These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

295 related articles for article (PubMed ID: 16239840)

  • 1. Genotype-phenotype analysis in childhood-onset Crohn's disease: NOD2/CARD15 variants consistently predict phenotypic characteristics of severe disease.
    Russell RK; Drummond HE; Nimmo EE; Anderson N; Smith L; Wilson DC; Gillett PM; McGrogan P; Hassan K; Weaver LT; Bisset M; Mahdi G; Satsangi J
    Inflamm Bowel Dis; 2005 Nov; 11(11):955-64. PubMed ID: 16239840
    [TBL] [Abstract][Full Text] [Related]  

  • 2. NOD2/CARD15 variants are associated with lower weight at diagnosis in children with Crohn's disease.
    Tomer G; Ceballos C; Concepcion E; Benkov KJ
    Am J Gastroenterol; 2003 Nov; 98(11):2479-84. PubMed ID: 14638352
    [TBL] [Abstract][Full Text] [Related]  

  • 3. CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease.
    Heliö T; Halme L; Lappalainen M; Fodstad H; Paavola-Sakki P; Turunen U; Färkkilä M; Krusius T; Kontula K
    Gut; 2003 Apr; 52(4):558-62. PubMed ID: 12631669
    [TBL] [Abstract][Full Text] [Related]  

  • 4. NOD2/CARD15 gene polymorphisms in Crohn's disease: a genotype- phenotype analysis.
    Heresbach D; Gicquel-Douabin V; Birebent B; D'halluin PN; Heresbach-Le Berre N; Dreano S; Siproudhis L; Dabadie A; Gosselin M; Mosser J; Semana G; Bretagne JF; Yaouanq J
    Eur J Gastroenterol Hepatol; 2004 Jan; 16(1):55-62. PubMed ID: 15095853
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association of NOD2/CARD15 variants with Crohn's disease in a Greek population.
    Gazouli M; Zacharatos P; Mantzaris GJ; Barbatis C; Ikonomopoulos I; Archimandritis AJ; Lukas JC; Papalambros E; Gorgoulis V
    Eur J Gastroenterol Hepatol; 2004 Nov; 16(11):1177-82. PubMed ID: 15489579
    [TBL] [Abstract][Full Text] [Related]  

  • 6. CARD15 gene mutations and risk for early surgery in pediatric-onset Crohn's disease.
    Kugathasan S; Collins N; Maresso K; Hoffmann RG; Stephens M; Werlin SL; Rudolph C; Broeckel U
    Clin Gastroenterol Hepatol; 2004 Nov; 2(11):1003-9. PubMed ID: 15551253
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Crohn's disease patients carrying Nod2/CARD15 gene variants have an increased and early need for first surgery due to stricturing disease and higher rate of surgical recurrence.
    Alvarez-Lobos M; Arostegui JI; Sans M; Tassies D; Plaza S; Delgado S; Lacy AM; Pique JM; Yagüe J; Panés J
    Ann Surg; 2005 Nov; 242(5):693-700. PubMed ID: 16244543
    [TBL] [Abstract][Full Text] [Related]  

  • 8. NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease.
    Gazouli M; Pachoula I; Panayotou I; Mantzaris G; Chrousos G; Anagnou NP; Roma-Giannikou E
    World J Gastroenterol; 2010 Apr; 16(14):1753-8. PubMed ID: 20380008
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Contribution of CARD15 variants in determining susceptibility to Crohn's disease in Sweden.
    Törkvist L; Noble CL; Lördal M; Sjöqvist U; Lindforss U; Nimmo ER; Russell RK; Löfberg R; Satsangi J
    Scand J Gastroenterol; 2006 Jun; 41(6):700-5. PubMed ID: 16716969
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic susceptibility has a more important role in pediatric-onset Crohn's disease than in adult-onset Crohn's disease.
    de Ridder L; Weersma RK; Dijkstra G; van der Steege G; Benninga MA; Nolte IM; Taminiau JA; Hommes DW; Stokkers PC
    Inflamm Bowel Dis; 2007 Sep; 13(9):1083-92. PubMed ID: 17476680
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Common NOD2/CARD15 and TLR4 Polymorphisms Are Associated with Crohn's Disease Phenotypes in Southeastern Brazilians.
    Tolentino YF; Elia PP; Fogaça HS; Carneiro AJ; Zaltman C; Moura-Neto R; Luiz RR; Carvalho Mda G; de Souza HS
    Dig Dis Sci; 2016 Sep; 61(9):2636-47. PubMed ID: 27107867
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autophagy gene ATG16L1 influences susceptibility and disease location but not childhood-onset in Crohn's disease in Northern Europe.
    Van Limbergen J; Russell RK; Nimmo ER; Drummond HE; Smith L; Anderson NH; Davies G; Gillett PM; McGrogan P; Weaver LT; Bisset WM; Mahdi G; Arnott ID; Wilson DC; Satsangi J
    Inflamm Bowel Dis; 2008 Mar; 14(3):338-46. PubMed ID: 18088053
    [TBL] [Abstract][Full Text] [Related]  

  • 13. NOD2/CARD15 and TNFA, but not IL1B and IL1RN, are associated with Crohn's disease.
    Ferreira AC; Almeida S; Tavares M; Canedo P; Pereira F; Regalo G; Figueiredo C; Trindade E; Seruca R; Carneiro F; Amil J; Machado JC; Tavarela-Veloso F
    Inflamm Bowel Dis; 2005 Apr; 11(4):331-9. PubMed ID: 15803022
    [TBL] [Abstract][Full Text] [Related]  

  • 14. NOD2/CARD15 mutation analysis and genotype-phenotype correlation in Jewish pediatric patients compared with adults with Crohn's disease.
    Weiss B; Shamir R; Bujanover Y; Waterman M; Hartman C; Fradkin A; Berkowitz D; Weintraub I; Eliakim R; Karban A
    J Pediatr; 2004 Aug; 145(2):208-12. PubMed ID: 15289769
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Toll-like receptor 4 and NOD2/CARD15 mutations in Hungarian patients with Crohn's disease: phenotype-genotype correlations.
    Lakatos PL; Lakatos L; Szalay F; Willheim-Polli C; Osterreicher C; Tulassay Z; Molnar T; Reinisch W; Papp J; Mozsik G; Ferenci P;
    World J Gastroenterol; 2005 Mar; 11(10):1489-95. PubMed ID: 15770725
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Carriage of CARD15 variants and smoking as risk factors for resective surgery in patients with Crohn's ileal disease.
    Laghi L; Costa S; Saibeni S; Bianchi P; Omodei P; Carrara A; Spina L; Contessini Avesani E; Vecchi M; De Franchis R; Malesci A
    Aliment Pharmacol Ther; 2005 Sep; 22(6):557-64. PubMed ID: 16167972
    [TBL] [Abstract][Full Text] [Related]  

  • 17. NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe?
    Arnott ID; Nimmo ER; Drummond HE; Fennell J; Smith BR; MacKinlay E; Morecroft J; Anderson N; Kelleher D; O'Sullivan M; McManus R; Satsangi J
    Genes Immun; 2004 Aug; 5(5):417-25. PubMed ID: 15190267
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Is age of onset of Crohn's disease governed by mutations in NOD2/caspase recruitment domains 15 and Toll-like receptor 4? Evaluation of a pediatric cohort.
    Leshinsky-Silver E; Karban A; Buzhakor E; Fridlander M; Yakir B; Eliakim R; Reif S; Shaul R; Boaz M; Lev D; Levine A
    Pediatr Res; 2005 Sep; 58(3):499-504. PubMed ID: 16148063
    [TBL] [Abstract][Full Text] [Related]  

  • 19. NOD2/CARD15 mutations in Croatian patients with Crohn's disease: prevalence and genotype-phenotype relationship.
    Cukovic-Cavka S; Vermeire S; Hrstic I; Claessens G; Kolacek S; Jakic-Razumovic J; Krznaric Z; Grubelic K; Radic D; Misak Z; Jadresin O; Rutgeerts P; Vucelic B
    Eur J Gastroenterol Hepatol; 2006 Aug; 18(8):895-9. PubMed ID: 16825909
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn's disease.
    Brand S; Staudinger T; Schnitzler F; Pfennig S; Hofbauer K; Dambacher J; Seiderer J; Tillack C; Konrad A; Crispin A; Göke B; Lohse P; Ochsenkühn T
    Inflamm Bowel Dis; 2005 Jul; 11(7):645-52. PubMed ID: 15973118
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.