000 01618 a2200397 4500
005 20250515194736.0
264 0 _c20100315
008 201003s 0 0 eng d
022 _a1090-2104
024 7 _a10.1016/j.bbrc.2009.11.088
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRoussel, Lucie
245 0 0 _aIL-17 primes airway epithelial cells lacking functional Cystic Fibrosis Transmembrane conductance Regulator (CFTR) to increase NOD1 responses.
_h[electronic resource]
260 _bBiochemical and biophysical research communications
_cJan 2010
300 _a505-9 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aCells, Cultured
650 0 4 _aCystic Fibrosis
_xcomplications
650 0 4 _aCystic Fibrosis Transmembrane Conductance Regulator
_xgenetics
650 0 4 _aEpithelial Cells
_ximmunology
650 0 4 _aHumans
650 0 4 _aInterleukin-17
_xmetabolism
650 0 4 _aInterleukin-8
_xmetabolism
650 0 4 _aLung
_ximmunology
650 0 4 _aNeutrophils
_ximmunology
650 0 4 _aNod1 Signaling Adaptor Protein
_xbiosynthesis
650 0 4 _aPseudomonas Infections
_ximmunology
650 0 4 _aPseudomonas aeruginosa
650 0 4 _aReceptors, Interleukin-17
_xbiosynthesis
650 0 4 _aRespiratory Mucosa
_ximmunology
650 0 4 _aToll-Like Receptor 4
_xbiosynthesis
700 1 _aRousseau, Simon
773 0 _tBiochemical and biophysical research communications
_gvol. 391
_gno. 1
_gp. 505-9
856 4 0 _uhttps://doi.org/10.1016/j.bbrc.2009.11.088
_zAvailable from publisher's website
999 _c19316273
_d19316273