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1 rugs for targeting to specific tissues (e.g. olfactory mucosa).
2 ransporters in mouse nasal tissue containing olfactory mucosa.
3 olated by DNA-affinity purification from rat olfactory mucosa.
4 rthologs are expressed preferentially in the olfactory mucosa.
5 f glial cell which can be harvested from the olfactory mucosa.
6 patterns of neural receptor activity on the olfactory mucosa.
7 roteins among non-neuronal cell types of the olfactory mucosa.
8 pression of the CYP1A2 gene in the liver and olfactory mucosa.
9 e immunostaining, and decreased depth in the olfactory mucosa.
10 found to be expressed at a high level in the olfactory mucosa.
11 o reacts to pressure pulses delivered to the olfactory mucosa.
12 hat excluded circulating antibodies from the olfactory mucosa.
13 cells are the major target cell type in the olfactory mucosa.
15 element and nuclear extracts from liver and olfactory mucosa, all of which were supershifted in the
16 , we transplanted lamina propria (LP) of the olfactory mucosa alone or in combination with cultured o
18 onstrated that EGFR mRNA is expressed in the olfactory mucosa and also in the positive control tissue
19 T) isozymes (alpha, mu, and pi) in the mouse olfactory mucosa and characterize the zonal expression o
20 owed by transplantation of lamina propria of olfactory mucosa and cultured olfactory ensheathing cell
21 CYP2A3 is expressed preferentially in rat olfactory mucosa and is believed to play important roles
22 nation reduced H5N1 virus replication in the olfactory mucosa and prevented subsequent virus spread t
24 Influenza A viruses can replicate in the olfactory mucosa and subsequently use the olfactory nerv
27 t studies point to an important role for the olfactory mucosa as a barrier to both respiratory pathog
29 e study combined psychophysical testing with olfactory mucosa biopsy analysis, single-cell RNA-Sequen
30 ytochrome P-450 isoform in the liver and the olfactory mucosa but is essentially not expressed in oth
31 ted with the CYP2A3 promoter in vivo, in rat olfactory mucosa, but essentially not in the liver where
33 f the CYP2A3 gene with nuclear extracts from olfactory mucosa, but not from liver, lung, kidney, or b
37 This mechanism of prion shedding from the olfactory mucosa could contribute to prion transmission.
38 ique immunologically relevant anatomy of the olfactory mucosa, describing what is known of olfactory
40 iseases, can readily enter the brain via the olfactory mucosa, have led to the hypothesis that Alzhei
41 ed with unique proteins detected only in the olfactory mucosa in electrophoretic mobility shift assay
42 research highlights the significant role of olfactory mucosa in nose-to-brain delivery, with an effi
44 ed rabbit P450s known to be expressed in the olfactory mucosa, including 1A2, 2A10/11, 2B4, 2E1, 2G1,
47 COVID-19 pandemic has demonstrated that the olfactory mucosa is an integral part of a heterogeneous
49 Furthermore, we show that NCX1 mRNA in rat olfactory mucosa is expressed as 8 alternative splice va
54 ll cultures (neurosphere-derived cells) from olfactory mucosa of schizophrenia patients have signific
55 y highlights the importance of including the olfactory mucosa, olfactory nerve, and CNS tissues in fu
56 e two major olfactory organs of rodents, the olfactory mucosa (OM) and the vomeronasal organ (VNO), u
58 antibody were determined for lung and nasal olfactory mucosa (OM) from Cyp2abfgs-null, CYP2A13-human
64 tion element potentially responsible for the olfactory mucosa-predominant expression of the CYP2A3 ge
65 gene and nuclear extracts from rat liver and olfactory mucosa revealed a single protected region corr
66 id not prevent H5N1 virus replication in the olfactory mucosa sufficiently, resulting in CNS invasion
67 stentacular cells and Bowman's glands of the olfactory mucosa suggests that these cells play a signif
68 scernibly different flux patterns across the olfactory mucosa that may contribute to the encoding of
69 n of flux (or imposed patterning) across the olfactory mucosa, that carries information concerning od
72 an NFI isoform previously identified in the olfactory mucosa, transactivated the CYP2A3 promoter, wh
75 nce delay and phagocytic dysfunction in aged olfactory mucosa were accompanied by a decline of phagoc