ライフサイエンスコーパス: stria

1 nuated the decreased vascular density in the stria.

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

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

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

5 A stria LGE pattern with subepicardial/midmyocardial distr

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

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

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

9 38+/-25 months, 6 of 27 (22%) athletes with stria pattern experienced malignant arrhythmic events su

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

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

12 ng neurons in the anterior bed nuclei of the stria terminalis (aBNST) make direct GABAergic inputs on

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

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

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

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

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

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

19 The anterior lateral bed nucleus of the stria terminalis (alBST) expresses glucagon-like peptide

20 ing, and the anteroventral bed nuclei of the stria terminalis (avBST) integrates homeostatic informat

21 he anteroventral region of bed nuclei of the stria terminalis (avBST) regulates glucocorticoid releas

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

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

24 eA CRF projections to the bed nucleus of the stria terminalis (BNST) and that inhibition of the CRF(C

25 neurons projecting to the bed nucleus of the stria terminalis (BNST) are also frequently contacted by

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

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

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

29 ng and CRF neurons in the bed nucleus of the stria terminalis (BNST) drive negative affective behavio

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

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

32 The bed nucleus of the stria terminalis (BNST) has been implicated in condition

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

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

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

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

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

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

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

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

41 receptor signaling in the bed nucleus of the stria terminalis (BNST) is a critical molecular substrat

42 The bed nucleus of the stria terminalis (BNST) is a critical node involved in s

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

44 The bed nucleus of the stria terminalis (BNST) is a sexually dimorphic region t

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

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

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

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

49 The bed nucleus of the stria terminalis (BNST) is part of the limbic-hypothalam

50 IGNIFICANCE STATEMENT The bed nucleus of the stria terminalis (BNST) is part of the limbic-hypothalam

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

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

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

54 e oval (ov) region of the Bed Nucleus of the Stria Terminalis (BNST) may be critical for monitoring e

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

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

57 the effects of CRF in the bed nucleus of the stria terminalis (BNST) of lactating mice during materna

58 ivation of lPBN efferents to the bed nucleus stria terminalis (BNST) or central amygdala (CEA) genera

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

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

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

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

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

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

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

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

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

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

69 se in PACAP levels in the bed nucleus of the stria terminalis (BNST), a brain area within the extende

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

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

72 The bed nucleus of the stria terminalis (BNST), a brain region of the extended

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

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

75 ed heteroreceptors in the bed nucleus of the stria terminalis (BNST), a key brain region in driving s

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

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

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

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

80 The bed nucleus of the stria terminalis (BNST), an integral part of the extende

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

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

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

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

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

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

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

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

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

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

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

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

93 rsomedial division of the bed nucleus of the stria terminalis (BNST), well connected to the amygdala,

94 in the oval region of the bed nucleus of the stria terminalis (BNST), which are activated by various

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

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

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

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

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

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

101 frontal cortex (mPFC) and bed nucleus of the stria terminalis (BNST).

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

103 nd neural activity in the bed nucleus of the stria terminalis (BNST).

104 al hypothalamus (VmH) and bed nucleus of the stria terminalis (BNST).

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

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

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

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

109 y within the medioventral bed nucleus of the stria terminalis (BNSTmv).

110 he principal component of the bed nucleus of stria terminalis (BNSTpr), a limbic center, in social in

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

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

113 cates that neurons in the bed nucleus of the stria terminalis (BST) generate anxiety-like behaviors,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

130 ransmission in the dorsal bed nucleus of the stria terminalis (dBNST), a region heavily implicated in

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

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

133 CeA and the dorsolateral bed nucleus of the stria terminalis (dlBST).

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

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

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

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

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

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

140 ns project to the ventral bed nucleus of the stria terminalis (vBNST), parabrachial nucleus (PBN), an

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

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

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

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

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

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

147 ior capsule region (including bed nucleus of stria terminalis and nucleus accumbens) remains investig

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

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

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

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

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

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

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

155 of a CeL to laterodorsal bed nucleus of the stria terminalis circuit that may be relevant to underst

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

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

158 SIC1A in the amygdala and bed nucleus of the stria terminalis in CO(2)-evoked and acid-evoked behavio

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

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

161 2 expression in the amygdala and bed nucleus stria terminalis in response to stress, whereas males ex

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

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

164 ed activation of anterior bed nucleus of the stria terminalis neurons was reduced in mice without GHR

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

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

167 their projections to the bed nucleus of the stria terminalis promotes feeding.

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

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

170 romedial hypothalamus and bed nucleus of the stria terminalis that undergo synaptic potentiation afte

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

172 icate that OT acts in the bed nucleus of the stria terminalis to induce avoidance of potentially dang

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

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

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

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

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

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

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

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

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

182 in regions, including the bed nucleus of the stria terminalis, amygdala, and locus coeruleus.

183 cortex, basal forebrain, bed nucleus of the stria terminalis, amygdala, diencephalon, and brainstem.

184 (i.e., nucleus accumbens, bed nucleus of the stria terminalis, amygdala, habenula, and raphe nucleus)

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

186 udate putamen, claustrum, bed nucleus of the stria terminalis, amygdaloid nucleus, ventral posterior

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

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

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

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

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

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

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

194 he medial amygdala (MeA), bed nucleus of the stria terminalis, and lateral septum.

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

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

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

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

199 romedial hypothalamus and bed nucleus of the stria terminalis, and these projections have opposing ef

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

201 regions: lateral septum, bed nucleus of the stria terminalis, and ventral tegmental area.

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

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

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

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

206 ular nucleus of the thalamus, bed nucleus of stria terminalis, basolateral amygdala, and medial prefr

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

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

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

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

211 , hypothalamus, amygdala, bed nucleus of the stria terminalis, hippocampus, ventral midbrain, periaqu

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

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

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

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

216 r and infralimbic areas), bed nucleus of the stria terminalis, periaqueductal gray, Barrington's nucl

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

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

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

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

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

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

223 eir subunits) such as the bed nucleus of the stria terminalis, the amgydala, and the hippocampus, as

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

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

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

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

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

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

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

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

232 scattered throughout the bed nucleus of the stria terminalis.

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

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

235 oject to the laterodorsal bed nucleus of the stria terminalis.

236 alamic nuclei, and in the bed nucleus of the stria terminalis.

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

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

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

240 ns, ventral pallidum, and bed nucleus of the stria terminalis.

241 -producing neurons in the bed nucleus of the stria terminalis.

242 e expression in the mouse bed nucleus of the stria terminalis.

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

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

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

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

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

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

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

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

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

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

253 The stria vascularis (SV) in the cochlea generates and maint

254 e organ of Corti (OC), spiral ganglion (SG), stria vascularis (SV), and afferent nerve fibres.

255 dependent on ion homeostasis mediated by the stria vascularis (SV).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

273 neural crest cells fail to migrate into the stria vascularis intermediate layer, resulting in a sign

274 The stria vascularis is a nonsensory structure that is essen

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

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

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

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

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

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

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

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

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

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

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

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

291 melanocyte-derived intermediate cells in the stria vascularis.

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

293 maintained in scala media, generated by the stria vascularis.

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

295 stemic circulation and the fluids inside the stria vascularis.

296 e progressive appearance of large lesions in stria vascularis.

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

298 nd structurally damaged blood vessels in the stria vascularis.

299 endocochlear potential due to atrophy of the stria vascularis.

300 egions medial to inner HCs as well as in the stria vascularis.