CARD15/NOD2 analyses in spondylarthropathy

被引：50

作者：

Miceli-Richard, C ^{[1
]}

Zouali, H

Lesage, S

Thomas, G

Hugot, JP

Said-Nahal, R

Breban, M

机构：

[1] Fdn Jean Daussete, CEPH, Paris, France

[2] Hop Cochin, AP HP, F-75674 Paris, France

[3] Univ Paris 05, Paris, France

来源：

ARTHRITIS AND RHEUMATISM | 2002年 / 46卷 / 05期

关键词：

D O I：

10.1002/art.10196

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：1405 / 1406

页数：2

共 12 条

[1]

AMOR B, 1990, REV RHUM, V57, P85

[2]

ARNETT FC, 1987, ARTHRITIS RHEUM, V31, P315

[3] ILEOCOLONOSCOPY IN SERONEGATIVE SPONDYLARTHROPATHY [J].

DEVOS, M ;

CUVELIER, C ;

MIELANTS, H ;

VEYS, E ;

BARBIER, F ;

ELEWAUT, A .

GASTROENTEROLOGY, 1989, 96 (02) :339-344

[4] THE EUROPEAN-SPONDYLARTHROPATHY-STUDY-GROUP PRELIMINARY CRITERIA FOR THE CLASSIFICATION OF SPONDYLARTHROPATHY [J].

DOUGADOS, M ;

VANDERLINDEN, S ;

JUHLIN, R ;

HUITFELDT, B ;

AMOR, B ;

CALIN, A ;

CATS, A ;

DIJKMANS, B ;

OLIVIERI, I ;

PASERO, G ;

VEYS, E ;

ZEIDLER, H .

ARTHRITIS AND RHEUMATISM, 1991, 34 (10) :1218-1227

[5] 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

[6] 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

[7] CARD15 mutations in Blau syndrome [J].

Miceli-Richard, C ;

Lesage, S ;

Rybojad, M ;

Prieur, AM ;

Manouvrier-Hanu, S ;

Häfner, R ;

Chamaillard, M ;

Zouali, H ;

Thomas, G ;

Hugot, JP .

NATURE GENETICS, 2001, 29 (01) :19-20

[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] Nod2, a Nod1/Apaf-1 family member that is restricted to monocytes and activates NF-κB [J].

Ogura, Y ;

Inohara, N ;

Benito, A ;

Chen, FF ;

Yamaoka, S ;

Núñez, G .

JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (07) :4812-4818

[10]

Said-Nahal R, 2000, ARTHRITIS RHEUM-US, V43, P1356, DOI 10.1002/1529-0131(200006)43:6<1356::AID-ANR20>3.0.CO

← 1 2 →