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1 ns disrupts the SI by preventing pollen tube inhibition.
2 y over TrkB and TrkC or promiscuous, pan-Trk inhibition.
3 who achieved sustained greater than 85% FLT3 inhibition.
4 eptides with respect to its mode of protease inhibition.
5 the high levels of cellular 2OG may preclude inhibition.
6 ed by intracellular Ca(2+)i chelation or CaM inhibition.
7 ), that may be attenuated through complement inhibition.
8 tocidal antimalarial activity and proteasome inhibition.
9  was partially reduced by genetic complement inhibition.
10  as well as a transient surge in feedforward inhibition.
11 mation of vAC was compromised upon endocytic inhibition.
12 ortant roles in T-cell co-stimulation and co-inhibition.
13  of picophytoplankton productivity including inhibition.
14 ion of lifespan, cardioprotection, and tumor inhibition.
15 h GABABRs are able to modulate fast synaptic inhibition.
16 positive emotional stimuli and enhanced fear inhibition.
17 ased motor neuron excitability and decreased inhibition.
18 either ignore inhibition or only include PAR inhibition.
19  did not demonstrate any advantage for COX-2 inhibition.
20 y aquatic enveloped virus diseases and their inhibition.
21 ely correlated with changes in intracortical inhibition.
22 c activity was not directly affected by BRD4 inhibition.
23 ation of tyrosine 447 (PY447) regulates auto-inhibition.
24 otch1 extracellular domain for activation or inhibition.
25 nd suggests an enzyme isomerization model of inhibition.
26 t androgen receptor (AR) regulates HR and AR inhibition activates the PARP pathway in vivo, thus inhi
27                           Altogether, the QS inhibition activity of the synthesized compounds is enco
28                        We find that lysosome inhibition alters their mobility and also decreases dend
29 ic knockout of STAT3, or its pharmacological inhibition, ameliorate skin fibrosis in experimental mou
30                        Moreover, optogenetic inhibition and ablation of VLS D2-MSNs causes, respectiv
31 artmentalization minimizes inevitable enzyme inhibition and alleviates constraints that self-inhibiti
32  of DNA replication stress and damage by ATR inhibition and cytarabine, and the ability of ATR inhibi
33 ding RNA (TINCR), which mediated both cancer-inhibition and differentiation-induction effects of ZNF7
34 ons in cortical pyramidal neurons: transient inhibition and longer-lasting excitation.
35 n of membrane proteins often leads to growth inhibition and perturbs central metabolism and this burd
36             Therefore, combining conjugation inhibition and promoting plasmid loss would be an effect
37                                       Hapten inhibition and the use of structurally unrelated hapten-
38 ination-induced H3-specific hemagglutination inhibition antibody responses, and consequently might af
39 oconversion rates and lower hemagglutination-inhibition antibody titer geometric mean fold increase a
40 lecules with novel and defined mechanisms of inhibition are thus needed to functionally characterize
41 g in nanomolar potencies in an ATP synthesis inhibition assay.
42 ibody binding, we conducted hemagglutination inhibition assays using virions and ISVPs.
43  against MN/10 and BJ/92 in hemagglutination inhibition assays.
44 eutic approach may be classical pathway (CP) inhibition at the level of early component C1.
45 nd genetic approaches, we confirm that HDAC6 inhibition augments in vitro efficacy of anti-CD20 mAbs
46 ufficient to quantify the effects of contact inhibition because they focus on data describing early t
47 nation for the previously baffling substrate-inhibition behavior of the enzyme.
48 quired for preventing the spread of synaptic inhibition between adjacent EB lamina.
49                             Interhemispheric inhibition between S1s and intracortical inhibition in t
50 inhibition (BRAFi) and combined BRAF and MEK inhibition (BRAFi and MEKi) therapies have markedly impr
51                                Targeted BRAF inhibition (BRAFi) and combined BRAF and MEK inhibition
52  for exploring mechanisms of virus infection inhibition by antibodies.
53              Mechanistic target of rapamycin inhibition by either nutrient starvation or use of an ac
54 ve studies included analysis of in vivo FLT3 inhibition by plasma inhibitory activity assay and indic
55 alidated by site-directed mutagenesis and by inhibition by small peptides that mimic the loop residue
56 and indicate that the catalyst is subject to inhibition by the product of the chloroacylation reactio
57 ated rare variant (M2145T) in TGEF2 impaired inhibition by the TGEF2 pleckstrin-homology domain, resu
58            Our findings show how GSK3 kinase inhibition can greatly enhance the mature character of N
59 nt aeration was mostly explained by periodic inhibition caused by free ammonia due to periodic transi
60 retion system (T1SS) and a contact-dependent inhibition (CDI) system.
61 py to Achieve Optimal Management of Platelet Inhibition (CHAMPION PCI, CHAMPION PLATFORM, and CHAMPIO
62                   Multiple forms of synaptic inhibition compartmentalized the GAC dendritic tree and
63 teomic profiling, we show that, in BL, HSP90 inhibition compromises the activity of the pivotal B-cel
64 tations in its interface, that has an MMP-14 inhibition constant (Ki ) of 0.9 pm, the strongest MMP-1
65                                    Even with inhibition constant, when inhibitory synchrony was highe
66 ro binding to the enzyme active site and for inhibition constants.
67 mon wet ARMD treatment, suggesting that VEGF inhibition could reduce cellular complement regulatory c
68 purified proteins at pH ranges in which PMEI inhibition differed between AtPMEI4 and AtPMEI9 had dist
69 increased by asparaginase, suggesting mTORC1 inhibition during asparaginase exposure is not driven vi
70 omain, and RhoA-GTP binding may relieve this inhibition during mitosis.
71 ing FoxM1 as a critical target for cyclin B1 inhibition during MVM infection.IMPORTANCE Replication o
72 , supporting the use of intensified platelet inhibition during the first year after STEMI.
73 s was independent on N supply because of the inhibition effect of the extreme rainfall event.
74  that PIP4Kgamma is a druggable target whose inhibition enhances productive autophagy and mHtt proteo
75 s precedes CD42b shedding and that apoptosis inhibition enriches the FV(+) HG/CD42b(+) MKs, leading t
76        More mature individuals with superior inhibition evidenced only context-specific profiles, rev
77 nstrated by qualitative and quantitative IgE inhibition experiments.
78 Analysis of these cells revealed that CDK4/6 inhibition failed to induce cell-cycle arrest or senesce
79 e and voriconazole have the greatest overall inhibition for all isolates of Acanthamoeba castellanii
80                                          Syk inhibition has been proposed as a new therapeutic approa
81 ng can be delicately controlled by GABAergic inhibition in a cell-type-specific manner.
82 s elicited by persistent PKC-2 activation or inhibition in AFD (or intestine) disclosed that PKC-2 re
83 tic induction of apoptosis and proliferation inhibition in AML cell lines.
84 sulting in superior therapeutic efficacy.MEK inhibition in breast cancer is associated with increased
85  However, a new study reports that RORgammat inhibition in CD4(+)CD8(+) thymocytes resulted in skewed
86 ble salutary effect of renal GPCR-Gbetagamma inhibition in CKD developed in a clinically relevant mur
87 may explain the decreased efficiency of HDAC inhibition in EOC, based on our data demonstrating that
88                                         DRP1 inhibition in human smooth muscle cells undergoing osteo
89 MAPK pathway signaling under continuous EGFR inhibition in osimertinib-sensitive cells.
90 le safety profile and showed consistent FLT3 inhibition in patients with relapsed or refractory acute
91 fication(s) in response to combined MEK/mTOR inhibition in PTEN-loss contexts and identified JAK1/STA
92          The time course of the Na-/K-ATPase inhibition in the cell culture was demonstrated by the c
93                                  Global IL-6 inhibition in the early phase after fracture reduced sys
94  is a prevailing mechanism for use-dependent inhibition in the nucleus accumbens core and dorsal stri
95 ric inhibition between S1s and intracortical inhibition in the S1 modulated the amplitude of the P25/
96 enase complex, caused a profound cell growth inhibition in tumour cells harbouring KRAS mutations.
97        Genetic knockdown and pharmacological inhibition in vascular smooth muscle cells reveal that c
98  disrupts the balance between excitation and inhibition in VTA dopamine neurons, while PDE4 inhibitio
99 d the cocaine-induced reduction of GABAergic inhibition in VTA dopamine neurons.
100 e actr10 mutation and pharmacological dynein inhibition in zebrafish result in failure to properly di
101  groups of (2S)-hesperetin are important for inhibition, in particular the phenyl-chroman moiety.
102  MeCP2 T158M degradation and that proteasome inhibition increased MeCP2 T158M levels.
103                       We found that PP1alpha inhibition increases steady-state levels of phosphorylat
104 hip between the change in magnitude of GABAA inhibition induced by tACS and the magnitude of GABAA in
105 on analysis for the association between RAAS inhibition-induced WRF, HF phenotype and outcome.
106                           Explaining why DLK inhibition is only partially protective, we identify leu
107 of lateral connections is very strong, or if inhibition is particularly weak, the network operates cl
108 The induction of SMARCA2 in response to EZH2 inhibition is required for apoptosis, but not for growth
109                        In contrast, synaptic inhibition is unaffected by changes in firing or CaMKIV
110 ML38 was essential for AtRALF1-mediated root inhibition, it appeared not to have an effect on the AtR
111 ory syncytial virus (RSV) infection, and its inhibition leads to exaggerated immunopathology.
112 nzyme (DcpS), but the mechanism whereby DcpS inhibition leads to therapeutic benefit is unclear.
113      These results suggest that altering ADP inhibition may be a mechanism of Hsp90 regulation.
114 or interactions were consistent with lateral inhibition mediated by retinal horizontal cells that rec
115                             During transient inhibition, MPH increased prefrontal activation for both
116 sease Control and Prevention standardized NA inhibition (NI) assay with oseltamivir, zanamivir, peram
117 n induced by tACS and the magnitude of GABAA inhibition observed during task-related synchronization
118  In vitro studies demonstrate that Ct growth inhibition occurs by interferon-gamma (IFN-gamma)-mediat
119  as modification of actin polymerization and inhibition of a broad range of actin-dependent functions
120 d dopamine release, suggesting that feedback inhibition of acetylcholine release was not involved.
121  actin regulates microtubule organization as inhibition of actin polymerization with a low dose of la
122                                However, both inhibition of adenylate cyclase A (ACA) with SQ22536 and
123 SPGs are required for Nogo-A-Delta20-induced inhibition of adhesion, cell spreading, and neurite outg
124 tantly, insulin prevented the AbetaO-induced inhibition of AMPK.
125 ndicated activation of caspase proteases and inhibition of arginine-specific proteases.
126                                      Rather, inhibition of ATP synthesis caused massive spontaneous v
127 duction of IBTKalpha and the UPR, along with inhibition of autophagic flux, was associated with progr
128                                We found that inhibition of autophagy by knocking down the core autoph
129 plicate selected experiments from the paper "Inhibition of BET recruitment to chromatin as an effecti
130               We show that brief optogenetic inhibition of BLA neurons around moments of aversive rei
131 ion activates the PARP pathway in vivo, thus inhibition of both AR and PARP is required for effective
132 K exerts its anti-tumor activity through the inhibition of c-Met-Ras-HO-1 axis; and it can have signi
133                                          The inhibition of CD4(+) T cells is dependent on TGF-beta, w
134 +) T cells is dependent on TGF-beta, whereas inhibition of CD8(+) T cells is dependent on TGF-beta an
135 ne up-regulated gene 1 (TUG1) induces marked inhibition of cell migration, invasion, and glycolysis t
136 12 was able to cause concentration-dependent inhibition of cell proliferation, yielding an IC50 value
137                                 In contrast, inhibition of CIN firing with the mu/delta selective opi
138                            Importantly, dual inhibition of CK1alpha and the proteasome synergisticall
139                                        Thus, inhibition of Clks might become a novel anticancer strat
140          Suppression of NFS1 cooperates with inhibition of cysteine transport to trigger ferroptosis
141 uclei, is believed to underlie the transient inhibition of DA neurons attributed to activation of the
142 etrahydrofolate (5-methylTHF) and subsequent inhibition of de novo thymidylate (dTMP) biosynthesis.
143 he concentration of FAEs and ECs through the inhibition of degrading enzymes has been considered to b
144 model, suggesting the importance of systemic inhibition of DGAT1 for body weight control.
145           These properties may contribute to inhibition of distinct NMDAR subpopulations by memantine
146 megaloblastic anemia, which results from the inhibition of DNA synthesis by trapping folate cofactors
147 (high) macrophages is strongly suppressed by inhibition of dynamin.
148 nd they show different susceptibility to the inhibition of early and immediate early viral gene expre
149 timicrobial resistance is represented by the inhibition of efflux pumps.
150                     Genetic or pharmacologic inhibition of EGFR tyrosine kinase activity or downstrea
151            Here, we report that silencing or inhibition of endogenous TAK1 in hepatoma cell lines lea
152 eration of cSCC cells and resulted in potent inhibition of extracellular signal-regulated kinase 1/2
153                 This result was true for the inhibition of FcgammaR signaling as well.
154                                              Inhibition of focal adhesion kinase (FAK) rescued SERT f
155  thrombin or FXa also enhanced TFPI-mediated inhibition of FXa approximately 12-fold in the presence
156 initiation factor 2 (eIF2alpha) resulting in inhibition of general protein synthesis.
157  H3 lysine 27 trimethylation (H3K27me3), and inhibition of genes related to epithelial-to-mesenchymal
158 ing FOXO1-dependent activation of G6pase and inhibition of glucokinase, respectively.
159                                              Inhibition of glutamine metabolism in ECs did not cause
160 et of rapamycin (mTOR) signaling pathway and inhibition of glycogen synthase kinase 3beta (GSK3beta).
161 n, while mutation of target serines and drug inhibition of GSK-3 activity coordinately induce both fo
162                                 We show that inhibition of HDAC6 activity significantly increases CD2
163                     In vivo, pharmacological inhibition of HDAC6 improved established PAH in two expe
164 specific antagonist that caused a pronounced inhibition of HDM-induced airway inflammation and goblet
165                                              Inhibition of hepatic mTOR in Am mice increased hepatic
166 ed with the overexpression of HIFs, specific inhibition of HIFs might represent a new powerful treatm
167 ass-I APM is due to histone deacetylation as inhibition of histone deacetylases (HDACs) not only indu
168 y antagonize infection with cell-free virus, inhibition of HIV-1 transmission from infected to uninfe
169                                              Inhibition of Hsp104 function in yeast cells leads to a
170 n in SKMEL28 human melanoma cells, following inhibition of Hsp90 and BRAF signaling using 17-AAG and
171 vated protein kinase, leading to synergistic inhibition of human leukemia cell viability.
172 for the important viral gene activator ICP0, inhibition of ICP0 expression by miR-H2 has been a major
173                                              Inhibition of ILK signaling, which is involved in cell m
174                                    Selective inhibition of individual ligands revealed that this sign
175             However, this can be reversed by inhibition of inflammatory cytokine production that can
176 tervention and ion replacement, we show that inhibition of K(+) transport abolishes RBC electrophysio
177                                              Inhibition of KCC2 activity in clonal MIN6 beta-cells in
178                                              Inhibition of KLK5-mediated effects may offer potential
179 n 7 (KLK7) are heparin-binding proteins, and inhibition of KLK7 by vaspin is accelerated by heparin.
180 one A-ring backbone are essential for potent inhibition of LasR/RhlR.
181                                              Inhibition of LDH activity by small hairpin ribonucleic
182 7 deficiency resolved plaque inflammation by inhibition of lesional inflammasome activation and reduc
183 BAA receptors was responsible for the direct inhibition of light-evoked spike responses, the slow inh
184 HIF-1 Conversely, silencing or pharmacologic inhibition of LOX activity blocked dissemination of colo
185 ding to LRP6 in in vitro binding assays, and inhibition of LRP6 or critical signaling cascades downst
186 ry effect of F4 was not mediated through the inhibition of MAPKs and NF-kappaB activation but was med
187                                     Further, inhibition of MARKs led to increased pathological alpha-
188                                              Inhibition of miR-204 protects against tunicamycin-induc
189 rial compounds; however, evidence for direct inhibition of MmpL3 activity is also lacking.
190 o cell death, over-acetylated tubulin led to inhibition of motility and mitosis.
191 ediated synaptotoxicity and demonstrate that inhibition of MT dynamics and accumulation of PTMs are d
192                                              Inhibition of mTOR strongly reduced the lysosomal efflux
193                                              Inhibition of mTORC1 with rapamycin induces PIM3 transcr
194 g the rho pathway rather than through direct inhibition of myosin.
195                                   Inversely, inhibition of NEDDylation by MLN4924 blocked proinflamma
196           Either genetic knockdown of p62 or inhibition of NF-kappaB sensitized tumor cells to CQ, re
197 an antioxidant, mitochondrial inhibitors, or inhibition of NO formation.
198 innervate the brainstem to drive feedforward inhibition of nociceptive neurons.
199                                              Inhibition of NOS2 and COX2 using amino-guanidine and as
200 C6 or Orai1 channels and caused only a minor inhibition of P2X1-dependent Ca(2+) entry.
201 eas a non-phosphorylatable S561A mutation or inhibition of Par1 kinase activity decreases SH3-GK inte
202 or of nuclear poly (ADP-ribose) polymerases (inhibition of PARP-1 > PARP-2 > PARP-3), following a sim
203                                  Optogenetic inhibition of pBNST CRFR2 neurons yielded opposite effec
204 almost completely blocked by pharmacological inhibition of phosphorylation of Akt.
205                                              Inhibition of PI3K-dependent exocytosis of TRPC6 is thou
206 , Ru-thio-chrysin displayed a 4-fold greater inhibition of platelet function and thrombus formation i
207                                              Inhibition of PLCgamma/PKC-induced mTOR activation impai
208 rs could help unveil the mechanisms by which inhibition of poly(ADP-ribose) polymerases (PARPs) elici
209 hallenges in achieving effective, persistent inhibition of polymerization of hemoglobin S.
210                          The pharmacological inhibition of PPP canceled the UCHL1-mediated radioresis
211 n and omega-conotoxin-MVIIC, consistent with inhibition of presynaptic TRPV1 channels by alpha2 adren
212  polar-lipid, and specifically phospholipid, inhibition of prion-seeded amyloid formation highlight t
213     Additionally, prediction analysis showed inhibition of proinflammatory regulators and activation
214 -mediated activation of protein kinase A and inhibition of Protein kinase B (AKT).
215                                     However, inhibition of PV(+) cells in either CA1 or mPFC eliminat
216                                              Inhibition of Ras nucleotide exchange is a promising new
217          Genetic, physiological, or chemical inhibition of respiratory processes elicited increased b
218                                              Inhibition of Rho-associated kinase (ROCK) prevented cyt
219                                     Targeted inhibition of Rho-associated kinase (ROCK)2 downregulate
220 ke receptor (RLR) signaling pathway involves inhibition of RIG-I K63-linked polyubiquitination and th
221 ed resistance to 2,4-D compared with IAA for inhibition of root growth, were also found to have less
222 : A tonically active, muscarinic cholinergic inhibition of rostral raphe pallidus (rRPa) neurons infl
223                                              Inhibition of signaling after ligand exposure selectivel
224 on of light-evoked spike responses, the slow inhibition of spiking activity required the activation o
225 n important function of tumor suppressor via inhibition of STAT3 phosphorylation in uterine epithelia
226                These effects translated into inhibition of superantigen-induced Th1 cell recruitment.
227 NgR1-3) acts as Abeta receptors mediating an inhibition of synapse assembly, plasticity, and learning
228                                    Selective inhibition of T-channels and global deletion of CaV 3.1
229                                              Inhibition of targetable proteins associated with drug r
230                                 VMH-specific inhibition of TBK-1 in mice with diet-induced obesity im
231 uppress autoimmune responses in vivo through inhibition of the autophagic machinery in DCs in a cytot
232                                        Thus, inhibition of the coactivation-function of Stat3 resulte
233                                              Inhibition of the conversion of glutamate to alpha-ketog
234 s prevented by genetic deletion of Slc6a2 or inhibition of the encoded transporter.
235 l potency to lineage priming is prevented by inhibition of the FGF/MAPK signalling pathway.
236                                Additionally, inhibition of the H3K27 demethylase JMJD3 in naive CD4 T
237                                              Inhibition of the insulin-like growth factor I receptor
238 e considerations regarding the mechanisms of inhibition of the lipid peroxidation in micelles, in vie
239           The current study examined whether inhibition of the neurokinin-1 receptor with a specific
240 , we show here that, besides its role in the inhibition of the NF-kappaB pathway, NLRC3 interferes wi
241 ect of ILT3.Fc on tumor cell growth involves inhibition of the p70S6K signaling pathway.
242 n directly activated by cAMP (Epac) provokes inhibition of the phospholipase C by an as yet unknown m
243          We show that stimulation of OXPHOS, inhibition of the PTP, or deletion of CypD increased hig
244 ther experiments suggested that NS1-mediated inhibition of the RIG-I-like receptor (RLR) signaling pa
245                                              Inhibition of the sarcoendoplasmic reticulum calcium tra
246  to consider for obtaining potent cell-based inhibition of this cancer metabolism target.
247  for the pro-metastatic effect of MSCs since inhibition of this chemotaxis abolished increased neutro
248 y influence clinical response to therapeutic inhibition of tonic BCR signaling in DLBCL.
249 ading to enhanced degradation of the mRNA or inhibition of translation.
250                         This induces a tonic inhibition of transmission at direct pathway synapses an
251                                              Inhibition of type 4 phosphodiesterase (PDE4) and elevat
252 e to modulation of host responses, including inhibition of type I interferon responses, suppression o
253                             For example, the inhibition of ubiquitin-specific protease 7 (USP7) resul
254 s no significant difference in the levels of inhibition of UVB-induced immunosuppression amongst mice
255                           Thus, we evaluated inhibition of virulence in P. aeruginosa by a designed p
256 es to uncontrolled cSCC growth by preventing inhibition of YAP/WBP2.
257  inductions of Na(+)K(+)/ATPases, and strong inhibitions of molt-related proteins such as chitinase a
258                            The effect of PDH inhibition on mast cell function was examined.
259 ergic interneurons that mediate feed-forward inhibition onto GCs.
260            Here we show that pharmacological inhibition or gene ablation of the Ep3 receptor in mice
261 rowth can be mitigated through pharmacologic inhibition or genome editing of these loci.
262 most other productivity models either ignore inhibition or only include PAR inhibition.
263                                              Inhibition or silencing of ROCK1 was sufficient to rescu
264 ption reflects a general influence of visual inhibition or whether the GABA levels of different corti
265 ibition and alleviates constraints that self-inhibition places on metabolism.
266 py to Achieve Optimal Management of Platelet Inhibition [PLATFORM]: NCT00385138; A Clinical Trial Com
267 y of the double rnhAB mutants to translation inhibition points to R-loops as precursors for R-lesions
268 tracts of examined Rosa species demonstrated inhibition potency towards production of some monitored
269                             Additional CXCR7 inhibition potentiated the effect of SDF-1 antagonism, m
270  our results, we suggest that HDAC1-specific inhibition prevents progenitor cells of the retina from
271 f these straight lines, an absolute scale of inhibition properties of the lipid peroxidation can be d
272 nprecedented pharmacological approach to MMP inhibition, providing an opportunity to improve selectiv
273  original consolidation by protein synthesis inhibition (PSI) begun shortly after training.
274 hibition in VTA dopamine neurons, while PDE4 inhibition reestablishes the balance between excitation
275                                          ACE inhibition relies on the formation of hydrogen bonds bet
276                                   Thus, HDAC inhibition restored HLA class-I surface expression in vi
277 DA neurons inhibited by, and the duration of inhibition resulting from, LHb stimulation.
278 C, based on our data demonstrating that HDAC inhibition specifically induces expression of IL-8/CXCL8
279 te their synergistic potential and their CYP inhibition strength in the aquatic invertebrate Gammarus
280  changes in astrocytes, including proteasome inhibition, stress kinase activation, mechanistic target
281              The structure-guided cell-based inhibition studies further demonstrate that these loops
282 in ligase substrate, and is reversed by RhoA inhibition, suggesting increased RhoA as an important me
283 phy (N=33), or both (N=63) during a response inhibition task.
284 rite-targeting excitation and soma-targeting inhibition (the latter contributes non-dipole-like featu
285  to early cytokine therapy, newer checkpoint inhibition therapies have also demonstrated activity.
286 tablishes the balance between excitation and inhibition through distinct mechanisms.
287 ition and cytarabine, and the ability of ATR inhibition to abrogate the G2 cell cycle checkpoint both
288 that Angptl4 does not link glucagon receptor inhibition to compensatory hyperglucagonemia or expansio
289 activity-dependent switch from GABA-mediated inhibition to excitation.
290 rose feeding experiments, and photosynthesis inhibition to tease apart the influences of light, metab
291                              Peripheral IL-1 inhibition using anakinra for 4 weeks does not result in
292 emia intermedia, Th3/(+) We observed that HO inhibition using tin protoporphyrin IX (SnPP) decreased
293 l-down experiments demonstrate that VEGF165b inhibition versus control increased VEGFR1-STAT3 binding
294                                              Inhibition was independent of IFNalpha, IFNbeta, IFNL1,
295                                              Inhibition was prevented by an antioxidant, mitochondria
296                       In the DLPFC, cortical inhibition was significantly decreased in patients with
297                                   Isradipine inhibition was splice variant and isoform dependent, wit
298 en by both attentional modulation and mutual inhibition, which have distinct selectivity (feature vs.
299 s renders lung SqCC vulnerable to glycolytic inhibition, while lung ADC exhibits significant glucose
300                                Combining ALK inhibition with other novel therapeutic modalities shoul

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