ライフサイエンスコーパス: sensory epithelium

1 n adjacent non-sensory cells of the cochlear sensory epithelium.

2 n the organ of Corti, the mammalian auditory sensory epithelium.

3 he stimulus impinges on large regions of the sensory epithelium.

4 sed pool of progenitor cells in the cochlear sensory epithelium.

5 t planar cell polarity (PCP) parallel to the sensory epithelium.

6 dividual cellular components of the auditory sensory epithelium.

7 ry hair cell ciliary bundles on the saccular sensory epithelium.

8 is as well as in different cell types of the sensory epithelium.

9 s distributed homogenously across the entire sensory epithelium.

10 noreactive hair cells present throughout the sensory epithelium.

11 dent on planar signals within the developing sensory epithelium.

12 pling between the otolith and the underlying sensory epithelium.

13 through the mucus that covers the olfactory sensory epithelium.

14 ng hair cell differentiation in the cochlear sensory epithelium.

15 th was complementary to TR expression in the sensory epithelium.

16 rel contains multiple representations of the sensory epithelium.

17 ating cell proliferation in mature inner ear sensory epithelium.

18 y upon these cells and other elements in the sensory epithelium.

19 cells, but not hair cells, of the vestibular sensory epithelium.

20 in alternating cell types in the developing sensory epithelium.

21 age and microglia-like cells increase in the sensory epithelium.

22 were also located in the basal region of the sensory epithelium.

23 duce regeneration in the mammalian inner ear sensory epithelium.

24 asal region close to the basal lamina in the sensory epithelium.

25 not in mitotic progenitors in the inner ear sensory epithelium.

26 cell cycle progression in damaged inner ear sensory epithelium.

27 numerous synapsin-reactive structures in the sensory epithelium.

28 f cells localized in the basal region of the sensory epithelium.

29 hroughout a zonally restricted region of the sensory epithelium.

30 proliferation in the mature avian vestibular sensory epithelium.

31 r-cell division in cultured avian vestibular sensory epithelium.

32 se to these endings remain intact within the sensory epithelium.

33 ceptor hair directional sensitivities on the sensory epithelium.

34 ls were supporting cells within the cochlear sensory epithelium.

35 tterning and proper function of the auditory sensory epithelium.

36 uster spatially segregated from the cochlear sensory epithelium.

37 ween functionally specialized regions of the sensory epithelium.

38 inery or more generally by disruption of the sensory epithelium.

39 pansion of Lgr5(+) cells within the cochlear sensory epithelium.

40 pensable for differentiation of the cochlear sensory epithelium.

41 ating proliferation in mature avian auditory sensory epithelium.

42 ries with their longitudinal position in the sensory epithelium.

43 ts by a large repertoire of receptors in the sensory epithelium.

44 patterning and alignment within the cochlear sensory epithelium.

45 atterning during development of the cochlear sensory epithelium.

46 acellular matrix that overlies the cochlea's sensory epithelium.

47 and straight after reaching the edge of the sensory epithelium.

48 sis, damaged hair cells are ejected from the sensory epithelium.

49 and afferent innervation within the repaired sensory epithelium.

50 distinct cellular expression in the auditory sensory epithelium.

51 ymidine labeled cells were identified in the sensory epithelium: (1) labeled cells with synaptic spec

52 st to the rapid decomposition process of the sensory epithelium after death (especially of the inner

53 tudy defines characteristics of the auditory sensory epithelium after hair cell loss.

54 middle saccule may reflect curvature of the sensory epithelium against the otolith.

55 expand to fill the resulting lesions in the sensory epithelium, an initial repair process that is de

56 eptor neurons in the middle layer of the VNO sensory epithelium and CB-immunoreactive glomeruli in th

57 l microscopy in whole mounts of the cochlear sensory epithelium and dissociated cell preparations.

58 localization of Nav1.6 was disrupted in the sensory epithelium and ganglion.

59 tion and patterning of the cochlear duct and sensory epithelium and loss of the dorsal cochlear nucle

60 GSH levels in the sensory epithelium and modiolus did not show significant

61 tion revealed marked atrophy of the cochlear sensory epithelium and neurons.

62 reduced macrophage recruitment into both the sensory epithelium and spiral ganglion and also resulted

63 ion of Rac1 in morphogenesis of the auditory sensory epithelium and stereociliary bundle.

64 Dying hair cells were retained within the sensory epithelium and supporting cells remained unexpan

65 critical for PCP regulation in the auditory sensory epithelium and that PTK7-SFK signaling regulates

66 cell proliferation in mature avian auditory sensory epithelium and that this signaling pathway may b

67 nitial patterning of connections between the sensory epithelium and the bulb is widely appreciated.

68 that includes an increase in the size of the sensory epithelium and the development of large ectopic

69 and abneural limbs adjacent to the cochlear sensory epithelium and the stroma of the crista ampullar

70 type I and type II, navigate together to the sensory epithelium and then diverge to contact inner hai

71 ox2 initially marks all cells in the nascent sensory epithelium and, in mouse, is required for sensor

72 erentiation of the cochlear inner sulcus and sensory epithelium, and deformity of the tectorial membr

73 hology, distribution of cell type within the sensory epithelium, and expression of odorant receptors

74 in the differentiation and patterning of the sensory epithelium, and in particular in the development

75 ls, neurofilament innervation in a thickened sensory epithelium, and otoconia, all of which are found

76 otrophin-3 (NT-3) have been localized to the sensory epithelium, and their respective high-affinity t

77 e mammalian cochlea, small vibrations of the sensory epithelium are amplified due to active electro-m

78 eas tympanic border cells (TBCs) beneath the sensory epithelium are proliferative.

79 otolith assembly atop specific cells of the sensory epithelium are unclear.

80 ated on mechanosensory hair cells within the sensory epithelium are unidirectionally oriented.

81 This study also establishes the vestibular sensory epithelium as a tractable tissue for analyzing P

82 groups had reduced silver grains over the VN sensory epithelium as had been reported previously with

83 hird rows, forming a distinct band along the sensory epithelium at its outer region.

84 n response to each IR pulse delivered to the sensory epithelium, at phase-locked rates up to 96 pulse

85 cal signals decrease, and development of the sensory epithelium becomes essentially independent from

86 responded to direct optical radiation of the sensory epithelium but did not respond to thermal stimul

87 receptor neurons widely distributed over the sensory epithelium, but these neurons then project to a

88 mately 200 mus pulse(-)(1)) delivered to the sensory epithelium by an optical fibre evoked profound c

89 by embryonic day 7, in the undifferentiated sensory epithelium by day 9, and in hair cells at embryo

90 decades it has been known that the olfactory sensory epithelium can act like a chromatograph, separat

91 a dramatic effect on the development of the sensory epithelium, causing a severe reduction in hair c

92 The auditory sensory epithelium, composed of mechano-sensory hair cel

93 Here we show that the adult utricular sensory epithelium contains cells that display the chara

94 expression pattern of miRNAs in the cochlear sensory epithelium, defined miRNA responses to acoustic

95 Expression of sox2 begins after the onset of sensory epithelium development and is regulated by Atoh1

96 f expression extends to the apex, and as the sensory epithelium differentiates Prox1 becomes restrict

97 y corresponds to the degree of hair cell and sensory epithelium differentiation, and Fgf10 expression

98 result of defective development of auditory sensory epithelium due to connexion dysfunction.

99 lastic force opposes growth of the utricular sensory epithelium during development, confines cellular

100 Cochlear sensory epithelium explants were prepared from postnatal

101 middle layer (middle 1/3) of the vomeronasal sensory epithelium express Gi alpha 2.

102 he deep layer (basal 1/3) of the vomeronasal sensory epithelium, express G(o alpha), and axons of the

103 trating specific expression in the olfactory sensory epithelium for approximately 800 OR genes previo

104 ts a potential role for Fgf20 in priming the sensory epithelium for hair cell formation.

105 sublethally damaged hair cells remain in the sensory epithelium for prolonged periods, acquiring supp

106 the utricle, saccule, and cochlear base but sensory epithelium formation is completely absent in the

107 ry epithelium and, in mouse, is required for sensory epithelium formation.

108 alone was significantly higher than that of sensory epithelium from utricle or saccule.

109 Within the sensory epithelium, hair cells are polarized in a stereo

110 The adult mammalian cochlear sensory epithelium houses two major types of cells, mech

111 For a given location in a sensory epithelium, however, the shape and polarity of a

112 M) couples a single calcified otolith to the sensory epithelium in the bluegill sunfish (Lepomis macr

113 ted in the development and patterning of the sensory epithelium in the cochlea, the organ of Corti.

114 olumnar epithelial cells located outside the sensory epithelium in the greater epithelial ridge, whic

115 The sensory epithelium in the mammalian cochlea (the organ o

116 y, we analyzed Lis1 function in the auditory sensory epithelium in the mouse.

117 stripe encompasses the full thickness of the sensory epithelium, including developing hair cells and

118 Label density of ampullar sensory epithelium incubated with 3H-QNB alone was signi

119 n, excess proliferation in the COUP-TFI(-/-) sensory epithelium indicates that the origin of the extr

120 upporting cells at the edges of the saccular sensory epithelium, indicating that these cells are a pr

121 Each individual sensory epithelium is composed of highly heterogeneous p

122 Correct patterning of the inner ear sensory epithelium is essential for the conversion of so

123 Because the inner ear sensory epithelium is highly conserved in all vertebrate

124 Previous studies have shown that the sensory epithelium is postmitotic, but it harbors cells

125 tor (Fgfr) 1 signaling within the developing sensory epithelium is required for the differentiation o

126 In the postnatal cochlea, the sensory epithelium is terminally differentiated, whereas

127 s demonstrate that cell proliferation in the sensory epithelium is very limited and is far below the

128 n of goldfish appears as a rosette, with the sensory epithelium lying along the proximal portion of e

129 x, the otoconial complex, which overlies the sensory epithelium (macula) and provides inertial mass t

130 mRNA for Cx36 was expressed in the olfactory sensory epithelium, main olfactory bulb and accessory ol

131 erentiate exclusively into hair cells as the sensory epithelium matures and elongates through a proce

132 sentation of a small, point-like area on the sensory epithelium may be a functional feature of primar

133 tes that gentamicin-induced apoptosis in the sensory epithelium occurs mainly during a 2 d treatment

134 ans of a mitotic mechanism in the vestibular sensory epithelium of adult mammals.

135 fference, we created excision lesions in the sensory epithelium of embryonic and 2-week-old mouse utr

136 id screening of a cDNA library made from the sensory epithelium of embryonic chick cochlea revealed a

137 are expressed in fewer cells in the cochlear sensory epithelium of Emx2 null mice.

138 stributions of Cx26 and Cx30 in the cochlear sensory epithelium of guinea pigs were examined by immun

139 The organ of Corti, the sensory epithelium of hearing in mammals, matures postna

140 ll death in the organ of Corti, the auditory sensory epithelium of mammals.

141 The sensory epithelium of rhinophores, tentacles, and mouth

142 nd/or aminoglycoside damage in the utricular sensory epithelium of the adult rat.

143 as also present in nerve bundles beneath the sensory epithelium of the ampulla.

144 It is concluded that the cells of the sensory epithelium of the chick utricle subjected to ami

145 Developmental remodeling of the sensory epithelium of the cochlea is required for the fo

146 in a complete disruption of formation of the sensory epithelium of the cochlea, including the develop

147 increase in macrophages associated with the sensory epithelium of the cochlea.

148 the connective tissue stroma underlying the sensory epithelium of the crista ampullaris of the semic

149 in the mouse inner ear are restricted to the sensory epithelium of the developing cristae ampularis,

150 ie and provide optimal stimulus input to the sensory epithelium of the gravity receptor in the inner

151 n humans frequently caused by defects in the sensory epithelium of the inner ear, composed of hair ce

152 scripts in liver and ovary, the CNS, and the sensory epithelium of the main auditory endorgan (saccul

153 The sensory epithelium of the mammalian cochlea comprises me

154 The sensory epithelium of the mammalian cochlea is composed

155 g aspects of the cellular pattern within the sensory epithelium of the mammalian cochlea is the prese

156 In the inner ear, it is found in the sensory epithelium of the organ of Corti and vestibular

157 these two cell types together constitute the sensory epithelium of the organ of Corti, which is the h

158 onstrated mouse claudin-14 expression in the sensory epithelium of the organ of Corti.

159 the ear, in particular, is expressed in the sensory epithelium of the vestibular organs but not of t

160 is assembled specifically above the macular sensory epithelium of the vestibule.

161 First discovered in the sensory epithelium of the visual and olfactory systems,

162 tudy, neurogenesis and cell migration in the sensory epithelium of the VNO were analyzed in opossums

163 The sensory epithelium of the vomeronasal organ (VNO) contai

164 osensory receptor neurons are located in the sensory epithelium of the vomeronasal organ (VNO).

165 a severe inner ear malformation, whereas the sensory epithelium of Ysb/Ysb mice shows abnormal develo

166 ell lesions and after transplantation of the sensory epithelium onto a chemically defined substrate.

167 ential therapeutic targets to promote either sensory epithelium or hair cell regeneration in mammals.

168 ds to otolith agenesis without affecting the sensory epithelium or other structures within the inner

169 surrounding supporting cells directly in the sensory epithelium or spiral ganglion neurons (SGNs).

170 The auditory sensory epithelium (organ of Corti), where sound waves a

171 an replicate to high levels in the olfactory sensory epithelium (OSE) in hamsters and that induction

172 In the auditory sensory epithelium, planar polarity of individual hair c

173 In the auditory sensory epithelium, Prox1 is initially expressed at embr

174 Microvilli of vomeronasal organ (VNO) sensory epithelium receptor cells project into the VNO l

175 structural repair, although a defect on the sensory epithelium remains in the form of an incompletel

176 r polarity information across the developing sensory epithelium remains unclear.

177 f hair cells from the mammalian cochlea, the sensory epithelium repairs to close the lesions but no n

178 n of early progenitor cells in the olfactory sensory epithelium represents an important challenge in

179 xpression analysis of miRNAs in the cochlear sensory epithelium revealed constitutive expression of 1

180 and lateral-line organ appeared normal, the sensory epithelium showed progressive signs of degenerat

181 As the sensory epithelium starts to differentiate, it is down-r

182 All of them are expressed in the rhinophore sensory epithelium, suggesting that Galphaq, Galphai, Ga

183 cells are located in the lumenal half of the sensory epithelium, suggesting that some may be newly ge

184 leukocytes in lesioned areas of the auditory sensory epithelium suggests they may not play a critical

185 The mammalian auditory sensory epithelium (the organ of Corti) contains a numbe

186 lusters of labeled cells were evident in the sensory epithelium, the nonsensory epithelium, and in ad

187 Centrally within the VNO sensory epithelium, the numbers of receptor cells with G

188 The mammalian auditory sensory epithelium, the organ of Corti, contains sensory

189 The mammalian auditory sensory epithelium, the organ of Corti, is a highly orde

190 ations of environmental infrared cues on the sensory epithelium through specific neuronal projections

191 mainly due to the inability of the cochlear sensory epithelium to replace lost mechanoreceptor cells

192 Olfactory receptor neurons project from the sensory epithelium to stereotyped targets within the olf

193 int-to-point topographic projection from the sensory epithelium to the CNS.

194 Cultured, posthatch avian auditory sensory epithelium treated with Acvr2a and Acvr2b inhibi

195 yos, a subpopulation of the cells within the sensory epithelium undergo apoptosis in a temporal gradi

196 ls and cellular organization of the auditory sensory epithelium was abnormal.

197 In addition, maturation of the cochlear sensory epithelium was delayed at the transition point b

198 of BrdU-labeled cells in the reconstituting sensory epithelium was greatly increased compared with t

199 receptor neurons in the middle layer of the sensory epithelium was immunostained with antibodies to

200 ral segregation of infrared afferents in the sensory epithelium was matched by a differential termina

201 roles in the differentiation of the auditory sensory epithelium, we evaluated hearing in a large grou

202 y 10), more cells in the basal region of the sensory epithelium were labeled than in the adult VNO, i

203 Sensory axons and adjacent non-sensory epithelium were not affected by these procedures

204 All critical cell types of the cochlear sensory epithelium were present in double mutant mice an

205 cells formed support cells in the utricular sensory epithelium were rescued.

206 in the basal region near the margins of the sensory epithelium where it meets the nonsensory epithel

207 n is particularly important for the auditory sensory epithelium, where deviations from the normal spa

208 dynamic range is established in the cochlear sensory epithelium, where functional subtypes of cochlea

209 precursor population that gives rise to the sensory epithelium, whereas treatment with Sonic hedgeho

210 e supporting cell population of the auditory sensory epithelium, which might mediate potassium cyclin

211 ls (SCs) of the postnatal mammalian auditory sensory epithelium, which unlike non-mammalian vertebrat

212 uiculatus that affords optical access to the sensory epithelium while mimicking its in vivo environme

213 ene choice and their distribution within the sensory epithelium, with each subset preferentially expr

214 organ suggest that PWs are initiated in the sensory epithelium within each olfactory lamella.

215 of the membrane marker FM1-43 in the intact sensory epithelium within the cochlear bone of the adult

216 osensory hair cells located in a specialized sensory epithelium within the inner ear.