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1            The selectivity in its peripheral inhibitory action may partly account for fremanezumab's
2 -proteosomal pathway and hence reversing the inhibitory action of Foxp3 on RORgammat activity.
3                               Because of its inhibitory action on the reproductive axis in other vert
4                                         This inhibitory action was not associated with overt circadia
5 st and may be attenuated when drugs with NHE inhibitory actions are given concomitantly.
6 osed of Az and geldanamycin, which have high inhibitory activities towards both Hsp70 and Hsp90, exhi
7 wever, the Az and imatinib hybrids have weak inhibitory activities towards Hsp70 and Abl, and display
8 lase and angiotensin converting enzyme (ACE) inhibitory activities were successfully identified using
9 N-FIV (3-1kDa) fractions showed the best ACE-inhibitory activities with IC50 values of 53.31 and 75.0
10                3a and 7c exhibited promising inhibitory activities with MICs ranging 1-8 mug/mL again
11 in vitro CB1R antagonist activities and iNOS inhibitory activities.
12 othelial progenitor EP cells) and the kinase inhibitory activity (toward both isolated kinases and EP
13 ur compounds were further screened for their inhibitory activity against recombinant HDAC1-3, HDAC6,
14 nalysis of in vivo FLT3 inhibition by plasma inhibitory activity assay and indicated improved overall
15 basophil activation and measurement of serum inhibitory activity for allergen-IgE binding to B cells
16 he absence of vivax invasion assays, binding-inhibitory activity of antibodies has been reported to b
17 ion.IMPORTANCE The greater ex vivo antiviral inhibitory activity of CD8(+) T cells from elite control
18  of this study was to evaluate the potential inhibitory activity of guarana extracts, after digestion
19                        The latter blocks the inhibitory activity of the autoinhibitor domain.
20 tioxidant capacity and the alpha-glucosidase inhibitory activity of the duodenal extract correlated w
21                                          The inhibitory activity of the non-digested and digested sam
22 ed comparable antioxidant capacity, stronger inhibitory activity on pancreatic lipase and comparable
23  dissociates it from 5'UTRs and relieves its inhibitory activity on RP mRNA translation.
24 and pepsin hydrolysates exhibited higher ACE-inhibitory activity than HT (P<0.05).
25 activity whereas a negative impact on lipase inhibitory activity was observed (p<.0001).
26                          GF WSP possessed NO inhibitory activity, and the strongest was GF121.
27 and selective Brr2 inhibitor 9 with helicase inhibitory activity.
28 N-benzylated derivative showed enhanced Clk1 inhibitory activity.
29  agents exerting partial FXR agonism and sEH inhibitory activity.
30 tor, or iniparib (n = 11), which has no PARP inhibitory activity.
31                          Thus, a decrease in inhibitory afferents to MNTB neurons should lead to grea
32        The resulting inhibitor combines high inhibitory affinity and selectivity with a good stabilit
33 uce persistent memory erasure even after the inhibitory agent is removed.
34 y arises in the inner plexiform layer, where inhibitory amacrine cells modulate the excitatory signal
35 ological character is dependent on vesicular inhibitory amino acid transporter-mediated signaling.
36 for additional research on the mitochondrial inhibitory and antiestrogenic effects of QUATS, includin
37                                  Optimum ACE-inhibitory and antioxidant activities of proteins separa
38 s and specificities, we predicted and tested inhibitory and cytotoxic NK potential on the basis of KI
39 We show that nAChRs are located on ascending inhibitory and descending excitatory presynaptic inputs
40  that PNN removal alters the balance between inhibitory and excitatory spiking activity directly.
41  combinations of intrinsic ion conductances, inhibitory and excitatory synaptic inputs that differ am
42 ested that C3b is responsible for the growth inhibitory and neurotoxic or anti-adhesion activities of
43                      We further verified the inhibitory and stimulatory functions of UbVs in cells.
44 cement factor can lead to the development of inhibitory antibodies, requiring the use of bypassing ag
45 ck of tolerance, leading to the formation of inhibitory antibodies.
46 ficiently expressed in Escherichia coli, and inhibitory assays demonstrated that it was a potent inhi
47 essed in amygdalar neurons of mice during an inhibitory avoidance task revealed that CaMKII activity
48 its ability to engage an MTSS1-Src-cortactin inhibitory axis.
49 tatively anti-Bd bacteria to determine if Bd-inhibitory bacteria are dominant microbiome members.
50 ype-specific contributions to the excitatory/inhibitory balance and circuit maturation.
51         GIRK channels mediate the actions of inhibitory brain neurotransmitters.
52 ts are caused by hyperphosphorylation of the inhibitory C-terminal tail of Lck.
53                                        Their inhibitory capacities through the involvement of tolerog
54 electrical coupling relates to a coordinated inhibitory chemical synapse formation between sparsely l
55                    GABAA receptors are brain inhibitory chloride ion channels.
56  signaling in interneuronal connectivity and inhibitory circuit formation.
57         By contrast, we identify a pull-push inhibitory circuit in frontal cortex that originates in
58 of learning depends on structured changes to inhibitory circuitry remains unclear.
59 though experience-dependent changes in brain inhibitory circuits are thought to play a key role durin
60 e variety of odorants.SIGNIFICANCE STATEMENT Inhibitory circuits in the olfactory bulb (OB) play a ma
61            In the main olfactory bulb (MOB), inhibitory circuits regulate the activity of principal c
62 omplement activation and genetic variants in inhibitory complement factor H (CFH) are also features o
63  prefrontal infusions of KYNA attenuated the inhibitory component of PFC LFP responses, a disruption
64 st excitatory component followed by a slower inhibitory component.
65 ment function identified a single complement inhibitory compound, termed cmp-5, and mechanistic studi
66 ore potent antimicrobial agents [VRE minimum inhibitory concentration (MIC) = 0.01-0.005 mug/mL] with
67                       The daptomycin minimum inhibitory concentration (MIC) was 4 mg/L in 78 (69.6%)
68                   (131)I-RPS-027, with a 50% inhibitory concentration (PSMA) of 15 nM and a dissociat
69 bility testing, and determination of minimum inhibitory concentration is conventionally performed by
70 ith a KD of 76 nM against BioA and a minimum inhibitory concentration of 1.7 muM (0.6 mug/mL) against
71                        Normally, the minimum inhibitory concentration of an antibiotic, the dosage at
72 acillin underdosing when facing high minimal inhibitory concentration pathogens.
73 tively correlated (r = -0.52; P =018) to 50% inhibitory concentration values.
74 und to GRPR with high affinity (half maximal inhibitory concentration, 1-2 nM).
75 azyl (DPPH) radical quenching potential (50% inhibitory concentration, IC50 approximately 0.59mg/mL)
76 ng susceptibility tests to determine minimum inhibitory concentrations for M. genitalium.
77 d clustering on the resulting excitatory and inhibitory connection patterns.
78 Syt1 and Syt2 at two types of fast-releasing inhibitory connections in the mammalian CNS: the medial
79 was as follows: processing speed ( r = .39), inhibitory control ( r = .34), working memory ( r = .28)
80 al gyrus (IFG)-one node in a corticothalamic inhibitory control (IC) network.
81  the first to show associations between poor inhibitory control and amphetamine reward sensitivity at
82                                  This subtle inhibitory control of plateau potential depends on the l
83 ed actions or interfering information (i.e., inhibitory control) are essential human cognitive abilit
84  reward-value coupled with an underdeveloped inhibitory control, and thus a hypersensitivity to rewar
85 rating motoneurons and decreased presynaptic inhibitory control.
86              In this respect diffuse noxious inhibitory controls (DNIC) are a unique form of endogeno
87 eases in excitability in both excitatory and inhibitory cortical neurons show that selective dysfunct
88 ibition and tACS acts on both excitatory and inhibitory cortical neurons.
89                                         With inhibitory coupling, ISR is quite robust.
90     Cardiomyocyte-directed expression of the inhibitory CREM isoform CREM-IbDeltaC-X in transgenic mi
91 f tyrosine kinase receptor AXL, an important inhibitory DC auto-regulator.
92 pectroscopy demonstrated that the N-terminal inhibitory domain (NID) is intrinsically disordered, yet
93 pecific APP isoforms contain Kunitz protease-inhibitory domains, which regulate the proteolytic activ
94 made by CCK(+)VGlut3(+) basket cells and the inhibitory drive they exerted on pyramidal cells were re
95 slational potential of this marker of spinal inhibitory dysfunction in human painful diabetic neuropa
96 pe A receptor function, indicative of spinal inhibitory dysfunction.
97 synaptic effects that disrupt the excitatory/inhibitory (E/I) balance.
98 ders arise from imbalances in excitatory and inhibitory (E/I) brain circuitry.
99 sis, and an increased ratio of excitatory to inhibitory (E/I) neurotransmission.
100 ent was antagonistic and had a minimal tumor inhibitory effect compared with individual agents.
101                                         This inhibitory effect of BECs was significantly reduced in t
102 ct of codon reassignment in the SGC, and the inhibitory effect of changes in the code on horizontal g
103 Moreover, Y470H and Y88F hDAT potentiate the inhibitory effect of cocaine on DA uptake and attenuate
104                                          The inhibitory effect of F4 was not mediated through the inh
105                                The strongest inhibitory effect of FA ( approximately 62%) appeared wh
106                                          The inhibitory effect of Lm211 is seen only in fibers of sma
107 nase II (CaMKII) was blocked with KN-93, the inhibitory effect of noradrenaline on the capsaicin-acti
108                                          The inhibitory effect of noradrenaline on TRPV1 channels was
109 these findings provide new insights into the inhibitory effect of SFN on HCC tumor angiogenesis as we
110  evidence for the enhancement of rapamycin's inhibitory effect on IL-1beta secretion by the IL-1 rece
111 ient to explain Pre1a's potent and selective inhibitory effect on the fast inactivation process of Na
112 r NOM) alone, whereas Zn+NOM showed a lesser inhibitory effect than its individual component (NOM) al
113                                         This inhibitory effect was determined by the length of the in
114                                    The PON-2 inhibitory effect was ENaC-specific, as PON-2 had no eff
115 letely ablated the activity of LLO, and this inhibitory effect was fully reversible by treatment with
116 ocumented external immune system with strong inhibitory effects against B. bassiana.
117 ter the expiry date and retained significant inhibitory effects against colon carcinoma (CaCo-2) cell
118  as a combination of terpenes, exerts growth inhibitory effects against colon carcinoma, suggesting a
119                                   These fear-inhibitory effects cannot be explained by changes in app
120 hate and Zn+NOM+orthophosphate) had stronger inhibitory effects compared to each inhibitor (Zn, ortho
121 ading during storage, although EDTA had some inhibitory effects in the early stages of storage.
122              To appropriate and redirect the inhibitory effects of CD200R signaling on transferred CD
123  protected SMIT1 activity from the otherwise inhibitory effects of cellular depolarization imposed by
124  antioxidant N-acetylcysteine attenuates the inhibitory effects of phenformin.
125  of culture conditions was further seen when inhibitory effects of short wavelength light were reduce
126                                    Selective inhibitory effects of zinc on cell proliferation in esop
127 e to non-targeted NPs showed markedly better inhibitory effects on apoptosis and oxidative/inflammato
128 ral stimulation and LHb lesions reversed the inhibitory effects on cocaine locomotion produced by per
129 ated that STAT1 nitration also mediates MDSC inhibitory effects on immune cells.
130 n in iPMd induced more frequent and powerful inhibitory effects on M1 outputs compared with iPMv.
131            These inhibitors exhibited strong inhibitory effects toward EGFR kinase activity and excel
132 e selected for their robust and reproducible inhibitory effects within the primary screening assay.
133   Interestingly, we observed the aggregation inhibitory efficacy of alpha/beta and alpha/gamma BSBHps
134 e inhibitor (CHMFL-BTK-11) which exerted its inhibitory efficacy through a covalent bond with BTK Cys
135 p isoform has shorter 5'UTR removing an auto-inhibitory element.
136 s designed to hybridize to other translation inhibitory elements in 5' UTRs.
137 ate activation of excitatory memory engrams, inhibitory engrams can make memories quiescent, stored i
138                                Such matched "inhibitory engrams" can form through homeostatic potenti
139 neural networks with balanced excitatory and inhibitory engrams, the release of innate responses and
140 suggested downregulated macrophage migration inhibitory factor (MIF) to be the most pertinent mediato
141 g of the human cytokine macrophage migration inhibitory factor (MIF).
142 kine (C-C motif) ligands 2 and 3, macrophage inhibitory factor, and chemokines mediating neutrophil a
143 tical models: 1) parallel activation of Fshb inhibitory factors (e.g. inhibin alpha and VGF nerve gro
144 Putative excitatory regular-spiking (RS) and inhibitory fast-spiking (FS) V1 cells had similar EPSP c
145 vestigated relative levels of activating and inhibitory FcgammaRs on brain-resident microglia followi
146                 Several peptides with DPP-IV inhibitory features or known activity were identified by
147 ese results indicate that patterning without inhibitory feedback is functional but fragile.
148 ivate Renshaw cells, which provide recurrent inhibitory feedback to the motor neurons.
149  targets except for the matR transcript, and inhibitory, for which glutamate is dispensable.
150  to ILD processing (excitatory from one ear, inhibitory from the other: EI cells) compare ILDs separa
151                                This putative inhibitory function could serve to increase the fidelity
152 n, directly interacts with, and relieves the inhibitory function of eukaryotic initiation factor 3f,
153  genetic evidence that Lrp4 mediates the Wnt inhibitory function of Wise and also modulates Wnt/beta-
154 r-specific neuroanatomy and neurofunction of inhibitory functions.
155  are innervated and regulated by neighboring inhibitory GABA cells.
156 ment of the major excitatory (glutamate) and inhibitory (gamma aminobutyric acid (GABA)) neurotransmi
157 alpha oscillations, believed to exert active inhibitory gating, downmodulate the temporal width of LR
158 t the phage genome-which encodes potentially inhibitory gene products-is still allowed to enter the c
159                                 By contrast, inhibitory Gi-DREADDs in the basolateral amygdala (BLA)
160 aRIIA, hFcgammaRIIIA, and hFcgammaRIIIB) and inhibitory (hFcgammaRIIB) hFcgammaR genes, has been inse
161 using a chemogenetic approach expressing the inhibitory hM4Di designer receptor exclusively activated
162 may offer diverse mechanisms for maintaining inhibitory homeostasis.SIGNIFICANCE STATEMENT Corelease
163  [RFRP-3; mammalian ortholog to gonadotropin-inhibitory hormone (GnIH)] in neuroendocrine control of
164 a network rate model with excitatory (E) and inhibitory (I) populations exhibiting a novel bistable r
165 ell activation is negatively regulated by an inhibitory IgG-receptor.
166 pmental disorder characterized by excitatory/inhibitory imbalance and dopamine (DA) dysfunction.
167 pendent T cell apoptosis and upregulation of inhibitory immune checkpoint molecules.
168 cells, and its counter-receptor, the myeloid inhibitory immunoreceptor SIRPalpha.
169                           Consistent with an inhibitory influence of inflammatory pathways on cardiac
170 lly different, but neither had a significant inhibitory influence on the endogenous rate of aerobic o
171 e a long-held view concerning the pattern of inhibitory input and provide results that agree with cur
172  pathway contains projections that convey an inhibitory input from the periphery to mesolimbic reward
173 indings on the integration of excitatory and inhibitory inputs in healthy cortical circuits and discu
174 nd precision (0-4 ms jitter) of synchrony of inhibitory inputs, along with the rates (0-100 spikes s(
175 g a ring network, we show how excitatory and inhibitory interactions can implement different computat
176 vation of p110delta (>300-fold) and disrupts inhibitory interactions from the nSH2, iSH2, and cSH2 do
177 ty between excitatory mitral cells (MCs) and inhibitory internal granule cells (IGCs), but the physio
178                         Distinct subtypes of inhibitory interneuron are known to shape diverse rhythm
179 e great majority of these cells also express inhibitory interneuron markers.
180 k-related synchronization of oscillations in inhibitory interneuronal circuits, supporting the hypoth
181 growth and synaptic integration of GABAergic inhibitory interneurons are essential for functional neu
182 perineuronal nets (PNNs) around fast-spiking inhibitory interneurons, in a rat model of TBI as well a
183 ng a subset of aromatase neurons as putative inhibitory interneurons.
184 hy progression and should not be a target of inhibitory interventions.
185 n be controlled combinatorially by different inhibitory ligands.
186 labeled axon terminals, which, in turn, form inhibitory-like synapses on auditory efferent somata.
187 y humans inherited activating KIR2DS4 and an inhibitory lineage III KIR, likely encoding a C1-specifi
188 tes T cell activation in both activating and inhibitory manners.
189 t targeting FimH with M4284, a high-affinity inhibitory mannoside, reduces intestinal colonization of
190    Here we delineated an inflammation-driven inhibitory mechanism of beige adipogenesis in obesity th
191 sual signals during blinks are suppressed by inhibitory mechanisms [3-6], so that small changes acros
192     These findings highlight the role of the inhibitory microenvironment and how CAR T cells can be f
193  cmp-5, and mechanistic studies of the cmp-5 inhibitory mode revealed it acts at the level of C5 acti
194 ificant reduction in detected excitatory and inhibitory monosynaptic connections.
195  RNA editing, localize to >20 excitatory and inhibitory neocortical neuron types defined by physiolog
196 pe and a unique human parvalbumin-expressing inhibitory neuron subtype.
197                                  Neocortical inhibitory neurons exhibit remarkably diverse morphology
198 erential and cooperative roles of SOM and PV inhibitory neurons in orchestrating specific cortical os
199 experimental designs targeting a majority of inhibitory neurons may be able to resolve this question.
200                                              Inhibitory neurons, although relatively few in number, e
201 edict that top-down signals primarily affect inhibitory neurons, whereas excitatory neurons are more
202 ominantly composed of fast-spiking, putative inhibitory neurons, which displayed unusually strong cou
203 e the coordinated activity of excitatory and inhibitory neurons.
204 etic stimulation which predominantly targets inhibitory neurons.
205 escued the imbalances between excitatory and inhibitory neurotransmission evident in Fmr1-KO mice.
206 nes do significantly alter the maturation of inhibitory neurotransmission in the cingulate region of
207 Accumulating evidence shows that glycinergic inhibitory neurotransmission in the spinal cord dorsal h
208  in the relative strengths of excitatory and inhibitory neurotransmission.
209 ila olfactory sensory neurons and found that inhibitory odors triggered outward receptor currents by
210 rents to MNTB neurons should lead to greater inhibitory output to the projections from this nucleus.
211 t that VISTA represents another compensatory inhibitory pathway in prostate tumors after ipilimumab t
212 ) are a unique form of endogenous descending inhibitory pathway since they can be easily evoked and q
213           This could be restored by blocking inhibitory pathways and, in particular, by supplementing
214 those targeting CTLA-4/B7 and the PD-1/PD-L1 inhibitory pathways, are now available for clinical use
215 ed PDH-E1alpha protein content and increased inhibitory PDH-E1alpha Ser(300) phosphorylation and FA o
216                                       DPP-IV inhibitory peptide sequences identified within camel and
217  Nine novel dipeptidyl peptidase IV (DPP-IV) inhibitory peptides (FLQY, FQLGASPY, ILDKEGIDY, ILELA, L
218  that can be specifically targeted by fusion-inhibitory peptides.
219 ew framework for developing effective fusion inhibitory peptides.
220 conditional KO/knockdown of GSK3beta reduced inhibitory phosphorylation of CRMP2 in RGCs and improved
221 tment of adherent platelets with PGI2 caused inhibitory phosphorylation of RhoA, reduced RhoA GTP-loa
222 g CDK inhibitors to reverse the constitutive inhibitory phosphorylation of T387 of U-STAT2 might enha
223 and, phosphatase PP2A-PP2R3B can remove this inhibitory phosphorylation.
224 ts reveal that nonmating behaviors drive AOB inhibitory plasticity and indicate that increased MC inh
225 he target of clinical investigation, gastric inhibitory polypeptide (GIP), as proof-of-principle pept
226  glucagon, ghrelin, cholecystokinin, gastric inhibitory polypeptide (GIP), glucagon-like peptide 1 (G
227 nscription factor 7-like 2 (TCF7L2), gastric inhibitory polypeptide receptor (GIPR), caveolin 2 (CAV2
228 n about both innocuous and painful touch and inhibitory populations that serve as a gate to prevent i
229                   OF increased depression of inhibitory postsynaptic currents (IPSCs) along IPSC trai
230 neurons presented frequencies of spontaneous inhibitory postsynaptic currents (sIPSCs) and spontaneou
231 showed an increased frequency of spontaneous inhibitory postsynaptic currents.
232 ffered an explanation for the differences in inhibitory potency between glucosyl and glucosaminyl der
233 ompatibility, and significantly enhanced the inhibitory potency of ATRA on HCC cell growth, improving
234 in vitro sliding velocity and attenuated the inhibitory potential of the allosteric myosin inhibitor
235 ns and angiotensin I-converting enzyme (ACE) inhibitory potentials.
236 ription to be presented, including off-cycle inhibitory processes, the source of amine and organoboro
237 tatory) processes laterally and glycinergic (inhibitory) processes medially.
238 chizophrenia, increasing confidence that P50 inhibitory processing can inform the development of inte
239 utamate-dominant excitatory to GABA-dominant inhibitory processing in early visual areas.
240 entity may impact the relative abundance and inhibitory properties of skin bacteria.
241 CS family genes encoding the STAT signalling inhibitory proteins SOCS1, SOCS3 and CISH were marked by
242 acrophages (TAM), which favors expression of inhibitory rather than activating Fcgamma receptors (Fcg
243 an in LPFC, resulting in a lower excitatory: inhibitory ratio and a greater dynamic range for signal
244                                         PD-1 inhibitory receptor blockade partially reversed T cell u
245 g T cell activation by stimulating a natural inhibitory receptor called leukocyte-associated Ig-like
246         We therefore determined and compared inhibitory receptor expression patterns of 2B4, CTLA-4,
247 y using Cal-Light to drive expression of the inhibitory receptor halorhodopsin (eNpHR), which respond
248                                          The inhibitory receptor signal regulatory protein-alpha (SIR
249                                              Inhibitory receptors expressed by T cells mediate tolera
250 k mechanisms by which negative selection and inhibitory receptors restrain TCR signaling to enforce b
251 is has provided impetus to identify other co-inhibitory receptors that could be exploited to enhance
252 t, precedes the expression of MHC-I-specific inhibitory receptors, and is modulated in an education-d
253  CD4 T cells following blocking of different inhibitory receptors, and we confirmed our results in a
254 i and regulates the surface level of NK-cell inhibitory receptors.
255 tive signals received through activating and inhibitory receptors.
256                           As anticipated for inhibitory reciprocal feedback between AR and PI3K/AKT s
257 oinhibited at a single site by either of two inhibitory regions, CBD and LAVP, which block substrate
258 e view that the lateral habenula establishes inhibitory relationships between stimuli and food outcom
259 etary rewards, and by applying excitatory or inhibitory repetitive transcranial magnetic stimulation
260                                     The slow inhibitory response defined an optimum frequency of pres
261                                              Inhibitory responses that diminished after repetitive AC
262 mic neurons gradually develop new, primarily inhibitory responses to reward-predictive cues across le
263 the decoy receptor IL-1R2 plays an important inhibitory role in local IL-1- and neutrophil-dependent
264 ess during wound healing, alpha9beta1 has an inhibitory role, suggesting that regulation of basement
265 ecedented resolution the distribution of the inhibitory scaffold protein gephyrin in response to prot
266  present the identification of new Cruzipain inhibitory scaffolds within the GlaxoSmithKline HAT (Hum
267 ction neuron (MSN) activity via monosynaptic inhibitory signaling.
268 is induced by TGFbeta and is mediated by the inhibitory SMAD, SMAD7.
269  cells with small interfering RNAs targeting inhibitory SMADs to analyze gene expression profiles.
270 that pharmacotherapies capable of increasing inhibitory spinal glycinergic neurotransmission hold in
271    This establishment of neuropil excitatory-inhibitory structure largely precedes dendritic arboriza
272 ty in the LTMR-RZ: seven excitatory and four inhibitory subtypes of interneurons exhibiting unique mo
273                  Similarly, we observed that inhibitory suppression of phasic noise generated by out-
274 notopic visual cortex largely due to reduced inhibitory surrounds.
275 atory and inhibitory synapses and facilitate inhibitory synapse adaptations.
276 oride transporter function at excitatory and inhibitory synapses and facilitate inhibitory synapse ad
277 how that Syt1 is weakly coexpressed at these inhibitory synapses and must be genetically inactivated
278 napses, with neuroligin 2 (NLGN2) limited to inhibitory synapses and neuroligin 1 (NLGN1) dominating
279 1 adenosine receptor activation and enhanced inhibitory synapses from the lateral subdivision of the
280                                The number of inhibitory synapses made by CCK(+)VGlut3(+) basket cells
281 ately 50% of glutamatergic synapses, but not inhibitory synapses, in culture.
282          Select pairs promote excitatory and inhibitory synapses, with neuroligin 2 (NLGN2) limited t
283 reby decreased the confinement of GABAARs at inhibitory synapses.
284  the accumulation of GABAARs and gephyrin at inhibitory synapses.
285 rs but differentially impaired excitatory or inhibitory synaptic functions in an isoform-specific man
286 e their selectivity both from excitatory and inhibitory synaptic inputs from other neurons and from t
287 ials interact with subsequent excitatory and inhibitory synaptic inputs remains unknown.
288 m computations by integrating excitatory and inhibitory synaptic inputs.
289 rin in response to protocols inducing LTP of inhibitory synaptic responses (iLTP).
290 inoid-dependent effects of corticosterone on inhibitory synaptic transmission in the rat PL were dete
291 ard enabling the study of diseases affecting inhibitory synaptic transmission.
292 in acute rat OB slices from both sexes, that inhibitory synchrony is evident in the spontaneous synap
293          Even with inhibition constant, when inhibitory synchrony was higher, excitation increased Cb
294 m that prevents Cdr1 colocalization with its inhibitory target Wee1 during osmotic stress.
295 timulation of excitatory corticothalamic and inhibitory tectothalamic terminals.
296  have little effect on evoked responses from inhibitory thalamic reticular nucleus and excitatory tec
297  onset of puberty, ovarian hormones increase inhibitory tone in the prefrontal cortex.
298  for Cl(-) and thus can be used as efficient inhibitory tools for optogenetics.
299           (S)-Orteronel was three times more inhibitory toward the conversion of 17alpha-hydroxypregn
300                 Further investigation in the inhibitory versus excitatory neuronal networks and micro

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