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1 profile with no signs of toxicity following intratracheal administration.
2 mor tissues persisted at least 14 days after intratracheal administration.
3 mor-targeted gene delivery in the setting of intratracheal administration.
4 ion, specifically in the upper airways after intratracheal administration.
5 vivo models in two species via intranasal or intratracheal administration.
6 riction and inflammation assays in rat after intratracheal administration.
7 iction and inflammation assays in rats after intratracheal administration.
8 targeted drug delivery through intranasal or intratracheal administration.
10 oth in vivo in the airway tract of mice upon intratracheal administration, and in vitro in bronchial
11 % lower in Abcc1 ((-/-)) rats, whereas after intratracheal administration, AUC(lung) was 352% higher
12 of M(pro) in the lungs of living mice after intratracheal administration but also permits optical ur
13 injection was performed in C57BL6 mice with intratracheal administration by Candida albicans or phos
15 Sixteen rats were studied 3 days after an intratracheal administration of 5 x 10(9) to 1 x 10(11)
25 Clenoliximab) on immune functions following intratracheal administration of adenoviral vectors in mu
29 odynamically, and animals were randomized to intratracheal administration of aerosolized AAV1 carryin
30 ic K-rasG12D allele that can be activated by intratracheal administration of an adenovirus expressing
31 cellular influx in the lung airway following intratracheal administration of an N-[1-(2-3-dioleyloxy)
32 lpha was induced in the lungs in response to intratracheal administration of Aspergillus fumigatus co
33 e to mainstream CS increases AHR after acute intratracheal administration of Aspergillus fumigatus ex
34 highly susceptible to lung injury caused by intratracheal administration of AV1-GFP, an early (E) re
38 F-beta1) is a critical mediator of ALI after intratracheal administration of bleomycin or Escherichia
40 ved in antibacterial defenses, and exogenous intratracheal administration of CG combined with NE does
49 a clinically relevant mouse model induced by intratracheal administration of hydrochloric acid and li
51 ion of the lungs of CBA/J mice following the intratracheal administration of K. pneumoniae (7 x 10(2)
52 te that HFH-11 mRNA levels are stimulated by intratracheal administration of keratinocyte growth fact
65 lation of neuraminidase (NA) 30 min prior to intratracheal administration of LPS increased polymorpho
67 nfections were initiated through noninvasive intratracheal administration of M. avium 724 in mice ind
69 antly reduced in C57BL/6 mice after a single intratracheal administration of modified vectors, and le
71 ct (HIV-LTR/luciferase (HLL)), we found that intratracheal administration of P. aeruginosa resulted i
72 bited augmented clearance 3 and 7 days after intratracheal administration of P. murina, which correla
74 sceptible throughout 8 wk to infection after intratracheal administration of Pseudomonas aeruginosa;
79 er examined the effect of IGFBP-5 in vivo by intratracheal administration of replication-deficient ad
83 nhibition of Fas gene expression in lungs by intratracheal administration of small interfering RNA co
86 ospholipids were found to increase following intratracheal administration of tBuOOH (36 mg/kg), but n
87 expression of FcgammaRIIA in the lung after intratracheal administration of the AdFcgammaRIIA enhanc
90 y drug accumulation in lungs and blood after intratracheal administration of the spray dried inhalabl
93 rachea of wild-type and Cxcr2(-/-) mice, but intratracheal administration of TNFalpha did not induce
94 ts, pulmonary gene transfer was performed by intratracheal administration of various amounts of an ad
96 experimental model used herein entailed six intratracheal administrations of methylnitrosourea (MNU)