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1 lowed by intracerebroventricular infusion of brain-derived neurotrophic factor.
2 sport and sorting of nerve growth factor and brain-derived neurotrophic factor.
3  and signaling responses to the neurotrophin brain-derived neurotrophic factor.
4 sport and sorting of nerve growth factor and brain-derived neurotrophic factor.
5  including complement 1q, interleukin 6, and brain-derived neurotrophic factor.
6 art through inositol 1,4,5-trisphosphate and brain-derived neurotrophic factor.
7 y protective role played by the neurotrophin brain-derived neurotrophic factor.
8 factors such as dopamine, noradrenaline, and brain-derived neurotrophic factor [3-7].
9            Osteopontin, chemokine ligand 23, brain derived neurotrophic factor and C-reactive protein
10 hich were accompanied with reduced levels of brain derived neurotrophic factor and neurotransmitters
11 e element-binding protein and an increase in brain-derived neurotrophic factor and c-FOS protein leve
12 specific set of genes, tyrosine hydroxylase, brain-derived neurotrophic factor and FK506 binding prot
13           These fragments directly sequester brain-derived neurotrophic factor and impair hippocampal
14 s of susceptibility or resilience, decreased brain-derived neurotrophic factor and increased phosphor
15 ntal area signaling molecules independent of brain-derived neurotrophic factor and indicate that grea
16 uced hippocampal signaling proteins, such as brain-derived neurotrophic factor and its downstream tar
17                    We previously showed that brain-derived neurotrophic factor and its receptor, TrkB
18 , and they secreted higher concentrations of brain-derived neurotrophic factor and nerve growth facto
19 rophages with E2 increased concentrations of brain-derived neurotrophic factor and neurotrophin 3, wh
20 R activation induced expression of c-Fos and brain-derived neurotrophic factor and phosphorylation of
21 stimulation procedure) and protein levels of brain-derived neurotrophic factor and related signaling
22                                   Cytokines, brain-derived neurotrophic factor and tumor necrosis fac
23 C range, 6 to 15), whereas pleotropin, FGF5, brain-derived neurotrophic factor, and Dickkopf WNT sign
24 trophic markers such as nerve growth factor, brain-derived neurotrophic factor, and glial cell-derive
25 ptor tropomyosin-related kinase B, binds the brain-derived neurotrophic factor, and has been shown to
26 rkA, TrkB, and TrkC) and their ligands (NGF, brain-derived neurotrophic factor, and neurotrophin 3) a
27 e expression neural-plasticity genes such as brain derived neurotrophic factor (BDNF) and its high af
28                    Neurotrophin-3 (Ntf3) and brain derived neurotrophic factor (Bdnf) are critical fo
29 S-induced structural plasticity, we measured brain derived neurotrophic factor (BDNF) in the visual c
30         One exception is the polymorphism in brain derived neurotrophic factor (BDNF), a critical neu
31 sion of synapsin-1, postsynaptic density 95, brain derived neurotrophic factor (BDNF), and stromal ce
32 ors, comprised of nerve growth factor (NGF), brain derived neurotrophic factor (BDNF), neurotrophin 3
33 rotrophin family: nerve growth factor (NGF), brain derived neurotrophic factor (BDNF), neurotrophin 3
34  polymorphism (rs6265) in the human gene for brain derived neurotrophic factor (BDNF).
35 y to stimulate cells to produce pro-survival brain derived neurotrophic factor (BDNF).
36                      At the molecular level, brain derived-neurotrophic factor (BDNF) represents an i
37 varepsilon4 non-carrier[varepsilon4(-)]) and brain-derived neurotrophic factor (BDNF(Val/Val), BDNF(M
38 nucleotide polymorphism in the gene encoding brain-derived neurotrophic factor (BDNF(Val66Met)) is as
39 found OH-PAHs were inversely associated with brain-derived neurotrophic factor (BDNF) (p < 0.05), and
40  age-related neuromuscular changes depend on brain-derived neurotrophic factor (BDNF) acting through
41 chemokine, CXCL-10, and its receptor, CXCR3, brain-derived neurotrophic factor (BDNF) and a receptor
42 f synaptic activity-induced genes, including brain-derived neurotrophic factor (Bdnf) and activity-re
43                     Membrane depolarization, brain-derived neurotrophic factor (BDNF) and forskolin a
44 rovide evidence that trophic factors such as brain-derived neurotrophic factor (BDNF) and glial cell
45                                              Brain-derived neurotrophic factor (BDNF) and its high af
46                                              Brain-derived neurotrophic factor (BDNF) and its recepto
47 d in D1-type MSNs of the NAc by signaling of brain-derived neurotrophic factor (BDNF) and its recepto
48                                              Brain-derived neurotrophic factor (BDNF) and its recepto
49                                              Brain-derived neurotrophic factor (BDNF) and its TrkB re
50 ponent involved in potentiated expression of brain-derived neurotrophic factor (BDNF) and memory foll
51 ubunits from 2B to 2A, which is dependent on brain-derived neurotrophic factor (BDNF) and metabotropi
52                   Neurotrophins particularly brain-derived neurotrophic factor (BDNF) and nerve growt
53 amining this issue because the neurotrophins brain-derived neurotrophic factor (BDNF) and neurotrophi
54 n (mTOR)-dependent structural plasticity via brain-derived neurotrophic factor (BDNF) and protein neo
55                                Expression of brain-derived neurotrophic factor (BDNF) and somatostati
56                 A parallel downregulation of brain-derived neurotrophic factor (BDNF) and somatostati
57 r (GR) and plasma corticosterone, as well as brain-derived neurotrophic factor (BDNF) and total perce
58 ells in the subgranular zone; mRNA levels of brain-derived neurotrophic factor (BDNF) and TrkB were a
59 val nucleus of the BNST (ovBNST), is rich in brain-derived neurotrophic factor (BDNF) and tropomyosin
60 ronal network in asthmatic airways driven by brain-derived neurotrophic factor (BDNF) and Tropomyosin
61  present study aimed to evaluate the role of brain-derived neurotrophic factor (BDNF) and tyrosine re
62 omodeoxyuridine [BrdU]) and those expressing brain-derived neurotrophic factor (BDNF) and vimentin, a
63  factors controlling GABAergic transmission, brain-derived neurotrophic factor (BDNF) appears to play
64 rlies BP, we hypothesized that cytokines and brain-derived neurotrophic factor (BDNF) are biomarkers
65  the actions of ovarian steroid hormones and brain-derived neurotrophic factor (BDNF) are highly conv
66    Serotonin (5-hydroxytryptamine, 5-HT) and brain-derived neurotrophic factor (BDNF) are two signali
67 ingle-cell transcriptome analysis identified brain-derived neurotrophic factor (Bdnf) as a STAT3 targ
68 enes for nucleotide oxidation and identified brain-derived neurotrophic factor (Bdnf) as a target of
69 rsal of age-dependent effects on hippocampal brain-derived neurotrophic factor (BDNF) BDNF-IX, BDNF-I
70               In particular, we knocked down brain-derived neurotrophic factor (Bdnf) bilaterally in
71 hanced gut motility, and increased levels of brain-derived neurotrophic factor (BDNF) but produced no
72 ious injuries by modulating the secretion of brain-derived neurotrophic factor (BDNF) by pulp fibrobl
73                                      Because brain-derived neurotrophic factor (BDNF) can modulate ve
74 ffect that positively correlated with plasma brain-derived neurotrophic factor (BDNF) concentrations.
75                           Deficits in muscle brain-derived neurotrophic factor (BDNF) correlate with
76 c imaging of these neurons, we observed that brain-derived neurotrophic factor (BDNF) enhances co-loc
77 ely increased myostatin (3-fold) and lowered brain-derived neurotrophic factor (BDNF) expression (0.6
78 oglial activation resulted in an increase in brain-derived neurotrophic factor (BDNF) expression and
79 cetylation marks, is necessary for enhancing brain-derived neurotrophic factor (BDNF) expression and
80 y abused drugs lead to changes in endogenous brain-derived neurotrophic factor (BDNF) expression in n
81                      Cocaine exposure alters brain-derived neurotrophic factor (BDNF) expression in t
82              Furthermore, while sustained PL brain-derived neurotrophic factor (BDNF) expression is r
83 tient cohorts revealed a correlation between brain-derived neurotrophic factor (BDNF) expression, ner
84 D striatal neurons; synthesis and release of brain-derived neurotrophic factor (BDNF) from WT cortica
85         Application of a NOTCH inhibitor and brain-derived neurotrophic factor (BDNF) further directe
86 legans, an intraexonic splicing event in the brain-derived neurotrophic factor (BDNF) gene generates
87 effects of ketamine are thought to depend on brain-derived neurotrophic factor (BDNF) genotype and do
88                                              Brain-derived neurotrophic factor (BDNF) has a crucial r
89                                              Brain-derived neurotrophic factor (BDNF) has a crucial r
90                   The over-expressed colonic brain-derived neurotrophic factor (BDNF) has been report
91                           In animal studies, brain-derived neurotrophic factor (BDNF) has been shown
92                                  One member, brain-derived neurotrophic factor (BDNF) has drawn much
93               The biosynthesis of endogenous brain-derived neurotrophic factor (BDNF) has thus far be
94                Circulating concentrations of brain-derived neurotrophic factor (BDNF) have been linke
95 s, could be enhanced by IN + FUS delivery of brain-derived neurotrophic factor (BDNF) in a toxin-base
96 anism involving E2-dependent upregulation of brain-derived neurotrophic factor (BDNF) in astrocytes,
97  found that retrograde axonal trafficking of brain-derived neurotrophic factor (BDNF) in DIV7 culture
98                                              Brain-derived neurotrophic factor (BDNF) in particular c
99 sion vector to induce enhanced expression of brain-derived neurotrophic factor (BDNF) in rat-derived
100 volvement of the glutamate AMPA receptor and brain-derived neurotrophic factor (BDNF) in the antidepr
101 inhibitory circuits, we examined the role of brain-derived neurotrophic factor (BDNF) in the assembly
102               Results Protein expressions of brain-derived neurotrophic factor (BDNF) in the BCCAO ra
103 -tau, and activated microglia and less total brain-derived neurotrophic factor (BDNF) in the cortex a
104 ment-binding protein (CREB) and induction of brain-derived neurotrophic factor (BDNF) in the medial p
105            Mechanisms controlling release of brain-derived neurotrophic factor (BDNF) in the mesolimb
106 Several miRNAs control the expression of the brain-derived neurotrophic factor (BDNF) in the prefront
107 present study was to investigate the role of brain-derived neurotrophic factor (BDNF) in the regenera
108                                Low levels of brain-derived neurotrophic factor (BDNF) increase the de
109 5hmC modifications at the promoter region of brain-derived neurotrophic factor (BDNF) increased, whic
110 ers of the antidepressant response including brain-derived neurotrophic factor (BDNF) induction and i
111                                              Brain-derived neurotrophic factor (BDNF) influences the
112                                  Infusion of brain-derived neurotrophic factor (BDNF) into the dmPFC
113                                              Brain-derived neurotrophic factor (BDNF) is a critical e
114                                              Brain-derived neurotrophic factor (BDNF) is a critical g
115                         Here, we report that brain-derived neurotrophic factor (BDNF) is a fasting-in
116                                              Brain-derived neurotrophic factor (BDNF) is a growth fac
117                             The neurotrophin brain-derived neurotrophic factor (BDNF) is a key regula
118                                              Brain-derived neurotrophic factor (BDNF) is a key regula
119                                              Brain-derived neurotrophic factor (BDNF) is a neurotroph
120                                              Brain-derived neurotrophic factor (BDNF) is a neurotroph
121          Studies suggest that dysfunction of brain-derived neurotrophic factor (BDNF) is a possible c
122                                              Brain-derived neurotrophic factor (BDNF) is a potent mod
123                                              Brain-derived neurotrophic factor (BDNF) is among the ke
124                                              Brain-derived neurotrophic factor (BDNF) is an active ne
125                                              Brain-derived neurotrophic factor (BDNF) is an activity-
126                                              Brain-derived neurotrophic factor (BDNF) is critical for
127                                              Brain-derived neurotrophic factor (BDNF) is essential fo
128                                              Brain-derived neurotrophic factor (BDNF) is expressed in
129                                We found that brain-derived neurotrophic factor (BDNF) is expressed in
130                                              Brain-derived neurotrophic factor (BDNF) is generated by
131                                              Brain-derived neurotrophic factor (BDNF) is implicated i
132                                              Brain-derived neurotrophic factor (BDNF) is known to hav
133 e nucleotide polymorphism (SNP) in precursor brain-derived neurotrophic factor (BDNF) is one of the e
134                                              Brain-derived neurotrophic factor (BDNF) is produced by
135                       In this study, we show brain-derived neurotrophic factor (BDNF) is required for
136                                              Brain-derived neurotrophic factor (BDNF) is widely accep
137 ombination treatment significantly increased brain-derived neurotrophic factor (BDNF) level and subve
138 eandrin does the following: (1) enhances the brain-derived neurotrophic factor (BDNF) level in the br
139 onal capacity of the rats and measured their brain-derived neurotrophic factor (BDNF) levels as a pro
140                                              Brain-derived neurotrophic factor (BDNF) levels in dopam
141 chronic exposure to drugs of abuse increases brain-derived neurotrophic factor (BDNF) levels in ventr
142                                    Low serum brain-derived neurotrophic factor (BDNF) levels measured
143  transforming growth factor (TGF)-beta1, and brain-derived neurotrophic factor (BDNF) levels were exa
144 sides pathological mHTT aggregation, reduced brain-derived neurotrophic factor (BDNF) levels, impaire
145                                      Reduced brain-derived neurotrophic factor (BDNF) may underlie ag
146                 This study addressed whether brain-derived neurotrophic factor (BDNF) mediates a tran
147                             The neurotrophin brain-derived neurotrophic factor (BDNF) mediates activi
148              Recent studies demonstrate that brain-derived neurotrophic factor (BDNF) might be associ
149 s are critical for cognitive flexibility and brain-derived neurotrophic factor (BDNF) modulates gluta
150 caloric status in normal mice and reduced in brain-derived neurotrophic factor (BDNF) mutants, which
151 showing a tonic sympatho-inhibitory role for brain-derived neurotrophic factor (BDNF) neurotransmissi
152   For comparison, the enhancement effects of brain-derived neurotrophic factor (BDNF) on the local pr
153 iated with transcriptional activation at the brain-derived neurotrophic factor (Bdnf) P4 promoter, wh
154 s, we investigated the relationships between brain-derived neurotrophic factor (BDNF) plasma concentr
155 dies have shown that neurotrophins including brain-derived neurotrophic factor (BDNF) play a role in
156                                              Brain-derived neurotrophic factor (BDNF) plays a central
157                                              Brain-derived neurotrophic factor (BDNF) plays a key rol
158         First, does temporary treatment with brain-derived neurotrophic factor (BDNF) prevent nerve d
159  hippocampal cannabinoid receptor type 1 and brain-derived neurotrophic factor (BDNF) protein levels
160 cting antidepressant ketamine: activation of brain-derived neurotrophic factor (BDNF) receptor TrkB,
161 may in part be caused by upregulation of the brain-derived neurotrophic factor (BDNF) receptor trkB.T
162 eL neurons was mediated by activation of the brain-derived neurotrophic factor (BDNF) receptor tropom
163                                              Brain-derived neurotrophic factor (BDNF) regulates diver
164                                              Brain-derived neurotrophic factor (BDNF) regulates neuro
165                                              Brain-derived neurotrophic factor (BDNF) regulates synap
166  to methionine (Met) polymorphism within the brain-derived neurotrophic factor (BDNF) sequence reduce
167  through a mechanism involving activation of brain-derived neurotrophic factor (BDNF) signaling and i
168 ct of NV-5138 is mediated by upregulation of brain-derived neurotrophic factor (BDNF) signaling and t
169                                              Brain-derived neurotrophic factor (BDNF) signaling in th
170 ial defeat stress (CSDS) in mice showed that brain-derived neurotrophic factor (BDNF) signaling in th
171 rylation of glucocorticoid receptors (GR) by brain-derived neurotrophic factor (BDNF) signaling integ
172                                              Brain-derived neurotrophic factor (BDNF) signaling regul
173                            Here we show that brain-derived neurotrophic factor (BDNF) signaling throu
174                                              Brain-derived neurotrophic factor (BDNF) signaling throu
175              Genetic evidence indicates that brain-derived neurotrophic factor (BDNF) signaling throu
176 ortex), integrating dopamine, glutamate, and brain-derived neurotrophic factor (BDNF) signaling, and
177 icate PTP1B in the regulation of the central brain-derived neurotrophic factor (BDNF) signaling.
178 hrough changes in hippocampal plasticity and brain-derived neurotrophic factor (BDNF) signaling.
179                                              Brain-derived neurotrophic factor (BDNF) signals through
180          Further, we describe a key role for brain-derived neurotrophic factor (BDNF) that is produce
181 otrophin receptor p75(NTR), required for pro-brain-derived neurotrophic factor (BDNF) to induce long-
182 , we conducted a candidate gene study on the Brain-derived neurotrophic factor (BDNF) Val66Met polymo
183 A SCIENTIFIC COMMENTARY ON THIS ARTICLE: The brain-derived neurotrophic factor (BDNF) Val66Met polymo
184 iants (SNVs) revealed that the gene encoding brain-derived neurotrophic factor (BDNF) was associated
185              Additionally, the expression of brain-derived neurotrophic factor (BDNF) was markedly de
186  population showed enhanced vulnerability to brain-derived neurotrophic factor (BDNF) withdrawal in t
187 ncreased binding of MeCP2 to the promoter of brain-derived neurotrophic factor (BDNF), a gene that is
188 lated tau protein and abnormal expression of brain-derived neurotrophic factor (BDNF), a key modulato
189 the leptin receptor (LepRb) colocalizes with brain-derived neurotrophic factor (BDNF), a key player i
190                                              Brain-derived neurotrophic factor (BDNF), a key player i
191                                              Brain-derived neurotrophic factor (BDNF), a member of th
192                                              Brain-derived neurotrophic factor (BDNF), a promising ne
193                                              Brain-derived neurotrophic factor (BDNF), a protein impo
194  neurogenic genes [e.g., SRY-box 21 (Sox21), brain-derived neurotrophic factor (Bdnf), and growth arr
195  IL-1beta (control) treatment increased NGF, brain-derived neurotrophic factor (BDNF), and IL-1beta g
196 vation of the mammary gland is controlled by brain-derived neurotrophic factor (BDNF), and sexually d
197 ell documented that neurotrophins, including brain-derived neurotrophic factor (BDNF), are severely a
198 ropeptides galanin and neuropeptide Y (NPY), brain-derived neurotrophic factor (BDNF), as well as neu
199 ssive effect through increasing the level of brain-derived neurotrophic factor (BDNF), but the underl
200 necessary for the many beneficial effects of brain-derived neurotrophic factor (BDNF), including dend
201 e neurotrophin receptor TrkB and its ligand, brain-derived neurotrophic factor (BDNF), is correlated
202 otrophic factors; nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), neurotrophin-3
203 on of TRKB and facilitated its activation by brain-derived neurotrophic factor (BDNF), observed as le
204 ted an effect of neurotrophins, particularly brain-derived neurotrophic factor (BDNF), on airway cont
205 ell line-derived neurotrophic factor (GDNF), brain-derived neurotrophic factor (BDNF), pleiotrophin (
206 CI, we expressed the axon guidance molecule, brain-derived neurotrophic factor (BDNF), selectively at
207 nization was used for measuring the level of brain-derived neurotrophic factor (BDNF), the expression
208 lasticity: the facilitation of plasticity by brain-derived neurotrophic factor (BDNF), the postsynapt
209 e of astrocytes is to synthesize and release brain-derived neurotrophic factor (BDNF), which is vital
210 hat human endothelial cells (HUVECs) secrete brain-derived neurotrophic factor (BDNF), which signific
211  stress-activated protein kinase 1 (MSK1), a brain-derived neurotrophic factor (BDNF)-activated enzym
212  increased the intracellular accumulation of brain-derived neurotrophic factor (BDNF)-activated TrkB
213 eptor inhibition of rat VP neurons through a brain-derived neurotrophic factor (BDNF)-dependent activ
214       Here, we report that Slitrk5 modulates brain-derived neurotrophic factor (BDNF)-dependent biolo
215 e, we show that deletion of the neurotrophin brain-derived neurotrophic factor (BDNF)-dependent GR-ph
216 KB), while PNN component aggrecan attenuates brain-derived neurotrophic factor (BDNF)-induced pTRKB i
217 e, we explore the involvement of the MNKs in brain-derived neurotrophic factor (BDNF)-stimulated prot
218 contributes to the retrograde trafficking of brain-derived neurotrophic factor (BDNF)-TrkB complexes
219 campal neurogenesis, and increased levels of brain-derived neurotrophic factor (BDNF).
220  levels similar or superior to the effect of brain-derived neurotrophic factor (BDNF).
221  the neuroplasticity-associated neurotrophin brain-derived neurotrophic factor (BDNF).
222 been associated with increased risk, such as brain-derived neurotrophic factor (BDNF).
223  be implicated in SZ, including the gene for brain-derived neurotrophic factor (BDNF).
224 i.e., clinically practicable) treatment with brain-derived neurotrophic factor (BDNF).
225 mediators that includes endocannabinoids and brain-derived neurotrophic factor (BDNF).
226 f the tyrosine kinase TRKB, the receptor for brain-derived neurotrophic factor (BDNF).
227             The canonical ligand for TrkB is brain-derived neurotrophic factor (BDNF).
228 r player in this process is the neurotrophin brain-derived neurotrophic factor (BDNF).
229 treating neurons with neurotrophins, such as brain-derived neurotrophic factor (BDNF).
230 triatal dopamine levels and loss of striatal brain-derived neurotrophic factor (BDNF).
231 requires activity-dependent transcription of brain-derived neurotrophic factor (BDNF).
232 n induced by the loss of cortically supplied brain-derived neurotrophic factor (BDNF).
233 ors (MOR), kappa opioid receptors (KOR), and brain-derived neurotrophic factor (BDNF).
234 ion in Lin28-regulated miRNAs, downstream of brain-derived neurotrophic factor (BDNF).
235 otentiation (LTP) that requires postsynaptic brain-derived neurotrophic factor (BDNF)/TrkB and presyn
236                                              Brain-derived-neurotrophic-factor (BDNF) has been shown
237 en identified, including semaphorins [4, 5], brain-derived neurotrophic factors (BDNFs) [6], UNC-6/Ne
238 els of synaptic plasticity markers including brain derived neurotrophic factor (BNDF) and phosphoryla
239                        Propofol enhanced pro-brain-derived neurotrophic factor/brain-derived neurotro
240 uT3, but decreased expression of hippocampal brain-derived neurotrophic factor, consistent with impai
241  neurogenesis via an increase in hippocampal brain-derived neurotrophic factor content.
242                                Smooth muscle brain-derived neurotrophic factor contributes to airway
243 100b, intercellular adhesion molecule-5, and brain-derived neurotrophic factor) daily during extracor
244 tably restored the cognitive impairment in a brain-derived neurotrophic factor-dependent manner.
245 urthermore, in stressed rats, the decline in brain-derived neurotrophic factor expression in the hipp
246 t contextual episodic memory and reduced HPC brain-derived neurotrophic factor expression, but did no
247  repair (Serpine1/PAI-1) and growth factors (brain-derived neurotrophic factor, fibroblast growth fac
248 f vascular endothelial growth factor (VEGF), brain-derived neurotrophic factor, fibroblast growth fac
249 ying a single-nucleotide polymorphism of the brain-derived neurotrophic factor gene (BDNF Val66Met),
250  mouse model of a common polymorphism in the brain-derived neurotrophic factor gene (BDNF) provides e
251                                              Brain-derived neurotrophic factor genetic variants were
252 erve growth factor, myelin protein zero, and brain derived neurotrophic factor in a 4AP dose dependen
253 vestigating neurogenesis; the measurement of brain derived neurotrophic factor in plasma is a distal
254  exposed to MeHg increased the expression of brain-derived neurotrophic factor in the IC, suggesting
255 th response protein 1, cyclooxygenase-2, and brain-derived neurotrophic factor in the PFC.
256 ases 5, accompanied by reduced expression of brain-derived neurotrophic factor, in the brains 61 week
257                                          The brain derived neurotrophic factor increased in all brain
258 n organotypic cultures of cerebellar slices, brain-derived neurotrophic factor increased RacGTP level
259 factor in the IC, suggesting that astrocytic brain-derived neurotrophic factor is a potent protectant
260                                        BDNF (brain-derived neurotrophic factor) is a member of the ne
261 (glutamic acid decarboxylase 67, Reelin, and brain-derived neurotrophic factor), leading to their hyp
262 promoted a sustained increase in hippocampal brain-derived neurotrophic factor level.
263  hippocampal long-term potentiation (LTP), a brain-derived neurotrophic factor-mediated (BDNF-mediate
264 sufficiency was accompanied by impairment of brain-derived neurotrophic factor-mediated dendritic gro
265  whereas intracerebroventricular infusion of brain-derived neurotrophic factor mimicked the action of
266 beta mRNA expression in females, and reduced brain derived neurotrophic factor mRNA in males.
267                                              Brain derived-neurotrophic factor mRNA was increased, bu
268 hins in the contralesional cortex, including brain-derived neurotrophic factor, nerve growth factor,
269 an increased expression of neural growth and brain derived neurotrophic factors (NGF, BDNF).
270 ways of CVD (eg, transcriptional regulation, brain-derived neurotrophic factor, nitric oxide, renin-a
271 surrounding control cells, mimicked by Bdnf (brain-derived neurotrophic factor) or Dcx RNAi, and resc
272 ous impact and implicates a role for the pro-brain-derived neurotrophic factor-p75 neurotrophin recep
273  expression of several key components of the brain derived neurotrophic factor pathway that were mark
274 rticosterone level in the circulation and of brain-derived neurotrophic factor, phosphorylated tropom
275 his study, we report for the first time that brain-derived neurotrophic factor potentiates vestibular
276                      We report here that pro-brain-derived neurotrophic factor (proBDNF) activates p7
277                    We report here that a pro-brain-derived neurotrophic factor (proBDNF)-dependent p7
278 ation of trkB.T1, a truncated isoform of the brain-derived neurotrophic factor receptor (BDNF), contr
279 ether, our data show that activity-dependent brain-derived neurotrophic factor release from molecular
280 vesicles (DCVs) containing a neuropeptide or brain-derived neurotrophic factor shows that the F-actin
281 ivity, likely due to selective impairment of brain-derived neurotrophic factor signaling via its rece
282                      Blockade of hippocampal brain-derived neurotrophic factor signaling with intrace
283 dependent gene transcription associated with brain-derived neurotrophic factor signaling within vHC-P
284 of convergent mechanisms including increased brain-derived neurotrophic factor signaling, increased s
285 s levels of a number of proteins linked with brain-derived neurotrophic factor signaling.
286 dent kinase II phosphorylated at Thr286, and brain-derived neurotrophic factor, suggesting a role for
287 n a microRNA-mediated pathway, downstream of brain-derived neurotrophic factor that affects insulin-l
288 T inhibition increased Na(+)-channel 1.2 and brain-derived neurotrophic factor transcription and boos
289  term depression was clearly diminished, and brain-derived neurotrophic factor treatment was unable t
290 presented are promising tools to investigate brain-derived neurotrophic factor/TrkB signaling with ti
291       Moreover, mutant mice display impaired brain-derived neurotrophic factor-tropomyosin receptor k
292 armacological approaches to test the role of brain-derived neurotrophic factor-tropomyosin-related ki
293                                  Deficits in brain-derived neurotrophic factor/tropomyosin-receptor-k
294 RIS activates two autocrine signaling loops, brain-derived neurotrophic factor/tyrosine kinase B rece
295                                              Brain-derived neurotrophic factor, via activation of tro
296                              Tissue level of brain-derived neurotrophic factor was assessed by enzyme
297         Recombinant human TrkB-Fc chimera or brain-derived neurotrophic factor was infused into the l
298         The level of antioxidant markers and brain-derived neurotrophic factor were altered in PINK1-
299 e to stimulate primary astrocytes to produce brain-derived neurotrophic factor, which does foster cog
300 al for lung cancer cell migration identified brain-derived neurotrophic factor, which stimulates cell

 
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