ライフサイエンスコーパス: oligodendrocyte progenitor cell

1 require technologies to generate functional oligodendrocyte progenitor cells.

2 lates cell cycle exit and differentiation in oligodendrocyte progenitor cells.

3 otential for recovery mediated by endogenous oligodendrocyte progenitor cells.

4 O mice revealed a specific deficit of NG2(+) oligodendrocyte progenitor cells.

5 s have dramatically increased numbers of CNS oligodendrocyte progenitor cells.

6 mmunocytochemically for oligodendrocytes and oligodendrocyte progenitor cells.

7 white matter is synthesized by proliferating oligodendrocyte progenitor cells.

8 ransplantation or manipulation of endogenous oligodendrocyte progenitor cells.

9 hondroitin sulfate proteoglycan expressed by oligodendrocyte progenitor cells.

10 tors of proliferation and differentiation of oligodendrocyte progenitor cells.

11 ns and mice, between reactive astrocytes and oligodendrocyte progenitor cells.

12 ves differentiation of oligodendrocytes from oligodendrocyte progenitor cells.

13 mote production of new oligodendrocytes from oligodendrocyte progenitor cells.

14 tire CNS after they have differentiated from oligodendrocyte progenitor cells.

15 ouse for voltage-operated Ca(2+) channels in oligodendrocyte progenitor cells.

16 mouse pluripotent epiblast stem-cell-derived oligodendrocyte progenitor cells.

17 ndent on the survival and differentiation of oligodendrocyte progenitor cells.

18 of betaT4-positive cells with A2B5-positive oligodendrocyte progenitor cells after transplantation (

19 peroxia showed a reduced capacity to protect oligodendrocyte progenitor cells against the toxic effec

20 We show a human-specific increase of oligodendrocyte progenitor cells and a decrease of matur

21 e of the TUJ-1-positive cells, A2B5-positive oligodendrocyte progenitor cells and A2B5-negative cells

22 by an expression pattern resembling that of oligodendrocyte progenitor cells and carries a distincti

23 and in our studies, primary cultures of both oligodendrocyte progenitor cells and differentiating oli

24 Both parenchymal oligodendrocyte progenitor cells and endogenous adult ne

25 he cellular factors involved in apoptosis of oligodendrocyte progenitor cells and oligodendrocytes, a

26 r for cell proliferation), NG2 (a marker for oligodendrocyte progenitor cells) and brain-derived neur

27 ind strong spatial segregation of microglia, oligodendrocyte progenitor cells, and astrocytes.

28 cific regulatory changes were accelerated in oligodendrocyte progenitor cells, and we highlight key b

29 Moreover, we showed that CNS oligodendrocyte progenitor cells are activated following

30 In the developing spinal cord, early oligodendrocyte progenitor cells are induced from the ve

31 Oligodendrocyte progenitor cells are stem cells in the c

32 ation that human embryonic stem cell-derived oligodendrocyte progenitor cells are susceptible to JC v

33 nical translation: first, transplantation of oligodendrocyte progenitor cells as a means of treating

34 vides direct evidence that targeting EGFR in oligodendrocyte progenitor cells at a specific time afte

35 However, myosin-1d was undetectable in oligodendrocyte progenitor cells at early and late time

36 alphavveta3 integrin may play in regulating oligodendrocyte progenitor cell behaviour, cells of the

37 pression of syntaxin 4 but not syntaxin 3 in oligodendrocyte progenitor cells but not immature oligod

38 PIKE-L expression is up-regulated when oligodendrocyte progenitor cells commit to differentiati

39 Both oligodendrocyte progenitor cell commitment and oligodend

40 strates a unique role for Olig1 in promoting oligodendrocyte progenitor cell commitment, differentiat

41 nriched for astrocytes, oligodendrocytes and oligodendrocyte progenitor cells containing the genes C4

42 mportant roles for Sox17 in controlling both oligodendrocyte progenitor cell cycle exit and different

43 nal LB supplementation promoted neuronal and oligodendrocyte progenitor cell development.

44 and constitutive ablation of NR1 in neonatal oligodendrocyte progenitor cells did not interrupt their

45 ous system (CNS) most often is the result of oligodendrocyte progenitor cells differentiating into my

46 elevant, FDA-approved compounds that promote oligodendrocyte progenitor cell differentiation and indu

47 Treg directly promoted oligodendrocyte progenitor cell differentiation and myel

48 endrocyte lineage cells completely inhibited oligodendrocyte progenitor cell differentiation and myel

49 CN3 is a matricellular protein that promotes oligodendrocyte progenitor cell differentiation and myel

50 tory supernatants also resulted in decreased oligodendrocyte progenitor cell differentiation without

51 also explore the effect of these changes on oligodendrocyte progenitor cell differentiation, which i

52 se activity is upregulated very early during oligodendrocyte progenitor cell differentiation.

53 myelin debris, which contains inhibitors of oligodendrocyte progenitor cell differentiation.

54 d neither a direct nor an indirect impact on oligodendrocyte progenitor cell differentiation.

55 enhancer (PIKE) expression by shRNA prevents oligodendrocyte progenitor cell differentiation.

56 romote remyelination by enhancing endogenous oligodendrocyte progenitor cells differentiation and by

57 NS cells expressing A2B5, an early marker in oligodendrocytes progenitor cell differentiation as well

58 ess and promotes precocious neurogenesis and oligodendrocyte progenitor cell elaboration.

59 cortex regions, while excitatory neurons and oligodendrocyte progenitor cells emerged as the major ce

60 We have previously shown that oligodendrocyte progenitor cells exhibit developmental s

61 TACE deficiency in oligodendrocyte progenitor cells following demyelination

62 brinogen inhibits nerve repair by preventing oligodendrocyte progenitor cells from differentiating in

63 Studies with oligodendrocyte progenitor cells from INK4a-/- mice indi

64 In purified cerebellar oligodendrocyte progenitor cells, glutamate receptor ago

65 56 regulates cortical lamination, whereas in oligodendrocyte progenitor cells, GPR56 controls develop

66 arative capabilities, and transplantation of oligodendrocyte progenitor cells, have generated substan

67 We discover sub-populations of human oligodendrocyte progenitor cells (hOPCs) including a pot

68 minimally invasive delivery of primary human oligodendrocyte progenitor cells (hOPCs) to the brain of

69 Oligodendrocyte progenitor cells identified by mAb A2B5

70 ely, from proliferating local astrocytes and oligodendrocyte progenitor cells in adult mice of both s

71 cal studies revealed that the recruitment of oligodendrocyte progenitor cells in response to demyelin

72 us studies have suggested the persistence of oligodendrocyte progenitor cells in the adult mammalian

73 e fifth major cell population that serves as oligodendrocyte progenitor cells in the postnatal CNS.

74 eration of human oligodendrocytes from human oligodendrocyte progenitor cells in vitro.

75 e-cell population is relatively enriched for oligodendrocyte-progenitor cells in the cortex versus th

76 Apoptosis of oligodendrocyte progenitor cells induced by growth facto

77 ly tune axonal diameter, promote re-entry of oligodendrocyte progenitor cells into the cell cycle, or

78 netic nanoparticles, and transplanted tagged oligodendrocyte progenitor cells into the spinal cord of

79 Generation of induced oligodendrocyte progenitor cells (iOPCs) from somatic fi

80 se embryonic and lung fibroblasts to induced oligodendrocyte progenitor cells (iOPCs) using sets of e

81 a novel mechanism by which proliferation of oligodendrocyte progenitor cells is regulated in the pos

82 er cell metabolic crosstalk during proneural/oligodendrocyte progenitor cell-like to mesenchymal-like

83 process formation were also inhibited in the oligodendrocyte progenitor cell line CG-4 after suppress

84 We show that oligodendrocyte progenitor cell lineage-associated GBMs

85 of transplanted cells co-labeled for NG2, an oligodendrocyte progenitor cell marker, but not for neur

86 urons and astrocytes remains the same, early oligodendrocyte progenitor cell markers are decreased in

87 As shown recently, failure in oligodendrocyte progenitor cell maturation contributes t

88 this mild inflammatory environment promotes oligodendrocyte progenitor cells maturation and myelin r

89 of an early oligodendrocytic promoter, these oligodendrocyte progenitor cells may be extracted and pu

90 on rather than uncontrolled proliferation of oligodendrocyte progenitor cells may have important impl

91 Endogenous oligodendrocyte progenitor cells may represent a viable

92 aling in establishing a motile phenotype for oligodendrocyte progenitor cell migration in vivo and il

93 immature oligodendrocyte-lineage cells, with oligodendrocyte progenitor cells more vulnerable to inju

94 bient RNA removal, we detect rare, committed oligodendrocyte progenitor cells not annotated in most p

95 Oligodendrocyte progenitor cell number decreased with ag

96 Many physiologically important activities of oligodendrocyte progenitor cells (O-2A cells), including

97 g development of the central nervous system, oligodendrocyte progenitor cells (O-2A) undergo an order

98 al and mesenchymal glioblastoma, relative to oligodendrocyte progenitor cells (Oli-Neu).

99 ed to the expansion of genetically wild-type oligodendrocyte progenitor cells, oligodendrocyte differ

100 Nonproliferating oligodendrocyte progenitor cells, oligodendrocytes, and

101 compression on the function and survival of oligodendrocyte progenitor cells/oligodendrocytes and ax

102 e found that AXIN2 was expressed in immature oligodendrocyte progenitor cells (OLPs) in white matter

103 ze the effects of BCNU on clonal cultures of oligodendrocyte progenitor cells-one of the best-charact

104 Recently, we showed oligodendrocyte progenitor cell (OPC) accumulation and r

105 Ca(2+) channels and receptors that regulate oligodendrocyte progenitor cell (OPC) and oligodendrocyt

106 In oligodendrocyte progenitor cell (OPC) cultures, IL-11 re

107 udies of TBI victims demonstrate significant oligodendrocyte progenitor cell (OPC) death post TBI; an

108 d Ca(2+) channels (L-VOCCs) are required for oligodendrocyte progenitor cell (OPC) development, we ge

109 n by acting at several critical steps during oligodendrocyte progenitor cell (OPC) development.

110 The effect of olesoxime on oligodendrocyte progenitor cell (OPC) differentiation an

111 d increases both adult mouse and adult human oligodendrocyte progenitor cell (OPC) differentiation, i

112 Reduced Serpine2 expression enhances oligodendrocyte progenitor cell (OPC) differentiation, p

113 s is enough to restrict them to an exclusive oligodendrocyte progenitor cell (OPC) fate during differ

114 Intrinsic and extrinsic inhibition of oligodendrocyte progenitor cell (OPC) function contribut

115 Revealing unknown cues that regulate oligodendrocyte progenitor cell (OPC) function in remyel

116 he ventral telencephalon were generated, but oligodendrocyte progenitor cell (OPC) generation was sev

117 se (MAPK)-dependent pathway is implicated in oligodendrocyte progenitor cell (OPC) lineage progressio

118 reased microglial phagocytosis, and improved oligodendrocyte progenitor cell (OPC) maturation in kits

119 re infants results in inflammation, arrested oligodendrocyte progenitor cell (OPC) maturation, and re

120 multiple sclerosis (PPMS) failed to promote oligodendrocyte progenitor cell (OPC) maturation, wherea

121 ibute to remyelination failure by perturbing oligodendrocyte progenitor cell (OPC) maturation.

122 This work describes the role of oligodendrocyte progenitor cell (OPC) microRNAs (miRNAs)

123 two nf1 orthologs in zebrafish and show that oligodendrocyte progenitor cell (OPC) numbers are increa

124 We further showed that young CSF boosts oligodendrocyte progenitor cell (OPC) proliferation and

125 Oligodendrocyte death and oligodendrocyte progenitor cell (OPC) proliferation duri

126 We have previously demonstrated that oligodendrocyte progenitor cell (OPC) proliferation is c

127 Dysregulation of oligodendrocyte progenitor cell (OPC) recruitment and ol

128 Human oligodendrocyte progenitor cell (OPC) specification and

129 We show that inhibition of PDE4D boosts oligodendrocyte progenitor cells (OPC) differentiation a

130 Oligodendrocytes differentiate from oligodendrocyte progenitor cells (OPC) in early postnata

131 erived growth factor receptor alpha-positive oligodendrocyte progenitor cells (OPC) located within th

132 ervous system (CNS) cell types revealed that oligodendrocyte progenitor cells (OPC), the largest popu

133 sion, instead promoting the proliferation of oligodendrocyte progenitor cells (OPC).

134 on landscape shift during differentiation of oligodendrocyte-progenitor cells (OPC).

135 alpha)-expressing stromal cells derived from oligodendrocytes progenitor cells (OPC) were discovered

136 ntiate human embryonic stem cells (hESCs) to oligodendrocyte progenitor cells (OPCs) according to dev

137 Oligodendrocyte progenitor cells (OPCs) account for appr

138 nsequences of disrupting Fth iron storage in oligodendrocyte progenitor cells (OPCs) after demyelinat

139 se genes was measured in primary neurons and oligodendrocyte progenitor cells (OPCs) after inflammato

140 Microarray analysis in oligodendrocyte progenitor cells (OPCs) after Sox17 atte

141 Metformin rejuvenates adult rat oligodendrocyte progenitor cells (OPCs) allowing more ef

142 isruption of the syntenic insulator in mouse oligodendrocyte progenitor cells (OPCs) allows an OPC-sp

143 AMPA stimulation of cultured oligodendrocyte progenitor cells (OPCs) also caused an i

144 in vitro primary rat embryonic cell model of oligodendrocyte progenitor cells (OPCs) and a mouse N20.

145 ation at the same site, eventually depleting oligodendrocyte progenitor cells (OPCs) and exhausting t

146 overexpressing mice harbor enlarged pools of oligodendrocyte progenitor cells (OPCs) and show greater

147 hogenetic protein (BMP) signaling pathway in oligodendrocyte progenitor cells (OPCs) and suppresses r

148 expression in the developing CNS identifies oligodendrocyte progenitor cells (OPCs) and whose activa

149 , both the proliferation and total number of oligodendrocyte progenitor cells (OPCs) appeared normal

150 ination and why remyelination is absent when oligodendrocyte progenitor cells (OPCs) are present.

151 Oligodendrocyte progenitor cells (OPCs) are specified fr

152 ouse forebrain, temporally distinct waves of oligodendrocyte progenitor cells (OPCs) arise from diffe

153 In the postnatal brain, oligodendrocyte progenitor cells (OPCs) arise from the s

154 termination of proliferation determines when oligodendrocyte progenitor cells (OPCs) can initiate dif

155 Oligodendrocyte progenitor cells (OPCs) can repair demye

156 Remyelination by oligodendrocyte progenitor cells (OPCs) can restore thes

157 In the CNS, oligodendrocyte progenitor cells (OPCs) differentiate in

158 In these conditions, resident oligodendrocyte progenitor cells (OPCs) differentiate in

159 ular mechanisms that drive the maturation of oligodendrocyte progenitor cells (OPCs) during the remye

160 l myelinating glial cells, centrally derived oligodendrocyte progenitor cells (OPCs) ectopically exit

161 Here, we report that oligodendrocyte progenitor cells (OPCs) express function

162 fish, we observed that prior to myelination, oligodendrocyte progenitor cells (OPCs) extend processes

163 factor-1 (IGF-1) provides neuroprotection to oligodendrocyte progenitor cells (OPCs) following cerebr

164 y also be a radial component of migration of oligodendrocyte progenitor cells (OPCs) from a ventral s

165 Migration of oligodendrocyte progenitor cells (OPCs) from proliferati

166 mice also exhibited an increased density of oligodendrocyte progenitor cells (OPCs) in CNS white mat

167 Oligodendrocyte progenitor cells (OPCs) in demyelinated

168 er agents with prodifferentiative effects on oligodendrocyte progenitor cells (OPCs) in rodent models

169 e show that the expression of Sox2 occurs in oligodendrocyte progenitor cells (OPCs) in rodent models

170 fficulties in generating pure populations of oligodendrocyte progenitor cells (OPCs) in sufficient qu

171 filtrative cells mirrors that of uncommitted oligodendrocyte progenitor cells (OPCs) in the developin

172 ion, and may contribute to the production of oligodendrocyte progenitor cells (OPCs) in the dorsal co

173 Oligodendrocyte progenitor cells (OPCs) in the postnatal

174 of human embryonic stem cell (hESC)-derived oligodendrocyte progenitor cells (OPCs) into adult rat s

175 Differentiation of oligodendrocyte progenitor cells (OPCs) into mature olig

176 n obligatory step for the differentiation of oligodendrocyte progenitor cells (OPCs) into myelinating

177 in disorders can be treated by transplanting oligodendrocyte progenitor cells (OPCs) into the affecte

178 Differentiation and maturation of oligodendrocyte progenitor cells (OPCs) involve the asse

179 The activation and proliferation of oligodendrocyte progenitor cells (OPCs) is a necessary s

180 ment.SIGNIFICANCE STATEMENT The migration of oligodendrocyte progenitor cells (OPCs) is an essential

181 ted failure to produce oligodendrocytes from oligodendrocyte progenitor cells (OPCs) is associated wi

182 cal changes, while in developing neurons and oligodendrocyte progenitor cells (OPCs) it induces cellu

183 t impairs recruitment and differentiation of oligodendrocyte progenitor cells (OPCs) leading to faile

184 lutamatergic synapses onto adult-born NG2(+) oligodendrocyte progenitor cells (OPCs) migrating from t

185 expression of the Tf receptor (Tfr) gene in oligodendrocyte progenitor cells (OPCs) on mice of eithe

186 t oligodendrocytes, whether by transplanting oligodendrocyte progenitor cells (OPCs) or by mobilizing

187 n which Tsc1 is deleted by Cre expression in oligodendrocyte progenitor cells (OPCs) or in premyelina

188 Neonatal engraftment by oligodendrocyte progenitor cells (OPCs) permits the myel

189 Oligodendrocyte progenitor cells (OPCs) persist in human

190 We show how Sox2 is expressed in oligodendrocyte progenitor cells (OPCs) preparing to und

191 ination of the central nervous system (CNS), oligodendrocyte progenitor cells (OPCs) proliferate and

192 In experimental models, oligodendrocyte progenitor cells (OPCs) rather than prev

193 Oligodendrocyte progenitor cells (OPCs) recruited to dem

194 Oligodendrocyte progenitor cells (OPCs) that are positiv

195 White matter stroke stimulates adjacent oligodendrocyte progenitor cells (OPCs) to divide and mi

196 isoprenoid and cholesterol synthesis, causes oligodendrocyte progenitor cells (OPCs) to migrate past

197 Here we explore the contribution of oligodendrocyte progenitor cells (OPCs) to pathological

198 er, direct injection of neural stem cells or oligodendrocyte progenitor cells (OPCs) to the lesion si

199 in which we targeted Notch1 inactivation to oligodendrocyte progenitor cells (OPCs) using Olig1Cre a

200 ation by blocking the differentiation of rat oligodendrocyte progenitor cells (OPCs) via modulation o

201 osis, induces pathologic quiescence in human oligodendrocyte progenitor cells (OPCs) via upregulation

202 Many chronically demyelinated lesions have oligodendrocyte progenitor cells (OPCs) within their bor

203 system (CNS) multipotent stem cells known as oligodendrocyte progenitor cells (OPCs)(2).

204 and support cytocompatible encapsulation of oligodendrocyte progenitor cells (OPCs), as well as thei

205 mong three macroglial progenitor populations-oligodendrocyte progenitor cells (OPCs), astrocytes and

206 plaque-associated Olig2- and NG2-expressing oligodendrocyte progenitor cells (OPCs), but not astrocy

207 rect effects on the myelinating potential of oligodendrocyte progenitor cells (OPCs), in addition to

208 In oligodendrocyte progenitor cells (OPCs), Lrp1 is require

209 By leveraging primary oligodendrocyte progenitor cells (OPCs), microglia-deple

210 In cultured oligodendrocyte progenitor cells (OPCs), Sox17 levels we

211 tly characterized by scarce undifferentiated oligodendrocyte progenitor cells (OPCs), suggesting the

212 gene expression profiling on purified murine oligodendrocyte progenitor cells (OPCs), the remyelinati

213 rve conduction, and the ectopic migration of oligodendrocyte progenitor cells (OPCs), the resident my

214 rotein fibronectin perturb the maturation of oligodendrocyte progenitor cells (OPCs), thereby impedin

215 oliferation is not altered in Seh1-deficient oligodendrocyte progenitor cells (OPCs), they fail to di

216 t transferrin receptor (Tfr) specifically in oligodendrocyte progenitor cells (OPCs), we have establi

217 Since one role of NG2 glia is that of oligodendrocyte progenitor cells (OPCs), we investigated

218 Oligodendrocyte progenitor cells (OPCs), which different

219 cells produces first motor neurons and then oligodendrocyte progenitor cells (OPCs), which migrate,

220 and generate de novo synapses with recruited oligodendrocyte progenitor cells (OPCs), which, early af

221 ocytes and with a reduction in proliferating oligodendrocyte progenitor cells (OPCs).

222 most PLP-EGFP-expressing cells gave rise to oligodendrocyte progenitor cells (OPCs).

223 the generation of new oligodendrocytes from oligodendrocyte progenitor cells (OPCs).

224 modulator of intracellular Ca(2+) levels in oligodendrocyte progenitor cells (OPCs).

225 CSPG4/NG2 is a hallmark protein of oligodendrocyte progenitor cells (OPCs).

226 lay a fundamental role in the development of oligodendrocyte progenitor cells (OPCs).

227 glial-restricted progenitors cells, known as oligodendrocyte progenitor cells (OPCs).

228 cytes arise from migratory and proliferative oligodendrocyte progenitor cells (OPCs).

229 ult human forebrain contain large numbers of oligodendrocyte progenitor cells (OPCs).

230 h activity could promote formation of excess oligodendrocyte progenitor cells (OPCs).

231 ing the autocrine Wnt/B-catenin signaling in oligodendrocyte progenitor cells (OPCs).

232 ngent upon the successful differentiation of oligodendrocyte progenitor cells (OPCs).

233 ng glycosaminoglycan (GAG) catabolism within oligodendrocyte progenitor cells (OPCs).

234 tes within or near the anticodon compared to oligodendrocyte progenitor cells (OPCs).

235 brate astrocytes, oligodendrocytes (OL), and oligodendrocyte progenitor cells (OPCs).

236 PSCs into neural progenitor cells (NPCs) and oligodendrocyte progenitor cells (OPCs).

237 umorigenic cell line and primary cultures of oligodendrocyte progenitor cells (OPCs).

238 stem cells (NSCs) and to a lesser extent in oligodendrocyte progenitor cells (OPCs).

239 emyelination by impairing differentiation of oligodendrocyte progenitor cells (OPCs).

240 myelin and myelin repair by differentiating oligodendrocyte progenitor cells (OPCs).

241 iated neuroinflammation, and an expansion of oligodendrocyte progenitor cells (OPCs).

242 liferation, migration and differentiation of oligodendrocyte progenitor cells (OPCs).

243 ig1-Cre-expressing cells reduces the pool of oligodendrocyte progenitor cells (OPCs).

244 endent on recruitment and differentiation of oligodendrocyte progenitor cells (OPCs).

245 ation, proliferation, and differentiation of oligodendrocyte progenitor cells (OPCs).

246 the autocrine Wnt/beta-catenin signaling in oligodendrocyte progenitor cells (OPCs).

247 nated is crucial to our understanding of how oligodendrocyte progenitor cells (OPs) develop into myel

248 Proliferative oligodendrocyte progenitor cells (OPs) express large, de

249 Genetic deletion of TACE in oligodendrocyte progenitor cells (OPs) induces premature

250 els to selectively delete TACE expression in oligodendrocyte progenitors cells (OPs), we found that T

251 Parenchymal oligodendrocyte progenitor cells (pOPCs) are considered

252 mbryonic forebrain, developmentally distinct oligodendrocyte progenitor cell populations and their pr

253 migration, survival, and differentiation of oligodendrocyte progenitor cells, precursors to myelin-f

254 and altered F-actin spreading at the tips of oligodendrocyte progenitor cell processes.

255 In the absence of ERK1/ERK2 signaling NG2(+) oligodendrocyte progenitor cells proliferated and differ

256 signaling increases neurogenesis and reduces oligodendrocyte progenitor cell proliferation (OPC) in t

257 infiltrates and demyelination, and increased oligodendrocyte progenitor cell proliferation and BDNF+

258 Oligodendrocyte progenitor cell proliferation was observ

259 el blocker tetraethylammonium also inhibited oligodendrocyte progenitor cell proliferation.

260 uced myelin were examined for remyelination, oligodendrocyte progenitor cells, reactive astrocytes, a

261 On the other hand, it is possible that oligodendrocyte progenitor cells remain undifferentiated

262 Npc1(-/-) oligodendrocyte progenitor cells reproduce impaired matu

263 Differentiation of oligodendrocyte progenitor cells requires activation of

264 gh combined doses of oral antibiotics impair oligodendrocyte progenitor cell responses during remyeli

265 blish that deletion of mTORC2 signaling from oligodendrocyte progenitor cells results in reduced myel

266 lack expression of Timp1 do not support rat oligodendrocyte progenitor cell (rOPC) differentiation,

267 enriched population of cells expressing the oligodendrocyte progenitor cell-specific marker NG2.

268 noted because Nkx2.2 promotes maturation of oligodendrocyte progenitor cells specified by expression

269 sis, remyelination can fail despite abundant oligodendrocyte progenitor cells, suggesting impairment

270 d with a truncated proliferative response of oligodendrocyte progenitor cells, suggesting that deplet

271 /or indirectly (via astrocytes) impact human oligodendrocyte progenitor cell survival and differentia

272 to eightfold greater number of proliferating oligodendrocyte progenitor cells than did wild-type (wt)

273 Solicitation of endogenous oligodendrocytes progenitor cells, the precursor of olig

274 w that miconazole and clobetasol function in oligodendrocyte progenitor cells through mitogen-activat

275 ibility of human embryonic stem cell-derived oligodendrocyte progenitor cells to infection with JC vi

276 y changes during the transition from A2B5(+) oligodendrocyte progenitor cells to premyelinating GalC(

277 man adult brain-derived oligodendrocytes and oligodendrocyte progenitor cells under conditions of met

278 Whereas LINGO-1 expressed by oligodendrocyte progenitor cells was previously identifi

279 ds for enhancing myelination from endogenous oligodendrocyte progenitor cells, we screened a library

280 two populations of NG2 proteoglycan-positive oligodendrocyte progenitor cells were identified that ex

281 Oligodendrocyte progenitor cells were not decreased in d

282 se developing axon-free nerves, 25 to 33% of oligodendrocyte progenitor cells were proliferating.

283 rability of O4+ preoligodendrocytes, whereas oligodendrocyte progenitor cells were resistant to insul

284 Oligodendrocyte progenitor cells were the cell type with

285 o explore the mechanism of redistribution of oligodendrocyte progenitor cells with compensatory myeli

286 S immune milieu and concurrent activation of oligodendrocyte progenitor cells with subsequent remyeli

287 ng inflammatory injury, oligodendrocytes and oligodendrocyte progenitor cells within lesion sites are