ライフサイエンスコーパス: peripheral nervous system

1 velopment of craniofacial structures and the peripheral nervous system.

2 anatomical and functional impairments in the peripheral nervous system.

3 rmally only produced by Schwann cells in the peripheral nervous system.

4 n of Notch-mediated cell fate choices in the peripheral nervous system.

5 mily, TRPM8, is a major cold receptor in the peripheral nervous system.

6 mpathetic neurons, to pattern the developing peripheral nervous system.

7 ptogenetic modulation of the spinal cord and peripheral nervous system.

8 ine (psychosine), accumulates in the CNS and peripheral nervous system.

9 then form the cranial sensory ganglia of the peripheral nervous system.

10 ence for a physiological role of NgR2 in the peripheral nervous system.

11 required for development and survival of the peripheral nervous system.

12 in a subpopulation of sensory neurons in the peripheral nervous system.

13 lling progenitor behavior in the central and peripheral nervous system.

14 n and transmission of noxious stimuli by the peripheral nervous system.

15 d for survival of neurons in the central and peripheral nervous system.

16 l connectivity and synaptic circuitry in the peripheral nervous system.

17 urodegenerative disorders of the central and peripheral nervous system.

18 the establishment of the myelin unit in the peripheral nervous system.

19 is hypomorphic and disease is limited to the peripheral nervous system.

20 specialized sensory neurons derived from the peripheral nervous system.

21 ously described myelination phenotype in the peripheral nervous system.

22 may arise proximally or distally within the peripheral nervous system.

23 , known mechanoreceptors of the lateral line peripheral nervous system.

24 l dynamics, migration and myelination in the peripheral nervous system.

25 tive MOR antagonist mainly acting within the peripheral nervous system.

26 zation (da) neurons of the Drosophila larval peripheral nervous system.

27 to form latent infections in neurons of the peripheral nervous system.

28 experiments with nerve growth factor in the peripheral nervous system.

29 ng cells, in particular Schwann cells of the peripheral nervous system.

30 vity for the central nervous system over the peripheral nervous system.

31 aM-dependent neuronal NOS in the central and peripheral nervous system.

32 al switch for controlling myelination in the peripheral nervous system.

33 antennular nerve as a representative of the peripheral nervous system.

34 under normal physiological conditions in the peripheral nervous system.

35 marcate an itch-specific labeled line in the peripheral nervous system.

36 r necessity during nerve degeneration in the peripheral nervous system.

37 ay a role in disorders of myelination in the peripheral nervous system.

38 lationships underpin the organization of the peripheral nervous system.

39 and other body parts, including central and peripheral nervous system.

40 an undecapeptide present in the CNS and the peripheral nervous system.

41 elination is crucial for the function of the peripheral nervous system.

42 y the levels at which they accumulate in the peripheral nervous system.

43 from aberrant development or function of the peripheral nervous system.

44 degeneration specific to the spinal cord and peripheral nervous system.

45 iple organs, often including the central and peripheral nervous system.

46 as a disease-modifying agent for the injured peripheral nervous system.

47 r neurodegenerative conditions involving the peripheral nervous system.

48 g that HHV-7 may also have a tropism for the peripheral nervous system.

49 of these disorders impact the central and/or peripheral nervous systems.

50 m of neurons and fibers in their central and peripheral nervous systems.

51 AL) is widely distributed in the central and peripheral nervous systems.

52 fornica) central and rat (Rattus norvegicus) peripheral nervous systems.

53 y key physiological roles in the central and peripheral nervous systems.

54 the predominant cell type in the central and peripheral nervous systems.

55 ed ion channels expressed in the central and peripheral nervous systems.

56 (AChRs) mediate signaling in the central and peripheral nervous systems.

57 loop receptors found in both the central and peripheral nervous systems.

58 d in signal transmission in both central and peripheral nervous systems.

59 functions, are ubiquitous in the central and peripheral nervous systems.

60 eptors widely distributed in the central and peripheral nervous systems.

61 t excitatory transmission in the central and peripheral nervous systems.

62 icants, many of which target the central and peripheral nervous systems.

63 rodevelopment and maintenance of central and peripheral nervous systems.

64 late many vital functions of the central and peripheral nervous systems.

65 ss of maternal Ube3a in the central, but not peripheral, nervous system.

66 Peripheral nervous system abnormalities, including neuro

67 primary immune reaction against gliomedin, a peripheral nervous system adhesion molecule, can be resp

68 display early and severe degeneration of the peripheral nervous system along with IF accumulation, bu

69 been recorded in other tissues including the peripheral nervous system and adrenal gland.

70 aS, including its ability to spread from the peripheral nervous system and along neuroanatomical trac

71 microtubule dynamics in vivo and ex vivo in peripheral nervous system and central nervous system neu

72 of maladaptive changes occurring within the peripheral nervous system and CNS.

73 eurodegenerative disorder affecting both the peripheral nervous system and CNS.

74 sition to migrate away and contribute to the peripheral nervous system and craniofacial skeleton.

75 chwann cells are the myelinating glia of the peripheral nervous system and dysfunction of these cells

76 These viruses efficiently invade the peripheral nervous system and establish lifelong latency

77 an pseudorabies virus (PRV), that infect the peripheral nervous system and have to travel long distan

78 in which Ikbkap expression is ablated in the peripheral nervous system and identify the steps in peri

79 y results from autoimmune destruction of the peripheral nervous system and is a component of the mult

80 r Tomosyn-2) is expressed in the central and peripheral nervous system and is known to inhibit neurot

81 eptor complex is primarily restricted to the peripheral nervous system and is selectively expressed b

82 Loss of Megf8 disrupts axon guidance in the peripheral nervous system and leads to defects in develo

83 order that primarily affects the central and peripheral nervous system and muscles and in the latter

84 uded abnormal results of function studies of peripheral nervous system and special senses, conduct di

85 nalyses have expanded our knowledge of early peripheral nervous system and spinal cord development.

86 virus that can cause infections in both the peripheral nervous system and the central nervous system

87 MR imaging of the peripheral nervous system and the limb-girdle muscle may

88 -/-) mice, which lack CB1 receptors from the peripheral nervous system and the spinal cord.

89 required to infect the Schwann cells of the peripheral nervous system and therefore may also be neur

90 y to defeat consecutive host barriers of the peripheral nervous system and together promote the poten

91 lucosan bodies accumulate in the central and peripheral nervous systems and are often associated with

92 (NPY) is widely expressed in the central and peripheral nervous systems and is proliferative for a ra

93 hR subtypes are expressed in the central and peripheral nervous systems and play a critical role in v

94 cases of neuroblastoma (NB), a cancer of the peripheral nervous system, and are thought to be the pri

95 ssue expression and has been found in brain, peripheral nervous system, and gastrointestinal tract.

96 expressed throughout development of the CNS, peripheral nervous system, and kidneys.

97 at control cross-talk between the cancer and peripheral nervous system, and possible interventions, u

98 activation of PI3K signaling in glia of the peripheral nervous system, and suggest that glycosyltran

99 rat (control) Chga expression in central and peripheral nervous systems, and found Chga protein to be

100 Injuries to the peripheral nervous system are major sources of disabilit

101 privileged tissues such as the brain and the peripheral nervous system are shielded from plasma prote

102 nd the redox state by CIH in the central and peripheral nervous systems associated with the chemorefl

103 In parallel, peripheral nervous system autoimmunity resembling chroni

104 In the peripheral nervous system, axoglial contact at the nodes

105 In the developing peripheral nervous system, axon-derived signals stimulat

106 In the peripheral nervous system, axonal neuregulin 1 type III

107 ry and stochastic simulations of central and peripheral nervous system axons from vertebrates and inv

108 kness in both the central nervous system and peripheral nervous system because reduced cleavage of Nr

109 ocular and non-ocular tissues including the peripheral nervous system, but its functions in these ti

110 investigated the role of glial cells in the peripheral nervous system by creating SMA mice selective

111 oprotein mostly expressed in the central and peripheral nervous systems by different cell types in ma

112 Mature neurons in the adult peripheral nervous system can effectively switch from a

113 neuropathies are inherited disorders of the peripheral nervous system caused by mutations in Schwann

114 at inhibits Notch signalling during multiple peripheral nervous system cell fate decisions.

115 e central spinal cord represents a source of peripheral nervous system cells.

116 Schwann cells myelinate distinct central and peripheral nervous system (CNS and PNS) domains along th

117 (SWCs), the myelinating glia of central and peripheral nervous system (CNS and PNS), respectively, r

118 expression in the central nervous system and peripheral nervous system consistent with the endogenous

119 These include much of the peripheral nervous system, craniofacial skeleton, smooth

120 abilities secondary to central and, perhaps, peripheral nervous system damage.

121 The regenerative capacity of the peripheral nervous system declines with age.

122 Successful myelination of the peripheral nervous system depends upon induction of majo

123 ral nervous system and identify the steps in peripheral nervous system development that are Ikbkap-de

124 During peripheral nervous system development, Schwann cells (SC

125 nd migration, which in turn is essential for peripheral nervous system development.

126 mmune cells, and, in response to danger, the peripheral nervous system directly communicates with the

127 of interest for the treatment of central and peripheral nervous system diseases associated with exces

128 get for the treatment of various central and peripheral nervous system disorders, including Parkinson

129 gical role of COMT inhibitors in central and peripheral nervous system disorders; (ii) to provide the

130 During development of the peripheral nervous system, excess neurons are generated,

131 n of HSV-1 in the CNS in comparison with the peripheral nervous system following ocular infection in

132 ) type III is involved in myelination of the peripheral nervous system, for which it requires proteol

133 Here, we demonstrate that Ifit2 protects the peripheral nervous system from VSV infection as well.

134 olytic activity in nerves and of central and peripheral nervous system function.

135 hat Spry3 is highly expressed in central and peripheral nervous system ganglion cells in mouse and hu

136 The peripheral nervous system has remarkable regenerative ca

137 In vertebrates, the peripheral nervous system has retained its regenerative

138 duced axonal degeneration in the central and peripheral nervous systems, has provided insight into a

139 However, its actions on the peripheral nervous system have been less characterized.

140 Several studies of VZV reactivation in the peripheral nervous system (herpes zoster) have been publ

141 et tissues, including skeletal muscle in the peripheral nervous system; however, the mechanisms by wh

142 ns that allow HSV to persist within the host peripheral nervous system, improved neuronal models are

143 ural ectoderm and together contribute to the peripheral nervous system in all vertebrates.

144 ng regulates inflammation in the central and peripheral nervous system in ALS, supporting therapeutic

145 cking and neurodevelopmental deficits in the peripheral nervous system in Down syndrome.

146 be essential for myelination of axons in the peripheral nervous system in fish and mice.

147 By showing involvement of the peripheral nervous system in MS, this proof-of-concept s

148 gnosis of ALS and suggest involvement of the peripheral nervous system in the ALS pathogenetic cascad

149 ssays with neural cells from the central and peripheral nervous system in vitro and shown to be indep

150 polyneuropathy, an autoimmune disease of the peripheral nervous system in which humoral immune respon

151 aggregates occurs widely in the central and peripheral nervous systems in Parkinson's disease (PD).

152 rved in our cases, involving the central and peripheral nervous system, include deafness, optic neuro

153 ate extensively and give rise to most of the peripheral nervous system, including sympathetic, parasy

154 uronal types cultured from mouse central and peripheral nervous systems, including excitatory and inh

155 ural connectivity throughout the central and peripheral nervous systems, including the removal of sup

156 portant, as this process underlies both mild peripheral nervous system infection and severe spread to

157 In the peripheral nervous system, infiltrating monocyte-derived

158 SC receptors that detect peripheral nervous system injury remain incompletely und

159 ities for emerging classes of prostheses and peripheral nervous system interface technologies.

160 nt (16 of 17 patients [94.1%]; P = .008) and peripheral nervous system involvement (5 of 17 patients

161 0 years, 1.64; 95% CI, 1.19-2.27; P = .003), peripheral nervous system involvement (HR, 6.75; 95% CI,

162 nervous system, although dysfunction of the peripheral nervous system is a common manifestation.

163 Schwann cell (SC) myelination in the peripheral nervous system is essential for motor functio

164 The progressive damage to the peripheral nervous system is irreversible although stric

165 in; however, the role of plasmalogens in the peripheral nervous system is poorly defined.

166 Myelination of the peripheral nervous system is required for axonal functio

167 ain hypersensitivity following injury to the peripheral nervous system, is common, greatly impairs qu

168 ose expression is normally restricted to the peripheral nervous system, is present in cerebellar Purk

169 Whether pain originates in the central or peripheral nervous system, it frequently becomes central

170 f sulfatides in the cells of the central and peripheral nervous system leading to the destruction of

171 ferentiation of central precursor cells into peripheral nervous system-like Schwann cells that remyel

172 3 as an important player in both central and peripheral nervous system maintenance.

173 widely used antitubulin cancer drugs on the peripheral nervous system may help guide clinical evalua

174 This novel POMT function in the peripheral nervous system may shed light on analogous fu

175 erivatives including neurons and glia of the peripheral nervous system, melanocytes, and bone and car

176 RS-mediated diseases specifically affect the peripheral nervous system-most commonly causing axonal p

177 in myelin protein zero, the main protein of peripheral nervous system myelin.

178 In some cases, however, Schwann cells, the peripheral nervous system myelinating glia, are found re

179 led receptor (aGPCR) Gpr126 is essential for peripheral nervous system myelination, although the mole

180 ription factor SOX10, which is essential for peripheral nervous system myelination.

181 milieu may be a promising novel strategy in peripheral nervous system neuritis.

182 as pseudorabies virus (PRV) invade axons of peripheral nervous system neurons and undergo retrograde

183 s heterozygosity strongly suppresses ectopic peripheral nervous system neurons in mir-279/996 mutants

184 erpesvirus infection is spread from axons of peripheral nervous system neurons to cells in peripheral

185 In the peripheral nervous system, obesity-driven alterations in

186 In the peripheral nervous system of Drosophila melanogaster, di

187 ponse after misfolding and deposition in the peripheral nervous system of mutant transthyretin.

188 that regulate visceral pain sensation in the peripheral nervous system of rats.

189 s emphasize the structural complexity of the peripheral nervous system of the siphon, and the importa

190 tion of ER stress is first quantified in the peripheral nervous system of type I diabetic rats.

191 Here, we examined the central and peripheral nervous systems of FE65-KO, FE65L1-KO and FE6

192 vels are strongly reduced in the central and peripheral nervous systems of p73 knockout mice.

193 chronic stress-induced visceral pain in the peripheral nervous systems of rats.

194 m do not regenerate, and even neurons in the peripheral nervous system often fail to regenerate to th

195 the development of cells in the central and peripheral nervous systems, olfactory epithelium and end

196 The requirement and influence of the peripheral nervous system on tissue replacement in mamma

197 investigating sleep, auditory functions and peripheral nervous system, ophthalmological studies incl

198 hat give rise to multiple derivatives of the peripheral nervous system, particularly, the sensory neu

199 herapeutic agents can affect the central and peripheral nervous systems, patients must undergo a proc

200 athological abnormalities recapitulating the peripheral nervous system phenotype of homozygous Egr2-n

201 esin acts as a signaling molecule regulating peripheral nervous system (PNS) and central nervous syst

202 of the major differences between the injured peripheral nervous system (PNS) and CNS is the pro- and

203 the context of the development of Drosophila peripheral nervous system (PNS) and neuromuscular juncti

204 nt and long-term viability of neurons in the peripheral nervous system (PNS) and retina.

205 Development and maintenance of the peripheral nervous system (PNS) are essential for an org

206 d natural incidence of ER stress in diabetic peripheral nervous system (PNS) argue for a major role o

207 protein that is constitutively expressed by peripheral nervous system (PNS) axons and Schwann cells.

208 vous system, mature neurons in the mammalian peripheral nervous system (PNS) can regenerate axons aft

209 Injury to the peripheral nervous system (PNS) causes a dramatic shift

210 al cells of vertebrate meninges and of their peripheral nervous system (PNS) connective tissue counte

211 cells (including Schwann cells; SCs) of the peripheral nervous system (PNS) could be purified and ex

212 metrical heminodes found in both the CNS and peripheral nervous system (PNS) during development.

213 and Notch signaling regulates the epidermal-peripheral nervous system (PNS) fate choice in tail midl

214 ithout poisoning, is associated with adverse peripheral nervous system (PNS) function.

215 Selective in vivo delivery of cargo to peripheral nervous system (PNS) has broad clinical and p

216 n, the contribution of hypoxic damage to the peripheral nervous system (PNS) has not been addressed.

217 High glucose levels in the peripheral nervous system (PNS) have been implicated in

218 ion of both central nervous system (CNS) and peripheral nervous system (PNS) in PD.

219 llowing central nervous system (CNS) but not peripheral nervous system (PNS) injury.

220 degenerative and regenerative events in the peripheral nervous system (PNS) is still to be establish

221 in these cells and in the myelination of the peripheral nervous system (PNS) is unknown.

222 Of patients presenting with pain or peripheral nervous system (PNS) manifestations, 39% were

223 chanosensory and chemosensory neurons of the peripheral nervous system (PNS) must signal to the motor

224 port that sulfated N-glycans are involved in peripheral nervous system (PNS) myelination.

225 o studies have shown that infected, cultured peripheral nervous system (PNS) neurons exhibited aberra

226 viruses that establish life-long latency in peripheral nervous system (PNS) neurons of their native

227 port of viral particles in axons of cultured peripheral nervous system (PNS) neurons.

228 es are neuroinvasive viruses that infect the peripheral nervous system (PNS) of infected hosts as an

229 Sensory and autonomic neurons of the peripheral nervous system (PNS) play a critical role in

230 ammals is severely limited, yet axons in the peripheral nervous system (PNS) regrow, albeit to a limi

231 he sensory organs and cells that make up the peripheral nervous system (PNS) relies on the activity o

232 N) neurons to understand whether ScNs of the peripheral nervous system (PNS) synapse with CN neurons

233 non-neuronal cells in the central (CNS) and peripheral nervous system (PNS) that nourish neurons and

234 Optogenetic control of the peripheral nervous system (PNS) would enable novel studi

235 contact with sensory neuron clusters of the peripheral nervous system (PNS), and blood cells (hemocy

236 (CNS), non-myelinating Schwann cells in the peripheral nervous system (PNS), and enteric glial cells

237 In the peripheral nervous system (PNS), developmental axon prun

238 immunoreactive neurons were detected in the peripheral nervous system (PNS), especially in lip and f

239 Schwann cells, the myelinating glia of the peripheral nervous system (PNS), originate from multipot

240 dant not only in the shk CNS but also in its peripheral nervous system (PNS), which, as in other "mye

241 raphs of the dorsal root entry zone show the peripheral nervous system (PNS)-CNS transition of regrow

242 Apparent peripheral nervous system (PNS)-like and central nervous

243 ) displays this role primarily affecting the peripheral nervous system (PNS).

244 ell as axon regeneration after injury in the peripheral nervous system (PNS).

245 research on nerve growth factor (NGF) in the peripheral nervous system (PNS).

246 n axonal myelination by Schwann cells in the peripheral nervous system (PNS).

247 and dendritic regeneration in the Drosophila peripheral nervous system (PNS).

248 is known about the disease pathology in the peripheral nervous system (PNS).

249 ss direct evidence for a similar role in the peripheral nervous system (PNS).

250 ertebrate development, the central (CNS) and peripheral nervous systems (PNS) arise from the neural p

251 h neurological disorders of both the CNS and peripheral nervous systems (PNS), yet few studies have d

252 Myelinating Schwann cells in the vertebrate peripheral nervous system rely on Brg1 (Smarca4) for ter

253 rentiation and subsequent myelination of the peripheral nervous system require the action of several

254 Development of a functional peripheral nervous system requires axons to rapidly inne

255 Maturation of the peripheral nervous system requires specification of axon

256 Brain and peripheral nervous system research conducted over the pa

257 s that efficiently transduce the central and peripheral nervous systems, respectively.

258 Understanding how the peripheral nervous system responds to electro-mechanical

259 rs that control Schwann cell myelination and peripheral nervous system responses to nerve injury.

260 itatory neurotransmission in the central and peripheral nervous systems, resulting in skeletal muscle

261 Analysis of the peripheral nervous system revealed that Schwann cells an

262 In the peripheral nervous system, Schwann cells (SCs) demonstra

263 In the peripheral nervous system, Schwann cells (SCs) radially

264 h Lewy body disease pathology in central and peripheral nervous system structures.

265 by NADPHd histochemistry in both central and peripheral nervous system structures.

266 physiology, and for treating diseases of the peripheral nervous system, such as chronic nausea, vomit

267 ificant perturbations in eye development and peripheral nervous system, suggesting novel targets in a

268 Schwann cells (SCs), ensheathing glia of the peripheral nervous system, support axonal survival and f

269 ectual disability and additional central and peripheral nervous system symptoms but an absence of fro

270 e stroma and pathogenic modifications to the peripheral nervous system that elevate metastatic capaci

271 Schwann cells are myelinating glia in the peripheral nervous system that form the myelin sheath.

272 AG) neuropathy, an autoimmune disease of the peripheral nervous system that is mediated by IgM autoan

273 Cocaine has actions in the peripheral nervous system that reliably precede--and thu

274 we present the structural components of the peripheral nervous system that underlie its susceptibili

275 During the development of the peripheral nervous system, the large number of apoptotic

276 Unfortunately, in contrast to axons from the peripheral nervous system, the limited capacity of regen

277 ause a persistent, lifelong infection in the peripheral nervous system, the virus remains within the

278 ls in at least two different settings in the peripheral nervous system: the pIIIb precursor of the ne

279 During the development of the peripheral nervous system there is extensive apoptosis,

280 en the aim of reading neural activity in the peripheral nervous system, this work has investigated an

281 an cause neuropathy in mice if it enters the peripheral nervous system through skin lesions; however,

282 Myelin insulates axons in the peripheral nervous system to allow rapid propagation of

283 rain stimulation can be used to "bypass" the peripheral nervous system to induce multisensory illusio

284 ranging from neurons and glial cells of the peripheral nervous system to pigment cells, fibroblasts

285 chwann cells, the myelin-making cells of the peripheral nervous system to remyelinate adult CNS axons

286 The central and peripheral nervous system transcriptomes of the spider C

287 ly, we evaluated primary human NF1-deficient peripheral nervous system tumors and found that MNKs are

288 nding of rare human hereditary neuropathies, peripheral nervous system tumors, and common degenerativ

289 defined neuronal subclasses within the mouse peripheral nervous system using an experimental strategy

290 Here we analyzed the role of Miz1 in the peripheral nervous system, using an early embryonic cond

291 alling factor controlling myelination in the peripheral nervous system, via signalling through ErbB t

292 tion require concurrent reinnervation by the peripheral nervous system, we hypothesized that cardiac

293 nown about the role of alpha6* nAChRs in the peripheral nervous system (where the asterisk denotes th

294 le is known about expression of UBE3A in the peripheral nervous system, where loss of maternal UBE3A

295 shown to be of particular importance in the peripheral nervous system with pharmacological and genet

296 ves our understanding of autoimmunity in the peripheral nervous system with potential relevance for h

297 p73 null mice also have impairments in the peripheral nervous system with reduced thermal sensitivi

298 Periaxin (PRX) is an abundant protein in the peripheral nervous system, with an important role in mye

299 ns extend our understanding of the zebrafish peripheral nervous system within a little-studied sensor

300 N9A gene, is preferentially expressed in the peripheral nervous system within sensory dorsal root gan