-
1
-
-
0035978533
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
|