

1

Deletion at 6q24.2-26 predicts longer survival of high-grade serous epithelial ovarian cancer patients.

Kamieniak MM, Rico D, Milne RL, Muñoz-Repeto I, Ibáñez K, Grillo MA, Domingo S, Borrego S, Cazorla A, García-Bueno JM, Hernando S, García-Donas J, Hernández-Agudo E, Y Cajal TR, Robles-Díaz L, Márquez-Rodas I, Cusidó M, Sáez R, Lacambra-Calvet C, Osorio A, Urioste M, Cigudosa JC, Paz-Ares L, Palacios J, Benítez J, García MJ. Kamieniak MM, et al. Among authors: benitez j. Mol Oncol. 2015 Feb;9(2):422-36. doi: 10.1016/j.molonc.2014.09.010. Epub 2014 Oct 5. Mol Oncol. 2015. PMID: 25454820 Free PMC article.

2

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. Among authors: benitez j. Int J Cancer. 2002 Feb 1;97(4):466-71. doi: 10.1002/ijc.1627. Int J Cancer. 2002. PMID: 11802208

3

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: benitez j. Int J Cancer. 2002 May 10;99(2):305-9. doi: 10.1002/ijc.10337. Int J Cancer. 2002. PMID: 11979449

4

Clustering of cancer-related mutations in a subset of BRCA1 alleles: a study in the Spanish population.

de la Hoya M, Sulleiro S, Osorio A, Díez O, Baiget M, Benítez J, Díaz-Rubio E, Caldés T. de la Hoya M, et al. Among authors: benitez j. Int J Cancer. 2002 Aug 10;100(5):618-9. doi: 10.1002/ijc.10527. Int J Cancer. 2002. PMID: 12124814

5

A rapid and easy method for multiple endocrine neoplasia type 1 mutation detection using conformation-sensitive gel electrophoresis.

Arancha C, Ruíz-Llorente S, Cascón A, Osorio A, Martínez-Delgado B, Benítez J, Robledo M. Arancha C, et al. Among authors: benitez j. J Hum Genet. 2002;47(4):190-5. doi: 10.1007/s100380200022. J Hum Genet. 2002. PMID: 12166655

6

Different incidence and pattern of p15INK4b and p16INK4a promoter region hypermethylation in Hodgkin's and CD30-Positive non-Hodgkin's lymphomas.

García MJ, Martínez-Delgado B, Cebrian A, Martínez A, Benítez J, Rivas C. García MJ, et al. Among authors: benitez j. Am J Pathol. 2002 Sep;161(3):1007-13. doi: 10.1016/S0002-9440(10)64261-7. Am J Pathol. 2002. PMID: 12213729 Free PMC article.

7

No mutations in the XRCC2 gene in BRCA1/2-negative high-risk breast cancer families.

Rodríguez-López R, Osorio A, Sánchez-Pulido L, De La Hoya M, Barroso A, Caldés T, Benítez J. Rodríguez-López R, et al. Among authors: benitez j. Int J Cancer. 2003 Jan 1;103(1):136-7. doi: 10.1002/ijc.10766. Int J Cancer. 2003. PMID: 12455067 No abstract available.

8

Molecular study of a new family with hereditary renal cell carcinoma and a translocation t(3;8)(p13;q24.1).

Meléndez B, Rodríguez-Perales S, Martínez-Delgado B, Otero I, Robledo M, Martínez-Ramírez A, Ruiz-Llorente S, Urioste M, Cigudosa JC, Benítez J. Meléndez B, et al. Among authors: benitez j. Hum Genet. 2003 Feb;112(2):178-85. doi: 10.1007/s00439-002-0848-6. Epub 2002 Nov 13. Hum Genet. 2003. PMID: 12522559

9

De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19.

Cigudosa JC, Odero MD, Calasanz MJ, Solé F, Salido M, Arranz E, Martínez-Ramirez A, Urioste M, Alvarez S, Cervera JV, MacGrogan D, Sanz MA, Nimer SD, Benitez J. Cigudosa JC, et al. Among authors: benitez j. Genes Chromosomes Cancer. 2003 Apr;36(4):406-12. doi: 10.1002/gcc.10180. Genes Chromosomes Cancer. 2003. PMID: 12619165 Free article.

10

Over-representation of two specific haplotypes among chromosomes harbouring BRCA1 mutations.

Osorio A, de la Hoya M, Rodríguez-López R, Granizo JJ, Díez O, Vega A, Durán M, Carracedo A, Baiget M, Caldés T, Benítez J. Osorio A, et al. Among authors: benitez j. Eur J Hum Genet. 2003 Jun;11(6):489-92. doi: 10.1038/sj.ejhg.5200969. Eur J Hum Genet. 2003. PMID: 12774043

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