Plataforma en Red
Banco Nacional de ADN Carlos III
Facebook Twitter YouTube
English Castellano
Banco Nacional de ADN Banco Nacional de ADN Banco Nacional de ADN Banco Nacional de ADN Banco Nacional de ADN Banco Nacional de ADN
Inicio » Publicaciones
Publicaciones relacionadas con el BNADN
CRIADO I, BLANCO E, RODRÍGUEZ-CABALLERO A, et al; EuroFlow PID Group and The Primary Health Care Group of Salamanca for the Study of MBL. Residual normal B-cell profiles in monoclonal B-cell lymphocytosis versus chronic lymphocytic leukemia. Leukemia. 2018 Jun 21. doi: 10.1038/s41375-018-0164-3
CRIADO I, RODRÍGUEZ-CABALLERO A, GUTIÉRREZ ML, et al; Primary Health Care Group of Salamanca for the Study of MBL. Low-count monoclonal B-cell lymphocytosis persists after seven years of follow up and is associated with a poorer outcome. Haematologica. 2018 Jul;103(7):1198-1208. doi: 10.3324/haematol.2017.183954.
NICOLETTI P, AITHAL GP, BJORNSSON ES, et al; International Drug-Induced Liver Injury Consortium, Drug-Induced Liver Injury Network Investigators, and International Serious Adverse Events Consortium. Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study. Gastroenterology. 2017 Apr;152(5):1078-1089. doi: 10.1053/j.gastro.2016.12.016.
VALVERDE L, ILLESCAS MJ, VILLAESCUSA P, et al. New clues to the evolutionary history of the main European paternal lineage M269: dissection of the Y-SNP S116 in Atlantic Europe and Iberia. Eur J Hum Genet. 2016 Mar;24(3):437-41. doi: 10.1038/ejhg.2015.114.
NICOLETTI P, WERK AN, SAWLE A, et al; International Drug-induced Liver Injury Consortium. HLA-DRB1*16: 01-DQB1*05: 02 is a novel genetic risk factor for flupirtine-induced liver injury. Pharmacogenet Genomics. 2016 May;26(5):218-24. doi: 10.1097/FPC.0000000000000209.
MUÑOZ-LÓPEZ A, ROMERO-MOYA D, PRIETO C, et al. Development Refractoriness of MLL-Rearranged Human B Cell Acute Leukemias to Reprogramming into Pluripotency. Stem Cell Reports. 2016 Oct 11;7(4):602-618. doi: 10.1016/j.stemcr.2016.08.013.
INFANTE M, DURÁN M, ACEDO A, et al.The highly prevalent BRCA2 mutation c.2808_2811del (3036delACAA) is located in a mutational hotspot and has multiple origins. Carcinogenesis. 2014. 2013 Nov;34(11):2505-11. doi: 10.1093/carcin/bgt272
BEDIAGA NG, MARICHALAR-MENDIA X, REY-BARJA N, et al. Polymorphisms in alcohol and tobacco metabolism genes in head and neck cancer in the Basque Country. J Oral Pathol Med. 2015 Nov;44(10):769-75. doi: 10.1111/jop.12305
PRIETO-FERNANDEZ E, BAETA M, NUÑEZ C, et al. A new 17 X-STR multiplex por forensic purposes. Forensic Science Internatonal: Genetics supplements series. 2015
RICHARD E, BRASIL S, BRISO-MONTIANO A, et al. Generation and characterization of two human iPSC lines from patients with methylmalonic acidemia cblB type. Stem Cell Res. 2018 Apr 5;29:143-147. doi: 10.1016/j.scr.2018.03.021
BARRAL-ARCA R, PISCHEDDA S, GÓMEZ-CARBALLA A, et al. Meta-Analysis of Mitochondrial DNA Variation in the Iberian Peninsula. PLoS One. 2016 Jul 21;11(7):e0159735. doi: 10.1371/journal.pone.0159735. eCollection 2016
MUÑOZ-LÓPEZ Á, VAN ROON EH, ROMERO-MOYA D, et al. Cellular Ontogeny and Hierarchy Influence the Reprogramming Efficiency of Human B Cells into Induced Pluripotent Stem Cells. Stem Cells. 2016 Mar;34(3):581-7. doi: 10.1002/stem.2303
BAZ-DÁVILA R, ESPINOZA-JIMÉNEZ A, RODRÍGUEZ-PÉREZ MDEL C, et al. Role of HIF1A, VEGFA and VEGFR2 SNPs in the Susceptibility and Progression of COPD in a Spanish Population. PLoS One. 2016 May 10;11(5):e0154998. doi: 10.1371/journal.pone.0154998. eCollection 2016
MARTÍNEZ-CRUZ B, MENDIZABAL I, HARMANT C, et al. Origins, admixture and founder lineages in European Roma. Eur J Hum Genet. 2016 Jun;24(6):937-43. doi: 10.1038/ejhg.2015.201
PRIETO-FERNÁNDEZ E, BAETA M, NÚÑEZ C, et al. Development of a new highly efficient 17 X-STR multiplex for forensic purposes. Electrophoresis. 2016 Jul;37(12):1651-8. doi: 10.1002/elps.201500546
BAETA M, ILLESCAS MJ, GARCÍA L, et al. Iberian allele frequency database for 10 X-STRs. Forensic Sci Int Genet. 2015 Nov;19:76-78. doi: 10.1016/j.fsigen.2015.06.009
RUANO EG, CANIVELL S, VIEIRA E. REV-ERB ALPHA polymorphism is associated with obesity in the Spanish obese male population. PLoS One. 2014 Aug 4;9(8):e104065. doi: 10.1371/journal.pone.0104065. eCollection 2014
GOMES DA SILVA AM1, SILBIGER VN. miRNAs as biomarkers of atrial fibrillation. Biomarkers. 2014 Dec;19(8):631-6. doi: 10.3109/1354750X.2014.954001
BYCROFT C, FERNÁNDEZ-ROZADILLA C, RUIZ-PONTE C, et al. Patterns of genetic differentiation and the footprints of historical migrations in the Iberian Peninsula. bioRxiv 250191; doi:
DAIMI H, HAJ KHELIL A, NEJI A, at al. Role of SCN5A coding and non-coding sequences in Brugada syndrome onset. What's behind the scenes? bioRxiv 218099; doi:
BAETA M, NÚÑEZ C, VILLAESCUSA P, et al. Assessment of a subset of Slowly Mutating Y-STRs for forensic and evolutionary studies. Forensic Sci Int Genet. 2018 May;34:e7-e12. doi: 10.1016/j.fsigen.2018.03.008.
HERRERO AB, GUTIÉRREZ NC. Targeting Ongoing DNA Damage in Multiple Myeloma: Effects of DNA Damage Response Inhibitors on Plasma Cell Survival. Front Oncol. 2017 May 19;7:98. doi: 10.3389/fonc.2017.00098. eCollection 2017.
NÚÑEZ C, BAETA M, IBARBIA N, et al. 17 to 23: A novel complementary mini Y-STR panel to extend the Y-STR databases from 17 to 23 markers for forensic purposes. Electrophoresis. 2017 Apr;38(7):1016-1021. doi: 10.1002/elps.201600313.
VILLAESCUSA P, ILLESCAS MJ, VALVERDE L, et al. Characterization of the Iberian Y chromosome haplogroup R-DF27 in Northern Spain. Forensic Sci Int Genet. 2017 Mar;27:142-148. doi: 10.1016/j.fsigen.2016.12.013.
TELL-MARTI G, PUIG-BUTILLE JA, POTRONY M, et al. A Common Variant in the MC1R Gene (p.V92M) is associated with Alzheimer's Disease Risk. J Alzheimers Dis. 2017;56(3):1065-1074. doi: 10.3233/JAD-161113.
Páginas: 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10
« volver
Universidad de Salamanca
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