CARD15/NOD2 mutational analysis in Japanese patients with Crohn's disease

被引：44

作者：

Sugimura, M ^{[1
]}

Kinouchi, Y ^{[1
]}

Takahashi, S ^{[1
]}

Aihara, H ^{[1
]}

Takagi, S ^{[1
]}

Negoro, K ^{[1
]}

Obana, N ^{[1
]}

Kojima, Y ^{[1
]}

Matsumoto, K ^{[1
]}

Kikuchi, T ^{[1
]}

Hiroki, M ^{[1
]}

Oomori, S ^{[1
]}

Shimosegawa, T ^{[1
]}

机构：

[1] Tohoku Univ, Grad Sch Med, Div Gastroenterol, Aoba Ku, Sendai, Miyagi 9808574, Japan

来源：

CLINICAL GENETICS | 2003年 / 63卷 / 02期

关键词：

D O I：

10.1046/j.0009-9163.2002.00174.x

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：160 / 162

页数：3

共 9 条

[1] The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease [J].

Cuthbert, AP ;

Fisher, SA ;

Mirza, MM ;

King, K ;

Hampe, J ;

Croucher, PJP ;

Mascheretti, S ;

Sanderson, J ;

Forbes, A ;

Mansfield, J ;

Schreiber, S ;

Lewis, CM ;

Mathew, CG .

GASTROENTEROLOGY, 2002, 122 (04) :867-874

[2] Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: a cohort study [J].

Hampe, J ;

Grebe, J ;

Nikolaus, S ;

Solberg, C ;

Croucher, PJP ;

Mascheretti, S ;

Jahnsen, J ;

Moum, B ;

Klump, B ;

Krawczak, M ;

Mirza, MM ;

Foelsch, UR ;

Vatn, M ;

Schreiber, S .

LANCET, 2002, 359 (9318) :1661-1665

[3] Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations [J].

Hampe, J ;

Cuthbert, A ;

Croucher, PJP ;

Mirza, MM ;

Mascheretti, S ;

Fisher, S ;

Frenzel, H ;

King, K ;

Hasselmeyer, A ;

MacPherson, AJS ;

Bridger, S ;

van Deventer, S ;

Forbes, A ;

Nikolaus, S ;

Lennard-Jones, JE ;

Foelsch, UR ;

Krawczak, M ;

Lewis, C ;

Schreiber, S ;

Mathew, CG .

LANCET, 2001, 357 (9272) :1925-1928

[4] Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease [J].

Hugot, JP ;

Chamaillard, M ;

Zouali, H ;

Lesage, S ;

Cézard, JP ;

Belaiche, J ;

Almer, S ;

Tysk, C ;

O'Morain, CA ;

Gassull, M ;

Binder, V ;

Finkel, Y ;

Cortot, A ;

Modigliani, R ;

Laurent-Puig, P ;

Gower-Rousseau, C ;

Macry, J ;

Colombel, JF ;

Sahbatou, M ;

Thomas, G .

NATURE, 2001, 411 (6837) :599-603

[5] Mapping of a susceptibility locus for Crohn's disease on chromosome 16 [J].

Hugot, JP ;

LaurentPuig, P ;

GowerRousseau, C ;

Olson, JM ;

Lee, JC ;

Beaugerie, L ;

Naom, I ;

Dupas, JL ;

VanGossum, A ;

Orholm, M ;

BonaitiPellie, C ;

Weissenbach, J ;

Mathew, CG ;

LennardJones, JE ;

Cortot, A ;

Colombel, JF ;

Thomas, G .

NATURE, 1996, 379 (6568) :821-823

[6] Lack of common NOD2 variants in Japanese patients with Crohn's disease [J].

Inoue, N ;

Tamura, K ;

Kinouchi, Y ;

Fukuda, Y ;

Takahashi, S ;

Ogura, Y ;

Inohara, N ;

Núñez, G ;

Kishi, Y ;

Koike, Y ;

Shimosegawa, T ;

Shimoyama, T ;

Hibi, T .

GASTROENTEROLOGY, 2002, 123 (01) :86-91

[7] CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease [J].

Lesage, S ;

Zouali, H ;

Cézard, JP ;

Colombel, JF ;

Belaiche, J ;

Almer, S ;

Tysk, C ;

O'Morain, C ;

Gassull, M ;

Binder, V ;

Finkel, Y ;

Modigliani, R ;

Gower-Rousseau, C ;

Macry, J ;

Merlin, F ;

Chamaillard, M ;

Jannot, AS ;

Thomas, G ;

Hugot, JP .

AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (04) :845-857

[8] A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease [J].

Ogura, Y ;

Bonen, DK ;

Inohara, N ;

Nicolae, DL ;

Chen, FF ;

Ramos, R ;

Britton, H ;

Moran, T ;

Karaliuskas, R ;

Duerr, RH ;

Achkar, JP ;

Brant, SR ;

Bayless, TM ;

Kirschner, BS ;

Hanauer, SB ;

Nuñez, G ;

Cho, JH .

NATURE, 2001, 411 (6837) :603-606

[9] Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12 [J].

Satsangi, J ;

Parkes, M ;

Louis, E ;

Hashimoto, L ;

Kato, N ;

Welsh, K ;

Terwilliger, JD ;

Lathrop, GM ;

Bell, JI ;

Jewell, DP .

NATURE GENETICS, 1996, 14 (02) :199-202

← 1 →