recent publications

• academic article

  • 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
  • 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
  • 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
  • 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
  • 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
  • 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