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1.
Bi-allelic loss-of-function variants in KIF21A cause severe fetal akinesia with arthrogryposis multiplex.
J Med Genet
; 60(1): 48-56, 2023 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-34740919
2.
Epistasis between Toll-like receptor-9 polymorphisms and variants in NOD2 and IL23R modulates susceptibility to Crohn's disease.
Am J Gastroenterol
; 104(7): 1723-33, 2009 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-19455129
3.
Novel genetic risk markers for ulcerative colitis in the IL2/IL21 region are in epistasis with IL23R and suggest a common genetic background for ulcerative colitis and celiac disease.
Am J Gastroenterol
; 104(7): 1737-44, 2009 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-19455118
4.
rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population.
Am J Gastroenterol
; 104(3): 665-72, 2009 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-19262523
5.
A polymorphism in the macrophage migration inhibitory factor gene is involved in the genetic predisposition of Crohn's disease and associated with cumulative steroid doses.
Hepatogastroenterology
; 54(75): 784-6, 2007.
Artículo
en Inglés
| MEDLINE | ID: mdl-17591062
6.
Role of the NFKB1 -94ins/delATTG promoter polymorphism in IBD and potential interactions with polymorphisms in the CARD15/NOD2, IKBL, and IL-1RN genes.
Inflamm Bowel Dis
; 12(7): 606-11, 2006 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-16804398
7.
Association of the ASP299GLY TLR4 polymorphism with COPD.
Respir Med
; 100(5): 892-6, 2006 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-16219455
8.
On the genetic involvement of apoptosis-related genes in Crohn's disease as revealed by an extended association screen using 245 markers: no evidence for new predisposing factors.
J Negat Results Biomed
; 4: 8, 2005 Nov 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-16318629
9.
CD14 expression on monocytes and soluble CD14 plasma levels in correlation to the promotor polymorphism of the endotoxin receptor CD14 gene in patients with inactive Crohn's disease.
Hepatogastroenterology
; 52(63): 808-11, 2005.
Artículo
en Inglés
| MEDLINE | ID: mdl-15966209
10.
Complex genetic predisposition in adult and juvenile rheumatoid arthritis.
BMC Genet
; 5: 2, 2004 Feb 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-15018649
11.
Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.
PLoS One
; 5(4): e10373, 2010 Apr 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-20454450
12.
The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German population.
Am J Gastroenterol
; 103(3): 682-91, 2008 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-18162085
13.
The 14-bp deletion polymorphism in the HLA-G gene displays significant differences between ulcerative colitis and Crohn's disease and is associated with ileocecal resection in Crohn's disease.
Int Immunol
; 19(5): 621-6, 2007 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-17446213
14.
rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants.
PLoS One
; 2(9): e819, 2007 Sep 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-17786191
15.
Polymorphisms in the interleukin-8 gene in patients with chronic obstructive pulmonary disease.
Electrophoresis
; 26(15): 2888-91, 2005 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-16007706
16.
A polymorphism of the bactericidal/permeability increasing protein (BPI) gene is associated with Crohn's disease.
J Clin Gastroenterol
; 39(4): 282-3, 2005 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-15758620
17.
A promotor polymorphism in the Interleukin 11 gene is associated with chronic obstructive pulmonary disease.
Electrophoresis
; 25(6): 804-8, 2004 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-15004839
18.
A polymorphism of the NFKBIA gene is associated with Crohn's disease patients lacking a predisposing allele of the CARD15 gene.
Int J Colorectal Dis
; 19(2): 153-6, 2004 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-13680285
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