ライフサイエンスコーパス: cervical spinal cord

1 receptors for phrenic LTF are located in the cervical spinal cord.

2 ibres after injury to these axons in the mid-cervical spinal cord.

3 rge motoneurons in the medulla oblongata and cervical spinal cord.

4 sensory tracts from the lumbar to the upper cervical spinal cord.

5 lumbar and sacral segments and the lowest in cervical spinal cord.

6 em preceded PrP(Sc) detection in the rostral cervical spinal cord.

7 axonal decussation and projection beyond the cervical spinal cord.

8 n into the C(1) and C(2) levels of the upper cervical spinal cord.

9 resent in the lumbar spinal cord than in the cervical spinal cord.

10 scores and transverse sectional area of the cervical spinal cord.

11 ganisation of the corticospinal tract in the cervical spinal cord.

12 nervous system development, focusing on the cervical spinal cord.

13 recurrent intramedullary PNET affecting the cervical spinal cord.

14 t that projects to the ventral region of the cervical spinal cord.

15 cipal trigeminal nucleus and caudally to the cervical spinal cord.

16 applied dorsally to the C2-C6 region of the cervical spinal cord.

17 mediated by NK1R+/SST+ neurons in the dorsal cervical spinal cord.

18 cipants underwent 3.0-T MRI of the brain and cervical spinal cord.

19 n of metabolic changes in the brain stem and cervical spinal cord.

20 ury (SCI) by applying MR spectroscopy in the cervical spinal cord.

21 n-like c-Fos immunoreactivity pattern in the cervical spinal cord.

22 er afferents onto common interneurons in the cervical spinal cord.

23 athways via retrograde tracing from the high cervical spinal cord.

24 in CST cell bodies and in axon terminals in cervical spinal cord.

25 nctionally integrate in the circuitry of the cervical spinal cord.

26 he prefrontal cortex and the lamina X of the cervical spinal cord.

27 icacy after transplantation into the injured cervical spinal cord.

28 n of SCI patients suffer contusion trauma to cervical spinal cord.

29 as they ascend in the dorsal columns of the cervical spinal cord.

30 nt of their physiological actions within the cervical spinal cord.

31 aptic responses require a bilaterally intact cervical spinal cord.

32 bral hemispheres, brainstem, cerebellum, and cervical spinal cord.

33 n content was elevated in the Gaa(-/-) mouse cervical spinal cord.

34 ion of both the white and grey matter of the cervical spinal cord.

35 MRI abnormalities were predominantly in the cervical spinal cord (103/118).

36 s into the contralesional gray matter of the cervical spinal cord administered 28 d after stroke indu

37 to restrict corticospinal sprouting in mouse cervical spinal cord after unilateral pyramidotomy.

38 ntrol subjects to undergo 7 T imaging of the cervical spinal cord and brain as well as conventional 3

39 cit movements and had few connections to the cervical spinal cord and distinctive cyto- and immunoarc

40 es, we demonstrated similar pathology in the cervical spinal cord and greater accumulation of glycoge

41 better corticospinal tract integrity in the cervical spinal cord and improved neurological outcomes

42 e growth of corticospinal tract axons in the cervical spinal cord and then use specific optogenetic a

43 e degeneration of motoneurons, mostly in the cervical spinal cord, and in the brain stem cranial moto

44 Thirty of them were acquired in cervical spinal cord, and the remaining 18 spectra were

45 stem-spinal and segmental projections to the cervical spinal cord are present at birth, skilled forel

46 in the midbrain/pons, medulla oblongata, and cervical spinal cord as defined on the individual's MRI

47 on tensor imaging of the mouse brainstem and cervical spinal cord at 117 mum x 117 mum in-plane resol

48 subjects were prospectively acquired in the cervical spinal cord at C2 above the level of injury bet

49 Strikingly, we find that cervical spinal cord Atoh1-lineage neurons form mainly t

50 s of MWF and f(M) in healthy human brain and cervical spinal cord (available online) and compared the

51 ctive for Zif268 protein were not present in cervical spinal cord before postnatal day (P) 6.

52 ted that corticospinal axons reach the lower cervical spinal cord by 24 weeks post-conceptional age (

53 enshaw cells, identified in human postmortem cervical spinal cord by their morphology, location and c

54 R mRNA in the adult rat and mouse brains and cervical spinal cords by using ISHH with novel cRNA prob

55 R and LE immunoreactivities in the adult rat cervical spinal cord (C3-C5).

56 BDA-labeled terminals in the ventral horn of cervical spinal cord (C4-C5) were immunoreactive for enk

57 lly sectioned dorsal column afferents in the cervical spinal cord (C4-C6) in adult squirrel monkeys.

58 sly that epidural stimulation of the lateral cervical spinal cord can evoke tactile sensations percei

59 ocal glucose hypermetabolism at the level of cervical spinal cord compression may predict an improved

60 humans, and we hypothesized that EES of the cervical spinal cord could antagonize opioid-induced res

61 vated by designer drugs (DREADDs) in the mid-cervical spinal cord could effectively stimulate phrenic

62 l and neuronal injury in mouse brainstem and cervical spinal cord could improve our understanding of

63 acquire functional images of both brain and cervical spinal cord (CSC) simultaneously and examined t

64 In the cervical spinal cord, CSP axons from S2 and M1 partly co

65 Purpose To identify MRI features of cervical spinal cord damage that could help predict disa

66 al column somatosensory pathway in the upper cervical spinal cord deactivates neurons in the hand reg

67 activity is similarly plastic in human lower cervical spinal cord development, with many changes occu

68 al nerve 12) and lateral motor column of the cervical spinal cord, displaying differential vulnerabil

69 asures and macromolecular MRI metrics in the cervical spinal cord, distal to the site of injury.

70 Cervical spinal cord, DRG, and forepaw skin were removed

71 nd strengthening of existing circuits in the cervical spinal cord due to a combination of afferent ta

72 ally applied electrical stimulation over the cervical spinal cord during structured rehabilitation.

73 at C3, with or without a transplant of fetal cervical spinal cord (embryonic day 14); unoperated pups

74 deficit; in contrast to forebrain, fyn(-/-) cervical spinal cord exhibited no reduction in myelin co

75 Epidural electrical stimulation (EES) at the cervical spinal cord facilitated motor activity in roden

76 to map functional connectivity of the human cervical spinal cord from C1 to C4 at 1 x 1 x 3-mm resol

77 he volume of brainstem, cerebellum and upper cervical spinal cord from three-dimensional MRIs acquire

78 d structural and quantitative imaging of the cervical spinal cord from which we calculated magnetizat

79 Cervical spinal cord GM atrophy is an accurate predictor

80 pendent predictors of EDSS score in PMS were cervical spinal cord GM CSA and brain GM volume (R(2) =

81 Logistic regression analysis identified cervical spinal cord GM CSA and T2 lesion volume as inde

82 An optimal cervical spinal cord GM CSA cut-off value of 11.1 mm(2)

83 Cervical spinal cord GM lesions may subsequently cause G

84 al funiculi FA, normalized brain volume, and cervical spinal cord GM T2 lesion volume (R(2) = 0.51).

85 multivariable analysis identified phenotype, cervical spinal cord gray matter (GM) cross-sectional ar

86 differed at various CNS regions in that the cervical spinal cord had the greatest rate of influx, wh

87 Cervical spinal cord imaging at 7 T was used to segment

88 distinct upper extremity movements onto the cervical spinal cord in accordance with established myot

89 show that a single session of TESS over the cervical spinal cord in individuals with incomplete chro

90 egional changes of glucose metabolism of the cervical spinal cord in patients with degenerative cervi

91 s clinico-pathological study we examined the cervical spinal cord in patients with primary and second

92 corticospinal tracts from the cortex to the cervical spinal cord in patients with various disease ph

93 electrodes over motor cortex and the dorsal cervical spinal cord in rats; motor evoked potentials (M

94 , we found neurons in the dorsal horn of the cervical spinal cord in which c-Fos and pseudorabies wer

95 ather patterns could predict the severity of cervical spinal cord injuries (CSCI) across the United S

96 ncy is the leading cause of death after high-cervical spinal cord injuries (SCIs).

97 es recovery of manual dexterity in rats with cervical spinal cord injuries.

98 To investigate the effects of cervical spinal cord injury (C-SCI) on cough reflex sens

99 lower limb muscles after chronic incomplete cervical spinal cord injury (iSCI), but the underlying m

100 -70 years with acute, complete or incomplete cervical spinal cord injury (neurological level of injur

101 Cervical spinal cord injury (SCI) alone did not affect b

102 Traumatic cervical spinal cord injury (SCI) can result in debilita

103 Cervical spinal cord injury (SCI) causes devastating los

104 ger muscle in humans with chronic incomplete cervical spinal cord injury (SCI) compared with age-matc

105 Respiratory dysfunction after cervical spinal cord injury (SCI) has not been examined

106 High-thoracic or cervical spinal cord injury (SCI) is associated with sev

107 Cervical spinal cord injury (SCI) leads to permanent imp

108 accuracy of prognostication in patients with cervical spinal cord injury (SCI) needs to be improved.

109 Humans with cervical spinal cord injury (SCI) often recover voluntar

110 Most individuals with cervical spinal cord injury (SCI) show increased muscle

111 s, as well as in monkeys subjected to either cervical spinal cord injury (SCI), Parkinson's disease (

112 After cervical spinal cord injury (SCI), people often recover

113 By 2 months after unilateral cervical spinal cord injury (SCI), respiratory motor out

114 ortical representations reorganize following cervical spinal cord injury (SCI).

115 preserved in humans with incomplete chronic cervical spinal cord injury (SCI).

116 of diaphragm paralysis associated with high cervical spinal cord injury (SCI).

117 ts with subcortical damage due to incomplete cervical spinal cord injury (SCI).

118 ss of T1-weighted images in 10 subjects with cervical spinal cord injury and 16 controls.

119 ls in 15 individuals with chronic incomplete cervical spinal cord injury and 17 uninjured participant

120 ped a low-cost portable BMI for survivors of cervical spinal cord injury and investigated it as a mea

121 mediated respiratory recovery following high cervical spinal cord injury and that activation of intra

122 ensory cortex of two human participants with cervical spinal cord injury and varied the stimulus ampl

123 This effect was just as strong in rats with cervical spinal cord injury as in uninjured rats, demons

124 Cervical spinal cord injury at birth permanently disrupt

125 te whether baclofen use and paralysis due to cervical spinal cord injury change the contractile prope

126 Neonatal cervical spinal cord injury disrupts not only locomotion

127 6-year-old man with tetraplegia secondary to cervical spinal cord injury enrolled in the ongoing Brai

128 d replacement from 7 weeks to 7 months after cervical spinal cord injury in four adult rhesus monkeys

129 erent acute anti-inflammatory treatments for cervical spinal cord injury in rats.

130 study were to determine the consequences of cervical spinal cord injury on forelimb motor function a

131 The extent of cervical spinal cord injury was measured on MR images ob

132 20, 2022, 463 patients with acute traumatic cervical spinal cord injury were screened, 334 were deem

133 indings of an individual with traumatic high-cervical spinal cord injury who coordinated reaching and

134 as investigated in an individual with a high cervical spinal cord injury, a 5-year absence of nearly

135 People with chronic tetraplegia, due to high-cervical spinal cord injury, can regain limb movements t

136 ese observations suggest that after neonatal cervical spinal cord injury, embryonic transplants suppo

137 rgo lesion-dependent plasticity after either cervical spinal cord injury, Parkinson's disease-like sy

138 Here we show that, after cervical spinal cord injury, the expression of chondroit

139 ween elbow flexor and extensor muscles after cervical spinal cord injury.

140 of the diaphragm is a severe consequence of cervical spinal cord injury.

141 intains recovery for prolonged periods after cervical spinal cord injury.

142 of skilled forelimb activity after neonatal cervical spinal cord injury.

143 c avenue for people with chronic, incomplete cervical spinal cord injury.

144 S-evoked percepts in three participants with cervical spinal cord injury.

145 function in people with chronic, incomplete cervical spinal cord injury.

146 n a study participant with quadriplegia from cervical spinal cord injury.

147 targeted multisegmental cell delivery to the cervical spinal cord is a promising therapeutic strategy

148 Electrical stimulation of the cervical spinal cord is gaining traction as a therapy fo

149 In the rostral cervical spinal cord, labelled axons projecting to the l

150 Three-day-old rats received a cervical spinal cord lesion at C3, with or without a tra

151 We also measured brain lesion volume, cervical spinal cord lesion number and cross-sectional a

152 ng neurotrophin-3 (NT-3) within and beyond a cervical spinal cord lesion site grafted with autologous

153 n atrophy (whole brain and gray matter), and cervical spinal cord lesions (T2LV) and atrophy.

154 Despite the prevalence of cervical spinal cord lesions and atrophy, brain patholog

155 tissue bridges at the epicenter of traumatic cervical spinal cord lesions in 24 subacute tetraplegic

156 netic resonance imaging of the brainstem and cervical spinal cord lesions resulting from damage to LM

157 Cervical spinal cord lesions were mapped voxel-wise as a

158 relevant pain circuitry locations following cervical spinal cord level (C)5/6 contusion (using both

159 tion activated SST-expressing neurons in the cervical spinal cord, likely interneurons, that communic

160 gravir and tenofovir), CSF (lamivudine), and cervical spinal cord/meninges (efavirenz); the lowest we

161 2-fold more CST axons decussated across the cervical spinal cord midline (approximately 12,000 axons

162 Here we characterise cervical spinal cord morphometric abnormalities in SCA1,

163 gulation nor neuronal death of brainstem and cervical spinal cord motor neurons and have markedly red

164 Conclusion Cervical spinal cord MRI involvement has a central role

165 Cervical spinal cord MRI was performed with three-dimens

166 ists transactivate TrkB receptors in the rat cervical spinal cord near phrenic motoneurons, thus indu

167 njections in lateral rectus eye muscle label cervical spinal cord neurons closely connected to abduce

168 investigated the functional response in the cervical spinal cord of 18 healthy human subjects (aged

169 heximide) were injected intrathecally in the cervical spinal cord of anesthetized rats.

170 stigated using immunocytochemical methods in cervical spinal cord of neonatal and adult rats.

171 tactile and nociceptive heat stimuli in the cervical spinal cord of nonhuman primates.

172 e the grey and white matter pathology in the cervical spinal cord of patients with early relapsing-re

173 brain hypermetabolism in the brain stem and cervical spinal cord of patients within the amyotrophic

174 ium bromide into the dorsal funiculus of the cervical spinal cord of the rat to induce zones of demye

175 of differentiating into astrocytes--into the cervical spinal cord of WT rats to reveal how mutant ast

176 nstrated that after transplantation into the cervical spinal cords of adult mice with severe combined

177 o astrocytes and reduced microgliosis in the cervical spinal cords of SOD1(G93A) rats.

178 thway were made in adult rats in the rostral cervical spinal cord or caudal medulla.

179 Three-day-old rats received a cervical spinal cord overhemisection with or without tra

180 nistration of the same doses of DAMGO to the cervical spinal cord produces a suppression of withdrawa

181 us system; necrotizing focal myelitis in the cervical spinal cord; radiculitis; neuritis and demyelin

182 From postmortem studies of eight human cervical spinal cords ranging in age from 11 to 35 weeks

183 stem cell transplantation into lumbar and/or cervical spinal cord regions in amyotrophic lateral scle

184 ys after dorsal column lesions (DCLs) in the cervical spinal cord relies on neural rewiring in the cu

185 We transplanted GRPs around cervical spinal cord respiratory motor neuron pools, the

186 Persons with long-standing injury to the cervical spinal cord resulting in complete or partial pa

187 termittent hypoxia induces plasticity in the cervical spinal cord, resulting in enhanced inspiratory

188 oracic segment and below, transection of the cervical spinal cord results in severely compromised exp

189 his, we utilised a collection of post-mortem cervical spinal cord samples and investigated seven DCM

190 objective of this study was to characterize cervical spinal cord (SC) changes in asymptomatic C9orf7

191 21 [49.2%], including one lesion observed at cervical spinal cord [SC] MRI) lesions.

192 Compression of cervical spinal cord secondary to cervical spondylosis o

193 Microinjections of glutamate into the upper cervical spinal cord significantly reduced (to 57% of co

194 ol involves similar circuits, located in the cervical spinal cord, suggesting that EES could also imp

195 with access to spinal motoneurons in primate cervical spinal cord that receive inputs from the periph

196 somatostatin (SST)-expressing neurons in the cervical spinal cord that were activated (c-Fos-positive

197 In the cervical spinal cord the number of corticospinal axons o

198 of ascending dorsal column afferents in the cervical spinal cord, the hand representation in the con

199 al nucleus and dorsal horns of the C(1/)C(2) cervical spinal cord: the trigeminocervical complex.

200 ontralateral red nucleus and the ipsilateral cervical spinal cord; this axonal plasticity is enhanced

201 occurred onto medial motoneuron pools in the cervical spinal cord; this sprouting was paralleled by f

202 inations of persons with acute injury to the cervical spinal cord to examine the time post-injury at

203 hondroitinase ABC was microinjected into the cervical spinal cord to induce localized plasticity of f

204 upper thoracic spinal segments relays in the cervical spinal cord to inhibit activity of lumbar spino

205 of nongenomic estrogen signaling within the cervical spinal cord to recover respiratory neuroplastic

206 , and the trigeminal sensory system from the cervical spinal cord to the midbrain.

207 In decerebrate, cervical spinal cord-transected male rats, the lumbosacr

208 Spinal L6-S2 dorsal horn neurons of cervical spinal cord-transected, decerebrate female rats

209 after 6.2 pmol), and completely abolished by cervical spinal cord transection at the C6 level.

210 Following cervical spinal cord transection, NaCN and also dinitrop

211 othetical scenario of a 2-yr old with a high cervical spinal-cord transection.

212 D), direct spinal connections from the upper cervical spinal cord (UC; C1 and C2) and the cervical en

213 esonance images from the mouse brainstem and cervical spinal cord using the actively decoupled, anato

214 iated virus type 8 (AAV8)-Gfa2 vector to rat cervical spinal cord ventral horn for targeting focal as

215 Reducing ephrinB2 in the cervical spinal cord ventral horn via viral-mediated shR

216 es respiratory-related rhythms recorded from cervical spinal cord ventral roots.

217 whether NPCs can be delivered to the injured cervical spinal cord via lumbar puncture using a mixed p

218 Human cervical spinal cord was derived at autopsy from 54 pati

219 tracts of the dorsolateral funiculus of the cervical spinal cord was investigated in cats.

220 The volume of the upper (C1-C3) cervical spinal cord was significantly correlated with a

221 tion of the dorsal white matter tract of the cervical spinal cord, we found that both lesioned dorsal

222 structural MRI of both the brainstem and the cervical spinal cord, we were able to identify a number

223 MT images of the cervical spinal cord were collected parallel to the inte

224 irst experiments, slices of embryonic day 16 cervical spinal cord were cultured for one, two or three

225 numbers of neurons in the dorsal horn of the cervical spinal cord were labeled, especially ipsilatera

226 produces homogeneous delivery throughout the cervical spinal cord white and gray matter and brain mot

227 ing-state functional MR imaging of the human cervical spinal cord with a 3.0-T clinical MR imaging un

228 re, we combined a computational model of the cervical spinal cord with experiments in macaque monkeys

229 Neurons in the upper cervical spinal cord, with descending propriospinal proj

230 ibution of multiple sclerosis lesions in the cervical spinal cord, with respect to clinical status.

231 97% in the lumber spinal cord and 91% in the cervical spinal cord, without changing the number of Opr

232 that pairing stimulation of motor cortex and cervical spinal cord would strengthen motor responses th