ライフサイエンスコーパス: choroid plexus

1 SF sources (including neural progenitors and choroid plexus).

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

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

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

5 xpression profiles were observed within each choroid plexus.

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

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

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

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

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

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

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

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

14 pithelial cell layer of the fourth ventricle choroid plexus.

15 lenoprotein genes were also expressed in the choroid plexus.

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

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

18 l engorgement and intense enhancement of the choroid plexus.

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

20 cells from the lateral and fourth ventricle choroid plexus.

21 ntribute to the vascular substructure of the choroid plexus.

22 a saturable efflux mechanism present at the choroid plexus.

23 white matter, hemispheric white matter, and choroid plexus.

24 bstantia nigra, but not the basal ganglia or choroid plexus.

25 pressed in kidney, in astrocytes, and in the choroid plexus.

26 ed with age); thalamus and white matter; and choroid plexus.

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

28 e effects of annexin A5 on Abeta toxicity in choroid plexus.

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

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

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

32 facial nucleus, 0.39 ug . g(-1) +/- 0.10 in choroid plexus, 0.29 ug . g(-1) +/- 0.05 in caudate-puta

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

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

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

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

37 ta (Abeta) deposits may cause impairments in choroid plexus, a specialised brain structure which form

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

39 Choroid plexus abnormalities have been implicated in bot

40 hese findings suggest the involvement of the choroid plexus across the psychosis spectrum with a pote

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

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

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

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

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

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 8 T cells resulted in lytic infection of the choroid plexus and ependymal lining, marked meningitis,

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

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

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

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

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

61 The choroid plexus and neocortex were additional structures

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

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

64 lammation-induced CCC phosphorylation in the choroid plexus and reduces cerebrospinal fluid (CSF) hyp

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

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

67 annexin A5 would exert a protective role in choroid plexus and this protection is lost as Abeta accu

68 rs that are secreted by distant neurons, the choroid plexus and vasculature.

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

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

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

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

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

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

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

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

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

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

79 , and the eye, and is secreted by the liver, choroid plexus, and retinal epithelium, respectively.

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

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

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

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

84 Choroid plexuses are the primary site of cerebrospinal f

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

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

87 Stromal choroid plexus BAMs are also considerably reduced.

88 e arrival of cephalic mesenchyme and stromal choroid plexus BAMs was only partially restricted.

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

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

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

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

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

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

95 Since the choroid plexus can mediate interaction between periphera

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

97 Choroid plexus carcinoma (CPC) is a rare brain tumor tha

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

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

100 This study describes new mouse models of choroid plexus carcinoma and uses them to investigate th

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

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

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

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

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

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

107 Choroid plexus carcinomas (CPCs) are poorly understood a

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

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

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

111 Choroid plexus cell cultures from rats were used to anal

112 Annexin A5 addition to choroid plexus cell cultures restored the Abeta-induced

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

114 expression of viral receptor ACE2 in mature choroid plexus cells expressing abundant lipoproteins, b

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

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

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

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

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

120 es previously identified in fourth ventricle choroid plexus cells.

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

122 The choroid plexus (ChP) epithelium is a source of secreted

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

124 Barrier properties of the choroid plexus (ChP) help protect the brain from the ext

125 Here we show that WNT5A is produced by the choroid plexus (ChP) of the developing hindbrain, but no

126 The choroid plexus (ChP) regulates brain development by secr

127 The CSF is produced by the choroid plexus (ChP), a protective epithelial barrier th

128 , resulting in leukocyte infiltration of the choroid plexus (ChP).

129 Choroid plexuses (ChPs) are vascularized secretory organ

130 % increase in (86)Rb(+) efflux from diabetic choroid plexus compared with controls.

131 ing in the dura mater, subdural meninges and choroid plexus consisted of distinct subsets with tissue

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

133 s, as well as choroid plexus familiality and choroid plexus covariance with clinical, cognitive, brai

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

135 We examined leukocyte trafficking via the choroid plexus (CP) following neonatal stroke in relatio

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

137 ffic into the brain via multiple routes, the choroid plexus (CP) has been identified as a uniquely ed

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

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

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

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

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

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

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

145 s the multiple drivers of disease, including choroid plexus CSF hypersecretion, ependymal denudation,

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

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

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

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

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

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

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

153 ipoprotein- and ACE2-expressing cells of the choroid plexus epithelial barrier.

154 hat TMEM67 is required for the regulation of choroid plexus epithelial cell fluid and electrolyte hom

155 Choroid plexus epithelial cells (CPECs) have essential d

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

157 ntial vanilloid 4 (TRPV4), in primary murine choroid plexus epithelial cells and immortalized cell li

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

159 ate that skeletal muscle myoblasts and brain choroid plexus epithelial cells are particularly suscept

160 live virus to demonstrate viral tropism for choroid plexus epithelial cells but little to no infecti

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

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

163 Protein localization in choroid plexus epithelial cells indicates that aquaporin

164 The choroid plexus epithelial cells may have selectively enh

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

166 s and astrocytes were sparsely infected, but choroid plexus epithelial cells underwent robust infecti

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

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

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

170 32 receptors/mum(2) on the apical surface of choroid plexus epithelial cells.

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

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

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

174 The choroid plexus epithelium (CPe) is primarily responsible

175 The choroid plexus epithelium (CPE) secretes higher volumes

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

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

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

179 ning for rh Bri2 BRICHOS was observed in the choroid plexus epithelium as well as in the cerebral cor

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

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

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

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

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

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

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

190 w that infection with SARS-CoV-2 damages the choroid plexus epithelium, leading to leakage across thi

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

192 vealed nuclear inclusions in hepatocytes and choroid plexus epithelium.

193 subset residing on the apical surface of the choroid plexus epithelium.

194 sing the cerebrospinal fluid produced by the choroid plexus epithelium.

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

196 AD choroid plexus exhibited progressive reduction of annexi

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

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

199 and axis II cluster A relatives, as well as choroid plexus familiality and choroid plexus covariance

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

201 carried out a mass proteomic-based study in choroid plexus from AD patients and we found several dif

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

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

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

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

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

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

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

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

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

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

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

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

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

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

216 CLIO-NPs were also found in the choroid plexus, indicating inflammation of the ventricul

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

218 The choroid plexus is an important physiological barrier and

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

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

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

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

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

234 order-associated meningeal, perivascular and choroid plexus macrophages.

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

236 The choroid plexus may be an important target in future rese

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 nate lymphoid cells (ILC2) accumulate in the choroid plexus of aged brains.

244 ed in the cerebral cortex, pineal gland, and choroid plexus of both rats and humans via in situ hybri

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

246 Strikingly, we identified the choroid plexus of the mouse lateral ventricle as the maj

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

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

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

250 9 also became detectable specifically in the choroid plexuses of the lateral and 3rd ventricles at E1

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

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

253 We optimized a protocol to generate choroid plexus organoids from hiPSCs and showed that pro

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

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

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

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

258 In choroid plexus primary cultures, Abeta administration re

259 loss of Folr1-mediated folate uptake at the choroid plexus, providing a therapeutic approach for neu

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

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

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

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

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

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

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

267 and photoreceptors, and the ciliary body and choroid plexus, the sources of aqueous humor and cerebro

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

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

270 bral folate delivery primarily occurs at the choroid plexus through FRalpha and PCFT; inactivation of

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

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

273 We used choroid plexus tissue samples and CSF from mild cognitiv

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

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

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

277 A previous choroid plexus transcriptomic analysis of schizophrenia

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

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

280 uable tools for understanding the biology of choroid plexus tumors and for testing novel approaches t

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

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

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

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

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

286 The purpose of this study was to examine choroid plexus volume in probands across the psychosis s

287 Choroid plexus volume was quantified (using FreeSurfer)

288 red with healthy control subjects; and total choroid plexus volume was significantly heritable.

289 Choroid plexus volume was significantly larger in proban

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

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

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

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

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

295 ion factor promoting PNN development, in the choroid plexus, where it is produced, as well as in parv

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

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

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