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Publicaciones relacionadas con el BNADN
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ORDOÑANA JR, REBOLLO-MESA I, CARRILLO E, et al. "The Murcia twin registry: a population-based registry of adult multiples in Spain". Twin Res Hum Genet. 2012 Oct 9:1-5.
CÉNIT MC, SIMEÓN CP, FONOLLOSA V, et al ; SPANISH SCLERODERMA GROUP. "No evidence of association between functional polymorphisms located within IL6R and IL6ST genes and systemic sclerosis". Tissue Antigens. 2012 Sep; 80(3):254-8.
ILLESCAS MJ, AZNAR JM, CARDOSO S, et al. "Genetic characterization of ten X-STRs in a population from the Spanish Levant". Forensic Sci Int Genet. 2012 Jul 5.
VAN DONGEN J, SLAGBOOM PE, DRAISMA HH, et al. "The continuing value of twin studies in the omics era". Nat Rev Genet. 2012 Aug 14;13(9):640-53.
SANCHEZ-JIMENO C, CUADRADO-CORRALES N, ALLER E, et al. "Recessive Dystrophic Epidermolysis Bullosa: The origin of the c.6527insC mutation in the Spanish population". Br J Dermatol. 2012 Jul 3.
JULIÀ A, TORTOSA R, HERNANZ JM, et al. "Risk variants for psoriasis vulgaris in a large case-control collection and association with clinical subphenotypes". Human Molecular Genetics. (in press, doi: 10.1093/hmg/dds295).
BENITO-SANZ S, AZA-CARMONA M, RODRÍGUEZ-ESTEVEZ A, et al. "Identification of the first PAR1 deletion encompassing upstream SHOX enhancers in a family with idiopathic short stature". Eur J Hum Genet. 2012 Jan; 20(1):125-7.
CELORRIO D, BUJANDA L, CASO C, et al. "A comparison of Val81Met and other polymorphisms of alcohol metabolising genes in patients and controls in Northern Spain". Alcohol. 2012 May 2.
BOSSINI-CASTILLO L, SIMEON CP, BERETTA L, et al; THE SPANISH SCLERODERMA GROUP. "A multicenter study confirms CD226 gene association with systemic sclerosis-related pulmonary fibrosis". Arthritis Res Ther. 2012 Apr 24; 14(2):R85.
TERUEL M, MARTIN JE, GÓMEZ-GARCÍA M, et al. "Lack of association of ACP1 gene with inflammatory bowel disease: a case-control study". Tissue Antigens. 2012 Jul; 80(1):61-64.
TERUEL M, SIMEON CP, BROEN J, et al. "Analysis of the association between CD40 and CD40 ligand polymorphisms and systemic sclerosis". Arthritis Res Ther. 2012 Jun 25; 14(3):R154.
PINO-YANES M, SÁNCHEZ-MACHÍN I, CUMPLIDO J, et al. "IL-1 receptor-associated kinase 3 gene (IRAK3) variants associate with asthma in a replication study in the Spanish population". J Allergy Clin Immunol. 2012 Feb;129(2):573-5, 575.
MARTÍN JE, BROEN JC, CARMONA D, et al. "Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up". Hum Mol Genet. 2012 Mar 9.
GAZQUEZ I, LOPEZ-ESCAMEZ JA, MORENO A, et al. "Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Menière’s disease in a European Caucasian population". DNA Cell Biol 2011 30 (9): 699-708.
BALLANA E, GONZALO E, GRAU E, et al. "Rare LEDGF/p75 genetic variants in white long-term nonprogressor HIV+ individuals". AIDS. 2012 Feb 20; 26(4): 527-8.
BALLANA E, RUIZ-DE ANDRES A, MOTHE B, et al. "Differential prevalence of the HLA-C -35 CC genotype among viremic long term non-progressor and elite controller HIV+ individuals". Immunobiology. 2012 Jan 8.
MARTÍN JE, ALIZADEH BZ, GONZÁLEZ-GAY MA, et al. "Evidence for PTPN22 R620W polymorphism as the sole common risk variant for rheumatoid arthritis in the 1p13.2 región". J Rheumatol. 2011 Nov; 38(11): 2290-6.
DÍAZ-GALLO LM, GARCIA S, ORTEGO-CENTENO N, et al. "Association study of BAK1 gene polymorphisms in Spanish rheumatoid arthritis and systemic lupus erythematosus cohorts". Ann Rheum Dis. 2012 Feb;71(2):314-6.
GARCÍA-BERMÚDEZ M, GONZÁLEZ-JUANATEY C, et al. "Lack of association of NAMPT rs9770242 and rs59744560 polymorphisms with disease susceptibility and cardiovascular risk in patients with rheumatoid arthritis". Clin Exp Rheumatol. 2011 Jul-Aug; 29(4): 681-8.
BOSSINI-CASTILLO L, SIMEON CP, BERETTA L, et al; SPANISH SCLERODERMA GROUP. "Confirmation of association of the macrophage migration inhibitory factor gene with systemic sclerosis in a large European population". Rheumatology (Oxford). 2011 Nov; 50(11): 1976-81.
BOSSINI-CASTILLO L, MARTIN JE, BROEN J, et al. "A GWAS follow-up study reveals the association of the IL12RB2 gene with systemic sclerosis in Caucasian populations". Hum Mol Genet. 2012 Feb 15;21(4):926-933.
CARMONA FD, GUTALA R, SIMEÓN CP, et al (SPANISH SCLERODERMA GROUP). "Novel identification of the IRF7 region as an anticentromere autoantibody propensity locus in systemic sclerosis". Ann Rheum Dis. 2012 Jan;71(1):114-9
MARTIN JE, CARMONA FD, BROEN JC, et al (SPANISH SCLERODERMA GROUP). "The autoimmune disease-associated IL2RA locus is involved in the clinical manifestations of systemic sclerosis". Genes Immun. 2011 Oct 20. doi: 10.1038/gene.2011.72.
CARMONA FD, SIMEON CP, BERETTA L, et al. "Association of a non-synonymous functional variant of the ITGAM gene with systemic sclerosis". Ann Rheum Dis. 2011 Nov;70 (11):2050-2.
CARMONA FD, SERRANO A, RODRÍGUEZ-RODRÍGUEZ L, et al. "A nonsynonymous functional variant of the ITGAM gene is not involved in biopsy-proven giant cell arteritis". J Rheumatol. 2011 Dec; 38(12):2598-601.
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Universidad de Salamanca
Nucleus
PRB2
Red de biobancos
Instituto Carlos III
Junta de Castilla y León
Union Europea
Banco Nacional de ADN
Edificio Multiusos I+D+i (Universidad de Salamanca)
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