BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

300 related articles for article (PubMed ID: 19103559)

  • 61. 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]  

  • 62. CARD15 gene polymorphisms in Serbian patients with Crohn's disease: genotype-phenotype analysis.
    Protic MB; Pavlovic ST; Bojic DZ; Krstic MN; Radojicic ZA; Tarabar DK; Stevanovic AZ; Karan Djurasevic TZ; Godjevac MV; Svorcan PV; Dapcevic BD; Jojic NZ
    Eur J Gastroenterol Hepatol; 2008 Oct; 20(10):978-84. PubMed ID: 18787464
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Role of ATG16L, NOD2 and IL23R in Crohn's disease pathogenesis.
    Naser SA; Arce M; Khaja A; Fernandez M; Naser N; Elwasila S; Thanigachalam S
    World J Gastroenterol; 2012 Feb; 18(5):412-24. PubMed ID: 22346247
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Analysis of the influence of OCTN1/2 variants within the IBD5 locus on disease susceptibility and growth indices in early onset inflammatory bowel disease.
    Russell RK; Drummond HE; Nimmo ER; Anderson NH; Noble CL; Wilson DC; Gillett PM; McGrogan P; Hassan K; Weaver LT; Bisset WM; Mahdi G; Satsangi J
    Gut; 2006 Aug; 55(8):1114-23. PubMed ID: 16469794
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Confirmation of the role of ATG16L1 as a Crohn's disease susceptibility gene.
    Cummings JR; Cooney R; Pathan S; Anderson CA; Barrett JC; Beckly J; Geremia A; Hancock L; Guo C; Ahmad T; Cardon LR; Jewell DP
    Inflamm Bowel Dis; 2007 Aug; 13(8):941-6. PubMed ID: 17455206
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Incidence of Crohn's disease and CARD15 mutation in a small township in Sicily.
    Cottone M; Renda MC; Mattaliano A; Oliva L; Fries W; Criscuoli V; Modesto I; Scimeca D; Maggio A; Casà A; Maisano S; Mocciaro F; Sferrazza A; Orlando A
    Eur J Epidemiol; 2006; 21(12):887-92. PubMed ID: 17160430
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease.
    Yamazaki K; Takazoe M; Tanaka T; Kazumori T; Nakamura Y
    J Hum Genet; 2002; 47(9):469-72. PubMed ID: 12202985
    [TBL] [Abstract][Full Text] [Related]  

  • 68. 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]  

  • 69. NOD2/CARD15 gene polymorphism in patients with inflammatory bowel disease: is Hungary different?
    Büning C; Molnar T; Nagy F; Lonovics J; Weltrich R; Bochow B; Genschel J; Schmidt H; Lochs H
    World J Gastroenterol; 2005 Jan; 11(3):407-11. PubMed ID: 15637755
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Classification of genetic profiles of Crohn's disease: a focus on the ATG16L1 gene.
    Grant SF; Baldassano RN; Hakonarson H
    Expert Rev Mol Diagn; 2008 Mar; 8(2):199-207. PubMed ID: 18366306
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Frequency of three common mutations of CARD15/NOD2 gene in Iranian IBD patients.
    Derakhshan F; Naderi N; Farnood A; Firouzi F; Habibi M; Rezvany MR; Javeri A; Bahari A; Balaii H; Rad MG; Aghazadeh R; Zali MR
    Indian J Gastroenterol; 2008; 27(1):8-11. PubMed ID: 18541930
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Genetic association between IL23R rs11209026 and rs10889677 polymorphisms and risk of Crohn's disease and ulcerative colitis: evidence from 41 studies.
    Zhu Y; Jiang H; Chen Z; Lu B; Li J; Shen X
    Inflamm Res; 2020 Jan; 69(1):87-103. PubMed ID: 31728561
    [TBL] [Abstract][Full Text] [Related]  

  • 73. CARD15 genotype-phenotype relationships in a small inflammatory bowel disease population with severe disease affection status.
    Crawford NP; Colliver DW; Eichenberger MR; Funke AA; Kolodko V; Cobbs GA; Petras RE; Galandiuk S
    Dig Dis Sci; 2007 Oct; 52(10):2716-24. PubMed ID: 17404888
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Variants of CARD15 are associated with an aggressive clinical course of Crohn's disease--an IG-IBD study.
    Annese V; Lombardi G; Perri F; D'Incà R; Ardizzone S; Riegler G; Giaccari S; Vecchi M; Castiglione F; Gionchetti P; Cocchiara E; Vigneri S; Latiano A; Palmieri O; Andriulli A
    Am J Gastroenterol; 2005 Jan; 100(1):84-92. PubMed ID: 15654786
    [TBL] [Abstract][Full Text] [Related]  

  • 75. High-resolution melting curve analysis for high-throughput genotyping of NOD2/CARD15 mutations and distribution of these mutations in Slovenian inflammatory bowel diseases patients.
    Mitrovič M; Potočnik U
    Dis Markers; 2011; 30(5):265-74. PubMed ID: 21734346
    [TBL] [Abstract][Full Text] [Related]  

  • 76. CARD15 gene polymorphisms in patients with spondyloarthropathies identify a specific phenotype previously related to Crohn's disease.
    Laukens D; Peeters H; Marichal D; Vander Cruyssen B; Mielants H; Elewaut D; Demetter P; Cuvelier C; Van Den Berghe M; Rottiers P; Veys EM; Remaut E; Steidler L; De Keyser F; De Vos M
    Ann Rheum Dis; 2005 Jun; 64(6):930-5. PubMed ID: 15539413
    [TBL] [Abstract][Full Text] [Related]  

  • 77. 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]  

  • 78. Perianal Crohn's disease: predictive factors and genotype-phenotype correlations.
    Kanaan Z; Ahmad S; Bilchuk N; Vahrenhold C; Pan J; Galandiuk S
    Dig Surg; 2012; 29(2):107-14. PubMed ID: 22440928
    [TBL] [Abstract][Full Text] [Related]  

  • 79. IGR2096a_1 T and IGR2198a_1 C alleles on IBD5 locus of chromosome 5q31 region confer risk for Crohn's disease in Hungarian patients.
    Lakner L; Csöngei V; Sarlós P; Járomi L; Sáfrány E; Varga M; Orosz P; Magyari L; Bene J; Miheller P; Tulassay Z; Melegh B
    Int J Colorectal Dis; 2009 May; 24(5):503-7. PubMed ID: 19214536
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Association between NOD2/CARD15 gene polymorphisms and Crohn's disease in Chinese Zhuang patients.
    Long WY; Chen L; Zhang CL; Nong RM; Lin MJ; Zhan LL; Lv XP
    World J Gastroenterol; 2014 Apr; 20(16):4737-44. PubMed ID: 24782627
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.