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2. CARD15 variants in patients with sporadic Parkinson's disease. Bialecka M; Kurzawski M; Klodowska-Duda G; Opala G; Juzwiak S; Kurzawski G; Tan EK; Drozdzik M Neurosci Res; 2007 Mar; 57(3):473-6. PubMed ID: 17174426 [TBL] [Abstract][Full Text] [Related]
3. CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies. van der Linde K; Boor PP; Houwing-Duistermaat JJ; Crusius BJ; Wilson PJ; Kuipers EJ; de Rooij FW Eur J Gastroenterol Hepatol; 2007 Jun; 19(6):449-59. PubMed ID: 17489054 [TBL] [Abstract][Full Text] [Related]
4. Variants of CARD15, TNFA and PTPN22 and susceptibility to Crohn's disease in the Czech population: high frequency of the CARD15 1007fs. Hradsky O; Lenicek M; Dusatkova P; Bronsky J; Nevoral J; Valtrova V; Kotalova R; Szitanyi P; Petro R; Starzykova V; Bortlik M; Vitek L; Lukas M; Cinek O Tissue Antigens; 2008 Jun; 71(6):538-47. PubMed ID: 18489434 [TBL] [Abstract][Full Text] [Related]
5. CARD15/NOD2 polymorphisms do not explain concordance of Crohn's disease in Swedish monozygotic twins. Halfvarson J; Bresso F; D'Amato M; Järnerot G; Pettersson S; Tysk C Dig Liver Dis; 2005 Oct; 37(10):768-72. PubMed ID: 16002353 [TBL] [Abstract][Full Text] [Related]
6. Mutations in CARD15 and smoking confer susceptibility to Crohn's disease in the Danish population. Ernst A; Jacobsen B; Østergaard M; Okkels H; Andersen V; Dagiliene E; Pedersen IS; Thorsgaard N; Drewes AM; Krarup HB Scand J Gastroenterol; 2007 Dec; 42(12):1445-51. PubMed ID: 17852840 [TBL] [Abstract][Full Text] [Related]
7. CARD15 gene mutations in periodontitis. Laine ML; Murillo LS; Morré SA; Winkel EG; Peña AS; van Winkelhoff AJ J Clin Periodontol; 2004 Oct; 31(10):890-3. PubMed ID: 15367194 [TBL] [Abstract][Full Text] [Related]
8. CARD15 mutations in patients with Crohn's disease in a homogeneous Spanish population. Núñez C; Barreiro M; Domínguez-Muñoz JE; Lorenzo A; Zapata C; Peña AS Am J Gastroenterol; 2004 Mar; 99(3):450-6. PubMed ID: 15056084 [TBL] [Abstract][Full Text] [Related]
9. Clinical applications of NOD2/CARD15 mutations in Crohn's disease. Barreiro-de Acosta M; Peña AS Acta Gastroenterol Latinoam; 2007 Mar; 37(1):49-54. PubMed ID: 17486745 [TBL] [Abstract][Full Text] [Related]
10. NOD2/CARD15 gene mutation is not associated with susceptibility to Wegener's granulomatosis. Newman B; Rubin LA; Siminovitch KA J Rheumatol; 2003 Feb; 30(2):305-7. PubMed ID: 12563685 [TBL] [Abstract][Full Text] [Related]
11. Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian population. Bianchi V; Maconi G; Ardizzone S; Colombo E; Ferrara E; Russo A; Tenchini ML; Porro GB Eur J Gastroenterol Hepatol; 2007 Mar; 19(3):217-23. PubMed ID: 17301648 [TBL] [Abstract][Full Text] [Related]
12. The 3020insC mutation of the NOD2/CARD15 gene in patients with periodontal disease. Folwaczny M; Glas J; Török HP; Mauermann D; Folwaczny C Eur J Oral Sci; 2004 Aug; 112(4):316-9. PubMed ID: 15279649 [TBL] [Abstract][Full Text] [Related]
13. Homozygosity for the CARD15 frameshift mutation 1007fs is predictive of early onset of Crohn's disease with ileal stenosis, entero-enteral fistulas, and frequent need for surgical intervention with high risk of re-stenosis. Seiderer J; Schnitzler F; Brand S; Staudinger T; Pfennig S; Herrmann K; Hofbauer K; Dambacher J; Tillack C; Sackmann M; Göke B; Lohse P; Ochsenkühn T Scand J Gastroenterol; 2006 Dec; 41(12):1421-32. PubMed ID: 17101573 [TBL] [Abstract][Full Text] [Related]
14. Epistasis between Toll-like receptor-9 polymorphisms and variants in NOD2 and IL23R modulates susceptibility to Crohn's disease. Török HP; Glas J; Endres I; Tonenchi L; Teshome MY; Wetzke M; Klein W; Lohse P; Ochsenkühn T; Folwaczny M; Göke B; Folwaczny C; Müller-Myhsok B; Brand S Am J Gastroenterol; 2009 Jul; 104(7):1723-33. PubMed ID: 19455129 [TBL] [Abstract][Full Text] [Related]
15. CARD15 gene variants and risk of reoperation in Crohn's disease patients. Maconi G; Colombo E; Sampietro GM; Lamboglia F; D'Incà R; Daperno M; Cassinotti A; Sturniolo GC; Ardizzone S; Duca P; Porro GB; Annese V Am J Gastroenterol; 2009 Oct; 104(10):2483-91. PubMed ID: 19638967 [TBL] [Abstract][Full Text] [Related]
16. Evidence of allelic heterogeneity for associations between the NOD2/CARD15 gene and ulcerative colitis among North Indians. Juyal G; Amre D; Midha V; Sood A; Seidman E; Thelma BK Aliment Pharmacol Ther; 2007 Nov; 26(10):1325-32. PubMed ID: 17892524 [TBL] [Abstract][Full Text] [Related]
17. Association of interleukin-1 receptor-associated kinase M (IRAK-M) and inflammatory bowel diseases. Weersma RK; Oostenbrug LE; Nolte IM; Van Der Steege G; Oosterom E; Van Dullemen HM; Kleibeuker JH; Dijkstra G Scand J Gastroenterol; 2007 Jul; 42(7):827-33. PubMed ID: 17558906 [TBL] [Abstract][Full Text] [Related]
18. Association between CARD15/NOD2 gene polymorphisms and paratuberculosis infection in cattle. Pinedo PJ; Buergelt CD; Donovan GA; Melendez P; Morel L; Wu R; Langaee TY; Rae DO Vet Microbiol; 2009 Mar; 134(3-4):346-52. PubMed ID: 18926647 [TBL] [Abstract][Full Text] [Related]
19. Host susceptibility to tuberculosis: CARD15 polymorphisms in a South African population. Möller M; Nebel A; Kwiatkowski R; van Helden PD; Hoal EG; Schreiber S Mol Cell Probes; 2007 Apr; 21(2):148-51. PubMed ID: 17113749 [TBL] [Abstract][Full Text] [Related]
20. Three common CARD15 mutations are not responsible for the pathogenesis of Crohn's disease in Iranians. Teimoori-Toolabi L; Vahedi H; Mollahajian H; Kamali E; Hajizadeh-Sikaroodi S; Zeinali S; Tabrizian T; Olfati G; Rashtak S; Malekzadeh F; Ghoddosi A; Malekzadeh R Hepatogastroenterology; 2010; 57(98):275-82. PubMed ID: 20583427 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]