CARD 15 gene mutations in sarcoidosis

被引:19
作者
Ho, LP
McMichael, AJ
Ho, LP
Davies, RJO
Gaber, K
Hugot, JP
Merlin, F
Hugot, JP
机构
[1] Univ Oxford, MRC, Human Immunol Unit, Weatherall Inst Mol Med, Oxford OX3 9DS, England
[2] Churchill Hosp, Oxford Ctr Resp Med, Oxford OX3 7IJ, England
[3] Royal Devon & Exeter Hosp, Exeter EX2 5DW, Devon, England
[4] FDn Jean Dausset, CEPH, Paris, France
[5] Hop Robert Debre, AP HP, INSERM U458, Paris, France
关键词
D O I
10.1136/thx.2004.036871
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
引用
收藏
页码:354 / 355
页数:2
相关论文
共 10 条
[1]   The molecular classification of the clinical manifestations of Crohn's disease [J].
Ahmad, T ;
Armuzzi, A ;
Bunce, M ;
Mulcahy-Hawes, K ;
Marshall, SE ;
Orchard, TR ;
Crawshaw, J ;
Large, O ;
De Silva, A ;
Cook, JT ;
Barnardo, M ;
Cullen, S ;
Welsh, KI ;
Jewell, DP .
GASTROENTEROLOGY, 2002, 122 (04) :854-866
[2]  
[Anonymous], 1999, Am J Respir Crit Care Med, V160, P736
[3]   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
[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]   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
[6]   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
[7]   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
[8]   HLA-DRB1*1101:: A significant risk factor for sarcoidosis in blacks and whites [J].
Rossman, MD ;
Thompson, B ;
Frederick, M ;
Maliarik, M ;
Iannuzzi, MC ;
Rybicki, BA ;
Pandey, JP ;
Newman, LS ;
Magira, E ;
Beznik-Cizman, B ;
Monos, D .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (04) :720-735
[9]   CARD15 gene mutations in sarcoidosis [J].
Schürmann, M ;
Valentonyte, R ;
Hampe, J ;
Müller-Quernheim, J ;
Schwinger, E ;
Schreiber, S .
EUROPEAN RESPIRATORY JOURNAL, 2003, 22 (05) :748-754
[10]   CARD15 mutations in familial granulomatosis syndromes [J].
Wang, XJ ;
Kuivaniemi, H ;
Bonavita, G ;
Mutkus, L ;
Mau, U ;
Blau, E ;
Inohara, N ;
Nunez, G ;
Tromp, G ;
Williams, CJ .
ARTHRITIS AND RHEUMATISM, 2002, 46 (11) :3041-3045