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 ad autoimmune autonomic neuropathy (AAN) and ganglionic acetylcholine receptor (AChR) autoantibodies.

3 Ganglionic acetylcholine receptor antibodies can be asso

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

5 nel (P/Q-type or N-type), potassium channel, ganglionic acetylcholine receptor, muscle acetylcholine

6 disorder associated with antibodies against ganglionic acetylcholine receptors.

7 o the N-terminal extracellular domain of the ganglionic AChR alpha3 subunit produce ganglionic AChR a

8 f the ganglionic AChR alpha3 subunit produce ganglionic AChR antibodies and develop signs of experime

9 onomic failure, and support the concept that ganglionic AChR antibodies are important diagnostically

10 in mice injected with rabbit IgG containing ganglionic AChR antibodies.

11 The demonstration that ganglionic AChR-specific IgG causes impaired autonomic s

12 mmunoreactivity was occasionally observed in ganglionic and internodal fibers.

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

14 Ganglionic and myocardial nerve sprouting and nerve dens

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

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

17 nd the SBP responses to phenylephrine during ganglionic blockade (BRBbolus: r=0.53; BRBslope: r=0.98,

18 to the SBP response to phenylephrine before ganglionic blockade (r=-0.78, P<0.0001).

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

20 Ganglionic blockade abolished the PVN-induced responses

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

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

23 Ganglionic blockade had no effect on the slope of the CF

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

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

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

27 Ganglionic blockade with hexamethonium caused greater fa

28 usion (BRBslope) during compared with before ganglionic blockade with trimethaphan.

29 different or greater in the older men before ganglionic blockade, but smaller during ganglionic block

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

31 During ganglionic blockade, which abolished the increase in MAP

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

33 eduction in arterial pressure in response to ganglionic blockade.

34 fore ganglionic blockade, but smaller during ganglionic blockade.

35 heart rate and mean arterial pressure to the ganglionic blocker hexamethonium and decreased urinary n

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

37 r changes were observed in the presence of a ganglionic blocker.

38 cardiopulmonary changes after treatment with ganglionic blocker.

39 1 stimulation was eliminated by splenectomy, ganglionic-blocker administration or beta2-adrenergic re

40 uency is a direct consequence of a decreased ganglionic burst rate.

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

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

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

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

45 cell cycle at early E2, prior to and during ganglionic condensation, and neurogenesis continues thro

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

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

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

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

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

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

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

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

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

55 rons appear to derive mainly from the caudal ganglionic eminence (CGE).

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

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

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

59 the frequency of embryonic day 14.5 (E14.5) ganglionic eminence (GE) progenitors that grew into neur

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

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

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

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

64 uction in the size of the Tlx mutant lateral ganglionic eminence (LGE) from embryonic day 14.5 onward

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

66 The lateral ganglionic eminence (LGE) is known to give rise to stria

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

68 known as Aldh1a3), is reduced in the lateral ganglionic eminence (LGE) of Gsh2 mutants.

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

70 ell cycle of progenitor cells in the lateral ganglionic eminence (LGE), the neuroepithelial precursor

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

94 Young neurons born in the medial ganglionic eminence (MGE) migrate a long distance dorsal

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

96 groups originate primarily within the medial ganglionic eminence (MGE) of the subcortical telencephal

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

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

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

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

101 2 in the ventricular zone (VZ) of the medial ganglionic eminence (MGE) using Olig2-Cre mice causes mo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

128 tion analysis, Gsh2 expression in the medial ganglionic eminence after E10.5 may negatively regulate

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

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

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

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

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

134 The lateral ganglionic eminence and rostral migratory stream develop

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

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

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

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

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

140 The medial ganglionic eminence exhibited unique patterns of progeni

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

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

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

144 Transplanting medial ganglionic eminence interneuron progenitors to introduce

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

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

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

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

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

150 GABAergic interneurons that originate in the ganglionic eminence of the ventral forebrain and incorpo

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

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

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

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

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

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

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

158 Enforced collapse of ganglionic eminence vessels and resultant periventricula

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

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

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

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

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

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

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

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

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

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

169 l lateral geniculate nucleus from the caudal ganglionic eminence, there is no obvious new source of p

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

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

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

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

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

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

176 5-HT(3A) receptors (5-HT(3A)Rs) and a medial ganglionic eminence-derived subpopulation lacking 5-HT(3

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

178 cell subpopulation derived from the lateral ganglionic eminence.

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

180 liferation of interneuron progenitors in the ganglionic eminence.

181 that originate developmentally in the caudal ganglionic eminence.

182 cephalic ventricular zone and not the medial ganglionic eminence.

183 cal interneurons that derive from the medial ganglionic eminence.

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

185 terneurons derived from the embryonic medial ganglionic eminence.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

217 cal neuroepithelium but not medial or caudal ganglionic eminences.

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

219 interneurons originating in the more distant ganglionic eminences.

220 The in vivo ganglionic environment directs the latent herpes simplex

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

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

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

224 9 deletion mutant resulted in a frequency of ganglionic infection at 3 days similar to that seen with

225 emporally localized, coincident with limited ganglionic infection.

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

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

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

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

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

231 ontal plane and terminate exclusively in the ganglionic layer.

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

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

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

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

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

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

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

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

240 ying this cancer as a potential initiator of ganglionic nAChR autoimmunity.

241 In addition, we found ganglionic nAChR protein in small-cell carcinoma lines,

242 muscle type and heteromeric neuronal (e.g., ganglionic) nAChRs.

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 tion factors in murine and bovine trigeminal ganglionic neurons.

265 sistently detected in a subset of trigeminal ganglionic neurons.

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

267 calcium in acutely dissociated vagal jugular ganglionic neurons.

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

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

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

271 e serum antibodies specific for the neuronal ganglionic nicotinic acetylcholine receptor (AChR).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

288 in IMR-32 and SH-SY5Y cells expressing human ganglionic receptors, and in TE-671 cells expressing hum

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

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