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Publicaciones relacionadas con el BNADN
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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.
GARCÍA-BERMÚDEZ M, LÓPEZ-MEJIAS R, RODRIGUEZ-RODRIGUEZ L, et al. "No evidence of association of the KLF12 gene with rheumatoid arthritis in Spanish and Dutch cohorts and a meta-analysis of published data". Hum Immunol. 2011 Sep;72(9):779-82.
TERUEL M, MARTIN JE, GONZÁLEZ-JUANATEY C, et al. "Association of acid phosphatase locus 1*C allele with the risk of cardiovascular events in rheumatoid arthritis patients". Arthritis Res Ther. 2011 Jul 18; 13(4): R116.
LÓPEZ-MEJÍAS R, GARCÍA-BERMÚDEZ M, GONZÁLEZ-JUANATEY C, et al. "Lack of association of IL6R rs2228145 and IL6ST/gp130 rs 2228044 gene polymorphisms with cardiovascular disease in patients with rheumatoid arthritis". Tissue Antigens. 2011 Dec; 78(6): 438-41.
F. JAVIER GARCÍA PALOMO. “Requerimientos físicos de las instalaciones de laboratorios biológicos: diferencias entre norma española y americana”. Biotecnología Sanitaria. Enero 2012 (nº 8). pp 3-11. ISSN: 2013-746X.
LÓPEZ-ESCAMEZ JA, SAENZ-LOPEZ P, GAZQUEZ I, et al. "Polymorphisms of CD16A and CD32 Fcy receptors and circulating immune complexes in Ménière’s disease: a case-control study". BMC Med Genet. 2011 Jan 5;12:2.
MARTÍNEZ-CRUZ B, ZIGLE J, SANZ P, et al; "Genographic Consortium. Multiplex single-nucleotide polymosphism typing of the human Y chromosome using TaqMan probes". Investig Genet. 2011 May 31;2:13.
DOCAMPO E, GIARDINA E, RIVEIRA-MUÑOZ E, et al. "Delection of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: a study in Spanish and Italian populations and meta-analysis". Arthritis Rheum. 2011 Jul; 63(7): 1860-5.
FERNÁNDEZ-MORENO M, TAMAYO M, SOTO-HERMIDA A, et al. "mtDNA haplogroup J Modulates telomere length and Nitric Oxide production". BMC Musculoskelet Disord. 2011 Dec 15; 12:283.
DANECEK P, AUTON A, ABECASIS G, et al; 1000 GENOMES PROJECT ANALYSIS GROUP. "The variant call format and VCFtools". Bioinformatics. 2011 Aug 1;27(15):2156-8.
MACKINTOSH C, ORDOÑEZ JL, GARCÍA-DOMÍNGUEZ DJ, et al. "1q gain and CDT2 overexpression underlie an aggressive and highly proliferative form of Ewing sarcoma". 2011. Oncogene. 2011 Aug 8. doi: 10.1038/onc.2011.317.
FORTIER I, DOIRON A, LITTLE J, et al; International Harmonization Initiative. "Is rigorous retrospective harmonization possible? Application of the DataSHaPER approach across 53 large studies". Int J Epidemiol. 2011 Oct; 40(5): 1314-28.
SZCZYPIORSKA M, SÁNCHEZ A, BARTOLOMÉ N, et al. "ERAP1 polymorphisms and haplotypes are associated with ankylosing spondylitis susceptibility and functional severity in a Spanish population". 2011. Rheumatology (Oxford). 2011 Nov; 50(11): 1969-75.
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Banco Nacional de ADN
Edificio Multiusos I+D+i (Universidad de Salamanca)
C/ Espejo s/n. 37007 Salamanca
Teléfono de contacto: 923294500. Ext. 5473
Edificio Multiusos I+D+i (Universidad de Salamanca)
C/ Espejo s/n. 37007 Salamanca
Teléfono de contacto: 923294500. Ext. 5473
