Showing 1 - 20 results of 20 for search 'Beutler, B', query time: 0.05s
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ZBTB1 is a determinant of lymphoid development. by Siggs, O, Li, X, Xia, Y, Beutler, B
Published 2012Journal article -
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X-linked cholestasis in mouse due to mutations of the P4-ATPase ATP11C. by Siggs, O, Schnabl, B, Webb, B, Beutler, B
Published 2011Journal article -
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NOVEL LYMPHOCYTE DEFICIENCIES REVEALED BY MOUSE FORWARD GENETICS by Siggs, O, Bull, K, Beutler, B, Cornall, R
Published 2012Conference item -
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Disruption of copper homeostasis due to a mutation of Atp7a delays the onset of prion disease. by Siggs, O, Cruite, J, Du, X, Rutschmann, S, Masliah, E, Beutler, B, Oldstone, M
Published 2012Journal article -
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The P4-type ATPase ATP11C is essential for B lymphopoiesis in adult bone marrow. by Siggs, O, Arnold, C, Huber, C, Pirie, E, Xia, Y, Lin, P, Nemazee, D, Beutler, B
Published 2011Journal article -
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iRhom2 is required for the secretion of mouse TNFα. by Siggs, O, Xiao, N, Wang, Y, Shi, H, Tomisato, W, Li, X, Xia, Y, Beutler, B
Published 2012Journal article -
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Increased susceptibility to DNA virus infection in mice with a GCN2 mutation. by Won, S, Eidenschenk, C, Arnold, C, Siggs, O, Sun, L, Brandl, K, Mullen, T, Nemerow, G, Moresco, E, Beutler, B
Published 2012Journal article -
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A forward genetic screen reveals roles for Nfkbid, Zeb1, and Ruvbl2 in humoral immunity. by Arnold, C, Pirie, E, Dosenovic, P, McInerney, G, Xia, Y, Wang, N, Li, X, Siggs, O, Karlsson Hedestam, G, Beutler, B
Published 2012Journal article -
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MyD88 signaling in nonhematopoietic cells protects mice against induced colitis by regulating specific EGF receptor ligands. by Brandl, K, Sun, L, Neppl, C, Siggs, O, Le Gall, S, Tomisato, W, Li, X, Du, X, Maennel, D, Blobel, C, Beutler, B
Published 2010Journal article -
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Soluble human TLR2 ectodomain binds diacylglycerol from microbial lipopeptides and glycolipids. by Jiménez-Dalmaroni, M, Radcliffe, C, Harvey, D, Wormald, M, Verdino, P, Ainge, G, Larsen, D, Painter, G, Ulevitch, R, Beutler, B, Rudd, P, Dwek, R, Wilson, I
Published 2015Journal article -
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A point mutation in the amino terminus of TLR7 abolishes signaling without affecting ligand binding. by Iavarone, C, Ramsauer, K, Kubarenko, A, Debasitis, J, Leykin, I, Weber, A, Siggs, O, Beutler, B, Zhang, P, Otten, G, D'Oro, U, Valiante, N, Mbow, M, Visintin, A
Published 2011Journal article -
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A mutation of Ikbkg causes immune deficiency without impairing degradation of IkappaB alpha. by Siggs, O, Berger, M, Krebs, P, Arnold, C, Eidenschenk, C, Huber, C, Pirie, E, Smart, N, Khovananth, K, Xia, Y, McInerney, G, Karlsson Hedestam, G, Nemazee, D, Beutler, B
Published 2010Journal article -
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An Slfn2 mutation causes lymphoid and myeloid immunodeficiency due to loss of immune cell quiescence. by Berger, M, Krebs, P, Crozat, K, Li, X, Croker, B, Siggs, O, Popkin, D, Du, X, Lawson, B, Theofilopoulos, A, Xia, Y, Khovananth, K, Moresco, E, Satoh, T, Takeuchi, O, Akira, S, Beutler, B
Published 2010Journal article -
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Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutations by Bull, K, Rimmer, A, Siggs, O, Miosge, L, Roots, C, Enders, A, Bertram, E, Crockford, T, Whittle, B, Potter, P, Simon, M, Mallon, A, Brown, S, Beutler, B, Goodnow, C, Lunter, G, Cornall, R
Published 2013Journal article -
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Systems analysis identifies an essential role for SHANK-associated RH domain-interacting protein (SHARPIN) in macrophage Toll-like receptor 2 (TLR2) responses. by Zak, D, Schmitz, F, Gold, E, Diercks, A, Peschon, J, Valvo, J, Niemistö, A, Podolsky, I, Fallen, S, Suen, R, Stolyar, T, Johnson, C, Kennedy, K, Hamilton, M, Siggs, O, Beutler, B, Aderem, A
Published 2011Journal article -
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RNA and imidazoquinolines are sensed by distinct TLR7/8 ectodomain sites resulting in functionally disparate signaling events. by Colak, E, Leslie, A, Zausmer, K, Khatamzas, E, Kubarenko, A, Pichulik, T, Klimosch, SN, Mayer, A, Siggs, O, Hector, A, Fischer, R, Klesser, B, Rautanen, A, Frank, M, Hill, A, Manoury, B, Beutler, B, Hartl, D, Simmons, A, Weber, A
Published 2014Journal article -
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Mutation of Fnip1 is associated with B-cell deficiency, cardiomyopathy, and elevated AMPK activity. by Siggs, O, Stockenhuber, A, Deobagkar-Lele, M, Bull, K, Crockford, T, Kingston, B, Crawford, G, Anzilotti, C, Steeples, V, Ghaffari, S, Czibik, G, Bellahcene, M, Watkins, H, Ashrafian, H, Davies, B, Woods, A, Carling, D, Yavari, A, Beutler, B, Cornall, R
Published 2016Journal article -
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ENU-induced phenovariance in mice: inferences from 587 mutations. by Arnold, C, Barnes, M, Berger, M, Blasius, A, Brandl, K, Croker, B, Crozat, K, Du, X, Eidenschenk, C, Georgel, P, Hoebe, K, Huang, H, Jiang, Z, Krebs, P, La Vine, D, Li, X, Lyon, S, Moresco, E, Murray, A, Popkin, D, Rutschmann, S, Siggs, O, Smart, N, Sun, L, Tabeta, K, Webster, V, Tomisato, W, Won, S, Xia, Y, Xiao, N, Beutler, B
Published 2012Journal article -
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Forward genetic analysis of mammalian immunity by Siggs, O, Owen Siggs
Published 2012Other Authors: “…Beutler, B…”
Thesis