戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 -stained with antibody to beta(III) Tubulin (neuronal marker).
2 c (SMC marker), Kit (ICC marker) and Pgp9.5 (neuronal marker).
3 ease in newborn cells expressing an immature neuronal marker.
4  function of this popular activity-dependent neuronal marker.
5        Elav has long served as the canonical neuronal marker.
6 ively in migrating neurons, and Hu, an early neuronal marker.
7 hus preceding that detected by using the pan-neuronal marker.
8 t at sites of plasticity, and TuJ1, an early neuronal marker.
9 hydroxyephedrine (HED), an established heart neuronal marker.
10 o decompressive craniectomy, we used NeuN, a neuronal marker.
11 aining was co-localized with that of NeuN, a neuronal marker.
12 rs develop persistent deficits in brain 5-HT neuronal markers.
13 ion of graft-derived cells expressing mature neuronal markers.
14 erentiated regions Sox1 co-labeled only with neuronal markers.
15 sitions within the DG and expressed immature neuronal markers.
16 ion of GFP-labeled cells to express immature neuronal markers.
17 neuronal counts or other immunohistochemical neuronal markers.
18 beled cells that expressed each of the eight neuronal markers.
19 rogenitor vimentin and nestin but not mature neuronal markers.
20  the neocortex and midbrain expressed mature neuronal markers.
21 U-labeled cells in the neostriatum expressed neuronal markers.
22 egions of the spinal cord that express motor neuronal markers.
23  and represses induction of immunophenotypic neuronal markers.
24 o staged by the expression of early and late neuronal markers.
25 uronal differentiation and expression of pan-neuronal markers.
26  immature, and they express only a subset of neuronal markers.
27 neurite extension and enhanced expression of neuronal markers.
28 s and decreased the expression of subsequent neuronal markers.
29 ffness of 700 Pa maximizes expression of pan-neuronal markers.
30  characterized by the expression of multiple neuronal markers.
31 of Pax3 expression and the absence of mature neuronal markers.
32  STAT3 reversed SPARC-mediated expression of neuronal markers.
33 ression of Notch signaling and expression of neuronal markers.
34 e cells were never colabeled with any of the neuronal markers.
35                   Most contained one or more neuronal markers; a few were positive for A2B5 and/or GF
36 d between brain volume and other putative MR neuronal markers also indicate that atrophy reflects axo
37 l dispersion was examined both with an early neuronal marker and through the focal application of DiI
38 SP showed increased immunoreactivity for the neuronal markers and a decrease in Notch1 expression and
39 rate of neurogenesis, based on expression of neuronal markers and cRNA microarray analyses.
40           Sling cells label with a number of neuronal markers and display electrophysiological proper
41 hologies, expressed retinal subtype-specific neuronal markers and displayed neuron-like physiological
42 mentation significantly enhanced cholinergic neuronal markers and facilitated induction of hippocampa
43                     Both populations express neuronal markers and have extensive dendritic arborizati
44  gonadal steroids, resulting in masculinized neuronal markers and male sexual behavior in female rats
45 , no precocious expression of differentiated neuronal markers and no interaction of REST with miR-21.
46            Many of the newborn cells express neuronal markers and show functional phenotypes relevant
47 expressed proliferation markers and immature neuronal markers and that lacked evidence of DNA damage
48 tion of precursor cells that express general neuronal markers and the granule cell marker RU49, but f
49               Improved methods for detecting neuronal markers and the retrograde tracer Fluoro-Gold (
50 tive for microtubule-associated protein 2 (a neuronal marker) and glial fibrillary acidic protein (an
51 biomarkers TUBB3 (melanocyte development and neuronal marker) and its upstream molecule FIG4 (phospha
52 eased the proportions of both beta-tubulin- (neuronal marker) and O4- (oligodendroglial marker) immun
53 lt tissues, characterization of an embryonic neuronal marker, and measurement of cellular proliferati
54 rotein gene product 9.5 (PGP 9.5), a general neuronal marker, and vasoactive intestinal peptide (VIP)
55 ave rise to myofibroblasts, cells expressing neuronal markers, and cells of uncharacterized phenotype
56 on of a neuronal morphology, upregulation of neuronal markers, and establishment of outward rectifyin
57 5) neurons ectopically expressed subcerebral neuronal markers, and extended their axons into subcereb
58 ion of the p21(WAF1) promoter, expression of neuronal markers, and neurite extension.
59 hese cells in the interstitial space express neuronal markers, and their number correlates with plasm
60 and contain cells immunopositive for the pan-neuronal markers ANNA-1 and PGP9.5, the inhibitory neuro
61    Immunohistochemical staining with the pan-neuronal marker, ANNA-1, revealed that the transplanted
62                     By E15, cells expressing neuronal markers are also PSA-NCAM immunoreactive and be
63 it is not known whether all cells expressing neuronal markers are capable of firing action potentials
64 nd sAPPalpha, but cells expressing GABAergic neuronal markers are overrepresented.
65 ression of neuronal subtype-specific and pan-neuronal markers, as well as into Schwann cells and sate
66               However, some cells expressing neuronal markers at E11.5 or E12.5 did not exhibit an ac
67  of neural crest-derived cells expresses pan-neuronal markers at early stages of ENS development (at
68       Of the cells colabeled with BrdU and a neuronal marker, at least half had an inhibitory phenoty
69 scence-activated cell sorting, expressed the neuronal marker beta III tubulin.
70 and vascular tissue that did not express the neuronal marker beta-III tubulin, but was positive for F
71  at the lesion border expressed the immature neuronal marker beta-tubulin, although a small percentag
72 re were confirmed by immunostaining with pan-neuronal marker, beta-III tubulin and two populations we
73 l differentiation media, a peak level of the neuronal marker, beta-tubulin III, was observed on vmIPN
74 d the neural progenitor marker nestin or the neuronal markers beta3-tubulin, syntaxin, and VC1.1 show
75 fferentiate into neurons and express the pan-neuronal markers, beta3-tubulin (Tuj1) and Hu showing th
76 ignificant increase in the expression of pan-neuronal markers (betaIII-tubulin, PGP 9.5) as well as m
77 ally homogenous population and that specific neuronal markers (Brn3 and neurofilament) can partly dis
78                        Here we show that the neuronal marker BRN3A/POU4F1 is expressed abundantly at
79 ury requires not only BrdU uptake and mature neuronal markers but also evidence showing absence of ap
80 teristics of granule neurons and expressed a neuronal marker by the 3-week time point.
81 a activation was assessed by quantifying the neuronal marker c-fos.
82       Further, fibers expressing the sensory neuronal markers calcitonin gene-related protein and sub
83 e neurochemically characterized by using six neuronal markers: calcitonin gene-related peptide (CGRP)
84 iation, and concomitant up-regulation of the neuronal markers calretinin and calbindin, as assessed b
85 these cells were neurons and coexpressed the neuronal markers class IIIbeta-tubulin or neuronal nucle
86 ion and ectopically expressed the early-born neuronal marker CTIP2.
87 ded proliferating progenitors expressing the neuronal marker Dcx (Doublecortin) in the SVZ and the DG
88 ression and observed increased expression of neuronal markers Dcx, Map2, and Tubb3.
89 labeled with BrdUrd coexpressed the immature neuronal markers doublecortin and proliferating cell nuc
90 GFR2/Flk-1 was colocalized with the immature neuronal marker, doublecortin (Dcx).
91 intenance, as Abl mutant photoreceptors lose neuronal markers during late pupal stages but do not re-
92 neurons, as evidenced by coexpression of mDA neuronal markers (e.g., TH, Pitx3, Nurr1, and Lmx1b) and
93              Subsequent to expression of the neuronal marker elav, dVDUP1 is up-regulated to varying
94 euronal morphologies and expressing multiple neuronal markers, even after downregulation of the exoge
95 sion proteins characteristic of EFT activate neuronal marker expression to confer a neural phenotype
96 f Tp53 rescues the decrease in proneural and neuronal marker expression, which is thus an off-target
97 ly regulate RA-induced neurite outgrowth and neuronal marker expression.
98 n and the disease-specific loss of autonomic neuronal marker expression.
99 CGE lineage, because of the lack of specific neuronal markers for these interneuron subtypes.
100               The expression patterns of the neuronal marker FOS were used to assess neurological act
101        Loss of N-acetylaspartate, a putative neuronal marker, from gray matter preceded that observed
102 cells, as determined by an overexpression of neuronal marker genes.
103 or in association with RA express the caudal neuronal marker Hoxc4.
104 ydroxylase expression in addition to the pan-neuronal marker Hu in nonneural ectoderm.
105 nsory ganglia, whereas expression of the pan-neuronal marker Hu is largely unperturbed; GABAergic and
106           Here, Dlx3, Dlx5, Pax6 and the pan-neuronal marker Hu serve as molecular labels to follow t
107  Immunostaining for active caspase-3 and the neuronal marker Hu specifically confirms the presence of
108 birth (P1), all CARTp-IR cells expressed the neuronal marker Hu.
109  between the muscle layers and expressed the neuronal marker Hu.
110  differentiate into neurons that express the neuronal markers Hu or calretinin.
111 fferentiation) and reduced the expression of neuronal markers, Hu antigen, and MAP2.
112 croscopic analysis and staining with the pan-neuronal marker HuC confirmed that this loss of dopamine
113 tion, and many newborn cells coexpressed the neuronal marker HuC/D at 30 days, suggesting they had di
114 were also immunopositive for the nociceptive neuronal markers IB4, TRPV1, CGRP, and substance P.
115 owing: 1) extraction, purification, and NeuN neuronal marker immunotagging of nuclei from adult human
116 rcentage of BrdUrd-labeled cells expressed a neuronal marker in the dentate gyrus than in either neoc
117 Notably, the loss of subcortical cholinergic neuronal markers in aged monkeys was nearly completely r
118 lts suggest that SPARC induces expression of neuronal markers in medulloblastoma cells through its in
119 peptide colocalizes with both astrocytic and neuronal markers in mouse nRT, and investigate the role
120 strated significant reductions in functional neuronal markers in subcortical brain regions in primate
121 ciculation and loss of expression of several neuronal markers in the embryonic peripheral and central
122 n promotes the expression of ectopic sensory neuronal markers in the lateral ectoderm, suggesting a r
123       These results indicate that changes in neuronal markers in the spinal cord can persist after ap
124 dU) incorporation and expression of immature neuronal markers in the subgranular zone (SGZ) of the hi
125 Here we sought to identify reliable efferent neuronal markers in the vestibular periphery of turtle,
126 oration of BrdUrd and expression of immature neuronal markers in two neuroproliferative regions: the
127 es the number of dividing cells that express neuronal markers in vitro.
128 thors measured N-acetylaspartate (a putative neuronal marker) in the right and left thalamus of 17 ma
129 BrdU-positive cells expressed NeuN, a mature neuronal marker, in regions of cortex undergoing targete
130  the STN neurochemical organization based on neuronal markers including parvalbumin (PV), calretinin
131 aracterized using antibodies against several neuronal markers, including those expressed by sensory n
132                                              Neuronal markers; including PGP9.5, GAP-43, acetylated t
133 (1)H MRS revealed age-dependent decreases in neuronal markers, increases in glial markers, but no det
134 nstrated that both excitatory and inhibitory neuronal markers labeled subpopulations of E2-BSA-FITC b
135 vealed that Wnt/beta-catenin antagonists and neuronal markers localized to a particular cell populati
136  (AD) is marked by cholinergic hypofunction, neuronal marker loss, and decreased nicotinic acetylchol
137 e in vitro observation that induction of the neuronal marker MAP-2 in metastatic melanoma cells is ac
138 luciferase-positive cells also expressed the neuronal marker MAP-2.
139                  Decreased expression of the neuronal marker MAP2 and synaptic markers PSD95 and syna
140 res were double-labeled against GABA and the neuronal marker MAP2, and the percentage of neurons that
141 orrespondingly, the expression of the mature neuronal markers Map2 a/b and neurofilament was increase
142  region, newly generated cells expressed the neuronal marker microtubule-associated protein-2, or neu
143 orated within the inner retina expressed the neuronal markers microtubule associated protein (MAP)-2
144 ry indicated that PR-ir colocalizes with the neuronal marker, microtubule associated protein-2, but n
145 h vimentin, and Olig2 was coexpressed with a neuronal marker, microtubule-associated protein 2.
146 in the lesioned brain with some labeled with neuronal marker mitogen-activated protein 2 and decorate
147 mber or volume correlated with levels of the neuronal marker N-acetyl aspartate (NAA).
148 ients showed reduced AN activation and lower neuronal marker N-acetylaspartate in prefrontal and pari
149 onal neurohistopathology and decrease of the neuronal marker N-acetylaspartate measured by HRMAS 1HMR
150 eurons, as revealed by the expression of the neuronal marker N-tubulin, is prevented by Xiro3 express
151 nd expression of a terminally differentiated neuronal marker, N-tubulin, was diminished upon loss of
152 tion factors, Xath3 and MyT1, as well as the neuronal markers, N-tubulin and elrC.
153 ransit amplifying cell marker MASH1, nor the neuronal marker NCAM.
154 oliferating cell nuclear antigen [PCNA]); of neuronal markers (nestin, neuron-specific class III beta
155  proliferating cell nuclear antigen [PCNA]), neuronal markers (nestin, neuron-specific class III beta
156  of cells that stained positive for both the neuronal marker NeuN and 5-bromo-2'-deoxyuridine (BrdU;
157  the cell proliferation marker BrdU with the neuronal marker NeuN and peptides revealed a marked stim
158 oform TASK-1 was mainly colocalized with the neuronal marker NeuN in hippocampal pyramidal neurons an
159            Double staining studies using the neuronal marker NeuN indicated that >90% of rAAV-transdu
160 calizing the bradykinin B2 receptor with the neuronal marker NeuN or the astrocytic marker glial fibr
161 x2(+) precursors acquired positivity for the neuronal marker NeuN over time and integrated into cellu
162 onal populations and dual labelling with the neuronal marker NeuN revealed 28.5+/-1.9% of NeuN labell
163 he 67-kDa isoform of GAD (GAD67), and 7) the neuronal marker NeuN was performed in mice expressing gr
164 ile 88 +/- 2% of SNc neurons labelled by the neuronal marker NeuN were co-labelled for the catecholam
165                                    Using the neuronal marker NeuN, almost every neuron in LS (> 90%)
166  soma) and exhibited immunoreactivity to the neuronal marker NeuN, and to glutamic acid decarboxylase
167    Klotho protein co-localized with both the neuronal marker NeuN, as well as, oligodendrocyte marker
168 entified in deeper cortical layers using the neuronal marker NeuN, showed a marked reduction in neuro
169 s labeled with BrdU (4 weeks) and the mature neuronal marker NeuN.
170     Some of these dividing cells express the neuronal marker NeuN.
171 iated with neurons, identified using the pan-neuronal marker NeuN.
172 e cells migrate into the GCL and express the neuronal markers NeuN and calbindin-D28k.
173 ns were immunolabeled with antibodies to the neuronal markers NeuN, glutamate, and calbindin-D28k, an
174 (Ad-DsRed-SP) elevated the expression of the neuronal markers NeuN, nestin, neurofilament, and MAP-2
175 oreactivity colocalized exclusively with the neuronal marker (NeuN) and did not colocalize with the s
176 hat beta-galactosidase is coexpressed with a neuronal marker (NeuN) and with parvalbumin and neuropep
177 r/CA3 border also were double-labeled with a neuronal marker (NeuN).
178 kers; doublecortin and PSA-NCAM as the early neuronal marker, NeuN to identify mature neurons, and gl
179           BrdU-positive VB cells coexpressed neuronal markers: NeuN, HuC/D, microtubule-associated pr
180 Pax3+ placode cells begin to express the pan-neuronal marker neurofilament while still in the ectoder
181  and/or double or triple immunostaining with neuronal markers neurofilament 200 (NF200) and choline a
182 er of 20.78 +/- 2.5 microm and expressed the neuronal markers neurofilament 200, betaIII-tubulin, pro
183          Over time, CHX10(+) cells expressed neuronal markers [neurofilament, NeuN, and vesicular glu
184 cells had neuronal morphology, expressed the neuronal marker neuron specific enolase, and were incorp
185 labeled cells primarily colocalized with the neuronal marker neuron-specific nuclear protein and rare
186 ochemistry and immunohistochemistry with the neuronal marker neuronal nuclear antigen (NeuN) in rat b
187  nNOS-IR positive cells contained IR for the neuronal marker neuronal nuclear antigen (NeuN), none of
188 n, new cells in the adult mPFC stain for the neuronal marker neuronal nuclear protein, although enhan
189 roglial marker OX-42 and not with either the neuronal marker neuronal-specific nuclear protein or the
190             These cells colocalized with the neuronal marker neuronal-specific nuclear protein.
191  measured using immunohistochemistry for the neuronal markers neuronal nuclear antigen and calbindin
192 tin immunoreactivity was co-localized with a neuronal marker (neuronal specific enolase).
193 us, a subset of which express the orexigenic neuronal marker, Neuropeptide-Y, and respond to fasting
194 istochemically with antisera against the pan-neuronal marker neurotubulin.
195 uding, neurite extension and upregulation of neuronal markers of differentiation.
196 nd for the first time, expression of typical neuronal markers of NT2/D1 differentiation.
197  Western blot analysis of PGP 9.5, a generic neuronal marker, of the colonic tissues were employed to
198 rast to MASH1, fails to induce expression of neuronal markers or a neuronal morphology, but does indu
199 ivity of "neuron"-like cells (expressing pan-neuronal markers or with neuronal morphology) in the gut
200 immunohistochemistry using PGP9.5 (a general neuronal marker) or CGRP (calcitonin gene-related peptid
201 c marker), microtubule-associated protein 2 (neuronal marker), or 2',3'-cyclic mononucleotide 3'-phos
202 unoreacted with antibodies either to NeuN, a neuronal marker, or to the 67-kDa isoform of glutamic ac
203  does not affect neurogenesis, expression of neuronal markers, or initial axonal growth.
204 ns survived and expressed the proprioceptive neuronal marker parvalbumin.
205 ion analysis of cells showed the presence of neuronal markers peripherin, PGP9.5, HuD, tau, synaptic
206 skin innervation, when antibodies to the pan-neuronal marker PGP (protein gene product) 9.5 were used
207     Total nerve density, revealed by the pan-neuronal marker PGP 9.5, was also greater after estrogen
208  the stem cell marker nestin but not the pan-neuronal marker PGP 9.5.
209 estrous rats and immunostained using the pan-neuronal marker PGP9.5 and specific markers for calciton
210 nd non-peptidergic nerve fibers with the pan-neuronal marker PGP9.5, the expression was significantly
211 d to be a subset of cells that expressed the neuronal marker PGP9.5.
212      Cultures were immunostained for the pan neuronal marker, PGP9.5, and TUNEL.
213 efined by coexpression of the proprioceptive neuronal marker pickpocket (ppk) and the sex-determinati
214  gene fruitless (fru) and the proprioceptive neuronal marker pickpocket (ppk) in the female reproduct
215 dult-formed cells, some of which expressed a neuronal marker, present in the bulb 3 weeks later.
216 at young neurons in adult rats show a mature neuronal marker profile and activity-induced immediate e
217 rine (NE) uptake-1 site density, sympathetic neuronal marker profiles, tissue-reduced glutathione/oxi
218 oxyuridine into cells that express the early neuronal marker protein doublecortin in the subventricul
219                   GSI treatment also induced neuronal marker protein expression, as shown by Western
220                      ORNs also expressed the neuronal marker protein gene product (PGP) 9.5 and the c
221                   Immunostaining for the pan-neuronal marker protein gene product (PGP) 9.5 revealed
222 e-labeling experiments using the nonspecific neuronal marker Protein Gene Product 9.5 were performed
223 escence, we labeled sections for the general neuronal marker, protein gene product 9.5.
224 rporation into cells that expressed immature neuronal marker proteins and increased cell number in cu
225 , we investigated the expression of immature neuronal marker proteins that signal the birth of new ne
226 of BCCAO, in the absence of focal changes of neuronal marker proteins.
227 d recovery in the levels of several striatal neuronal markers severely impaired in R6/2 mice.
228 s 14 and 18, combined with immunolabeling of neuronal markers, showed that subpopulations of central
229 e GLI3 repressor and increase in the ventral neuronal markers specified by SHH.
230 xA8 in AnxA8-depleted cells led to decreased neuronal marker staining, and normal cell growth as judg
231 osed to growth factors and low levels of pan-neuronal markers such as beta-III-tubulin.
232 s that EWS/ETS proteins induce expression of neuronal markers such as BRN3A in EFT by showing that th
233 eled cells that do not express aromatase nor neuronal markers such as Hu or NeuN in the POM and other
234 not only Neurog1 and Neurod1 but also mature neuronal markers such as neurofilament, indicating that
235 creased apoptosis, and reduced expression of neuronal markers such as neuron specific enolase and bet
236 on, we found that reprogrammed CMs expressed neuronal markers such as Tuj1, Map2, and NCAM.
237          At week 3 post-transduction, mature neuronal markers such as vGlut and synapsin were observe
238            BrdU labeling was associated with neuronal markers, such as Hu and betaIII tubulin.
239                                              Neuronal markers, such as neurofilament, have been detec
240 ranular layer was co-localized with an early neuronal marker, suggesting that caspase-mediated apopto
241  do proliferate after injury and can express neuronal markers, suggesting a latent neurogenic capacit
242 o dorsal interneurons possessing appropriate neuronal markers, synaptic proteins and functional neuro
243 ical analysis was performed to analyze three neuronal markers: synaptophysin, microtubule-associated
244  began to extend neurites, and expressed the neuronal markers tau, NeuN, neurofilament 200 kDa, and g
245 ochlea are improperly innervated and express neuronal markers that are not normally expressed in thes
246      Although the cells aberrantly expressed neuronal markers, they retained their pigmented CE cell
247 ase marker bromodeoxyuridine (BrdU) and used neuronal markers to characterize new cells at different
248                                 The immature neuronal marker TUC-4 (TOAD/Ulip/CRMP-4) was used to def
249  to 4-fold increase in the expression of the neuronal markers Tuj1 and doublecortin.
250              As cells started to express the neuronal markers Tuj1 and tyrosine hydroxylase (TH) at E
251 yte-specific phenotype marker (MART-1) and a neuronal marker (Tuj1) revealed a subpopulation of melan
252 ic dividing cells, respectively, exhibited a neuronal marker (TuJ1).
253 thors measured N-acetylaspartate (a putative neuronal marker), using in vivo proton magnetic resonanc
254 age-specific markers such as TUBB3, an early neuronal marker; vWF, VEGFA, VEGFC and IL-8, endothelial
255 f neuron-specific enolase messenger RNA as a neuronal marker was also determined in these brain areas
256 s antibodies 2 days postviral injection: the neuronal marker was the transcription factor SOX1; early
257 owing that the number of cells expressing V2 neuronal markers was drastically diminished in gata2 nul
258 th antibodies against PKD1/PKD2 and PKD3 and neuronal markers, we found that PKDs were expressed in r
259 units, calcium-binding proteins, and general neuronal markers, we selectively labeled various OSN typ
260  In addition, some cells expressing an early neuronal marker were mis-localised at the ventricular su
261                                              Neuronal markers were also reduced up to 40%, and hippoc
262 pmental regulatory transcription factors and neuronal markers were analyzed in the alar hypothalamus
263 pmental regulatory transcription factors and neuronal markers were analyzed in the basal hypothalamus
264 pmental regulatory transcription factors and neuronal markers were analyzed in the hypothalamus of th
265                                              Neuronal markers were assessed by reverse-transcription
266         Subsequently, quail cells expressing neuronal markers were found in the chick ciliary ganglio
267  Cells colabeled for BrdU and five different neuronal markers were observed within the primary somato
268 -induced neurite outgrowth and expression of neuronal markers were reduced in this model.
269 udy, selective CB(1) receptor antibodies and neuronal markers were used to identify and characterise
270 arcoma family tumors (ESFTs or EFTs) express neuronal markers, which indicates they may originate fro
271               We used antibodies against the neuronal markers zn-12, acetylated tubulin, and human ne

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top