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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
ALFONSO A, VIEYTES MR, BOTANA LM. Yessotoxin, a Promising Therapeutic Tool. Mar Drugs. 2016 Jan 28;14(2). pii: E30. doi: 10.3390/md14020030
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.
RODRIGUEZ-RODRIGUEZ L, RAMÓN LAMAS J, ABÁSOLO L, et al. The rs3771863 single nucleotide polymorphism of the TACR1 gene is associated to a lower risk of sicca syndrome in fibromyalgia patients. Clin Exp Rheumatol. 2015 Jan-Feb;33(1 Suppl 88):S33-40.
FERNÁNDEZ-ARAUJO A, ALFONSO A, et al. Key role of phosphodiesterase 4A (PDE4A) in autophagy triggered by yessotoxin. Toxicology. 2015 Mar 2;329:60-72. doi: 10.1016/j.tox.2015.01.004.
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.
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.
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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
