NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2 - Test2 - elhamkhani - TriplyDB

NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2

NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2

http://www.wikidata.org/entity/Q28247419

about

Genetics and Therapeutics in Pediatric Ulcerative Colitis: the Past, Present and Future From genetics of inflammatory bowel disease towards mechanistic insights Role of genetics in pediatric inflammatory bowel disease The genetics of complex cholestatic disorders Deregulation of intestinal anti-microbial defense by the dietary additive, maltodextrin The diagnostic approach to monogenic very early onset inflammatory bowel disease Rac Attack: Modulation of the Small GTPase Rac in Inflammatory Bowel Disease and Thiopurine Therapy Genetics of inflammatory bowel disease from multifactorial to monogenic forms Functional genomics identifies negative regulatory nodes controlling phagocyte oxidative burst An inflammatory bowel disease-risk variant in INAVA decreases pattern recognition receptor-induced outcomes Differential diagnosis in ulcerative colitis in an adolescent: Chronic granulomatous disease needs extra attention.A Nationwide Study of Severe and Protracted Diarrhoea in Patients with Primary Immunodeficiency Diseases The role of the innate and adaptive immune system in pediatric inflammatory bowel disease.NOX2-dependent regulation of inflammation Mutations in tetratricopeptide repeat domain 7A result in a severe form of very early onset inflammatory bowel disease.Reactive oxygen species deficiency induces autoimmunity with type 1 interferon signature.Rac2-deficiency leads to exacerbated and protracted colitis in response to Citrobacter rodentium infection Serum protein profiling of adults and children with Crohn disease.Phagocyte NADPH oxidase restrains the inflammasome in ANCA-induced GN Influence of NADPH oxidase on inflammatory response in primary intestinal epithelial cells in patients with ulcerative colitis.Role of altered intestinal microbiota in systemic inflammation and cardiovascular disease in chronic kidney disease.Association between NCF4 rs4821544T/C polymorphism and inflammatory bowel disease risk in Caucasian: a meta-analysis.A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report Defects in NADPH Oxidase Genes NOX1 and DUOX2 in Very Early Onset Inflammatory Bowel Disease Voltage-Gated Proton Channels as Novel Drug Targets: From NADPH Oxidase Regulation to Sperm Biology Network Modeling of Crohn's Disease Incidence.Maintaining intestinal health: the genetics and immunology of very early onset inflammatory bowel disease.Opportunities and challenges of whole-genome and -exome sequencing.Profiles of microRNA networks in intestinal epithelial cells in a mouse model of colitis.Animal models of human granulocyte diseases.Colitis susceptibility in p47(phox-/-) mice is mediated by the microbiome.Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease.Association between a multi-locus genetic risk score and inflammatory bowel disease.p40phox expression regulates neutrophil recruitment and function during the resolution phase of intestinal inflammation.Impact of exome sequencing in inflammatory bowel disease.NASPGHAN single-topic symposium: discovering the future of pediatric IBD care.A CARD9 polymorphism is associated with decreased likelihood of persistent conjugated hyperbilirubinemia in intestinal failure.Allelic heterogeneity in NCF2 associated with systemic lupus erythematosus (SLE) susceptibility across four ethnic populations.Small GTPases of the Ras superfamily regulate intestinal epithelial homeostasis and barrier function via common and unique mechanisms.Germline variation in NCF4, an innate immunity gene, is associated with an increased risk of colorectal cancer

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NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2

http://www.wikidata.org/entity/Q28247419

description

2012 nî lūn-bûn

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2012 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2012 թվականի հուլիսին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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NADPH oxidase complex and IBD ...... lts in reduced binding to RAC2

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NADPH oxidase complex and IBD ...... lts in reduced binding to RAC2

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NADPH oxidase complex and IBD ...... lts in reduced binding to RAC2

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NADPH oxidase complex and IBD ...... lts in reduced binding to RAC2

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NADPH oxidase complex and IBD ...... lts in reduced binding to RAC2

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NADPH oxidase complex and IBD ...... lts in reduced binding to RAC2

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NADPH oxidase complex and IBD ...... lts in reduced binding to RAC2

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NADPH oxidase complex and IBD ...... lts in reduced binding to RAC2

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NADPH oxidase complex and IBD ...... lts in reduced binding to RAC2

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NADPH oxidase complex and IBD ...... lts in reduced binding to RAC2

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Aleixo M Muise

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Anne M Griffiths

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Cong-Hui Guo

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David C Wilson

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Grace Y Lam

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Jack Satsangi

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John H Brumell

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Juan Cristóbal Gana

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Judy H Cho

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Mark S Silverberg

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P2860

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Common variants at five new loci associated with early-onset inflammatory bowel disease

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

Genes for two autosomal recessive forms of chronic granulomatous disease assigned to 1q25 (NCF2) and 7q11.23 (NCF1)

PLINK: a tool set for whole-genome association and population-based linkage analyses

Human neutrophil immunodeficiency syndrome is associated with an inhibitory Rac2 mutation

The International HapMap Project

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1028-1035

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738769

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7

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Andrew D. Paterson

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21900546

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