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1 und that p-eIF2a was decreased when PTEN was depleted.
2 anced AIDS, in whom CD8+ T cells may also be depleted.
3 tion of the more volatile component as it is depleted.
4 get proteins that are, or can be, methionine-depleted.
5 mbrane potentials when calcium stores become depleted.
6 oops was exacerbated when both proteins were depleted.
7 types similar to those observed when ClpP is depleted.
9 xperiments using Trib1 (-/-) mice that had a depleted ability to develop M2 macrophages and other in-
11 hanistically, we demonstrated that, in FANCM-depleted ALT cells, BRCA1 and BLM help to resolve the te
12 still form, but acidic cluster proteins are depleted, although several other CCV components were eit
14 hat upon metastasis to the brain, TRPA1 gets depleted, an effect triggered by the transfer of TRPA1-t
16 ression of Kras(G12D) were crossed with Lcn2-depleted animals and fed isocaloric diets with varying a
17 nkG expression increased ENaC activity while depleting AnkG reduced ENaC-mediated Na(+) transport.
23 d in the growth media as a carbon source was depleted around the fungi, suggesting its uptake and con
24 ding protein (Igfbp) genes when Ng2/Cspg4 is depleted at tumor initiation, but not when Ng2/Cspg4 is
25 age oxidative stress, yet glutamine is often depleted at tumor sites owing to excessive cellular cons
26 host ATM and gammaherpesvirus infection, we depleted ATM specifically in B cells, a cell type critic
30 ed relationship between host and microbiota, depleting bacterial populations critical for the mainten
32 e low-dose chemotherapy conditioning regimen depleted blood lymphocytes and increased serum interleuk
33 hage populations of wild-type mice with Nrp1-depleted bone marrow-derived macrophages (BMDM) confers
36 s was attributed to the existence of regions depleted by aggregates of certain sizes in the parent br
39 acellular Ca(2+) ([Ca(2+) ]i ) in ASMCs with depleted Ca(2+) -stores in response to increased [Ca(2+)
41 d to HemW was actively transferred to a heme-depleted, catalytically inactive nitrate reductase, rest
42 In cynomolgus monkeys, SGN-CD19B effectively depleted CD20(+) B lymphocytes in peripheral blood and l
49 culture conditions to maintain mitochondrial-depleted cells for up to 30 d with minimal loss of viabi
51 NP overexpression rescues furrowing in MKlp2-depleted cells in an INCENP-actin binding-dependent mann
53 ve imaging of meiotic divisions in condensin-depleted cells showed repeated nuclear stretching and co
54 lk1 itself (self-priming) increased in MYPT1-depleted cells showing that MYPT1 provides a molecular l
55 itochondrial electron transport chain, mtDNA-depleted cells still maintain mitochondria and many mito
60 erately enhanced compared to that in the Cbl-depleted cells, suggesting that the Cbl-Nectin-1 interac
61 Microarray analysis of IRE1alpha- and XBP1-depleted cells, validation using RNA cleavage assays, an
67 defective mitochondria, compromised OXPHOS, depleted cellular ATP, and altered cellular metabolism p
72 To test this, we use the UAS/Gal4 system to deplete CFI proteins from neural tissue and observe that
74 coexisting with a Lalpha phase, or ceramide depleted, coexisting with a Lbeta phase, depending on th
77 cted growth rate under nitrogen-replete and -deplete conditions, as well as the effect of external ca
78 e water-deprived but not under food- or salt-depleted conditions, indicating that the hedonic value o
80 +) T cell responses to cross-presented Ag by depleting cross-presenting conventional dendritic cells.
81 tration of C1572 suppressed tumor growth and depleted CSCs in a manner correlated with diminished MYC
82 small-molecule natural product, selectively depletes CSCs in a dose-dependent fashion in human tripl
84 ctions with SIVmac239, but not with Delta5G, deplete CXCR3(+) CCR5(+) CD4(+) T (Th1) cells during the
85 15) combined 2 small molecules-decitabine to deplete DNMT1 and tetrahydrouridine (THU) to inhibit cyt
87 Cx43-beta-tubulin molecular interaction was depleted due to protein-protein interaction between vira
92 onoclonal antibody that directly and rapidly depletes eosinophils, reduces asthma exacerbations, and
93 etween the abilities of Tg and Tg analogs to deplete ER Ca(2+) stores and their detrimental effects o
95 l by eliciting excessive EnR stress and also depletes ERalpha expression/function, we propose SGK3 in
97 factors involved in the common pathway were depleted (factor II, V, X), which corresponded to increa
101 tion, we performed Hi-C experiments on cells depleted for the Forkhead transcription factors, Fkh1 an
102 t climate change and industrial fishing have depleted forage fish stocks in this system [10, 11].
103 expression of CXCL10, CXCR3(+) T cells were depleted from blood in the SIVmac239-infected animals.
104 ional knockout mouse in which the protein is depleted from muscle progenitors at embryonic day 8.5 (M
106 nd profiled transcripts that are enriched or depleted from select subsets of ribosomes within embryon
108 The Arabidopsis thaliana strain Cvi has depleted gene body methylation relative to the reference
109 Furthermore, these results suggest that depleted glutathione levels, which occur in aging and st
110 s or genetic inhibition of glycogen synthase depletes glycogen stores and extends the lifespan of ani
111 tion-free conditioning regimen with a T-cell-depleted graft to eliminate radiation exposure and minim
114 but microbiota analysis revealed a severely depleted gut microbiota with concomitant opportunistic p
118 ion changes were partially relieved in Ki-67-depleted hTERT-RPE1 cells by codepletion of the Rb check
119 in 1, was particularly inhibited in ataxin-3-depleted human cell lines and mouse primary neurons, and
121 pre-incubated with alpha-gal or protein G to deplete IgG Ab. alpha-Gal-specific IgG1-4 Ab in individu
122 protein mice) transplantation in bone marrow-depleted IL10KO mice (IL10KO chimeric mice) reduced tran
128 (promoters, UTRs, and introns), while being depleted in coding and intergenic regions, and these fin
129 ar mycorrhizal fungi (AMF) are significantly depleted in H. forsteriana on volcanic soil, relative to
132 species and the Sphingomonodaceae family and depleted in members of the Mogibacteriaceae family and L
136 nic mouse model in which FlnA is selectively depleted in myeloid cells, such as neutrophils, we show
137 uN, a neuronal maturity marker, is strangely depleted in suprachiasmatic nucleus (SCN) neurons, and m
138 enhanced decoding of specific mRNAs that are depleted in terminally differentiating/enucleating cells
140 es, as SODA/DeltasodA cultures were strongly depleted in this infective form and more susceptible to
141 of the lunar interior must be significantly depleted in volatile elements and compounds and that vol
144 11A, suggesting that the enhancing effect of depleting IRF2 on replication of the SPI-1 mutant was in
145 ately 40-55% of this population had small or depleted iron stores (i.e., SF concentration </=30 mug/L
147 (CRP plus AGP), the estimated prevalence of depleted iron stores increased by 7-25 and 2-8 absolute
148 tantially change the estimated prevalence of depleted iron stores.Our results lend support for the us
151 ased the abundance of dipeptide metabolites, depleted key tricarboxylic acid cycle metabolites, and s
152 ckpoint but does require the kinetochore, as depleting kinetochore components prevents the error-indu
154 oalescence that promote homogeneous, species-depleted landscapes; and (g) deliberate culture and rele
155 ene and lipid-tail carbons result in greatly depleted lipid density within confined regions of the me
156 fluorescence microscopy, we show that CDCP1 depletes lipids from cytoplasmic lipid droplets (LDs) th
157 their crystallization, confirming a volatile-depleted lunar interior source with homogeneous delta(66
160 divergent roles in homeostasis and fibrosis: depleting macrophages in control mice protected from acu
161 ice protected from acute insult; conversely, depleting macrophages in fibrotic liver weakened the hep
163 ruginosa mutants defective in growth in iron-depleted media and find that gene PA2374, proximal to th
166 ore, raising serum calcium levels in Cyp27b1-depleted mice directly increased FGF23 levels and indire
167 although not completely protected, mast cell-depleted mice displayed less organ atrophy and fibrosis
169 s is demonstrated by the finding that CD301b-depleted mice exhibit delayed wound closure in vivo, whi
170 nsity was maintained in young satellite cell-depleted mice regardless of running, although it was mod
172 cued in RAG2(-/-), IFN-gamma(-/-), or T cell depleted mice, suggesting IFN-gamma and T cell mediated
178 ConA was administered i.v. to control or HSC-depleted mice; hepatic histopathology and cytokines/chem
179 except for glucose and histidine, which were depleted more slowly than predicted, and proline, glycin
180 t defense by degrading human mucin-2 (MUC2), depleting mucin stores and inducing differential gene ex
181 CCK-8 levels to mimic pancreatitis, Munc18c-depleted (Munc18c(+/-)) mouse acini exhibited a reductio
182 icient, lymphocyte-deficient, and neutrophil-depleted murine hosts revealed that neutrophil-phage syn
183 s or body weight gain in the rat, whereas it depleted muscle carnitine content (all moieties), increa
185 ization and greater lipid oxidation in HDAC3-depleted muscles, a fuel switch caused by the activation
190 ve role for the microbiome, treatment of pDC-depleted neonates with the microbial-derived metabolite
192 on loss of B cell self-tolerance in vivo, we depleted neutrophils at different stages of disease.
193 e cotransporter 2 inhibitor (dapagliflozin), depleting neutrophils or Kupffer cells, or inhibiting S1
194 The extent to which depletion processes deplete non-EV particles is incompletely understood, but
195 rable concentrated salt solution after being depleted of bodily sodium despite never having tasted sa
197 ained on the surface of cells that have been depleted of Cbl; and (iii) that in cells infected with a
199 e-radiolabeling experiments with human cells depleted of CIA1, CIA2A, CIA2B, or MMS19 revealed that C
200 bulk DNA synthesis or activate Chk1 in cells depleted of Claspin, or when Chk1 was depleted or subjec
202 btained within seven days of ARDS onset, was depleted of high abundance proteins and labeled for iTRA
203 the RNR catalytic activity in yeast mutants depleted of individual components of the mitochondrial i
205 ve effect of etifoxine was abolished in mice depleted of microglia by using a colony-stimulating fact
206 n vitro, human LS174T goblet-like cells were depleted of mucus and had elevated levels of MUC2 mRNA e
207 opsy specimens exposed to G. duodenalis were depleted of mucus, and in vivo mice infected with G. duo
211 nd secondary parasitemia was similar in mice depleted of platelets by mAb-injection just before infec
213 nsitivity of Chlamydomonas reinhardtii cells depleted of the chloroplast protein PGRL1 was rescued by
214 ongevity studies combined; all but three are depleted of the life-shortening alleles in older Biobank
215 has been mostly injected back into pressure-depleted oil-producing reservoirs for enhanced oil recov
216 .3(K27M)-driven lesions are clonal, H3K27me3 depleted, Olig2 positive, highly proliferative, and diff
218 xyloglucan was allowed to bind to xyloglucan-depleted onion walls, CBM76 labelling gave positive evid
219 tions where the histone demethylase KDM4A is depleted or inactive, H3K9me3 accumulates at the HIF-1al
223 sturbance to the global carbon(C)-cycle, and depleted oxygen in Earth's oceans resulting in marine ma
225 PI3K and phospholipase Cgamma, enzymes that deplete plasma membrane phosphatidylinositol 4,5-bisphos
236 specific guanine nucleotide exchange factor, depleting Rac1 results in the loss of most of mesenchyma
237 sal striatum of dopamine-intact and dopamine-depleted rats during two brain states, respectively defi
244 Whereas lambda somatic mutants from the depleted sample displayed evidence of positive selection
246 nd explored a combined targeting strategy to deplete senescent cholangiocytes and ASFs from fibrotic
248 EV particles is incompletely understood, but depleted serum is associated with reduced viability and
249 sical complement pathway using TNT003 or C1q-depleted serum significantly reduced adhesion of monocyt
251 onclusions that conventional harvests do not deplete SOC in the mineral soil have been a function of
252 fluids, derived from external, isotopically depleted sources, metasomatized the granites, which resu
256 th when activation was triggered in vitro by depleting stabilizing Ca(2+) from solubilized Env and wh
260 cks, we identified significantly enriched or depleted structure motifs relative to earlier rounds.
262 change is masking ozone recovery from ozone-depleting substances in some regions and will increasing
264 s to the occurrence of phosphorus-bearing, N-depleted surface waters, which encourages N2 fixation, t
265 ized with minocycline or rifampicin (RIF) to deplete symbionts, block embryogenesis, and stop microfi
267 istent with these results, we found that Ver-depleted telomeres form RPA and gammaH2AX foci, like the
268 aginalis and other anaerobic bacteria, which depleted tenofovir by metabolism more rapidly than targe
269 due to a precursor mRNA splicing defect that depletes the protein GON4-like (GON4L) in B cell progeni
272 the anthelmintic albendazole (ABZ) and drugs depleting the filarial endosymbiont Wolbachia, a proven
273 ence among the NUDIX hydrolases, we pairwise deplete them generating an epistatic interaction map, ev
274 enileukin diftitox and other suppressor cell-depleting therapies may be useful adjunctive, host-direc
277 gnaling drives PUMA expression, specifically depleting these stem-like tumor cells; increases their s
278 A, since patients express autoantibodies and depleting this cell type is a successful therapeutic app
281 l-replete) or tamoxifen (Tam, satellite cell-depleted) treated at 4 months of age and were then allow
282 isting anti-CD25 antibodies were observed to deplete Treg cells in the periphery, upregulation of the
286 , allergic disorders, and graft rejection by depleting undesired disease-causing T cells while keepin
292 ng the virulence of P. aeruginosa in albumin-depleted versus albumin-rich infection sites and an unde
293 ce of relatively young, very dense, nutrient-depleted water during the LGM (18 ky to 21 ky ago).
297 Examination of the Kupffer's vesicle in Gle1-depleted zebrafish revealed compromised ciliary beating
298 imulated numerically the evolution of the CH-depleted zone and the dissolution of the cement surfaces
299 ghted the importance of the portlandite (CH)-depleted zone and the surface dissolution zone in the CO
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