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1 e geometry that links the environment to the sensory epithelium.
2 progressive differentiation of the auditory sensory epithelium.
3 pecialized epithelium-like cells outside the sensory epithelium.
4 acellular matrix that overlies the cochlea's sensory epithelium.
5 and straight after reaching the edge of the sensory epithelium.
6 sis, damaged hair cells are ejected from the sensory epithelium.
7 and afferent innervation within the repaired sensory epithelium.
8 distinct cellular expression in the auditory sensory epithelium.
9 he stimulus impinges on large regions of the sensory epithelium.
10 t planar cell polarity (PCP) parallel to the sensory epithelium.
11 hair cell orientation along the plane of the sensory epithelium.
12 dividual cellular components of the auditory sensory epithelium.
13 ry hair cell ciliary bundles on the saccular sensory epithelium.
14 is as well as in different cell types of the sensory epithelium.
15 s distributed homogenously across the entire sensory epithelium.
16 noreactive hair cells present throughout the sensory epithelium.
17 dent on planar signals within the developing sensory epithelium.
18 e (TM), an acellular structure overlying the sensory epithelium.
19 through the mucus that covers the olfactory sensory epithelium.
20 ng hair cell differentiation in the cochlear sensory epithelium.
21 lls spanning the length of the spiral-shaped sensory epithelium.
22 th was complementary to TR expression in the sensory epithelium.
23 rel contains multiple representations of the sensory epithelium.
24 ating cell proliferation in mature inner ear sensory epithelium.
25 y upon these cells and other elements in the sensory epithelium.
26 cells, but not hair cells, of the vestibular sensory epithelium.
27 in alternating cell types in the developing sensory epithelium.
28 age and microglia-like cells increase in the sensory epithelium.
29 were also located in the basal region of the sensory epithelium.
30 duce regeneration in the mammalian inner ear sensory epithelium.
31 asal region close to the basal lamina in the sensory epithelium.
32 not in mitotic progenitors in the inner ear sensory epithelium.
33 cell cycle progression in damaged inner ear sensory epithelium.
34 numerous synapsin-reactive structures in the sensory epithelium.
35 f cells localized in the basal region of the sensory epithelium.
36 hroughout a zonally restricted region of the sensory epithelium.
37 proliferation in the mature avian vestibular sensory epithelium.
38 r-cell division in cultured avian vestibular sensory epithelium.
39 se to these endings remain intact within the sensory epithelium.
40 ceptor hair directional sensitivities on the sensory epithelium.
41 ls were supporting cells within the cochlear sensory epithelium.
42 in the brainstem and innervate the cochlear sensory epithelium.
43 ell transcriptomics of the mouse vomeronasal sensory epithelium.
44 limiting or preventing further damage to the sensory epithelium.
45 bular ganglion and the stroma underlying the sensory epithelium.
46 m to limit or to avoid further damage to the sensory epithelium.
47 n adjacent non-sensory cells of the cochlear sensory epithelium.
48 inery or more generally by disruption of the sensory epithelium.
49 atterning during development of the cochlear sensory epithelium.
50 n the organ of Corti, the mammalian auditory sensory epithelium.
51 sed pool of progenitor cells in the cochlear sensory epithelium.
52 pling between the otolith and the underlying sensory epithelium.
53 tterning and proper function of the auditory sensory epithelium.
54 uster spatially segregated from the cochlear sensory epithelium.
55 ween functionally specialized regions of the sensory epithelium.
56 pansion of Lgr5(+) cells within the cochlear sensory epithelium.
57 pensable for differentiation of the cochlear sensory epithelium.
58 ating proliferation in mature avian auditory sensory epithelium.
59 ries with their longitudinal position in the sensory epithelium.
60 ts by a large repertoire of receptors in the sensory epithelium.
61 patterning and alignment within the cochlear sensory epithelium.
62 ymidine labeled cells were identified in the sensory epithelium: (1) labeled cells with synaptic spec
63 e vestibular ganglion and stroma beneath the sensory epithelium, (2) preserved hair cells and support
64 dependently of traveling waves, and that the sensory epithelium achieves active amplification by oper
65 firing of groups of nearby hair cells in the sensory epithelium, activity that is conveyed to auditor
66 st to the rapid decomposition process of the sensory epithelium after death (especially of the inner
69 expand to fill the resulting lesions in the sensory epithelium, an initial repair process that is de
70 eptor neurons in the middle layer of the VNO sensory epithelium and CB-immunoreactive glomeruli in th
71 l microscopy in whole mounts of the cochlear sensory epithelium and dissociated cell preparations.
73 All the extra hair cells (HCs) within the sensory epithelium and Kolliker's organ contained mechan
74 tion and patterning of the cochlear duct and sensory epithelium and loss of the dorsal cochlear nucle
77 in the arrangement of the otoliths into the sensory epithelium and otogelin/otogelin-like proteins t
78 reduced macrophage recruitment into both the sensory epithelium and spiral ganglion and also resulted
80 Dying hair cells were retained within the sensory epithelium and supporting cells remained unexpan
81 critical for PCP regulation in the auditory sensory epithelium and that PTK7-SFK signaling regulates
82 cell proliferation in mature avian auditory sensory epithelium and that this signaling pathway may b
83 nitial patterning of connections between the sensory epithelium and the bulb is widely appreciated.
84 that includes an increase in the size of the sensory epithelium and the development of large ectopic
85 and abneural limbs adjacent to the cochlear sensory epithelium and the stroma of the crista ampullar
86 type I and type II, navigate together to the sensory epithelium and then diverge to contact inner hai
88 ox2 initially marks all cells in the nascent sensory epithelium and, in mouse, is required for sensor
89 ar ganglion cells and the stroma beneath the sensory epithelium, and (4) CD3-positive T-lymphocyte in
90 erentiation of the cochlear inner sulcus and sensory epithelium, and deformity of the tectorial membr
91 hology, distribution of cell type within the sensory epithelium, and expression of odorant receptors
92 in the differentiation and patterning of the sensory epithelium, and in particular in the development
93 ls, neurofilament innervation in a thickened sensory epithelium, and otoconia, all of which are found
94 otrophin-3 (NT-3) have been localized to the sensory epithelium, and their respective high-affinity t
95 e mammalian cochlea, small vibrations of the sensory epithelium are amplified due to active electro-m
99 This study also establishes the vestibular sensory epithelium as a tractable tissue for analyzing P
100 groups had reduced silver grains over the VN sensory epithelium as had been reported previously with
102 n response to each IR pulse delivered to the sensory epithelium, at phase-locked rates up to 96 pulse
103 cal signals decrease, and development of the sensory epithelium becomes essentially independent from
104 responded to direct optical radiation of the sensory epithelium but did not respond to thermal stimul
105 sensory cell fate and formation of auditory sensory epithelium, but how it activates gene expression
106 receptor neurons widely distributed over the sensory epithelium, but these neurons then project to a
107 mately 200 mus pulse(-)(1)) delivered to the sensory epithelium by an optical fibre evoked profound c
108 by embryonic day 7, in the undifferentiated sensory epithelium by day 9, and in hair cells at embryo
110 decades it has been known that the olfactory sensory epithelium can act like a chromatograph, separat
111 a dramatic effect on the development of the sensory epithelium, causing a severe reduction in hair c
115 The organ of Corti, the auditory mammalian sensory epithelium, contains two types of mechanotransdu
116 expression pattern of miRNAs in the cochlear sensory epithelium, defined miRNA responses to acoustic
117 Six1 binding at different stages of auditory sensory epithelium development and find that Six1-bindin
118 Expression of sox2 begins after the onset of sensory epithelium development and is regulated by Atoh1
119 with increasing age: Gene programs promoting sensory epithelium development loses chromatin accessibi
120 f expression extends to the apex, and as the sensory epithelium differentiates Prox1 becomes restrict
121 y corresponds to the degree of hair cell and sensory epithelium differentiation, and Fgf10 expression
123 lastic force opposes growth of the utricular sensory epithelium during development, confines cellular
126 he deep layer (basal 1/3) of the vomeronasal sensory epithelium, express G(o alpha), and axons of the
127 trating specific expression in the olfactory sensory epithelium for approximately 800 OR genes previo
129 sublethally damaged hair cells remain in the sensory epithelium for prolonged periods, acquiring supp
130 the utricle, saccule, and cochlear base but sensory epithelium formation is completely absent in the
134 ea at postnatal day (P) 1 and found that the sensory epithelium had doubled in size but the length of
136 Despite alterations in the structure of the sensory epithelium, hair cells within the cochlea of Gjb
141 M) couples a single calcified otolith to the sensory epithelium in the bluegill sunfish (Lepomis macr
142 ted in the development and patterning of the sensory epithelium in the cochlea, the organ of Corti.
143 olumnar epithelial cells located outside the sensory epithelium in the greater epithelial ridge, whic
148 stripe encompasses the full thickness of the sensory epithelium, including developing hair cells and
150 n, excess proliferation in the COUP-TFI(-/-) sensory epithelium indicates that the origin of the extr
151 upporting cells at the edges of the saccular sensory epithelium, indicating that these cells are a pr
157 patterning, differentiation of the auditory sensory epithelium is precisely timed and follows a stee
158 tor (Fgfr) 1 signaling within the developing sensory epithelium is required for the differentiation o
160 s demonstrate that cell proliferation in the sensory epithelium is very limited and is far below the
161 n of goldfish appears as a rosette, with the sensory epithelium lying along the proximal portion of e
162 x, the otoconial complex, which overlies the sensory epithelium (macula) and provides inertial mass t
163 mRNA for Cx36 was expressed in the olfactory sensory epithelium, main olfactory bulb and accessory ol
164 erentiate exclusively into hair cells as the sensory epithelium matures and elongates through a proce
165 sentation of a small, point-like area on the sensory epithelium may be a functional feature of primar
166 tes that gentamicin-induced apoptosis in the sensory epithelium occurs mainly during a 2 d treatment
168 circumferential F-actin bands throughout the sensory epithelium of cultured utricles that were isolat
169 fference, we created excision lesions in the sensory epithelium of embryonic and 2-week-old mouse utr
170 id screening of a cDNA library made from the sensory epithelium of embryonic chick cochlea revealed a
172 stributions of Cx26 and Cx30 in the cochlear sensory epithelium of guinea pigs were examined by immun
176 protein synthesis were downregulated in the sensory epithelium of P0 cochlea lacking Jag1 Finally, u
182 reside together with supporting cells in the sensory epithelium of the cochlea, called the organ of C
183 in a complete disruption of formation of the sensory epithelium of the cochlea, including the develop
185 the connective tissue stroma underlying the sensory epithelium of the crista ampullaris of the semic
186 in the mouse inner ear are restricted to the sensory epithelium of the developing cristae ampularis,
187 ie and provide optimal stimulus input to the sensory epithelium of the gravity receptor in the inner
188 n humans frequently caused by defects in the sensory epithelium of the inner ear, composed of hair ce
190 scripts in liver and ovary, the CNS, and the sensory epithelium of the main auditory endorgan (saccul
193 g aspects of the cellular pattern within the sensory epithelium of the mammalian cochlea is the prese
194 One of the most striking aspects of the sensory epithelium of the mammalian cochlea, the organ o
195 enriched in open chromatin of the developing sensory epithelium of the mouse cochlea, we investigated
196 red SARS-CoV-2 S RBD mostly binds to the non-sensory epithelium of the olfactory organ and causes sev
198 these two cell types together constitute the sensory epithelium of the organ of Corti, which is the h
200 the ear, in particular, is expressed in the sensory epithelium of the vestibular organs but not of t
203 tudy, neurogenesis and cell migration in the sensory epithelium of the VNO were analyzed in opossums
206 a severe inner ear malformation, whereas the sensory epithelium of Ysb/Ysb mice shows abnormal develo
207 ell lesions and after transplantation of the sensory epithelium onto a chemically defined substrate.
208 ential therapeutic targets to promote either sensory epithelium or hair cell regeneration in mammals.
209 ds to otolith agenesis without affecting the sensory epithelium or other structures within the inner
210 surrounding supporting cells directly in the sensory epithelium or spiral ganglion neurons (SGNs).
211 ent and that its continued expression in the sensory epithelium orchestrates critical aspects of phys
213 an replicate to high levels in the olfactory sensory epithelium (OSE) in hamsters and that induction
217 structural repair, although a defect on the sensory epithelium remains in the form of an incompletel
219 f hair cells from the mammalian cochlea, the sensory epithelium repairs to close the lesions but no n
220 n of early progenitor cells in the olfactory sensory epithelium represents an important challenge in
221 xpression analysis of miRNAs in the cochlear sensory epithelium revealed constitutive expression of 1
222 and lateral-line organ appeared normal, the sensory epithelium showed progressive signs of degenerat
224 All of them are expressed in the rhinophore sensory epithelium, suggesting that Galphaq, Galphai, Ga
225 cells are located in the lumenal half of the sensory epithelium, suggesting that some may be newly ge
226 leukocytes in lesioned areas of the auditory sensory epithelium suggests they may not play a critical
227 i, a highly derived and rigorously patterned sensory epithelium that acts to convert auditory stimuli
229 lusters of labeled cells were evident in the sensory epithelium, the nonsensory epithelium, and in ad
233 A striking feature of the mammalian cochlear sensory epithelium, the organ of Corti, is the cellular
236 ations of environmental infrared cues on the sensory epithelium through specific neuronal projections
237 t of Activin A signaling within the auditory sensory epithelium times the longitudinal gradient of ha
238 ling are required in the developing auditory sensory epithelium to control cochlear duct elongation a
239 mainly due to the inability of the cochlear sensory epithelium to replace lost mechanoreceptor cells
240 Olfactory receptor neurons project from the sensory epithelium to stereotyped targets within the olf
243 yos, a subpopulation of the cells within the sensory epithelium undergo apoptosis in a temporal gradi
246 In addition, maturation of the cochlear sensory epithelium was delayed at the transition point b
247 of BrdU-labeled cells in the reconstituting sensory epithelium was greatly increased compared with t
248 receptor neurons in the middle layer of the sensory epithelium was immunostained with antibodies to
249 ral segregation of infrared afferents in the sensory epithelium was matched by a differential termina
250 roles in the differentiation of the auditory sensory epithelium, we evaluated hearing in a large grou
251 y 10), more cells in the basal region of the sensory epithelium were labeled than in the adult VNO, i
253 All critical cell types of the cochlear sensory epithelium were present in double mutant mice an
255 in the basal region near the margins of the sensory epithelium where it meets the nonsensory epithel
256 n is particularly important for the auditory sensory epithelium, where deviations from the normal spa
257 dynamic range is established in the cochlear sensory epithelium, where functional subtypes of cochlea
258 precursor population that gives rise to the sensory epithelium, whereas treatment with Sonic hedgeho
259 ient of terminal mitosis within the auditory sensory epithelium, which constitutes a novel mechanism
260 e supporting cell population of the auditory sensory epithelium, which might mediate potassium cyclin
261 ls (SCs) of the postnatal mammalian auditory sensory epithelium, which unlike non-mammalian vertebrat
262 uiculatus that affords optical access to the sensory epithelium while mimicking its in vivo environme
263 e fetal inner ear prior to maturation of the sensory epithelium will optimally restore sensory functi
264 of the sensory domain, resulting in a wider sensory epithelium with ectopic inner hair cell formatio
265 ene choice and their distribution within the sensory epithelium, with each subset preferentially expr
267 of the membrane marker FM1-43 in the intact sensory epithelium within the cochlear bone of the adult