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 ents associated with establishing PCP in the utricle.
2 caudal ends that fuse to form the prostatic utricle.
3 supporting cell proliferation in the mature utricle.
4 on spontaneous hair cell death in the chick utricle.
5 II beta-tubulin and beta-actin from the same utricle.
6 al canal and ampulla, as well as part of the utricle.
7 myosin Ibeta in hair bundles of the bullfrog utricle.
8 om hair cells in the epithelium of the mouse utricle.
9 evelopment of a murine vestibular organ, the utricle.
10 -Seq) of hair cell regeneration in the chick utricle.
11 liferation in a murine vestibular organ, the utricle.
12 nd Pcdh15 and were not detected in the chick utricle.
13 ifferentiation, and PCP establishment in the utricle.
14 en supporting cells in the gravity-sensitive utricle.
15 mechanoelectrical transduction in the turtle utricle.
16 the vestibular dark cells in the ampulla and utricle.
17 he dissection and culture of the adult mouse utricle.
18 d recovery in saccules comparable to that in utricles.
19 eat-shocked utricles and the nonheat-shocked utricles.
20 g cells into hair cells in cisplatin-treated utricles.
21 epithelium of embryonic and 2-week-old mouse utricles.
22 ecipitated from purified hair bundles of rat utricle, 2w was the only site A variant detected; moreov
23 munolocalization of HCN protein in the mouse utricle, a mechanosensitive organ that contributes to th
24 l phenotype during regeneration in the avian utricle, a vestibular organ that detects linear accelera
25 hic evidence that, in cultured postnatal rat utricles, a substantial number of hair cells can survive
27 ere we show that HC damage in neonatal mouse utricle activates the Wnt target gene Lgr5 in striolar s
28 We asked whether hair cells of the mouse utricle adapt, and if so, whether the adaptation was sim
33 in both hair cells and support cells in the utricle and basilar papilla, and its expression does not
35 zed within sensory epithelia of the saccule, utricle and cochlea throughout development and into adul
36 ells and surrounding cells, from cochlea and utricle and from E16 to P7, we performed a comprehensive
37 lar canal crista, as well as a fusion of the utricle and saccule endolymphatic spaces into a common u
41 ect in tlt homozygous mice is limited to the utricle and saccule of the inner ear, which completely l
42 The defect in het mutants is limited to the utricle and saccule of the inner ear, which completely l
43 nuclei and cerebellum similar to that of the utricle and saccule suggest that the primary role of the
46 a from experimental preparations of ampulla, utricle and saccule were found to be significantly highe
49 hatic duct and sac, in distinct areas of the utricle and saccule, and in the external sulcus region w
51 splatin-induced hair cell death in the mouse utricle and suggest that treatment with EGCG may be a us
52 find that only a subset of hair cells in the utricle and the crista ampullaris express BK channels.
54 onditional hair cell ablation in adult mouse utricles and demonstrates that hair cells are spontaneou
55 d STAT1 phosphorylation in cisplatin-treated utricles and resulted in concentration-dependent increas
56 ibular hair cell renewal in ototoxin-damaged utricles and the maturation of stereociliary bundle morp
58 epletion of sensory cells in the saccule and utricle, and a complete loss of the horizontal semicircu
60 maining sensory epithelia (posterior crista, utricle, and cochlea) that closely corresponds to the de
61 and ventral projections from the saccule and utricle, and medial and dorsal projections from the lage
65 ncluding three semicircular canals, saccule, utricle, and their associated sensory organs, detects an
66 sed within the striolar reversal zone of the utricle, and we show here that this regionalized express
67 ELISA in the media surrounding heat-shocked utricles, and depletion of HSP70 from the media abolishe
71 nd medial extrastriolar (MES) regions of the utricle at embryonic day 11.5 (E11.5), while cells in th
73 elow 5 Hz, within the frequency range of the utricle, but because it was incomplete, substantial resp
74 e/Cwe animals had very few hair cells in the utricle, but their ampullae and cochlea were devoid of a
75 iled to induce proliferation in neonatal rat utricles, but brief (</=1 hr) exposures to forskolin or
76 ve ablation of hair cells in the adult mouse utricle by inserting the human diphtheria toxin receptor
78 ated for their ability to reduce the size of utricles (comedolytic activity) in a rhino mouse model o
79 ratio was significantly elevated in rda/rda utricles compared with controls, and the level of ARF6-G
80 this we used neomycin to kill hair cells in utricles cultured from mice of different ages and found
81 close proximity between the saccules and the utricles, deeply grooved sulci on the saccular otoliths,
91 ter photobleaching (FRAP) of SC junctions in utricles from mice that express a gamma-actin-GFP fusion
93 pha were assayed in organo-typic cultures of utricles from the mature, undamaged (normal) chicken inn
98 w that HES7 is specifically expressed during utricle hair cell regeneration and closely parallels the
102 th widely expressed in the cochlear duct and utricle in an overlapping pattern, suggesting coexpressi
103 bundles in the extrastriolar regions of the utricle in Ptprq(-/-) mice become significantly longer t
104 ia also occurs in the striolar region of the utricle in Ptprq(-/-) mice, but is not accompanied by ha
106 contrast to adults, HC ablation in neonatal utricles in vivo recruits Lgr5+ cells to regenerate stri
107 at high levels in stereocilia of the chicken utricle, in an approximate 1:1 molar ratio with radixin.
109 in different regions of the lagena, saccule, utricle, macula neglecta, and cristae was characterized
110 n other annexin genes are expressed in mouse utricles, mass spectrometry showed that none were presen
111 st that gravity-sensing hair cells in murine utricles may increase in number during neonatal developm
112 cluded hypospadias, opacification of a small utricle (not in the patient with hypospadias), ejaculato
113 ulin, along with that for beta-actin, in the utricle of chicks after hair cell damage both in vitro a
117 ked specific structures such as the cochlea, utricle, or saccule throughout late IE development.
118 Ventral to the mid-level of the presumptive utricle, Otx1 and Otx2 were co-expressed, in regions suc
119 the number of BK-positive hair cells in the utricle peaks in juvenile rats and declines in early adu
124 periods, total RNA was extracted from single utricles, reverse transcribed to cDNA and the cDNA ampli
125 hich triggers proliferation and restores the utricle's growth; interfering with Yap's activity revers
126 ave a misshapen and smaller ear with a fused utricle, saccule, and cochlea and absent horizontal cana
128 e numbers of hair cells differentiate in the utricle, saccule, and cochlear base but sensory epitheli
129 ferents from the three otolithic organs (the utricle, saccule, and lagena) project to the intermediat
130 t, including the mature semicircular canals, utricle, saccule, cochlear duct, endolymphatic duct and
131 lia of the three mechanoreceptor organs, the utricle/saccule, cristae, and cochlea, with distinct typ
132 munoreactive sensory epithelia of the macula utricle, sacule, and crista ampullaris, and the membrano
137 cells of the sensory epithelium of the chick utricle subjected to aminoglycoside-induced damage under
138 nner ear endorgans (the saccule, lagena, and utricle) synapse directly on the ipsilateral M-cell, the
140 agena as two separate pouches ventral to the utricle, the lungfish has a single large ventral pouch t
141 the anterior crista, the lateral crista, the utricle, the saccule, and both the basilar papilla and l
143 Although sparse, the projections of the utricle to the flocculus/ventral paraflocculus suggest a
145 and organ cultures of the chick cochlea and utricle, we found that cisplatin treatment caused apopto
150 he number of otoconia in the saccule and the utricle, were consistently observed in the Raldh3 mutant
151 mainly in the medial striolar region of the utricle, where they constitute at most 12% of hair cells
152 abundant in a subpopulation of cells in the utricle, which undergoes continual postembryonic hair ce
153 three semicircular canals extending from the utricle, with the typical hair cell orientations, but th
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。