Detalhe da pesquisa
1.
The intracellular sensor NOD2 induces microRNA-29 expression in human dendritic cells to limit IL-23 release.
Immunity;
39(3): 521-36, 2013 Sep 19.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24054330
2.
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.
Nat Genet;
39(7): 827-9, 2007 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17558408
3.
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
Nat Genet;
39(7): 830-2, 2007 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17554261
4.
Association of a functional variant in the Wnt co-receptor LRP6 with early onset ileal Crohn's disease.
PLoS Genet;
8(2): e1002523, 2012.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22393312
5.
Genetic factors conferring an increased susceptibility to develop Crohn's disease also influence disease phenotype: results from the IBDchip European Project.
Gut;
62(11): 1556-65, 2013 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23263249
6.
Subclinical mucosal inflammation in diarrhea-predominant irritable bowel syndrome (IBS) in a tropical setting.
Scand J Gastroenterol;
47(6): 619-24, 2012 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22486731
7.
Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.
Gastroenterology;
136(2): 523-9.e3, 2009 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19068216
8.
Characterization of inflammatory bowel disease with urinary metabolic profiling.
Am J Gastroenterol;
104(6): 1435-44, 2009 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19491857
9.
Contribution of histological, serological, and genetic factors to the clinical heterogeneity of adult-onset coeliac disease.
Scand J Gastroenterol;
44(9): 1076-83, 2009.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19593686
10.
The genetic basis of inflammatory bowel disease.
Dig Dis;
27(4): 428-42, 2009.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19897957
11.
Two-stage candidate gene study of chromosome 3p demonstrates an association between nonsynonymous variants in the MST1R gene and Crohn's disease.
Inflamm Bowel Dis;
14(4): 500-7, 2008 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18200509
12.
Indeterminate colitis: a review of the concept--what's in a name?
Inflamm Bowel Dis;
14(6): 850-7, 2008 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18213696
13.
Cancer in patients with ulcerative colitis, Crohn's disease and coeliac disease: record linkage study.
Eur J Gastroenterol Hepatol;
20(4): 297-304, 2008 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18334873
14.
Pneumococcal infection in patients with coeliac disease.
Eur J Gastroenterol Hepatol;
20(7): 624-8, 2008 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18679063
15.
Contribution of the novel inflammatory bowel disease gene IL23R to disease susceptibility and phenotype.
Inflamm Bowel Dis;
13(9): 1063-8, 2007 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17508420
16.
Confirmation of the role of ATG16L1 as a Crohn's disease susceptibility gene.
Inflamm Bowel Dis;
13(8): 941-6, 2007 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17455206
17.
Muramyl dipeptide and toll-like receptor sensitivity in NOD2-associated Crohn's disease.
Lancet;
365(9473): 1794-6, 2005.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15910952
18.
Genetics of inflammatory bowel disease: the role of the HLA complex.
World J Gastroenterol;
12(23): 3628-35, 2006 Jun 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16773677
19.
A common CTLA4 haplotype associated with coeliac disease.
Eur J Hum Genet;
13(4): 440-4, 2005 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15657618
20.
Clinical implications of inflammatory bowel disease genetics on phenotype.
Inflamm Bowel Dis;
11(1): 56-61, 2005 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15674114