Menéndez MJ - Search Results

1

Genetic polymorphism of N-acetyltransferase-2, glutathione S-transferase-M1, and cytochromes P450IIE1 and P450IID6 in the susceptibility to head and neck cancer.

González MV, Alvarez V, Pello MF, Menéndez MJ, Suárez C, Coto E. González MV, et al. Among authors: menendez mj. J Clin Pathol. 1998 Apr;51(4):294-8. doi: 10.1136/jcp.51.4.294. J Clin Pathol. 1998. PMID: 9659241 Free PMC article.

2

Mutation analysis of the p53, APC, and p16 genes in the Barrett's oesophagus, dysplasia, and adenocarcinoma.

González MV, Artímez ML, Rodrigo L, López-Larrea C, Menéndez MJ, Alvarez V, Pérez R, Fresno MF, Pérez MJ, Sampedro A, Coto E. González MV, et al. Among authors: menendez mj. J Clin Pathol. 1997 Mar;50(3):212-7. doi: 10.1136/jcp.50.3.212. J Clin Pathol. 1997. PMID: 9155671 Free PMC article.

3

Deletion and methylation of the tumour suppressor gene p16/CDKN2 in primary head and neck squamous cell carcinoma.

González MV, Pello MF, López-Larrea C, Suárez C, Menéndez MJ, Coto E. González MV, et al. Among authors: menendez mj. J Clin Pathol. 1997 Jun;50(6):509-12. doi: 10.1136/jcp.50.6.509. J Clin Pathol. 1997. PMID: 9378820 Free PMC article.

4

Loss of heterozygosity and mutation analysis of the p16 (9p21) and p53 (17p13) genes in squamous cell carcinoma of the head and neck.

González MV, Pello MF, López-Larrea C, Suárez C, Menéndez MJ, Coto E. González MV, et al. Among authors: menendez mj. Clin Cancer Res. 1995 Sep;1(9):1043-9. Clin Cancer Res. 1995. PMID: 9816078

5

Lack of association between protocadherin 11-X/Y (PCDH11X and PCDH11Y) polymorphisms and late onset Alzheimer's disease.

Miar A, Alvarez V, Corao AI, Alonso B, Díaz M, Menéndez M, Martínez C, Calatayud M, Morís G, Coto E. Miar A, et al. Brain Res. 2011 Apr 6;1383:252-6. doi: 10.1016/j.brainres.2011.01.054. Epub 2011 Jan 27. Brain Res. 2011. PMID: 21276771

6

The Sp1/Egr1-tandem repeat polymorphism in the 5-lipoxygenase gene promoter is not associated with late onset Alzheimer disease.

Alvarez V, González P, Corao AI, Menéndez M, Lahoz CH, Martínez C, Calatayud M, Morales B, Coto E. Alvarez V, et al. Alzheimer Dis Assoc Disord. 2008 Apr-Jun;22(2):177-80. doi: 10.1097/WAD.0b013e3181572046. Alzheimer Dis Assoc Disord. 2008. PMID: 18525291

7

A family with a milder form of adult dominant polycystic kidney disease not linked to the PKD1 (16p) or PKD2 (4q) genes.

Ariza M, Alvarez V, Marín R, Aguado S, López-Larrea C, Alvarez J, Menéndez MJ, Coto E. Ariza M, et al. Among authors: menendez mj. J Med Genet. 1997 Jul;34(7):587-9. doi: 10.1136/jmg.34.7.587. J Med Genet. 1997. PMID: 9222969 Free PMC article.

8

Factor V Leiden (R506Q) and risk of venous thromboembolism: a case-control study based on the Spanish population.

García-Gala JM, Alvarez V, Pinto CR, Soto I, Urgellés MF, Menéndez MJ, Carracedo C, López-Larrea C, Coto E. García-Gala JM, et al. Among authors: menendez mj. Clin Genet. 1997 Oct;52(4):206-10. doi: 10.1111/j.1399-0004.1997.tb02548.x. Clin Genet. 1997. PMID: 9383024

9

SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V.

Sánchez-Ferrero E, Coto E, Beetz C, Gámez J, Corao AI, Díaz M, Esteban J, del Castillo E, Moris G, Infante J, Menéndez M, Pascual-Pascual SI, López de Munaín A, Garcia-Barcina MJ, Alvarez V; Genetics of Spastic Paraplegia study group. Sánchez-Ferrero E, et al. Among authors: menendez m. Clin Genet. 2013 Mar;83(3):257-62. doi: 10.1111/j.1399-0004.2012.01896.x. Epub 2012 May 21. Clin Genet. 2013. PMID: 22571692

10

Amyloid precursor protein gene (APP) variation in late-onset Alzheimer's disease.

Miar A, Alvarez V, Corao AI, Díaz M, Alonso B, Martínez C, Calatayud MT, Menéndez M, Morís G, Coto E. Miar A, et al. J Mol Neurosci. 2011 Sep;45(1):5-9. doi: 10.1007/s12031-011-9510-x. Epub 2011 Mar 22. J Mol Neurosci. 2011. PMID: 21424791

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