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Publicaciones relacionadas con el BNADN
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.
MUNIESA CA, VERDE Z, DIAZ-UREÑA G, et al. Telomere Length in Elite Athletes. Int J Sports Physiol Perform. 2017 Aug;12(7):994-996. doi: 10.1123/ijspp.2016-0471. Epub 2016 Dec 5.
PINHEIRO MB, MOROSOLI JJ, COLODRO-CONDE L, et al. Genetic and environmental influences to low back pain and symptoms of depression and anxiety: A population-based twin study. J Psychosom Res. 2018 Feb;105:92-98. doi: 10.1016/j.jpsychores.2017.12.007. Epub 2017 Dec 6
VIDAL-TABOADA JM, PUGLIESE M, SALVADÓ M, et al. KATP Channel Expression and Genetic Polymorphisms Associated with Progression and Survival in Amyotrophic Lateral Sclerosis. Mol Neurobiol. 2018 Feb 28. doi: 10.1007/s12035-018-0970-7
LÓPEZ-LÓPEZ A, GELPI E, LOPATEGUI DM, et al. Association of the CX3CR1-V249I Variant with Neurofibrillary Pathology Progression in Late-Onset Alzheimer's Disease. Mol Neurobiol. 2018 Mar;55(3):2340-2349. doi: 10.1007/s12035-017-0489-3. Epub 2017 Mar 25
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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