ライフサイエンスコーパス: olfactory mucosa

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 o reacts to pressure pulses delivered to the olfactory mucosa.

9 pression of the CYP1A2 gene in the liver and olfactory mucosa.

10 e immunostaining, and decreased depth in the olfactory mucosa.

11 found to be expressed at a high level in the olfactory mucosa.

12 ) in intercellular signaling pathways in the olfactory mucosa after target ablation.

13 element and nuclear extracts from liver and olfactory mucosa, all of which were supershifted in the

14 , we transplanted lamina propria (LP) of the olfactory mucosa alone or in combination with cultured o

15 nt stimuli, namely mechanical stimuli to the olfactory mucosa and a large number of amino acids.

16 onstrated that EGFR mRNA is expressed in the olfactory mucosa and also in the positive control tissue

17 T) isozymes (alpha, mu, and pi) in the mouse olfactory mucosa and characterize the zonal expression o

18 owed by transplantation of lamina propria of olfactory mucosa and cultured olfactory ensheathing cell

19 CYP2A3 is expressed preferentially in rat olfactory mucosa and is believed to play important roles

20 nation reduced H5N1 virus replication in the olfactory mucosa and prevented subsequent virus spread t

21 event influenza virus replication within the olfactory mucosa and subsequent spread to the CNS.

22 Influenza A viruses can replicate in the olfactory mucosa and subsequently use the olfactory nerv

23 n of CR-ir olfactory receptor neurons in the olfactory mucosa and their bulbar projections.

24 application of horseradish peroxidase to the olfactory mucosa and were subsequently sacrificed.

25 rat CYP2A3, which has been detected in human olfactory mucosa as well as in liver.

26 ytochrome P-450 isoform in the liver and the olfactory mucosa but is essentially not expressed in oth

27 ted with the CYP2A3 promoter in vivo, in rat olfactory mucosa, but essentially not in the liver where

28 We have found OPs in monkey olfactory mucosa, but none in rodents.

29 f the CYP2A3 gene with nuclear extracts from olfactory mucosa, but not from liver, lung, kidney, or b

30 The olfactory mucosa can serve as a conduit for a number of

31 In the olfactory mucosa containing the olfactory receptor neuro

32 This mechanism of prion shedding from the olfactory mucosa could contribute to prion transmission.

33 nervous system (CNS) anterogradely from the olfactory mucosa following intranasal infection.

34 iseases, can readily enter the brain via the olfactory mucosa, have led to the hypothesis that Alzhei

35 ed with unique proteins detected only in the olfactory mucosa in electrophoretic mobility shift assay

36 to obtain the cells from the more accessible olfactory mucosa in the nasal lining.

37 ed rabbit P450s known to be expressed in the olfactory mucosa, including 1A2, 2A10/11, 2B4, 2E1, 2G1,

38 The mouse olfactory mucosa is a complex chemosensory tissue compos

39 The rodent olfactory mucosa is characterized by a mosaic of gene ex

40 Furthermore, we show that NCX1 mRNA in rat olfactory mucosa is expressed as 8 alternative splice va

41 Inserted in the olfactory mucosa lining of the nasal cavity, they are ex

42 ociated with CYP2A13 promoter in vivo in the olfactory mucosa of CYP2A13-transgenic mice.

43 own to cause tissue-specific toxicity in the olfactory mucosa of rodents at very low doses.

44 e-specific toxicity at very low doses in the olfactory mucosa of rodents.

45 ll cultures (neurosphere-derived cells) from olfactory mucosa of schizophrenia patients have signific

46 y highlights the importance of including the olfactory mucosa, olfactory nerve, and CNS tissues in fu

47 e two major olfactory organs of rodents, the olfactory mucosa (OM) and the vomeronasal organ (VNO), u

48 antibody were determined for lung and nasal olfactory mucosa (OM) from Cyp2abfgs-null, CYP2A13-human

49 The olfactory mucosa (OM) is exposed to environmental agents

50 rion protein in cerebrospinal fluid (CSF) or olfactory mucosa (OM) samples.

51 ptors and cell adhesion molecules across the olfactory mucosa (OM).

52 liver, nasal-associated lymphoid tissue, and olfactory mucosa (OM).

53 tion element potentially responsible for the olfactory mucosa-predominant expression of the CYP2A3 ge

54 gene and nuclear extracts from rat liver and olfactory mucosa revealed a single protected region corr

55 id not prevent H5N1 virus replication in the olfactory mucosa sufficiently, resulting in CNS invasion

56 stentacular cells and Bowman's glands of the olfactory mucosa suggests that these cells play a signif

57 scernibly different flux patterns across the olfactory mucosa that may contribute to the encoding of

58 n of flux (or imposed patterning) across the olfactory mucosa, that carries information concerning od

59 The olfactory mucosa, the organ of smell in the nose, is a n

60 the anterograde spread of the virus from the olfactory mucosa to the bulb.

61 an NFI isoform previously identified in the olfactory mucosa, transactivated the CYP2A3 promoter, wh

62 different tissue compartments (e.g. kidney, olfactory mucosa) via organic anions.

63 Biopsies of the skin and olfactory mucosa were obtained, and expression levels of