戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 the mechanotransduction complex in zebrafish vestibular hair cells.
2 ined transcriptomes of developing and mature vestibular hair cells.
3 nner hair cells, spiral ganglion neurons and vestibular hair cells.
4 nglion neurons (VGN) innervating the type II vestibular hair cells.
5 ssion, reminiscent of two subtypes of native vestibular hair cells.
6 cholinergic efferents innervating peripheral vestibular hair cells.
7  mechanotransduction complex in auditory and vestibular hair cells.
8 the tips of stereocilia of both cochlear and vestibular hair cells.
9 l mouse cochlear hair cells but persisted in vestibular hair cells.
10 ve distinct functional roles in cochlear and vestibular hair cells.
11 ctures at the apical surface of auditory and vestibular hair cells.
12 atment caused apoptosis of both auditory and vestibular hair cells.
13 f data concerning BK expression in mammalian vestibular hair cells.
14 esponse, and normal transduction currents in vestibular hair cells.
15 myosin-1c is required for fast adaptation in vestibular hair cells.
16  tips of the stereocilia of the cochlear and vestibular hair cells.
17  signaling events that regulate the death of vestibular hair cells.
18 in the apoptotic destruction of auditory and vestibular hair cells.
19 h1-null mice failed to generate cochlear and vestibular hair cells.
20 ptation of mechanoelectrical transduction in vestibular hair cells.
21 on, regeneration, and apoptosis of mammalian vestibular hair cells.
22 ou4f3 expression in cochlear hair cells than vestibular hair cells, administration of a low dose of D
23                    Little is known about how vestibular hair cells adopt a Type I or Type II identity
24 upport to calyceal synaptic contact with the vestibular hair cell and that Caspr is required for the
25  is conveyed by a central "striolar" zone of vestibular hair cells and afferent neurons in the inner
26                                              Vestibular hair cells and afferents were counterstained
27 detected in stereocilia of both cochlear and vestibular hair cells and also along the apical surface
28 ly as embryonic day 16.5 in the auditory and vestibular hair cells and associated ganglionic neurons,
29 form in hair bundles of outer hair cells and vestibular hair cells and is the predominant PMCA of hai
30 enrichment of relatively pure populations of vestibular hair cells and non-sensory cells including su
31 y hair cells and deafness in mice, a loss of vestibular hair cells and overt behavioral defects chara
32 ing, disease, and trauma can lead to loss of vestibular hair cells and permanent vestibular dysfuncti
33 ted in maturing (myosin VIIA immunoreactive) vestibular hair cells and subsequently in the underlying
34 are significant signaling regions of type II vestibular hair cells and suggest that type II hair cell
35 used dual patch-clamp recordings from turtle vestibular hair cells and their afferent neurons to show
36 tial fraction of the Cy3-ATP tip labeling in vestibular hair cells, and so this novel preparation cou
37 Brn-3c protein is found only in auditory and vestibular hair cells, and the Brn-3a and Brn-3b protein
38                    In mammals, type I and II vestibular hair cells are defined by their shape, contac
39                Significantly, adult pRb(-/-) vestibular hair cells are functional, and pRb(-/-) mice
40 zd9, whereas the main receptors expressed in vestibular hair cells are Fzd1 and Fzd7, in addition to
41                                              Vestibular hair cells are mechanoreceptors critical for
42        Our results suggest that cochlear and vestibular hair cells are the primary regulators of auto
43                                          How vestibular hair cells are tuned to transduce dynamic sti
44                                 Auditory and vestibular hair cell bundles exhibit active mechanical o
45                                          The vestibular hair cell-calyx synapse supports a mysterious
46 he M-like conductances in mouse auditory and vestibular hair cells can include KCNQ4 subunits and may
47 -rich stereocilia elongation in auditory and vestibular hair cells, causing deafness and balance defe
48 located in the apical region of cochlear and vestibular hair cells, consists of alternating, cross-li
49 s spectrometry shows that bundles from chick vestibular hair cells contain a complete set of proteins
50 resonance seen in many types of auditory and vestibular hair cells contributes to frequency selectivi
51  development of hair bundles in cochlear and vestibular hair cells, controlling hair bundle morphogen
52              The hair bundle of auditory and vestibular hair cells converts mechanical stimuli into e
53  cause of vestibular dysfunction is arguably vestibular hair cell damage, which can result from an ar
54    In a wild-type mouse, during auditory and vestibular hair cell development, myosin XVa appears at
55          Accordingly, whole cell currents of vestibular hair cells did not differ between genotypes.
56 ally redundant FGF ligands may contribute to vestibular hair cell differentiation and supports a deve
57                                   Lesions of vestibular hair cells disrupt the characteristic firing
58 ects reflect a complete loss of auditory and vestibular hair cells during the late embryonic and earl
59 r promising translational avenue to treating vestibular hair cell dysfunction is the potential develo
60                      Both type I and type ll vestibular hair cells express the alpha9 and alpha10 sub
61                                 Cochlear and vestibular hair cells from PCDH15-deficient mice also sh
62 nd that, whereas the basolateral membrane of vestibular hair cells from the frog saccule extrudes H+
63         We conclude that HCN1 contributes to vestibular hair cell function and the sense of balance.
64                                              Vestibular hair cells have a distinct planar cell polari
65                                       Type I vestibular hair cells have large K+ currents that, like
66 otions and tilt are detected by two types of vestibular hair cells (HCs) with strikingly different mo
67                    Mammals have two types of vestibular hair cell, I and II, with unique morphologica
68 ion is a specific and early marker of Type-I vestibular hair cell identity.
69                Thus, natural regeneration of vestibular hair cells in adult mice is limited in total
70 that, following acute destruction of ~95% of vestibular hair cells in adult mice, ~20% regenerate nat
71  and ultrastructure of efferent terminals on vestibular hair cells in alpha9, alpha10, and alpha9/10
72 ibe unique morphological features of type II vestibular hair cells in mature rodents (mice and gerbil
73 ion mixture resulted in the return of type 1 vestibular hair cells in ototoxin-damaged cristae, and i
74 sition of the kinocilium is reversed between vestibular hair cells in the cristae of the semicircular
75                                              Vestibular hair cells in the inner ear encode head movem
76 often result in degeneration of cochlear and vestibular hair cells in the inner ear.
77 ers (ANF), spiral ganglion neurons (SGN) and vestibular hair cells in the saccule, utricle and semici
78  occurred to OHC, IHC, ANF, SGN and only the vestibular hair cells in the striola region of the saccu
79 ir cells had many features of mature type II vestibular hair cells, including polarized mechanosensit
80                   The molecular diversity of vestibular hair cells indicates a functional diversity t
81 cochlear outer hair cells and some groups of vestibular hair cells, indicating that Jag1 is required
82 type I hair cell, and the basolateral type I vestibular hair cell is NR-1 immunoreactive.
83  Myo1c to stereociliary tips of cochlear and vestibular hair cells is disrupted by treatments that br
84        Additionally, Ocm immunoreactivity in vestibular hair cells is present as early as E18 and is
85 te the effect of hydrostatic pressure on the vestibular hair cells located in the labyrinth of the do
86 al yet distinct roles of pRb in cochlear and vestibular hair cell maturation, function, and survival
87 o suggest that persistent TMC2 expression in vestibular hair cells may preserve vestibular function i
88 cadherin 15 has been described for a teleost vestibular hair-cell model and mammalian organ of Corti
89 ning (i.e., light paired with stimulation of vestibular hair cells) modifies the kinetics of presynap
90 spiral and vestibular ganglia, inner ear and vestibular hair cell neurons in the vestibuloacoustic sy
91                  We transfected auditory and vestibular hair cells of organotypic cultures generated
92               I(h) has been characterized in vestibular hair cells of the inner ear, but its molecula
93 ble intracellular damage to the auditory and vestibular hair cells of the inner ear.
94 tional co-activator regulated by miR-135b in vestibular hair cells of the mouse inner ear as well as
95                  In contrast to the cochlea, vestibular hair cells of the murine utricle have some re
96 ransduction is impaired in cochlear, but not vestibular, hair cells of early postnatal Vlgr1/del7TM m
97 ted in a significant and age-related loss of vestibular hair cells only in the saccule.
98 monly associated with damage to cochlear and vestibular hair cells or neurons.
99 t expression patterns: some are specific for vestibular hair cells, others for cochlear hair cells, a
100 component, to trace development of the SO in vestibular hair cells over the first postnatal week.
101 nd PMCA2 isozymes holds for rat auditory and vestibular hair cells; PMCA2a is the only PMCA isoform i
102 pe of CNGA3 transcript in a purified teleost vestibular hair cell preparation with immunolocalization
103   Treatment with GF I significantly enhanced vestibular hair cell renewal in ototoxin-damaged utricle
104         Sensory transduction in auditory and vestibular hair cells requires expression of transmembra
105 t and mechanical stimulation of the animal's vestibular hair cells resulted in an increase in the exc
106 efined immunolocalization in rat and chicken vestibular hair cells showed that CLIC5 is limited to th
107        Confocal imaging of isolated bullfrog vestibular hair cells shows that the bundle membrane seg
108 ings of light and presynaptic stimulation of vestibular hair cells (simulating light-rotation pairing
109 the localization of BK channels in mammalian vestibular hair cells, specifically in rat vestibular ne
110      In adult mice, the sudden death of most vestibular hair cells stimulates the production of new h
111 coupled receptors as a result of presynaptic vestibular hair cell stimulation.
112 n inner hair cells and in type I and type II vestibular hair cells suggests a functional role in hair
113 fferentially expressed genes in auditory and vestibular hair cells suggests that GFI1 serves differen
114                   In contrast, many pRb(-/-) vestibular hair cells survive and continue to divide in
115 ion (MET) by cochlear hair cells, but not by vestibular hair cells that co-express CIB2 and CIB3.
116  model based on Myo7a mutation, cochlear and vestibular hair cells, the main inner ear cell types aff
117 ctions, owing to the failure of cochlear and vestibular hair cells to differentiate properly.
118 vey excitatory stimuli from inner ear type I vestibular hair cells to postsynaptic calyx nerve termin
119                                              Vestibular hair cells transmit information about head po
120               However, it is unclear whether vestibular hair cells undergo similar degeneration in co
121 ethods to demonstrate that utricular type II vestibular hair cells undergo turnover in adult mice und
122 carinic receptors (mAChRs), are expressed by vestibular hair cells (VHCs).
123                            In frog and mouse vestibular hair cells, we found that the rate of fast ad
124 s, a robust model for mammalian auditory and vestibular hair cells, we identified a urea-thiophene ca
125 sing the Brn 3.1 knockout mouse, which lacks vestibular hair cells, we recently described a major rol
126  found at calyx terminals ensheathing type I vestibular hair cells where it may be localized pre- or
127 oad punctate cytoplasmic distribution in the vestibular hair cells, whereas it was detected in the en
128               The sense of balance relies on vestibular hair cells, which detect head motions.
129 completely envelopes one or more presynaptic vestibular hair cells, which transmits mechanosensory si

 
Page Top