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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
34 l survival at both 1 and 2 weeks after nerve crush (1 week, 79% vs. 55%; 2 weeks, 60% vs. 31%).
35                        The force required to crush a live urchin was reduced in animals reared in low
36 several partial to nearly complete but badly crushed adult crania.
37 fective when the action potentials evoked in crushed afferents were prevented from propagating into t
38 otential activity restricted to the axons of crushed afferents.
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
41 even increase the stretch reflex after nerve crush and by difference to nerve transection.
42  per week starting 1 week before optic nerve crush and continuing for 6 weeks.
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
45 -positive after injury caused by optic nerve crush and NMDA injection.
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
49 erve crush, or immediately after optic nerve crush and then every 2 days for four weeks.
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
53 ic terms were fitted to compare TRT of nerve-crushed and control eyes over time.
54 nd lyophilisation for apple samples (chunks, crushed and juice).
55                                 The pulp was crushed and mixed with water prior to HS-SPME analysis,
56 that the square prism is more resilient when crushed and provides a mechanism for preserving articula
57                            Tender leaves are crushed and washed by running water before eating.
58 th the protocone (pestle) of the upper molar crushing and grinding in the talonid basin (mortar) on t
59 ng upper and lower molars, probably for dual crushing and grinding.
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
65                 Using mouse optic nerve (ON) crush as a CNS injury model, we and others have found th
66                      Using mouse optic nerve crush as a model for CNS traumatic injury, we performed
67 ons into the spinal cord after a dorsal root crush as well as substantial axon regrowth in the crush-
68           In this study, we describe a nerve crush assay in Drosophila melanogaster to study injury s
69 anced locomotor recovery after sciatic nerve crush, associated to an improvement in key pro-regenerat
70         Confirming results after optic nerve crush, astrocytes in glaucomatous optic nerves had thick
71  in freeze-dried pomace from whole than from crushed berries.
72        During maceration, a reduction in the crushed berry skin break force of more than 15% occurred
73         Thirty-six hours after the CSTs were crushed bilaterally, nocturnal NAT was decreased by 99%.
74 saurs could not run rapidly, were capable of crushing bite forces, had accelerated growth rates and k
75  interference competition in the presence of crushed bladderwort.
76 ong treatments, but growth was greatest with crushed bladderwort.
77                                          The crushed bones are then chopped and incubated for 1 h at
78             Virgin olive oils produced by co-crushing both varieties in two different proportions, re
79 with skin testing using native extracts from crushed buds and leaves.
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
82 y, the source might be ice warmed, melted or crushed by tectonic motions.
83                  Males tended to suffer from crushing by the sow more than females and statistically
84                        Using the multicenter CRUSH-C cohort, genotype-specific rates of advanced fibr
85 oceprevir-based triple therapy at 6 centers (CRUSH-C consortium) were retrospectively assessed.
86 4 bar pCO2 into a capillary tube packed with crushed calcite.
87 ze and high mandibular strength confer shell-crushing capability matched only by other extinct mollus
88                                  Optic nerve crush caused rapid (10-20 minutes), irreversible reducti
89 rve crush and received no treatment or nerve crush combined with intravitreous treatment of the affec
90 velocities consequent to acute sciatic nerve crush compared with wild-type control animals.
91 yses showed a >3-fold faster absorption with crushed compared with whole prasugrel.
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
95                     We used the intensity of crushing damage on differing surface zones of the stones
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
98             The decision between peeling and crushing depends on the cortical tension determined by t
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
104                                  Optic nerve crush, excitotoxicity, and elevated intraocular pressure
105                                        Nerve-crushed eyes showed an initial period of thickening, fol
106 ts, such as rapidly growing plant leaves and crushed foils.
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
109                                          The crushing force required for breaking the tube was reduce
110                          After sciatic nerve crush, functional recovery in vivo was retarded in SNS-g
111 lity sand layer overlying a low-permeability crushed granite layer containing a NAPL mixture of indan
112            Leaching experiments with freshly crushed granodiorite, the dominant bedrock, showed that
113 ic retinoschisis can very rarely occur after crush head injury, but remain specific for shaken baby s
114                    At 11 d after optic nerve crush, hnRNP K underwent significant translocation into
115 d by reducing impulse-evoked transmission in crushed IA afferents, then restoring synaptic activity s
116                     Purge and cold-trap with crushed ice serving as condensation nuclei achieved reco
117 mote regeneration after brachial dorsal root crush in adult rats.
118  to the brainstem after brachial dorsal root crush in adult rats.
119 eurons (MNs) by IA afferents 3 d after nerve crush in anesthetized adult rats.
120 ion cell axon regeneration after optic nerve crush in mice.
121 egeneration of optic nerve axons after nerve crush in vivo.
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
124                                     If nerve crush initiates IA EPSP enlargement as proposed by reduc
125 glutamate or NMDA was injected directly into crush-injured rat sciatic nerves, ERK1/2 phosphorylation
126                                  After large crush injuries across the entire spinal cord, ependyma-d
127 s surviving blunt and penetrating trauma and crush injuries have subsequent complications that lead t
128 uctures and swirling debris inflict numerous crush injuries, fractures, and serious wounds.
129 ognition of potential complications, such as crushing injuries or nerve damage, must be sought.
130  Wistar rats (n=26) underwent either carotid crush injury (mural thrombosis model) or embolic stroke
131 terminating inflammation after sciatic nerve crush injury and promoting regeneration.
132                               In the carotid crush injury animals, biodistribution analysis confirmed
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
135 mmation and regeneration after sciatic nerve crush injury in mice.
136                                Sciatic nerve crush injury in rats induced expression of the ER chaper
137 tion, acute kidney injury by gentamicin, and crush injury in spinal cord cells.
138 ronal death in Nf1+/- mice after optic nerve crush injury is also attenuated by rolipram treatment in
139                                  Optic nerve crush injury leads to rapid elevation of DLK protein, fi
140                Similarly, in the optic nerve crush injury model, MAB228 and AG490 neutralizes dominan
141 n effects of the growth factor artemin after crush injury of the dorsal spinal nerve roots in rats.
142                       Mice received complete crush injury or control laminectomy at either thoracic l
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
145           Within 3 days after an optic nerve crush injury to one eye, primary transcript levels of NF
146                        One day sciatic nerve crush injury triggered a robust increase in UPR-associat
147                                              Crush injury up-regulates kon expression downstream of N
148 lowing sterile injury, ischemia reperfusion, crush injury, and autoimmune-mediated tissue damage.
149                                        After crush injury, animals received either 8.3 mg/kg (332,000
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
152                               In response to crush injury, sciatic nerves in scLRP1(-/-) mice showed
153  cell body to axon predominantly after nerve crush injury, suggesting that it encodes a growth-associ
154                        Following optic nerve crush injury, the mpz:egfp transgene was strongly up-reg
155                            After dorsal root crush injury, the ROCKII(-/-) mice recovered use of the
156 overy occurred in mice after a sciatic nerve crush injury, there was little return of motor function
157            Using an infraorbital optic nerve crush injury, we show that reducing beta-catenin-depende
158  protected from degeneration following nerve crush injury.
159 neration following retro-orbital optic nerve crush injury.
160 arly axonal regeneration after sciatic nerve crush injury.
161  of mouse sciatic nerve distal segment after crush injury.
162 egrowth tapered off around 2 weeks after the crush injury.
163 s gangrene, necrotizing fasciitis, and acute crush injury.
164 axons into the spinal cord after dorsal root crush injury.
165 emyelination is severely delayed after nerve-crush injury.
166 ation and delayed RGC loss after optic nerve crush injury.
167 10 is rapidly expressed by macrophages after crush injury.
168  nerves starting between 2 and 3 weeks after crush injury.
169  to a level equivalent of that observed with crush injury.
170 ation in animal models following axotomy and crush injury.
171 unctional recovery after incomplete cervical crush injury; (2) either of these cell types is preferab
172                         When a thin sheet is crushed into a small three-dimensional volume, it invari
173 rofile of RGC degeneration after optic nerve crush is characterized by a two-phase exponential decay
174              Better recovery following nerve crush is commonly attributed to superior reconnection of
175 tion of the distal nerve stump after a nerve crush is greatly delayed when there is increased potassi
176                                              Crushing is a key step during olive oil extraction.
177 y bag is poorly packed and liable to tear or crush its contents, or a tool is firmly attached to a ta
178 cot seeds as well as beverages prepared from crushed kernels.
179  as well as substantial axon regrowth in the crush-lesioned optic nerve.
180        Our in vivo analysis of dorsal column crush lesions confirms the close association between NG2
181 cm) consisting of clay without AC as well as crushed limestone were also tested.
182                    Eleven eyes from 11 nerve crush mice (baseline age 76 +/- 11.8 days) and eight eye
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
185                      By using an optic nerve crush model that results in the death of the majority of
186 xonal regeneration in vivo in an optic nerve crush model when given intraocularly without lens damage
187                           In the optic nerve crush model, 37%, 87%, and 93% of Rbpms-positive cells w
188 of photoreceptor degeneration and in a nerve crush model.
189                           One week after the crush, more neurons survived in the rtACS-treated group
190             We demonstrate that extract from crushed muscle upregulates Sca-1 expression in myoblasts
191 up (n=250), 89% of culotte (n=75) and 72% of crush (n=169) cases were completed successfully with fin
192 colchicine blockade of axon transport in the crushed nerve.
193                              Furthermore, in crushed nerves of c-Jun OE/+ mice, where c-Jun levels ar
194             Nearly all neurons in ganglia of crushed nerves that were Sox11 immunopositive showed col
195 Half of the individuals were inoculated with crushed nodules, whereas the other half remained uninocu
196                             Three days after crush, nuclear atrophy was restricted to ganglion cells
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
199                      Four weeks after axonal crush of sciatic nerve, TDP-43 transgenic mice remained
200                                          The crushing of superhydrophobic polymer multilayers destroy
201                             The effect of co-crushing on phenolics, ester volatiles and banana nuance
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.
204  retina and that is activated by optic nerve crush (ONC).
205 h RGC loss in the mouse model of optic nerve crush (ONC).
206 le to that exhibited by rats receiving nerve crush only.
207  an anti-allodynic effect, compared to nerve crush-only control rats.
208  cells that infiltrate the brain after nerve crush or contusion actually protect neurons from injury.
209       Using either spinal cord dorsal column crush or contusion injury models, miR-155 deletion impro
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-
212  ErbB2 (caErbB2) selectively in SCs after DR crush or transection.
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
216 eels as if the calvarial bones are deformed, crushed, or broken.
217  10, and 50, respectively, after optic nerve crush (P < 0.001; n = 5).
218  after crush and by 32% at three weeks after crush (P<0.05 at both time points).
219                                   In a nerve crush paradigm, mitochondrial clusters form sequentially
220  report the structure of the grains (intact, crushed, partially milled) in foods, and 5) describe the
221                                        After crush, peripherin and ubiquitin levels remained also sig
222                                           Co-crushing Picual:Local (80:20) provided a significant enh
223 d RGC survival following partial optic nerve crush (pONC) injury.
224           In STEMI patients undergoing PPCI, crushed prasugrel leads to faster drug absorption, and c
225                 Compared with whole tablets, crushed prasugrel led to reduced P2Y12 reaction units by
226  platelet reactivity rates were reduced with crushed prasugrel.
227       This study sought to determine whether crushing prasugrel is associated with more favorable dru
228 udies have investigated the PK/PD effects of crushing prasugrel.
229 ly evolved as a defense in response to shell-crushing predators.
230 nced transmission at the central synapses of crushed primary sensory afferents through a mechanism th
231    A cohort of mice not exposed to the nerve crush procedure served as control.
232                   Seven days after the nerve crush procedure, rats were treated with HBO2 at 3.5 atm
233                                       The co-crushing process improved sensory and health properties
234 treal injection of MT-I/II after optic nerve crush promotes axonal regeneration.
235                                 At 3 d after crush, quantitative analysis revealed nearly a twofold i
236 with greater success following injuries that crush rather than sever the nerve.
237 ils as well as those resulting from their co-crushing reach values which are required by EU legislati
238                         However, after nerve crush, reflex muscle forces during stretch do recover af
239 on cell (RGC) degeneration after optic nerve crush remained unaffected upon microglia depletion, alth
240                                  Optic nerve crush rescued the circadian period of Myk/+ behavior, hi
241 o integrated functions: grasping ability and crushing resistance.
242                                          The crushed rock material is subsequently deposited in headw
243                      The volatile profile of crushed rocket leaves (Eruca sativa and Diplotaxis tenui
244          Analysis of a cross-sectioned and a crushed sample by combining scanning microscopic X-ray d
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
250 d retinal ganglion fibers extending past the crush site.
251 w along SC processes past the transection or crush site.
252  regions proximal, within, and distal to the crush site.
253              The evaluation and evolution of crushed skin mechanical properties during maceration-fer
254                        The dried raisin, the crushed soda can, and the collapsed bicycle inner tube e
255                                  Adjacent to crush spinal cord injury (SCI), reactive astrocytes exhi
256 roteins is reduced by nearly 80% following a crush spinal cord injury in adult male rats, 7 days post
257                            After optic nerve crush, staining for multiple markers of regenerating axo
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
263 nisms of Ani/Neo combination in acute lethal crush syndrome (CS).
264 wder X-ray diffractograms of the powders and crushed tablets show evidence of the formation of new cr
265 l 60-mg loading dose (LD) either as whole or crushed tablets.
266                                              Crushing tablets has been suggested to lead to more favo
267 st) and manufacturing techniques (orthodox, "crush, tear, curl").
268 st) and manufacturing techniques (orthodox, "crush, tear, curl").
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
271                                           In crushing tests live urchins mostly ruptured at sutures b
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
274 around the liposome or actively compress and crush the liposome.
275 ) by HIV patients and non-infected teens who crush the pills and smoke the powder for its psychoactiv
276           To assess in vivo regeneration, we crushed the optic nerve and examined retinal ganglion fi
277 , but the reaction rate could be enhanced by crushing the AB sample to increase its contact area with
278 usts (Locusta migratoria) were axotomized by crushing the base of the antenna.
279                We have previously shown that crushing the optic nerve induces death of retinal gangli
280  We tested these possibilities in rats after crushing the tibial nerve (TN), and using Vesicular GLUt
281                At one week after optic nerve crush, the proportion of fluorescent retinal neurons ret
282 ferent sizes and weights without dropping or crushing them.
283     The analysis of samples drawn from grape crush through malolactic fermentation in four varieties
284                       Mouse liver was gently crushed through a fine mesh with and without in vivo per
285                               Along with the crushed type specimen from Italy, these specimens have a
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
288 brief, the tibia and femora are isolated and crushed using a pestle and mortar.
289 hanistic model of AVNs stating that arteries crush veins remains somewhat unchallenged despite the la
290                        Tmax was shorter with crushed vs whole tablets (P = .047).
291                            Acute optic nerve crush was used to examine neuronal atrophy in the gangli
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
295                Adult rats with sciatic nerve crush were immediately and systemically injected BMMC th
296 hereas the axons detected 6 mm distal to the crush were increased.
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
300 amage induced by scraping from substratum or crushing with glass beads.

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