Pages that link to "Q28050119"
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The following pages link to Jack Satsangi (Q28050119):
Displayed 50 items.
- Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (Q22251069) (← links)
- Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease (Q22251082) (← links)
- Meta-analysis and imputation refines the association of 15q25 with smoking quantity (Q24273244) (← links)
- TLE1 modifies the effects of NOD2 in the pathogenesis of Crohn's disease (Q24307593) (← links)
- Tuberous sclerosis-2 (TSC2) regulates the stability of death-associated protein kinase-1 (DAPK) through a lysosome-dependent degradation pathway (Q24313169) (← links)
- The intermediate filament protein, vimentin, is a regulator of NOD2 activity (Q24337903) (← links)
- Common variants at five new loci associated with early-onset inflammatory bowel disease (Q24600801) (← links)
- Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci (Q24618592) (← links)
- Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls (Q24628710) (← links)
- Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects (Q24631241) (← links)
- Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease (Q24644398) (← links)
- IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease (Q24645890) (← links)
- Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (Q24646663) (← links)
- Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region (Q24657139) (← links)
- Danish cohort of monozygotic inflammatory bowel disease twins: Clinical characteristics and inflammatory activity (Q24658606) (← links)
- NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2 (Q28247419) (← links)
- Association of DLG5 and inflammatory bowel disease across populations (Q28289728) (← links)
- Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases (Q28394008) (← links)
- Analysis of germline GLI1 variation implicates hedgehog signalling in the regulation of intestinal inflammatory pathways (Q28474285) (← links)
- Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 (Q28943305) (← links)
- Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility (Q29614872) (← links)
- Negligible impact of rare autoimmune-locus coding-region variants on missing heritability (Q30415780) (← links)
- Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry (Q30426245) (← links)
- Technology insight: the application of proteomics in gastrointestinal disease (Q33289727) (← links)
- Dysregulation of human beta-defensin-2 protein in inflammatory bowel disease (Q33484190) (← links)
- Genetic variation in the familial Mediterranean fever gene (MEFV) and risk for Crohn's disease and ulcerative colitis (Q33507084) (← links)
- Association of genetic variants of the chemokine receptor CCR5 and its ligands, RANTES and MCP-2, with outcome of HCV infection (Q33974291) (← links)
- Cigarette smoke extract (CSE) delays NOD2 expression and affects NOD2/RIPK2 interactions in intestinal epithelial cells (Q34023974) (← links)
- Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease. (Q34341147) (← links)
- Prevalence of CARD15/NOD2 mutations in Caucasian healthy people (Q34576207) (← links)
- Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship (Q34899429) (← links)
- Systematic review: the role of breastfeeding in the development of pediatric inflammatory bowel disease (Q34982695) (← links)
- Azathioprine and anti-TNF alpha therapies in Crohn's disease: a review of pharmacology, clinical efficacy and safety (Q35044577) (← links)
- Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes (Q35104679) (← links)
- The impact of different DNA extraction kits and laboratories upon the assessment of human gut microbiota composition by 16S rRNA gene sequencing (Q35106510) (← links)
- Changes to serum sample tube and processing methodology does not cause Intra-Individual [corrected] variation in automated whole serum N-glycan profiling in health and disease (Q35241750) (← links)
- Pathogenesis of Crohn's disease (Q35659341) (← links)
- Inflammatory bowel disease associates with proinflammatory potential of the immunoglobulin G glycome (Q35670608) (← links)
- Pharmacogenetics and inflammatory bowel disease: progress and prospects. (Q35787609) (← links)
- Molecular genetics of Crohn's disease (Q35789560) (← links)
- Genetic sharing and heritability of paediatric age of onset autoimmune diseases. (Q36249776) (← links)
- Multidrug resistance (MDR1) gene in inflammatory bowel disease: a key player? (Q36292830) (← links)
- Molecular genetics in gastroenterology: from research success to clinical application? (Q36304098) (← links)
- The hedgehog signalling pathway in the gastrointestinal tract: implications for development, homeostasis, and disease (Q36312266) (← links)
- Autologous stem-cell transplantation in treatment-refractory Crohn's disease: an analysis of pooled data from the ASTIC trial (Q36369998) (← links)
- Novel susceptibility genes in inflammatory bowel disease (Q36446297) (← links)
- New genes in inflammatory bowel disease: lessons for complex diseases? (Q36456702) (← links)
- Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study (Q36468290) (← links)
- Two-stage genome-wide methylation profiling in childhood-onset Crohn's Disease implicates epigenetic alterations at the VMP1/MIR21 and HLA loci. (Q36530028) (← links)
- Clinical utility and diagnostic accuracy of faecal calprotectin for IBD at first presentation to gastroenterology services in adults aged 16-50 years (Q36696950) (← links)