Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15(-) Crohn's disease patients

scientific article

Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15(-) Crohn's disease patients is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1006843569
P356DOI10.1038/EJHG.2009.50
P932PMC publication ID2986636
P698PubMed publication ID19337309
P5875ResearchGate publication ID24249076

P50authorJavier MartinQ55089349
Emilio Gómez de la ConchaQ55526452
Jezabel VaradeQ56956278
Miguel Fernández-ArqueroQ117265209
Elena UrcelayQ48293032
P2093author name stringMiguel Angel López-Nevot
Alfonso Martínez
Ana Márquez
Carlos Taxonera
Manuel Díaz-Rubio
Juan Luis Mendoza
María Gómez-García
Gema Robledo
P2860cites workA frameshift mutation in NOD2 associated with susceptibility to Crohn's diseaseQ22251291
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsQ24550675
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetesQ24652324
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's diseaseQ27860821
Risk alleles for multiple sclerosis identified by a genomewide studyQ29614890
Bacterial ligands generated in a phagosome are targets of the cytosolic innate immune systemQ33280634
CD209 in inflammatory bowel disease: a case-control study in the Spanish populationQ33309481
A functional variant in the CD209 promoter is associated with DQ2-negative celiac disease in the Spanish populationQ33867573
A genome-wide association study identifies KIAA0350 as a type 1 diabetes geneQ34651283
Variation within the CLEC16A gene shows consistent disease association with both multiple sclerosis and type 1 diabetes in Sardinia.Q34863892
Deficient host-bacteria interactions in inflammatory bowel disease? The toll-like receptor (TLR)-4 Asp299gly polymorphism is associated with Crohn's disease and ulcerative colitisQ35596664
Role of the MHC2TA gene in autoimmune diseases.Q35759959
Divergent roles for C-type lectins expressed by cells of the innate immune systemQ35914429
Myeloid C-type lectins in innate immunityQ36655901
Collaboration between the innate immune receptors dectin-1, TLRs, and Nods.Q36938606
New links to the pathogenesis of Crohn disease provided by genome-wide association scansQ36984901
Suppressor of cytokine signaling 1 negatively regulates Toll-like receptor signaling by mediating Mal degradationQ40328896
Suppressor of cytokine signalling 1 in lymphocytes regulates the development of intestinal inflammation in miceQ42243167
Association of the macrophage migration inhibitory factor gene polymorphisms with inflammatory bowel disease.Q42843666
Classification of inflammatory bowel diseaseQ44185737
Polymorphisms of the lipopolysaccharide-signaling complex in inflammatory bowel disease: association of a mutation in the Toll-like receptor 4 gene with ulcerative colitisQ47318019
Suppressor of cytokine signaling-1 regulates inflammatory bowel disease in which both IFNgamma and IL-4 are involved.Q53637040
Toll-like receptor-1, -2, and -6 polymorphisms influence disease extension in inflammatory bowel diseases.Q54625562
P433issue10
P407language of work or nameEnglishQ1860
P921main subjectCrohn's diseaseQ1472
P304page(s)1304-8
P577publication date2009-10-01
P1433published inEuropean Journal of Human GeneticsQ2155433
P1476titleSpecific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15(-) Crohn's disease patients
P478volume17

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cites work (P2860)
Q24609382A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis
Q24634112A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis
Q37980033Autoimmune Addison disease: pathophysiology and genetic complexity.
Q58727397CLEC16A regulates splenocyte and NK cell function in part through MEK signaling
Q83000727Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus
Q27335170Fine mapping and functional studies of risk variants for type 1 diabetes at chromosome 16p13.13
Q38084534From Identification to Characterization of the Multiple Sclerosis Susceptibility Gene CLEC16A.
Q37774322Function of the intestinal epithelium and its dysregulation in inflammatory bowel disease.
Q44943791GOP-1 promotes apoptotic cell degradation by activating the small GTPase Rab2 in C. elegans
Q37585015Genes involved in type 1 diabetes: an update
Q36249776Genetic sharing and heritability of paediatric age of onset autoimmune diseases.
Q34065263Genome-wide association filtering using a highly locus-specific transmission/disequilibrium test
Q43184075IBD candidate genes and intestinal barrier regulation
Q56898663Interaction between CTLA4 gene and IBD5 locus in Hungarian Crohn's disease patients
Q33892035Multiple sclerosis susceptibility alleles in African Americans.
Q60445325Multiple sclerosis-associated single-nucleotide polymorphisms in CLEC16A correlate with reduced SOCS1 and DEXI expression in the thymus
Q34469229Polymorphisms in the inflammatory genes CIITA, CLEC16A and IFNG influence BMD, bone loss and fracture in elderly women
Q27003222Role of genetics in the diagnosis and prognosis of Crohn's disease
Q35638770Role of genetics in the diagnosis and prognosis of Crohn's disease
Q37454468Susceptibility to ulcerative colitis in Hungarian patients determined by gene-gene interactions
Q35902390Systemic Lupus Erythematosus Patients Exhibit Reduced Expression of CLEC16A Isoforms in Peripheral Leukocytes
Q61803777The Autoimmune Disorder Susceptibility Gene Restrains NK Cell Function in YTS NK Cell Line and Knockout Mice
Q38874311The Autoimmunity-Associated Gene CLEC16A Modulates Thymic Epithelial Cell Autophagy and Alters T Cell Selection.

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