Benítez J - Search Results

1

A novel candidate region linked to development of both pheochromocytoma and head/neck paraganglioma.

Cascón A, Ruiz-Llorente S, Rodríguez-Perales S, Honrado E, Martínez-Ramírez A, Letón R, Montero-Conde C, Benítez J, Dopazo J, Cigudosa JC, Robledo M. Cascón A, et al. Among authors: benitez j. Genes Chromosomes Cancer. 2005 Mar;42(3):260-8. doi: 10.1002/gcc.20139. Genes Chromosomes Cancer. 2005. PMID: 15609347

2

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

3

Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma.

Cascon A, Ruiz-Llorente S, Cebrian A, Telleria D, Rivero JC, Diez JJ, Lopez-Ibarra PJ, Jaunsolo MA, Benitez J, Robledo M. Cascon A, et al. Among authors: benitez j. Eur J Hum Genet. 2002 Aug;10(8):457-61. doi: 10.1038/sj.ejhg.5200829. Eur J Hum Genet. 2002. PMID: 12111639

4

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

5

Cytogenetic characterization reveals that the SAM-1 erythroid cell line is derived from K-562 cells.

Alvarez S, MacGrogan D, Rodriguez-Perales S, Martinez-Ramirez A, Urioste M, Benitez J, Nimer SD, Cigudosa JC. Alvarez S, et al. Among authors: benitez j. Blood. 2002 Nov 1;100(9):3435-6. doi: 10.1182/blood-2002-07-2328. Blood. 2002. PMID: 12412578 Free article. No abstract available.

6

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

7

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.

8

Coincidental LOH regions in mouse and humans: evidence for novel tumor suppressor loci at 9q22-q34 in non-Hodgkin's lymphomas.

Meléndez B, Cuadros M, Robledo M, Rivas C, Fernández-Piqueras J, Martínez-Delgado B, Benítez J. Meléndez B, et al. Among authors: benitez j. Leuk Res. 2003 Jul;27(7):627-33. doi: 10.1016/s0145-2126(02)00278-3. Leuk Res. 2003. PMID: 12681362

9

G12S and H50R variations are polymorphisms in the SDHD gene.

Cascón A, Ruiz-Llorente S, Cebrián A, Letón R, Tellería D, Benítez J, Robledo M. Cascón A, et al. Among authors: benitez j. Genes Chromosomes Cancer. 2003 Jun;37(2):220-1. doi: 10.1002/gcc.10212. Genes Chromosomes Cancer. 2003. PMID: 12696072 No abstract available.

10

Polymorphisms G691S/S904S of RET as genetic modifiers of MEN 2A.

Robledo M, Gil L, Pollán M, Cebrián A, Ruíz S, Azañedo M, Benitez J, Menárguez J, Rojas JM. Robledo M, et al. Among authors: benitez j. Cancer Res. 2003 Apr 15;63(8):1814-7. Cancer Res. 2003. PMID: 12702567

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