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
Resultados
MANILS J, GÓMEZ D, SALLA-MARTRET M, et al. "Multifaceted role of TREX2 in the skin defense against UV-induced skin carcinogénesis". Oncotarget. 2015 Jun 15.
TELL-MARTI G, PUIG-BUTILLE JA, POTRONY M, et al. "The MC1R melanoma risk variant p.R160W is associated with Parkinson disease". Ann Neurol. 2015 May;77(5):889-94. doi: 10.1002/ana.24373. Epub 2015 Mar 13.
ACOSTA-HERRERA M, PINO-YANES M, BLANCO J, et al. "Common variants of NFE2L2 gene predisposes to acute respiratory distress syndrome in patients with severe sepsis"; GRECIA and GEN-SEP networks. Crit Care. 2015 Jun 16;19:256. doi: 10.1186/s13054-015-0981-y.
ACOSTA-HERRERA M, PINO-YANES M, MA SF, et al. "Fine mapping of the myosin light chain kinase gene (MYLK) replicates the association with asthma in populations of Spanish descent". J Allergy Clin Immunol. 2015 May 26. pii: S0091-6749(15)00587-4. doi: 10.1016/j.jaci.2015.04.025.
VIDAL-TABOADA JM, LOPEZ-LOPEZ A, SALVADO M, et al. "UNC13A confers risk for sporadic ALS and influences survival in a Spanish cohort". J Neurol. 2015 Jul 11.
LÓPEZ-MEJÍAS R, GENRE F, SEVILLA PÉREZ B, et al. "Association of HLA-B*41:02 with Henoch-Schönlein Purpura (IgA Vasculitis) in Spanish individuals irrespective of the HLA-DRB1 status". Arthritis Res Ther. 2015 Apr 14;17(1):102.
DELANEAU O, MARCHINI J. 1000 Genomes Project Consortium; "Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel"; Nat Commun. 2014 Jun 13;5:3934. doi: 10.1038/ncomms4934.
LOPEZ-LOPEZ A, GAMEZ J, SYRIANI E, et al. "CX3CR1 is a modifying gene of survival and progression in amyotrophic lateral sclerosis". PLoS One. 2014 May 7;9(5):e96528. doi: 10.1371/journal.pone.0096528. eCollection 2014.
MÁRQUEZ A, SOLANS R, HERNÁNDEZ-RODRÍGUEZ J, et al. "A Candidate Gene Approach Identifies an IL33 Genetic Variant as a Novel Genetic Risk Factor for GCA". PLoS One. 2014 Nov 19;9(11):e113476.
LÓPEZ-MEJÍAS R, GENRE F, PÉREZ BS, et al. "HLA-DRB1 association with Henoch-Schonlein purpura". Arthritis Rheumatol. 2014 Dec 2. doi: 10.1002/art.38979
FERRÁN A, ALEGRET JM, SUBIRANA I, et al. "Association Between rs2200733 and rs7193343 Genetic Variants and Atrial Fibrillation in a Spanish Population, and Meta-analysis of Previous Studies". Rev Esp Cardiol (Engl Ed). 2014 Oct;67(10):822-9. doi: 10.1016/j.rec.2013.12.019.
IVORRA JL, RIVERO O, COSTAS J, et al. "Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain". Schizophr Res. 2014 Oct;159(1):107-13. doi: 10.1016/j.schres.2014.07.004
CASH TP, PITA G, DOMÍNGUEZ O, et al. "Exome sequencing of three cases of familial exceptional longevity". Aging Cell. 2014 Aug 12. doi: 10.1111/acel.12261
CARRERAS-TORRES R, KUNDU S, ZANETTI D, et al. "Genetic risk score of NOS gene variants associated with myocardial infarction correlates with coronary incidence across Europe". PLoS One. 2014 May 7;9(5):e96504. doi: 10.1371/journal.pone.0096504.
LÓPEZ S, GARCÍA O, YURREBASO I, et al. "The interplay between natural selection and susceptibility to melanoma on allele 374F of SLC45A2 gene in a South European population". PLoS One. 2014 Aug 5;9(8):e104367. doi: 10.1371/journal.pone.0104367.
BOTIGUÉ LR, HENN BM, GRAVEL S, et al. "Gene flow from North Africa contributes to differential human genetic diversity in southern Europe". Proc Natl Acad Sci USA. 2013 Jul 16;110(29):11791-6. doi: 10.1073/pnas.1306223110
JULIÀ A, DOMÈNECH E, CHAPARRO M, et al. "A genome-wide association study identifies a novel locus at 6q22.1 associated with ulcerative colitis". Hum Mol Genet. 2014 Jul 31.
DIAZ-GALLO LM, SIMEON CP, BROEN JC, et al; SPANISH SCLERODERMA GROUP. "Implication of IL-2/IL-21 region in systemic sclerosis genetic susceptibility". Ann Rheum Dis. 2013 Jul;72(7):1233-8. doi: 10.1136/annrheumdis-2012-202357
RODRÍGUEZ-CABALLERO A, HENRIQUES A, CRIADO I, et al. "Subjects with chronic lymphocytic leukaemia-like B-cell clones with stereotyped B-cell receptors frequently show MDS-associated phenotypes on myeloid cells". Br J Haematol. 2014 Sep 24. doi: 10.1111/bjh.13127
COLONNA V, AYUB Q, CHEN Y, et al. "Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences". Genome Biol. 2014 Jun 30;15(6):R88
LOPEZ-LOPEZ A, GAMEZ J, SYRIANI E, et al. "CX3CR1 is a modifying gene of survival and progression in amyotrophic lateral sclerosis". PLoS One. 2014 May 7;9(5):e96528. doi: 10.1371/journal.pone.0096528. eCollection
PINO-YANES M, CORRALES A, ACOSTA-HERRERA M, et al. "HLA-DRB1*15:01 allele protects from asthma susceptibility". J Allergy Clin Immunol. 2014 Jul 14. pii: S0091-6749(14)00770-2. doi: 10.1016/j.jaci.2014.05.031.
ARGENTE J, FLORES R, GUTIÉRREZ-ARUMÍ A, et al. "Defective minor spliceosome mRNA processing results in isolated familial growth hormone deficiency". EMBO Mol Med. 2014 Mar;6(3):299-306. doi: 10.1002/emmm.201303573. Epub 2014 Jan 30
MAYES MD, BOSSINI-CASTILLO L, GORLOVA O, et al. "Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis". Am J Hum Genet. 2014 Jan 2;94(1):47-61. doi: 10.1016/j.ajhg.2013.12.002.
DOCAMPO E, ESCARAMÍS G, GRATACÒS M, et al. "Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system". Pain. 2014 Jun;155(6):1102-9. doi: 10.1016/j.pain. 2014.02.016. Epub 2014 Feb 26.
Páginas: 1 | 2 | 3 | 4
« volver
Universidad de Salamanca
Nucleus
PRB2
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
Top