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Publicaciones relacionadas con el BNADN
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LÓPEZ-LÓPEZ A, GELPI E, LOPATEGUI DM, VIDAL-TABOADA JM. Association of the CX3CR1-V249I Variant with Neurofibrillary Pathology Progression in Late-Onset Alzheimer's Disease. Mol Neurobiol. 2017 Mar 25. doi: 10.1007/s12035-017-0489-3.
SERRA-JUHÉ C, MARTOS-MORENO GÁ, BOU DE PIERI F, et al. Novel genes involved in severe early-onset obesity revealed by rare copy number and sequence variants. PLoS Genet. 2017 May 10;13(5):e1006657. doi: 10.1371/journal.pgen.1006657. eCollection 2017 May.
ORDOÑANA JR, SÁNCHEZ ROMERA JF, COLODRO-CONDE L, CARRILLO E, et al. The Murcia Twin Registry. A resource for research on health-related behaviour. Gac Sanit. 2017 Mar 8. pii: S0213-9111(16)30259-X. doi: 10.1016/j.gaceta.2016.10.008
FERNÁNDEZ-GUTIÉRREZ B, PERROTTI PP, GISBERT JP, et al;IMID Consortium. Cardiovascular disease in immune-mediated inflammatory diseases: A cross-sectional analysis of 6 cohorts. Medicine (Baltimore). 2017 Jun;96(26):e7308. doi: 10.1097/MD.0000000000007308
GAGO-DÍAZ M, BRION M, GALLEGO P, et al. The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study. J Mol Cell Cardiol. 2017 Jan;102:3-9. doi: 10.1016/j.yjmcc.2016.11.012. Epub 2016 Nov 25.
DÍEZ P, IBARROLA N, DÉGANO RM, LÉCREVISSE et al. A systematic approach for peptide characterization of B-cell receptor in chronic lymphocytic leukemia cells. Oncotarget. 2017 Jun 27;8(26):42836-42846. doi: 10.18632/oncotarget.17076.
CARRERAS-TORRES R, FERRAN A, ZANETTI D, et al. Population structure from NOS genes correlates with geographical differences in coronary incidence across Europe. Am J Phys Anthropol. 2016 Dec;161(4):634-645. doi: 10.1002/ajpa.23063. Epub 2016 Aug 8.
POTRONY M, PUIG-BUTILLE JA, AGUILERA P, el al. Prevalence of MITF p.E318K in Patients With Melanoma Independent of the Presence of CDKN2A Causative Mutations. JAMA Dermatol. 2016 Apr;152(4):405-12. doi: 10.1001/jamadermatol.2015.4356
BARRETO-LUIS A, CORRALES A, ACOSTA-HERRERA M, et al. A pathway-based association study reveals variants from Wnt signalling genes contributing to asthma susceptibility.. Clin Exp Allergy. 2017 Jan 12. doi: 10.1111/cea.12883
BARRETO-LUIS A, PINO-YANES M, CORRALES A, et al. Genome-wide association study in Spanish identifies ADAM metallopeptidase with thrombospondin type 1 motif, 9 (ADAMTS9), as a novel asthma susceptibility gene. J Allergy Clin Immunol. 2016 Mar;137(3):964-6. doi: 10.1016/j.jaci.2015.09.051
POZNIK GD, XUE Y, MENDEZ FL, et al; 1000 GENOMES PROJECT CONSORTIUM. Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences. Tyler-Smith C. Nat Genet. 2016 Jun;48(6):593-9. doi: 10.1038/ng.3559.
JULIÀ A, GONZÁLEZ I, FERNÁNDEZ-NEBRO A, et al. A genome-wide association study identifies SLC8A3 as a susceptibility locus for ACPA-positive rheumatoid arthritis. Rheumatology (Oxford). 2016 Jun;55(6):1106-11. doi: 10.1093/rheumatology/ kew035. Epub 2016 Mar 15.
GAMARRA D, ELCOROARISTIZABAL X, FERNÁNDEZ-MARTÍNEZ M, DE PANCORBO MM. Association of the C47T Polymorphism in SOD2 with Amnestic Mild Cognitive Impairment and Alzheimer's Disease in Carriers of the APOEε4 Allele. Dis Markers. 2015;2015:746329. doi: 10.1155/2015/746329. Epub 2015 Dec 1.
PRIETO-FERNÁNDEZ E, NÚÑEZ C, BAETA M, et al. Forensic Spanish allele and haplotype database for a 17 X-STR panel. Forensic Sci Int Genet. 2016 Sep;24:120-3. doi: 10.1016/j.fsigen.2016.06.016. Epub 2016 Jun 22.
FREIRE-ARADAS A, PHILLIPS C, MOSQUERA-MIGUEL A, et al. Development of a methylation marker set for forensic age estimation using analysis of public methylation data and the Agena Bioscience EpiTYPER system. Forensic Sci Int Genet. 2016 Sep;24:65-74. doi: 10.1016/j.fsigen.2016.06.005. Epub 2016 Jun 8.
ALONSO A, JULIÀ A, VINAIXA M, et al; IMID Consortium. Urine metabolome profiling of immune-mediated inflammatory diseases. BMC Med. 2016 Sep 8;14(1):133. doi: 10.1186/s12916-016-0681-8.
SÁNCHEZ-LANZAS R, ALVAREZ-CASTELAO B, BERMEJO T, et al. Protein degradation in a LAMP-2-deficient B-lymphoblastoid cell line from a patient with Danon disease. Biochim Biophys Acta. 2016 Aug;1862(8):1423-32. doi: 10.1016/j.bbadis.2016.04.014. Epub 2016 Apr 26
MUCIENTES A, MÁRQUEZ A, CORDERO-COMA M, et al. Specific association of IL17A genetic variants with panuveitis. Br J Ophthalmol. 2015 Apr;99(4):566-70. doi: 10.1136/bjophthalmol-2014-306106.
BOSSINI-CASTILLO L, DE KOVEL C, KALLBERG H, et al. A genome-wide association study of rheumatoid arthritis without antibodies against citrullinated peptides. Ann Rheum Dis. 2015 Mar;74(3):e15. doi: 10.1136/annrheumdis-2013-204591.
LÓPEZ-ISAC E, CAMPILLO-DAVO D, BOSSINI-CASTILLO L, et at. Influence of TYK2 in systemic sclerosis susceptibility: a new locus in the IL-12 pathway. Ann Rheum Dis. 2015 Sep 2. pii: annrheumdis-2015-208154. doi: 10.1136/annrheumdis-2015-208154
COSTAS J, CARRERA N, ALONSO P, et al. Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia. Transl Psychiatry. 2016 Mar 29;6:e768. doi: 10.1038/tp.2016.34.
LÓPEZ-ISAC E, MARTÍN JE, ASSASSI S, et al. Cross-disease Meta-analysis of Genome-wide Association Studies for Systemic Sclerosis and Rheumatoid Arthritis Reveals IRF4 as a New Common Susceptibility Locus. Arthritis Rheumatol. 2016 Apr 25. doi: 10.1002/art.39730.
LÓPEZ-MEJÍAS R, GENRE F, REMUZGO-MARTÍNEZ S, et al. Interleukin 1 beta (IL1ß) rs16944 genetic variant as a genetic marker of severe renal manifestations and renal sequelae in Henoch-Schönlein purpura. Clin Exp Rheumatol. 2016 Feb 1.
MARTÍNEZ-ROBLES E, YEBRA-BANGO M, MELLOR-PITA S, et al. Genotypic distribution of common variants of endosomal toll like receptors in healthy Spanish women. A comparative study with other populations. Gene. 2016 Mar 1;578(1):32-7. doi: 10.1016/j.gene.2015.12.004.
BARRETO-LUIS A, PINO-YANES M, CORRALES A, et al. Genome-wide association study in Spanish identifies ADAM metallopeptidase with thrombospondin type 1 motif, 9 (ADAMTS9), as a novel asthma susceptibility gene. J Allergy Clin Immunol. 2016 Mar;137(3):964-6. doi: 10.1016/j.jaci.2015.09.051
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University of Salamanca
Nucleus
PRB2
Biobanks Network
Institute Carlos III
Junta de Castilla y León
European Union
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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