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1 loss is delayed in SkpA mutants after nerve crush.
2 (-/-) compared with control mice after nerve crush.
3 l neurons of Thy1-CFP mice after optic nerve crush.
4 ell bodies at both 21 days and 3 months post-crush.
5 5%), as well as RGC loss (88%) 1 month after crush.
6 ting mice were challenged with sciatic nerve crush.
7 may protect RGC health following optic nerve crush.
8 aged weekly for four weeks after optic nerve crush.
9 als at 1, 2, 3 and 4 weeks after optic nerve crush.
10 e growth and synaptic remodeling after nerve crush.
11 r injury but still apparent at 2 months post-crush.
12 imaged again prior to unilateral optic nerve crush.
13 line injection immediately after optic nerve crush.
14 elopment and during regeneration after nerve crush.
15 ted remyelination of the sciatic nerve after crush.
16 ld-type and fat-1 mice after a sciatic nerve crush.
17 recovered to supranormal levels after nerve crush.
18 nction after experimental glaucoma and nerve crush.
19 restoring the stretch reflex following nerve crush.
20 eneration of sensory axons after dorsal root crush.
21 n cell axonal regeneration after optic nerve crush.
22 ks, and at weeks 10 and 50 after optic nerve crush.
23 ell as axonal regeneration after optic nerve crush.
24 ssion was examined in rats after optic nerve crush.
25 y increases the loss of ChAT following nerve crush.
26 en the motor neurons are challenged by nerve crush.
27 lysis of AIS and node disruption after nerve crush.
28 xon growth in an animal model of optic nerve crush.
29 ano, Tempranillo and Grenache, destemmed and crushed.
30 iberate a methane-rich volatile component on crushing.
31 cooling treatment (CT) of olive paste after crushing.
32 inducible shell morphology on resistance to crushing.
33 ore and at different times after optic nerve crush 1.5 mm behind the eye, followed by TUJ1-positive R
37 fective when the action potentials evoked in crushed afferents were prevented from propagating into t
39 n in adult rat spinal cord after dorsal root crush and adeno-associated virus transgene expression in
40 the control group by 28% at two weeks after crush and by 32% at three weeks after crush (P<0.05 at b
43 red in CLU(-/-) mice following sciatic nerve crush and impaired regeneration nerve fibers through CLU
44 ia MEK/ERK signaling and after sciatic nerve crush and Neto2(-/-) neurons from adult mice have stunte
46 s and in eyes that received (1) a mild nerve crush and no treatment, (2) a single intravitreal inject
47 ation and sprouting of the optic nerve after crush and of supraspinal tracts after spinal cord injury
48 m cats that underwent unilateral optic nerve crush and received no treatment or nerve crush combined
50 -1 promoter activation following optic nerve crush and whether this effect targets the earlier quick
51 ile compounds was observed when samples were crushed and analysed by SPME-GC-MS, in comparison to und
52 observed that, although carbon-60 cages were crushed and became amorphous, the solvent molecules rema
56 that the square prism is more resilient when crushed and provides a mechanism for preserving articula
58 th the protocone (pestle) of the upper molar crushing and grinding in the talonid basin (mortar) on t
60 ocesses like reuse, conching, concentration, crushing and storage enhance the amount of PAHs in some
61 otoneurons during regeneration (21 days post crush) and after they reinnervate muscle (3 months).
62 vels of bladderwort presence (functional and crushed) and measured bluegill responses (survival and g
63 of AIS and loss of nodes within days of the crush, and complete loss of nodes 1 week after injury.
64 oplasmic levels in motor neurons after nerve crush, and the relocalization of TDP-43 to the nucleus w
67 ons into the spinal cord after a dorsal root crush as well as substantial axon regrowth in the crush-
69 anced locomotor recovery after sciatic nerve crush, associated to an improvement in key pro-regenerat
74 saurs could not run rapidly, were capable of crushing bite forces, had accelerated growth rates and k
80 regulin 1 impaired remyelination after nerve crush, but did not affect Schwann cell proliferation ass
81 led retinal ganglion cells after optic nerve crush, but remarkable had no influence on their degenera
87 ze and high mandibular strength confer shell-crushing capability matched only by other extinct mollus
89 rve crush and received no treatment or nerve crush combined with intravitreous treatment of the affec
92 perties of the resulting partially amorphous crushed compound are closed to those of the other yellow
93 , alkaline conditions were induced by adding crushed concrete (pH 12.33 +/- 0.07), a filtered concret
94 2030 and 2050, an increase in the uptake in crushed concrete, from 12,000 tonnes today to 200,000 an
96 hannel activity, recordings made after nerve crush demonstrated that the distal stump does not fire a
97 xtension and synaptic remodeling after nerve crush, demonstrating the importance of cGMP in these pro
99 Swallowing oral solid dosage forms whole or crushing/dissolving them and mixing with water were the
100 ces, such as resources that are difficult to crush (e.g. hard-shelled organisms) and assimilate (e.g.
101 report a dinosaur clutch containing several crushed eggs and embryonic material ascribed to the mega
102 ount a massive defensive wound response that crushes eggs of the pest insect; in contrast, naive Nort
103 ophthalmoscope before and after optic nerve crush every week, and fluorescent spots were counted man
107 = 5) before optic nerve crush, weekly after crush for 3 weeks, and at weeks 10 and 50 after optic ne
108 was maintained in the second two weeks after crush for both the cream cheese vehicle study and water
111 lity sand layer overlying a low-permeability crushed granite layer containing a NAPL mixture of indan
113 ic retinoschisis can very rarely occur after crush head injury, but remain specific for shaken baby s
115 d by reducing impulse-evoked transmission in crushed IA afferents, then restoring synaptic activity s
122 le showed precise re-innervation after nerve crush, inaccurate regeneration after correct repair, mor
123 ed that HBO2 significantly reduced the nerve crush-induced allodynia; this anti-allodynic effect of H
125 glutamate or NMDA was injected directly into crush-injured rat sciatic nerves, ERK1/2 phosphorylation
127 s surviving blunt and penetrating trauma and crush injuries have subsequent complications that lead t
130 Wistar rats (n=26) underwent either carotid crush injury (mural thrombosis model) or embolic stroke
133 cidence may be increased as a result of mass crush injury casualties or prolonged evacuation times.
134 Remyelinated axons were evident 20 d after crush injury in control mice, yet were largely absent in
138 ronal death in Nf1+/- mice after optic nerve crush injury is also attenuated by rolipram treatment in
141 n effects of the growth factor artemin after crush injury of the dorsal spinal nerve roots in rats.
143 t of adult mice with LiCl after facial nerve crush injury stimulated the expression of myelin genes,
144 ofile of laser ablation is more similar to a crush injury than the precision removal of individual ce
148 lowing sterile injury, ischemia reperfusion, crush injury, and autoimmune-mediated tissue damage.
150 when combined with retro-orbital optic nerve crush injury, lengthy growth of severed retinal ganglion
151 of MMP-9-PEX into sciatic nerves, 24 h after crush injury, robustly increased phosphorylation of ERK1
153 cell body to axon predominantly after nerve crush injury, suggesting that it encodes a growth-associ
156 overy occurred in mice after a sciatic nerve crush injury, there was little return of motor function
171 unctional recovery after incomplete cervical crush injury; (2) either of these cell types is preferab
173 rofile of RGC degeneration after optic nerve crush is characterized by a two-phase exponential decay
175 tion of the distal nerve stump after a nerve crush is greatly delayed when there is increased potassi
177 y bag is poorly packed and liable to tear or crush its contents, or a tool is firmly attached to a ta
183 We have used the adult mouse facial nerve crush model and adult-onset conditional disruption of th
184 ieback as well as an adult rat dorsal column crush model of spinal cord injury, we found that multipo
186 xonal regeneration in vivo in an optic nerve crush model when given intraocularly without lens damage
191 up (n=250), 89% of culotte (n=75) and 72% of crush (n=169) cases were completed successfully with fin
195 Half of the individuals were inoculated with crushed nodules, whereas the other half remained uninocu
197 accuracy of peripheral re-innervation by (i) crush of both nerves; (ii) correct repair of median to m
198 e explained by structural preservation after crush of Ia afferent synapses on regenerating motoneuron
202 in axonal regeneration following optic nerve crush (ONC) in adult zebrafish, which fully recover from
203 urvival of retinal neurons after optic nerve crush (ONC) in rodent models of visual system injury.
208 cells that infiltrate the brain after nerve crush or contusion actually protect neurons from injury.
210 Ralpha, even when challenged by facial nerve crush or the injection-associated trauma, thereby sugges
211 t RBPMS cells are lost following optic nerve crush or transection at 3 weeks, and all Brn3a-, SMI-32-
213 Tracheal tubes in mutant larvae are often crushed or twisted, although tracheal patterning and mat
214 rare injuries that result from severe, broad crushing or blast forces involving dorsopalmar compressi
215 ither one time immediately after optic nerve crush, or immediately after optic nerve crush and then e
220 report the structure of the grains (intact, crushed, partially milled) in foods, and 5) describe the
230 nced transmission at the central synapses of crushed primary sensory afferents through a mechanism th
237 ils as well as those resulting from their co-crushing reach values which are required by EU legislati
239 on cell (RGC) degeneration after optic nerve crush remained unaffected upon microglia depletion, alth
245 e/cytokine PCR array of the nerve 24 h after crush showed a 2- to 4-fold increase in the expression o
246 sis of the sciatic nerve at 11 d after nerve crush showed that the number of regenerating axons in th
247 ayer deposition (ALD) of alumina followed by crushing showed significantly improved selectivity to ac
248 cal stimulation of the nerve proximal to the crush site did, in fact, eliminate enlargement but was,
249 ons in thy1-YFPH mice elongated through a DR crush site, but not a transection site, and grew along t
256 roteins is reduced by nearly 80% following a crush spinal cord injury in adult male rats, 7 days post
258 g the considered double-stenting techniques, crush stenting (integrated values of TAWSS=1.18.10(-4) N
259 heir mesoscale geometry can facilitate large crushing strains with high energy absorption, optical ba
260 nths, in addition to polymer scaffold radial crush strength and molecular weight (M(W)) at 3, 6, and
261 ebrile monkey in Uganda's Zika Forest and in crushed suspensions of the Aedes mosquito, which is one
262 However, after ganglion cell axons were crushed, synaptic receptors showed greater lateral mobil
264 wder X-ray diffractograms of the powders and crushed tablets show evidence of the formation of new cr
269 When double stenting is considered, the crush technique with the use of a thin-strut stent may r
270 sels were systematically stented (culotte or crush techniques) with mandatory kissing balloon dilatat
272 te RGC axons more robustly after optic nerve crush than wild-type littermates under normal conditions
273 ntent of iridoids was obtained in juice from crushed than from whole berries, and in freeze-dried pom
275 ) by HIV patients and non-infected teens who crush the pills and smoke the powder for its psychoactiv
277 , but the reaction rate could be enhanced by crushing the AB sample to increase its contact area with
280 We tested these possibilities in rats after crushing the tibial nerve (TN), and using Vesicular GLUt
283 The analysis of samples drawn from grape crush through malolactic fermentation in four varieties
286 awley rats were subjected to a sciatic nerve crush under anesthesia and mechanical thresholds were as
287 rves of one eye from each C57Bl/6 mouse were crushed under direct visualization for 3 seconds, 1 mm p
289 hanistic model of AVNs stating that arteries crush veins remains somewhat unchallenged despite the la
292 ged 6 to 9 months (n = 5) before optic nerve crush, weekly after crush for 3 weeks, and at weeks 10 a
293 g in the vehicle group following optic nerve crush were 36 +/- 8, 18 +/- 6, 13 +/- 10, 12 +/- 4, 13 +
294 g retinal areas before and after optic nerve crush were compared, and the fluorescent spots were coun
297 in the retina immediately after optic nerve crush, whilst levels were suppressed in regenerating opt
298 luorescent spots was found after optic nerve crush with 18.6% +/- 2.3%, 11.3% +/- 3.4%, 8.8% +/- 5.3%
299 ioxidant-rich and flavour-rich VOOs, when co-crushing with a higher proportion of Brava olives, satis
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