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Results: 1-7 |
Results: 7
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
Authors: Wildin, RS Ramsdell, F Peake, J Faravelli, F Casanova, JL Buist, N Levy-Lahad, E Mazzella, M Goulet, O Perroni, L Bricarelli, FD Byrne, G McEuen, M Proll, S Appleby, M Brunkow, ME
Citation: Rs. Wildin et al., X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy, NAT GENET, 27(1), 2001, pp. 18-20
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3
Authors: Bennett, CL Christie, J Ramsdell, F Brunkow, ME Ferguson, PJ Whitesell, L Kelly, TE Saulsbury, FT Chance, PF Ochs, HD
Citation: Cl. Bennett et al., The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3, NAT GENET, 27(1), 2001, pp. 20-21
Disruption of a new forkhead/winged-helix protein, scurfin, results in thefatal lymphoproliferative disorder of the scurfy mouse
Authors: Brunkow, ME Jeffery, EW Hjerrild, KA Paeper, B Clark, LB Yasayko, SA Wilkinson, JE Galas, D Ziegler, SF Ramsdell, F
Citation: Me. Brunkow et al., Disruption of a new forkhead/winged-helix protein, scurfin, results in thefatal lymphoproliferative disorder of the scurfy mouse, NAT GENET, 27(1), 2001, pp. 68-73
A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA -> AAUGAA) leads to the IPEX syndrome
Authors: Bennett, CL Brunkow, ME Ramsdell, F O'Briant, KC Zhu, Q Fuleihan, RL Shigeoka, AO Ochs, HD Chance, PF
Citation: Cl. Bennett et al., A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA -> AAUGAA) leads to the IPEX syndrome, IMMUNOGENET, 53(6), 2001, pp. 435-439
The amount of scurfin protein determines peripheral T cell number and responsiveness
Authors: Khattri, R Kasprowicz, D Cox, T Mortrud, M Appleby, MW Brunkow, ME Ziegler, SF Ramsdell, F
Citation: R. Khattri et al., The amount of scurfin protein determines peripheral T cell number and responsiveness, J IMMUNOL, 167(11), 2001, pp. 6312-6320
Bone dysplasia sclerosteosis results from loss of the SOST gene product, anovel cystine knot-containing protein
Authors: Brunkow, ME Gardner, JC Van Ness, J Paeper, BW Kovacevich, BR Proll, S Skonier, JE Zhao, L Sabo, PJ Fu, YH Alisch, RS Gillett, L Colbert, T Tacconi, P Galas, D Hamersma, H Beighton, P Mulligan, JT
Citation: Me. Brunkow et al., Bone dysplasia sclerosteosis results from loss of the SOST gene product, anovel cystine knot-containing protein, AM J HU GEN, 68(3), 2001, pp. 577-589
Cellular and molecular characterization of the scurfy mouse mutant
Authors: Clark, LB Appleby, MW Brunkow, ME Wilkinson, JE Ziegler, SF Ramsdell, F
Citation: Lb. Clark et al., Cellular and molecular characterization of the scurfy mouse mutant, J IMMUNOL, 162(5), 1999, pp. 2546-2554
Risultati: 1-7 |