ライフサイエンスコーパス: non-neuronal cell

1 on in cocultured neurons when expressed in a non-neuronal cell.

2 SIEH, suggesting that this is mediated via a non-neuronal cell.

3 REZ, forming presynaptic terminal endings on non-neuronal cells.

4 cribed before, and appear to be specific for non-neuronal cells.

5 that is critical for regulated exocytosis in non-neuronal cells.

6 naling pathways, to promote the migration of non-neuronal cells.

7 p2) as an interaction partner of MICAL-L1 in non-neuronal cells.

8 ry for high affinity binding to neuronal and non-neuronal cells.

9 or REST silences neuronal gene expression in non-neuronal cells.

10 or that targets a group of neuronal genes in non-neuronal cells.

11 ate filaments (IFs) both in neurons and many non-neuronal cells.

12 epigenetic suppression of neuronal genes in non-neuronal cells.

13 in the differentiation and proliferation of non-neuronal cells.

14 flp-10 is expressed in both neurons and non-neuronal cells.

15 SEMA3B has emerged as a tumor suppressor in non-neuronal cells.

16 T and NFkappaB in the suppression of TAC1 in non-neuronal cells.

17 osis-inducing activity in neurons but not in non-neuronal cells.

18 te smoke, can stimulate the proliferation of non-neuronal cells.

19 including cell replacement, targeted to the non-neuronal cells.

20 the cultures were 50-60% neuronal and 40-50% non-neuronal cells.

21 activity of anti-P2X7 receptor antibodies on non-neuronal cells.

22 anscriptional repressor of neuronal genes in non-neuronal cells.

23 ments, leading to neuronal gene silencing in non-neuronal cells.

24 , little is known regarding this receptor in non-neuronal cells.

25 ndent inhibition of BzATP-evoked currents in non-neuronal cells.

26 ng more prominent in primary neurons than in non-neuronal cells.

27 nd non-neuronal cells, only neurons, or only non-neuronal cells.

28 ivated after destruction of both neurons and non-neuronal cells.

29 tentacular cells, and several other kinds of non-neuronal cells.

30 s the expression of neuron-specific genes in non-neuronal cells.

31 identified as a stress-responsive protein in non-neuronal cells.

32 ted the differentiation of both neuronal and non-neuronal cells.

33 es in neuronal cells and their repression in non-neuronal cells.

34 ng NR2A mRNA than that in glial cultures and non-neuronal cells.

35 is differentially regulated in neuronal and non-neuronal cells.

36 promoted expression of neuronal features in non-neuronal cells.

37 used increased levels of ROS in neuronal and non-neuronal cells.

38 ted a novel mRNA splice variant of nPTB from non-neuronal cells.

39 us-dependent gene expression in neuronal and non-neuronal cells.

40 functional activity of nPTB in neuronal and non-neuronal cells.

41 expression of neuronal phenotypic traits in non-neuronal cells.

42 nd causes formation of nuclear aggregates in non-neuronal cells.

43 ive in retinal neurons compared with retinal non-neuronal cells.

44 dependent transport pathways in neuronal and non-neuronal cells.

45 chanism significantly different from that in non-neuronal cells.

46 activities of these IRESs are comparable in non-neuronal cells.

47 ar to be similar to those used in asymmetric non-neuronal cells.

48 ting of clathrin-coated vesicles by Hsc70 in non-neuronal cells.

49 sting that GAK acts as an auxilin homolog in non-neuronal cells.

50 l role in the life and death of neuronal and non-neuronal cells.

51 In contrast, promoter activity is low in non-neuronal cells.

52 nits are thought to be restricted largely to non-neuronal cells.

53 R-positive neurons as well as nAchR-negative non-neuronal cells.

54 o the tubulovesicular recycling endosomes in non-neuronal cells.

55 tment to the plasma membrane of neuronal and non-neuronal cells.

56 ellular Ca2+ wave initiation in neuronal and non-neuronal cells.

57 t-synaptic localization and/or expression in non-neuronal cells.

58 ively inhibit the reverse mode of the NCE in non-neuronal cells.

59 cular supporting cells, and several types of non-neuronal cells.

60 rment of cell migration on ATF4 reduction in non-neuronal cells.

61 mice and expression of WT and mutant Dcx in non-neuronal cells.

62 mission in the brain and are also present in non-neuronal cells.

63 ZBP1 at serine 181 (Ser181) was described in non-neuronal cells.

64 rogeneity and the contribution of effects of non-neuronal cells.

65 sing a large consortium of neuronal genes in non-neuronal cells.

66 wn to accumulate in filopodia in neurons and non-neuronal cells.

67 ost had different activities in neuronal vs. non-neuronal cells.

68 and intercellular signaling in neuronal and non-neuronal cells.

69 ir chaperone-like function when expressed in non-neuronal cells.

70 ents a slow form of exocytosis found in many non-neuronal cells.

71 reducing milieu and suppresses apoptosis in non-neuronal cells.

72 or responsive to the interaction of FMNs and non-neuronal cells.

73 In NHE5-transfected non-neuronal cells, activation of AMPK by the AMP mimeti

74 subset of bronchial epithelial cells and in non-neuronal cells adjacent to neurovascular bundles in

75 For example, Bcl-2 does not protect non-neuronal cells against taxol, a microtubule-stabiliz

76 PtdInsPKI gamma-90 is expressed in non-neuronal cells, albeit at much lower levels than in

77 40% of spinal cord motor neurons, with other non-neuronal cells also transduced.

78 otic BH3-only protein, promotes apoptosis of non-neuronal cells, although the mechanisms involved rem

79 erences in the regulome between neuronal and non-neuronal cells and ascribes putative functional role

80 d internalization of pre-formed fibrils into non-neuronal cells and dopaminergic neurons matched the

81 nscheduled accumulation of neuronal mRNAs in non-neuronal cells and ensures coordinated upregulation

82 es and cortical neurons, but was inactive in non-neuronal cells and glia.

83 nteracted functionally with NgR1-p75/TROY in non-neuronal cells and in brain lysates, mediating RhoA

84 tional processing regulates OPA1 function in non-neuronal cells and moreover, aberrant processing of

85 ecipitation experiments in both neuronal and non-neuronal cells and mouse brain.

86 le pathways within the neurovascular unit in non-neuronal cells and neurons during acute or chronic C

87 t study, the expression of P2X7 receptors in non-neuronal cells and neurons isolated from dorsal root

88 etergent insoluble membrane (DIM) domains of non-neuronal cells and neurons that fulfill the criteria

89 L4 retention in the endoplasmic reticulum in non-neuronal cells and neurons, and blocked NL4 transpor

90 type A receptor subunits were coexpressed in non-neuronal cells and neurons.

91 rillion cells in the human brain and include non-neuronal cells and postmitotic neurons identified by

92 for regulating distinct actin structures in non-neuronal cells and presumably in growth cones.

93 how that sacsin localizes to mitochondria in non-neuronal cells and primary neurons and that it inter

94 ndent internalization of HA-DAT expressed in non-neuronal cells and rat dopaminergic neurons.

95 Bak and Bax are functionally redundant in non-neuronal cells and represent a mitochondrial converg

96 ged activation of the same HSP subset in the non-neuronal cells and severe morphological damage in bo

97 REST is expressed in non-neuronal cells and stem/progenitor neuronal cells, i

98 rst trafficking regulatory role for Crmp2 in non-neuronal cells and support a model in which Crmp2 is

99 h lysosome-associated membrane protein II in non-neuronal cells and with synaptophysin in neuronal ce

100 degenerative disease predominantly occurs in non-neuronal cells, and in the brain, alphaBc is mainly

101 s were decreased in the presence of Fbxo2 in non-neuronal cells, and increased in both cultured hippo

102 ivatives are taken up into both neuronal and non-neuronal cells, and into resealed chromaffin granule

103 atives, including CNS and olfactory neurons, non-neuronal cells, and olfactory ensheathing glia, all

104 VP motif shapes mitochondria in neuronal and non-neuronal cells, and that CaN-mediated Drp1 dephospho

105 type Ca(2+) channels can be reconstituted in non-neuronal cells, and that RGS2 can selectively block

106 CAN channels in many non-neuronal cells are blocked by non-steroidal antiinfl

107 ion cells, indicating that interactions with non-neuronal cells are likely to play an important role

108 n activation of glutamate receptors on these non-neuronal cells are not known.

109 hwann cells and haploinsufficiency of Nf1 in non-neuronal cells are required for tumorigenesis.

110 le in neuronal and neuroendocrine but not in non-neuronal cells as a GTP-dependent switch between reg

111 (c) impaired cytoskeleton function, and (d) non-neuronal cells as modifiers of the ALS phenotype.

112 ed in the regulation of integrin function in non-neuronal cells, as well as in the regulation of grow

113 o M-1, Hep G2, or human embryonic kidney 293 non-neuronal cells at similar concentrations.

114 her, these data suggest that, in contrast to non-neuronal cells, Bif-1 is essential for the maintenan

115 organelles involved in matrix remodeling in non-neuronal cells but not described in neural structure

116 ical effects on sodium channels expressed in non-neuronal cells, but may primarily cause loss of func

117 lly activated H-Ras fails to activate Rin in non-neuronal cells, but results in potent stimulation of

118 ceptors (nAChRs) are present on neuronal and non-neuronal cells, but while in neurons, nAChRs are cat

119 r further reduced GluR2 promoter activity in non-neuronal cells by 30-47%.

120 bsent from brain tissue and was generated in non-neuronal cells by alternative splicing to include fi

121 battery of neuronal differentiation genes in non-neuronal cells by binding to a specific consensus DN

122 the expression of neuronal-specific genes in non-neuronal cells by recruiting histone deacetylases (H

123 rmines the fates of a number of neuronal and non-neuronal cells by regulating the expression of multi

124 Neuronal gene transcription is repressed in non-neuronal cells by the repressor element 1 (RE-1)-sil

125 ts also indicate that primary changes within non-neuronal cells can affect mutant SOD1-induced diseas

126 ate that human brain cells (both neurons and non-neuronal cells) can be aneuploid and that the result

127 In non-neuronal cells, CD2AP, like other adaptor proteins,

128 In non-neuronal cells, coexpression of human NgR1, p75 and

129 the p50 subunit of dynactin in neuronal and non-neuronal cell cultures abolished the association bet

130 nged agonist activation of P2X7 receptors in non-neuronal cells did not lead to cytolytic pore format

131 causes the accumulation of the aggregates in non-neuronal cells, differentiated neuroblastoma cells,

132 Distinct from MLK3, which was identified in non-neuronal cells, DLK and MKK7 were detected predomina

133 dicates that Ras and MEKK3, a MEK5 kinase in non-neuronal cells, do not play a significant role in BD

134 However, in non-neuronal cells, DOX also inhibits the expression of

135 sed transiently in a variety of neuronal and non-neuronal cells during restricted periods of embryoni

136 ns exhibited unique features not observed in non-neuronal cells, e.g., the lack of RE1 motifs and an

137 In non-neuronal cells, EHD1 (Eps15 homology-domain containi

138 ptiPrep gradients and then from neuronal and non-neuronal cells expressing only endogenous proteins.

139 in regular arrays by precise positioning of non-neuronal cells expressing synaptic proteins, while a

140 sable for the assembly of focal adhesions in non-neuronal cells, FAK activity is required for the for

141 d suppression of a Notch repressor to assign non-neuronal cell fate.

142 t, but here we show that CDK5 is required in non-neuronal cells for the DNA-damage response and, in p

143 ized to begin when pioneer axons extend over non-neuronal cells, forming tracts guiding follower axon

144 There are also occasional non-neuronal cells found to arise from ckPCs.

145 -polyethylene tri-block copolymers, protects non-neuronal cells from traumatic injuries and rescues h

146 nduced, but not constitutive, exocytosis, in non-neuronal cells GTP- and GDP-bound Rab11b inhibited c

147 neurons during development, but its role in non-neuronal cells has been less studied.

148 Although growth factor activation of ERK5 in non-neuronal cells has been shown to contribute to cell

149 to as high or low based on transcription in non-neuronal cells) has been investigated in a number of

150 al cells, but its expression and function in non-neuronal cells have remained poorly characterized.

151 Previous studies in non-neuronal cells have shown that Bif-1 is proapoptotic

152 Recent studies in non-neuronal cells have shown that the tumor suppressor

153 regulators of actin cytoskeletal dynamics in non-neuronal cells; however, their neuronal functions ar

154 small GTPases in regulating this process in non-neuronal cells identifies them as candidate signalli

155 the activity of ubiquitous JNK1 and JNK2 in non-neuronal cells, impacting the signaling pathway that

156 ults are consistent with previous reports in non-neuronal cells, implicating the importance of caveol

157 d regulate the function of many neuronal and non neuronal cells in adult organisms.

158 ctive and specific silencing in neuronal and non-neuronal cells in culture and in the DRG of mice in

159 This method has been adapted to non-neuronal cells in mice and to neurons in fish and fl

160 Rods form abundantly in the cytoplasm of non-neuronal cells in response to many treatments that i

161 RNA and protein are detected transiently in non-neuronal cells in several regions of the early CNS,

162 activity was also observed in FMRP-deficient non-neuronal cells in the absence of gp1 mGluRs.

163 ctor Neurogenin2 can induce new neurons from non-neuronal cells in the adult neocortex and striatum w

164 omicroniotaalpha meaning 'glue') pertains to non-neuronal cells in the central (CNS) and peripheral n

165 nteract directly with nicotinic receptors on non-neuronal cells in the developing lung, and that simi

166 In non-neuronal cells in the fly, dHIP14 protein is found i

167 dings demonstrate acute induction of HO-1 in non-neuronal cells in the injured spinal cord.

168 ssion of Hsp27 was localized to neuronal and non-neuronal cells in the inner layers of the retina.

169 , and further highlight the critical role of non-neuronal cells in the pathogenesis of ALS.

170 ed the number and proportion of neuronal and non-neuronal cells in the primary sensory areas of the n

171 ration of neuronal synapses onto transfected non-neuronal cells in the so-called artificial synapse-f

172 eptor CCR2 was expressed in neurons and some non-neuronal cells in the spinal cord.

173 t rather involves a dysregulated response by non-neuronal cells in the surrounding neuropil.

174 sses of previously inaccessible neuronal and non-neuronal cells in vivoSIGNIFICANCE STATEMENT Instruc

175 to induce Ca2+ release than do a variety of non-neuronal cells (including astrocytes, hepatocytes, e

176 Non-neuronal cells, including astrocytes, shape motor ne

177 nd report that p53 protein also increases in non-neuronal cells, including microglia.

178 Studies in non-neuronal cells indicate that actin cytoskeletal regu

179 Data from non-neuronal cells indicate that taxol-induced apoptosis

180 Previous work in non-neuronal cells indicates that presenilin-1 (PS1) ass

181 Contact with a neuroligin-expressing non-neuronal cell induces formation of presynaptic termi

182 heterologous expression of APLP1 or APLP2 in non-neuronal cells induces presynaptic differentiation i

183 In non-neuronal cells, integrins are critical modulators of

184 We review how non-neuronal cells interact with nociceptive neurons by

185 nt progenitor that gives rise to neurons and non-neuronal cells is a basal cell, whereas the progenit

186 fficient because damage to other neurons and non-neuronal cells is common in retinal and optic nerve

187 superoxide dismutase 1 (SOD1) action within non-neuronal cells is implicated in damage to spinal mot

188 st, synchronous spontaneous activity between non-neuronal cells is mediated more locally.

189 MP levels in both dissociated neurons and in non-neuronal cells, isoproterenol significantly stimulat

190 uR6D and GluR6E are exclusively expressed in non-neuronal cells, it is likely that these receptor sub

191 On the other hand, inactivation of TTP in non-neuronal cells leads to dramatic upregulation of mul

192 cell types (a number of neuronal as well as non-neuronal cell lineages) are generated at characteris

193 s by a mechanism quite distinct from that of non-neuronal cell lines and emphasize the importance of

194 lencer reduced promoter activity in glia and non-neuronal cell lines by two- to threefold, was withou

195 In PC6-3 cells, but not non-neuronal cell lines, Bgamma specifically promoted lo

196 non-denaturing conditions from neuronal and non-neuronal cell lines, brain tissue and living human c

197 nce transcription from neuronal promoters in non-neuronal cell lines, but its function during normal

198 In immortalized non-neuronal cell lines, SMN has been shown to form a ri

199 regulate UBQLN1 in a variety of neuronal and non-neuronal cell lines.

200 n control of expression between neuronal and non-neuronal cell lines.

201 the A2V mutant confirming earlier data from non-neuronal cell lines.

202 tested AR-12 in prion infected neuronal and non-neuronal cell lines.

203 IL-1-induced c-fos mRNA-positive cells were non-neuronal cells located in barrier regions of the bra

204 Non-neuronal cells may be pivotal in neurodegenerative d

205 In analogy to non-neuronal cells, metalloproteinases (ADAM10/17) are i

206 eral investigations support the concept that non-neuronal cells (microglia, astroglia, oligodendrogli

207 Modulation of P2X7 receptors in non-neuronal cells might have impact on peripheral senso

208 ry factors dynactin and LIS1 in neuronal and non-neuronal cell migration.

209 nhibits axonal extension, but does not alter non-neuronal cell morphology.

210 e TRPA1 channels heterologously expressed in non-neuronal cells, mouse neurons and zebrafish neurons

211 In motile non-neuronal cells, myosin-II binds and exerts force upo

212 In non-neuronal cells, neuron-restrictive silencer factor (

213 Glial cells comprise most of the non-neuronal cells of the brain and peripheral nervous s

214 l interactions between neurons and glia, the non-neuronal cells of the nervous system.

215 ocal signaling pathways between neuronal and non-neuronal cells offer new opportunities for disease m

216 lls, can consist of a mixture of neurons and non-neuronal cells, only neurons, or only non-neuronal c

217 l alpha subunits heterologously expressed in non-neuronal cells or natively expressed in a murine neu

218 Neuronal and non-neuronal cells overexpressing green fluorescent prot

219 xagonal bundles in neurite-like processes in non-neuronal cells overexpressing Tau, cell-free reconst

220 ma cells expressing endogenous Tau, in human non-neuronal cells overexpressing wild-type Tau, and in

221 alpha7 is also expressed in non-neuronal cells, particularly immune cells, where it

222 cally required in the gut endoderm tissue, a non-neuronal cell population, where it mediates adhesion

223 ecognized, nonsynaptic functions in specific non-neuronal cell populations in the nervous system.

224 ithelial Bowman's gland acinar cells, two OE non-neuronal cell populations involved with inhalant bio

225 euron development, we suggest that these two non-neuronal cell populations might play an important ro

226 and maturation of a variety of neuronal and non-neuronal cell populations, including those involved

227 In contrast, there was no increase in the non-neuronal cell populations.

228 he motor neurons, without contamination from non-neuronal cells present in CNS.

229 ectonically defined clusters of degenerating non-neuronal cells, probably astrocytes, were found.

230 blast cell were frequently duplicated, while non-neuronal cells produced by the posterior daughter ce

231 egular exercise training induces significant non-neuronal cell proliferation in the hypothalamus of o

232 Furthermore, ectopic expression of Shep1 in non-neuronal cells promotes cell migration through a col

233 ous system signaling, AChE can also modulate non-neuronal cell properties, although it remains contro

234 In non-neuronal cells, protein phosphatase 5 (PP5) has been

235 Infected non-neuronal cells release neurotoxic factors such as th

236 Overexpression of functional NMDAR in non-neuronal cells results in cell death by excitotoxici

237 matidia, while ectopic expression of Dip3 in non-neuronal cells results in photoreceptor loss.

238 rier in mice and signal to both neuronal and non-neuronal cells (see the related article beginning on

239 Studies in non-neuronal cells show that c-Jun N-terminal kinases (J

240 ationic currents by P2X receptor agonists in non-neuronal cells showed a rank order of BzATP > ATP >

241 Non-neuronal cells showed clear transcriptional response

242 In contrast to previous data on non-neuronal cells showing an MHC-evoked increase in cal

243 In non-neuronal cells, SIRT2 has been shown to function as

244 of RanBPM cooperates with PlexinA1 to reduce non-neuronal cell spreading and strongly inhibit axonal

245 trafficking have been studied extensively in non-neuronal cells such as fibroblasts and significant a

246 Accumulating evidence suggests that non-neuronal cells such as immune cells, glial cells, ke

247 Display events are much rarer in non-neuronal cells, such as fibroblasts and astrocytes.

248 ed vesicles formed at the plasma membrane of non-neuronal cells suggesting that an auxilin homolog ma

249 ate a hypoxia signal transduction pathway in non-neuronal cells that culminates in the stabilization

250 n drive promoter activity in a wide range of non-neuronal cells that express little or no endogenous

251 etic modifications that are distinct between non-neuronal cells that give rise to neurons and those t

252 Thus, the destruction of both neurons and non-neuronal cells that is caused by MeBr activates two

253 e LNv cells appear to target a population of non-neuronal cells that resides at the base of the eye.

254 ollectively demonstrate that, in contrast to non-neuronal cells, the apoptotic activity of p53 in pos

255 in-coupled receptor subtypes activate ERK in non-neuronal cells, the coupling of G(i/o) to ERK is tig

256 udies point to a significant contribution by non-neuronal cells, the glia--especially astrocytes and

257 hat neuronal MTs are more stable than MTs in non-neuronal cells, the molecular mechanisms underlying

258 In both neurons and non-neuronal cells, the PTC caused substantial loss of m

259 In non-neuronal cells, the PTP has been implicated as a Ca2

260 often-stuttering behavior of single pores in non-neuronal cells, through which small molecules trickl

261 Direct reprogramming of non-neuronal cells to generate new neurons is a promisin

262 NIPA1 localized in transfected neuronal and non-neuronal cells to the Golgi complex, a subset of syn

263 ted by the Akt/GSK3beta signaling cascade in non-neuronal cells to trigger rapid, dysregulated CME.

264 tanding the cellular actions of MCH by using non-neuronal cells transfected with the MCH receptor gen

265 ted that MCH activated potassium channels in non-neuronal cells transfected with the MCH receptor gen

266 Here we show that unlike in non-neuronal cells, Tsc2-deficient neurons have increase

267 Whether non-neuronal cells tune touch receptors through active o

268 ain are propagated faithfully in this single non-neuronal cell type.

269 everely abnormal nuclear membranes, although non-neuronal cell types appear normal.

270 o the toxic accumulation of PAP in yeast and non-neuronal cell types in mice [4, 5].

271 We examined the major non-neuronal cell types in the CNS for expression of TLR

272 Enteric glia also interact with various non-neuronal cell types in the gut wall such as enterocy

273 ence that in different species, glial cells, non-neuronal cell types in the nervous system are crucia

274 zonal expression profiles of proteins among non-neuronal cell types of the olfactory mucosa.

275 ro induces Parkin-mediated mitophagy in many non-neuronal cell types or neuronal cell lines.

276 ons, and differentiated PC-12 cells, but not non-neuronal cell types or undifferentiated PC-12 cells.

277 ngevity, and activate the UPR(ER) in distal, non-neuronal cell types through a cell-nonautonomous mec

278 the contributions of different neuronal and non-neuronal cell types to hypothalamic inflammatory pro

279 Both neuronal and non-neuronal cell types transfected with casp-9-CTD were

280 A few non-neuronal cell types were detected, including microgl

281 to examine the distribution of neuronal and non-neuronal cell types within and surrounding layer I n

282 he P2Y(1) receptor was not detected in other non-neuronal cell types.

283 L associations, were unexpectedly present in non-neuronal cell types.

284 inhibiting transcription in a wide range of non-neuronal cell types.

285 in the vagal ganglia was likely derived from non-neuronal cell types.

286 OMC mRNA and precursor protein expression in non-neuronal cells varies to a great degree as to the ex

287 ription of numerous neuron-specific genes in non-neuronal cells via recruitment of two independent hi

288 ne-rich domains), which induces apoptosis in non-neuronal cells via the cytosolic/mitochondrial pathw

289 r of MAPK/ERK and androgens activate CREB in non-neuronal cells, we investigated whether androgens ac

290 In contrast to non-neuronal cells, we now report that in neurons Bif-1

291 In contrast to non-neuronal cells, we show here that the ICP4 locus cas

292 ty was effective in cultured muscle, whereas non-neuronal cells were agrin insensitive.

293 ripheral "olfactory organ." NADPH-d-reactive non-neuronal cells were detected in the periphery and we

294 To study this neuronal and non-neuronal cells were transfected with either wild typ

295 ancer cells, whereas 7% of the REST peaks in non-neuronal cells were ubiquitously called and <25% wer

296 Past studies did not consider the role of non-neuronal cells, which are now known to play an impor

297 indirect mechanism of action for Bk via the non-neuronal cells, which may perform a nociceptive role

298 d high, persistent reporter gene activity in non-neuronal cells while an independent expression casse

299 lacZ reporter was predominantly expressed in non-neuronal cells, with only 29% co-expression with CGR

300 xpression of the dopaminergic D2 receptor in non-neuronal cells within the brain.