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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
SEGURA V, VALERO ML, CANTERO L, et al. In-Depth Proteomic Characterization of Classical and Non-Classical Monocyte Subsets. Proteomes. 2018 Feb 5;6(1). pii: E8. doi: 10.3390/proteomes6010008
UMBRIA M, RAMOS A, CANER J, e al. Involvement of mitochondrial haplogroups in myocardial infarction and stroke: A case-control study in Castile and Leon (Spain) population. Mitochondrion. 2017 Dec 16. pii: S1567-7249(17)30024-7. doi: 10.1016/j.mito.2017.12.004
CRIADO I, MUÑOZ-CRIADO S, RODRÍGUEZ-CABALLERO A, et al; Primary Health Care Group of Salamanca for the Study of MBL. Host virus and pneumococcus-specific immune responses in high-count monoclonal B-cell lymphocytosis and chronic lymphocytic leukemia: implications for disease progression. Haematologica. 2017 Jul;102(7):1238-1246. doi: 10.3324/haematol.2016.159012. Epub 2017 Apr 6
PINHEIRO MB, MOROSOLI JJ, FERREIRA ML, et al. Genetic and environmental contributions to sleep quality and low back pain: a population-based twin study. Psychosom Med. 2017 Dec 13. doi: 10.1097/PSY.0000000000000548
GÓMEZ-TORTOSA E, RUGGIERO M, SAINZ MJ, et al. SORL1 variants in familiar alzheimer´s disease. Journal of Alzheimer Disease. 2017
ORTIZ-FERNÁNDEZ L, MONTES-CANO MA, GARCÍA-LOZANO JR, et al. PTPN22 is not associated with Behçet's disease. Study spanning the complete gene region in the Spanish population and meta-analysis of the functional variant R620W. Clin Exp Rheumatol. 2016 Apr 1
BOSSINI-CASTILLO L, CAMPILLO-DAVÓ D, LÓPEZ-ISAC E, et al; Spanish Scleroderma Group. An MIF Promoter Polymorphism Is Associated with Susceptibility to Pulmonary Arterial Hypertension in Diffuse Cutaneous Systemic Sclerosis. J Rheumatol. 2017 Oct;44(10):1453-1457. doi: 10.3899/jrheum.161369. Epub 2017 Jul 1.
MÁRQUEZ A, CORDERO-COMA M, MARTÍN-VILLA JM, et al. New insights into the genetic component of non-infectious uveitis through an Immunochip strategy. J Med Genet. 2017 Jan;54(1):38-46. doi: 10.1136/jmedgenet-2016-104144
LOPEZ-ISAC E, BOSSINI-CASTILLO L, PALMA AB, et al. Analysis of ATP8B4 F436L Missense Variant in a Large Systemic Sclerosis Cohort. Arthritis Rheumatol. 2017 Jun;69(6):1337-1338. doi: 10.1002/art.40058. Epub 2017 May 9.
GÓMEZ-TORTOSA E, VAN DER ZEE J, RUGGIERO M, et al; EU EOD Consortium. Familial primary lateral sclerosis or dementia associated with Arg573Gly TBK1 mutation. J Neurol Neurosurg Psychiatry. 2017 Nov;88(11):996-997. doi: 10.1136/jnnp-2016-315250.
HISADO-OLIVA A, RUZAFA-MARTIN A, SENTCHORDI L, et al. Mutations in C-natriuretic peptide (NPPC): a novel cause of autosomal dominant short stature. Genet Med. 2017 Jun 29. doi: 10.1038/gim.2017.66
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.
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Edificio Multiusos I+D+i (Universidad de Salamanca)
C/ Espejo s/n. 37007 Salamanca
Teléfono de contacto: 923294500. Ext. 5473
