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1 ua/CIC maintains peripheral immune tolerance by suppressing aberrant activation of adaptive immunity.
2 their proper development and maturation and by suppressing aberrant proliferation mediated by the T
4 evelopment and progression of renal fibrosis by suppressing activation and expression of multiple pro
5 vent neuroinflammation and neurodegeneration by suppressing activation of innate and adaptive immune
6 ough inhibition of renal fibroblasts and EMT by suppressing activation of multiple profibrotic signal
7 gluteofemoral adipose tissue (AT) expansion by suppressing adipogenesis and increasing gluteal adipo
9 rosis can potentially be treated effectively by suppressing allele-specific genes using small interfe
10 es both innate and adaptive immune responses by suppressing alpha-SYN-induced microglia and macrophag
11 x vivo, ibuprofen also affected Sertoli cell by suppressing AMH production and mRNA expression of AMH
12 itor may more effectively treat glioblastoma by suppressing an important temozolomide resistance mech
13 A1AR) protects against cisplatin ototoxicity by suppressing an inflammatory response initiated by ROS
14 e (AMPK), which regulates energy homeostasis by suppressing anabolic and activating catabolic process
17 hesis that people can attenuate future fears by suppressing anticipatory simulations of dreaded event
18 inhibited the AAA development in AdAPN mice by suppressing aortic inflammatory cell infiltration, me
19 with doxorubicin, paclitaxel, or carboplatin by suppressing apoptosis and upregulating NF-kappaB Over
22 ng antagonist sgp130Fc ameliorated emphysema by suppressing augmented alveolar type II cell apoptosis
23 y for enhancing responses to EGFR inhibitors by suppressing AURKA-driven residual disease and acquire
24 re moderately effective at reversing disease by suppressing autoimmune inflammation in the skin and p
26 the maintenance of immunological homeostasis by suppressing autoreactive T cells in liver and lung.
27 plant hormone auxin, prevents bud outgrowth by suppressing auxin canalization and export from axilla
32 rs, we show that foretinib protected neurons by suppressing both known degenerative pathways and a ne
33 ting oncogenic and tumor suppressive effects by suppressing both tumor suppressive mRNAs and oncogeni
34 may enhance (or intensify) cryptosporidiosis by suppressing C. parvum-induced cell turnover and caspa
36 and extent of inflammatory cell infiltration by suppressing canonical BMP signaling, thereby providin
38 which EZH2 controls GC B cell proliferation by suppressing CDKN1A, enabling cell cycle progression w
41 ing allows management as a chronic condition by suppressing circulating viral load to allow for a nea
42 (QDs) enhances triplet energy transfer (TET) by suppressing competitive charge transfer from QDs to m
47 ve mechanical resilience of flexible devices by suppressing crack formation upon stretching and bendi
48 that miR-23a prevents ROS-elicited necrosis by suppressing cyclophilin D (PPIF), a regulator of ROS
49 Talpha1 in regulating mitochondrial function by suppressing CYP2E1 expression at multiple levels.
51 ve molecule that promotes beta-cell survival by suppressing DDR signaling and attenuating DNA damage-
52 e excitability of SLC5A11-expressing neurons by suppressing dKCNQ channels, thereby conferring the hu
54 luding DNA repair and inflammatory response, by suppressing downstream targets IKBKB, WEE1, FGF2, RAD
57 y a convergent strategy of TE load reduction by suppressing element origination in their independent
58 c cells and functions to favor NHEJ over HDR by suppressing end resection, which is the rate-limiting
60 signaling in cancer cells promotes survival by suppressing endogenous DNA damage, and may control ce
61 rated the enhancement of dendritic formation by suppressing endogenous TRIO, and similarly decreasing
62 ardiac fibrosis and functional deterioration by suppressing endothelial autophagy and promoting endot
64 tment efficacy against multiple malignancies by suppressing epigenetic hypermethylation in tumor cell
65 and mucous metaplasia following RV infection by suppressing epithelial cell innate cytokine expressio
66 pound 13d alleviates ER stress in beta-cells by suppressing ER stress-mediated activation of all thre
68 10 also indirectly supports humoral immunity by suppressing excessive IFN-gamma, which induces T-bet
69 T (Treg) cells prevent autoimmune disorders by suppressing excessive lymphocyte activity, but how in
70 vo activity of these cells, at least in part by suppressing excitatory drive from PBN inputs onto CRF
71 ng two-distinct stages of positive selection by suppressing expression levels of pro-apoptotic molecu
72 plored as a novel therapy for CRPC treatment by suppressing expression of AR and AR splice variants t
73 n of GPR30 by G-1 enhanced cholelithogenesis by suppressing expression of cholesterol 7alpha-hydroxyl
74 l self-renewal and reprogram immune response by suppressing expression of immune checkpoint genes, es
75 ion protects against fatty liver development by suppressing expression of peroxisome proliferator-act
76 , promoted apoptosis in BAP1-deficient cells by suppressing expression of the prosurvival genes Bcl2
77 ration, clonogenic ability, and invasiveness by suppressing extracellular signal-regulated kinases 1/
80 glucose production and promotes lipogenesis by suppressing FOXO1-dependent activation of G6pase and
81 of tau in GABAergic interneurons impairs AHN by suppressing GABAergic transmission and disinhibiting
82 ance and lineage determination of stem cells by suppressing genes that regulate cellular differentiat
84 impairs upper airway dilator muscle activity by suppressing glutamatergic input from PH premotoneuron
85 at IL-9 reduces autoimmune neuroinflammation by suppressing GM-CSF production by CD4(+) T cells throu
86 y, a major issue for Sb(2)Se(3), is resolved by suppressing growth kinetics via close space sublimati
87 llee effects can limit species distributions by suppressing growth rates of peripheral populations wh
92 ugs might prove to be an effective treatment by suppressing HK2 infectivity in diseases where these v
95 n may, therefore, increase TB susceptibility by suppressing IFN-gamma and IL-17A production during th
97 f immune effector molecules, including iNOS, by suppressing IFN-gamma-JAK-STAT1 transcription-factor
98 ly reduced late, but not early, infarct size by suppressing IGF-1 degradation and, consequently, dimi
99 asis-related proinflammatory gene expression by suppressing IkappaBzeta induction in keratinocytes.
100 the differentiation of inflammatory T cells by suppressing IL-10 expression through histone demethyl
101 i-TNF-alpha therapy may act at least in part by suppressing IL-22BP and point toward a more specific
104 uate sleep has deleterious effects on health by suppressing immunity and promoting inflammation.
105 mprovements of survival and cardiac function by suppressing infiltration of multiple kinds of inflamm
108 tection against IR-induced intestinal injury by suppressing inflammation and nitrosative stress and u
110 ated inflammation in the injured brain areas by suppressing inflammatory cytokines expression whereas
111 predisposes to invasive pneumococcal disease by suppressing inflammatory processes of the upper respi
112 with Kv4.2 channel and promotes its function by suppressing inhibitory modulation by cAMP-protein kin
113 hyperresponsiveness and airway inflammation by suppressing innate and adaptive antiviral responses a
114 Ca(2+) influx maintained the quiescent state by suppressing insulin-like growth factor (IGF)-mediated
115 that ATM kinase promotes Alt-EJ-mediated CSR by suppressing interchromosomal translocations independe
116 m changes in bone marrow-derived macrophages by suppressing interleukin 1beta, CD68, and phagocytosis
117 orate the pathological outcomes of infection by suppressing interleukin 6 production in the brain.
118 ysmetabolism and improves muscle performance by suppressing intramuscular fat deposits, Phospho-AKT l
119 environment at the distant organ sites, and by suppressing invasive properties of the cancer cells.
120 pneumoniae responds to exogenous fatty acids by suppressing its de novo biosynthetic pathway and excl
128 C pyramidal neuron responses to MThal inputs by suppressing local feed-forward GABA signaling from pa
129 astatic process of lung cancer cells in vivo by suppressing local invasion and distant colonization.
132 hown to exacerbate motor symptoms of DA loss by suppressing M(4)-autoreceptor-Galpha (i/o) signaling
133 reatine reprogrammed macrophage polarization by suppressing M(interferon-gamma [IFN-gamma]) yet promo
134 d enhance the anti-neoplasia effect of BPTES by suppressing malignant cells' glucose utilization.
135 nhibited alpha-SYN-induced neuroinflammation by suppressing microglial activation, macrophage and CD4
136 drive this learning-induced memory mechanism by suppressing microRNA-mediated translational silencing
137 a-secretase system decreases neuronal losses by suppressing miR-212 and increasing its target surviva
142 data establish that MNT synergizes with MYC by suppressing MYC-driven apoptosis, and that it does so
143 n modeled responses to MYCN-directed therapy by suppressing MYCN expression in MYCN-driven retinoblas
144 Intriguingly, Deltex2 inhibits myogenesis by suppressing MyoD transcription, and the Deltex2 knock
146 ndependent, prosurvival pathway in the heart by suppressing necroptotic signaling, which may serve as
147 SI-09, phenocopied the effects of Epac1 null by suppressing neointima formation and proliferative VSM
148 Microglia respond to neuronal activation by suppressing neuronal activity, and ablation of microg
149 ve regulation of acute inflammatory response by suppressing NF-kappaB activation and proinflammatory
150 KDM3C demonstrates anti-inflammatory effects by suppressing NF-kappaB signaling and osteoclastogenesi
152 (GM-CSF)-induced CD103(+) DC differentiation by suppressing NF-kappaB, STAT1/5, and p38 activation.
153 tor of HIV-1 gene-expression and replication by suppressing NF-kappaB-mediated activation of viral tr
154 a positively regulates inflammatory response by suppressing NKRF production, which might be targeted
155 tPA deficit attenuated functional hyperemia by suppressing NMDAR-dependent nitric oxide production d
156 oting sleep during the night but not the day by suppressing nocturnal arousal and hyperactivity.
157 n detectors improves motion discriminability by suppressing noise generated by the local structure of
158 niche pinwheel structures, at least in part by suppressing Notch activation in radial glial cells, w
160 suggest that the A1AR provides otoprotection by suppressing NOX3 and inflammation in the cochlea and
161 androgen-independent prostate cancer growth by suppressing nuclear receptor-mediated oxidative stres
162 el components in high dynamic range mixtures by suppressing one-bond (13)C satellite signals in (1)H
165 Teriparatide increases osteoblast numbers by suppressing osteoblast apoptosis and activating bone-
166 oading regulates subchondral bone remodeling by suppressing osteoclast development, and prevents degr
167 emonstrate that Hdac3 controls bone modeling by suppressing osteoclast lineage cell responsiveness to
168 f OA, knee loading exerts protective effects by suppressing osteoclastogenesis through Wnt signaling,
169 ore, knee loading exerted protective effects by suppressing osteoclastogenesis through Wnt signaling.
172 ductance enhances rate coding in place cells by suppressing out-of-field excitation and by limiting d
173 atory role in lineage-committed tissue cells by suppressing overactivation of multiple signalling pat
174 9 acts as a regulator of cellular metabolism by suppressing oxidation of fatty acids, and thus adapts
175 ion alleviated IRI and improved OLT survival by suppressing p-p38 upregulation, ROS induction, and HM
176 d the capacity of macrophages to proliferate by suppressing p21 expression to halt their differentiat
177 2 promotes breast cancer early dissemination by suppressing p38, but how Her2 downregulates p38 is un
179 ductive and effector sites of oral tolerance by suppressing peripheral regulatory T cell (pTreg) conv
180 layed in AMPKalpha2 cKO mice were alleviated by suppressing PERK activity pharmacologically or geneti
181 ll proliferation, survival, and tumor growth by suppressing PI3K/mTOR/Akt activities in mouse models
182 phogenesis and modulates thermomorphogenesis by suppressing PIF4 activity, through a reduction in PIF
183 microbes can favor or improve insect fitness by suppressing plant defenses and detoxifying defensive
185 tion may protect against cerebral I/R injury by suppressing post-ischemic apoptosis, whereas heavy et
189 ficantly attenuated early/acute inflammation by suppressing pro-inflammatory cytokines (TNF-alpha, IL
190 diolipin inhibits resolution of inflammation by suppressing production of anti-inflammatory IL-10 by
192 ith maturation and commitment to iNKT1 cells by suppressing proliferation and Opa1-related mitochondr
193 ion of aberrant neovessels into the vitreous by suppressing proliferation of endothelial cells (EC) i
195 rmation of a more reactive phenotype enabled by suppressing proteolytic cleavage of sIL-6R from IL-6R
196 whether structural changes shape adaptation by suppressing recombination or by creating new mutation
197 r, vitamin D may also promote renoprotection by suppressing renin transcription through cross-talk be
198 increased spontaneous EPSC (sEPSC) frequency by suppressing RIM1alpha-facilitated CaV2.2 expression i
199 2 has a role in protecting cartilage from OA by suppressing Runx2-induced Adamts5 via Runx2 poly-ubiq
200 MAGE-B2, increases cellular stress tolerance by suppressing SG formation through translational inhibi
202 marrow-derived cells and limits inflammation by suppressing signaling through stimulatory receptors.
205 gic advantage to singlet fission solar cells by suppressing singlet dissociation at optimal driving f
206 thora sojae effector PSR1 promotes infection by suppressing small RNA biogenesis in plant hosts.
209 that VP reduces Src kinase phosphorylation: by suppressing Src using the inhibitor dasatinib and siR
210 ulatory protein protects against nephropathy by suppressing STAT-mediated cell responses to diabetic
211 lopment of psoriasis in various mouse models by suppressing STAT3-mediated IkappaBzeta expression.
212 moting environmental condition, acts in part by suppressing stomatal defense and is linked to hormone
213 dings, technology was developed to treat RHT by suppressing sympathetic activity with electrical stim
214 Furthermore, we find that NCA promotes sleep by suppressing synaptic release from a dispersed wake-pr
215 en implicated in immune regulation, not only by suppressing T cell responses but also by regulating a
217 of TCF4, we created an in vivo model of PTHS by suppressing Tcf4 expression in rat prefrontal neurons
218 al growth factor (VEGF) secretion in Mos/Mps by suppressing TGFbeta1 signalling and subsequently inhi
220 ge performance could potentially be obtained by suppressing the (La,Sr)O termination and stabilizing
221 hat MHC-matching reduces the immune response by suppressing the accumulation of microglia (Iba-1+) an
222 ith improvement in progression-free survival by suppressing the activating mutation and preventing th
223 demonstrate that Notch maintains type II NBs by suppressing the activation of earmuff (erm) by Pointe
225 gm1 negatively regulates IL-1beta maturation by suppressing the activation of the NLRP3 inflammasome.
226 ctivation of transcription of the BIC genes, by suppressing the activity of CONSTITUTIVE PHOTOMORPHOG
228 he inhibitory effect of the spacing was lost by suppressing the activity of Ras or mitogen-activated
229 ated macrophages (TAMs) support tumor growth by suppressing the activity of tumor-infiltrating T cell
230 pancreatitis in EtOH-sensitized acinar cells by suppressing the adaptive unfolded protein response si
231 affects the RNA remodeling ability of LAF-1 by suppressing the affinity, dynamics, and annealing act
233 y shaping the architecture of the tumour and by suppressing the antitumour activities of immune cells
235 tion, regulates miRNA abundance and function by suppressing the biogenesis of ribosomal RNA-derived s
236 viate pain and reduce fever and inflammation by suppressing the biosynthesis of prostacyclin (PGI2) a
238 ecular strategy to adapt to hot environments by suppressing the efficiency of TRPV1-mediated heat det
239 novel class of NRF2 activators that function by suppressing the enzymatic activity of an epigenetic r
240 not Tyr(701)) and STAT1 luciferase activity by suppressing the ERK1/2, p38, and JNK mitogen-activate
242 inhibition in an experience-dependent manner by suppressing the expression of EphB4; PV cells hemizyg
243 0 protected LRP5/6(DeltaCD11c) mice from CAC by suppressing the expression of inflammatory factors.
245 beta inhibits macrophage foam cell formation by suppressing the expression of key genes implicated in
246 reover, BCL11A promotes cancer cell invasion by suppressing the expression of muscleblind-like splici
247 ed against renal ischemia-reperfusion injury by suppressing the expression of proinflammatory genes a
248 er engagement of the B cell antigen receptor by suppressing the expression of the autoimmune suppress
249 node that switches off antimigratory miR-198 by suppressing the expression of the regulatory factor,
250 d that IDR-1002 reduced sterile inflammation by suppressing the expression of transmembrane G protein
252 The coating results in superior performance by suppressing the formation of Li dendrites and inactiv
253 ify chromatin and to support DNA replication by suppressing the formation of R-loops (DNA/RNA-hybrids
254 The compounds likely enhanced cell viability by suppressing the formation of reactive oxygen species
255 increase in the yield of expected runoff RNA by suppressing the formation of undesired longer RNA byp
258 ally, mir156 mutations enhance seed dormancy by suppressing the gibberellin (GA) pathway through de-r
259 , simvastatin improved restenosis indicators by suppressing the HIF-1alpha/calpains/MMP2/TGF-beta1 pa
260 essential for facilitating biotrophic growth by suppressing the host oxidative burst-the first line o
261 thelialization, and collagen deposition, and by suppressing the inflammatory response and apoptosis.
264 stricts the EHT of lymphoid-myeloid lineages by suppressing the mannosyltransferase alg2 and sialyltr
266 hieve more control over the mode selectivity by suppressing the mode that has the highest gain (i.e.
267 onstrates that Ubx stabilizes lineage choice by suppressing the multipotency encoded in the genome vi
268 r stress counteracts endothelial dysfunction by suppressing the pro-inflammatory non-canonical TGF-be
269 ally expanded CD8(+) T cells inhibit disease by suppressing the proliferation of MOG-specific CD4(+)
270 When the population is further increased by suppressing the radiative recombination rate with the
271 s strong evidence that the brain compensates by suppressing the retinal motion due to self-motion, ho
272 yclosporine into the aqueous phase, probably by suppressing the solubilization capability of the mice
273 utes to female germline stem cell unipotency by suppressing the somatic program and is potentially in
274 l monitoring of genetic and protein circuits by suppressing the spectral cross-talk among multiple fl
277 miR-200 family promotes the epithelial state by suppressing the Zeb1/Zeb2 epithelial gene transcripti
278 INB1) limited the activity of those caspases by suppressing their caspase-recruitment domain (CARD) o
281 represents a promising therapeutic strategy by suppressing therapy-induced senescence-associated CSC
282 AAL(S) reduced the severity of acute AAD by suppressing tissue eosinophils and inflammation, mucu
283 hibit experimental fungal keratitis in mouse by suppressing TLR4 and inflammatory cytokines such as T
284 dendritic cell (DC) responses, specifically by suppressing TLR4 signalling to inhibit Th1/Th17-drive
286 naive CD8(+) T cells required for activation by suppressing TMEM20, a negative regulator of Ca(2+) ex
287 meostasis, it blocked osteoclast development by suppressing transcription factors c-Fos and JunB, but
289 overed that OCTR-1 regulates innate immunity by suppressing translation and the unfolded protein resp
290 nt role in modulating disease-risk in humans by suppressing tumour progression, decreasing inflammati
291 s expressing a LIF transgene reduce fibrosis by suppressing type 2 immunity and highlight a novel app
292 he FGF19-SHP-LSD1 axis maintains homeostasis by suppressing unnecessary autophagic breakdown of cellu
295 ferentiation-related gene expression profile by suppressing Wnt pathway activity and reducing mesench
297 umor suppressor, which inhibits tumor growth by suppressing Wnt/beta-catenin signaling in lung adenoc
298 ppears to modify the specificity of the MAPK by suppressing Y kinase and enhancing S/T kinase activit