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2 ssociated proapoptotic transcription factor, protected fibroblasts from 5-aza only when the cytotoxic
4 oughness, or in adjacent micro-porosity, can protect the surface from a strong wettability alteration
6 irus (VACV) infection were less effective at protecting mice from a lethal pulmonary challenge with V
7 ins (OMPs) have shown encouraging results in protecting mice from A. baumannii infection, but monoclo
8 ane, establishes an impermeable barrier that protects the cell from a number of stressors in the envi
13 reatment with an inhibitor of MCJ expression protects liver from acetaminophen-induced liver injury a
16 rate that the biosafety level 4 (BSL-4) suit protects workers from aerosols in a BSL-4 environment us
19 ow flavonoid compounds have the potential to protect the brain from aging and neurodegenerative disea
22 ubtilis has rendered the engineered bacteria protected against phages from all three major families o
23 ntranasal administration of exogenous Sema3E protects mice from allergic asthma by reducing eosinophi
24 though antigen application before conception protected WT progeny from allergy, it aggravated allergi
25 ) that modulate transcriptional networks and protect cells from alpha-synuclein (alphaSyn) toxicity.
27 es the cationic exopolysaccharide Pel, which protects bacteria from aminoglycoside antibiotics and co
28 Tfh cells decreased IgE antibody levels and protected mice from anaphylaxis, without affecting Th2 c
32 tial for these inhibitory TRAIL receptors to protect hHSC from apoptosis opens new avenues for progno
33 ts both its kinase end RNase activities, and protects cells from apoptosis both in vitro and in vivo.
35 cellular antiadrenergic therapeutic strategy protecting the heart from arrhythmia and contractile dys
37 ude that O-AS function as direct defenses to protect plants from attack by both native pathogenic fun
40 microbial layer around the colony that helps protect the brood from bacterial pathogen infection, res
41 acrophage-specific in vivo knockdown of Irf5 protected ZDF rats from beta-cell loss and hyperglycemia
43 Besides enzyme entrapment, the obtained gels protected the transducer from biofouling, enabling the r
44 d and licensed dengue vaccine that failed to protect seronegative individuals from breakthrough or en
45 nvironmental conditions as an ion sensor and protects Caulobacter from calcium deficiency stress, a u
49 a polymer known as peptidoglycan (PG), which protects the cell from changes in osmotic pressure and s
52 bit IRI in adoptive transfer experiments and protected mice from cisplatin- and doxorubicin-induced n
54 r show that the clinical isolates frequently protect each other from clinically relevant antibiotics.
56 cells, but not intestinal epithelial cells, protects mice from colitis-induced intestinal cancer and
57 TOR or MAPK signaling cascades, which act to protect the parasite from complement-mediated and osmoti
58 zed that KSHV miRNAs target human GADD45B to protect cells from consequences of DNA damage, which can
59 that addition of a specific bpy-diol ligand protects unprotected peptides from Cu(II) -mediated oxid
60 at lacked Fabp4/Fabp5 were less effective at protecting mice from cutaneous viral infection, and lung
61 ressor PTEN into the nucleus and in so doing protects it from cytoplasmic proteins that cause PTEN de
62 hereas the X-ray beam is often attenuated to protect the detector from damage caused by intense Bragg
64 sults reveal a novel mechanism as to how WRN protects telomere integrity from damage and telomere ero
67 es are specialized chromatin structures that protect chromosome ends from dangerous processing events
68 izing properties, and possess the ability to protect nerve cells from death at the calcium overload c
69 how that IDGF2 is independent of insulin and protects cells from death caused by serum deprivation, t
70 oxp1 Elevating expression of isoform-A or -D protects cortical neurons from death caused by the expre
71 that in mice the transcription factor STAT3 protects these cells from death and contributes to maint
74 e-stranded DNA (ssDNA) with high affinity to protect it from degradation and prevent secondary struct
75 omic plants expressing proinsulin and GAD to protect the autoantigens from degradation in an oral vac
78 ttenuated FoxO-mediated murf1 expression and protected sarcomeres from degradation in ncx1-deficient
79 ies, but also creates a steric hindrance for protecting the glycoproteins from degradation by proteas
80 tablish that the PhoP-activated protein MgtC protects PhoP from degradation by outcompeting ClpS for
81 gic or genetic inhibition of Cdc25A activity protects neurons from delayed death in vitro and in vivo
84 e role during nutrient starvation, autophagy protects cells from detachment-induced cell death, terme
86 matic adolescent hAPP mice was sufficient to protect these mice from developing cognitive impairment.
87 ta7) just before and following SIV infection protected rhesus macaques from developing AIDS and parti
89 the CB1 gene (Ati-CB1-KO) was sufficient to protect adult mice from diet-induced obesity and associa
93 monstrate that KSHV miRNAs are important for protecting infected cells from DNA damage responses.
94 X)-dependent, and apocynin, a NOX inhibitor, protected cells from double-strand breaks induced by HDM
95 ular ROS, and interference with either event protects bacteria from double-stranded DNA breakage and
97 ion in mice afflicted with p53-mutant tumors protected them from doxorubicin-induced neutropenia and
98 ound BGP-15 improved mitochondrial function, protecting neurons from dying in vitro and in vivo, and
99 alling through the SMAD1 and SMAD3 pathways, protecting the endothelium from endothelial-to-mesenchym
101 with HA35 normalized these changes and also protected mice from ethanol-induced liver and intestinal
102 xpression and in cholesterol uptake, further protecting macrophages from excessive lipid accumulation
103 complete dendritic stripping following rtACS protects neurons from excitotoxic cell death by silencin
105 tb) administration, and has shown ability to protect animals from exposure to a pesticide, paraoxon a
106 hly crosslinked ECM impeded drug permeation, protecting tumor cells from exposure to small-molecule d
107 ecombination factors BRCA1, BRCA2, and RAD51 protect these structures from extended nucleolytic degra
108 chromatin compaction by nucleosome stacking protects nucleosomal DNA from external forces up to 4 pi
109 ical memory following cell culture expansion protects MSCs from fibrogenesis in the host wound enviro
111 eutic targeting of PLD4 using specific siRNA protected mice from folic acid-induced kidney fibrosis a
118 e transporter expressed highly in the liver, protects mice from high-fat diet-induced and aging-induc
119 evidence has revealed that SLC13A5 deletion protects mice from high-fat diet-induced hepatic steatos
120 patic gluconeogenesis in the mouse liver but protects mice from high-fat diet-induced hyperglycemia.
121 rom an evolutionarily ancient mechanism that protects photosynthetic bacteria from high light stress,
122 olysaccharides (CPSs) play multiple roles in protecting bacteria from host and environmental factors,
123 HVEM-specific HSV-1 neutralizing antibodies protect mice from HSV-1 eye disease, indicating the crit
125 ditional analyses revealed that FGF2 priming protected cultured DPCs from hydrogen-peroxide-induced c
127 ese cells toward proinflammatory phenotypes, protecting the kidney from hypertensive injury and fibro
128 These studies suggest that while the ISR protects OPCs from hypoxia in vitro, it does not appear
129 teract with the environment, particularly to protect pathogens from immune surveillance and host defe
130 gly, we discovered that TrxR1/NADPH directly protects PTP1B from inactivation when present during the
131 etylation, and the presence of purified CobB protects TopA from inactivation by such non-enzymatic ac
133 asite traversal and development, and did not protect mice from infection with PfCSP transgenic Plasmo
134 generation of the skin's barrier in order to protect the body from infection and dehydration and to h
135 in astrocytes regulates BBB permeability and protects the cerebellum from infection and immunopatholo
136 EETs at sites of airway epithelial damage to protect the host from infections in patients with chroni
137 tributions to public health needs and better protect the public from infectious disease often motivat
142 tibody from a single injection of VRC01 mRNA protects humanized mice from intravenous HIV-1 challenge
145 ogenetic C1 neuron (C1) stimulation (10 min) protected mice from ischemia-reperfusion injury (IRI).
146 ., Mulholland, M., Zhang, W. mTOR activation protects liver from ischemia/reperfusion-induced injury
151 e the efficacy of the HMP Airdrive system to protect liver grafts from lethal ischemic damage before
152 m previously infected mice was sufficient to protect uninfected mice from lethal pathogen challenge.
153 s responsive to favipiravir treatment, which protected all animals from lethal disease and reduced se
155 elicited neutralizing antibody responses and protected mice from lethal VEEV and EEEV challenges at 1
159 FA are dynamically regulated and function to protect EC from lipotoxic stress and provide FA for meta
162 und, surprisingly, that neutrophils serve to protect the host from LPS-induced lethal inflammation.
163 ctively, our results demonstrate that YW3-56 protects animals from LPSS, and CitH3 is a reliable biom
164 RNA nucleotides in the drug binding site can protect cells from macrolide-induced killing, even with
167 nitor of lipoprotein trafficking tasked with protecting the cell from mislocalized lipoproteins.
169 ibodies, including the broadly binding ones, protected mice from mortality despite lacking neutraliza
170 ocytosis by macrophages and neutrophils, and protected mice from MRSA infection in two model systems.
171 21(Waf1/Cip1) blocks the ability of Foxp1 to protect neurons from mut-Htt-induced neurotoxicity.
172 ogenomics platform to identify strategies to protect neuronal cells from mutant huntingtin induced de
173 bservation indicates that MMR preferentially protects genes from mutation and has important consequen
174 the AMPK-TORC1 metabolic checkpoint, thereby protecting tumour cells from MYC-driven cell death, and
175 er wild-type or a nonfunctional SpeA mutant, protects mice from nasopharyngeal infection; however, on
176 n protection mutualisms, defensive symbionts protect their hosts from natural enemies, including para
177 all molecule TNFR inhibitor R-7050 partially protected hyperoxaluric mice from nephrocalcinosis and C
178 esence of G70S protein was not sufficient to protect mice from neurodegeneration in G70S/- mice, show
180 hat forms an efficient permeation barrier to protect the cell from noxious compounds (1)(,)(2) .
181 st, yKu70/80 rapidly localizes to the break, protecting DNA ends from nuclease accessibility, and rec
182 s support a novel nuclear role for SmgGDS in protecting malignant cells from nucleolar stress, thus p
183 R in the renal proximal tubule cells did not protect the mice from obesity, but markedly attenuated t
188 eract inhibition by unfair competition: MLCP protects pCPI-17 from other phosphatases, while pCPI-17
190 f Myc in osteoclasts increases bone mass and protects mice from ovariectomy-induced (OVX-induced) ost
202 nregulates p53 transcription and selectively protects noncancerous cells from p53-dependent apoptosis
206 ion of Clostridiales, but not Bacteroidales, protected neonatal mice from pathogen infection and abro
207 release of antimicrobials into the tears and protected the eye from pathogenic Candida albicans or Ps
211 skin microbiome acts as an important barrier protecting our body from pathogens and other environment
212 s Akt activation and osteoclastogenesis, and protects mice from pathological bone loss in disease mod
213 tive, interleukin-10-positive T cells, which protect animals from pathology, increased after malaria
215 stabilizes the 5 end of the guide strand by protecting it from phosphatases and 5-to-3 exonucleases.
216 5-Vinylphosphonate modification of siRNAs protects them from phosphatases, and improves silencing
222 s the deubiquitinase activity of ataxin 3 to protect beclin 1 from proteasome-mediated degradation an
223 t tunnel to host the elongating new peptide, protect it from proteolytic digestion, and guide its eme
225 more efficacious than Esc(1-21) and LL-37 in protecting host from pulmonary bacterial infection after
226 and ATP synthesis at a level high enough to protect M. tuberculosis from Q203-induced bacterial deat
227 nhibition of glutathione biosynthesis, which protects cells from reactive metabolites, increased the
229 dern stormwater management practices are not protecting surface waters from road salt contamination a
235 otection.In meiosis I centromeric cohesin is protected by Sgo2 from Separase-mediated cleavage ensuri
237 novel glycosylation-dependent mechanism that protects tumor cells from serum growth factor withdrawal
238 malaria-endemic areas of Africa, where they protect children from severe and uncomplicated Plasmodiu
239 g bNAbs CR6261 and CR9114 have been shown to protect mice from severe disease following challenge wit
240 can antagonize TLR4 activation in vitro and protect mice from severe influenza infection, most likel
241 especially those with p53-mutant tumors, may protect them from severe chemotoxicity while allowing tr
242 laxis with the ABL kinase inhibitor imatinib protected the mice from severe IgE-mediated anaphylaxis.
243 py approach for IFNgammaR1 deficiency, which protects mice from severe mycobacterial infections, ther
244 ptosis in a mammalian expression system, and protected cortical neurons from slow excitotoxic injury
245 with RTX before radiation exposure partially protected podocytes from SMPDL3b loss, cytoskeletal remo
246 ne marrow mesenchymal stromal cells (BM-MSC) protect AML blasts from spontaneous and chemotherapy-ind
248 chanical therapy have the clear potential to protect hindlimb function from such adverse influence.
249 the aforementioned conformational switch can protect nitrogenase from such damage, confirming that th
251 at outside-xylem hydraulic vulnerability can protect the xylem from tensions that would induce emboli
253 CNS we reasoned that brain aromatization may protect circuits from the threats of peripheral infectio
254 observations suggest that FGF2 priming might protect DPCs from the post-trauma microenvironment in wh
255 ctors present in the CNS may physiologically protect neurons from the deleterious impact of AbetaOs.
256 lts suggest that using money to buy time can protect people from the detrimental effects of time pres
257 the two-dimensional (2D) high-mobility plane protect the semiconductor from the effect of dynamic dis
258 ha and modified its ubiquitination status to protect Topo IIalpha from the proteasomal degradation in
259 facilitate nuclear import and simultaneously protect unassembled RpL4 from the cellular degradation m
260 le methods to test water supplies onsite can protect vulnerable communities from the impact of contam
261 ulating PGRP-SB2 selectively in the fat body protected animals from the deleterious effects of overnu
264 ains of V. cholerae, which are thought to be protected only from the toxicity of their own effectors.
265 s thought to be a glutathione precursor, NAC protected primary astrocytes from the toxicity of the pr
266 es in vitro and in vivo KCNQ2/3 coexpression protected SMIT1 activity from the otherwise inhibitory e
268 etry genetic pathway as a key determinant in protecting A. baumannii from the bactericidal activity o
269 oting gametocyte-to-ookinete development and protecting ookinetes from the mosquito complement-like r
270 different function in Plasmodium falciparum, protecting ookinetes from the mosquito immune response.
271 ial cells form a barrier that is critical in protecting the host from the hostile luminal environment
272 njugation, transport, and excretion, thereby protecting the liver from the harmful effects of bile ac
274 tial component of the shelterin complex that protects chromosome ends from the DNA damage response ma
275 ys demonstrated that the optimized inhibitor protects macrophages from the toxicity of lethal factor.
277 am to the eC surface without breaking vacuum protects the surface from the environment after fabricat
278 ch, whereas stimulation of alpha4beta2-nAChR protected delay cells from these deleterious effects.
281 contribution of biallelic RELA expression in protecting stromal cells from TNF-mediated cell death, t
284 thesis that myeloperoxidase inhibition could protect hematopoietic cells from TOP2 poison-mediated ge
285 rated that keratinocyte-derived GC synthesis protected skin from topical phorbol 12-myristate 13-acet
286 hort duration, these efficient nanofactories protect human cells from toxic reactive oxygen species f
287 inhibitor of NF-kappaB-inducing kinase (NIK) protects liver from toxin-induced inflammation, oxidativ
288 utaneous immunization with neoglycoconjugate protected mice from transnasal challenge with the highly
290 ether, we demonstrate that Dnmt3a and Dnmt3b protect the epidermis from tumorigenesis and that squamo
292 idues on RNF157 disrupts binding to CDH1 and protects RNF157 from ubiquitination and degradation.
293 onfers resistance to high oxygen tension and protects cells from undergoing ferroptosis in response t
294 In conclusion, melatonin and its metabolites protect melanocytes from UVB-induced DNA damage and oxid
295 y therefore investigated whether fat feeding protected mice from ventilator-induced lung injury.
299 particularly during pregnancy and lactation, protects offspring from WD-induced developmental program
300 nt IL6 to LysM-Cre; Egfr(f/f) mice given DSS protected them from weight loss and restored epithelial
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