戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

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 plement 1q, interleukin 6, and brain-derived neurotrophic factor.
2 ositol 1,4,5-trisphosphate and brain-derived neurotrophic factor.
3 ole played by the neurotrophin brain-derived neurotrophic factor.
4 cerebroventricular infusion of brain-derived neurotrophic factor.
5 ing of nerve growth factor and brain-derived neurotrophic factor.
6  responses to the neurotrophin brain-derived neurotrophic factor.
7 ing of nerve growth factor and brain-derived neurotrophic factor.
8 olved both immunomodulation and induction of neurotrophic factors.
9  antidepressants by increasing production of neurotrophic factors.
10 sturbances of developing processes involving neurotrophic factors.
11  in the CA3 area and increased expression of neurotrophic factors.
12 matory response to injury and a reduction in neurotrophic factors.
13 ing mesenchymal stem cells (MSCs) to secrete neurotrophic factors.
14 ed to the receptors of multiple hormones and neurotrophic factors.
15 s dopamine, noradrenaline, and brain-derived neurotrophic factor [3-7].
16  protein analyses of glial cell-line-derived neurotrophic factor, a crucial factor in ureteric bud br
17                                              Neurotrophic factors, a family of secreted proteins that
18 essing, is also a neurotrophic factor, named neurotrophic factor-alpha1 (NF-alpha1) and has important
19 ovel N-terminal-truncated carboxypeptidase E/neurotrophic factor-alphal variants in embryonic mouse b
20 eopontin, chemokine ligand 23, brain derived neurotrophic factor and C-reactive protein (CRP) were fu
21 f genes, tyrosine hydroxylase, brain-derived neurotrophic factor and FK506 binding protein 5.
22 h the secreted APP ectodomain that acts as a neurotrophic factor and full-length APP forming trans-ce
23 e fragments directly sequester brain-derived neurotrophic factor and impair hippocampal long-term pot
24 RET ligand/coreceptor complex, glial-derived neurotrophic factor and its coreceptor, exhibit improved
25 al signaling proteins, such as brain-derived neurotrophic factor and its downstream targets vs. contr
26      We previously showed that brain-derived neurotrophic factor and its receptor, TrkB, in the dorso
27 reted higher concentrations of brain-derived neurotrophic factor and nerve growth factor than NCSC-SC
28  neurotrophic factor, and glial cell-derived neurotrophic factor and release axon-guidance molecules
29                     Cytokines, brain-derived neurotrophic factor and tumor necrosis factor beta, were
30 on relationship studies on this new class of neurotrophic factors and also assist in evaluation of th
31                             Tumor release of neurotrophic factors and axonal guidance molecules likel
32 exert neuroprotection through the release of neurotrophic factors and clearance of neurotoxic glutama
33 separated signals initiated by extracellular neurotrophic factors and nuclear DNA damage are integrat
34 hysical exercise increases the expression of neurotrophic factors and stimulates neuronal growth, res
35 eleterious events, such as downregulation of neurotrophic factors and synaptic proteins.
36 atural growth factor glial cell line-derived neurotrophic factor, and are selective for cells express
37 s such as nerve growth factor, brain-derived neurotrophic factor, and glial cell-derived neurotrophic
38 in-related kinase B, binds the brain-derived neurotrophic factor, and has been shown to play an impor
39 ytokines on monoaminergic neurotransmission, neurotrophic factors, and measures of synaptic plasticit
40                                              Neurotrophic factors are candidates for treating epileps
41 s than neurons or astrocytes and that CSPG4E neurotrophic factors are diminished early in AD, with no
42 olome profiling, vitamin-D, inflammatory and neurotrophic factors are in progress.
43                    NGFR(hi) cells induce the neurotrophic factor BDNF, which contributes to T cell re
44 ymorphism in the gene encoding brain-derived neurotrophic factor (BDNF(Val66Met)) is associated with
45 were inversely associated with brain-derived neurotrophic factor (BDNF) (p < 0.05), and interquartile
46 L-10, and its receptor, CXCR3, brain-derived neurotrophic factor (BDNF) and a receptor tyrosine-prote
47 ivity-induced genes, including brain-derived neurotrophic factor (Bdnf) and activity-regulated cytosk
48                                Brain-derived neurotrophic factor (BDNF) and its high affinity recepto
49                                Brain-derived neurotrophic factor (BDNF) and its receptor TrkB are cru
50 d in potentiated expression of brain-derived neurotrophic factor (BDNF) and memory following HDAC inh
51     Neurotrophins particularly brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF)
52 dent structural plasticity via brain-derived neurotrophic factor (BDNF) and protein neo-synthesis.
53   A parallel downregulation of brain-derived neurotrophic factor (BDNF) and somatostatin (SST), a mar
54 sma corticosterone, as well as brain-derived neurotrophic factor (BDNF) and total percent DNA methyla
55  the BNST (ovBNST), is rich in brain-derived neurotrophic factor (BDNF) and tropomyosin receptor kina
56 in asthmatic airways driven by brain-derived neurotrophic factor (BDNF) and Tropomyosin receptor kina
57 ypothesized that cytokines and brain-derived neurotrophic factor (BDNF) are biomarkers for BP.
58 f ovarian steroid hormones and brain-derived neurotrophic factor (BDNF) are highly convergent on brai
59 5-hydroxytryptamine, 5-HT) and brain-derived neurotrophic factor (BDNF) are two signaling molecules t
60 nscriptome analysis identified brain-derived neurotrophic factor (Bdnf) as a STAT3 target gene with n
61 pendent effects on hippocampal brain-derived neurotrophic factor (BDNF) BDNF-IX, BDNF-IV and BDNF-I t
62 In particular, we knocked down brain-derived neurotrophic factor (Bdnf) bilaterally in the OFC or gen
63 by modulating the secretion of brain-derived neurotrophic factor (BDNF) by pulp fibroblasts.
64 itively correlated with plasma brain-derived neurotrophic factor (BDNF) concentrations.
65             Deficits in muscle brain-derived neurotrophic factor (BDNF) correlate with neuromuscular
66 hese neurons, we observed that brain-derived neurotrophic factor (BDNF) enhances co-localization of d
67 myostatin (3-fold) and lowered brain-derived neurotrophic factor (BDNF) expression (0.6-fold) in the
68 ion resulted in an increase in brain-derived neurotrophic factor (BDNF) expression and a reduction in
69 ks, is necessary for enhancing brain-derived neurotrophic factor (BDNF) expression and improved memor
70 urthermore, while sustained PL brain-derived neurotrophic factor (BDNF) expression is required for me
71 revealed a correlation between brain-derived neurotrophic factor (BDNF) expression, nerve density, an
72 raexonic splicing event in the brain-derived neurotrophic factor (BDNF) gene generates a truncated mR
73 amine are thought to depend on brain-derived neurotrophic factor (BDNF) genotype and dose.
74     The over-expressed colonic brain-derived neurotrophic factor (BDNF) has been reported to be assoc
75                    One member, brain-derived neurotrophic factor (BDNF) has drawn much attention due
76  Circulating concentrations of brain-derived neurotrophic factor (BDNF) have been linked to cancer, n
77 hanced by IN + FUS delivery of brain-derived neurotrophic factor (BDNF) in a toxin-based PD mouse mod
78 g E2-dependent upregulation of brain-derived neurotrophic factor (BDNF) in astrocytes, and subsequent
79 trograde axonal trafficking of brain-derived neurotrophic factor (BDNF) in DIV7 cultures of E18 corti
80                                Brain-derived neurotrophic factor (BDNF) in particular can confer neur
81 he glutamate AMPA receptor and brain-derived neurotrophic factor (BDNF) in the antidepressant-like ef
82 Results Protein expressions of brain-derived neurotrophic factor (BDNF) in the BCCAO rats treated wit
83 vated microglia and less total brain-derived neurotrophic factor (BDNF) in the cortex and/or hippocam
84 was to investigate the role of brain-derived neurotrophic factor (BDNF) in the regenerative ability o
85 idepressant response including brain-derived neurotrophic factor (BDNF) induction and increased phosp
86                                Brain-derived neurotrophic factor (BDNF) influences the differentiatio
87                                Brain-derived neurotrophic factor (BDNF) is a critical effector of dep
88                                Brain-derived neurotrophic factor (BDNF) is a critical growth factor i
89           Here, we report that brain-derived neurotrophic factor (BDNF) is a fasting-induced myokine
90                                Brain-derived neurotrophic factor (BDNF) is a growth factor that plays
91                                Brain-derived neurotrophic factor (BDNF) is a key regulator of the mor
92 es suggest that dysfunction of brain-derived neurotrophic factor (BDNF) is a possible contributor to
93                                Brain-derived neurotrophic factor (BDNF) is a potent modulator of brai
94                                Brain-derived neurotrophic factor (BDNF) is generated by proteolytic c
95                                Brain-derived neurotrophic factor (BDNF) is implicated in both Meth ef
96 olymorphism (SNP) in precursor brain-derived neurotrophic factor (BDNF) is one of the earliest SNPs t
97         In this study, we show brain-derived neurotrophic factor (BDNF) is required for the antimanic
98                                Brain-derived neurotrophic factor (BDNF) is widely accepted for its in
99 atment significantly increased brain-derived neurotrophic factor (BDNF) level and subventricular zone
100 he following: (1) enhances the brain-derived neurotrophic factor (BDNF) level in the brain; (2) reduc
101 of the rats and measured their brain-derived neurotrophic factor (BDNF) levels as a proxy of neuronal
102   This study addressed whether brain-derived neurotrophic factor (BDNF) mediates a transsynaptic effe
103 ecent studies demonstrate that brain-derived neurotrophic factor (BDNF) might be associated with nico
104  for cognitive flexibility and brain-derived neurotrophic factor (BDNF) modulates glutamate plasticit
105  in normal mice and reduced in brain-derived neurotrophic factor (BDNF) mutants, which are severely o
106 nscriptional activation at the brain-derived neurotrophic factor (Bdnf) P4 promoter, which is require
107 n that neurotrophins including brain-derived neurotrophic factor (BDNF) play a role in chronic inflam
108                                Brain-derived neurotrophic factor (BDNF) plays a central pivotal role
109                                Brain-derived neurotrophic factor (BDNF) plays a key role in the patho
110 annabinoid receptor type 1 and brain-derived neurotrophic factor (BDNF) protein levels were measured.
111 essant ketamine: activation of brain-derived neurotrophic factor (BDNF) receptor TrkB, facilitation o
112  caused by upregulation of the brain-derived neurotrophic factor (BDNF) receptor trkB.T1, a truncated
113                                Brain-derived neurotrophic factor (BDNF) regulates neuronal survival a
114        At the molecular level, brain derived-neurotrophic factor (BDNF) represents an important playe
115 hanism involving activation of brain-derived neurotrophic factor (BDNF) signaling and induction of LT
116 is mediated by upregulation of brain-derived neurotrophic factor (BDNF) signaling and that NV-5138 tr
117                                Brain-derived neurotrophic factor (BDNF) signaling in the dorsolateral
118 ess (CSDS) in mice showed that brain-derived neurotrophic factor (BDNF) signaling in the mesolimbic d
119 ucocorticoid receptors (GR) by brain-derived neurotrophic factor (BDNF) signaling integrates both pat
120                                Brain-derived neurotrophic factor (BDNF) signaling regulates synaptic
121 enetic evidence indicates that brain-derived neurotrophic factor (BDNF) signaling through the TrkB re
122              Here we show that brain-derived neurotrophic factor (BDNF) signaling through tyrosine ki
123  in hippocampal plasticity and brain-derived neurotrophic factor (BDNF) signaling.
124                                Brain-derived neurotrophic factor (BDNF) signals through its high affi
125 er, we describe a key role for brain-derived neurotrophic factor (BDNF) that is produced in the brain
126 tor p75(NTR), required for pro-brain-derived neurotrophic factor (BDNF) to induce long-term depressio
127  a candidate gene study on the Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism, a gene
128 evealed that the gene encoding brain-derived neurotrophic factor (BDNF) was associated with ADHD at B
129 dditionally, the expression of brain-derived neurotrophic factor (BDNF) was markedly decreased in the
130 ein and abnormal expression of brain-derived neurotrophic factor (BDNF), a key modulator of neuronal
131                                Brain-derived neurotrophic factor (BDNF), a key player in regulating s
132 eptor (LepRb) colocalizes with brain-derived neurotrophic factor (BDNF), a key player in the pathophy
133                                Brain-derived neurotrophic factor (BDNF), a member of the neurotrophin
134 mammary gland is controlled by brain-derived neurotrophic factor (BDNF), and sexually dimorphic seque
135 in-1, postsynaptic density 95, brain derived neurotrophic factor (BDNF), and stromal cell-derived fac
136  that neurotrophins, including brain-derived neurotrophic factor (BDNF), are severely affected in Alz
137 anin and neuropeptide Y (NPY), brain-derived neurotrophic factor (BDNF), as well as neuroinflammatory
138 hrough increasing the level of brain-derived neurotrophic factor (BDNF), but the underlying mechanism
139 ly: nerve growth factor (NGF), brain derived neurotrophic factor (BDNF), neurotrophin 3 (NT3), and ne
140 rs; nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3), and g
141  facilitated its activation by brain-derived neurotrophic factor (BDNF), observed as levels of phosph
142 of neurotrophins, particularly brain-derived neurotrophic factor (BDNF), on airway contractility [ vi
143 ed neurotrophic factor (GDNF), brain-derived neurotrophic factor (BDNF), pleiotrophin (PTN), and NT-3
144 ed the axon guidance molecule, brain-derived neurotrophic factor (BDNF), selectively at the location
145 s is to synthesize and release brain-derived neurotrophic factor (BDNF), which is vital for neuronal
146 thelial cells (HUVECs) secrete brain-derived neurotrophic factor (BDNF), which significantly stimulat
147 ted protein kinase 1 (MSK1), a brain-derived neurotrophic factor (BDNF)-activated enzyme downstream o
148 t deletion of the neurotrophin brain-derived neurotrophic factor (BDNF)-dependent GR-phosphorylation
149  component aggrecan attenuates brain-derived neurotrophic factor (BDNF)-induced pTRKB in cortical neu
150 pa opioid receptors (KOR), and brain-derived neurotrophic factor (BDNF).
151 egulated miRNAs, downstream of brain-derived neurotrophic factor (BDNF).
152 (rs6265) in the human gene for brain derived neurotrophic factor (BDNF).
153  cells to produce pro-survival brain derived neurotrophic factor (BDNF).
154 nesis, and increased levels of brain-derived neurotrophic factor (BDNF).
155 r or superior to the effect of brain-derived neurotrophic factor (BDNF).
156 TP) that requires postsynaptic brain-derived neurotrophic factor (BDNF)/TrkB and presynaptic cyclic A
157              We report that a muscle-derived neurotrophic factor, BDNF, rescues synaptic and muscle f
158 d their ability to produce astrocyte-derived neurotrophic factors, BDNF and IGF-1, and the glutamate
159 bust downregulation of the astrocyte-derived neurotrophic factors, BDNF and IGF-1, as well as the ast
160  SMF on the gene expression and secretion of neurotrophic factors- BDNF and NT3 was quantified.
161 c plasticity markers including brain derived neurotrophic factor (BNDF) and phosphorylated CREB, both
162                         These data show that neurotrophic factors can selectively promote the surviva
163                            Cerebral dopamine neurotrophic factor (CDNF) is expressed in the brain and
164                            Cerebral dopamine neurotrophic factor (CDNF) protects dopaminergic neurons
165                            Exogenous ciliary neurotrophic factor (CNTF) administration promotes the s
166                                      Ciliary neurotrophic factor (CNTF) has been tested in clinical t
167 ng DCs, which were a major source of ciliary neurotrophic factor (CNTF) in the cornea.
168      We previously demonstrated that ciliary neurotrophic factor (CNTF) promotes process outgrowth fr
169  to early postnatal treatment with a ciliary neurotrophic factor (CNTF) small-molecule peptide mimeti
170 s of hepatocyte growth factor (HGF), ciliary neurotrophic factor (CNTF), and Artemin through specific
171 , including oncostatin (OSM), IL-11, ciliary neurotrophic factor (CNTF), and leukemia inhibitor facto
172 tor, fibroblast growth factor-2, and ciliary neurotrophic factor (CNTF), and the implantation of eMSC
173 /insulin-like growth factor 1 (IGF1)/ciliary neurotrophic factor (CNTF), induces regrowth of retinal
174 its OPC proliferation by stimulating ciliary neurotrophic factor (CNTF)-mediated signaling through re
175 ons that were maintained under subsaturating neurotrophic factor conditions operates under cholinergi
176                  Smooth muscle brain-derived neurotrophic factor contributes to airway hyperreactivit
177  the cognitive impairment in a brain-derived neurotrophic factor-dependent manner.
178 c factors, nor intravenous administration of neurotrophic factors (either through protein or gene del
179  stressed rats, the decline in brain-derived neurotrophic factor expression in the hippocampus and sh
180 pisodic memory and reduced HPC brain-derived neurotrophic factor expression, but did not affect anxie
181  permissive, all-in-one niche which provides neurotrophic factors, extracellular matrix molecules, ce
182 dent of a coreceptor glial cell line-derived neurotrophic factor family receptor alpha, which is requ
183 onse cytokine of the glial cell line-derived neurotrophic factor family within the TGF-beta superfami
184 rturin (NRTN), a member of the glial-derived neurotrophic factor family, was identified from an embry
185            Hippocampal concentrations of the neurotrophic factor fibroblast growth factor 2 (FGF2) ar
186 othelial growth factor (VEGF), brain-derived neurotrophic factor, fibroblast growth factor-2, and cil
187 ne1/PAI-1) and growth factors (brain-derived neurotrophic factor, fibroblast growth factors, platelet
188 sion and function of glial cell line-derived neurotrophic factor (GDNF) and its receptor tyrosine kin
189                      Glial cell line-derived neurotrophic factor (GDNF) binds GDNF family receptor al
190                      Glial cell line-derived neurotrophic factor (GDNF) binds the GFRalpha1 receptor,
191 roach for delivering glial cell line-derived neurotrophic factor (GDNF) directly to the hippocampus o
192 ceptor tyrosine kinase for the glial derived neurotrophic factor (GDNF) family ligands (GFLs), during
193 apeutic potential of glial cell line-derived neurotrophic factor (GDNF) has been studied extensively
194 reased expression of glial cell line-derived neurotrophic factor (GDNF) in injured muscle and increas
195 gated the effects of glial cell line-derived neurotrophic factor (GDNF) in Parkinson's disease, using
196 iphasic function for glial cell line-derived neurotrophic factor (GDNF) in the development and subseq
197 whether administration of glial cell derived neurotrophic factor (GDNF) induces enteric nervous syste
198                      Glial cell line-derived neurotrophic factor (GDNF) is a growth factor that regul
199                      Glial cell line-derived neurotrophic factor (GDNF) is a protein that is required
200   We had previously found that glial derived neurotrophic factor (GDNF) is reduced in SMA astrocytes.
201    The effects of neither glial cell-derived neurotrophic factor (GDNF) nor serotonin are additive wi
202 s have reported that glial cell line-derived neurotrophic factor (GDNF) promotes IEB function, the me
203  Delivery of ectopic glial cell line-derived neurotrophic factor (GDNF) promotes the function, plasti
204 d ex vivo to produce glial cell line-derived neurotrophic factor (GDNF) readily migrate to the mouse
205          Here we identify glial cell-derived neurotrophic factor (GDNF) receptor alpha-like (GFRAL) a
206 binding neuropeptide glial-cell-line-derived neurotrophic factor (GDNF) to increase cocaine intake wa
207 raocular muscle with glial cell line-derived neurotrophic factor (GDNF) to produce a strabismus in in
208 rophin-3 (NT-3), and glial cell line-derived neurotrophic factor (GDNF) were analysed by specific enz
209 addition of tetracycline, glial cell-derived neurotrophic factor (GDNF), and dibutyryl cAMP.
210 cs to CNS, including glial cell line-derived neurotrophic factor (GDNF), and produce potent effects i
211 tial potency of NGF, glial cell line-derived neurotrophic factor (GDNF), brain-derived neurotrophic f
212 raspinally expressed glial cell line-derived neurotrophic factor (GDNF), but not the removal of chond
213 protein (sAPP)beta, sAPPalpha, glial-derived neurotrophic factor (GDNF), P-T181-tau, and P-S396-tau w
214 nucleotide polymorphism of the brain-derived neurotrophic factor gene (BDNF Val66Met), in a way that
215 f a common polymorphism in the brain-derived neurotrophic factor gene (BDNF) provides examples of how
216 ctor, myelin protein zero, and brain derived neurotrophic factor in a 4AP dose dependent manner.
217 urogenesis; the measurement of brain derived neurotrophic factor in plasma is a distal proxy and furt
218 Hg increased the expression of brain-derived neurotrophic factor in the IC, suggesting that astrocyti
219 ramework for the combined therapeutic use of neurotrophic factors in degenerative motor neuron diseas
220  sexual divergence involves higher secretion neurotrophic factors in tears, which in turn modulate ge
221 ving DPCs could increase the availability of neurotrophic factors in the lesion site, thereby promoti
222                            The brain derived neurotrophic factor increased in all brain regions with
223 IC, suggesting that astrocytic brain-derived neurotrophic factor is a potent protectant in the IC.
224 s for cardiotrophin-like cytokine (CLCF1), a neurotrophic factor known to modulate B and myeloid cell
225  decarboxylase 67, Reelin, and brain-derived neurotrophic factor), leading to their hypermethylation,
226 blot analysis revealed significantly altered neurotrophic factor levels in diabetic rat corneas, whic
227                      Glial cell-line-derived neurotrophic factor levels were significantly reduced at
228 scriptional targets downstream of long-range neurotrophic factor ligand/receptor signaling that promo
229 covered that mesencephalic astrocyte-derived neurotrophic factor (MANF) can revert defective RyR2-ind
230 ling induced mesencephalic astrocyte-derived neurotrophic factor (MANF) in innate immune cells.
231              Mesencephalic astrocyte-derived neurotrophic factor (MANF) is a neurotrophic factor that
232  much of the mesencephalic astrocyte-derived neurotrophic factor (MANF) is retained in the endoplasmi
233              Mesencephalic astrocyte-derived neurotrophic factor (MANF) localizes to the ER lumen and
234 then induces mesencephalic astrocyte-derived neurotrophic factor (MANF), an ER-resident protein with
235                               Muscle-derived neurotrophic factors may offer therapeutic promise for t
236 at depended on muscle type, a combination of neurotrophic factors may optimally rescue neuromuscular
237 ong-term potentiation (LTP), a brain-derived neurotrophic factor-mediated (BDNF-mediated) process res
238 ession in females, and reduced brain derived neurotrophic factor mRNA in males.
239                                Brain derived-neurotrophic factor mRNA was increased, but immunoreacti
240 Cs, and up-regulates the expression of their neurotrophic factors mRNA in vitro.
241 ved in proneuropeptide processing, is also a neurotrophic factor, named neurotrophic factor-alpha1 (N
242 tions in L1, where VM engages neuron-derived neurotrophic factor (NDNF+) cells in L1a and MD drives v
243 ected from 72 h serum-free DPSC cultures and neurotrophic factors; nerve growth factor (NGF), brain-d
244  disruption of the prototypic target-derived neurotrophic factor NGF leads to aberrant subtype-restri
245 g, transcriptional regulation, brain-derived neurotrophic factor, nitric oxide, renin-angiotensin).
246 e striatum and the ventral midbrain, without neurotrophic factors, nor intravenous administration of
247 ission, the upregulation of neurogenesis and neurotrophic factors, normalizing hypothalamic-pituitary
248 nd oligodendrocytes, and increased levels of neurotrophic factors NT-3, GDNF and BDNF.
249 tinic acetylcholine receptors (nAChR) during neurotrophic factor (NTF)-dependent excitatory synaptoge
250                                    Deficient neurotrophic factors of CSPG4-type neural cell exosomes
251 this, we here screened 66 combinations of 12 neurotrophic factors on pure, highly viable, and standar
252    This approach can be generalized to other neurotrophic factors or molecules that act in a paracrin
253  several key components of the brain derived neurotrophic factor pathway that were marked by m6A.
254                                     Numerous neurotrophic factors promote the survival of developing
255 T1, a truncated isoform of the brain-derived neurotrophic factor receptor (BDNF), contributes to glio
256 ophin-like cytokine factor 1 (CLCF1)-ciliary neurotrophic factor receptor (CNTFR) signaling axis in l
257                                      Ciliary neurotrophic factor receptor alpha subunit (CNTFRalpha)
258  of other important cargoes, such as the p75 neurotrophic factor receptor was minimally altered in mu
259 lso found that death receptor 6, but not p75 neurotrophic factor receptor, is required for transition
260      Zebrafish carrying a null mutation in a neurotrophic factor receptor, Ret, displayed defects in
261      This calcium flux is accompanied by p75 neurotrophic factor receptor-Rho-actin-dependent expansi
262  axon in response to trophic withdrawal, p75 neurotrophic factor receptor-RhoA signaling governs the
263 hat ShcD binds to active Ret, TrkA, and TrkB neurotrophic factor receptors predominantly via its phos
264 a show that activity-dependent brain-derived neurotrophic factor release from molecularly distinct vH
265 e-activated glucocorticoid receptor (GR) and neurotrophic factor release.
266 ed differentiation, functionality as well as neurotrophic factor release.
267 osure on oligodendrocyte differentiation and neurotrophic factors secretion.
268  transcription associated with brain-derived neurotrophic factor signaling within vHC-PrL projectors
269 mechanisms including increased brain-derived neurotrophic factor signaling, increased synthesis of sy
270 number of proteins linked with brain-derived neurotrophic factor signaling.
271 understanding on the molecular mechanisms of neurotrophic factor signaling.
272 d neural circuitry through the activation of neurotrophic factor signalling(3,4).
273 ed regulation of AKT activity emanating from neurotrophic-factor stimulation and endogenous DNA damag
274  phosphorylated at Thr286, and brain-derived neurotrophic factor, suggesting a role for Abeta in syna
275  by producing antiinflammatory cytokines and neurotrophic factors, support myelin production, and rem
276 G4 cells export in exosomes higher levels of neurotrophic factors than neurons or astrocytes and that
277 cyte-derived neurotrophic factor (MANF) is a neurotrophic factor that is also localized in the endopl
278 ing hypothalamic insulin signaling.MANF is a neurotrophic factor that is secreted but also mediates t
279 target because it is a relatively unexplored neurotrophic factor that modulates intracellular neuropl
280 nd survival.SIGNIFICANCE STATEMENT BDNF is a neurotrophic factor that regulates plastic changes in th
281  critical in upregulating gene expression of neurotrophic factors that are important in regulating ce
282 ;C* brain also led to enhanced expression of neurotrophic factors that have roles in neuronal surviva
283 ervous system, they function proximal to the neurotrophic factors that regulate cell survival, differ
284          These data show that HUVECs secrete neurotrophic factors that significantly enhance axonal g
285 take and has recently been shown to act as a neurotrophic factor to control the development of area p
286 meostasis, whereas target cells also produce neurotrophic factors to promote sympathetic innervation(
287 ncreased Na(+)-channel 1.2 and brain-derived neurotrophic factor transcription and boosted Na(+) curr
288 promising tools to investigate brain-derived neurotrophic factor/TrkB signaling with tight spatial an
289 , mutant mice display impaired brain-derived neurotrophic factor-tropomyosin receptor kinase B-depend
290 approaches to test the role of brain-derived neurotrophic factor-tropomyosin-related kinase B (BDNF-T
291 d increased expression of the angiogenic and neurotrophic factors VEGFA and IL7.
292                                Brain-derived neurotrophic factor, via activation of tropomyosin recep
293                      The production of major neurotrophic factors was equivalent in FGF2-treated and
294           Rather than a conventional peptide neurotrophic factor, we identified a prominent lipid com
295 vel of antioxidant markers and brain-derived neurotrophic factor were altered in PINK1-KO-PBMCs and b
296   Rat models of brain metastasis and ciliary neurotrophic factor were used to induce astrocyte reacti
297 ation, such as firing activity or release of neurotrophic factors were shown to be required for the g
298 s that dental pulp stem cells (DPSC) secrete neurotrophic factors which play an important role in neu
299  primary astrocytes to produce brain-derived neurotrophic factor, which does foster cognitive functio
300   CRADD/caspase-2 signaling is implicated in neurotrophic factor withdrawal- and amyloid-beta-induced

 
Page Top