ライフサイエンスコーパス: basilar papilla

1 e ortholog of alpha9 in the chick's cochlea (basilar papilla).

2 auditory subdivision, the cochlear duct, or basilar papilla.

3 r cell ejection from the proximal end of the basilar papilla.

4 bryonic day 11 (E11) of the developing chick basilar papilla.

5 is expressed early in the development of the basilar papilla.

6 cells from the frog sacculus and the turtle basilar papilla.

7 f cell proliferation in both the utricle and basilar papilla.

8 lectrically tuned auditory organ, the turtle basilar papilla.

9 lication of ACh to hair cells in the chicken basilar papilla.

10 s caused by the acoustic injury to the chick basilar papilla.

11 tributions of KCa channel isoforms along the basilar papilla.

12 oximal (mid-frequency) region of the chicken basilar papilla.

13 sectional anatomical pathology of the BWC's basilar papilla.

14 e is expressed at higher levels in the chick basilar papilla after acoustic overstimulation.

15 rn blot analysis of total RNA from the chick basilar papilla after noise trauma revealed increased le

16 a macula, whereas SFRP2 is maintained in the basilar papilla along with Fzd10 and Wnt7b.

17 Most notably, the basilar papilla, an auditory organ, contained infected s

18 o the apical or low frequency portion of the basilar papilla and coincided with maximal expression of

19 tage 20, the lateral crista at stage 22, the basilar papilla and lagena at stage 23, the macula utric

20 ista, the utricle, the saccule, and both the basilar papilla and lagenar macula form.

21 mately characteristic frequency) between the basilar papilla and NM is established as cochlear nerve

22 those studies, the surface anatomy of BWC's basilar papilla and sacculus was examined utilizing scan

23 ons and in peripheral fibers innervating the basilar papilla and synapsing at the base of hair cells.

24 r cells and support cells in the utricle and basilar papilla, and its expression does not change duri

25 Damaged hair cells in the avian basilar papilla are replaced by regenerative proliferati

26 Flanking the basilar papilla are Wnt7a, Wnt9a, Wnt11, and SFRP2 on th

27 f the substructural alterations in the chick basilar papilla at the earliest signs of hair cell degen

28 g the developing tonotopic axis of the chick basilar papilla (BP) identified a gradient of Bmp7.

29 the hearing organ of the chicken, called the basilar papilla (BP), after cellular differentiation.

30 ly phases of cell orientation in the chicken basilar papilla (BP), Vangl2 is present at supporting ce

31 of efferent fibers that innervate the chick basilar papilla (BP).

32 ation pathways among supporting cells in the basilar papilla but not in the utricular macula.

33 ed in most support cells in the mature chick basilar papilla but not in vestibular organs of the chic

34 neural edge of the avian auditory organ, the basilar papilla, by embryonic day 5 (E5).

35 ment sufficient to destroy hair cells in the basilar papilla causes a rapid, transient downregulation

36 ll ears tested, even in non-TM species whose basilar papilla contained as few as 50-60 hair cells.

37 The avian basilar papilla contains tall and short hair cells, with

38 Interestingly, hair cells in the avian basilar papilla demonstrate both electrical resonance an

39 cells that reenter the mitotic cycle in the basilar papilla do not express detectable levels of FGFR

40 Finally, in contrast to the chick basilar papilla, ectopic activation of Notch signaling d

41 the position of their cell bodies along the basilar papilla, foreshadowing the tonotopic mapping obs

42 o the cochlear nerve, cochlear ganglion, and basilar papilla (i.e., avian cochlea) in fixed tissue an

43 s after drug-induced hair cell damage to the basilar papilla in an opposite way to that found in the

44 ations within the apical half of the chicken basilar papilla in vivo and found broadly-tuned travelli

45 in the middle region along the length of the basilar papilla in which, in one cell, the terminals occ

46 junctions connecting supporting cells of the basilar papilla, in which its immunofluorescence colocal

47 ecursor during HC regeneration in the mature basilar papilla is consistent with their developmental h

48 re, frequency tuning within the apical avian basilar papilla is not mechanical, and likely derives fr

49 The avian basilar papilla is tonotopically organized; hair cells i

50 onotopic mapping observed between NM and the basilar papilla later in development.

51 In the basilar papilla, nuclear cProx1 expression is down-regul

52 ry brainstem, the cochlear ganglion, and the basilar papilla of chicks from embryonic (E) day 5 to E2

53 eural may express neurofilament and that the basilar papilla of the neonatal chicken is not morpholog

54 In the chicken cochlea (the basilar papilla or BP), dying hair cells are extruded fr

55 m 1 to 8-20 weeks, whereas hair cells in the basilar papilla remained morphologically intact out to 2

56 uditory sensory organ (the lagena macula and basilar papilla, respectively), which each have a distin

57 ut patches from hair cells along the chicken basilar papilla revealed 'tonotopic' gradations in calci

58 Light microscopic observations of the basilar papilla stained with the same antibody confirmed

59 ore severe at the apex and midsection of the basilar papilla than at the base.

60 tion density among hair cells of the chick's basilar papilla (the avian analog of the mammalian Organ

61 ontribute to the structural integrity of the basilar papilla, the maintenance of the ionic barrier at

62 A semi-intact preparation of the chick basilar papilla was developed to study calcium-dependent

63 In the chicken's basilar papilla, we found numerous isoforms of KCa chann

64 tion, but it is absent from all cells in the basilar papilla, which is mitotically quiescent.