메뉴 건너뛰기




Volumn 20, Issue 10, 2008, Pages 978-984

CARD15 gene polymorphisms in Serbian patients with Crohn's disease: Genotype-phenotype analysis

Author keywords

CARD15 gene; Crohn's disease; Genotype phenotype analysis

Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 15;

EID: 53549127562     PISSN: 0954691X     EISSN: None     Source Type: Journal    
DOI: 10.1097/MEG.0b013e328302f45e     Document Type: Article
Times cited : (13)

References (52)
  • 2
    • 26944491174 scopus 로고    scopus 로고
    • Etiology and pathogenesis of inflammatory bowel disease
    • Schmidt C, Stallmach A. Etiology and pathogenesis of inflammatory bowel disease. Minerva Gastroenterol Dietol 2005; 51:127-145.
    • (2005) Minerva Gastroenterol Dietol , vol.51 , pp. 127-145
    • Schmidt, C.1    Stallmach, A.2
  • 3
    • 0342844290 scopus 로고    scopus 로고
    • The epidemiology and the pathogenesis of inflammatory bowel disease
    • Karlinger K, Gyorke T, Mako E, Mester A, Tarjan Z. The epidemiology and the pathogenesis of inflammatory bowel disease. Eur J Radiol 2000; 35:154-167.
    • (2000) Eur J Radiol , vol.35 , pp. 154-167
    • Karlinger, K.1    Gyorke, T.2    Mako, E.3    Mester, A.4    Tarjan, Z.5
  • 5
    • 0030451868 scopus 로고    scopus 로고
    • Incidence of inflammatory bowel disease across Europe: Is there a difference between north and south? Results of the European Collaborative Study on Inflammatory Bowel Disease (EC- IBD)
    • Shivananda S, Lennard-Jones J, Logan R, Fear N, Price A, Carpenter L, van Blankenstein M. Incidence of inflammatory bowel disease across Europe: is there a difference between north and south? Results of the European Collaborative Study on Inflammatory Bowel Disease (EC- IBD). Gut 1996; 39:690-697.
    • (1996) Gut , vol.39 , pp. 690-697
    • Shivananda, S.1    Lennard-Jones, J.2    Logan, R.3    Fear, N.4    Price, A.5    Carpenter, L.6    van Blankenstein, M.7
  • 6
    • 4344671141 scopus 로고    scopus 로고
    • NOD2/CARD 15, TRL4 and CD14 mutation in Scottish and Irish Crohn's disease patients: Evidence for genetic heterogeneity within Europe?
    • Arnott IDR, Nimmo ER, Drummond HE, Fennell J, Smith BRK, MacKinlay E, et al. NOD2/CARD 15, TRL4 and CD14 mutation in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe? Genes Immun 2004; 5:417-425.
    • (2004) Genes Immun , vol.5 , pp. 417-425
    • Arnott, I.D.R.1    Nimmo, E.R.2    Drummond, H.E.3    Fennell, J.4    Smith, B.R.K.5    MacKinlay, E.6
  • 9
    • 0033773642 scopus 로고    scopus 로고
    • Concordance of inflammatory bowel disease among Danish twins. Results of nationwide study
    • Orholm M, Binder V, Sorensen Tl, Rasmussen LP, Kyvik KO. Concordance of inflammatory bowel disease among Danish twins. Results of nationwide study. Scand J Gastroenterol 2000; 35:1075-1081.
    • (2000) Scand J Gastroenterol , vol.35 , pp. 1075-1081
    • Orholm, M.1    Binder, V.2    Sorensen, T.3    Rasmussen, L.P.4    Kyvik, K.O.5
  • 10
    • 0035978651 scopus 로고    scopus 로고
    • Association of NOD2 leucine rich repeat variants with susceptibility to Crohn's disease
    • Hugot JP, Chamaillard M, Zouali H, Lesage S, Cezard JP Belaiche J, et al. Association of NOD2 leucine rich repeat variants with susceptibility to Crohn's disease. Nature 2001 ; 411:599-603.
    • (2001) Nature , vol.411 , pp. 599-603
    • Hugot, J.P.1    Chamaillard, M.2    Zouali, H.3    Lesage, S.4    Cezard, J.P.5    Belaiche, J.6
  • 11
    • 0035895992 scopus 로고    scopus 로고
    • a Nod 1/Apaf-1 family member that is restricted to monocytes and activates NF- kappa B
    • Ogura Y, Inohara N, Benito A, Chen FF, Yamaoka S, Ninez G. Nod 2, a Nod 1/Apaf-1 family member that is restricted to monocytes and activates NF- kappa B. J Biol Chem 2001; 276:4812-4818.
    • (2001) J Biol Chem , vol.276 , pp. 4812-4818
    • Ogura, Y.1    Inohara, N.2    Benito, A.3    Chen, F.F.4    Yamaoka, S.5    Ninez, G.6
  • 12
    • 0036201577 scopus 로고    scopus 로고
    • CARD 15/NOD 2 mutational analyses and genotype- phenotype correlation in 612 patients with inflammatory bowel disease
    • Lesage S, Zouali H, Cezard JP, Colombel JP, Belaiche J, Aimer S, et al. CARD 15/NOD 2 mutational analyses and genotype- phenotype correlation in 612 patients with inflammatory bowel disease. Am J Hum Genet 2002; 70:845-857.
    • (2002) Am J Hum Genet , vol.70 , pp. 845-857
    • Lesage, S.1    Zouali, H.2    Cezard, J.P.3    Colombel, J.P.4    Belaiche, J.5    Aimer, S.6
  • 14
    • 11144279151 scopus 로고    scopus 로고
    • Differential effect of NOD2 variants on Crohn's disease risk and phenotype in diverse populations
    • Economou M, Trikalinos TA, Loizou KT, Tsianos EV, loannidis J P. Differential effect of NOD2 variants on Crohn's disease risk and phenotype in diverse populations. Am J Gastroenterol 2004; 99:2393-2404.
    • (2004) Am J Gastroenterol , vol.99 , pp. 2393-2404
    • Economou, M.1    Trikalinos, T.A.2    Loizou, K.T.3    Tsianos, E.V.4    loannidis, J.P.5
  • 15
    • 2442429216 scopus 로고    scopus 로고
    • Clinical relevance of Advances in Genetic and Pharmacogenetics of IBD
    • Ahmad T, Tamboli PC, Jewel D, Colombel JF. Clinical relevance of Advances in Genetic and Pharmacogenetics of IBD. Gastroenterology 2004; 126:1533-1549.
    • (2004) Gastroenterology , vol.126 , pp. 1533-1549
    • Ahmad, T.1    Tamboli, P.C.2    Jewel, D.3    Colombel, J.F.4
  • 16
    • 34347357508 scopus 로고    scopus 로고
    • Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients
    • Yamazaki K, Onouchi Y, Takazoe M, Kubo M, Nakamura Y, Hata A. Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients. J Hum Genet 2007; 52:575-583.
    • (2007) J Hum Genet , vol.52 , pp. 575-583
    • Yamazaki, K.1    Onouchi, Y.2    Takazoe, M.3    Kubo, M.4    Nakamura, Y.5    Hata, A.6
  • 17
    • 0002338546 scopus 로고    scopus 로고
    • Racial differences in NOD2 variation: Characterization of NOD2 in African American with Crohn's disease
    • Bonen DK, Nicolae DL, Moran T, Turkyilmaz MA, Ramos R, Karaliukas R, et al. Racial differences in NOD2 variation: characterization of NOD2 in African American with Crohn's disease. Gastroenterology 2002; 122 (Suppl):A29.
    • (2002) Gastroenterology , vol.122 , Issue.SUPPL.
    • Bonen, D.K.1    Nicolae, D.L.2    Moran, T.3    Turkyilmaz, M.A.4    Ramos, R.5    Karaliukas, R.6
  • 18
    • 0037379286 scopus 로고    scopus 로고
    • CARD 15/NOD2 gene variants are associated with family occurring and complicated forms of Crohn's disease
    • Heliö T, Halme L, Lappalainen M, Fodstad H, Paavola-Sakki P, Turunen U, et al. CARD 15/NOD2 gene variants are associated with family occurring and complicated forms of Crohn's disease. Gut 2003; 52:558-562.
    • (2003) Gut , vol.52 , pp. 558-562
    • Heliö, T.1    Halme, L.2    Lappalainen, M.3    Fodstad, H.4    Paavola-Sakki, P.5    Turunen, U.6
  • 20
    • 33745843677 scopus 로고    scopus 로고
    • Cukovic-Cavka S, Vermeire S, Hrstic I, Claessens Q, Kolacek S, Jakic-Razumovic J, Krznaric Z NOD2/CARD 15 mutations in Croatians patients with Crohn's disease: prevalence and genotype - phenotype relationship. Eur J Gastroenterohepatol 2006; 18:895-899.
    • Cukovic-Cavka S, Vermeire S, Hrstic I, Claessens Q, Kolacek S, Jakic-Razumovic J, Krznaric Z NOD2/CARD 15 mutations in Croatians patients with Crohn's disease: prevalence and genotype - phenotype relationship. Eur J Gastroenterohepatol 2006; 18:895-899.
  • 21
    • 9144223009 scopus 로고    scopus 로고
    • Prevalence of the NOD2/CARD 15 gene and relation to phenotype in Spanish patients with Crohn Disease
    • Mendoza JL, Murillo LS, Fernandez L, Pena SA, Lana R, Urcelay E, et al. Prevalence of the NOD2/CARD 15 gene and relation to phenotype in Spanish patients with Crohn Disease. Scand J Gastroenterol 2003; 12:1235-1240.
    • (2003) Scand J Gastroenterol , vol.12 , pp. 1235-1240
    • Mendoza, J.L.1    Murillo, L.S.2    Fernandez, L.3    Pena, S.A.4    Lana, R.5    Urcelay, E.6
  • 22
    • 12144289474 scopus 로고    scopus 로고
    • Card 15 mutations in an Italian population: Leu 1007fsinsC but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's disease
    • Vavassori P, Borgiani P, Biancone L, D'Apice MR, Blanco Gdel V, Vallo L, et al. Card 15 mutations in an Italian population: Leu 1007fsinsC but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's disease. Inflamm Bowel Dis 2004; 10:116-121.
    • (2004) Inflamm Bowel Dis , vol.10 , pp. 116-121
    • Vavassori, P.1    Borgiani, P.2    Biancone, L.3    D'Apice, M.R.4    Blanco Gdel, V.5    Vallo, L.6
  • 23
    • 33847062913 scopus 로고    scopus 로고
    • Association of NOD2/Card 15 mutations on Crohn's disease phenotype in an Italian population
    • Bianchi V, Maconi G, Ardizzone S, Colombo E, Ferrara E, Russo A, et al. Association of NOD2/Card 15 mutations on Crohn's disease phenotype in an Italian population. Eur J Gastroenterol 2007; 19:217-223.
    • (2007) Eur J Gastroenterol , vol.19 , pp. 217-223
    • Bianchi, V.1    Maconi, G.2    Ardizzone, S.3    Colombo, E.4    Ferrara, E.5    Russo, A.6
  • 29
    • 33144468326 scopus 로고    scopus 로고
    • European evidence based consensus on the diagnosis and management of Crohn's disease definition and diagnosis
    • Stange EF, Travis SPL, Vermeire S, Beglinger C, Kupcinskas L, Geboes K, et al. European evidence based consensus on the diagnosis and management of Crohn's disease definition and diagnosis. Gut 2006; 55:1-15.
    • (2006) Gut , vol.55 , pp. 1-15
    • Stange, E.F.1    Travis, S.P.L.2    Vermeire, S.3    Beglinger, C.4    Kupcinskas, L.5    Geboes, K.6
  • 30
    • 33646778482 scopus 로고    scopus 로고
    • The Montreal classification of inflammatory bowel disease: Controversies, consensus, and implications
    • Satsangi J, Silvber MS, Vermeire S, Colombel J-F. The Montreal classification of inflammatory bowel disease: controversies, consensus, and implications. Gut 2006; 55:749-753.
    • (2006) Gut , vol.55 , pp. 749-753
    • Satsangi, J.1    Silvber, M.S.2    Vermeire, S.3    Colombel, J.-F.4
  • 31
    • 48249126370 scopus 로고    scopus 로고
    • The European consensus on ulcerative colitis: New horizons?
    • Stange EF, Travis SP The European consensus on ulcerative colitis: new horizons? Gut 2008; 57:1029-1031.
    • (2008) Gut , vol.57 , pp. 1029-1031
    • Stange, E.F.1    Travis, S.P.2
  • 35
    • 0037062228 scopus 로고    scopus 로고
    • Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: A cohort study
    • Hampe J, Grebe J, Nikolaus S, Solberg C, Croucher PJ, Mascherati S, et al. Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: a cohort study. Lancet 2002; 359:1661-1665.
    • (2002) Lancet , vol.359 , pp. 1661-1665
    • Hampe, J.1    Grebe, J.2    Nikolaus, S.3    Solberg, C.4    Croucher, P.J.5    Mascherati, S.6
  • 36
    • 18444381172 scopus 로고    scopus 로고
    • CARD 15 genetic variation in a Quebec population: Prevalence, genotype- phenotype relationship, and haplotype structure
    • Vermeire S, Wild G, Kocher K, Cousinaeu J, Dufresne L, Bitton A, et al. CARD 15 genetic variation in a Quebec population: prevalence, genotype- phenotype relationship, and haplotype structure. Am J Hum Genet 2002; 71:74-83.
    • (2002) Am J Hum Genet , vol.71 , pp. 74-83
    • Vermeire, S.1    Wild, G.2    Kocher, K.3    Cousinaeu, J.4    Dufresne, L.5    Bitton, A.6
  • 37
    • 25444505341 scopus 로고    scopus 로고
    • Crohn's disease is associated with polymorphism of Card 15/ NOD2 gene in a Hungarian population
    • Nagy Z, Karádi O, Rumi G, Rumi G Jr, Pár A, Mózsik G, et al. Crohn's disease is associated with polymorphism of Card 15/ NOD2 gene in a Hungarian population. Ann N Y Acad Sci 2005; 1051:45-51.
    • (2005) Ann N Y Acad Sci , vol.1051 , pp. 45-51
    • Nagy, Z.1    Karádi, O.2    Rumi, G.3    Rumi Jr, G.4    Pár, A.5    Mózsik, G.6
  • 38
    • 26544458865 scopus 로고    scopus 로고
    • Mutations of NOD 2 gene weakly correlate with Vienna classification of Crohn's disease (SD)
    • Annese V, Latino A, Andreoli A, Astegiano M, Bollani B, Campieri M, et al. Mutations of NOD 2 gene weakly correlate with Vienna classification of Crohn's disease (SD). Gastroenterology 2002; 122 (Suppl):A-296.
    • (2002) Gastroenterology , vol.122 , Issue.SUPPL.
    • Annese, V.1    Latino, A.2    Andreoli, A.3    Astegiano, M.4    Bollani, B.5    Campieri, M.6
  • 39
    • 0036202885 scopus 로고    scopus 로고
    • The contribution of NOD gene mutation to the risk and the site of disease in inflammatory bowel disease
    • Cuthbert AP, Fisher SA, Mirza MM, King K, Hampe J, Croucher PJ, et al. The contribution of NOD gene mutation to the risk and the site of disease in inflammatory bowel disease. Gastroenterology 2002; 122:867-874.
    • (2002) Gastroenterology , vol.122 , pp. 867-874
    • Cuthbert, A.P.1    Fisher, S.A.2    Mirza, M.M.3    King, K.4    Hampe, J.5    Croucher, P.J.6
  • 40
    • 0036897460 scopus 로고    scopus 로고
    • Variation at Card 15/ NOD2 in familial and sporadic cases of Crohn's disease in the Ashkenazi Jewish population
    • Zhou Z, Lin XY, Akolkar PN, Gulwani-Akolkar B, Levine J, Katz S, Silver J. Variation at Card 15/ NOD2 in familial and sporadic cases of Crohn's disease in the Ashkenazi Jewish population. Am J Gastroenterol 2002; 97:3095-3101.
    • (2002) Am J Gastroenterol , vol.97 , pp. 3095-3101
    • Zhou, Z.1    Lin, X.Y.2    Akolkar, P.N.3    Gulwani-Akolkar, B.4    Levine, J.5    Katz, S.6    Silver, J.7
  • 42
    • 0036080129 scopus 로고    scopus 로고
    • The c-insertion mutation of NOD 2 gene is associated with fistulizing and fibrostenotic phenotypes in Crohn's disease
    • Radlmayr M, Török HP, Martin K, Folwaczny C. The c-insertion mutation of NOD 2 gene is associated with fistulizing and fibrostenotic phenotypes in Crohn's disease. Gastroenterology 2002; 122:2091-2092.
    • (2002) Gastroenterology , vol.122 , pp. 2091-2092
    • Radlmayr, M.1    Török, H.P.2    Martin, K.3    Folwaczny, C.4
  • 43
    • 0036725827 scopus 로고    scopus 로고
    • Mutations in NOD2 are associated with fibrostenoting disease in patients with Crohn's disease
    • Abreu MT, Taylor KD, Lin YC, Han T, Giaennie J, Landers CJ, et al. Mutations in NOD2 are associated with fibrostenoting disease in patients with Crohn's disease. Gastroenterology 2002; 123:679-688.
    • (2002) Gastroenterology , vol.123 , pp. 679-688
    • Abreu, M.T.1    Taylor, K.D.2    Lin, Y.C.3    Han, T.4    Giaennie, J.5    Landers, C.J.6
  • 44
    • 0035897904 scopus 로고    scopus 로고
    • Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations
    • Hampe J, Cuthbert A, Croucher PJ, Mirza MM, Masheretti S, Fisher S, et al. Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations. Lancet 2001; 357:1925-1928.
    • (2001) Lancet , vol.357 , pp. 1925-1928
    • Hampe, J.1    Cuthbert, A.2    Croucher, P.J.3    Mirza, M.M.4    Masheretti, S.5    Fisher, S.6
  • 45
    • 0037379422 scopus 로고    scopus 로고
    • Early development of structuring or penetrating pattern in Crohn's disease is influenced by disease location, number of flares, and smoking but not by NOD2/CARD15 genotype
    • Louis E, Michel V, Hugot PJ, Reenaers C, Fontaine F, Delforge M, et al. Early development of structuring or penetrating pattern in Crohn's disease is influenced by disease location, number of flares, and smoking but not by NOD2/CARD15 genotype. Gut 2003; 52:552-557.
    • (2003) Gut , vol.52 , pp. 552-557
    • Louis, E.1    Michel, V.2    Hugot, P.J.3    Reenaers, C.4    Fontaine, F.5    Delforge, M.6
  • 47
    • 18644366895 scopus 로고    scopus 로고
    • Response to infliximab treatment in Crohn's disease is not associated with mutations in the Card 15(NOD2) gene: An analysis in 534 patients from two multicenter, prospective GCP-level trials
    • Masherattti S, Hampe J, Croucher PJ, Nikolaus S, Andus T, Schuber S, et al. Response to infliximab treatment in Crohn's disease is not associated with mutations in the Card 15(NOD2) gene: an analysis in 534 patients from two multicenter, prospective GCP-level trials. Pharmacogenetics 2003; 12:509-515.
    • (2003) Pharmacogenetics , vol.12 , pp. 509-515
    • Masherattti, S.1    Hampe, J.2    Croucher, P.J.3    Nikolaus, S.4    Andus, T.5    Schuber, S.6
  • 48
    • 27644562698 scopus 로고    scopus 로고
    • Crohn's disease patients carrying NOD2/CARD 15 gene variants have an increased and early need for first surgery due to stricturising disease and higher rate of surgical recurrence
    • Alvarez-Lobos M, Arostegui J, Sans M, Tassies D, Plaza S, Delgado S, et al. Crohn's disease patients carrying NOD2/CARD 15 gene variants have an increased and early need for first surgery due to stricturising disease and higher rate of surgical recurrence. Ann Surg 2005; 242:693-700.
    • (2005) Ann Surg , vol.242 , pp. 693-700
    • Alvarez-Lobos, M.1    Arostegui, J.2    Sans, M.3    Tassies, D.4    Plaza, S.5    Delgado, S.6
  • 49
    • 34848850085 scopus 로고    scopus 로고
    • The genetics of inflammatory bowel disease
    • Cho JH, Weaver CT. The genetics of inflammatory bowel disease. Gastroenterology 2007; 133:1327-1339.
    • (2007) Gastroenterology , vol.133 , pp. 1327-1339
    • Cho, J.H.1    Weaver, C.T.2
  • 50
    • 0142021798 scopus 로고    scopus 로고
    • Update on the genetics of inflammatory bowel disease
    • Duerr RH. Update on the genetics of inflammatory bowel disease. J Clin Gastroenterol 2003; 37:358-367.
    • (2003) J Clin Gastroenterol , vol.37 , pp. 358-367
    • Duerr, R.H.1
  • 51
    • 10844229057 scopus 로고    scopus 로고
    • Genotypes and phenotypes in Crohn's disease: Do they help in clinical management?
    • Gasche C, Grundtner P. Genotypes and phenotypes in Crohn's disease: do they help in clinical management? Gut 2005; 54:162-167.
    • (2005) Gut , vol.54 , pp. 162-167
    • Gasche, C.1    Grundtner, P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.