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1                                              CNTF and neurturin expression in the cochlear nucleus wa
2                                              CNTF binds to high or low affinity receptor complexes co
3                                              CNTF immunoreactivity was observed on astrocytes and oli
4                                              CNTF increased STAT3 phosphorylation in WT and SOCS3kd m
5                                              CNTF increases rapidly and greatly following traumatic o
6                                              CNTF induced an extensive activation of astrocytes, whic
7                                              CNTF induces a decrease in rhodopsin expression and an i
8                                              CNTF reduced diabetes incidence and islet apoptosis in W
9                                              CNTF treatment resulted in a dose-dependent increase in
10                                              CNTF viral transduction maintained rhodopsin expression
11                                              CNTF was identified in a subset of type B cells that lab
12                                              CNTF was increased and also expressed by neurons.
13                                              CNTF, anti-CNTF antibodies, and antibodies to the encaps
14                                              CNTF-/- mice had more extensive tissue loss and similar
15                                              CNTF-receptor complex members, CNTFRalpha, LIFRbeta and
16                                              CNTF/LIF/STAT3 signaling has been shown to promote their
17 le sclerosis, cortical neurons up regulate a CNTF-mediated neuroprotective signalling pathway.
18                                 In addition, CNTF secreted by GSNO-treated astrocytes enhanced the di
19                                 In addition, CNTF treatment resulted in increased numbers and dispers
20                                Additionally, CNTF combined with FGF2 enhanced the formation of prolif
21 d motor neurons, indicating that these adult CNTF receptors play no essential survival role in this m
22         As shown by immunoprecipitation, all CNTF variants retained the ability to bind to CNTFR.
23 lated cell implant is semipermeable to allow CNTF to reach the retina.
24 ression in the OC of deafened rats, although CNTF was expressed throughout the time that SGNs were dy
25                 However, CNTF and its analog CNTF(Ax15) activate leptin-like pathways in the hypothal
26  were quantified (by Western blot analysis), CNTF stimulation leading to the upregulation of connexin
27 enic response is indirect; that is, NT-3 and CNTF first bind to nascent neurons in the DRG--which the
28       Here we demonstrate that both NT-3 and CNTF induce distinct dose-dependent responses on cells i
29                          In the OC, NT-3 and CNTF showed a postnatal increase in expression approxima
30                                     NT-3 and CNTF, which normally increase postnatally, had significa
31 xon regeneration, Muller cell activation and CNTF production in the retina without affecting retinal
32  (NT-3), BDNF, GDNF, neurturin, artemin, and CNTF-in the OC and cochlear nucleus at various ages from
33 T, with CNTF and the combination of BDNF and CNTF reducing mfERG responses.
34                  The combination of BDNF and CNTF rescued more photoreceptors than either factor alon
35 fter PDT, although a combination of BDNF and CNTF rescues more photoreceptors.
36 ons of BDNF, CNTF, a combination of BDNF and CNTF, or PEDF in one eye and PBS in the other 2 days bef
37 hic factor (CNTF), a combination of BDNF and CNTF, or pigment epithelial cell-derived growth factor (
38 eurotrophic factor receptor (CNTFRalpha) and CNTF (0.83 nM) responsiveness in connexin 43 upregulatio
39 ctor receptor alpha subunit (CNTFRalpha) and CNTF play important roles in neuron survival, glial diff
40      Western blotting showed that leptin and CNTF(Ax15) activated Stat3 and ERK1/2 pathway in culture
41 By quantitative PCR, interleukin-6, LIF, and CNTF mRNA increased but with significantly different tim
42                         NT-3, neurturin, and CNTF were most abundant in the postnatal hearing OC; CNT
43  adenomatus polyposis coli (APC(+)) OLs, and CNTF significantly increased the percentage of APC(+) OL
44 endogenous neuroprotective system (TRPV1 and CNTF on astrocytes, and CNTFRalpha on dopamine neurons)
45                                   CNTF, anti-CNTF antibodies, and antibodies to the encapsulated cell
46 these patients were evaluated for CNTF, anti-CNTF antibodies, and antibodies to the encapsulated cell
47 that only CV-1 was as biologically active as CNTF.
48                                   Astroglial CNTF expression was not affected by diffusible neuronal
49  demonstrate that aspirin-induced astroglial CNTF was also functionally active and that supernatants
50                Here, we show that astroglial CNTF expression in the adult mouse striatum is increased
51 ts received intravitreal injections of BDNF, CNTF, a combination of BDNF and CNTF, or PEDF in one eye
52                                      Because CNTF can potentiate FGF-2 expression, we examined the di
53                                      Because CNTF exerts anti-obesogenic effects in adipocytes and NP
54                                      Because CNTF is predominantly expressed in the nervous system, t
55                                   Thus, both CNTF and FGF-2 are present in regions of elevated OPC pr
56 to the complex cellular responses induced by CNTF in diseased retinas.
57 0 in rods also demolishes neuroprotection by CNTF and prevents further activation of Muller glia.
58 esponse to NMDA-induced retinal damage or by CNTF or FGF2 in the absence of retinal damage.
59 eased, and TSPO protein was overexpressed by CNTF-activated astrocytes.
60  better understanding of the roles played by CNTF receptors in adult MNs.
61                        Retinal protection by CNTF in rcd1 dogs was accompanied by a significant incre
62 TAT3, a transcription factor up-regulated by CNTF and to a lesser extent FGF-2, was also detected.
63 y assigned to receive s.c. recombinant CNTF (CNTF(Ax15); 0.1 mg x kg(-1) per day; n = 11) calorie-res
64                                Both combined CNTF-BDNF and BDNF overexpression alone had no statistic
65 /Interleukin-6/IL-6Ralpha hexameric complex, CNTF/CNTF-Ralpha heterodimerizes gp130 and LIF-R via non
66                               In conclusion, CNTF protects mice against streptozotocin-induced diabet
67                                 Constitutive CNTF production resulted in sustained activation of cyto
68        In addition, eyes treated with 1 ng/d CNTF demonstrated significantly greater retinal sensitiv
69                    Eyes treated with 10 ng/d CNTF demonstrated significantly greater retinal sensitiv
70 gical control and infusion groups of 10 ng/d CNTF, 1 ng/d CNTF, and PBS vehicle control.
71  and infusion groups of 10 ng/d CNTF, 1 ng/d CNTF, and PBS vehicle control.
72  and wounded corneas, resulting in decreased CNTF and impaired sensory nerve innervation and regenera
73                                   By 28 dpi, CNTF expression was significantly higher along lesion bo
74 P (CNTF3, and CNTF4) studies received an ECT-CNTF implant, designated as "NT-501," in one eye.
75                                Thus, ectopic CNTF-mediated activation of STAT3 restored axon elongati
76 ted viral vectors (type 2) containing either CNTF, BDNF, or both, with saline-injected eyes and nonin
77 amine the in vivo roles played by endogenous CNTF receptors in adult motor neuron survival and ChAT m
78 strating a developmental role for endogenous CNTF receptor signaling.
79 acological treatments to increase endogenous CNTF levels for neuroprotection.
80 ion with our previous study, that endogenous CNTF receptor signaling can protect MNs against toxic in
81   Together, the data suggest that endogenous CNTF receptor signaling in type B stem cells inhibits ad
82                                 The enhanced CNTF expression in GSNO-treated astrocytes was ascribed
83 TF receptor alpha (CNTFRalpha), an essential CNTF receptor component, is greatly increased in skeleta
84 d reinnervation in normal corneas, exogenous CNTF accelerated nerve regeneration in the wounded corne
85 elucidate a cellular mechanism for exogenous CNTF-triggered neuroprotection and provide insight into
86 ding diseases, the target cells of exogenous CNTF and its mechanism of action remain poorly understoo
87                    We propose that exogenous CNTF initially targets Muller glia, and subsequently ind
88  of the muscle itself, even though exogenous CNTF has been shown to affect these functions.
89 monstrated by supplementation with exogenous CNTF in vitro and siRNA knockdown in vivo.
90  treatment of previously preserved explants, CNTF responsiveness was 174% +/- 23% (P = 0.023; 4 pairs
91 cytes of the SVZ and dentate gyrus expressed CNTF and were close to dopaminergic terminals.
92 ombined treatment with OPC grafts expressing CNTF can enhance remyelination and facilitate functional
93 ant adeno-associated virus (rAAV) expressing CNTF was injected subretinally, for transduction of peri
94                 Ciliary neurotrophic factor (CNTF) acts as a potent neuroprotective agent in multiple
95                 Ciliary neurotrophic factor (CNTF) administration maintains, protects, and promotes t
96       Exogenous ciliary neurotrophic factor (CNTF) administration promotes the survival of motor neur
97 oop, increasing ciliary neurotrophic factor (CNTF) and basic fibroblast growth factor (bFGF) producti
98 re, we examined ciliary neurotrophic factor (CNTF) and fibroblast growth factor-2 (FGF-2) expression,
99 uent release of ciliary neurotrophic factor (CNTF) and leukaemia inhibitory factor (LIF) potently pro
100 anisms by which ciliary neurotrophic factor (CNTF) and other neurotrophic molecules modify the axonal
101 y, we evaluated ciliary neurotrophic factor (CNTF) delivered via an intraocular encapsulated cell tec
102 ch sprouting is ciliary neurotrophic factor (CNTF) expressed in local spinal neurons.
103                 Ciliary neurotrophic factor (CNTF) has been shown to be expressed after brain lesions
104 ctors including ciliary neurotrophic factor (CNTF) in astrocytes in a dose-dependent manner.
105 major source of ciliary neurotrophic factor (CNTF) in the cornea.
106 d expression of ciliary neurotrophic factor (CNTF) in the rds mutant mouse retina.
107 n, the cytokine ciliary neurotrophic factor (CNTF) induces hypophagia and increases signal transducti
108 of the cytokine ciliary neurotrophic factor (CNTF) into the rat striatum, in the absence of neurodege
109                 Ciliary neurotrophic factor (CNTF) is a neurotrophic factor with therapeutic potentia
110                 Ciliary neurotrophic factor (CNTF) is a potent neural cytokine with very low expressi
111                 Ciliary neurotrophic factor (CNTF) is a promyelinating trophic factor, and the mechan
112                 Ciliary neurotrophic factor (CNTF) is important for the survival and outgrowth of ret
113 ting induced by ciliary neurotrophic factor (CNTF) is qualitatively different from the sprouting indu
114                 Ciliary neurotrophic factor (CNTF) is undergoing testing in human clinical trials to
115 ed induction of ciliary neurotrophic factor (CNTF) mRNA.
116       Exogenous ciliary neurotrophic factor (CNTF) promotes motor neuron (MN) survival following trau
117                 Ciliary neurotrophic factor (CNTF) promotes photoreceptor survival but also suppresse
118 educes, whereas ciliary neurotrophic factor (CNTF) promotes, neurogenesis.
119                 Ciliary neurotrophic factor (CNTF) protects pancreatic islets against cytokine-induce
120 that endogenous ciliary neurotrophic factor (CNTF) receptor signaling may inhibit neuronal differenti
121 reatment with a ciliary neurotrophic factor (CNTF) small-molecule peptide mimetic, Peptide 021 (P021)
122 ty trial, human ciliary neurotrophic factor (CNTF) was delivered by cells transfected with the human
123 upregulation of ciliary neurotrophic factor (CNTF) was observed within the retina following optic ner
124                 Ciliary neurotrophic factor (CNTF) was the most effective neurotrophic factor to prom
125 termine whether ciliary neurotrophic factor (CNTF), a combination of BDNF and CNTF, or pigment epithe
126 h factor (HGF), ciliary neurotrophic factor (CNTF), and Artemin through specific activation of their
127 R, the cytokine Ciliary Neurotrophic Factor (CNTF), and its alpha receptor (CNTF-Ralpha).
128 s, particularly ciliary neurotrophic factor (CNTF), as potential anti-obesity therapeutics.
129 factor 1 (IGF1)/ciliary neurotrophic factor (CNTF), induces regrowth of retinal axons and formation o
130 gs treated with ciliary neurotrophic factor (CNTF), to examine the effect of a neuroprotective stimul
131                 Ciliary neurotrophic factor (CNTF), which acts parallel to leptin in the hypothalamus
132 s production of ciliary neurotrophic factor (CNTF), which prevents the active degeneration of dopamin
133 roliferation by ciliary neurotrophic factor (CNTF).
134 he neurotrophin ciliary neurotrophic factor (CNTF).
135 useful protein [ciliary neurotrophic factor (CNTF)].
136  pro-OL differentiation and survival factors CNTF and FGF-2.
137 ce to DA fouling of a carbon nanotube fiber (CNTF) microelectrode to a traditional carbon fiber (CF)
138                                       First, CNTF protein was quantified using Western blots, which r
139  signaling in SVZ NSP cells, with a "floxed" CNTF receptor alpha (CNTFRalpha) mouse line and a gene c
140 mples from these patients were evaluated for CNTF, anti-CNTF antibodies, and antibodies to the encaps
141 lly characterize cells containing functional CNTF receptors.
142 viable cells with minimal cell loss and gave CNTF output at levels previously shown to be therapeutic
143                     After light damage GDNF, CNTF, and BDNF mRNA levels dropped 14- to 16-fold in the
144                      The survival of grafted CNTF-OPCs increased fourfold compared with EGFP-OPCs.
145                                     However, CNTF and its analog CNTF(Ax15) activate leptin-like path
146  Intravitreal injection of recombinant human CNTF protein in rat results in a series of biochemical a
147 entivirus to deliver the same secreted human CNTF used in clinical trials to a mouse model of RP.
148 elivered by cells transfected with the human CNTF gene and sequestered within capsules that were surg
149 on and rarely grow extrasynaptically even if CNTF is administered chronically.
150 ogenesis was reduced by approximately 20% in CNTF-/- mice, confirming the endogenous role of CNTF.
151 lost endogenous membrane-bound CNTFRalpha in CNTF signaling, suggesting the potential of an adjuvant
152                                 CE damage in CNTF-modulated explants and corneal buttons from explant
153  treatments did not diminish the increase in CNTF after MCAO.
154 n blot, there was a quantitative increase in CNTF and BDNF expression in retinas exposed to single vi
155           CE cell connexin-43 mRNA levels in CNTF-treated and (rhCNTFRalpha+CNTF)-treated paired corn
156 type mice by approximately 25-75% but not in CNTF-/- littermates or in the SVZ of mice infused with C
157 umber of neuroblasts in wild-type but not in CNTF-/- littermates.
158 ervation did not affect SVZ proliferation in CNTF-/- mice, suggesting that the dopaminergic innervati
159 % more per year in sham-treated eyes than in CNTF-treated eyes (P < 0.001, linear mixed model), and c
160 ree(2) more per year in sham-treated than in CNTF-treated eyes (P = 0.002, linear mixed model).
161 ntial of an adjuvant rhCNTFRalpha therapy in CNTF-therapy.
162 retinal layers were significantly thicker in CNTF-treated eyes than in sham-treated eyes (P < 0.005).
163  ischemia does not seem to directly increase CNTF, as intrastriatal injection of an ischemic solution
164 ent with the D2 agonist quinpirole increased CNTF mRNA in the SVZ and hippocampal formation, and in c
165                      Significantly increased CNTF was detected in spared white and gray matter betwee
166 vates astrocytes and Muller cells, increases CNTF levels in the retina and leads to enhanced retinal
167 ine-aspartic acid) blocking peptides induced CNTF expression, which was dependent on transcription.
168        We conclude that NO signaling induces CNTF expression in astrocytes that favors the beneficial
169                      Intracerebroventricular CNTF(Ax15) decreased 24 h food intake and body weight in
170 romoted by suppression of CASP2 and CASP6 is CNTF-dependent and mediated through the JAK/STAT signall
171  for 5 days with citrate buffer or 0.1 mg/kg CNTF before receiving 80 mg/kg streptozotocin.
172 ), showed a significant binding in the lenti-CNTF-injected striatum that was saturated and displaced
173                                    Likewise, CNTF inhibited apoptosis in WT but not in SOCS3kd MIN6 c
174  role in progenitor survival and maturation, CNTF acts as a chemoattractant and participates in the r
175 pports hindlimb motor neurons through c-Met; CNTF supports subsets of axial motor neurons through CNT
176                                    Moreover, CNTF elevates the expression of LIF and endothelin 2, th
177                                    Moreover, CNTF reduced NFkappaB activation and required down-regul
178                             Morphologically, CNTF treatment causes a shortening of rod outer segments
179        Unconditional disruption of the mouse CNTF receptor alpha (CNTFRalpha) gene leads to MN loss,
180 at, although neither motor neuron nor muscle CNTF receptors play a significant, nonredundant role in
181 e most abundant in the postnatal hearing OC; CNTF and neurturin most abundant in the cochlear nucleus
182                  Intravitreal application of CNTF further enhances axon regeneration from SOCS3-delet
183         Moreover, therapeutic application of CNTF reduced body weight in mice and humans.
184  show first that subcutaneous application of CNTF to levator auris longus muscles of adult mice evoke
185 hich may rely on the low-affinity binding of CNTF to the IL-6R.
186 VZ) cells in vivo with low concentrations of CNTF to anatomically characterize cells containing funct
187                  The intraocular delivery of CNTF in the encapsulated cell implant appeared to be saf
188 ibitor of the JAK/STAT pathway downstream of CNTF signalling).
189 gression analysis to calculate the effect of CNTF and BDNF.
190                        The overall effect of CNTF is to negatively regulate the phototransduction mac
191 re urgently needed to evaluate the effect of CNTF treatment in patients with inherited retinal degene
192  rhCNTFRalpha decreased the effectiveness of CNTF.
193  an intracellular mediator of the effects of CNTF and other neurotrophic cytokines, acts locally in a
194  abrogation of aspirin-induced expression of CNTF by siRNA knockdown of CREB, the presence of a conse
195 we examined the spatiotemporal expression of CNTF in cross-sections spanning the injury site.
196 lial activation, increases the expression of CNTF in culture, and subsequently increases the number o
197 rin increased mRNA and protein expression of CNTF in primary mouse and human astrocytes in a dose- an
198 n previously that constitutive expression of CNTF prevents photoreceptor death but alters the retinal
199 ohistochemistry to analyze the expression of CNTF receptor alpha (CNTFRalpha) in mouse retina and opt
200                                Expression of CNTF receptor alpha (CNTFRalpha), an essential CNTF rece
201                                Expression of CNTF was also analysed.
202 ation, together with autocrine expression of CNTF, was involved in glioma growth regulation.
203 PKA, abrogated aspirin-induced expression of CNTF.
204 ntly enhanced in animals receiving grafts of CNTF-OPCs.
205 al acuity) received the high-dose implant of CNTF.
206  not BDNF, and caused a delayed induction of CNTF mRNA.
207                                 Induction of CNTF signalling and the anti-apoptotic molecule, Bcl2, t
208 eated with chronic intravitreous infusion of CNTF.
209                  We found that low levels of CNTF halt photoreceptor death, improve photoreceptor mor
210 xotomy, even though there are high levels of CNTF in the optic nerve.
211                  The calculated half-life of CNTF in the vitreous continuously delivered by ECT impla
212                          The localization of CNTF receptors (CNTFRalpha) to the sarcolemma in C57BL/6
213 ight contribute to IL-6R/CNTFR plasticity of CNTF.
214 olecule, Bcl2, known down stream products of CNTF signalling were also increased in MS cortical neuro
215  (western, immunohistochemistry) products of CNTF-related genes.
216 sus cAMP-response element in the promoter of CNTF, and the recruitment of CREB and CREB-binding prote
217                            Quantification of CNTF-dependent proliferation of CNTFR.gp130.LIFR express
218                                  The rate of CNTF secretion from the explants and the corresponding v
219           Therefore, stringent regulation of CNTF may be necessary for its therapeutic application in
220 F-/- mice, confirming the endogenous role of CNTF.
221            Furthermore, an ectopic source of CNTF in adult healthy brains changes SVZ-derived neural
222 ast partially mediated by an upregulation of CNTF expression seen after lens injury.
223 enhanced green fluorescent protein (EGFP) or CNTF and transplanted into the contused adult thoracic s
224 rocytes induced by either thyroid hormone or CNTF was also abrogated by IFN-gamma.
225  to the anorectic action of either leptin or CNTF(Ax15), implying a crucial role for S6K1 in modulati
226  were used as vehicle versus CNTF-treated or CNTF- versus (rhCNTFRalpha+CNTF)-treated (24 hours, 37 d
227                                   Persistent CNTF signaling also caused enhanced phosphorylation of S
228                     NT-501 implants produced CNTF consistently over a 2-year period.
229 opic analysis of the full-length gp130/LIF-R/CNTF-Ralpha/CNTF quaternary complex elucidates an asymme
230 s of the full-length gp130/LIF-R/CNTF-Ralpha/CNTF quaternary complex elucidates an asymmetric structu
231                    Ten participants received CNTF implants in one eye.
232 ificantly increased in animals that received CNTF-OPC grafts compared with all other groups.
233 cipated in a phase 2 clinical trial received CNTF delivered by an encapsulated cell technology implan
234           Importantly, 75% of rats receiving CNTF-OPC grafts recovered transcranial magnetic motor-ev
235                                    Recently, CNTF has been evaluated in clinical trials for the inher
236 ophic Factor (CNTF), and its alpha receptor (CNTF-Ralpha).
237 andomly assigned to receive s.c. recombinant CNTF (CNTF(Ax15); 0.1 mg x kg(-1) per day; n = 11) calor
238 paminergic denervation in adult mice reduced CNTF mRNA by approximately 60%, whereas systemic treatme
239                   Cocultured neurons reduced CNTF expression in astrocytes, which was prevented by li
240 e receptor gp130 gene in Muller glia reduces CNTF-dependent photoreceptor survival and prevents phosp
241                  By multivariate regression, CNTF had a significant protective effect, with 15% less
242 en neurons and astrocytes normally represses CNTF expression and that neuronal dysfunction causes a r
243 RNA levels in CNTF-treated and (rhCNTFRalpha+CNTF)-treated paired corneas averaged (mean+/-SEM) 0.26+
244 s CNTF-treated or CNTF- versus (rhCNTFRalpha+CNTF)-treated (24 hours, 37 degrees C), followed by anal
245                      Interestingly, secreted CNTF was responsible for increased expression of glial f
246 Here, we aimed to generate a CNTFR-selective CNTF variant (CV).
247                      These data confirm that CNTF can exert a protective effect in experimental glauc
248 deo time-lapse imaging), we demonstrate that CNTF controls the directed migration of SVZ-derived prog
249         Among these cytokines, we found that CNTF, IL-11, and Clcf1/Crlf1a can stimulate optic axon r
250                         We hypothesized that CNTF and FGF-2 would increase after SCI, especially in r
251            This Phase I trial indicated that CNTF is safe for the human retina even with severely com
252                        While indicating that CNTF receptors can promote adult MN survival, the data d
253 ied using Western blots, which revealed that CNTF protein continually rose through 28 days post injur
254                                 We show that CNTF controls the migration of subventricular zone (SVZ)
255 n acute model of demyelination, we show that CNTF is strongly re-expressed after lesion and is involv
256                 Echocardiography showed that CNTF(Ax15) reduced cardiac hypertrophy [posterior wall t
257                  These findings suggest that CNTF delivered by the encapsulated cell technology impla
258                 These data also suggest that CNTF receptors may promote adult MN survival and that ap
259                      These data suggest that CNTF-mediated retinal neuroprotection may be a novel the
260 ent-binding protein) was enhanced across the CNTF gene promoter in GSNO treated astrocytes.
261                                 Although the CNTF might have a higher intrinsic RC constant, thus lim
262 s of rhCNTFRalpha (8.3 nM) in augmenting the CNTF (0.83 nM) effect was tested.
263 us limiting its high-frequency behavior, the CNTF shows a significantly higher durability than the CF
264 us neuregulin activity completely blocks the CNTF-induced proliferation and reduces about half of the
265 on of 100 muM DA, the signal measured by the CNTF microelectrode shows a 2-h window over which no dec
266                      Clinical studies of the CNTF derivative Axokine revealed intolerance at higher c
267 w that the CNTF-binding alpha-subunit of the CNTF receptor (CNTFRalpha) is released from injured tiss
268 nd adult-onset conditional disruption of the CNTF receptor alpha (CNTFRalpha) gene to directly examin
269 ibody targeted to the gp130 component of the CNTF receptor) and AG490 (an inhibitor of the JAK/STAT p
270                    Moreover, blockade of the CNTF-specific receptor CNTFRalpha induced sensory nerve
271 rating retina, whereas studies show that the CNTF-binding alpha-subunit of the CNTF receptor (CNTFRal
272 ment of CREB and CREB-binding protein to the CNTF promoter by aspirin suggest that aspirin increases
273 tural features with CNTF and signals via the CNTF receptor tripartite complex comprised of CNTFRalpha
274 tion normally regulates neurogenesis through CNTF.
275 inergic system promotes neurogenesis through CNTF.
276 ns and leads to behavioural recovery through CNTF receptor alpha (CNTFRalpha) on nigral dopamine neur
277 y nerve innervation and regeneration through CNTF and that diabetes reduces DC populations in UW and
278                                        Thus, CNTF mediates dopaminergic innervation- and D2 receptor-
279 ing site from cardiotrophin-like cytokine to CNTF.
280 scue from cell death, continuous exposure to CNTF changed photoreceptor cell profiles, especially res
281 lpha from axons renders RGCs unresponsive to CNTF, thereby contributing to regenerative failure and d
282                                       Unlike CNTF, our studies have revealed that NP also substantial
283 e novel observations suggest that NP, unlike CNTF, may not be a viable obesity therapeutic.
284 an donor corneas were used as vehicle versus CNTF-treated or CNTF- versus (rhCNTFRalpha+CNTF)-treated
285  the explants and the corresponding vitreous CNTF levels were evaluated for each time point.
286                        Disruption of in vivo CNTF receptor signaling in SVZ NSP cells, with a "floxed
287          The data also indicate that in vivo CNTF receptors play very different roles in adult and em
288 to different patterns of initiation: whereas CNTF-induced sprouts emerge randomly from the surface of
289                                      Whether CNTF-induced changes in rods are through the same mechan
290       This has caused concerns about whether CNTF is detrimental to the function of photoreceptors be
291         For this reason, we assessed whether CNTF protects mice against streptozotocin-induced diabet
292  trophic factor, and the mechanisms by which CNTF expression could be increased in the brain are poor
293                                        While CNTF neutralization retarded reinnervation in normal cor
294 eit with a much lower affinity compared with CNTF.
295 OCS3 knockdown MIN6 cells were cultured with CNTF, IL1beta, or both.
296 ares functional and structural features with CNTF and signals via the CNTF receptor tripartite comple
297 ttermates or in the SVZ of mice infused with CNTF antibodies.
298 elivered by ECT implants was 51 months, with CNTF levels statistically equivalent between the 6- and
299 oved retinal function 1 week after PDT, with CNTF and the combination of BDNF and CNTF reducing mfERG
300                      Combined treatment with CNTF and BoTX produces exceptionally robust extratermina

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