ライフサイエンスコーパス: nasal administration

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1 A similar pattern occurred following nasal administration.

2 vivo studies showed mucosal absorption after nasal administration.

3 ung epithelial cells in vivo following intra-nasal administration.

4 induced in DBA/1 mice was studied after the nasal administration (before disease induction) of 1 of

5 No drug CSF uptake was detected after nasal administration of a DFO water solution.

6 Nasal administration of a modulatory APL of the heat-sho

7 Previously, we showed that nasal administration of a naked cDNA plasmid expressing

8 Our results demonstrate that chronic nasal administration of Abeta peptide can induce an immu

9 e showed that blocking IL-10 concurrent with nasal administration of Ag abolished the disease-suppres

10 Nasal administration of alanine 183 did not lead to dete

11 More important, nasal administration of an adenovirus expressing a compl

12 Nasal administration of an APL of Hsp60 180-188 induces

13 t mucosal tolerance in EAG can be induced by nasal administration of an immunodominant peptide from t

14 Nasal administration of an oil-in-water nanoemulsion (NE

15 We have found that nasal administration of anti-CD3 mAb attenuated lupus de

16 Nasal administration of antigens is effective in inducin

17 mouse model can be effectively suppressed by nasal administration of cardiac myosin (CM).

18 Here we report that nasal administration of CD3-specific antibody ameliorate

19 Nasal administration of CM effectively reduced the sever

20 responses in the respiratory tract following nasal administration of encapsulated antigens.

21 Nasal administration of exogenous Hcrt-1 restored social

22 Collectively, these data suggest that the nasal administration of GAD65 peptides induces a Th2 cel

23 We previously reported that prior nasal administration of highly attenuated Bordetella per

24 rate that tumor immunity can be achieved via nasal administration of mRNA.

25 t mucosal tolerance in EAG can be induced by nasal administration of recombinant rat alpha3(IV)NC1 an

26 tolerance in EAG by examining the effect of nasal administration of recombinant rat alpha3(IV)NC1.

27 Here, we demonstrate that subcutaneous or nasal administration of small-molecule MC activators wit

28 Nasal administration of specific autoantigens has been r

29 These effects were not induced by nasal administration of synthetic epitopes of diphtheria

30 holine receptor (TAChR), to demonstrate that nasal administration of synthetic sequences of the TAChR

31 Thereafter, weekly nasal administration of the antigen was given until the

32 or nasal tissues following a single oral or nasal administration of the bacteria, respectively.

33 Moreover, nasal administration of the immunosuppressant drug FTY72

34 ificantly different from that seen following nasal administration of these vectors to mouse lung (rAA

35 rance in EAG by examining the effects of the nasal administration of this peptide after the onset of

36 In this study, we show that nasal administration of virus-like particles (VLPs) befo

37 hology studies in rats after 5 days repeated nasal administration showed that Solutol HS15 had no tox

38 Nasal administration to rats of 200 mug DFO encapsulated

39 After nasal administration, virus moved down the olfactory ner

40 te bioavailabilities obtained by DCH and MCD nasal administration were 6% and 15%, respectively.

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