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
  • Arnold, C. N., Xia, Y., Lin, P., Ross, C., Schwander, M., Smart, N. G., Muller, U., Beutler, B. Rapid identification of a disease allele in mouse through whole genome sequencing and bulk segregation analysis Genetics  2011 187:633-641  DOI:10.1534/genetics.110.124586  PMID:21196518  PMCID:PMC3063661
  • Siggs, O. M., Berger, M., Krebs, P., Arnold, C. N., Eidenschenk, C., Huber, C., Pirie, E., Smart, N. G., Khovananth, K., Xia, Y., McInerney, G., Hedestam, G. B. K., et al. A mutation of Ikbkg causes immune deficiency without impairing degradation of IκBα Proceedings of the National Academy of Sciences of the United States of America  2010 107:3046-3051  DOI:10.1073/pnas.0915098107  PMID:20133626  PMCID:PMC2840324
  • Blasius, A. L., Arnold, C. N., Georgel, P., Rutschmann, S., Xia, Y., Lin, P., Ross, C., Li, X. H., Smart, N. G., Beutler, B. Slc15a4, AP-3, and Hermansky-Pudlak syndrome proteins are required for Toll-like receptor signaling in plasmacytoid dendritic cells Proceedings of the National Academy of Sciences of the United States of America  2010 107:19973-19978  DOI:10.1073/pnas.1014051107  PMID:21045126  PMCID:PMC2993408
  • 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