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1 100 mul of Streptococcus pneumoniae (6B) per naris.
2 s fully restored 10 d after reopening of the naris.
3 d by peripheral olfactory deafferentation or naris blockade confirms that functional neural activity
4                       Neither bulbectomy nor naris closure affected TUNEL labeling in layer III.
5                                   Unilateral naris closure also produced enhanced TUNEL labeling, alt
6 adult wild-type mice subjected to unilateral naris closure and the olfactory bulbs of neonatal Er81 w
7             Our findings indicate that while naris closure caused a marked decrease in P2-OSN number
8 rvalbumin expression were not age dependent: naris closure from P30-P60 caused similar substantial de
9                             Using reversible naris closure in both juvenile and adult mice, we distor
10 deprivation studies that employed unilateral naris closure in neonatal rats demonstrated down-regulat
11          Long-Evans rats received unilateral naris closure on postnatal day 1 (PN1) or sham surgery.
12 s were examined from rats that had undergone naris closure or sham surgery on either postnatal day 1
13                         The adult unilateral naris closure paradigm was employed to establish a causa
14                                   Unilateral naris closure resulted in down-regulation of c-Fos and F
15 ture neurons, the consequences of unilateral naris closure were assessed in young adult rats.
16 l olfactory deprivation caused by unilateral naris closure, a manipulation that attenuates electrical
17 one half the nasal epithelium via unilateral naris closure, a manipulation that attenuates physiologi
18 on-independent forms of MAP2 is unchanged by naris closure, the total amount of the protein per unit
19 dor deprivation produced by adult unilateral naris closure.
20 of sensory input by unilateral and permanent naris closure.
21                  This effect is abolished by naris closure.
22 on the duration but not the time of onset of naris closure.
23 n whose expression was the least affected by naris closure.
24  ipsilateral and contralateral to the sealed naris compared to controls.
25 yer Ia was reduced ipsilateral to the sealed naris compared to undeprived controls.
26 , by injection of rhodamine-dextran into one naris, demonstrated that UEA(+) processes in microglomer
27 ation, TH expression is downregulated as the naris is closed and then upregulated upon naris reopenin
28 d noncarriers at three nasal sites (anterior naris, middle meatus, and sphenoethmoidal recess).
29   Here we show through experiments with both naris-occluded and anosmic mice that odorant-induced act
30 sis and immunocytochemistry, that unilateral naris occlusion (UNO) on postnatal day 1 alters OMP immu
31 zyme Cyp2a5 in sustentacular cells, and both naris occlusion and methimazole altered the abundance of
32 preference memory can be lateralized through naris occlusion as the anterior commissure is not yet fu
33   Sensory deprivation, induced by unilateral naris occlusion at birth, slowed the morphological devel
34 urons and the respiratory epithelia, because naris occlusion decreased expression of the xenobiotic c
35 t Long-Evans hooded rats received unilateral naris occlusion or a control manipulation and were sacri
36    Male and female rats underwent unilateral naris occlusion or sham surgery on either post-natal day
37                                   Unilateral naris occlusion resulted in elevated glomerular BACE lab
38 stressors was reduced by blocking a nostril (naris occlusion).
39               Methimazole's effects overcame naris occlusion, and the unfolded protein response was i
40                              With unilateral naris occlusion, the acute BDNF-induced tyrosine phospho
41 , we performed both permanent and reversible naris occlusion, which blocks odorant access to the nasa
42 xamined the effect of adult-onset unilateral naris occlusion, which reduces olfactory bulb afferent e
43 munoprecipitation experiments and unilateral naris occlusions were used to investigate whether the vo
44 sal cavity by surgically closing an external naris on P1 resulted in a gradual increase in TUNEL-posi
45 he naris is closed and then upregulated upon naris reopening.
46 xamine this hypothesis, we obtained anterior-naris samples from military trainees with cutaneous absc
47 e air stream entering the ventral tip of the naris traveled to the olfactory slit, and then passed th

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