ライフサイエンスコーパス: nasal epithelium

1 ating all of the cell types found within the nasal epithelium.

2 d by a marked paucity of motile cilia in the nasal epithelium.

3 s in the rainbow trout (Oncorhynchus mykiss) nasal epithelium.

4 g had a similar effect on gene expression in nasal epithelium.

5 infant airway transcriptome by sampling the nasal epithelium.

6 eceptors expressed by sensory neurons in the nasal epithelium.

7 tent of CFTR function in the sweat gland and nasal epithelium.

8 ares an apical distribution with CFTR in rat nasal epithelium.

9 trigeminal ganglion (TG) which innervate the nasal epithelium.

10 t cells were excluded from both the lens and nasal epithelium.

11 d several nonocular sites, such as heart and nasal epithelium.

12 dicate that bitter substances applied to the nasal epithelium activate the trigeminal nerve and evoke

13 on, infectious virus was recovered only from nasal epithelium; after intratracheal inoculation, it wa

14 l ganglion cells with sensory endings in the nasal epithelium also have branches reaching directly in

15 stem, beginning at embryonic day 11.5 in the nasal epithelium and at embryonic day 16.5 in the olfact

16 ed robust biofilms that were adherent to the nasal epithelium and displayed architectural attributes

17 osensory cells that reach the surface of the nasal epithelium and form synaptic contacts with trigemi

18 been implicated in S. aureus colonization of nasal epithelium and is therefore a key virulence factor

19 terial rhinosinusitis is an infection of the nasal epithelium and paranasal sinus mucosa, usually cau

20 ive TRP channels in chemesthesis in oral and nasal epithelium and suggest that TRPV3 may be a molecul

21 ce shows that Pax6 has distinct roles in the nasal epithelium and the principal tissue components of

22 are trapped on the mucous layer coating the nasal epithelium and upper respiratory tract, and are cl

23 induced at embryonic day 15.5 in epidermis, nasal epithelium, and surface of the tongue.

24 isrupts miRNA expression profiles within the nasal epithelium, and these alterations likely influence

25 Nuclear Yellow was injected into the dorsal nasal epithelium, and True Blue was injected into the ol

26 fects arise during embryogenesis and, in the nasal epithelium, appear to be independent of any change

27 To determine the usefulness of the nasal epithelium as a pre-screen for lung-directed thera

28 PLUNC (palate, lung, and nasal epithelium associated) is a 25-kDa secreted protei

29 of P. multocida organisms isolated from the nasal epithelium at the end of the experiment (R2 = 0.86

30 The short palate, lung, nasal epithelium clone (PLUNC) 1 (SPLUNC1) protein is a

31 otid secretory protein (PSP) and palate-lung-nasal epithelium clone (PLUNC) are novel secretory prote

32 nnate immune proteins of the palate lung and nasal epithelium clone (PLUNC) family in patients with C

33 protein is a member of the palate, lung, and nasal epithelium clone (PLUNC) family, also known as bac

34 Palate, lung, and nasal epithelium clone (Plunc, now renamed Splunc1) is a

35 The short palate, lung, and nasal epithelium clone (SPLUNC)1 protein is secreted in

36 Short palate, lung, and nasal epithelium clone 1 (SPLUNC1) protein is a recently

37 Short palate, lung, and nasal epithelium clone 1 (SPLUNC1) protein is highly exp

38 dies demonstrate that long palate, lung, and nasal epithelium clone 1 protein (LPLUNC1) is involved i

39 s with similarity to PLUNC (palate, lung and nasal epithelium clone), which is itself related to the

40 , which we call plunc (for palate, lung, and nasal epithelium clone; GenBankTM accession number U6917

41 n the proportions of epithelial cells in the nasal epithelium, compared with marked neutrophil inflam

42 We obtained biopsies of nasal epithelium containing ORNs from RTT patients and a

43 n and fluid transport in the sweat gland and nasal epithelium demonstrated the presence of functional

44 re BM-derived epithelial cells in the GI and nasal epithelium detected in CFTR-/- transplanted mice p

45 Rat nasal epithelium displayed robust immunoreactivity that

46 CREB regulation in CF is betaarr2-dependent, nasal epithelium excised from wt mice (Cftr +/+; betaarr

47 f genes that are differentially expressed in nasal epithelium following lesioning of the olfactory bu

48 y inefficient at initiating infection of the nasal epithelium following vaccination, and therefore, a

49 tigen distribution, being largely limited to nasal epithelium for intranasally infected guinea pigs a

50 transcriptome"), we found that bronchial and nasal epithelium from non-smokers were most similar in g

51 esting factors necessary for colonization on nasal epithelium, genetic determinants of nasal carriage

52 fferentially expressed between CF and non-CF nasal epithelium (>/=1.5-fold, P</=0.05).

53 mination were examined in rats in which each nasal epithelium had been irrigated with 0.1-0.5 ml 5% z

54 plunc mRNA was expressed in nasal epithelium, heart, lung, thymus, and salivary glan

55 TP and its metabolite UDP on polarized human nasal epithelium (HNE), and have compared the pharmacolo

56 The nasal epithelium is an important target site for chemica

57 helium are transcriptionally distinct and CF nasal epithelium is not a good surrogate for the lung re

58 The nasal epithelium is richly invested with peptidergic (su

59 P production in TG neurons projecting to the nasal epithelium is transiently increased after TDI expo

60 ium was inflammatory response, whereas in CF nasal epithelium it was amino acid metabolism.

61 and near-exclusion of mutant cells from the nasal epithelium mirrored the behaviour of mutant cells

62 d human airway epithelia in vitro and to the nasal epithelium of cystic fibrosis mice in vivo.

63 This defect is particularly striking in the nasal epithelium of E2f4-/- mice where ciliated cells ar

64 When vitamin C was instilled into the nasal epithelium of human subjects, it effectively activ

65 AAV5 to efficiently transduce the lungs and nasal epithelium of mice after repeated administration.

66 magnitude of the potential difference across nasal epithelium of mice homozygous for the most common

67 alters miRNA expression profiles within the nasal epithelium of nonhuman primates.

68 dministration of an adenovirus vector to the nasal epithelium of patients with CF with five escalatin

69 ane conductance regulator (CFTR) gene to the nasal epithelium of patients with cystic fibrosis.

70 sion, function, and regulation of TJs in the nasal epithelium of patients with house dust mite (HDM)-

71 an provide CFTR activity in the GI tract and nasal epithelium of recipient cystic fibrosis mice.

72 is related to JSRV but induces tumors in the nasal epithelium of sheep and goats.

73 length that is expressed in the presumptive nasal epithelium of the mouse embryo.

74 particles in CF mice produces changes in the nasal epithelium potential difference assay, consistent

75 exclusively on free nerve endings within the nasal epithelium, requiring that trigeminal irritants di

76 l cells evoked by weak (i.e., perithreshold) nasal epithelium shocks (1.0 Hz) in 17/18 cells (mean In

77 e inactivation of olfactory receptors in the nasal epithelium significantly reduced responses to intr

78 Olfrs localized to overlapping zones of the nasal epithelium, suggesting regional biases, but not to

79 saturable binding of [18F]GV1-57 in primate nasal epithelium, supporting its translational potential

80 leptin administered directly to the brain or nasal epithelium suppresses seizures via direct effects

81 By extending to the surface of the nasal epithelium, these chemosensory cells serve to expa

82 plunc was expressed in nasal epithelium, thymus, and salivary gland during embr

83 nating others, despite leaving the path from nasal epithelium to PC intact.

84 by blocking odorant passage to one half the nasal epithelium via unilateral naris closure, a manipul

85 SP nerve fiber density in nasal epithelium was significantly increased 12, 24, and

86 The order of efficiency for nasal epithelium was: Ba2+ > clofilium >>> TEA = azimili

87 IL-19 is highly expressed in the metaplastic nasal epithelium when compared to normal or hyperplastic

88 Similarly, fused is highly expressed in the nasal epithelium, where fused knockouts display bilatera

89 ograde transport by olfactory neurons in the nasal epithelium, which may limit the utility of this ro

90 tigen redirection occurred mainly across the nasal epithelium without subsequent transport along olfa