-
1
-
-
0019964811
-
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
-
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
-
3
-
-
0026021277
-
Spontaneous degenerative polyarthritis in male New Zealand black/KN mice
-
Nakamura K, Kashiwazaki S, Takagishi K, Tsukamoto Y, Morohoshi Y, Nakano T, et al. Spontaneous degenerative polyarthritis in male New Zealand black/KN mice. Arthritis Rheum 1991;34:171-9.
-
(1991)
Arthritis Rheum
, vol.34
, pp. 171-179
-
-
Nakamura, K.1
Kashiwazaki, S.2
Takagishi, K.3
Tsukamoto, Y.4
Morohoshi, Y.5
Nakano, T.6
-
4
-
-
0026719592
-
Characterization of a spontaneously occurring arthritis in male DBA/1 mice
-
Nordling C, Karlsson-Parra A, Jansson L, Holmdahl R, Klareskog L. Characterization of a spontaneously occurring arthritis in male DBA/1 mice. Arthritis Rheum 1992;35:717-22.
-
(1992)
Arthritis Rheum
, vol.35
, pp. 717-722
-
-
Nordling, C.1
Karlsson-Parra, A.2
Jansson, L.3
Holmdahl, R.4
Klareskog, L.5
-
5
-
-
0026650488
-
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
-
6
-
-
0029813721
-
Grouped caging predisposes male mice to ankylosing enthesopathy
-
Weinreich S, Capkova J, Hoebe-Hewryk B, Boog C, Ivanyi P. Grouped caging predisposes male mice to ankylosing enthesopathy. Ann Rheum Dis 1996;55:645-7.
-
(1996)
Ann Rheum Dis
, vol.55
, pp. 645-647
-
-
Weinreich, S.1
Capkova, J.2
Hoebe-Hewryk, B.3
Boog, C.4
Ivanyi, P.5
-
7
-
-
0033857242
-
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
-
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
-
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
-
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
-
12
-
-
0037320641
-
SAP couples Fyn to SLAM immune receptors
-
Chan B, Lanyi A, Song HK, Griesbach J, Simarro-Grande M, Poy F, et al. SAP couples Fyn to SLAM immune receptors. Nat Cell Biol 2003;5:155-60.
-
(2003)
Nat Cell Biol
, vol.5
, pp. 155-160
-
-
Chan, B.1
Lanyi, A.2
Song, H.K.3
Griesbach, J.4
Simarro-Grande, M.5
Poy, F.6
-
13
-
-
17344372694
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
25
-
-
1942532044
-
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
-
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
-
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
-
28
-
-
0027981524
-
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
-
Reardon W, Winter RM, Rutland P, Pulleyn U, Jones BM, Malcolm S. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome. Nat Genet 1994;8:98-103.
-
(1994)
Nat Genet
, vol.8
, pp. 98-103
-
-
Reardon, W.1
Winter, R.M.2
Rutland, P.3
Pulleyn, U.4
Jones, B.M.5
Malcolm, S.6
-
29
-
-
0028113931
-
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
-
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
-
31
-
-
0029242747
-
FGFR2 mutations in Pfeiffer syndrome
-
Lajeunie E, Ma HW, Bonaventure J, Munnich A, Le Merrer M, Renier D. FGFR2 mutations in Pfeiffer syndrome. Nat Genet 1995;9:108.
-
(1995)
Nat Genet
, vol.9
, pp. 108
-
-
Lajeunie, E.1
Ma, H.W.2
Bonaventure, J.3
Munnich, A.4
Le Merrer, M.5
Renier, D.6
-
32
-
-
0029109137
-
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
-
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
-
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
-
35
-
-
0142103924
-
Dependence on interferon-gamma for the spontaneous occurrence of arthritis in DBA/1 mice
-
Matthys P, Lories RJ, De Klerck B, Heremans H, Luyten FP, Billiau A. Dependence on interferon-gamma for the spontaneous occurrence of arthritis in DBA/1 mice. Arthritis Rheum 2003;48:2983-8.
-
(2003)
Arthritis Rheum
, vol.48
, pp. 2983-2988
-
-
Matthys, P.1
Lories, R.J.2
De Klerck, B.3
Heremans, H.4
Luyten, F.P.5
Billiau, A.6
|