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Serveur d'exploration sur Pittsburgh - Analysis (UK)

Index « Auteurs » - entrée « Thomas D. Walters »
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Thomas D. Nolin < Thomas D. Walters < Thomas Essinger-Hileman  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 2.
Ident.Authors (with country if any)Title
000739 (2012) Aleixo M. Muise [Canada] ; WEI XU [Canada] ; Cong-Hui Guo [Canada] ; Thomas D. Walters [Canada] ; Victorien M. Wolters [Canada] ; Ramzi Fattouh [Canada] ; Grace Y. Lam [Canada] ; PINGZHAO HU [Canada] ; Ryan Murchie [Canada] ; Mary Sherlock [Canada] ; Juan Cristobal Gana [Chili] ; Richard K. Russell [Jamaïque] ; Michael Glogauer [Canada] ; Richard H. Duerr [États-Unis] ; Judy H. Cho [États-Unis] ; Charlie W. Lees [Royaume-Uni] ; Jack Satsangi [Royaume-Uni] ; David C. Wilson [Royaume-Uni] ; Andrew D. Paterson [Canada] ; Anne M. Griffiths [Canada] ; Mark S. Silverberg [Canada] ; John H. Brumell [Canada]NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2
000835 (2011) Aleixo M. Muise [Canada] ; Wei Xu [Canada] ; Cong-Hui Guo [Canada] ; Thomas D. Walters [Canada] ; Victorien M. Wolters [Canada] ; Ramzi Fattouh [Canada] ; Grace Y. Lam [Canada] ; Pingzhao Hu [Canada] ; Ryan Murchie [Canada] ; Mary Sherlock [Canada] ; Juan Crist Bal Gana [Chili] ; Richard K. Russell ; Michael Glogauer [Canada] ; Richard H. Duerr [États-Unis] ; Judy H. Cho [États-Unis] ; Charlie W. Lees [Royaume-Uni] ; Jack Satsangi [Royaume-Uni] ; David C. Wilson [Royaume-Uni] ; Andrew D. Paterson [Canada] ; Anne M. Griffiths [Canada] ; Mark S. Silverberg [Canada] ; John H. Brumell [Canada]NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2

List of associated KwdEn.i

Nombre de
documents		Descripteur
2Gastroenterology
2Oxidase
2Ulcerative colitis
1Association study
1Autosomal
1Bonferroni correction threshold
1Bowel
1Bowel disease
1Candidate gene approach
1Chromosome
1Chronic granulomatous disease
1Cohort
1Colitis
1Colonic
1Crohn disease
1Discovery cohort
1Early onset
1Early onset bowel disease
1Edinburgh
1Genet
1Genetics
1Genetics consortium
1Granulomatous
1Gwas
1Healthy controls
1Heterozygote
1Identification
1Ileal
1Ileal disease
1Ileocolonic
1Mutation
1Nadph
1Nadph oxidase
1Ncf2
1Ncf2 variant
1Ncf4
1Neutrophil
1Neutrophil dysfunction
1Niddk
1Novel variant
1Nox2
1Nox2 nadph oxidase
1Online
1Online supplement
1Ontario
1Pathogenesis
1Perianal
1Perianal disease
1Phagocyte
1Phenotype
1Phenotypic description
1Polymorphism
1Proc natl acad
1Rac2
1Rac2 snps
1Recessive
1Replication
1Replication cohort
1Sick children
1Sinai hospital
1Snp
1Subphenotype analysis
1Susceptibility
1Validation
1Validation cohorts
1Variant
1Water molecule

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