ライフサイエンスコーパス: stria

1 smaller numbers found in the dorsal acoustic stria.

2 CN before exiting the CN via the commissural stria.

3 nucleus via the dorsal and ventral acoustic stria and at its medial border.

4 ranular insular area; bed nuclei of terminal stria; anterior hypothalamic area; arcuate, paraventricu

5 ranular insular area; bed nuclei of terminal stria; anterior hypothalamus; paraventricular, arcuate,

6 A stria LGE pattern with subepicardial/midmyocardial distr

7 iral ganglion neurons, supporting cells, and stria ligament in the inner ear.

8 e previously unidentified bed nucleus of the stria medullaris (BNSM).

9 thalamocortical and corticothalamic tracts), stria medullaris, stria terminalis, and hippocampal comm

10 yelinated, and they exit the dorsal acoustic stria of the injected cochlear nucleus to cross the brai

11 38+/-25 months, 6 of 27 (22%) athletes with stria pattern experienced malignant arrhythmic events su

12 Isolated nonischemic LV LGE with a stria pattern may be associated with life-threatening ar

13 All athletes with stria pattern showed ventricular arrhythmias with a pred

14 rojecting to the anterior bed nucleus of the stria terminalis (aBNST), but not to other brain areas i

15 tion of AgRP --> anterior bed nucleus of the stria terminalis (aBNST)vl projections, distinct from Ag

16 te region of the anterior bed nucleus of the stria terminalis (aBST) as a candidate for fulfilling th

17 ibed, anterior part of the bed nuclei of the stria terminalis (aBST) that houses stress-sensitive, PV

18 ic neurons within anterior bed nuclei of the stria terminalis (aBST) that integrates and relays inhib

19 d portion of the anterior bed nucleus of the stria terminalis (aBST), which we previously identified

20 anted DBS electrodes from the bed nucleus of stria terminalis (BNST area) in 12 patients (5 OCD, 7 MD

21 hippocampus, the lateral bed nucleus of the stria terminalis (BNST) and globus pallidus at 60 and 12

22 mRNA within the amygdala, bed nucleus of the stria terminalis (BNST) and paraventricular nucleus of t

23 nucleus (PVN) or into the bed nucleus of the stria terminalis (BNST) but not into the ventral tegment

24 Because the bed nucleus of the stria terminalis (BNST) contributes to fear- and anxiety

25 ine (NE) signaling in the bed nucleus of the stria terminalis (BNST) could have a role in mediating t

26 (MeA) and reduced in the bed nucleus of the stria terminalis (BNST) during novelty exposure, regardl

27 The bed nucleus of the stria terminalis (BNST) exerts a coordinated modulation

28 ong these structures, the bed nucleus of the stria terminalis (BNST) has been implicated in emotional

29 The anterior bed nucleus of the stria terminalis (BNST) has been recognized as a critica

30 ediated mechanisms in the bed nucleus of the stria terminalis (BNST) have a pivotal role in stress-in

31 rprising new role for the bed nucleus of the stria terminalis (BNST) in the coordinated modulation of

32 The bed nucleus of the stria terminalis (BNST) in the forebrain shows sexual di

33 entral amygdala (CeA) and bed nucleus of the stria terminalis (BNST) in the genesis of fear versus an

34 determined the effect of bed nucleus of the stria terminalis (BNST) injections of nor-BNI (4 mug/sid

35 The bed nucleus of the stria terminalis (BNST) is a brain region important for

36 The bed nucleus of the stria terminalis (BNST) is a critical region for alcohol

37 The bed nucleus of the stria terminalis (BNST) is a key component of the CNS st

38 iously, we found that the bed nucleus of the stria terminalis (BNST) is also necessary for the enhanc

39 The bed nucleus of the stria terminalis (BNST) is critical in mediating states

40 The bed nucleus of the stria terminalis (BNST) is implicated in anxiety and rew

41 The bed nucleus of the stria terminalis (BNST) is implicated in defensive respo

42 renergic signaling in the bed nucleus of the stria terminalis (BNST) is thought to be a source of thi

43 The bed nucleus of the stria terminalis (BNST) is thought to generate anxiety-l

44 Because the bed nucleus of the stria terminalis (BNST) lies immediately adjacent to the

45 ere we tested whether the bed nucleus of the stria terminalis (BNST) mediates anxiogenic effects of O

46 de (PACAP) systems in the bed nucleus of the stria terminalis (BNST) mediates many consequences of ch

47 effects of lesions of the bed nucleus of the stria terminalis (BNST) on conditioned fear and anxiety.

48 The bed nucleus of the stria terminalis (BNST) plays an important role in fear,

49 receptors (AR) within the bed nucleus of the stria terminalis (BNST) reduce stress-reward interaction

50 lter BI and metabolism in the bed nucleus of stria terminalis (BNST) region and that individual diffe

51 ic neuronal groups in the bed nucleus of the stria terminalis (BNST) related to anxiety and reward ci

52 levels of peptide in the bed nucleus of the stria terminalis (BNST) than isolated animals.

53 al manner to activate the bed nucleus of the stria terminalis (BNST) to drive stress- or cue-induced

54 iveness of neurons of the bed nucleus of the stria terminalis (BNST) to infralimbic cortex (ILCx) exc

55 xcitotoxic lesions of the bed nucleus of the stria terminalis (BNST) to that of sham rats.

56 CRF projections from the bed nucleus of the stria terminalis (BNST) to the VTA, CRF neurons in this

57 he amygdala (BlA), or the bed nucleus of the stria terminalis (BNST) were evaluated on excessive inta

58 KOR are expressed in the bed nucleus of the stria terminalis (BNST), a brain region associated with

59 e of CRF receptors in the bed nucleus of the stria terminalis (BNST), a brain region implicated in st

60 ines are found within the bed nucleus of the stria terminalis (BNST), a brain relay nucleus in the ex

61 ar dopamine levels is the bed nucleus of the stria terminalis (BNST), a CRF-rich component of the ext

62 e neural mechanism in the bed nucleus of the stria terminalis (BNST), a limbic brain region involved

63 tudy 5-HT inputs into the bed nucleus of the stria terminalis (BNST), a major subdivision of the exte

64 atory transmission in the bed nucleus of the stria terminalis (BNST), a region critical to the integr

65 e distinct regions of the bed nucleus of the stria terminalis (BNST), a structure that mediates behav

66 hors examined whether the bed nucleus of the stria terminalis (BNST), an area involved in stress and

67 us of the amygdala (CeA), bed nucleus of the stria terminalis (BNST), and insular cortex (IC).

68 e amygdala (CeA), lateral bed nucleus of the stria terminalis (BNST), and nucleus accumbens shell (NA

69 ergic transmission in the bed nucleus of the stria terminalis (BNST), and that ex vivo induction of t

70 periqueductal gray (PAG), bed nucleus of the stria terminalis (BNST), anterior cingulate cortex (ACC)

71 ar gustatory cortex (IC), bed nucleus of the stria terminalis (BNST), central nucleus of the amygdala

72 he gustatory cortex (GC), bed nucleus of the stria terminalis (BNST), central nucleus of the amygdala

73 Focusing on the bed nucleus of the stria terminalis (BNST), CRF-R1 and CRF-R2 mRNA expressi

74 he amygdala (CeA) and the bed nucleus of the stria terminalis (BNST), each of which has been implicat

75 e CeA, or the neighboring bed nucleus of the stria terminalis (BNST), initiates bouts of fictive call

76 in the dorsal and ventral bed nucleus of the stria terminalis (BNST), lateral septum, and nucleus acc

77 ain regions including the bed nucleus of the stria terminalis (BNST), medial preoptic area (MPOA), pa

78 d amygdala, including the bed nucleus of the stria terminalis (BNST), modulates fear and anxiety, but

79 ubfields of the amygdala, bed nucleus of the stria terminalis (BNST), optic tectum, various tegmental

80 lateral and ventrolateral bed nucleus of the stria terminalis (BNST), recruitment of G(q)-linked rece

81 s of the amygdala and the bed nucleus of the stria terminalis (BNST), respectively.

82 ptic nuclei, the anterior bed nucleus of the stria terminalis (BNST), the anterior paraventricular nu

83 require NA inputs to the bed nucleus of the stria terminalis (BNST), vehicle or saporin toxin conjug

84 e lateral division of the bed nucleus of the stria terminalis (BNST), which forms part of the circuit

85 elated regions, including the bed nucleus of stria terminalis (BNST), which is implicated in sustaine

86 medial amygdala (MeA) and bed nucleus of the stria terminalis (BNST), which mediate the female-stimul

87 s a tiny brain region-the bed nucleus of the stria terminalis (BNST)-in the body's stress response an

88 ly increase long-duration bed nucleus of the stria terminalis (BNST)-mediated aversive responses (ie,

89 , lateral septum (LS), or bed nucleus of the stria terminalis (BNST).

90 ateral amygdala (BLA) and bed nucleus of the stria terminalis (BNST).

91 xpression of PACAP in the bed nucleus of the stria terminalis (BNST).

92 cessing; the amygdala and bed nucleus of the stria terminalis (BNST).

93 leus accumbens (NAc), and bed nucleus of the stria terminalis (BNST)], whereas protracted alcohol abs

94 nterolateral group of the bed nucleus of the stria terminalis (BNSTALG ) is a critical modulator of a

95 lateral cell group of the bed nucleus of the stria terminalis (BNSTALG).

96 eAL) and the dorsolateral bed nucleus of the stria terminalis (BNSTDL) coordinate the expression of s

97 ry few VP-ir cells in the bed nucleus of the stria terminalis (BST) and none in the suprachiasmatic n

98 The bed nucleus of the stria terminalis (BST) and the medial amygdala (MeA) are

99 The bed nuclei of the stria terminalis (BST) are critically important for inte

100 dala (Ce) and the lateral bed nucleus of the stria terminalis (BST) are highly similar regions that s

101 a cluster comprising the bed nucleus of the stria terminalis (BST) in rats expressing contextual anx

102 The rat bed nuclei of the stria terminalis (BST) is an important part of the cereb

103 evidence suggest that the bed nucleus of the stria terminalis (BST) is well positioned to relay limbi

104 opressin (AVP) within the bed nucleus of the stria terminalis (BST) of adult brain is dependent upon

105 ed the hypothesis that the bed nuclei of the stria terminalis (BST) provides this compensatory plasti

106 sion of GAD67 mRNA in the bed nucleus of the stria terminalis (BST) was minimally affected by acute r

107 acting on neurons of the bed nucleus of the stria terminalis (BST), a component of extended amygdala

108 synaptic terminals in the bed nuclei of the stria terminalis (BST), a projection area for mPFC corti

109 of amniotes has been the bed nucleus of the stria terminalis (BST), but numerous recent investigatio

110 ld was iontophoresed into the bed nucleus of stria terminalis (BST), central nucleus of the amygdala

111 d shell), olfactory tubercle, bed nucleus of stria terminalis (BST), medial, central, cortical, and b

112 the amygdala (Ce) and the bed nucleus of the stria terminalis (BST), the two major subdivisions of th

113 connected regions of the bed nucleus of the stria terminalis (BST).

114 e anteromedial area of the bed nuclei of the stria terminalis (BSTam) is the relatively undifferentia

115 anteromedial) group of the bed nuclei of the stria terminalis (BSTamg), which also includes the more

116 The lateral bed nucleus of the stria terminalis (BSTL) is involved in mediating anxiety

117 In the lateral bed nucleus of the stria terminalis (BSTL), neither PPT nor DPN affected PR

118 solateral division of the bed nucleus of the stria terminalis (BSTld), part of the critical brain are

119 The medial bed nucleus of the stria terminalis (BSTm) influences both social approach

120 beling in the POM, medial bed nucleus of the stria terminalis (BSTm), and periaqueductal gray (PAG).

121 and oval division of the bed nucleus of the stria terminalis (BSTov), which form part of the central

122 principal division of the bed nuclei of the stria terminalis (BSTp).

123 ed Fos: the posteromedial bed nucleus of the stria terminalis (BSTPM), posteromedial amygdala (MeP),

124 ne release in the ventral bed nucleus of the stria terminalis (BSTv) with the alpha2-autoreceptor ant

125 The ventrolateral bed nucleus of the stria terminalis (BSTvl) receives direct input from two

126 inly to the ventrolateral bed nucleus of the stria terminalis (BSTvl), the pre-locus coeruleus (pre-L

127 ctor (CRF) neurons in the bed nucleus of the stria terminalis (CRF(BNST)) in mice.

128 The dorsolateral bed nucleus of the stria terminalis (dlBnST) has a critical role in the exp

129 hlighted the dorsolateral bed nucleus of the stria terminalis (dlBST) as a structure putatively invol

130 The juxtacapsular bed nucleus of the stria terminalis (jcBNST) is activated in response to ba

131 dial preoptic area/medial bed nucleus of the stria terminalis (mPOA/BSTm), and the highest AR express

132 djacent posterior part of the bed nucleus of stria terminalis (pBNST).

133 ntral part of the anterior bed nuclei of the stria terminalis (presently discussed as being involved

134 litude of IPSPs evoked by stimulation of the stria terminalis (ST).

135 The ventral bed nucleus of the stria terminalis (vBNST) has been implicated in stress-i

136 repinephrine-rich ventral bed nucleus of the stria terminalis (vBNST).

137 he anterior ventrolateral bed nucleus of the stria terminalis (vlBST).

138 extended amygdala (i.e., bed nucleus of the stria terminalis [BNST] and medial amygdala [MeA]), and

139 rtical structures such as the bed nucleus of stria terminalis and amygdala.

140 noradrenaline transmission in bed nucleus of stria terminalis and central amygdala, and dopamine, CRF

141 her regions including the bed nucleus of the stria terminalis and central amygdala.

142 osterior subnuclei of the bed nucleus of the stria terminalis and lateral septum.

143 ed in the anterior cingulate, bed nucleus of stria terminalis and perirhinal area of oxytocin pretrea

144 asolateral amygdala (BLA) inputs through the stria terminalis and projects back to the anterior BLA a

145 amygdalostriatal transition area (AStr) and stria terminalis and scattered throughout the bed nucleu

146 activation of D2R in the bed nucleus of the stria terminalis and the central amygdala.

147 leus of the amygdala, the bed nucleus of the stria terminalis and the medial preoptic nucleus.

148 s neuronal cluster, and between amygdala and stria terminalis bed nucleus.

149 n of the thalamus and the bed nucleus of the stria terminalis but not in the insular cortex.

150 amygdala AT1 receptor and bed nucleus of the stria terminalis c-Fos messenger RNA levels.

151 gdalohippocampal area and bed nucleus of the stria terminalis correlated positively with individual d

152 th triggered increases in bed nucleus of the stria terminalis dorsal (BNSTd) and lateral septum (LS).

153 ewise, in vivo intra-oval bed nucleus of the stria terminalis DRD1 pharmacological blockade reduced l

154 eriment 1, lesions of the bed nucleus of the stria terminalis had no influence on CTA or COA acquisit

155 iventricular nucleus, and bed nucleus of the stria terminalis in a distribution consistent with previ

156 oles for the anteroventral bed nuclei of the stria terminalis in inhibiting both stress hormone outpu

157 igher in the encapsulated bed nucleus of the stria terminalis in males than females for all four vole

158 ACAP signaling within the bed nucleus of the stria terminalis in mediating the consequences of stress

159 2 expression in the amygdala and bed nucleus stria terminalis in response to stress, whereas males ex

160 r fibers were observed in the nucleus of the stria terminalis in the telencephalon; habenular nucleus

161 T neurons in the amygdala and bed nucleus of stria terminalis inhibit MCH cells.

162 in the lateral septum and bed nucleus of the stria terminalis neurons.

163 cells in the medioventral bed nucleus of the stria terminalis of female mice but not male mice.

164 RXFP3 antagonist into the bed nucleus of the stria terminalis significantly decreased self-administra

165 a-Helical CRF9-41 in the bed nucleus of the stria terminalis suggested that this area is a site at w

166 ated cellular processes in the region of the stria terminalis that extended into the presumptive BSTp

167 (D1-LTPGABA) in the oval bed nucleus of the stria terminalis that was positively correlated with mot

168 ed in the medial amygdala/bed nucleus of the stria terminalis to lateral septum circuit.

169 nhibitory projection from bed nucleus of the stria terminalis to patch/exo-patch neurons was revealed

170 can act on neurons of the bed nucleus of the stria terminalis to reduce food intake via the IL-18 rec

171 binding in the posterior bed nucleus of the stria terminalis was greater in males irrespective of ag

172 d from lateral septum and bed nucleus of the stria terminalis were Fos-activated during cocaine CPP i

173 ng output (via the CNA or bed nucleus of the stria terminalis) that in turn regulates pontine REM gen

174 ippocampus, amygdala, and bed nucleus of the stria terminalis).

175 R) in the medial anterior bed nucleus of the stria terminalis, a key brain area that controls social

176 creased metabolism in the bed nucleus of the stria terminalis, a key component of the central extende

177 d stress behaviors (i.e., bed nucleus of the stria terminalis, amygdala, periaqueductal gray, raphe a

178 nucleus of the amygdala, bed nucleus of the stria terminalis, and a transition area in the shell of

179 nucleus of the amygdala, bed nucleus of the stria terminalis, and a transition area in the shell of

180 pituitary, hypothalamus, bed nucleus of the stria terminalis, and amygdala.

181 in the stress-responsive bed nucleus of the stria terminalis, and bilateral injections of RXFP3 anta

182 changes (caudate putamen, bed nucleus of the stria terminalis, and CA1 region of the hippocampus).

183 the amygdala and anterior bed nucleus of the stria terminalis, and densely to the lateral hypothalamu

184 The dorsal and hippocampal cingulum bundle, stria terminalis, and fornix were investigated as region

185 d corticothalamic tracts), stria medullaris, stria terminalis, and hippocampal commissure.

186 ions of the amygdala, the bed nucleus of the stria terminalis, and hippocampus.

187 laustrum, lateral septum, bed nucleus of the stria terminalis, and in many hypothalamic regions inclu

188 striatal transition area, bed nucleus of the stria terminalis, and medial habenular nucleus display a

189 nucleus of the amygdala, bed nucleus of the stria terminalis, and medial parvocellular paraventricul

190 gyrus polymorphic layer, bed nucleus of the stria terminalis, and paraventricular nucleus of the hyp

191 tral nucleus of the amygdala, bed nucleus of stria terminalis, and posterior ventral tegmental area.

192 ession in medial preoptic nuclei, bed nuclei stria terminalis, and the arcuate nucleus.

193 a, the oval nucleus of the bed nuclei of the stria terminalis, and the paraventricular nucleus of the

194 ons such as the amygdala, bed nucleus of the stria terminalis, and ventral forebrain.

195 the central amygdala, the bed nucleus of the stria terminalis, and visceral cortices were infected co

196 on Fos expression in the bed nucleus of the stria terminalis, another forebrain area implicated in s

197 able contributions of the bed nucleus of the stria terminalis, anterior insula, and thalamus during t

198 in the lateral septum and bed nucleus of the stria terminalis, as well as in several other limbic sit

199 n, EphA5 protein was found in the claustrum, stria terminalis, barrel cortex, and striatal patches, a

200 visualized in the cortex, bed nucleus of the stria terminalis, central amygdala, hypothalamic paraven

201 In the medioventral bed nucleus of the stria terminalis, defeat increased Oxt messenger RNA, to

202 uctures such as amygdala, bed nucleus of the stria terminalis, dorsal raphe, and lateral hypothalamus

203 itudinal fasciculus, bilateral fornix (cres)/stria terminalis, genu and splenium of the corpus callos

204 in the nucleus accumbens, bed nucleus of the stria terminalis, hippocampus, and cortex.

205 actory bulb, cerebral cortex, bed nucleus of stria terminalis, hippocampus, habenular nucleus, amygda

206 ells were observed in the bed nucleus of the stria terminalis, hypothalamic paraventricular, supraopt

207 ctions from the posterior bed nucleus of the stria terminalis, mesocortical structures and the hippoc

208 In the bed nucleus of the stria terminalis, one of several nuclei in a neural circ

209 nPGi was prominent in the bed nucleus of the stria terminalis, paraventricular nucleus (PVN), posteri

210 accumbens shell, lateral bed nucleus of the stria terminalis, paraventricular nucleus of the hypotha

211 nd a larger volume of the bed nucleus of the stria terminalis, paraventricular nucleus, and medial am

212 e nucleus, preoptic area, bed nucleus of the stria terminalis, paraventricular thalamus, periaqueduct

213 ctions with the amygdala, bed nucleus of the stria terminalis, periaqueductal gray, hippocampus, and

214 und in the hippocampal cingulum, fornix, and stria terminalis, posterior corona radiata, and superior

215 effects on the hippocampal cingulum, fornix, stria terminalis, posterior corona radiata, and superior

216 ricular nucleus (PVN) and the bed nucleus of stria terminalis, revealed global pattern changes in tra

217 ncountered in the septum, bed nucleus of the stria terminalis, substantia innominata, various thalami

218 (dmPFC), anterior insula, bed nucleus of the stria terminalis, thalamus, and midbrain consistently ac

219 teral septal nucleus, the bed nucleus of the stria terminalis, the fundus striati, the amygdala, the

220 sal forebrain structures, the bed nucleus of stria terminalis, the lateral preoptic area, the entoped

221 ygdala and to the lateral bed nucleus of the stria terminalis, the latter region receiving comparativ

222 eptum, the basal ganglia, bed nucleus of the stria terminalis, the thalamus including paraventricular

223 onal pathways specific to the amygdala (i.e. stria terminalis, ventral amygdalofugal pathway and unci

224 in specific nuclei of the bed nucleus of the stria terminalis, which plays essential roles in anxiety

225 and then to the principal bed nucleus of the stria terminalis, which suppresses territorial aggressio

226 fference in ERbeta in the bed nucleus of the stria terminalis, with males showing greater expression

227 examined areas, including the bed nucleus of stria terminalis,medial amygdala, and medial parabrachia

228 containing neurons of the bed nucleus of the stria terminalis.

229 neurons project into the bed nucleus of the stria terminalis.

230 esponse to high-frequency stimulation of the stria terminalis.

231 and the posterior lateral bed nucleus of the stria terminalis.

232 central amygdala, and the bed nucleus of the stria terminalis.

233 nnections that project primarily through the stria terminalis.

234 projection structure-the bed nucleus of the stria terminalis.

235 t of the CeA and into the bed nucleus of the stria terminalis.

236 scattered throughout the bed nucleus of the stria terminalis.

237 r commissure nucleus, and bed nucleus of the stria terminalis.

238 s no changes were observed within the BLA or stria terminalis.

239 dial extended amygdala and bed nuclei of the stria terminalis; basal telencephalic cholinergic and no

240 ended amygdala (primarily the bed nucleus of stria terminalis; BST), on the whole, the BST contained

241 prachiasmatic nucleus and bed nucleus of the stria terminalis; however, there are extensive VP-ir fib

242 nd principal nuclei of the bed nuclei of the stria terminalis; the caudate-putamen; the globus pallid

243 of the amygdala (ACe) and bed nucleus of the stria terminals (BnST), regions that are afferent to PVN

244 r commissure (IPAC, 56%), bed nucleus of the stria terminals (BNST, 59%), and medial preoptic area (M

245 , hippocampus, amygdala, caudate, and fornix/stria terminals.

246 alamus, raphe nuclei, and bed nucleus of the stria terminals.

247 traverse the midline in the ventral acoustic stria (VAS) are primarily located in the ventral cochlea

248 n proteins in the endothelial barrier of the stria vascularis (intrastrial fluid-blood barrier) throu

249 ing that the intermediate cells (ICs) of the stria vascularis (StV) express outward K+ current that r

250 The stria vascularis (StV) of the cochlear duct is the stati

251 In the previously reported S1pr2(-/-) mice, stria vascularis abnormalities, organ of Corti degenerat

252 ts principally from degeneration of cochlear stria vascularis and decline of the endocochlear potenti

253 Both marginal cells of the stria vascularis and hair cells express Trpml3 mRNA.

254 artery, which supplies blood directly to the stria vascularis and protects its capillary bed from hig

255 tissues, increased E2F1 and apoptosis in the stria vascularis and spiral ganglion neurons of the inne

256 Ngb was not present in the stria vascularis and the inner and outer hair cells.

257 tribution of nonsensory cell networks in the stria vascularis and the sensory region toward the matur

258 ing was restricted to the basal cells in the stria vascularis and was also detectable in the spiral g

259 barrier properties of tight junctions of the stria vascularis appeared intact in a biotin tracer assa

260 in the human cochlea, and they point to the stria vascularis as an important therapeutic target for

261 licated apoptosis in the spiral ganglion and stria vascularis because of mitochondrial reactive oxyge

262 paratus of renal glomerular podocytes and in stria vascularis cells of the inner ear, consistent with

263 Gelatin zymography of extracts from the stria vascularis confirmed these findings.

264 berrations in outer and inner hair cells and stria vascularis defects, leading to deafness in the var

265 hepatocyte growth factor (HGF) signaling in stria vascularis development for the first time and that

266 ochlear potential, indicative of significant stria vascularis dysfunction, but without obvious signs

267 Aberrant splicing of Fgfr2 blocked stria vascularis formation due to erroneous ligand usage

268 he relation of this developmental process to stria vascularis function is currently unknown.

269 n of transcripts in the WT versus Nr3b2(-/-) stria vascularis has identified a set of genes that is l

270 le's loop and for potassium secretion by the stria vascularis in the inner ear.

271 The stria vascularis is a nonsensory structure that is essen

272 Vascular disturbance within the stria vascularis is a potential mechanism that leads to

273 embranes in the cochlea, suggesting that the stria vascularis is the primary site of cochlear pathoge

274 ss structures of the endolymphatic space and stria vascularis observed at the light microscope level

275 acrophage-like melanocytes (PVM/Ms) from the stria vascularis of mice aged between P10 and P15 (P, po

276 anently impaired expression of KCNJ10 in the stria vascularis of Pit1(dw) mice, which likely contribu

277 rporation of the melanocytes into the future stria vascularis of the cochlear duct requires c-MET sig

278 owth factor (Hgf) is expressed in the future stria vascularis of the cochlear epithelium.

279 ll barriers and the capillary bed within the stria vascularis of the S1P(2) receptor-null mice showed

280 used a decrease in VEGF expression levels in stria vascularis vessels.

281 evealed that pericytes on capillaries of the stria vascularis were closely associated with the endoth

282 permeability of a biotin-based tracer in the stria vascularis were unaltered.

283 Explants of stria vascularis, 'mini-chips', are selectively cultured

284 lesions in the cochlea were found within the stria vascularis, a barrier epithelium containing the pr

285 We found that hair cells, marginal cells of stria vascularis, and other cells lining the cochlear an

286 was observed to leak from capillaries of the stria vascularis, and pericytes lost their tight associa

287 high throughput of K(+) across cells of the stria vascularis, conferred partly by the activity of Ki

288 y outer hair cells (OHCs), inner hair cells, stria vascularis, spiral ganglia, and surrounding nerves

289 vity delineated blood vessels located in the stria vascularis, spiral ligament, sub-basilar region, s

290 tin accumulation is consistently high in the stria vascularis, the region of the cochlea that maintai

291 hin the organ of Corti, spiral ganglion, and stria vascularis, which are known targets of cisplatin o

292 ced by 4 and 8 weeks old in mutants, and the stria vascularis, which generates the EP, showed degener

293 ner hair cells or a reduced thickness of the stria vascularis.

294 stemic circulation and the fluids inside the stria vascularis.

295 e progressive appearance of large lesions in stria vascularis.

296 articular in the cochlear organ of Corti and stria vascularis.

297 nd structurally damaged blood vessels in the stria vascularis.

298 at Kir4.1 confers the outflow of K(+) in the stria vascularis.

299 melanocyte-derived intermediate cells in the stria vascularis.

300 , forming the intermediate cell layer of the stria vascularis.