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1 e ortholog of alpha9 in the chick's cochlea (basilar papilla).
2 evels within the chicken auditory organ: the basilar papilla.
3  auditory subdivision, the cochlear duct, or basilar papilla.
4 r cell ejection from the proximal end of the basilar papilla.
5 bryonic day 11 (E11) of the developing chick basilar papilla.
6 is expressed early in the development of the basilar papilla.
7 f cell proliferation in both the utricle and basilar papilla.
8 lectrically tuned auditory organ, the turtle basilar papilla.
9  cells from the frog sacculus and the turtle 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 lication of ACh to hair cells in the chicken basilar papilla.
14  sectional anatomical pathology of the BWC's basilar papilla.
15 e is expressed at higher levels in the chick basilar papilla after acoustic overstimulation.
16 he changes in gene expression in the chicken basilar papilla after aminoglycoside antibiotic-induced
17 rn blot analysis of total RNA from the chick basilar papilla after noise trauma revealed increased le
18 a macula, whereas SFRP2 is maintained in the basilar papilla along with Fzd10 and Wnt7b.
19                            Most notably, the basilar papilla, an auditory organ, contained infected s
20 o the apical or low frequency portion of the basilar papilla and coincided with maximal expression of
21 tage 20, the lateral crista at stage 22, the basilar papilla and lagena at stage 23, the macula utric
22 ista, the utricle, the saccule, and both the basilar papilla and lagenar macula form.
23 mately characteristic frequency) between the basilar papilla and NM is established as cochlear nerve
24  those studies, the surface anatomy of BWC's basilar papilla and sacculus was examined utilizing scan
25 ons and in peripheral fibers innervating the basilar papilla and synapsing at the base of hair cells.
26 r cells and support cells in the utricle and basilar papilla, and its expression does not change duri
27              Damaged hair cells in the avian basilar papilla are replaced by regenerative proliferati
28                                 Flanking the basilar papilla are Wnt7a, Wnt9a, Wnt11, and SFRP2 on th
29 f the substructural alterations in the chick basilar papilla at the earliest signs of hair cell degen
30 g the developing tonotopic axis of the chick basilar papilla (BP) identified a gradient of Bmp7.
31 the hearing organ of the chicken, called the basilar papilla (BP), after cellular differentiation.
32                    In the chick cochlea, the basilar papilla (BP), proximal (high-frequency) HCs, are
33 ly phases of cell orientation in the chicken basilar papilla (BP), Vangl2 is present at supporting ce
34  of efferent fibers that innervate the chick basilar papilla (BP).
35 ation pathways among supporting cells in the basilar papilla but not in the utricular macula.
36 ed in most support cells in the mature chick basilar papilla but not in vestibular organs of the chic
37 neural edge of the avian auditory organ, the basilar papilla, by embryonic day 5 (E5).
38 ment sufficient to destroy hair cells in the basilar papilla causes a rapid, transient downregulation
39 ll ears tested, even in non-TM species whose basilar papilla contained as few as 50-60 hair cells.
40                                    The avian basilar papilla contains tall and short hair cells, with
41       Interestingly, hair cells in the avian basilar papilla demonstrate both electrical resonance an
42  cells that reenter the mitotic cycle in the basilar papilla do not express detectable levels of FGFR
43            Finally, in contrast to the chick basilar papilla, ectopic activation of Notch signaling d
44  the position of their cell bodies along the basilar papilla, foreshadowing the tonotopic mapping obs
45 o the cochlear nerve, cochlear ganglion, and basilar papilla (i.e., avian cochlea) in fixed tissue an
46 s after drug-induced hair cell damage to the basilar papilla in an opposite way to that found in the
47 ations within the apical half of the chicken basilar papilla in vivo and found broadly-tuned travelli
48 in the middle region along the length of the basilar papilla in which, in one cell, the terminals occ
49 junctions connecting supporting cells of the basilar papilla, in which its immunofluorescence colocal
50 ecursor during HC regeneration in the mature basilar papilla is consistent with their developmental h
51 re, frequency tuning within the apical avian basilar papilla is not mechanical, and likely derives fr
52                                    The avian basilar papilla is tonotopically organized; hair cells i
53 onotopic mapping observed between NM and the basilar papilla later in development.
54                                       In the basilar papilla, nuclear cProx1 expression is down-regul
55 ry brainstem, the cochlear ganglion, and the basilar papilla of chicks from embryonic (E) day 5 to E2
56 eural may express neurofilament and that the basilar papilla of the neonatal chicken is not morpholog
57                  In the chicken cochlea (the basilar papilla or BP), dying hair cells are extruded fr
58 m 1 to 8-20 weeks, whereas hair cells in the basilar papilla remained morphologically intact out to 2
59 priate position along the chick cochlea, the basilar papilla, requires that nascent HCs determine the
60 uditory sensory organ (the lagena macula and basilar papilla, respectively), which each have a distin
61 ut patches from hair cells along the chicken basilar papilla revealed 'tonotopic' gradations in calci
62        Light microscopic observations of the basilar papilla stained with the same antibody confirmed
63 ore severe at the apex and midsection of the basilar papilla than at the base.
64               The avian hearing organ is the basilar papilla that, in sharp contrast to the mammalian
65 tion density among hair cells of the chick's basilar papilla (the avian analog of the mammalian Organ
66 ontribute to the structural integrity of the basilar papilla, the maintenance of the ionic barrier at
67       A semi-intact preparation of the chick basilar papilla was developed to study calcium-dependent
68                             In the chicken's basilar papilla, we found numerous isoforms of KCa chann
69 tion, but it is absent from all cells in the basilar papilla, which is mitotically quiescent.