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Publicaciones relacionadas con el BNADN
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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.
PINO-YANES M, CORRALES A, BASALDÚA S, et al. "North African influences and potential bias in case-control association studies in the Spanish population". PLoS One. 2011 Mar 30; 6(3):e18389.
BENITO-SANZ S, ARAGONES A, GRACIA R, et al. "A non-pathogenic pseudoautosomal region 1 copy number variant downstream of SHOX". Am J Med Genet A. 2011 Apr; 155A(4): 935-7.
CHINCILLA A, DAIMI H, LOZANO-VELASCO E, et al. "PITX2 insufficiency leads to atrial electrical and structural remodeling linked to arrhythmogenesis". Cir Cardiovasc Genet. 2011 Jun;4(3):269-79.
ANDERSON CA, BOUCHER G, LEES CW et al. "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47". Nature Genetics. 2011 Mar; 43(3): 246-52.
BENITO-SANZ S, BARROSO E, HEINE-SUÑER D, et al. "Clinical and molecular evaluation of SHOX/PAR1 duplications in Lèri-Weill dyschondrosteosis (LWD) and idiopathic short stature (ISS)". J Clin Endocrinol Metab. 2011 Feb; 96(2): E404-12.
SÁNCHEZ A, SZCZYPIORSKA M, JUANOLA X, et al. "Association of the intergenic single-nucleotide polymorphism rs10865331 (2p15) with ankylosing spondylitis in a Spanish population". 2010. J Rheumatol; 2010 Nov; 37(11):2345-7.
GARCÍA MONTERO AC, REGALADO AM. "Políticas de calidad de un biobanco". Viure en Salut, n. 83, año 2010. pp 12-13.
FRANKE A, McGOVERN DP, BARRETT JC et al. "Genome-wide meta-analysis increases to 71 the number of confirmed Crohn’s disease susceptibility loci". Nature Genetics. 2010 Dec; 42(12):1118-25.
FORTIER I, BURTON PR, ROBSON PJ et al. "Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies". Int J Epidemiol. 2010 Oct; 39(5):1383-93.
LAAYOUNI H, CALAFELL F, BERTRANPETIT J. "A genome-wide survey does not show the genetic distinctiveness of Basques". Hum Genet. 2010 Apr;127(4):455-8
VARGAS-ALARCÓN G, FRAGOSO JM, CRUZ-ROBLES D, et al. "Association of adrenergic receptor gene polymorphisms with different fibromyalgia syndrome domains". Arthritis Rheum. 2009 Jul;60(7):2169-73.
VILLAMÓN E, PIQUERAS M, MACKINTOSH C, et al. "Comparison of different techniques for the detection of genetic risk-identifying chromosomal gains and losses in neuroblastoma". Virchows Archiv. 2008 Jul;453(1):47-55.
RUBIO-CABEZAS O, DIAZ GONZALEZ F, ARAGONES A, et al. "Permanent neonatal diabetes caused by a homozygous nonsense mutation in the glucokinase gene". Pediatr Diabetes. 2008 Jun; 9(3 Pt 1):245-9.
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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)
C/ Espejo s/n. 37007 Salamanca
Teléfono de contacto: 923294500. Ext. 5473
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