Scripps VIVO scripps research logo

  • Index
  • Log in
  • Home
  • People
  • Organizations
  • Research
  • Events
Search form
As of April 1st VIVO Scientific Profiles will no longer updated for faculty, and the link to VIVO will be removed from the library website. Faculty profile pages will continue to be updated via Interfolio. VIVO will continue being used behind the scenes to update graduate student profiles. Please contact helplib@scripps.edu if you have questions.
How to download citations from VIVO | Alternative profile options
placeholder image
Publications in VIVO
 
    Export Publications Table
co-author
Co-author Network
map of science
Map of Science

Smart, N. G.

share the uri
  • Publications
scroll to property group menus

Publications

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
    • 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
    • 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
    • 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
    • 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

©2022 The Scripps Research Institute | Terms of Use | Powered by VIVO

  • About
  • Contact Us
  • Support