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1 ould occur after unilateral axotomy via C(2) hemisection.
2 al hemidiaphragm paralyzed by C2 spinal cord hemisection.
3 ragm paralyzed by an ipsilateral spinal cord hemisection.
4  implant was tested in a rat model of dorsal hemisection.
5 obstacle, an increase that disappeared after hemisection.
6 ponses were lost or reduced after the second hemisection.
7  right ipsilesional hindlimb after the first hemisection.
8 substantially reduces the effects of lateral hemisection.
9 ation, before being reduced after the second hemisection.
10 h and beyond the lesion gap of a spinal cord hemisection.
11 er, a complete spinalization below the first hemisection.
12 ays to phrenic motoneurons below a C2 spinal hemisection.
13 lowing Fluoro-Gold injections, caudal to the hemisection.
14 cending axonal projections after spinal cord hemisection.
15 rhizotomy and midthoracic dorsal spinal cord hemisection.
16 the spinal cord gray matter after unilateral hemisection.
17 vity in the phrenic nerve ipsilateral to the hemisection.
18  activity indicating a functionally complete hemisection.
19 d-phrenic pathways after left C2 spinal cord hemisection.
20 l ND from 1 to 14 days following spinal cord hemisection.
21 n neurons of the ND and RN after spinal cord hemisection.
22 ity of phrenic motoneurons ipsilateral to C2 hemisection.
23 naltered in the RN neurons after spinal cord hemisection.
24 us monkeys that had undergone C7 spinal cord hemisection.
25  with wild-type controls after spinal dorsal hemisection.
26 rounding dysgranular S1 contralateral to the hemisection.
27  intrathecally after midthoracic dorsal over-hemisection.
28 mbs occurred less frequently after staggered hemisections.
29 icantly decreased after the first and second hemisections.
30  remained largely unaffected after staggered hemisections.
31  largely remained unaffected after staggered hemisections.
32 leus following an ipsilateral C2 spinal cord hemisection and 30-day survival period.
33 al performance after both T10 lateral spinal hemisection and a unilateral cortical stroke.
34                      Two months following T8 hemisection and Bcl-2/LacZ DNA injection, there was no s
35 ve significant neuroprotective effects after hemisection and compression SCI and can directly affect
36 eft hindlimb extensors early after the first hemisection and delayed short-latency responses in the r
37 multiple experimental data on the effects of hemisection and selective silencing or activation of V1
38 rated motor axon regeneration beyond both C5 hemisection and T3 complete transection sites.
39 uniculus on one side, dorsal and over-dorsal hemisections, and subtotal transections that spared pred
40 n the present study, the consequences of T13 hemisection are examined acutely at 45 min in MR neurons
41 t 28 days after injury, the effects of acute hemisection are unknown and predicted to be different th
42 renic nucleus 30 days after a C2 spinal cord hemisection as compared to nonhemisected controls.
43                                  Spinal cord hemisection at C(2) (C(2) SH), sparing the dorsal column
44                              Cervical spinal hemisection at C2 (SH) removes premotor drive to phrenic
45                                       Spinal hemisection at C2 reveals caudal synaptic pathways that
46 eurons whose axons were severed by a lateral hemisection at C3 (HX) and in lateral vestibular nucleus
47  lesions at thoracic level 9 (T9) or lateral hemisection at cervical level 5 (C5), our results reveal
48 ormation with spinal neurons, or caudal to a hemisection at L2/3, to assess restoration of function b
49 capability of cats after a unilateral spinal hemisection at T10 to cope with such a demanding locomot
50 /6 mice) and MRL/MpJ mice underwent a dorsal hemisection at T9 (thoracic vertebra 9).
51 hamsters were subjected to right spinal cord hemisection at the C7/T1 vertebral level.
52      We performed, in 9 adult cats, a spinal hemisection at thoracic level 10 and then a complete spi
53 sing microarrays, 24 voxel images of coronal hemisections at the level of the hippocampus of both the
54                                 Following C5 hemisections, athymic rats were treated with patches loa
55 acteristics of hindlimb locomotion following hemisection based on altered interactions between spinal
56                  Acutely, ipsilateral to the hemisection, both spontaneous and evoked activity of MR
57 uced at the first time point after the first hemisection, but partially recovered at the second time
58 N neurons occurred at L-1 ipsilateral to T-8 hemisection by 14 days, which reached 31% at 2 months an
59 our understanding of the effects of cervical hemisection (C(2) SH) on diaphragm muscle (DIAm) EMG act
60 ience such as required for adaptation to the hemisection, can remarkably respond to subsequent locomo
61                             After the second hemisection, cats required balance assistance to perform
62 e cells were grafted into a partial cervical hemisection cavity that completely interrupted one RST.
63 siRhoA, and p21) in experimental spinal cord hemisection, contusion, or transection on locomotor reco
64 irst (right T5-T6) and second (left T10-T11) hemisections, coordination of the fore- and hindlimbs wa
65 phase durations following a thoracic lateral hemisection during treadmill locomotion in tied-belt (eq
66 oro-gold labeling experiments following a T1 hemisection established that, as in the rat, the hamster
67 imental series, animals were subjected to T1 hemisection, followed by transplantation of a predegener
68 irst (right T5-T6) and second (left T10-T11) hemisections, forelimb-hindlimb co-ordination was altere
69 terminals was also found to be longer in the hemisection group (0.36 +/- 0.022 microns) as compared t
70 te terminals was significantly longer in the hemisection group (0.37 +/- 0.013 microns) as compared t
71 nes per terminal, however, is greater in the hemisection group (1.45 +/- 0.03) than in the control gr
72                         To test whether C(2) hemisection had induced a supraspinal change in respirat
73  Animals in which T13 was inserted caudal to hemisection had significantly less spasticity and muscle
74 l tract (CST) axons after spinal cord dorsal hemisection has yielded conflicting results.
75 icits induced by chronic midthoracic lateral hemisection (HX) injury: (1) synaptic transmission to lu
76                           Chronic unilateral hemisection (HX) of the adult rat spinal cord diminishes
77 clicality in female rats after a spinal cord hemisection (HX), implantation of EMG wires into selecte
78 ur different donors into a subtotal cervical hemisection in adult female rats and found that cells in
79  investigated following unilateral C4 spinal hemisection in adult rats.
80 h the hindlimbs after a thoracic spinal cord hemisection in adult rats.
81                               After a spinal hemisection in cats, locomotor plasticity occurring at t
82                                 After dorsal hemisection in the midthoracic cord, CST axons did not s
83 eatment with PUFAs after lateral spinal cord hemisection in the rat.
84 ion site, but not caudal to it, after dorsal hemisection in the transgenic mice.
85 injury (SCI) were evaluated by T9 cord level hemisection in wild-type mice (C57BL/6J and Bax+/+ mice)
86 spinal delivery of Ch'ase ABC, following T10 hemisections in adult cats, enhances adaptive movement f
87  before and after staggered lateral thoracic hemisections in cats.
88                                        After hemisection, inactivation of only V2b interneurons led t
89 function in all animals 1 month following C2 hemisection induced paralysis.
90  paradigm, we recently demonstrated that the hemisection induces durable changes in the symmetry of l
91 titive antagonist at the time of spinal cord hemisection induces significant regeneration of corticos
92           Rats then received cervical dorsal hemisection injuries and salmon fibrin was injected into
93                         Mice received dorsal hemisection injuries at thoracic level 6-7, which comple
94 gene targeting starting 8 weeks after spinal hemisection injury and monitored locomotion in the open
95                                       Spinal hemisection injury at T13 results in development of perm
96              Indeed, in a spinal cord dorsal hemisection injury model, we observed a significant impa
97 s can be efficiently delivered to a cervical hemisection injury site by intrathecal delivery at the l
98  were transplanted into an acute spinal cord hemisection injury with microvessels aligned with the ro
99                               After a dorsal hemisection injury, increased corticospinal and raphespi
100  within hours, days, or weeks following a C2 hemisection injury.
101 ssion in each V2a subtype 5 d following a C2 hemisection injury.
102 unctional recovery after mid-thoracic dorsal hemisection injury.
103                Three months after C5 lateral hemisections, iPSCs survived and differentiated into neu
104                                        After hemisection, ipsilesional knee flexor activation remaine
105 laterally in adult Sprague-Dawley rats by T8 hemisection, leaving the contralateral (left) CN as an i
106 k into the C5 spinal cord, having bypassed a hemisection lesion at C3.
107                            Two weeks after a hemisection lesion at C3/4, with embryonic spinal tissue
108 ere then grafted to acute spinal cord dorsal hemisection lesion cavities.
109 otor skills, but only in animals with dorsal hemisection lesions as opposed to dorsal column lesions.
110  cell grafts placed within sites of right C7 hemisection lesions in the rhesus macaque.
111 so be observed in human patients with spinal hemisection lesions.SIGNIFICANCE STATEMENT Following uni
112  by Basso Mouse Scale score following dorsal hemisection, likely due to developmental defects in the
113 f reticulospinal fiber growth after cervical hemisection, local rewiring of axotomized projections at
114       The present study uses a rodent spinal hemisection model of SCI in which mechanical and thermal
115 old-neural stem cells unit into an adult rat hemisection model of SCI promoted long-term improvement
116 t rats or the injury site in a dorsal column hemisection model of spinal cord injury, a population of
117 to promote motor recovery after SCI in a rat hemisection model when delivered in their original stem
118                              Utilizing a rat hemisection model, diaphragm function and paralysis was
119                               Unilateral T13 hemisection of the rat spinal cord produces a model of c
120                Contralateral and ipsilateral hemisection of the spinal cord (C5/C6) produced the same
121 g of corticospinal tract fibers after dorsal hemisection of the spinal cord did not reveal an obvious
122                    In this rare condition, a hemisection of the spinal cord typically leaves one side
123 .SIGNIFICANCE STATEMENT Following unilateral hemisection of the spinal cord, reticulospinal projectio
124                            Distal and medial hemisections of the endotracheal tube were assessed to q
125                                       Dorsal hemisections of the mid thoracic cord did not alter the
126  before and after staggered lateral thoracic hemisections of the spinal cord in cats.
127 perimental results confirmed many effects of hemisection on cat locomotion predicted by our simulatio
128 roxytryptamine prevented the effects of C(2) hemisection on contralateral phrenic neurogram amplitude
129 cats before and after a mid-thoracic lateral hemisection on the right side in the same locomotor cond
130 eks 1-2 and 7-8 after a lateral mid-thoracic hemisection on the right side of the cord while they neg
131 al segments] with a contralateral transverse hemisection one segment anterior to the hindlimb enlarge
132 ipsilateral hindlimb than did animals with a hemisection only.
133                              In animals with hemisections only, corticospinal, brainstem-spinal, and
134      Recovery of motor function after dorsal hemisection or complete transection of the spinal cord i
135           Using a staggered thoracic lateral hemisections paradigm, we investigated changes in intral
136 crease in complete clearance over time after hemisection paralleled the recovery of muscle activation
137 nerves before and after two thoracic lateral hemisections placed on opposite sides of the cord at 9-
138               In contrast, animals receiving hemisections plus transplants exhibited growth of these
139 C inhibitor, Go6976, into the site of dorsal hemisection promotes regeneration of dorsal column axons
140 atterns in the spinal turtle with transverse hemisection provided support for the concept of bilatera
141 tivity and relative stability after cervical hemisection raise speculation for potentially diverse ro
142 alyzed, ventilated, and spinally injured (C2 hemisection) rats that were exposed to either normoxia o
143                                       Spinal hemisection reduced immunostaining of the ipsilateral do
144                         The thoracic lateral hemisection represents an experimental model of an incom
145 EP1 40 to rats with mid-thoracic spinal cord hemisection results in significant axon growth of the co
146  number of NSPCs in a mouse model of lateral hemisection SCI during the acute stage.
147 d improved locomotion after staggered double hemisection SCI in mice.
148 al and serotonergic fibers in a rat cervical hemisection SCI model.
149 and spatial distribution in a double-lateral hemisection SCI mouse model.
150                         In a rat model of C2 hemisection SCI, we expressed the axon guidance molecule
151  as diminished paw drag often observed after hemisection.SIGNIFICANCE STATEMENT This paper introduces
152 hite matter 3-7 mm rostral and caudal to the hemisection site 8 d after injury.
153 he normal spinal cord, or just caudal to the hemisection site.
154                          Also, in rat T9-T10 hemisection spinal cord injury (SCI), we demonstrated th
155 rticospinal and serotonergic fibers in a rat hemisection spinal cord injury model.
156  acutely vulnerable in response to T8 dorsal hemisection spinal cord injury.
157 ing Ryk antibodies into the dorsal bilateral hemisectioned spinal cord either prevented the retractio
158                     In animals 28 days after hemisection, spontaneous activity of MR neurons was comp
159 the intact cord but lose this function after hemisection, suggesting that they are activated by input
160 ulation in the spinal turtle with transverse hemisection supports the concept that hip extensor circu
161                         After a lateral left hemisection (T10), cats recovered stepping with both hin
162  oxide (NO) production following spinal cord hemisection tends to lead to neurodegeneration in neuron
163 rainstem respiratory motor output after C(2) hemisection that coincided with the spontaneous recovery
164  in the lumbar spinal cord after T13 lateral hemisection that correlated with emergence of mechanical
165 es in hindlimb muscles early after the first hemisection that partially recovered with left superfici
166                         Additional rats with hemisections that received NT-3 continuously via mini-pu
167             Lesions included subtotal dorsal hemisections that spared only the lateral half of the do
168 on our model, we hypothesized that following hemisection the contralesional ('intact', left) side of
169                      Therefore, after spinal hemisection the time course of changes in NF mRNA expres
170                           At weeks 1-2 after hemisection, the ipsilesional right hindlimb contacted o
171 als in the phrenic nucleus was reduced after hemisection, the number of 5-HT terminals in the hemisec
172                          With a chronic left hemisection, the number of muscle nerves displaying loco
173                           At weeks 7-8 after hemisection, the proportion of complete clearance increa
174                              We used lateral hemisection to model central neuropathic pain and herpes
175  an intact spinal cord or after a unilateral hemisection to walk with a precise foot placement on the
176  cord injury, we administered C7 spinal cord hemisections to adult rhesus monkeys and analyzed behavi
177 lap debridement, apically repositioned flap, hemisection, tunneling or extraction, to regenerative th
178 very of locomotor functions following spinal hemisection, using chemogenetic tools to selectively sil
179 s subjected to an ipsilateral C2 spinal cord hemisection was confirmed electrophysiologically 24 h af
180                 Intensive LTM training after hemisection was found to change features of locomotion,
181 mmetrical state of locomotion induced by the hemisection was retained durably after the subsequent sp
182 labeling patterns following lateral cervical hemisection was then addressed.
183                     In our simulations, the 'hemisection' was always applied to the right side.
184                             Four weeks after hemisection, we administered multiple intraparenchymal C
185 ether lumbar segments of cats with a chronic hemisection were able to generate fictive locomotion-tha
186 matosensory cortex (S1) contralateral to the hemisection were determined using standard multiunit map
187  responses in all four limbs after staggered hemisections, which correlated with altered coordination
188 spinal networks were indeed modified after a hemisection with a clear asymmetry between left and righ
189 n green monkeys underwent right C5/6 lateral hemisection with evidence of persistent disuse of the ri
190          We report that 6 weeks after dorsal hemisection with peripheral conditioning lesion, C3(-/-)
191 f spatially and temporally separated lateral hemisections with or without the excitotoxic ablation of
192 d male hamsters were subjected to a right T1 hemisection, with half of the operated animals immediate
193 found redistribution of weight support after hemisection, with reduced diagonal supports and increase

 
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