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1 exocytosis of synaptic vesicles at the mouse auditory hair cell.
2 in the afferent neural projections to gerbil auditory hair cells.
3 timulus amplification during transduction in auditory hair cells.
4 (s) of each individual GNAI protein in mouse auditory hair cells.
5 es and the sensory transduction apparatus in auditory hair cells.
6 echanoelectrical transducer (MET) channel in auditory hair cells.
7 ganization and maintenance of stereocilia in auditory hair cells.
8 he growth and maintenance of hair bundles in auditory hair cells.
9 predominant influence on frequency tuning in auditory hair cells.
10 lls, and is no longer expressed in postnatal auditory hair cells.
11 fferent roles in terminal differentiation of auditory hair cells.
12 nt is a hallmark of functional maturation in auditory hair cells.
13  is shorter than normal with about 60% fewer auditory hair cells.
14 quency tuning in nonmammalian vestibular and auditory hair cells.
15 frequently branched to contact both types of auditory hair cells.
16 membrane compartments such as stereocilia of auditory hair cells.
17 by destruction and regeneration of inner ear auditory hair cells.
18 isms for controlling hair bundle position in auditory hair cells.
19 ctors that are essential for the function of auditory hair cells.
20 hanoelectrical transducer currents in turtle auditory hair cells adapt to maintained stimuli via a Ca
21                                      Loss of auditory hair cells (AHCs) is a major cause of human dea
22  Light microscopy tools allow for imaging of auditory hair cells along the full length of the cochlea
23  severely shortened with a reduced number of auditory hair cells and cellular organization of the aud
24 ce of mechanosensory function in postmitotic auditory hair cells and could help identify elusive comp
25 ns in Ptprq cause the loss of high-frequency auditory hair cells and deafness in mice, a loss of vest
26 ons are forming their final connections with auditory hair cells and nerve fibers, can lead to profou
27                       However, protection of auditory hair cells and neurons from CDDP-induced damage
28 ng noise-induced peroxisome proliferation in auditory hair cells and neurons.
29 itors under these conditions was examined in auditory hair cells and neurons.
30 rotein that is essential for the survival of auditory hair cells and normal hearing in mice, possibly
31               A loss of cilia also occurs in auditory hair cells and olfactory sensory neurons.
32 llular structure that comprises two types of auditory hair cells and several types of nonsensory supp
33 lia bundle and affects long-term function of auditory hair cells and spiral ganglion neurons.
34                                              Auditory hair cells and supporting cells arise in a wave
35 sins are critical for the normal function of auditory hair cells and the function and maintenance of
36              The physiological maturation of auditory hair cells and their innervation requires preci
37               The V-shaped hair bundles atop auditory hair cells and their uniform orientation are ma
38                         NF-M was detected in auditory hair cells and VIIIth cranial nerve neurons.
39 minently located in lateral-line hair cells, auditory hair cells, and ciliated epidermal cells of dev
40 owing that chordotonal organs and vertebrate auditory hair cells are developmentally related and that
41           Herein, we show that gaps in mouse auditory hair cells are largely repaired within 1 week o
42 Stereocilia maintenance is essential because auditory hair cells are not renewed in mammals.
43                                              Auditory hair cells are surrounded on their basolateral
44                            In adult mammals, auditory hair cells are unable to regenerate, and damage
45 omponent of the mechanotransducer channel in auditory hair cells, but the protein organization and ch
46    Sound stimuli vibrate the hair bundles on auditory hair cells, but the resulting motion attributab
47  The cell membranes in the hair bundle of an auditory hair cell confront a difficult task as the bund
48                                              Auditory hair cells contain mechanotransduction channels
49                                       Turtle auditory hair cells contain multiple isoforms of the por
50                          We report here that auditory hair cells contain two molecularly distinct mec
51 hanoelectrical transduction (MET) channel in auditory hair cells converts sound into electrical signa
52  In transfected cells and in vivo transduced auditory hair cells, cysteine mutagenesis experiments de
53 exposure causes oxidative stress, leading to auditory hair cell damage.
54 n changes in chicken supporting cells during auditory hair cell death.
55                                              Auditory hair cell defect is a major cause of hearing im
56 g hair bundle, the mechanosensory antenna of auditory hair cells, depends on the poorly characterized
57        We report that in contrast to matured auditory hair cells, depletion of membrane cholesterol i
58 e deaf and exhibit no mechanotransduction in auditory hair cells, despite the presence of tip links t
59                      In the absence of Dll1, auditory hair cells develop early and in excess, in agre
60                                              Auditory hair cells developed normally in Pls1 KO, but i
61 vered alterations in cochlear morphogenesis, auditory hair cell differentiation, and cell fate specif
62                                    Mammalian auditory hair cells do not spontaneously regenerate, unl
63            In contrast, regeneration of lost auditory hair cells does not occur in deafened mammals,
64 mechanotransducer currents in turtle and rat auditory hair cells during rapid deflections of the hair
65                                           In auditory hair cells, electrical tuning results from memb
66 edback available to a bird by killing either auditory hair cells encoding higher frequencies or those
67 rganization, F-actin-enriched stereocilia of auditory hair cells evidenced structural disorganization
68                          To this end, turtle auditory hair cells from high- (317 +/- 27 Hz) and low-f
69                                              Auditory hair cells from nonmammalian vertebrates are el
70                    The viral transduction of auditory hair cells from Pjvk (-/-) mice in vivo with bo
71 ic degradation of peroxisomes (pexophagy) in auditory hair cells from wild-type, but not pejvakin-def
72 a nonsensory structure that is essential for auditory hair cell function by maintaining potassium con
73                                              Auditory hair cell function requires proper assembly and
74                       During transduction in auditory hair cells, hair bundle deflection opens mechan
75 ice, abnormally short stereocilia bundles of auditory hair cells have numerous stereocilia links and
76             Unlike mammals, birds regenerate auditory hair cells (HCs) after injury.
77                              Adult mammalian auditory hair cells (HCs) and their associated supportin
78                                    Mammalian auditory hair cells (HCs) are inserted into a well struc
79 AAV) vectors for hearing disorders targeting auditory hair cells (HCs).
80 P(2) pool in the cell syncytia that supports auditory hair cells; (ii) spatially graded impairment of
81 ells in the cochlea, and the regeneration of auditory hair cells in adult mammals.
82 opment, morphology, or Ca(2+) homeostasis of auditory hair cells in the first two postnatal weeks.
83                 The frequency sensitivity of auditory hair cells in the inner ear varies with their l
84 rmanent moderate deafness due to the loss of auditory hair cells in the inner ear.
85 n the cristae of the semicircular canals and auditory hair cells in the organ of Corti.
86           The distinctive planar polarity of auditory hair cells is evident in the polarized organiza
87 gs show that MET current adaptation in mouse auditory hair cells is modulated similarly by extracellu
88                Hearing loss due to damage to auditory hair cells is normally irreversible because mam
89 ggests that regeneration/repair of mammalian auditory hair cells is possible during the early neonata
90 ive microvilli-like stereocilia crowning the auditory hair cells, is essential to hearing.
91 th muscle relaxation and frequency tuning of auditory hair cells, large-conductance calcium-activated
92 th calcium imaging of hair bundles in turtle auditory hair cells located near the high-frequency end
93                                              Auditory hair cells of birds, unlike hair cells in the m
94                                              Auditory hair cells of shaker-2 mice have very short ste
95  compared the mechanotransduction current in auditory hair cells of young normal-hearing littermates,
96                                       In the auditory hair cells of young postnatal mice and rats, a
97  OHC genes and with digenic mutations in the auditory hair cells, potentially expanding therapeutics
98                                              Auditory hair cells preferentially express Fzd2 and Fzd9
99                                              Auditory hair cells receive olivocochlear efferent inner
100 ral, spatial, and morphologic progression of auditory hair cell regeneration in chicks after a single
101 rds; the chick is the best-studied model for auditory hair cell regeneration.
102                                              Auditory hair cells represent one of the most prominent
103                             Mature mammalian auditory hair cells require transmembrane channel-like 1
104            Mechanoelectrical transduction at auditory hair cells requires highly specialized stereoci
105                                          The auditory hair cell resting potential is critical for pro
106 h highly differentiated apical surfaces: (i) auditory hair cells, revealing the presence of nanoscale
107 essential for synaptic vesicle exocytosis at auditory hair cell ribbon synapses.
108 nce, can explain the seasonal enhancement of auditory hair cell sensitivity to the frequency content
109 resent in the tallest rows of stereocilia in auditory hair cells, structures not traditionally though
110 hat paired-pulse plasticity at an adult frog auditory hair cell synapse depends on pulse duration and
111 iate glutamatergic transmission at the adult auditory hair cell synapse.
112 ge, we identified newly regenerated, nascent auditory hair cells that express genes linked to termina
113                          We found that mouse auditory hair cells that lack tip links due to genetic m
114 ver, nonmammalian vertebrates can regenerate auditory hair cells that restore sensory function.
115       Direct comparisons between neighboring auditory hair cells that were different only with respec
116 nbiased, and comprehensive image analysis of auditory hair cells that work well either with imaging d
117                                    In turtle auditory hair cells, the filtering properties are establ
118       In terminally differentiated mammalian auditory hair cells, tip links are subjected to sound-in
119                                              Auditory hair cells transduce sound to the brain, and in
120 -scaffold protein involved in vestibular and auditory hair cell transduction, is also expressed by pr
121                                  The loss of auditory hair cells triggers repair responses within the
122 we measured hair bundle compliance in turtle auditory hair cells under different conditions that alte
123          These observations demonstrate that auditory hair cells undergo a rapid and controlled proce
124                                    Using rat auditory hair cells, we characterize a mechanism, separa
125 ucleus and the supporting cells of the outer auditory hair cells were named, died in 1863 aged 29.
126 rt evidence for proton release from bullfrog auditory hair cells when they are held at more physiolog
127  mechanistic model for vesicle exocytosis in auditory hair cells where the rate of vesicle recruitmen
128      Hearing requires proper function of the auditory hair cell, which is critically dependent upon i

 
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