ライフサイエンスコーパス: turbinate

1 iated lymphoid tissue lining the trachea and turbinate.

2 a dark crusted lesion developed on her nasal turbinate.

3 h grass or ragweed extracts on each inferior turbinate.

4 rgeted the olfactory epithelium in the nasal turbinates.

5 ion, but not on day 3, and only in the nasal turbinates.

6 icates to high titers in the lungs and nasal turbinates.

7 mainly in ventral and lateral regions of the turbinates.

8 ed that bovine FLUDV replicated in the nasal turbinate and lungs of guinea pigs at high titers and wa

9 grams/ml) detected four bands in solubilized turbinate and tracheal epithelial cells (53.7, 31.2, 28.

10 High viral titers were obtained from nasal turbinates and lung tissues of directly inoculated anima

11 cterized by microscopic lesions in the nasal turbinates and lungs of all ferrets; however, Sw30 infec

12 ficant defects in viral replication in nasal turbinates and lungs.

13 s of infectious virus were detected in nasal turbinates and nasal wash samples of A(H3N2)v-inoculated

14 lage abnormalities in the basicranium, nasal turbinates and trachea.

15 s were collected by brushing of the inferior turbinates, and gene expression was interrogated by RNA-

16 > medium turbinate posterior (MTP) > medium turbinate anterior (MTA).

17 ptica is necessary to produce the lesions of turbinate atrophy and bronchopneumonia in pigs infected

18 Moderate turbinate atrophy and bronchopneumonia were found in mos

19 in a significant increase in the severity of turbinate atrophy induced by P. multocida compared with

20 given the parent strains, while there was no turbinate atrophy or pneumonia in pigs challenged with t

21 oxin (DNT), which has been implicated in the turbinate atrophy seen in cases of atrophic rhinitis.

22 Mild to moderate turbinate atrophy was apparent in pigs inoculated with s

23 was terminated on day 37, and the extent of turbinate atrophy was determined by using a morphometric

24 mild but statistically significant degree of turbinate atrophy.

25 24 h after challenge, and bilateral inferior turbinate biopsies were obtained 24 h after challenge, w

26 al swab samples, 71.7% (81 of 113) for nasal turbinate biopsy samples, 19.5% (22 of 113) for blood sa

27 That is, the reassortants grew well in nasal turbinates, but only sporadically (if at all) in the tra

28 milar in primary differentiated ferret nasal turbinate cells, and similar viral titers were measured

29 ted NP patients for comparison with inferior turbinates collected from healthy controls.

30 nt mice have reduced complexity of the nasal turbinates, decreased sensory innervation of the OB, red

31 ificant relationship between the severity of turbinate degeneration and the number of P. multocida or

32 l the pigs were euthanized and the extent of turbinate degeneration was assessed by using a morphomet

33 virus to replicate more efficiently in nasal turbinate epithelium and subsequently transmit between f

34 ovine choroid plexus (CP), testes (OAT-T3), turbinate (FLT), and intestinal carcinoma (ST6) cell lin

35 tors were moderately restricted in the nasal turbinates, highly restricted in lungs, and genetically

36 mu isozyme reveal that the lateral olfactory turbinates I, Ib, II, IIb, and III display a greater int

37 ulted in sloughing off of the OSE from nasal turbinates into the lumen of the nasal airway.

38 o significantly reduce viral titers in nasal turbinates, lungs, and olfactory bulbs.

39 ase chain reaction in nasal vestibule, nasal turbinate mucosa, and peripheral blood samples, along wi

40 ow levels of virus were present in the nasal turbinates of a few hamsters at 14 days p.i.

41 ilar viral titers were measured in the nasal turbinates of infected ferrets.

42 t in pigs inoculated with strain 4609, while turbinates of those infected with strain DBB25 developed

43 m only 1 of 12 animals and only in the nasal turbinates on a single day.

44 have recoverable virus in the lungs or nasal turbinates on days 3 or 5 postinfection and did not deve

45 Nasal turbinates or swabs were collected from wild ducks, gees

46 regional differences in the order: inferior turbinate posterior (ITP) > medium turbinate posterior (

47 inferior turbinate posterior (ITP) > medium turbinate posterior (MTP) > medium turbinate anterior (M

48 onvoluted peripheral channels of the ethmoid turbinates project to the ventral MOB.

49 ity within the olfactory tissue, the lateral turbinate regions displayed a higher level of activity w

50 nasal neurectomy combined with the inferior turbinate surgery between April in 2005 and March in 200

51 nasal neurectomy combined with the inferior turbinate surgery for severe perennial allergic rhinitis

52 nasal neurectomy combined with the inferior turbinate surgery is effective in alleviating clinical s

53 he nose and higher virus titers in the nasal turbinates than intratracheal inoculation.

54 olon, select lymph nodes, small bowel, nasal turbinates, the genital tract and lung.

55 riety of solid and liquid specimens, such as turbinate tissue homogenate and lung lavage fluid, as we

56 nd porcine respiratory coronavirus (PRCV) in turbinate tissue homogenate.

57 tologic lung, lymph node, trachea, and nasal turbinate tissue sections.

58 of CFU per gram of tissue recovered from the turbinate, trachea, and lung also demonstrated significa

59 ized groups: nasal septum variations, middle turbinate variations, uncinate process variations, and e

60 Nasal scrapings from both inferior turbinates were obtained before and 24 h after challenge

61 agent isolated from the squirt Ecteinascidia turbinate, which alkylates DNA in the minor groove at GC