Coto E - Search Results

1

Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy.

Valdés-Mas R, Gutiérrez-Fernández A, Gómez J, Coto E, Astudillo A, Puente DA, Reguero JR, Álvarez V, Morís C, León D, Martín M, Puente XS, López-Otín C. Valdés-Mas R, et al. Among authors: coto e. Nat Commun. 2014 Oct 29;5:5326. doi: 10.1038/ncomms6326. Nat Commun. 2014. PMID: 25351925 Free article.

2

Characterization of B27 haplotypes by oligotyping and genomic sequencing in the Mexican Mestizo population with ankylosing spondylitis: juvenile and adult onset.

López-Larrea C, Gonzalez-Roces S, Peña M, Dominguez O, Coto E, Alvarez V, Moreno M, Hernandez O, Burgos-Vargas R, Gorodezky C. López-Larrea C, et al. Among authors: coto e. Hum Immunol. 1995 Jul;43(3):174-80. doi: 10.1016/0198-8859(94)00156-k. Hum Immunol. 1995. PMID: 7558934

3

Genetic detection of the silent allele (*Q0) in hereditary deficiencies of the human complement C6, C7, and C9 components.

Alvarez V, Coto E, Setién F, Spath PJ, López-Larrea C. Alvarez V, et al. Among authors: coto e. Am J Med Genet. 1995 Feb 13;55(4):408-13. doi: 10.1002/ajmg.1320550405. Am J Med Genet. 1995. PMID: 7762578

4

Molecular analysis of HLA-B27 haplotypes in Caucasoids. Frequencies of B27-Cw in Jewish and Spanish populations.

González-Roces S, Brautbar C, Peña M, Dominguez O, Coto E, Alvarez V, Segal R, López-Larrea C. González-Roces S, et al. Among authors: coto e. Hum Immunol. 1994 Oct;41(2):127-34. doi: 10.1016/0198-8859(94)90005-1. Hum Immunol. 1994. PMID: 7860357

5

A physical map of two clusters containing the genes for six proinflammatory receptors.

Alvarez V, Coto E, Setién F, López-Larrea C. Alvarez V, et al. Among authors: coto e. Immunogenetics. 1994;40(2):100-3. doi: 10.1007/BF00188171. Immunogenetics. 1994. PMID: 8026857

6

A physical map of the human complement component C6, C7, and C9 genes.

Setién F, Alvarez V, Coto E, DiScipio RG, López-Larrea C. Setién F, et al. Among authors: coto e. Immunogenetics. 1993;38(5):341-4. doi: 10.1007/BF00210475. Immunogenetics. 1993. PMID: 8344719

7

Molecular evolution of the N-formyl peptide and C5a receptors in non-human primates.

Alvarez V, Coto E, Setién F, González-Roces S, López-Larrea C. Alvarez V, et al. Among authors: coto e. Immunogenetics. 1996;44(6):446-52. doi: 10.1007/BF02602806. Immunogenetics. 1996. PMID: 8824156

8

Characterization of interleukin-8 receptors in non-human primates.

Alvarez V, Coto E, Setién F, Gonzalez S, Gonzalez-Roces S, López-Larrea C. Alvarez V, et al. Among authors: coto e. Immunogenetics. 1996;43(5):261-7. doi: 10.1007/BF02440993. Immunogenetics. 1996. PMID: 9110929

9

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: coto e. 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.

10

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: coto e. 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.

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