ライフサイエンスコーパス: ganglionic

1 eceptor was most frequent (78%), followed by ganglionic acetylcholine receptor (20%), voltage-gated K

2 Ganglionic acetylcholine receptor antibodies can be asso

3 rently recognized as biomarkers of AGID, the ganglionic acetylcholine receptor autoantibody is the on

4 disorder associated with antibodies against ganglionic acetylcholine receptors.

5 ptor, muscarinic-2 receptors, AChR-nicotinic ganglionic alpha-3 receptors and calcium channels (N and

6 t showed >10 muM binding affinity toward the ganglionic alpha3beta4 receptor apart from showing selec

7 e action of 17 analogues of PhTX-343 against ganglionic (alpha3beta4) and brain (alpha4beta2) nAChRs

8 It is organized in ridges of ganglionic and molecular layers, oriented perpendicular

9 Ganglionic and myocardial nerve sprouting and nerve dens

10 segment (L2-L5) and regions (preganglionic, ganglionic and postganglionic).

11 attached to cell surfaces of Vero cells and ganglionic axons in cell culture as efficiently as wild-

12 axotomy (transection) or injury of the post-ganglionic axons.

13 (reduction in intra-arterial BP during acute ganglionic blockade [GB] with intravenous trimethaphan)

14 Ganglionic blockade abolished the PVN-induced responses

15 KO did not change the heart rate response to ganglionic blockade and exercise.

16 cardiorespiratory effects were prevented via ganglionic blockade and were enhanced in chronic heart f

17 en NG2KO and control islets was abolished by ganglionic blockade or by weaning the mice on a carbohyd

18 Elimination of SNA by ganglionic blockade produced a larger fall in MAP in rat

19 ase in mean arterial pressure in response to ganglionic blockade was higher in PTP1B knockout mice (-

20 Ganglionic blockade with hexamethonium caused greater fa

21 We conclude that during ganglionic blockade, the SVR response to systemic ADRB2

22 e to ADRB2 agonist terbutaline (Terb) during ganglionic blockade.

23 eduction in arterial pressure in response to ganglionic blockade.

24 sis, seven individuals were infused with the ganglionic blocker trimetaphan before and after an 8 h e

25 cardiopulmonary changes after treatment with ganglionic blocker.

26 1 stimulation was eliminated by splenectomy, ganglionic-blocker administration or beta2-adrenergic re

27 eptibility depended on injury of central pre-ganglionic but not peripheral postganglionic sympathetic

28 referentially expressed on highly functional ganglionic CD8(+) T cells during acute and latent HSV-1

29 rs driving the infiltration and retention of ganglionic CD8s, we examined several HSV recombinants th

30 yed expressions in ganglia suggest that most ganglionic cells retain their proliferative capacities a

31 coexpresses Id2 and ENH in the cytoplasm of ganglionic cells.

32 P-mediated insulin release by activating non-ganglionic cholinergic neurons that innervate the islets

33 stem, with the majority of axons confined to ganglionic connectives and commissures, suggesting a cen

34 no differences in viral load at dorsal root ganglionic (DRG) neurons at day 4 postinfection (p.i.) f

35 We show that dorsal root ganglionic (DRG) neurons produced little type I IFNs in

36 m medial ganglionic eminence (MGE) or caudal ganglionic eminence (CGE) progenitors.

37 bset of NGCs lacking nNOS arises from caudal ganglionic eminence (CGE) progenitors.

38 died; however, so far the role of the caudal ganglionic eminence (CGE), a posterior subpallial domain

39 the lateral ganglionic eminence (LGE) caudal ganglionic eminence (CGE), and septum, including loss of

40 In the hippocampal CA1, caudal ganglionic eminence (CGE)-derived interneurons are recru

41 lionic eminence (MGE)-derived but not caudal ganglionic eminence (CGE)-derived interneurons.

42 within the ventral telencephalon, the caudal ganglionic eminence (CGE).

43 interneurons that originate from the caudal ganglionic eminence (CGE).

44 t integration of INs derived from the caudal ganglionic eminence (CGE).

45 that the ITCs arise from the dorsal lateral ganglionic eminence (dLGE) and migrate in the lateral mi

46 We found that dorsal lateral ganglionic eminence (dLGE)-derived olfactory bulb intern

47 ncer (Dlx5/6ei) in embryonic day 13.5 medial ganglionic eminence (E13.5 MGE).

48 the progenitor zones in the pallium, lateral ganglionic eminence (LGE) and medial ganglionic eminence

49 f3 in the subventricular zone of the lateral ganglionic eminence (LGE) at embryonic day 13.5 may unde

50 tion phenotypes, particularly in the lateral ganglionic eminence (LGE) caudal ganglionic eminence (CG

51 ere we report that activin A induces lateral ganglionic eminence (LGE) characteristics in nascent neu

52 essed in neuronal progenitors of the lateral ganglionic eminence (LGE) in the ventral telencephalon.

53 The embryonic lateral ganglionic eminence (LGE) is thought to be the site of o

54 tinct neuronal subtypes derived from lateral ganglionic eminence (LGE) progenitors at specific embryo

55 es neural progenitor identity in the lateral ganglionic eminence (LGE), despite upregulating the neur

56 rgic interneurons (GABA INs), or the lateral ganglionic eminence (LGE), which generate GABA INs that

57 d such that they acquire a subset of lateral ganglionic eminence (LGE)-specific properties at the exp

58 direct pathways are generated in the lateral ganglionic eminence (LGE).

59 ity defined by their position in the lateral ganglionic eminence (LGE).

60 that the first OLPs originate in the medial ganglionic eminence (MGE) and anterior entopeduncular ar

61 precursors--including those from the medial ganglionic eminence (MGE) and OB--fail to generate neuro

62 Progenitor cells in the medial ganglionic eminence (MGE) and preoptic area (PoA) give r

63 ortical) telencephalon, including the medial ganglionic eminence (MGE) and preoptic area.

64 rupts interneuron neurogenesis in the medial ganglionic eminence (MGE) and, more importantly, that es

65 hermore, Nkx2.1(+) progenitors in the medial ganglionic eminence (MGE) are misspecified such that the

66 terneuron precursors derived from the medial ganglionic eminence (MGE) can induce a second period of

67 ed GABAergic precursor cells from the medial ganglionic eminence (MGE) can migrate and differentiate

68 gic progenitor cells derived from the medial ganglionic eminence (MGE) can reverse mechanical hyperse

69 Embryonic medial ganglionic eminence (MGE) cells transplanted into the ad

70 en described, a system modeling human medial ganglionic eminence (MGE) development, a critical ventra

71 itory interneuron precursors from the medial ganglionic eminence (MGE) enhances GABAergic signaling i

72 In the developing telencephalon, the medial ganglionic eminence (MGE) generates many cortical and vi

73 The medial ganglionic eminence (MGE) gives rise to the majority of

74 lateral ganglionic eminence (LGE) and medial ganglionic eminence (MGE) in the subpallium has been wel

75 cursors of GABAergic neurons from the medial ganglionic eminence (MGE) into adult mouse spinal cord a

76 of precursor cells from the embryonic medial ganglionic eminence (MGE) into early postnatal neocortex

77 embryonic inhibitory neurons from the medial ganglionic eminence (MGE) into postnatal visual cortex m

78 GABAergic interneurons from the mouse medial ganglionic eminence (MGE) into the adult mouse spinal co

79 In the ventral telencephalon, the medial ganglionic eminence (MGE) is a major source of cortical

80 The medial ganglionic eminence (MGE) is an embryonic forebrain stru

81 report that mosaic elimination in the medial ganglionic eminence (MGE) of Smo, a key effector of SHH

82 urons targeting cells by lineage from medial ganglionic eminence (MGE) or caudal ganglionic eminence

83 show that Prdm16 expression in mouse medial ganglionic eminence (MGE) progenitors is required for ma

84 Caudally situated medial ganglionic eminence (MGE) progenitors receive high level

85 ) IvCs and NGCs are both derived from medial ganglionic eminence (MGE) progenitors under control of t

86 e the two major subtypes generated by medial ganglionic eminence (MGE) progenitors.

87 y, it resulted in a partial rescue of medial ganglionic eminence (MGE) properties, including interneu

88 ST(+)) interneuron (IN) production in medial ganglionic eminence (MGE) secondary progenitors in mice.

89 king ALK4 in GABAergic neurons of the medial ganglionic eminence (MGE) showed marked deficits in dist

90 2 in the ventricular zone (VZ) of the medial ganglionic eminence (MGE) using Olig2-Cre mice causes mo

91 several cIN subtypes derive from the medial ganglionic eminence (MGE), a transient ventral telenceph

92 ient embryonic structure known as the medial ganglionic eminence (MGE), but how the remarkable divers

93 rgic interneuron progenitors from the medial ganglionic eminence (MGE), can overcome the mechanical h

94 cid (GABA) interneurons, derived from medial ganglionic eminence (MGE), is implicated in disorders of

95 RNA sequencing on the mouse embryonic medial ganglionic eminence (MGE), the major birthplace for CINs

96 cycle regulation was examined in the medial ganglionic eminence (MGE), the major source of PV intern

97 BAergic precursors from the embryonic medial ganglionic eminence (MGE), the source of neocortical par

98 ortical interneurons originate in the medial ganglionic eminence (MGE), where the signaling molecule

99 eurons, but not by progenitors in the medial ganglionic eminence (MGE), which generate cortical GABAe

100 apoptosis is mediated by inputs from medial ganglionic eminence (MGE)-derived but not caudal ganglio

101 mbryos harboring tdTomato-fluorescent medial ganglionic eminence (MGE)-derived cortical GABAergic int

102 Interestingly, compared with medial ganglionic eminence (MGE)-derived cortical interneuron p

103 Medial ganglionic eminence (MGE)-derived GABAergic cortical int

104 or the differentiation of a subset of medial ganglionic eminence (MGE)-derived neurons, but are dispe

105 Medial ganglionic eminence (MGE)-derived somatostatin (SST)+ an

106 o telencephalic excitatory neurons or medial ganglionic eminence (MGE)-like inhibitory neurons.

107 Medial ganglionic eminence (MGE)-like interneuron precursors de

108 irected differentiation of hPSCs into medial ganglionic eminence (MGE)-like progenitors and their mat

109 of immature neurons derived from the medial ganglionic eminence (MGE).

110 e embryonic subpallium, including the medial ganglionic eminence (MGE).

111 ortical interneurons generated in the medial ganglionic eminence (MGE).

112 enitors that primarily resides in the medial ganglionic eminence (MGE).

113 s, including those originating in the medial ganglionic eminence (MGE).

114 rneurons (CINs) that originate in the medial ganglionic eminence (MGE).

115 enitor cells from embryonic medial or caudal ganglionic eminence (MGE, CGE) were made in a well-chara

116 rived from the cortical anlage (CTXOE03) and ganglionic eminence (STROC05), as well as an adult EC li

117 re as the homologue of the mammalian lateral ganglionic eminence (the adult caudatoputamen in mammals

118 ere as the homologue of the mammalian medial ganglionic eminence (the adult pallidum in mammals).

119 lantation of cells from the embryonic medial ganglionic eminence (the major origin of cerebral cortic

120 m progenitors located in the ventral lateral ganglionic eminence (vLGE).

121 urons, are generated from the ventral medial ganglionic eminence and dorsal preoptic area based on fa

122 for inhibitory cells derived from the medial ganglionic eminence and few expressed VGAT, found in GAB

123 odeoxyuridine (BrdU) labeling in the lateral ganglionic eminence and frontal cortical neuroepithelium

124 al glial progenitors in the embryonic medial ganglionic eminence and preoptic area preferentially dev

125 p, develops domains equivalent to the medial ganglionic eminence and rhombic lip, resembling the gnat

126 The lateral ganglionic eminence and rostral migratory stream develop

127 an increase in cell death within the lateral ganglionic eminence and rostral migratory stream.

128 racteristics are found in the dorsal lateral ganglionic eminence and ventrolateral palliumembryonic r

129 (CIG)) mice, conditionally deleting Arx from ganglionic eminence derived neurons including cortical i

130 each of which labels a subset of GABAergic, ganglionic eminence derived neurons.

131 , whereas ventral neuronal specification and ganglionic eminence development in the Shh(N/-) telencep

132 om common precursors generated in the medial ganglionic eminence during embryogenesis.

133 The medial ganglionic eminence exhibited unique patterns of progeni

134 forebrain progenitors of the dorsal lateral ganglionic eminence from Pax6 mutant Small Eye (Pax6(Sey

135 tering, and markers revealed that the caudal ganglionic eminence generated a greater proportion of co

136 dicate that the volumes of basal ganglia and ganglionic eminence increase along with that of the whol

137 Transplanting medial ganglionic eminence interneuron progenitors to introduce

138 -type embryonic interneurons from the medial ganglionic eminence into the prefrontal cortex of neonat

139 architecture of the human SVZ at the lateral ganglionic eminence late in the second trimester of deve

140 nd ectopic persistence of the dorsal lateral ganglionic eminence marker Sp8.

141 he anterior entopeduncular area-basal medial ganglionic eminence of mammals).

142 In addition, unlike in the ganglionic eminence of the embryonic forebrain where Oli

143 rototypic GPe neurons derive from the medial ganglionic eminence of the embryonic subpallium and expr

144 n of pulvinar neurons has been observed, the ganglionic eminence of the telencephalon.

145 d then patterned to NKX2.1-expressing medial ganglionic eminence progenitors by simple treatment with

146 embryonic inhibitory neurons from the medial ganglionic eminence reinstate ocular dominance plasticit

147 ibitory interneurons derived from the medial ganglionic eminence represent the largest cohort of GABA

148 rast with the cortex, most stem cells in the ganglionic eminence SVZ did not maintain radial fibers o

149 restricted to neural progenitor cells in the ganglionic eminence that are fated to differentiate into

150 ring their migration from the dorsal lateral ganglionic eminence through maturity.

151 pment, interneurons migrate from the ventral ganglionic eminence to the cerebral cortex within severa

152 neurons, from their generation in the medial ganglionic eminence up to their settlement in the AC, ex

153 Enforced collapse of ganglionic eminence vessels and resultant periventricula

154 everely impaired proliferation in the medial ganglionic eminence without grossly altering differentia

155 only RG cells isolated from the subpallium (ganglionic eminence) generate CalR(+) or GABA(+) cells,

156 ented novel genetic evidence that the caudal ganglionic eminence, a distinct subpallial progenitor zo

157 uroepithelium had hemorrhages in the cortex, ganglionic eminence, and thalamus, as well as abnormal v

158 nterneurons that are derived from the medial ganglionic eminence, as most studies have examined this

159 between intermediate zones of the thalamus, ganglionic eminence, hypothalamus, and cortical preplate

160 kx2.1, which is expressed only in the medial ganglionic eminence, is not.

161 erative areas examined: embryonic neocortex, ganglionic eminence, midbrain, retina, hindbrain, and sp

162 ogenitors, derived from the embryonic medial ganglionic eminence, migrate long distances following tr

163 lls within the caudate nucleus adjoining the ganglionic eminence, potentially a waiting compartment.

164 In the medial ganglionic eminence, the NKX2-1 transcription factor con

165 iption factors normally found in the lateral ganglionic eminence, to prevent precocious differentiati

166 The PL develops next to the caudal ganglionic eminence, which generates inhibitory interneu

167 We deleted mouse Nf1 from the medial ganglionic eminence, which gives rise to both oligodendr

168 Our findings establish ganglionic eminence-dependent rules for early synaptic i

169 tly expressed in the prethalamus and lateral ganglionic eminence-derived corridor and on corticofugal

170 ta suggest that Satb1 is required for medial ganglionic eminence-derived interneuron differentiation,

171 ates the differentiation of two major medial ganglionic eminence-derived interneuron populations and

172 revealed that O-LM cells parse into a caudal ganglionic eminence-derived subpopulation expressing 5-H

173 5-HT(3A) receptors (5-HT(3A)Rs) and a medial ganglionic eminence-derived subpopulation lacking 5-HT(3

174 nversion of some MGE progenitors to a caudal ganglionic eminence-like, bipolar calretinin-expressing

175 ls within the ventricular zone of the medial ganglionic eminence.

176 terneurons derived from the embryonic medial ganglionic eminence.

177 ibits cell migration from the MGE and caudal ganglionic eminence.

178 cell subpopulation derived from the lateral ganglionic eminence.

179 rn MSNs within their birthplace, the lateral ganglionic eminence.

180 that originate developmentally in the caudal ganglionic eminence.

181 cephalic ventricular zone and not the medial ganglionic eminence.

182 liferation of interneuron progenitors in the ganglionic eminence.

183 sion of Nkx2-1 leads to a loss of the medial ganglionic eminence.

184 essed later in the forebrain itself (lateral ganglionic eminence; LGE) starting at E12.5, suggesting

185 ity arising from either the caudal or medial ganglionic eminences (CGE and MGE).

186 eral ganglionic eminences (LGEs), and caudal ganglionic eminences (CGEs) between preterm-born [born o

187 ortical interneurons (CINs) originate in the ganglionic eminences (GEs) and migrate tangentially to t

188 wave of OLPs from the lateral and/or caudal ganglionic eminences (LGE and CGE).

189 ion of progenitors in the lateral and medial ganglionic eminences (LGE and MGE).

190 medial ganglionic eminences (MGEs), lateral ganglionic eminences (LGEs), and caudal ganglionic emine

191 lly expressed ventrally in the telencephalic ganglionic eminences (Mash1, Dlx2 and Gsh2) are upregula

192 igin in the embryo from the medial or caudal ganglionic eminences (MGE and CGE).

193 nic lineage from either the medial or caudal ganglionic eminences (MGE and CGE).

194 fate-mapping of the mouse medial and caudal ganglionic eminences (MGE and CGE, respectively), from w

195 ared interneuronal progenitors in the medial ganglionic eminences (MGEs), lateral ganglionic eminence

196 lation of Dlx1/2 genes in the ventral medial ganglionic eminences and adjacent regions of the septum,

197 We characterized the developing human ganglionic eminences and found that the subventricular z

198 tion and ERK signaling in progenitors of the ganglionic eminences and had fewer SST(+) and VIP(+) int

199 thalamus, parts of the hypothalamus, and the ganglionic eminences and their derivatives in the subpal

200 V)-expressing cells, are born in the ventral ganglionic eminences during mid-gestation and then migra

201 re hippocampus as well as lateral and medial ganglionic eminences exhibited a 20-30% reduction in mit

202 sponding to the mammalian medial and lateral ganglionic eminences generated medium spiny neurons foun

203 Cortical interneurons arise from the ganglionic eminences in the ventral telencephalon and mi

204 al interneurons within the medial and caudal ganglionic eminences of the developing telencephalon.

205 neuron migration from the medial and caudal ganglionic eminences to the cerebral cortex in slice pre

206 nterneurons from their place of birth in the ganglionic eminences to their place of terminal differen

207 s, Dlx6(LacZ) is expressed in the developing ganglionic eminences, and their derivatives.

208 cal interneurons originate in the subpallial ganglionic eminences, but their developmental origins in

209 al GPe neurons originate from lateral/caudal ganglionic eminences, express the transcription factor F

210 an cortical interneurons are produced in the ganglionic eminences, including an enormous contribution

211 interneurons, most of which originate in the ganglionic eminences, take distinct tangential migratory

212 neural progenitors of the lateral and median ganglionic eminences, two protrusions of the ventral tel

213 estricted progenitors are located within the ganglionic eminences, using Dlx5/6-Cre-ires-EGFP (Dlx5/6

214 d the ventricular-subventricular zone of the ganglionic eminences, whereas at midgestation (20 GW), t

215 interneurons originating in the more distant ganglionic eminences.

216 inhibited in cortical ventricular zones and ganglionic eminences.

217 er from the medial (MGE) or the caudal (CGE) ganglionic eminences.

218 cal neuroepithelium but not medial or caudal ganglionic eminences.

219 tures such as the medial, lateral, or caudal ganglionic eminences.

220 itosis marker p-H3 showed down-regulation in ganglionic eminences.

221 id hormone 20-hydroxyecdysone (20E) regulate ganglionic fusion, but little is known about the cellula

222 bination results in the greatest decrease in ganglionic HSV loads.

223 In this study, we show that ganglionic HSV-specific CD8(+) T cells exhibit a higher

224 PD-L1 mediated reduced functional avidity of ganglionic HSV-specific CD8(+) T cells.

225 9 deletion mutant resulted in a frequency of ganglionic infection at 3 days similar to that seen with

226 emporally localized, coincident with limited ganglionic infection.

227 ssion of acute poliomyelitis and dorsal root ganglionic inflammation rarely observed in CD4(+/+) mice

228 erve fibers, including the afferent endings, ganglionic initial segments, and nodes of Ranvier.

229 The ganglionic input in songbirds, which is not present in d

230 at these fibers terminate exclusively in the ganglionic layer below the molecular layer where paralle

231 olecular layer, with fine axon arbors in the ganglionic layer.

232 nsverse plane, with local collaterals in the ganglionic layer.

233 ontal plane and terminate exclusively in the ganglionic layer.

234 mes of the photoreceptor, inner nuclear, and ganglionic layers and in the lens of 9 dpf ethanol-expos

235 ayer or proliferate in both the granular and ganglionic layers.

236 mprise two distinct subtypes dictated by the ganglionic location of their cell bodies.

237 icroM) completely prevented the induction of ganglionic LTD (gLTD).

238 ral neuron types in the intermediate ventral ganglionic mass in the annelid.

239 eral and significantly more prevalent in the ganglionic masses from males (38%) than females (21%).

240 monal events previously shown to choreograph ganglionic migration and fusion.

241 (GPI-MFas II) to study cell adhesion during ganglionic migration and fusion.

242 mide (a protein synthesis inhibitor) blocked ganglionic movement and the concomitant increase in TM-M

243 was to evaluate the changes of left stellate ganglionic nerve activity (SGNA) and left thoracic vagal

244 ned following compression injury to the post-ganglionic nerves.

245 ter 30 min a similar cerebello-thalamo-basal ganglionic network was seen as in explicit learning.

246 We observed ganglionic neuroendocrine neoplasms, lesions not associa

247 Serologic testing revealed both ganglionic neuronal acetylcholine receptor and N-type vo

248 rus was tested for the ability to enter into ganglionic neuronal axons in cell culture of explanted r

249 ion (gKDelta31-68 mutation) failed to infect ganglionic neurons after ocular infection of mice.

250 events the virus from successfully infecting ganglionic neurons after ocular infection of mice.

251 ter primary infection, VZV becomes latent in ganglionic neurons along the entire neuraxis.

252 ed SVV antigen in the lung alveolar wall, in ganglionic neurons and nonneuronal cells, and in skin an

253 omic balance, functional remodelling of post-ganglionic neurons and reduced inflammation.

254 se revealed a progressive loss of adrenergic ganglionic neurons and reduction of cardiac sympathetic

255 ion in monoclonal antibody (MAb) A5-positive ganglionic neurons and that a 2.8-kb portion of the HSV-

256 During HSV-1 latency, some ganglionic neurons are surrounded by CD8 T cells, and it

257 quently detected in ORF2-positive trigeminal ganglionic neurons of latently infected, but not mock-in

258 rons that reside in the spinal cord and post-ganglionic neurons that comprise a chain of vertebral sy

259 in sympathetic, but not parasympathetic, pre-ganglionic neurons were required to regulate energy expe

260 s are induced by dexamethasone in trigeminal ganglionic neurons within 1.5 h after dexamethasone trea

261 ses varicella in primates, becomes latent in ganglionic neurons, and reactivates to produce zoster.

262 neurons, including cholinergic autonomic pre-ganglionic neurons, are required to control energy and g

263 ory and vestibular hair cells and associated ganglionic neurons, with its expression being higher in

264 lla, after which the virus becomes latent in ganglionic neurons.

265 tion factors in murine and bovine trigeminal ganglionic neurons.

266 sistently detected in a subset of trigeminal ganglionic neurons.

267 ox), after which the virus becomes latent in ganglionic neurons.

268 calcium in acutely dissociated vagal jugular ganglionic neurons.

269 t virus failed to enter into the axoplasm of ganglionic neurons.

270 ed by extensive interactions of pre-and post-ganglionic neurons.

271 s and had no detectable effects on muscle or ganglionic nicotinic receptor subtypes, indicating a mar

272 wn that upon reactivation of latent virus in ganglionic organ cultures all genes are derepressed at o

273 tive factor, inducing HSV gene expression in ganglionic organ cultures harboring latent virus and inc

274 We also reported that in the ganglionic organ cultures incubated in medium containing

275 Elsewhere we have reported the use of ganglionic organ cultures that enable rapid reactivation

276 ding to reactivation, we examined the use of ganglionic organ cultures that enable rapid reactivation

277 l, each accelerates viral gene expression in ganglionic organ cultures.

278 NA; (iii) ATF3 is induced nearly 100-fold in ganglionic organ cultures; and (iv) ATF3 plays a key rol

279 (b) R111 did not spontaneously reactivate in ganglionic organ cultures; however, viral genes were exp

280 alpha3 and beta4 subunits to form the major ganglionic postsynaptic nicotinic receptor subtype.

281 It is known that ganglionic primordia initially emerge early and simultan

282 ed intraperitoneally to counterstain cardiac ganglionic principal neurons (PNs).

283 y-associated transcript (LAT) in spontaneous ganglionic reactivation by examining ganglia latently in

284 Studying spontaneous ganglionic reactivation of HSV in the mouse TG allows a

285 associated with a known trigger, spontaneous ganglionic reactivation of HSV-1 may be a better model o

286 that KOS dlLAT1.8 had a rate of spontaneous ganglionic reactivation very similar to that of HSV-1 (K

287 t local inhibitory interactions within inter-ganglionic regions, mediated by Eph/ephrins, and adhesiv

288 ating neurons, we argue that improving their ganglionic retention and function may offer a strategy i

289 ession by HSV-1 influences the formation and ganglionic retention of CD8(+) T cell populations, we de

290 n neurons, Bergmann glia, Schwann cells, and ganglionic satellite cells.

291 ly expressed in latently infected trigeminal ganglionic sensory neurons.

292 mouse, however, there is often only a single ganglionic structure situated alone in the vagus nerve.

293 ought to be related to dysfunctions in basal ganglionic structures of the brain.

294 The different markers did not reveal ganglionic subdivisions or physical compartmentalization

295 able antibody-mediated disorder of autonomic ganglionic synaptic transmission.

296 ave relevance late in development in vivo as ganglionic transmission and the effectiveness of BDNF ov

297 o play a role in modulation of the autonomic ganglionic transmission and to complement the vasodilato

298 s are found in autonomic ganglia and mediate ganglionic transmission.

299 y of defects in peripheral neuromuscular and ganglionic transmission.

300 ferentially modulate the agonist activity at ganglionic vs central nAChR subtypes, so that improved s