ライフサイエンスコーパス: choroid plexus

1 tyrosin in neurons of affected areas and the choroid plexus.

2 yme dispase, from the mouse fourth ventricle choroid plexus.

3 pithelial cell layer of the fourth ventricle choroid plexus.

4 lenoprotein genes were also expressed in the choroid plexus.

5 ctor T cells via the cerebrospinal fluid and choroid plexus.

6 strongly expressed EGFP, as did cells in the choroid plexus.

7 l engorgement and intense enhancement of the choroid plexus.

8 s were elevated over those in non-neoplastic choroid plexus.

9 cells from the lateral and fourth ventricle choroid plexus.

10 ntribute to the vascular substructure of the choroid plexus.

11 a saturable efflux mechanism present at the choroid plexus.

12 e2-lacZ-expressing cells into vessels of the choroid plexus.

13 -NT in cells adhering to the vasculature and choroid plexus.

14 used was the isolated Ringer perfused sheep choroid plexus.

15 g sheaths of blood vessels and stroma of the choroid plexus.

16 d biosynthesis and secretion of TTR from the choroid plexus.

17 a could be observed in the parenchyma of the choroid plexus.

18 dwarfing, male sterility, anemia, and cystic choroid plexus.

19 ite in all brain regions examined except the choroid plexus.

20 oparticles (NPs) using SVCT2 transporters of choroid plexus.

21 inding sites overlapped in kidney and in the choroid plexus.

22 ephalic) versus fourth ventricle (hindbrain) choroid plexus.

23 lt2st3 was found in the olfactory organs and choroid plexus.

24 xpression profiles were observed within each choroid plexus.

25 es, astroglial cells, leptomeninges, and the choroid plexus.

26 e perilesional cortex, lesion core zone, and choroid plexus.

27 (PSGL-1-receptor) was mainly detected at the choroid plexus.

28 ession in the epithelial cells of testis and choroid plexus.

29 he brain, where klotho levels are highest in choroid plexus.

30 least in part, to activation of cells in the choroid plexus.

31 c role in the development and functioning of choroid plexuses.

32 They did not occur in other parts of the choroid plexuses.

33 eneration of all the epithelial cells in the choroid plexuses.

34 ween RP and SP with SIVE were less marked in choroid plexus (29.6 versus 12.8 infected cells/mm(2), r

35 Using primary cultures of rat choroid plexus, a brain tissue that secretes CSF and abu

36 ork in this lab demonstrates that the normal choroid plexus, a primary component of the blood-cerebro

37 cephalic neuroectoderm expressing Wnt1; that choroid plexus, a secretory epithelium important for pat

38 SV11 mice develop tumors of the choroid plexus, a specialization of the ependymal lining

39 y high levels of A2AAR were expressed on the choroid plexus, a well-established CNS lymphocyte entry

40 rogenesis and reestablished IFN-II-dependent choroid plexus activity, which is lost in aging.

41 ide analysis of aged mice, we found that the choroid plexus, an interface between the brain and the c

42 are highly expressed in rodent meninges and choroid plexus, anatomical regions relevant to CSF physi

43 tigated the influx of leukocytes through the choroid plexus and acute induction of nuclear factor-kap

44 tor of cerebrospinal fluid (CSF) both at the choroid plexus and at the astrocytic end feet and defect

45 -mediated [(14)C]ALA transport from blood to choroid plexus and blood to CSF.

46 and the polarized expression of Mrp4 in the choroid plexus and brain capillary endothelial cells ind

47 expressed in blood vessels, neurons, and the choroid plexus and co-localized with glial fibrillary ac

48 ated with antiviral response, at the brain's choroid plexus and demonstrate its negative influence on

49 s that inhabit the parenchyma, meninges, and choroid plexus and discuss their roles in CNS homeostasi

50 urons, oligodendrocytes, astrocytes, and the choroid plexus and ependymal cells.

51 omoter, gene expression is detectable in the choroid plexus and ependymal epithelium by immunohistoch

52 We also examined gene expression in the choroid plexus and found several growth factors that are

53 rder) membrane vesicles isolated from bovine choroid plexus and in intact CP tissue from cow and rat.

54 tion was seen in the epithelial cells of the choroid plexus and in tanycytes at the third ventricle,

55 structural changes in the epithelium of the choroid plexus and in the ependyma, such as asymmetrical

56 in the cell nuclei of the epithelium of the choroid plexus and in the ependymal cells surrounding th

57 cked expression of PEPT2 mRNA and protein in choroid plexus and kidney, tissues in which PepT2 is nor

58 TTR is expressed at high levels in the choroid plexus and known to bind Abeta peptides and modu

59 ssues of the mouse with the exception of the choroid plexus and leptomeninges of the brain, where it

60 enhancers driving expression of Igf2 in the choroid plexus and leptomeninges, tissues where the gene

61 lia and perivascular macrophages, as well as choroid plexus and meningeal macrophages, dendritic cell

62 several regions of the brain, including the choroid plexus and meninges.

63 The choroid plexus and neocortex were additional structures

64 AQP1 is expressed in the choroid plexus and participates in forming cerebrospinal

65 cted expression of KCC3a in the hippocampus, choroid plexus and piriform cortex, as well as KCC4 in t

66 observed in the specialized epithelia of the choroid plexus and renal tubules and in connective tissu

67 ment proteins in the epithelial cells of the choroid plexus and the brain microvasculature in post-mo

68 Thus, Slit2, which is expressed by the choroid plexus and the septum, acts as a chemorepulsive

69 and piriform cortex, as well as KCC4 in the choroid plexus and the suprachiasmatic nucleus of the hy

70 n this research was the visualization of the choroid plexus and ventricular system, which seems to be

71 Because TTR is localized primarily in choroid plexus and, as a soluble monomer, in CSF, we con

72 se of this work was to determine whether the choroid plexus and/or the brain capillaries, a primary c

73 iated with increase in CSF production by the choroid plexus, and abnormal subcommissural organ.

74 al organ, median eminence, area postrema and choroid plexus, and accumulation of radioactivity at the

75 and hair follicles, gall bladder epithelium, choroid plexus, and biliary epithelium.

76 techniques involving brain/cord capillaries, choroid plexus, and CSF are needed.

77 etected in the heart, blood vessels, testes, choroid plexus, and in the ventral spinal cord.

78 layed weak COX-2 expression in the meninges, choroid plexus, and larger blood vessels.

79 es in the brain on glial cells, cells of the choroid plexus, and leukocytes.

80 r of SIV-infected cells in brain parenchyma, choroid plexus, and meninges from 17 macaques that devel

81 Both transporters are absent from the choroid plexus, and only GLAST mRNA is found in the subc

82 rived structures, including the vasculature, choroid plexus, and pial membranes.

83 he most dorsal telencephalic derivative, the choroid plexus, and that BMP signaling plays an essentia

84 that the myeloid cells enter the CNS via the choroid plexus, and that they may be infected during the

85 CA areas of the hippocampus, pontine nuclei, choroid plexus, and the cerebellum.

86 dymal cells of the ventricles, meninges, and choroid plexus; and the arcuate nucleus of the hypothala

87 The hindbrain roof plate and choroid plexus are essential organizing centers for indu

88 xpressed in rat lateral and fourth ventricle choroid plexus are very similar.

89 Choroid plexuses are the primary site of cerebrospinal f

90 exploit the biological effectiveness of the choroid plexus as a portal of entry into the brain.

91 rain inflammation, our findings pinpoint the choroid plexus as an important target for future researc

92 ospinal fluid, suggesting passage across the choroid plexus as well.

93 In contrast, expression of meningeal and choroid plexus-associated P selectin was upregulated 2 h

94 the transport kinetics of leptin across the choroid plexus (blood-CSF barrier) in isolation from the

95 ng the ventricles (CSF-brain barrier) or the choroid plexus (blood-CSF barrier).

96 ociated with leucocyte infiltration into the choroid plexus, brain cell death, and deficits in motiva

97 Aquaporin 4 (AQ4) is not expressed in the choroid plexus but is expressed in the astrocytic end fe

98 ocampal gyrus, amygdala, fusiform gyrus, and choroid plexus but not in other brain regions.

99 geal and parenchymal microvasculature and in choroid plexus by means of Western blot analysis and imm

100 Temporary disruption of the choroid plexus by microbubble-enhanced ultrasound is the

101 peculate that a fraction of D18G made by the choroid plexus can be transiently tetramerized by the lo

102 Since the choroid plexus can mediate interaction between periphera

103 lly engineered mouse carcinoma models, brain choroid plexus carcinoma (CPC) and prostate, to test the

104 TgT121;p53+/- mice, which invariably develop choroid plexus carcinoma (CPC), and nine age-matched hea

105 ma (n = 1), glioblastoma multiforme (n = 1), choroid plexus carcinoma (n = 2), and Burkitt lymphoma (

106 ), atypical teratoid rhabdoid tumor (n = 2), choroid plexus carcinoma (n = 2), and pineoblastoma (n =

107 Here we report the generation of a choroid plexus carcinoma cell line; Children's Cancer Ho

108 reshly isolated mouse ependymoma, glioma and choroid plexus carcinoma cells expressing red fluorescen

109 entiation having histological resemblance to choroid plexus carcinoma in this series.

110 tumor (n = 1), malignant glioma (n = 1), and choroid plexus carcinoma, (n = 1).

111 ryonal brain tumors such as medulloblastoma, choroid plexus carcinoma, and primary neuroectodermal tu

112 The diagnosis of choroid plexus carcinomas (CPC) in addition to MRTs in f

113 Choroid plexus carcinomas (CPCs) are poorly understood a

114 all survival in a cohort of 29 patients with choroid plexus carcinomas, a characteristic LFS tumor (P

115 tion rate in children presenting with ACC or choroid plexus carcinomas, and in females with breast ca

116 Endoscopic third ventriculostomy with choroid plexus cauterization (ETV-CPC) is an alternative

117 A 2005 bp clone was isolated from a rat choroid plexus cDNA library using a probe for ClC-2.

118 ort that ACIII localizes to primary cilia on choroid plexus cells and some astrocytes in the brain, w

119 the ENTV Env and sheep choroid plexus cells, choroid plexus cells stably expressing the JSRV Env prot

120 l types (eg, neurons, endothelial cells, and choroid plexus cells), most notably microglia and/or mac

121 oductive JCV infection of leptomeningeal and choroid plexus cells, and limited parenchymal involvemen

122 C) can affect expression of claudin-1 in rat choroid plexus cells, and we observed a correlation betw

123 th either the JSRV or the ENTV Env and sheep choroid plexus cells, choroid plexus cells stably expres

124 ber of different cell types, including brain choroid plexus cells, human endothelial cells, H9 cells,

125 n limited to tumors of lymphoid, breast, and choroid plexus cells.

126 es previously identified in fourth ventricle choroid plexus cells.

127 r was correlated with cytokine production by choroid plexus cells.

128 the brain, EGFP+ cells were detected in the choroid plexus, cerebellum, and cerebrum, where the perc

129 and of CRF2 (but not CRF1) receptors in the choroid plexus, certain hypothalamic nuclei, the nucleus

130 the source of cerebrospinal fluid (CSF), the choroid plexus (ChP) has been one of the most understudi

131 Choroid plexuses (ChPs) are vascularized secretory organ

132 % increase in (86)Rb(+) efflux from diabetic choroid plexus compared with controls.

133 ormal basal-to-apical fluid transport in the choroid plexus; conversely, AQP1 block with 500 mum Cd2+

134 flop isoforms of GluR-B RNA varied among the choroid plexus, cortex, hippocampus, olfactory bulb, and

135 od circulation, the epithelial layers of the choroid plexus (CP) are constitutively populated with CD

136 The choroid plexus (CP) forms the blood-cerebrospinal fluid

137 vestigated the roles of VEGF and TGF-beta in choroid plexus (CP) integrity and function in adult mice

138 expression was detected in kidney, liver, or choroid plexus (CP) of Oat3(-/-) mice.

139 cells to the CNS involves activation of the choroid plexus (CP) of the brain for leukocyte trafficki

140 The mechanism and membrane localization of choroid plexus (CP) organic anion transport were determi

141 Choroid plexus (CP) produces the cerebrospinal fluid (CS

142 The choroid plexus (CP) that forms the blood-CSF barrier (BC

143 forms of leptin receptor) expression in the choroid plexus (CP) was unchanged by high-fat diet or le

144 y members might mediate choline transport in choroid plexus (CP), the handling of choline by cloned t

145 Free (64)Cu uptake in rat choroid plexus (CP), where the blood-cerebrospinal fluid

146 f T4 from cerebrospinal fluid (CSF) into the choroid plexuses (CP) and ventricular brain regions, and

147 id transport assays with confluent polarized choroid plexus cultures showed that AQP1 current activat

148 s were calculated for the following markers: choroid plexus cyst, thickened nuchal fold, echogenic in

149 d a close relationship between meningeal and choroid plexus DCs (m/chDCs) and spleen DCs.

150 11(+) mice develop spontaneous tumors of the choroid plexus due to expression of SV40 Tag as a transg

151 res, including cortical hem, hippocampus and choroid plexus, either failed to form or were hypoplasti

152 oreover, our findings suggest that hindbrain choroid plexus endothelial cells, as compared to other v

153 ein were also present in epithelial cells of choroid plexus, ependyma, and meninges.

154 The staining in choroid plexus epithelia was unaffected by chronic metab

155 al Z310 cell line which was derived from rat choroid plexus epithelia, leading to a compartmental shi

156 F barrier (BCSFB) consists of a monolayer of choroid plexus epithelial (CPE) cells that maintain CNS

157 However, experiments in choroid plexus epithelial cell primary cultures indicate

158 Choroid plexus epithelial cells (CPECs) have essential d

159 Transcriptome analysis of FACS-purified choroid plexus epithelial cells also predicts their cell

160 This BCSFB is formed by the choroid plexus epithelial cells and is important in main

161 Choroid plexus epithelial cells express inward-rectifyin

162 A sheet of choroid plexus epithelial cells extends into each cerebr

163 CNS) microvascular endothelial cells and the choroid plexus epithelial cells form the endothelial blo

164 ls were observed in whole-cell recordings of choroid plexus epithelial cells isolated from ClC-2 knoc

165 f this study was to determine the ability of choroid plexus epithelial cells to volume regulate when

166 Native 5-HT2C receptors in choroid plexus epithelial cells were evaluated using flu

167 ion to Shh acting on the progenitor pool for choroid plexus epithelial cells, as previously shown, it

168 r NBCe2 results in significant remodeling of choroid plexus epithelial cells, including abnormal mito

169 5-HT(2C) receptor endogenously expressed in choroid plexus epithelial cells, we implemented a strate

170 tion was measured in primary cultures of rat choroid plexus epithelial cells, which endogenously expr

171 -HCO(3)(-) exchangers, contributes to RVI in choroid plexus epithelial cells.

172 32 receptors/mum(2) on the apical surface of choroid plexus epithelial cells.

173 sion identifies the primordium for hindbrain choroid plexus epithelial cells; Math1, for mossy fiber

174 Recently, the remote brain choroid plexus epithelium (CP) was identified as a porta

175 The choroid plexus epithelium (CPe) is primarily responsible

176 The choroid plexus epithelium (CPE) secretes higher volumes

177 n roof plate epithelium (hRPe) and hindbrain choroid plexus epithelium (hCPe) produce morphogens and

178 alization at the basolateral membrane of the choroid plexus epithelium and in the apical membrane of

179 Our data identify the choroid plexus epithelium as a novel source of IL-6 in E

180 ory vesicles and integration into endogenous choroid plexus epithelium following intraventricular inj

181 In contrast, in choroid plexus epithelium from NKCC1 null mice, SPAK imm

182 t Sonic hedgehog (Shh) produced by hindbrain choroid plexus epithelium induces the extensive vascular

183 fic inactivation of the pRb pathway in brain choroid plexus epithelium initiates tumorigenesis and in

184 to increase the permeability of immortalized choroid plexus epithelium monolayers in vitro.

185 However, the choroid plexus epithelium remains an obstacle to deliver

186 Immunohistochemical analysis of choroid plexus epithelium revealed co-expression of NKCC

187 derived C3 activates the C3a receptor in the choroid plexus epithelium to disrupt the blood-CSF barri

188 endothelial cells and high expression in the choroid plexus epithelium which regulates lymphocyte imm

189 nusoidal blood vessels, including podocytes, choroid plexus epithelium, and hepatocytes, as well as i

190 e central nervous system, including neurons, choroid plexus epithelium, and the brain microvasculatur

191 ss of cilia leads to altered function of the choroid plexus epithelium, as evidenced by elevated intr

192 adial glia, mature astrocytes, ependyma, and choroid plexus epithelium, but not in neurons.

193 trongly at the ventricular-facing surface of choroid plexus epithelium.

194 vealed nuclear inclusions in hepatocytes and choroid plexus epithelium.

195 their extravasation and passage through the choroid plexus epithelium; these infected myeloid cells

196 These results indicate that rat choroid plexus expresses the ClC-2 variant that was orig

197 and P-glycoprotein at the apical side of the choroid plexus facilitates an influx transport mechanism

198 , recognizing apoJ, which is abundant in the choroid plexus, facilitating Abeta clearance from the br

199 t only the most dorsalmedial derivative, the choroid plexus, failed to be specified or differentiate.

200 onsistent results (over the brain, neck, and choroid plexus) for background when SPECT/CT misalignmen

201 We analyzed postmortem choroid plexus from FXTAS and control subjects, and foun

202 tically induced water transport was rapid in choroid plexus from wild-type mice and reduced by fivefo

203 ths and vascular surface area fundamental to choroid plexus functions, but does not induce the more s

204 arise, in part, from regional differences in choroid plexus gene expression, we defined the transcrip

205 controls); and at 28 days, rats were killed, choroid plexuses harvested, and protein extracted.

206 ll as around it (in the meningeal spaces and choroid plexus) has been shown to be important for brain

207 human brain, with relatively high levels in choroid plexus, hippocampus and prefrontal cortex.

208 Association of C. neoformans with the choroid plexus, however, was not detected during up to 1

209 macrophages accumulated in the meninges and choroid plexus in early inflammation and in the perivasc

210 er, was detected at the apical aspect of the choroid plexus in FVB mice.

211 res of authentic DCs within the meninges and choroid plexus in healthy mouse brains.

212 rin and its receptor were upregulated in the choroid plexus in restless legs syndrome.

213 ining was reduced in the epithelial cells of choroid plexus in restless legs syndrome.

214 and also into non-neural tissues such as the choroid plexus in the brain and the retinal pigment epit

215 including the nasal mucosa and the ependyma/choroid plexus in the brain.

216 Our findings suggest involvement of the choroid plexus in the pathogenesis of CRPS.

217 These changes in expression may affect choroid plexus ion balance and thus significantly affect

218 -) mice, early leukocyte recruitment via the choroid plexus is enhanced, and IL-6 is elevated, which

219 le and non-saturable mechanisms and that the choroid plexus is involved in the regulation of leptin a

220 The cGMP-gated conductance in the choroid plexus is lost with targeted knockdown of AQP1 b

221 The secretory function of the choroid plexus is mediated by specific transport systems

222 2) showed that hematogenous infection of the choroid plexus is not a significant route of virus sprea

223 llelic (non-imprinted) expression within the choroid plexus is restricted to the epithelium, and we p

224 n of ion channels in the epithelial cells of choroid plexus isolated from the lateral ventricle of th

225 expression of the prolactin receptor in the choroid plexus, it has been hypothesized that the recept

226 pathway activity were also present in human choroid plexus lesions, and receptor mRNA levels in papi

227 The choroid plexus lining the four ventricles in the brain i

228 The BCSFB is situated at choroid plexuses located in the lateral, third, and four

229 The choroid plexus, located in brain ventricles, has receive

230 CSF is secreted continuously by the choroid plexus, located in the lateral, third and fourth

231 SVZ stem cell niche is the lateral ventricle choroid plexus (LVCP), a primary producer of CSF.

232 Perivascular, subdural meningeal and choroid plexus macrophages are non-parenchymal macrophag

233 macrophages and populations of meningeal and choroid plexus macrophages in normal brains and in brain

234 e populations, with the notable exception of choroid plexus macrophages, which had dual origins and a

235 However, some secretory epithelia (choroid plexus, Malpighian tubule, rectal gland, etc.) h

236 te itself to specify the expression of early choroid plexus markers.

237 Our data suggest that the roof plate and choroid plexus may be formed of functional units that ar

238 E expression was increased in the RVLM, PVH, choroid plexus, median preoptic nucleus, and organosum v

239 SIT1 mRNA was also expressed in the choroid plexus, microglia, and meninges of the brain and

240 Because the choroid plexus normally controls the production and comp

241 The choroid plexus, obtained at autopsy, from 18 neurologica

242 Therefore, the meninges and choroid plexus of a steady-state brain contain DCs that

243 at immunoreactive TTR was 41.5% lower in the choroid plexus of nicotine-treated rats compared with th

244 iary body is similar in many respects to the choroid plexus of the brain, and we demonstrated previou

245 of the caudal end of the fourth ventricular choroid plexus of the rat and mouse revealed 1-4 small,

246 ds to compare water permeability in isolated choroid plexus of wild-type vs. AQP1 null mice, as well

247 ffect of diabetes on ion transporters in the choroid plexuses of streptozotocin (STZ)-induced diabeti

248 9 also became detectable specifically in the choroid plexuses of the lateral and 3rd ventricles at E1

249 expressed in kidney, parathyroid glands, and choroids plexus of the brain.

250 brainstem and hippocampus (areas containing choroid plexus) of nicotine SA rats.

251 expression of simian virus 40 (SV40) TAg in choroid plexus or intestinal villi requires at least one

252 rent set of factors may be more essential to choroid plexus outgrowth.

253 They were microscopically highly similar to choroid plexus papillomas in humans, with an ongoing pro

254 cells, as previously shown, it also acts on choroid plexus pericytes, and together serves the import

255 as binding of (11)C-dihydroergotamine in the choroid plexus, pituitary gland, and venous sinuses as e

256 M [Ca2+]) there was no significant change in choroid plexus PMCA (Western Blots) compared to normocal

257 Choroid plexus precursors remained proliferative and did

258 temporal lobe regions (amygdala, hippocampus/choroid plexus region of interest) compared to younger c

259 ina lacks tissue equivalents of meninges and choroid plexus, rich sources of dendritic cells in brain

260 AQP1 deletion did not affect choroid plexus size or structure.

261 afficking of dye-positive monocytes into the choroid plexus stromata and perivascular spaces in the c

262 nt in the circumventricular organs including choroid plexus, subfornical organ, median eminence, and

263 tructures, such as the kidney, yolk sac, and choroid plexus, suggests a possible general role of Ctsh

264 iral protein expression were detected in the choroid plexus, the olfactory bulb, and in cells borderi

265 Phospholemman was particularly enriched in choroid plexus, the organ that secretes CSF in the ventr

266 iated with the Na,K-ATPase in cerebellum and choroid plexus: the proteins copurified after detergent

267 transporting epithelia, including kidney and choroid plexus, this cAMP-dependent signal transduction

268 tes from its primary production sites at the choroid plexus through the brain ventricles to reach the

269 tinual growth and expansion of the hindbrain choroid plexus throughout development.

270 d a selective and enriched expression in the choroid plexus tissue.

271 r family responsible for dipeptide uptake in choroid plexus tissue.

272 expressed highly in ependymal cells and the choroid plexus, tissues involved in the production and c

273 The ability of the choroid plexus to produce and degrade beta-amyloid, in a

274 Every individual with a choroid plexus tumor (eight of eight) and 14 of 21 indiv

275 ic CD8(+) T cells in the control of advanced choroid plexus tumor progression using large tumor Ag (T

276 bryonic day 9.5 mice causes the formation of choroid plexus tumors (CPTs).

277 V11 (H2(b)) mice develop rapidly progressing choroid plexus tumors due to expression of full-length T

278 at the control of advanced stage spontaneous choroid plexus tumors is associated with the induction o

279 ansfer into SV11 mice bearing advanced-stage choroid plexus tumors.

280 y the importance of VEGF-A in maintenance of choroid plexus vasculature and ependymal cells.

281 te yet functionally dependent structures-the choroid plexus vasculature and its ensheathing epitheliu

282 xtent, CD4(+) lymphocytes into the meninges, choroid plexus, ventricles, and parenchyma of the brain.

283 , we serendipitously found a 21% increase in choroid plexus volume in 12 patients suffering from comp

284 in (7.5 pmol l(-1)) at the blood face of the choroid plexus was 21.1+/-5.7%, which was greater than e

285 The efflux of the K(+) analog (86)Rb(+) from choroid plexus was also studied.

286 hydrolysis-resistant dipeptide) in isolated choroid plexus was essentially ablated (i.e. residual ac

287 d-cerebrospinal fluid barrier in the brain's choroid plexus was impaired.

288 In addition, secretion of new CSF by the choroid plexuses was significantly decreased with leptin

289 Background K+ and Cl- currents in the choroid plexus were dissected from AQP1 currents using C

290 dition, the parenchymal microvasculature and choroid plexus were strongly immunoreactive for mGluR1 a

291 Epithelial cells of the choroid plexus, where initial CCL20-induced leukocyte re

292 issues in which it is expressed, such as the choroid plexus, where the extracellular milieu is at neu

293 y nuclei, ependyma lining the ventricles and choroid plexus which was not observed after CRF.

294 inward-rectifying anion conductance in mouse choroid plexus, which must therefore express a novel inw

295 ial ventricles, the roof plate gives rise to choroid plexus, which regulates the internal environment

296 ptor antagonist were highly localized to the choroid plexus, which showed evidence of structural abno

297 amplified a 238 bp fragment of mRNA from rat choroid plexus, which was 99 % identical to the 5' seque

298 macrophages were present in the meninges and choroid plexus with AIDS.

299 m Cell, Silva-Vargas et al. (2016) show that choroid plexus, within the lateral ventricles of the adu

300 n, Cre activity was mainly restricted to the choroid plexus, without significant recombination detect