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
    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
    [J]. 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
    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
    [J]. GASTROENTEROLOGY, 2002, 122 (04) : 867 - 874
  • [4] Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
    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
    [J]. NATURE, 2001, 411 (6837) : 599 - 603
  • [5] CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease
    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
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (04) : 845 - 857
  • [6] CARD15 mutations in Blau syndrome
    Miceli-Richard, C
    Lesage, S
    Rybojad, M
    Prieur, AM
    Manouvrier-Hanu, S
    Häfner, R
    Chamaillard, M
    Zouali, H
    Thomas, G
    Hugot, JP
    [J]. NATURE GENETICS, 2001, 29 (01) : 19 - 20
  • [7] A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
    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
    [J]. NATURE, 2001, 411 (6837) : 603 - 606
  • [8] HLA-DRB1*1101:: A significant risk factor for sarcoidosis in blacks and whites
    Rossman, MD
    Thompson, B
    Frederick, M
    Maliarik, M
    Iannuzzi, MC
    Rybicki, BA
    Pandey, JP
    Newman, LS
    Magira, E
    Beznik-Cizman, B
    Monos, D
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (04) : 720 - 735
  • [9] CARD15 gene mutations in sarcoidosis
    Schürmann, M
    Valentonyte, R
    Hampe, J
    Müller-Quernheim, J
    Schwinger, E
    Schreiber, S
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2003, 22 (05) : 748 - 754
  • [10] CARD15 mutations in familial granulomatosis syndromes
    Wang, XJ
    Kuivaniemi, H
    Bonavita, G
    Mutkus, L
    Mau, U
    Blau, E
    Inohara, N
    Nunez, G
    Tromp, G
    Williams, CJ
    [J]. ARTHRITIS AND RHEUMATISM, 2002, 46 (11): : 3041 - 3045