recent publications
-
academic article
- Brandl, K., Tomisato, W., Li, X. H., Neppl, C., Pirie, E., Falk, W., Xia, Y., Moresco, E. M. Y., Baccala, R., Theofilopoulos, A. N., Schnabl, B., Beutler, B. Yip1 domain family, member 6 (Yipf6) mutation induces spontaneous intestinal inflammation in mice Proceedings of the National Academy of Sciences of the United States of America 2012 109:12650-12655 DOI:10.1073/pnas.1210366109 PMID:22802641 PMCID:PMC3412000
- Rutschmann, S., Crozat, K., Li, X., Du, X., Hanselman, J. C., Shigeoka, A. A., Brandl, K., Popkin, D. L., McKay, D. B., Xia, Y., Moresco, E. M. Y., Beutler, B. Hypopigmentation and maternal-zygotic embryonic lethality caused by a hypomorphic mbtps1 mutation in mice G3-Genes Genomes Genetics 2012 2:499-504 DOI:10.1534/g3.112.002196 PMID:22540041 PMCID:PMC3337478
- Won, S., Eidenschenk, C., Arnold, C. N., Siggs, O. M., Sun, L., Brandl, K., Mullen, T. M., Nemerow, G. R., Moresco, E. M. Y., Beutler, B. Increased susceptibility to DNA virus infection in mice with a GCN2 mutation Journal of Virology 2012 86:1802-1808 DOI:10.1128/jvi.05660-11 PMID:22114338 PMCID:PMC3264364
- Arnold, C. N., Barnes, M. J., Berger, M., Blasius, A. L., Brandl, K., Croker, B., Crozat, K., Du, X., Eidenschenk, C., Georgel, P., Hoebe, K., Huang, H., et al. ENU-induced phenovariance in mice: Inferences from 587 mutations BMC Research Notes 2012 5:577 DOI:10.1186/1756-0500-5-577 PMID:23095377 PMCID:PMC3532239
- Brandl, K., Sun, L., Neppl, C., Siggs, O. M., Le Gall, S. M., Tomisato, W., Li, X. H., Du, X., Maennel, D. N., Blobel, C. P., Beutler, B. MyD88 signaling in nonhematopoietic cells protects mice against induced colitis by regulating specific EGF receptor ligands Proceedings of the National Academy of Sciences of the United States of America 2010 107:19967-19972 DOI:10.1073/pnas.1014669107 PMID:21041656 PMCID:PMC2993336
- Xiao, N. M., Eidenschenk, C., Krebs, P., Brandl, K., Blasius, A. L., Xia, Y., Khovananth, K., Smart, N. G., Beutler, B. The tpl2 mutation sluggish impairs type i ifn production and increases susceptibility to group b streptococcal disease Journal of Immunology 2009 183:7975-7983 DOI:10.4049/jimmunol.0902718 PMID:19923465
- Brandl, K., Rutschmann, S., Li, X. H., Du, X., Xiao, N. M., Schnabl, B., Brenner, D. A., Beutler, B. Enhanced sensitivity to DSS colitis caused by a hypomorphic Mbtps1 mutation disrupting the ATF6-driven unfolded protein response Proceedings of the National Academy of Sciences of the United States of America 2009 106:3300-3305 DOI:10.1073/pnas.0813036106 PMID:19202076 PMCID:PMC2651297
- Blasius, A. L., Brandl, K., Crozat, K., Xia, Y., Khovananth, K., Krebs, P., Smart, N. G., Zampolli, A., Ruggeri, Z. M., Beutler, B. A. Mice with mutations of Dock7 have generalized hypopigmentation and white-spotting but show normal neurological function Proceedings of the National Academy of Sciences of the United States of America 2009 106:2706-2711 DOI:10.1073/pnas.0813208106 PMID:19202056 PMCID:PMC2650330