E G de la Concha
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Explore the profile of E G de la Concha including associated specialties, affiliations and a list of published articles.
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91
Citations
855
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Recent Articles
1.
Espino-Paisan L, de la Calle H, Fernandez-Arquero M, Figueredo M, de la Concha E, Urcelay E, et al.
Diabetologia
. 2011 May;
54(8):2033-7.
PMID: 21559886
Aims/hypothesis: A complex region covering numerous genes in 12q13 was first associated with type 1 diabetes in the Wellcome Trust Case-Control Consortium (WTCCC) study. Two studies performed in a white...
2.
Blanco-Kelly F, Alvarez-Lafuente R, Alcina A, Abad-Grau M, de las Heras V, Lucas M, et al.
Genes Immun
. 2010 Oct;
12(2):145-8.
PMID: 20962851
TNFRSF6B and TNFRSF14 genes were recently associated with Crohn's disease and rheumatoid arthritis. TNFRSF14 is known as herpes virus entry mediator (HVEM), and herpes viruses have been involved in the...
3.
Dema B, Fernandez-Arquero M, Maluenda C, Polanco I, Figueredo M, de la Concha E, et al.
Tissue Antigens
. 2010 Aug;
77(1):62-4.
PMID: 20796250
Alterations in intestinal epithelial permeability could underlie inflammatory bowel disease (IBD) and celiac disease (CeD) etiology, as supported by previous association studies. One related gene, DLG5 [discs, large homologue 5...
4.
de Leon A, de la Serna J, Santiago J, Sevilla C, Fernandez-Arquero M, de la Concha E, et al.
Neurogastroenterol Motil
. 2010 Apr;
22(7):734-8, e218.
PMID: 20367798
Background: Idiopathic achalasia is a primary esophageal motor disorder of unknown etiology. Different evidences have been reported in support of achalasia as the result of an autoimmune and inflammatory process...
5.
Cenit M, Alcina A, Marquez A, Mendoza J, Diaz-Rubio M, de las Heras V, et al.
Genes Immun
. 2010 Mar;
11(3):264-8.
PMID: 20200543
STAT3 (signal transducer and activator of transcription 3) signaling is a critical component of Th17-dependent autoimmune processes. Genome-wide association studies (GWAS) have revealed the role of the STAT3 gene in...
6.
Marquez A, Cenit M, Nunez C, Mendoza J, Taxonera C, Diaz-Rubio M, et al.
Genes Immun
. 2009 Aug;
10(7):631-5.
PMID: 19657358
Genome-wide studies highlighted the effect in Crohn's disease (CD) and ulcerative colitis (UC) susceptibility of single nucleotide polymorphisms (SNPs) in 3p21, where BSN (bassoon), MST1 (macrophage stimulating-1) and MST1R (MST1...
7.
Dema B, Martinez A, Fernandez-Arquero M, Maluenda C, Polanco I, de la Concha E, et al.
Genes Immun
. 2009 Jul;
10(7):659-61.
PMID: 19626039
Celiac disease (CD) is an inflammatory condition affecting small bowel and triggered by gluten (or related proteins) ingestion in genetic susceptible individuals. Polymorphisms in three genes, SERPINE2, PPP6C and PBX3,...
8.
Cenit M, Blanco-Kelly F, de las Heras V, Bartolome M, de la Concha E, Urcelay E, et al.
Mult Scler
. 2009 Jun;
15(8):913-7.
PMID: 19556317
Background: Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system. Interferon-beta is the most usual therapy in relapsing-remiting MS. However, approximately 50% of the treated patients...
9.
Dema B, Martinez A, Fernandez-Arquero M, Maluenda C, Polanco I, de la Concha E, et al.
J Med Genet
. 2009 Jun;
46(9):617-9.
PMID: 19542083
Background And Aims: Genome-wide association studies in coeliac disease (CD) have resulted in the finding of eight new genetic regions associated with disease susceptibility. However, a replication study performed in...
10.
Varade J, Ramon Lamas J, Rodriguez L, Fernandez-Arquero M, Loza-Santamaria E, Jover J, et al.
Ann Rheum Dis
. 2009 Jun;
68(7):1230-2.
PMID: 19525409
No abstract available.