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ATERIDO A, PALAU N, DOMÈNECH E,et al. Genetic association between CD96 locus and immunogenicity to anti-TNF therapy in Crohn's disease. Pharmacogenomics J. 2019 May 2. doi: 10.1038/s41397-019-0090-4.
MUÑOZ-GONZÁLEZ JI, ÁLVAREZ-TWOSE I, JARA-ACEVEDO M, et al. Frequency and prognostic impact of KIT and other genetic variants in indolent systemic mastocytosis. Blood. 2019 Aug 1;134(5):456-468. doi: 10.1182/blood.2018886507.
NICOLETTI P, BARRETT S, MCEVOY L, et al. Shared Genetic Risk Factors Across Carbamazepine-Induced Hypersensitivity Reactions. Clin Pharmacol Ther. 2019 May 7. doi: 10.1002/cpt.1493
FERNÁNDEZ-SANTIAGO R, MARTÍN-FLORES N, ANTONELLI F, et al; International Parkinson's Disease Genomics Consortium, Martí MJ, Ezquerra M, Malagelada C. SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease. Mov Disord. 2019 Jun 24. doi: 10.1002/mds.27770.
BARRIO PA, MARTÍN P, ALONSO A, et al; DNASEQEX Consortium. Massively parallel sequence data of 31 autosomal STR loci from 496 Spanish individuals revealed concordance with CE-STR technology and enhanced discrimination power. Forensic Sci Int Genet. 2019 Jun 14;42:49-55. doi: 10.1016/j.fsigen.2019.06.009.
VEGA ALONSO AT, ORDAX DÍEZ A, LOZANO ALONSO JE, et al; en nombre del grupo de investigación del estudio del Riesgo de enfermedad cardiovascular en Castilla y León. Validation of the SCORE index and SCORE for old people in the Castilla y Léon cardiovascular disease risk cohort. Hipertens Riesgo Vasc. 2019 Mar 26. pii: S1889-1837(19)30017-0. doi: 10.1016/j.hipert.2019.02.002
NICOLETTI P, AITHAL GP, CHAMBERLAIN TC, et al; Drug-Induced Liver Injury due to Flucloxacillin: Relevance of Multiple Human Leukocyte Antigen Alleles. International Drug-Induced Liver Injury Consortium (iDILIC). Clin Pharmacol Ther. 2019 Jul;106(1):245-253. doi: 10.1002/cpt.1375
ATERIDO A, CAÑETE JD, TORNERO J, et al. Genetic variation at the glycosaminoglycan metabolism pathway contributes to the risk of psoriatic arthritis but not psoriasis. Ann Rheum Dis. 2019 Mar;78(3). pii: e214158. doi: 10.1136/annrheumdis-2018-214158.
BYCROFT C, FERNANDEZ-ROZADILLA C, RUIZ-PONTE C, et al. Patterns of genetic differentiation and the footprints of historical migrations in the Iberian Peninsula.Nat Commun. 2019 Feb 1;10(1):551. doi: 10.1038/s41467-018-08272-w.
UMBRIA M, RAMOS A, CANER J, et al. Involvement of mitochondrial haplogroups in myocardial infarction and stroke: A case-control study in Castile and Leon (Spain) population. Mitochondrion. 2019 Jan;44:1-6. doi: 10.1016/j.mito.2017.12.004
VILLAESCUSA P, PALENCIA-MADRID L, CAMPANER MA, et al. Effective resolution of the Y chromosome sublineages of the Iberian haplogroup R1b-DF27 with forensic purposes. Int J Legal Med. 2019 Jan;133(1):17-23. doi: 10.1007/s00414-018-1936-z
VELÁZQUEZ C, ESTEBAN-CARDEÑOSA EM, LASTRA E, et al. A PALB2 truncating mutation: Implication in cancer prevention and therapy of Hereditary Breast and Ovarian Cancer. Breast. 2019 Feb;43:91-96. doi: 10.1016/j.breast.2018.11.010.
ANALES JM, IÑARRAIRAEGUI M, ARBELAIZ A, et al. Serum Metabolites as Diagnostic Biomarkers for Cholangiocarcinoma, Hepatocellular Carcinoma, and Primary Sclerosing Cholangitis. Hepatology. 2019 Aug;70(2):547-562. doi: 10.1002/hep.30319
TERUEL-MONTOYA R, LUENGO-GIL G, VALLEJO F, et al. Differential miRNA expression profile and proteome in plasma exosomes from patients with paroxysmal nocturnal hemoglobinuria Sci Rep. 2019 Mar 5;9(1):3611. doi: 10.1038/s41598-019-40453-5.
MONTALBAN G, BONACHE S, MOLES-FERNÁNDEZ A, et al. Screening of BRCA1/2 deep intronic regions by targeted gene sequencing identifies the first germline BRCA1 variant causing pseudoexon activation in a patient with breast/ovarian cancer. J Med Genet. 2018 Nov 24. pii: jmedgenet-2018-105606. doi: 10.1136/jmedgenet-2018-105606.
ATERIDO A, CAÑETE JD, TORNERO J, et al. Genetic variation at the glycosaminoglycan metabolism pathway contributes to the risk of psoriatic arthritis but not psoriasis. Ann Rheum Dis. 2018 Dec 14. pii: annrheumdis-2018-214158. doi: 10.1136/annrheumdis-2018-214158.
VELÁZQUEZ C, ESTEBAN-CARDEÑOSA EM, LASTRA E, et al. A PALB2 truncating mutation: Implication in cancer prevention and therapy of Hereditary Breast and Ovarian Cancer. Breast. 2018 Nov 29;43:91-96. doi: 10.1016/j.breast.2018.11.010
MUÑOZ-GONZÁLEZ JI, JARA-ACEVEDO M, ALVAREZ-TWOSE I, et al. Impact of somatic and germline mutations on the outcome of systemic mastocytosis. Blood Adv. 2018 Nov 13;2(21):2814-2828. doi: 10.1182/bloodadvances.2018020628.
GONZÁLEZ-SERNA D, ORTIZ-FERNÁNDEZ L, VARGAS S, et al. Association of a rare variant of the TNFSF13B gene with susceptibility to Rheumatoid Arthritis and Systemic Lupus Erythematosus. Sci Rep. 2018 May 29;8(1):8195. doi: 10.1038/s41598-018-26573-4
HERRAIZ-MARTÍNEZ A, LLACH A, TARIFA C, et al. The 4q25 variant rs13143308T links risk of atrial fibrillation to defective calcium homeostasis. Cardiovasc Res. 2018 Aug 14. doi: 10.1093/cvr/cvy215.
BANALES JM, IÑARRAIRAEGUI M, ARBELAIZ A, et al. Serum metabolites as diagnostic biomarkers for cholangiocarcinoma, hepatocellular carcinoma and primary sclerosing cholangitis. Hepatology. 2018 Oct 16. doi: 10.1002/hep.30319
MARQUETA-GRACIA JJ, ÁLVAREZ-ÁLVAREZ M, BAETA M, et al. Differentially methylated CpG regions analyzed by PCR-high resolution melting for monozygotic twin pair discrimination. Forensic Sci Int Genet. 2018 Nov;37:e1-e5. doi: 10.1016/j.fsigen.2018.08.013
VILLAESCUSA P, PALENCIA-MADRID L, CAMPANER MA, et al. Effective resolution of the Y chromosome sublineages of the Iberian haplogroup R1b-DF27 with forensic purposes. Int J Legal Med. 2018 Sep 18. doi: 10.1007/s00414-018-1936-z.
GENESCÀ E, LAZARENKOV A, MORGADES M, et al. Frequency and clinical impact of CDKN2A/ARF/CDKN2B gene deletions as assessed by in-depth genetic analyses in adult T cell acute lymphoblastic leukemia. J Hematol Oncol. 2018 Jul 24;11(1):96. doi: 10.1186/s13045-018-0639-8.
HERNANDEZ-PACHECO N, GUILLEN-GUIO B, ACOSTA-HERRERA M, et al; GEN-SEP Network. A vascular endothelial growth factor receptor gene variant is associated with susceptibility to acute respiratory distress syndrome. Intensive Care Med Exp. 2018 Jul 9;6(1):16. doi: 10.1186/s40635-018-0181-6.
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University of Salamanca
Nucleus
PRB2
Biobanks Network
Institute Carlos III
Junta de Castilla y León
European Union
Banco Nacional de ADN
Edificio Multiusos I+D+i (Universidad de Salamanca)
C/ Espejo s/n. 37007 Salamanca
Teléfono de contacto: 923294500. Ext. 5473
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