Linking risk conferring mutations in NCF4 to functional consequences in Crohn's disease
about
Mechanisms of Microbe-Host Interaction in Crohn's Disease: Dysbiosis vs. Pathobiont SelectionGenetic disorders coupled to ROS deficiencyReactive oxygen species deficiency induces autoimmunity with type 1 interferon signature.Association between NCF4 rs4821544T/C polymorphism and inflammatory bowel disease risk in Caucasian: a meta-analysis.Defects in NADPH Oxidase Genes NOX1 and DUOX2 in Very Early Onset Inflammatory Bowel DiseaseLinkage between genotype and immunological phenotype in Crohn's diseaseProfiles of microRNA networks in intestinal epithelial cells in a mouse model of colitis.p40phox expression regulates neutrophil recruitment and function during the resolution phase of intestinal inflammation.Allelic heterogeneity in NCF2 associated with systemic lupus erythematosus (SLE) susceptibility across four ethnic populations.Germline variation in NCF4, an innate immunity gene, is associated with an increased risk of colorectal cancerThe role of autophagy in Crohn's disease.Immune deficiency vs. immune excess in inflammatory bowel diseases-STAT3 as a rheo-STAT of intestinal homeostasis.The NOD2insC polymorphism is associated with worse outcome following ileal pouch-anal anastomosis for ulcerative colitis.Genetic polymorphism in ATG16L1 gene is associated with adalimumab use in inflammatory bowel disease.Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients with Crohn's Disease.
P2860
Q26774688-F1A4A62A-80A7-4C1F-AAFE-93B36D7CE9CBQ26799545-A4DC94FA-BCF1-4398-B256-D715E4DA500CQ34471099-CE5E86B8-5DC1-42D4-AD1C-32B295B0CE2FQ35750595-BDDAA3CD-8DEE-4A98-A0BC-55C6A970D4EBQ35964479-6B99E785-1EE5-4E2F-8C14-A3E34182A7B1Q36138115-041D553E-0B31-4D30-B348-4780878D7036Q36357175-00298215-8498-4A12-9863-AE5D38494C79Q37192211-F9FBE4DA-835F-426B-B865-DA8540C2B4C8Q37593029-AF59F106-8BE0-454A-B202-7A68D5CBB933Q37626295-BF08DEB2-B996-493B-84A6-D1770CF67764Q38202872-FF94654E-3131-4BD4-A64C-E69A42197D94Q38558749-7E8FEF54-DD59-49AB-9778-38B19C11F1A8Q43727523-642072E2-BCA3-4E50-ABF7-8B7B899C8BF5Q47328767-D6E59C1A-5919-4E7D-960B-86591187179BQ49896599-81E8ABE9-0BDE-467D-9824-29C75622BF1F
P2860
Linking risk conferring mutations in NCF4 to functional consequences in Crohn's disease
description
2012 nî lūn-bûn
@nan
2012 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Linking risk conferring mutations in NCF4 to functional consequences in Crohn's disease
@ast
Linking risk conferring mutations in NCF4 to functional consequences in Crohn's disease
@en
Linking risk conferring mutations in NCF4 to functional consequences in Crohn's disease
@nl
type
label
Linking risk conferring mutations in NCF4 to functional consequences in Crohn's disease
@ast
Linking risk conferring mutations in NCF4 to functional consequences in Crohn's disease
@en
Linking risk conferring mutations in NCF4 to functional consequences in Crohn's disease
@nl
prefLabel
Linking risk conferring mutations in NCF4 to functional consequences in Crohn's disease
@ast
Linking risk conferring mutations in NCF4 to functional consequences in Crohn's disease
@en
Linking risk conferring mutations in NCF4 to functional consequences in Crohn's disease
@nl
P2093
P1433
P1476
Linking risk conferring mutations in NCF4 to functional consequences in Crohn's disease
@en
P2093
C J van der Woude
G M Fuhler
J J Deuring
M P Peppelenbosch
R Somasundaram
P304
1097; author reply 1097-8
P356
10.1136/GUTJNL-2011-301344
P407
P577
2012-07-01T00:00:00Z