ライフサイエンスコーパス: cervical spinal cord

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

2 axonal decussation and projection beyond the cervical spinal cord.

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

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

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

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

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

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

9 recurrent intramedullary PNET affecting the cervical spinal cord.

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

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

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

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

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

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

16 icacy after transplantation into the injured cervical spinal cord.

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

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

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

20 aptic responses require a bilaterally intact cervical spinal cord.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

76 Cervical spinal cord injury at birth permanently disrupt

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

78 Neonatal cervical spinal cord injury disrupts not only locomotion

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

99 2-fold more CST axons decussated across the cervical spinal cord midline (approximately 12,000 axons

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

120 Compression of cervical spinal cord secondary to cervical spondylosis o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

136 Following cervical spinal cord transection, NaCN and also dinitrop

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

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

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

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

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

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

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

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

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

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

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

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

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

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