메뉴 건너뛰기




Volumn 65, Issue 10, 2006, Pages 1273-1278

Genetic characterisation of spontaneous ankylosing arthropathy with unique inheritance from Fas-deficient strains of mice

Author keywords

[No Author keywords available]

Indexed keywords

FAS ANTIGEN;

EID: 33750350867     PISSN: 00034967     EISSN: None     Source Type: Journal    
DOI: 10.1136/ard.2005.050526     Document Type: Article
Times cited : (5)

References (35)
  • 1
    • 0019964811 scopus 로고
    • A spontaneous rheumatoid arthritis-like disease in MRL/l mice
    • Hang L, Theofilopoulos AN, Dixon FJ. A spontaneous rheumatoid arthritis-like disease in MRL/l mice. J Exp Med 1982;155:1690-701.
    • (1982) J Exp Med , vol.155 , pp. 1690-1701
    • Hang, L.1    Theofilopoulos, A.N.2    Dixon, F.J.3
  • 2
    • 0025681421 scopus 로고
    • Spontaneous rheumatoid-like arthritis in a lime of mice sensitive to collagen-induced arthritis
    • Bouvet JP, Couderc J, Bouthiller Y, Franc B, Ducailar A, Mouton D. Spontaneous rheumatoid-like arthritis in a lime of mice sensitive to collagen-induced arthritis. Arthritis Rheum 1990;33:1716-22.
    • (1990) Arthritis Rheum , vol.33 , pp. 1716-1722
    • Bouvet, J.P.1    Couderc, J.2    Bouthiller, Y.3    Franc, B.4    Ducailar, A.5    Mouton, D.6
  • 5
    • 0026650488 scopus 로고
    • Genetic, hormonal and behavioural influence on spontaneously developing arthritis in normal mice
    • Holmdahl R, Jansson L, Andersson M, Jonsson R. Genetic, hormonal and behavioural influence on spontaneously developing arthritis in normal mice. Clin Exp Immunol 1992;88:467-72.
    • (1992) Clin Exp Immunol , vol.88 , pp. 467-472
    • Holmdahl, R.1    Jansson, L.2    Andersson, M.3    Jonsson, R.4
  • 7
    • 0033857242 scopus 로고    scopus 로고
    • T lymphocytes are not required for the spontaneous development of entheseal ossification leading to marginal ankylosis in the DBA/1 mouse
    • Corthay A, Hansson AS, Holmdahl R. T lymphocytes are not required for the spontaneous development of entheseal ossification leading to marginal ankylosis in the DBA/1 mouse. Arthritis Rheum 2000;43:844-51.
    • (2000) Arthritis Rheum , vol.43 , pp. 844-851
    • Corthay, A.1    Hansson, A.S.2    Holmdahl, R.3
  • 9
    • 0032190081 scopus 로고    scopus 로고
    • The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM
    • Sayos J, Wu C, Morra M, Wang N, Zhang X, Allen D, et al. The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM. Nature 1998;395:462-9.
    • (1998) Nature , vol.395 , pp. 462-469
    • Sayos, J.1    Wu, C.2    Morra, M.3    Wang, N.4    Zhang, X.5    Allen, D.6
  • 10
    • 0034889004 scopus 로고    scopus 로고
    • Regulation of SLAM-mediated signal transduction by SAP, the X-linked lymphoproliferative gene product
    • Latour S, Gish G, Helgason CD, Humphries RK, Pawson T, Veillette A. Regulation of SLAM-mediated signal transduction by SAP, the X-linked lymphoproliferative gene product. Nat Immunol 2001;2:681-90.
    • (2001) Nat Immunol , vol.2 , pp. 681-690
    • Latour, S.1    Gish, G.2    Helgason, C.D.3    Humphries, R.K.4    Pawson, T.5    Veillette, A.6
  • 11
    • 0037322612 scopus 로고    scopus 로고
    • Binding of SAP SH2 domain to FynT SH3 domain reveals a novel mechanism of receptor signalling in immune regulation
    • Latour S, Roncagalli R, Chen R, Bakinowski M, Shi X, Schwartzberg PL, et al. Binding of SAP SH2 domain to FynT SH3 domain reveals a novel mechanism of receptor signalling in immune regulation. Nat Cell Biol 2003;5:149-54.
    • (2003) Nat Cell Biol , vol.5 , pp. 149-154
    • Latour, S.1    Roncagalli, R.2    Chen, R.3    Bakinowski, M.4    Shi, X.5    Schwartzberg, P.L.6
  • 13
    • 17344372694 scopus 로고    scopus 로고
    • Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene
    • Coffey AJ, Brooksbank RA, Brandau O, Oohashi T, Howell GR, Bye JM, et al. Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene. Nat Genet 1998;20:129-35.
    • (1998) Nat Genet , vol.20 , pp. 129-135
    • Coffey, A.J.1    Brooksbank, R.A.2    Brandau, O.3    Oohashi, T.4    Howell, G.R.5    Bye, J.M.6
  • 14
    • 19344372415 scopus 로고    scopus 로고
    • SAP controls the cytolytic activity of CD8+ T cells against EBV-infected cells
    • Dupre L, Andolfi G, Tangye SG, Clementi R, Locatelli F, Arico M, et al. SAP controls the cytolytic activity of CD8+ T cells against EBV-infected cells. Blood 2005;105:4383-9.
    • (2005) Blood , vol.105 , pp. 4383-4389
    • Dupre, L.1    Andolfi, G.2    Tangye, S.G.3    Clementi, R.4    Locatelli, F.5    Arico, M.6
  • 15
    • 0035350808 scopus 로고    scopus 로고
    • SAP controls T cell responses to virus and terminal differentiation of TH2 cells
    • Wu C, Nguyen KB, Pien GC, Wang N, Gullo C, Howie D, et al. SAP controls T cell responses to virus and terminal differentiation of TH2 cells. Nat Immunol 2001;2:410-14.
    • (2001) Nat Immunol , vol.2 , pp. 410-414
    • Wu, C.1    Nguyen, K.B.2    Pien, G.C.3    Wang, N.4    Gullo, C.5    Howie, D.6
  • 16
    • 0034294836 scopus 로고    scopus 로고
    • Defective NK cell activation in X-linked lymphoproliferative disease
    • Benoit L, Wang X, Pabst HF, Dutz J, Tan R. Defective NK cell activation in X-linked lymphoproliferative disease. J Immunol 2000;165:3549-53.
    • (2000) J Immunol , vol.165 , pp. 3549-3553
    • Benoit, L.1    Wang, X.2    Pabst, H.F.3    Dutz, J.4    Tan, R.5
  • 17
    • 0034664724 scopus 로고    scopus 로고
    • Functional requirement for SAP in 2B4-mediated activation of human natural killer cells as revealed by the X-linked lymphoproliferative syndrome
    • Tangye SG, Phillips JH, Lanier LL, Nichols KE. Functional requirement for SAP in 2B4-mediated activation of human natural killer cells as revealed by the X-linked lymphoproliferative syndrome. J Immunol 2000;165:2932-6.
    • (2000) J Immunol , vol.165 , pp. 2932-2936
    • Tangye, S.G.1    Phillips, J.H.2    Lanier, L.L.3    Nichols, K.E.4
  • 18
    • 20144387328 scopus 로고    scopus 로고
    • Regulation of NKT cell development by SAP, the protein defective in XLP
    • Nichols KE, Hom J, Gong SY, Ganguly A, Ma CS, Cannons JL, et al. Regulation of NKT cell development by SAP, the protein defective in XLP. Nat Med 2005;11:340-5.
    • (2005) Nat Med , vol.11 , pp. 340-345
    • Nichols, K.E.1    Hom, J.2    Gong, S.Y.3    Ganguly, A.4    Ma, C.S.5    Cannons, J.L.6
  • 19
    • 15444374149 scopus 로고    scopus 로고
    • Defective NKT cell development in mice and humans lacking the adapter SAP, the X-linked lymphoproliferative syndrome gene product
    • Pasquier B, Yin L, Fondaneche MC, Relouzat F, Bloch-Queyrat C, Lambert N, et al. Defective NKT cell development in mice and humans lacking the adapter SAP, the X-linked lymphoproliferative syndrome gene product. J Exp Med 2005;201:695-701.
    • (2005) J Exp Med , vol.201 , pp. 695-701
    • Pasquier, B.1    Yin, L.2    Fondaneche, M.C.3    Relouzat, F.4    Bloch-Queyrat, C.5    Lambert, N.6
  • 20
    • 0028877463 scopus 로고
    • Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
    • Lander E, Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 1995;11:241-7.
    • (1995) Nat Genet , vol.11 , pp. 241-247
    • Lander, E.1    Kruglyak, L.2
  • 21
    • 0028224156 scopus 로고
    • Precision mapping of quantitative trait loci
    • Zeng ZB. Precision mapping of quantitative trait loci. Genetics 1994;136:1457-68.
    • (1994) Genetics , vol.136 , pp. 1457-1468
    • Zeng, Z.B.1
  • 22
    • 0028151261 scopus 로고
    • Empirical threshold values for quantitative trait mapping
    • Churchill GA, Doerge RW. Empirical threshold values for quantitative trait mapping. Genetics 1994;138:963-71.
    • (1994) Genetics , vol.138 , pp. 963-971
    • Churchill, G.A.1    Doerge, R.W.2
  • 23
    • 0019426077 scopus 로고
    • Progressive ankylosis, a new skeletal mutation in the mouse
    • Sweet HO, Green MC. Progressive ankylosis, a new skeletal mutation in the mouse. J Hered 1981;72:87-93.
    • (1981) J Hered , vol.72 , pp. 87-93
    • Sweet, H.O.1    Green, M.C.2
  • 24
    • 0031761219 scopus 로고    scopus 로고
    • Histopathology of murine ankylosing enthesopathy
    • Eulderink F, Ivanyi P, Weinreich S. Histopathology of murine ankylosing enthesopathy. Pathol Res Pract 1998;194:797-803.
    • (1998) Pathol Res Pract , vol.194 , pp. 797-803
    • Eulderink, F.1    Ivanyi, P.2    Weinreich, S.3
  • 25
    • 1942532044 scopus 로고    scopus 로고
    • Ankylosing enthesitis, dactylitis, and onychoperiostitis in male DBA/1 mice: A model of psoriatic arthritis
    • Lories RJ, Matthys P, de Vlam K, Derese I, Luyten FP. Ankylosing enthesitis, dactylitis, and onychoperiostitis in male DBA/1 mice: a model of psoriatic arthritis. Ann Rheum Dis 2004;63:595-8.
    • (2004) Ann Rheum Dis , vol.63 , pp. 595-598
    • Lories, R.J.1    Matthys, P.2    De Vlam, K.3    Derese, I.4    Luyten, F.P.5
  • 26
    • 20444478272 scopus 로고    scopus 로고
    • Modulation of bone morphogenetic protein signaling inhibits the onset and progression of ankylosing enthesitis
    • Lories RJ, Derese I, Luyten FP. Modulation of bone morphogenetic protein signaling inhibits the onset and progression of ankylosing enthesitis. J Clin Invest 2005;115:1571-9.
    • (2005) J Clin Invest , vol.115 , pp. 1571-1579
    • Lories, R.J.1    Derese, I.2    Luyten, F.P.3
  • 27
    • 20144379789 scopus 로고    scopus 로고
    • Accelerating effect of an MRL gene locus on the severity and onset of arthropathy in DBA/1 mice
    • Oishi H, Miyazaki T, Mizuki S, Kamogawa J, Lu LM, Tsubaki T, et al. Accelerating effect of an MRL gene locus on the severity and onset of arthropathy in DBA/1 mice. Arthritis Rheum 2005;52:959-66.
    • (2005) Arthritis Rheum , vol.52 , pp. 959-966
    • Oishi, H.1    Miyazaki, T.2    Mizuki, S.3    Kamogawa, J.4    Lu, L.M.5    Tsubaki, T.6
  • 29
    • 0028113931 scopus 로고
    • Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2 [correction appears in Nat Genet 1995;9:451]
    • Jabs EW, Li X, Scott AF, Meyers G, Chen W, Eccles M, et al. Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2 [correction appears in Nat Genet 1995;9:451]. Nat Genet 1994;8:275-9.
    • (1994) Nat Genet , vol.8 , pp. 275-279
    • Jabs, E.W.1    Li, X.2    Scott, A.F.3    Meyers, G.4    Chen, W.5    Eccles, M.6
  • 30
    • 0028798546 scopus 로고
    • Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
    • Wilkie AO, Slaney SF, Oldridge M, Poole MD, Ashworth GJ, Hockley AD, et al. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nat Genet 1995;9:165-72.
    • (1995) Nat Genet , vol.9 , pp. 165-172
    • Wilkie, A.O.1    Slaney, S.F.2    Oldridge, M.3    Poole, M.D.4    Ashworth, G.J.5    Hockley, A.D.6
  • 32
    • 0029109137 scopus 로고
    • Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes
    • Rutland P, Pulleyn U, Reardon W, Baraitser M, Hayward R, Jones B, et al. Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes. Nat Genet 1995;9:173-6.
    • (1995) Nat Genet , vol.9 , pp. 173-176
    • Rutland, P.1    Pulleyn, U.2    Reardon, W.3    Baraitser, M.4    Hayward, R.5    Jones, B.6
  • 33
    • 0035957343 scopus 로고    scopus 로고
    • A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes
    • Hajihosseini MK, Wilson S, De Moerlooze L, Dickson C. A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes. Proc Natl Acad Sci USA 2001;98:3855-60.
    • (2001) Proc Natl Acad Sci USA , vol.98 , pp. 3855-3860
    • Hajihosseini, M.K.1    Wilson, S.2    De Moerlooze, L.3    Dickson, C.4
  • 34
    • 4344689004 scopus 로고    scopus 로고
    • A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis
    • Eswarakumar VP, Horowitz MC, Locklin R, Morriss-Kay GM, Lonai P. A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis. Proc Natl Acad Sci USA 2004;101:12555-60.
    • (2004) Proc Natl Acad Sci USA , vol.101 , pp. 12555-12560
    • Eswarakumar, V.P.1    Horowitz, M.C.2    Locklin, R.3    Morriss-Kay, G.M.4    Lonai, P.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.