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HERRERO AB, SAN MIGUEL J, GUTIERREZ NC. Deregulation of DNA double-strand break repair in multiple myeloma: implications for genome stability. PLoS One. 2015 Mar 19;10(3):e0121581. doi: 10.1371/journal.pone.0121581.
BUJ R, MALLONA I, DÍEZ-VILLANUEVA A, et al. Quantification of Unmethylated Alu (QUAlu): a tool to assess global hypomethylation in routine clinical samples. Oncotarget. 2016 Feb 7. doi: 10.18632/oncotarget.7233.
JULIÀ A, BLANCO F, FERNÁNDEZ-GUTIERREZ B, et al. Genome-Wide Association Study Identifies IRX1 as a Risk Locus for Rheumatoid Factor Positivity in Rheumatoid Arthritis. Arthritis Rheumatol. 2016 Jan 27. doi: 10.1002/art.39591.
JULIÀ A, PINTO JA, GRATACÓS J, et al. A deletion at ADAMTS9-MAGI1 locus is associated with psoriatic arthritis risk. Ann Rheum Dis. 2015 Oct;74(10):1875-81. doi: 10.1136/annrheumdis-2014-207190. Epub 2015 May 19.
ATERIDO A, JULIÀ A, FERRÁNDIZ C, et al. Genome-Wide Pathway Analysis Identifies Genetic Pathways Associated with Psoriasis. J Invest Dermatol. 2015 Dec 29. pii: S0022-202X(15)00242-0. doi: 10.1016/j.jid.2015.11.026.
POTRONY M, PUIG-BUTILLE JA, AGUILERA P, et al. Prevalence of MITF p.E318K in Patients With Melanoma Independent of the Presence of CDKN2A Causative Mutations. JAMA Dermatol. 2015 Dec 9:1-8. doi: 10.1001/jamadermatol.2015.4356.
LEON RODRIGUEZ DA, SERRANO LOPERA A, CORDERO-COMA M,et al. "Study of association of CTLA4 gene variants to non-anterior uveítis". Tissue Antigens. 2015 Nov;86(5):373-6. doi: 10.1111/tan.12668. Epub 2015 Sep 16.
THE 1000 GENOMES PROJECT CONSORTIUM. AUTON A, BROOKS LD, DURBIN RM, et al. "A global reference for human genetic variation". Nature. 2015; 526: 68-74. doi:10.1038/nature15393.
PETER H. SUDMANT, TOBIAS RAUSCH, EUGENE J. GARDNER, et al; THE 1000 GENOMES PROJECT CONSORTIUM. "An integrated map of structural variation in 2,504 human genomes". Nature. 2015; 526: 75-81. doi:10.1038/nature15394.
LÓPEZ-MEJÍAS R, GENRE F, REMUZGO-MARTÍNEZ S, et al. "Role of PTPN22 and CSK gene polymorphisms as predictors of susceptibility and clinical heterogeneity in patients with Henoch-Schönlein purpura (IgA vasculitis)". Arthritis Res Ther. 2015 Oct 13;17:286. doi: 10.1186/s13075-015-0796-x.
MAYADO A, TEODOSIO C, GARCIA-MONTERO AC, et al. "Increased IL6 plasma levels in indolent systemic mastocytosis patients are associated with high risk of disease progression". Leukemia. 2015 Jul 8. doi: 10.1038/leu.2015.176.
JARA-ACEVEDO M, TEODOSIO C, SANCHEZ-MUÑOZ L, et al. "Detection of the KIT D816V mutation in peripheral blood of systemic mastocytosis: diagnostic implications". Mod Pathol. 2015 Aug;28(8):1138-49. doi: 10.1038/modpathol.2015.72. Epub 2015 Jun 12.
FERNÁNDEZ-ARAUJO A, SÁNCHEZ JA, ALFONSO A, et al. "Different toxic effects of YTX in tumor K-562 and lymphoblastoid cell lines". Front Pharmacol. 2015 Jun 17;6:124. doi: 10.3389/fphar.2015.00124. eCollection 2015.
ALONSO A, DOMÈNECH E, JULIÀ A, et al. "Identification of risk loci for Crohn's disease phenotypes using a genome-wide association study". Gastroenterology. 2015 Apr;148(4):794-805. doi: 10.1053/j.gastro.2014.12.030. Epub 2014 Dec 31.
MANILS J, GÓMEZ D, SALLA-MARTRET M, et al. "Multifaceted role of TREX2 in the skin defense against UV-induced skin carcinogénesis". Oncotarget. 2015 Jun 15.
TELL-MARTI G, PUIG-BUTILLE JA, POTRONY M, et al. "The MC1R melanoma risk variant p.R160W is associated with Parkinson disease". Ann Neurol. 2015 May;77(5):889-94. doi: 10.1002/ana.24373. Epub 2015 Mar 13.
ACOSTA-HERRERA M, PINO-YANES M, BLANCO J, et al. "Common variants of NFE2L2 gene predisposes to acute respiratory distress syndrome in patients with severe sepsis"; GRECIA and GEN-SEP networks. Crit Care. 2015 Jun 16;19:256. doi: 10.1186/s13054-015-0981-y.
ACOSTA-HERRERA M, PINO-YANES M, MA SF, et al. "Fine mapping of the myosin light chain kinase gene (MYLK) replicates the association with asthma in populations of Spanish descent". J Allergy Clin Immunol. 2015 May 26. pii: S0091-6749(15)00587-4. doi: 10.1016/j.jaci.2015.04.025.
VIDAL-TABOADA JM, LOPEZ-LOPEZ A, SALVADO M, et al. "UNC13A confers risk for sporadic ALS and influences survival in a Spanish cohort". J Neurol. 2015 Jul 11.
LÓPEZ-MEJÍAS R, GENRE F, SEVILLA PÉREZ B, et al. "Association of HLA-B*41:02 with Henoch-Schönlein Purpura (IgA Vasculitis) in Spanish individuals irrespective of the HLA-DRB1 status". Arthritis Res Ther. 2015 Apr 14;17(1):102.
DELANEAU O, MARCHINI J. 1000 Genomes Project Consortium; "Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel"; Nat Commun. 2014 Jun 13;5:3934. doi: 10.1038/ncomms4934.
LOPEZ-LOPEZ A, GAMEZ J, SYRIANI E, et al. "CX3CR1 is a modifying gene of survival and progression in amyotrophic lateral sclerosis". PLoS One. 2014 May 7;9(5):e96528. doi: 10.1371/journal.pone.0096528. eCollection 2014.
MÁRQUEZ A, SOLANS R, HERNÁNDEZ-RODRÍGUEZ J, et al. "A Candidate Gene Approach Identifies an IL33 Genetic Variant as a Novel Genetic Risk Factor for GCA". PLoS One. 2014 Nov 19;9(11):e113476.
LÓPEZ-MEJÍAS R, GENRE F, PÉREZ BS, et al. "HLA-DRB1 association with Henoch-Schonlein purpura". Arthritis Rheumatol. 2014 Dec 2. doi: 10.1002/art.38979
FERRÁN A, ALEGRET JM, SUBIRANA I, et al. "Association Between rs2200733 and rs7193343 Genetic Variants and Atrial Fibrillation in a Spanish Population, and Meta-analysis of Previous Studies". Rev Esp Cardiol (Engl Ed). 2014 Oct;67(10):822-9. doi: 10.1016/j.rec.2013.12.019.
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Edificio Multiusos I+D+i (Universidad de Salamanca)
C/ Espejo s/n. 37007 Salamanca
Teléfono de contacto: 923294500. Ext. 5473
