메뉴 건너뛰기




Volumn 64, Issue 20, 2004, Pages 7245-7247

NOD2 3020insC alone is not sufficient for colorectal cancer predisposition

Author keywords

[No Author keywords available]

Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 15;

EID: 5644298412     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: 10.1158/0008-5472.CAN-04-2364     Document Type: Article
Times cited : (33)

References (17)
  • 1
    • 0035978533 scopus 로고    scopus 로고
    • A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
    • Lond
    • Ogura Y, Bonen DK, Inohara N, et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature (Lond) 2001;411:603-6.
    • (2001) Nature , vol.411 , pp. 603-606
    • Ogura, Y.1    Bonen, D.K.2    Inohara, N.3
  • 2
    • 0035978651 scopus 로고    scopus 로고
    • Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
    • Lond
    • Hugot JP, Chamaillard M, Zouali H, et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature (Lond) 2001;411:599-603.
    • (2001) Nature , vol.411 , pp. 599-603
    • Hugot, J.P.1    Chamaillard, M.2    Zouali, H.3
  • 3
    • 18444381172 scopus 로고    scopus 로고
    • CARD15 genetic variation in a Quebec population: Prevalence, genotype-phenotype relationship, and haplotype structure
    • Vermeire S, Wild G, Kocher K, et al. CARD15 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
  • 4
    • 0036201577 scopus 로고    scopus 로고
    • CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease
    • Lesage S, Zouali H, Cezard JP, et al. CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease. Am J Hum Genet 2002;70:845-57.
    • (2002) Am J Hum Genet , vol.70 , pp. 845-857
    • Lesage, S.1    Zouali, H.2    Cezard, J.P.3
  • 5
    • 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, et al. Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations. Lancet 2001; 357:1925-8.
    • (2001) Lancet , vol.357 , pp. 1925-1928
    • Hampe, J.1    Cuthbert, A.2    Croucher, P.J.3
  • 6
    • 1842666807 scopus 로고    scopus 로고
    • NOD2 3020insC frameshift mutation is not associated with inflammatory bowel disease in Chinese patients of Han nationality
    • Guo QS, Xia B, Jiang Y, Qu Y, Li J. NOD2 3020insC frameshift mutation is not associated with inflammatory bowel disease in Chinese patients of Han nationality. World J Gastroenterol 2004;10:1069-71.
    • (2004) World J Gastroenterol , vol.10 , pp. 1069-1071
    • Guo, Q.S.1    Xia, B.2    Jiang, Y.3    Qu, Y.4    Li, J.5
  • 7
    • 0036306951 scopus 로고    scopus 로고
    • Lack of common NOD2 variants in Japanese patients with Crohn's disease
    • Inoue N, Tamura K, Kinouchi Y, et al. Lack of common NOD2 variants in Japanese patients with Crohn's disease. Gastroenterology 2002;123:86-91.
    • (2002) Gastroenterology , vol.123 , pp. 86-91
    • Inoue, N.1    Tamura, K.2    Kinouchi, Y.3
  • 8
    • 0037379286 scopus 로고    scopus 로고
    • CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease
    • Helio T, Halme L, Lappalainen M, et al. CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease. Gut 2003;52: 558-62.
    • (2003) Gut , vol.52 , pp. 558-562
    • Helio, T.1    Halme, L.2    Lappalainen, M.3
  • 9
    • 0036373539 scopus 로고    scopus 로고
    • 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. Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease. J Hum Genet 2002;47:469-72.
    • (2002) J Hum Genet , vol.47 , pp. 469-472
    • Yamazaki, K.1    Takazoe, M.2    Tanaka, T.3    Kazumori, T.4    Nakamura, Y.5
  • 10
    • 0035895992 scopus 로고    scopus 로고
    • Nod2, a Nod1/Apaf-1 family member that is restricted to monocytes and activates NF-kappaB
    • Ogura Y, Inohara N, Benito A, et al. Nod2, a Nod1/Apaf-1 family member that is restricted to monocytes and activates NF-kappaB. J Biol Chem 2001;276:4812-8.
    • (2001) J Biol Chem , vol.276 , pp. 4812-4818
    • Ogura, Y.1    Inohara, N.2    Benito, A.3
  • 11
    • 0033591330 scopus 로고    scopus 로고
    • Nod1, an Apaf-1-like activator of caspase-9 and nuclear factor-kappaB
    • Inohara N, Koseki T, del Peso L, et al. Nod1, an Apaf-1-like activator of caspase-9 and nuclear factor-kappaB. J Biol Chem 1999;274:14560-7.
    • (1999) J Biol Chem , vol.274 , pp. 14560-14567
    • Inohara, N.1    Koseki, T.2    Del Peso, L.3
  • 12
    • 0035474227 scopus 로고    scopus 로고
    • The NOD: A signaling module that regulates apoptosis and host defense against pathogens
    • Inohara N, Nunez G. The NOD: a signaling module that regulates apoptosis and host defense against pathogens. Oncogene 2001;20:6473-81.
    • (2001) Oncogene , vol.20 , pp. 6473-6481
    • Inohara, N.1    Nunez, G.2
  • 13
    • 12144287610 scopus 로고    scopus 로고
    • The NOD2 3020insC mutation and the risk of colorectal cancer
    • Kurzawski G, Suchy J, Kladny J, et al. The NOD2 3020insC mutation and the risk of colorectal cancer. Cancer Res 2004;64:1604-6.
    • (2004) Cancer Res , vol.64 , pp. 1604-1606
    • Kurzawski, G.1    Suchy, J.2    Kladny, J.3
  • 14
    • 0034129240 scopus 로고    scopus 로고
    • Population-based molecular detection of hereditary nonpolyposis colorectal cancer
    • Salovaara R, Loukola A, Kristo P, et al. Population-based molecular detection of hereditary nonpolyposis colorectal cancer. J Clin Oncol 2000;18:2193-200.
    • (2000) J Clin Oncol , vol.18 , pp. 2193-2200
    • Salovaara, R.1    Loukola, A.2    Kristo, P.3
  • 15
    • 0032555020 scopus 로고    scopus 로고
    • Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease
    • Aaltonen LA, Salovaara R, Kristo P, et al. Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. N Engl J Med 1998;338:1481-7.
    • (1998) N Engl J Med , vol.338 , pp. 1481-1487
    • Aaltonen, L.A.1    Salovaara, R.2    Kristo, P.3
  • 16
    • 4344671141 scopus 로고    scopus 로고
    • 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, et al. NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe? Genes Immun 2004;5:417-25.
    • (2004) Genes Immun , vol.5 , pp. 417-425
    • Arnott, I.D.1    Nimmo, E.R.2    Drummond, H.E.3
  • 17
    • 0037265610 scopus 로고    scopus 로고
    • Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations
    • Croucher PJ, Mascheretti S, Hampe J, et al. Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations. Eur J Hum Genet 2003;11:6-16.
    • (2003) Eur J Hum Genet , vol.11 , pp. 6-16
    • Croucher, P.J.1    Mascheretti, S.2    Hampe, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.