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1 rphyrins through substrate reduction therapy by inhibiting 5-aminolevulinate synthase 2 (ALAS2), the
3 , i.e., the suppression of cancer metastasis by inhibiting a crucial protein-protein interaction invo
4 s to drive the differentiation of PC12 cells by inhibiting a nuclease that promotes RNA-induced silen
7 ins that stabilize actin filaments (F-actin) by inhibiting actin polymerization and depolymerization.
8 HIV-1 exerts broad immunosuppressive effects by inhibiting activation of the transcription factor NF-
12 ing circulating IGF1, insulin and leptin and by inhibiting AKT-mTOR signalling via upregulation of EG
14 ells may regulate periodontitis pathogenesis by inhibiting alveolar bone loss through directly blocki
15 cupoints following MO treatment were reduced by inhibiting AMPA and NMDA receptors in the spinal cord
16 t and synaptic depotentiation were disrupted by inhibiting AMPAR internalization via intra-NAc shell
18 ownstream sequences into an ectopic S region by inhibiting and promoting their dynamic alignment with
19 L-18 production favors bacterial persistence by inhibiting antimicrobial peptide production and, at t
20 is mechanism also protects cancerous tissues by inhibiting antitumor immune cells in hypoxic and extr
24 d to be a potential target of cancer therapy by inhibiting Aurora B or survivin in different types of
25 helial cells, inhibits degradation of Kif19a by inhibiting autophagy, a cellular recycling mechanism
27 events ISO-induced apoptosis of kidney cells by inhibiting Bax protein upregulation and caspase-3 act
28 roved chemotherapy and radiotherapy response by inhibiting BCSC self-renewal and associated pluripote
29 te that BBR antagonizes beta-catenin pathway by inhibiting beta-catenin translation and mTOR activity
30 ading suppresses tumor growth and osteolysis by inhibiting bone resorption and enhancing bone formati
31 presents a "two-pronged" anticancer strategy by inhibiting both critical growth-promoting cell signal
32 mpaired HCC progression in vitro and in vivo by inhibiting both tumor cell proliferation and migratio
35 ow that C5aR2 is protective in intestinal IR by inhibiting C5aR1-mediated neutrophil recruitment to t
38 in acetylation and tumour cell proliferation by inhibiting calcineurin and NFATc3 activation in mouse
40 ling IL-1alpha/beta release from neutrophils by inhibiting caspase-8-dependent apoptosis and Ripk1-Ri
41 orrelated with neuronal activity and blocked by inhibiting caspases in presynaptic neurons, implicati
42 t losartan can exert antimetastatic activity by inhibiting CCR2 signaling and suppressing monocyte re
44 Pom1 controls the timing of mitotic entry by inhibiting Cdr2, which forms stable membrane-associat
47 inhibited new nephron formation after injury by inhibiting cell proliferation, and resulted in loss o
48 reticulata blocks signaled active avoidance by inhibiting cells in the pedunculopontine tegmental nu
49 edunculopontine tegmental nucleus (PPT), not by inhibiting cells in the superior colliculus or thalam
52 S256, and induces AQP2 membrane accumulation by inhibiting clathrin-mediated endocytosis and increasi
54 such multisensory conflicts can be minimized by inhibiting core cortical areas of the subordinate sen
60 own in MCF10A H-RAS(V12) breast cancer cells by inhibiting de novo proline biosynthesis and impairing
61 d interference with menaquinone biosynthesis by inhibiting demethylmenaquinone methyltransferase and
64 Potentiating radiotherapy and chemotherapy by inhibiting DNA damage repair is proposed as a therape
65 athway should further sensitize cancer cells by inhibiting DNA repair, thereby increasing the respons
68 ommencing gene transcription that is reduced by inhibiting EGFR, down-regulating FUS, or expressing F
69 icate that the specific reduction of H3K9me2 by inhibiting EHMT1/2 during nuclear reprogramming impac
72 chiral nanowire structures can be suppressed by inhibiting electron transport in a helical way to dim
73 ation of NuMA1 stabilizes the developing AIS by inhibiting endocytosis and removal of AIS proteins.
75 sine nucleotides, denoted as (p)ppGpp, which by inhibiting energy requiring molecular pathways help b
76 gatekeeper that responds to decreases in ATP by inhibiting energy-consuming anabolic processes and pr
77 e dichotomous functions of the two receptors by inhibiting ET(A)R with macitentan, an ET(A)R antagoni
79 3 blocked plasmid replication, respectively, by inhibiting expression or function of the plasmid repl
81 cells and cellular migration were attenuated by inhibiting F. nucleatum host-cell binding and entry u
82 is to potentiate endocannabinoid signalling by inhibiting fatty acid amide hydrolase (FAAH), the enz
84 repare" pathways processing-predicted inputs by inhibiting feedforward gamma rhythms and associated s
85 tion of Cd under reducing condition possibly by inhibiting ferrihydrite transformation and recapturin
88 venting virus membrane fusion with cells and by inhibiting fusion of infected cells (syncytialization
89 inal mTOR alone lowers plasma glucose levels by inhibiting glucose production in rodents with diabete
91 were developed to lower blood glucose levels by inhibiting glucose reabsorption in the proximal tubul
94 and genetic landscape, and can be exploited by inhibiting glutathione peroxidase 4 (GPX4) with small
95 -induced ferroptosis but not in that induced by inhibiting glutathione peroxidase-4 (GPX4), the most
96 through the synthetic pathways was maximized by inhibiting glycolate export from the chloroplast.
98 nts dissemination of a gut-resident pathogen by inhibiting goblet cell-mediated bacterial translocati
101 pendent and ligand-independent Met signaling by inhibiting HGF binding to Met and inducing receptor d
105 uggest that IFN-gamma blocks VZV replication by inhibiting IE62 function in a cell line-dependent man
106 uggest that IFN-gamma blocks VZV replication by inhibiting IE62 function in a cell line-dependent man
107 b was exerting its beneficial effects in HLH by inhibiting IFN-gamma signaling or by targeting signal
108 spider Atrax robustus, induces pain in mice by inhibiting inactivation of voltage-gated sodium (Na(V
109 ig-I or Mda5 deficiency reduced HSPC numbers by inhibiting inflammatory signals that were in turn enh
110 the CD47-SIRPA axis suppresses phagocytosis by inhibiting inside-out activation of integrin signalin
111 bacteria, H-NS promotes the cellular fitness by inhibiting intragenic transcription from AT-rich targ
113 ty of pathogen associated molecular patterns by inhibiting IRF3 and NF-kappaB nuclear transport.
114 ssory protein MRAP2 altered GHSR1a signaling by inhibiting its constitutive activity, as well as by e
118 sion through regulation of its promoters and by inhibiting its presentation through interaction with
121 f PTPN22 at Ser(751) prolonged its half-life by inhibiting K48-linked ubiquitination and impairing re
123 sition of proteins proximal to KRAS, notably by inhibiting KRAS proximity to the SNARE vesicular tran
124 te Wnt targets including c-Myc and Cyclin D1 by inhibiting LEF transcriptional activity in GC cells.
127 ion of atherosclerosis induced periodontitis by inhibiting local, systemic and vascular inflammation,
129 l ligation and puncture (CLP)-induced sepsis by inhibiting lung inflammation, leukocyte apoptosis, an
130 way dysregulates degradation of Cx43, either by inhibiting lysosomal activity or suppressing the leve
131 that GRK2 can function as a tumor suppressor by inhibiting MALT1 and provide a roadmap for developing
132 HPV16E7 protein promotes MAP4 stability by inhibiting MAP4 phosphorylation- mediated degradation
133 yer that minimizes the generation of bubbles by inhibiting mass transport along a vertical direction.
134 reased omental metastasis at least partially by inhibiting MCP-1 secretion from adipocytes independen
138 t Rik-203 facilitates neural differentiation by inhibiting miR-101a-3p's ability to reduce GSK-3beta
139 lung tumor development and brain metastasis by inhibiting mitochondrial bioenergetics, stimulating t
140 causes toxicity by binding to hemoglobin and by inhibiting mitochondrial cytochrome c oxidase (CcO),
142 consistent with AimB promoting MreB dynamics by inhibiting monomer-monomer assembly interactions, rep
145 er, impaired the maturation of NLGN4 protein by inhibiting N-linked glycosylation at an adjacent resi
148 ildren affected by Dravet syndrome, possibly by inhibiting neuronal lactate dehydrogenase 5 isoenzyme
150 therapeutic benefits of LCD NP are achieved by inhibiting neutrophil-mediated inflammatory macrophag
152 LPS activated murine macrophages (RAW 264.7) by inhibiting NF-kappaB activation and its nuclear trans
154 the balance of short and long 3'UTR isoforms by inhibiting NMD, in addition to its previously describ
161 s to the OB impede early olfactory signaling by inhibiting OB output neurons, thereby dynamically gat
163 n induced by prolonged calcifying conditions by inhibiting osteogenic differentiation and increases i
164 ypothesis that SOD3 preserves HA homeostasis by inhibiting oxidative and enzymatic hyaluronidase-medi
166 2 promotes breast cancer early dissemination by inhibiting p38, but the downstream pathway in this pr
170 Citrate is known to suppress glycolysis by inhibiting phosphofructokinase-1 and activate glucone
171 activate the unfolded protein response (UPR) by inhibiting phosphoglucomutase activity and causing th
174 gger oligodendrogenesis from precursor cells by inhibiting platelet-derived growth factor receptor-al
176 alignant transformation of predisposed cells by inhibiting pro-apoptotic signals and activating tumor
177 st that S100A8 and S100A9 regulate psoriasis by inhibiting production of IL-17A and -F, thereby, to o
182 ownstream target of WNT5B, which was blocked by inhibiting RAC1, a prominent regulator of C-JUN activ
184 s by counteracting MYC-induced apoptosis and by inhibiting RB1 function, thereby promoting cell-cycle
185 ogen-induced spine elimination was prevented by inhibiting reactive oxygen species (ROS) generation o
186 AMPK's ability to maintain redox homeostasis by inhibiting reactive oxygen species production and mai
187 cells reduced the level of MMP-1 expression by inhibiting recruitment of NF-kappaB to the MMP-1 prom
188 s negative feedback over apoptotic signaling by inhibiting recruitment of the key proapoptotic protei
191 PS1/gamma-secretase mediates axon growth by inhibiting RhoA signaling and cleaving EphA3 independ
192 Parkin axis negatively regulates necroptosis by inhibiting RIPK1-RIPK3 complex formation; this regula
196 utic to block pathological axon degeneration by inhibiting SARM1, an approach that may be applied cli
197 sponse and induction of immunological memory by inhibiting secondary tumor growth upon re-challenge w
199 not monomeric, beta-arrestin2 increases tau by inhibiting self-interaction of the autophagy cargo re
200 e de novo synthesis pathway of sphingolipids by inhibiting serine palmitoyl transferase in response t
204 Shh, we found that CBs reduced Shh signaling by inhibiting Smoothened (Smo), while Shh mRNA or a CB1
205 nent [Ca(2+)]cyt spikes that were attenuated by inhibiting SOCE, underlining the relevance of these [
206 re to MIS during the first six days of life, by inhibiting specification of the stroma, dysregulates
207 a signaling, also blocked IFN-beta responses by inhibiting STAT1/STAT2-mediated transcription in infe
209 protrusions could be effectively suppressed by inhibiting subcellular mitochondrial trafficking.
210 to possess blood glucose lowering properties by inhibiting sugar transporters in the small intestine
211 of RAGE blocks the effects of IL-13 and IL-4 by inhibiting sustained STAT6 activation and downstream
212 in sensory nerves to regulate bone formation by inhibiting sympathetic activity through the central n
214 at filgotinib suppresses HIV-1 transcription by inhibiting T cell activation and by modulating RNA sp
215 ell subset that controls antibody production by inhibiting T follicular helper (Tfh)-mediated help to
216 -2 prevents retrograde trafficking of toxins by inhibiting TA-protein targeting, describes a general
217 e primarily affects urinary bladder function by inhibiting TC generation and afferent nerve activity,
218 riment to downregulate the osteoclast number by inhibiting Th1 and Th17 cells, which governed the new
219 ptor on T cells mitigates renal fibrogenesis by inhibiting Th1 differentiation and renal accumulation
220 sruption by direct actin depolymerization or by inhibiting the actin driver nonmuscle myosin II (NMII
222 ins repress the expression of their own gene by inhibiting the activity of the CLOCK (CLK) and CYCLE
223 its cell motility and promotes S-phase entry by inhibiting the activity of the master regulator, CtrA
224 ng the pore-forming proteins Bax and Bak and by inhibiting the anti-apoptotic proteins Bcl-XL, Bcl-2
225 s, the Martinotti cells, gate top down input by inhibiting the apical dendrites of pyramidal cells in
226 GABAergic VTA neurons may limit wakefulness by inhibiting the arousal-promoting VTA glutamatergic an
228 ungal effect on susceptible Fusarium species by inhibiting the ATPase activity of their myosin class
229 es by MAP65-1 confers resistance to severing by inhibiting the binding of KTN1 and identifies the str
231 em cells (EPSCs) from individual blastomeres by inhibiting the critical molecular pathways that predi
232 erminus indicated that light stabilizes ACS5 by inhibiting the degradation mechanism that acts throug
233 by which plants fine-tune defense responses by inhibiting the degradation of a positive player in pl
235 so reduced thrombin-mediated EC permeability by inhibiting the disassembly of VE-cadherin at adherens
237 romatin needed for viral gene expression and by inhibiting the DNA damage response, makes the genome
238 damaging DNA, and (c) sustaining the damage by inhibiting the DNA repair protein poly(ADP-ribose) po
239 r JH action arrested vitellogenesis, in part by inhibiting the expression of doublesex (Dsx), a key t
240 n spheno-occipital synchondrosis development by inhibiting the expression of genes involved in chondr
244 ubiquitin at Thr12 (pUbT12) controls the DDR by inhibiting the function of 53BP1, a key factor for DN
245 h rate is thought to favor species exclusion by inhibiting the growth of less competitive species.
246 ose that Nrf2 activates a metastatic program by inhibiting the heme- and Fbxo22-mediated degradation
247 idence that this "oncohistone" mutation acts by inhibiting the histone methyltransferase PRC2, the de
249 ne, TNF-alpha, regulates skeletal myogenesis by inhibiting the interaction of SP1 with the Fbxl2 core
250 nuclear accumulation of PER-TIM heterodimers by inhibiting the interaction of TIM and nuclear export
251 so decreases the non-radiative rate constant by inhibiting the intramolecular motions of the incorpor
252 and pharmacological suppression of the ISR, by inhibiting the ISR-inducing double-stranded RNA-activ
254 st commonly used antihypertensives, function by inhibiting the L-type voltage-gated Ca(2+) (Ca(v) ) c
256 indlin-2 maintains alpha-tubulin acetylation by inhibiting the microtubule-associated deacetylase his
257 opose lowering neuronal mitochondrial Ca(2+) by inhibiting the mitochondrial Ca(2+) uniporter as a no
259 and that they prevent expression of the tic by inhibiting the nascent excitation released by the tic
260 Similarly, we filter out unintended noise by inhibiting the native SoxRS-mediated oxidative stress
261 s G6PD, the rate-limiting enzyme of the PPP, by inhibiting the newly identified E3 ligase TIRM21 and
262 to viral infection and inflammatory stimuli by inhibiting the NF-kappaB and type I interferon (IFN-I
263 rowth of tRXRalpha-mediated colorectal tumor by inhibiting the NF-kappaB-IL-6-STAT3 signaling cascade
264 splicing pathway restricts axon regeneration by inhibiting the nonconventional splicing of Xbp1 mRNA
265 motes the photosensitizing effect of porSMNs by inhibiting the pai-pai stacking interactions of the p
268 une system responses to infection and injury by inhibiting the production of tumor necrosis factor (T
269 RNAPII was reduced, which could be reverted by inhibiting the proteasome, indicating proteasomal deg
270 duce transcriptional changes in target cells by inhibiting the proteolytic processing of full-length
271 ults suggest that danazol exerts a CS effect by inhibiting the STAT3 pathway in MDR cancer cells and
272 wth and metastasis by inducing apoptosis and by inhibiting the STAT3 signaling pathway in cancer cell
273 from ER calcium release and were attenuated by inhibiting the store-operated calcium entry (SOCE) ch
274 ity improves myoblast differentiation partly by inhibiting the synthesis, not the degradation, of ID1
275 human neuroblastoma with TERT overexpression by inhibiting the TERT-associated gene expression networ
276 entinostat, disrupts the premetastatic niche by inhibiting the trafficking of MDSCs through the downr
277 cRel expression blocked ASC differentiation by inhibiting the transcription factor Blimp1, and in wi
278 containing miR-26a prevented muscle atrophy by inhibiting the transcription factor forkhead box O1.
279 tic function, enforces glycolytic metabolism by inhibiting the transport of pyruvate into the mitocho
282 e resulting oligomers to neuroblastoma cells by inhibiting their binding to the cellular membranes.
283 te transformation of LMP1-expressing B cells by inhibiting their differentiation to plasma cells.
284 omoters to induce their gene expression, and by inhibiting their interaction with phyB in the light.
285 maintained CAV1 and integrin protein amounts by inhibiting their lysosomal degradation through its en
289 es FcepsilonRI expression on dendritic cells by inhibiting transcription factor binding to its promot
293 e of these correlated networks was disrupted by inhibiting vCA1 shock responses during memory encodin
295 2-AG directly modulates pathogen function by inhibiting virulence programs essential for successfu
298 olorectal cancer tumor organoids (tumoroids) by inhibiting Wnt/beta-catenin signaling via induction o
300 stricts cell proliferation in animal tissues by inhibiting Yes-associated protein (YAP or YAP1) and T