コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 itor alone did not alter gestational length, treatment with 15-PGDH inhibitor + PGE2 or metabolism-re
2 leven (4%) of the 274 patients had PHD after treatment with (177)Lu-DOTATATE: 8 patients (2.9%) devel
5 eek break, followed by a cycle of 3 weeks of treatment with a 1-week break, until disease progression
8 the anti-CSF-1 receptor protected mice after treatment with a blocking antibody directed against PD-1
10 sing senescent cells in INK-ATTAC mice or by treatment with a combination of the senolytic drugs dasa
15 starting the study, or had received previous treatment with a poly(ADP-ribose) polymerase inhibitor.
17 -1 blocks nuclear localization of LysRS, but treatment with a reverse transcriptase inhibitor does no
22 between bacterial taxa in the protist-grazed treatments with a higher proportion of positive correlat
23 ease and conducting clinical trials of these treatments, with a focus on preventing congenital centra
26 ction (MI) of 12365 patients enrolled in the Treatment With Adenosine Diphosphate Receptor Inhibitors
28 ings demonstrate that combining electrolytic treatment with aerobic biodegradation may be a promising
29 play high Akt activation and that a combined treatment with AKT inhibitors causes synergistic tumour
32 tive medications, or relapse while receiving treatment with alternative medications were included in
33 ith refractoriness, ineligibility to receive treatment with alternative medications, or relapse while
38 ion phase, patients who had progressed after treatment with an EGFR tyrosine kinase inhibitor receive
39 l lineB double bond in 6 was achieved by the treatment with an isonitrile, which led to the formation
46 2 cells impaired epithelial integrity, while treatment with anti-TNF-alpha or anti-IL-4Ralpha monoclo
47 olated from liver biopsy led to the targeted treatment with anti-tumor necrosis factor-alpha, which w
48 th Nlrp12 deficency were reversed equally by treatment with antibodies targeting inflammatory cytokin
50 sfunction With Multimodality Imaging and Its Treatment with Anticoagulation) were included in this an
54 mTOR-induced cap-dependent translation, pre-treatment with AR antagonists including bicalutamide inc
55 cterized potential predictive biomarkers for treatment with AsiDNA, a novel first-in-class DNA repair
56 ts presented a good clinical response to the treatment, with at least stable disease, and only 1 had
58 formation was further supported by exogenous treatment with autophagy inducer tamoxifen, which rescue
60 n's lymphoma and peripheral T-cell lymphoma, treatment with bendamustine alone only achieves modest i
61 se prion disease were completely restored by treatment with benzyl quinolone carboxylic acid (BQCA) a
62 removal of a terminal beta-GlcNAc moiety by treatment with beta-N-acetylglucosaminidase and selectiv
64 results from a study comparing initial HIV-1 treatment with bictegravir-a novel INSTI with a high in-
66 ractory or relapsed myeloma who had received treatment with bortezomib, an immunomodulatory drug, or
67 ere insensitive to AtRALF1, and simultaneous treatment with both AtRALF1 and CML38 proteins restored
69 F are found in 50% of melanomas and although treatment with BRAF inhibitors (BRAFi) is effective, res
70 c and TfR gene expression was decreased upon treatment with BRD4 inhibitors and c-MYC small interferi
71 harmacological inhibition of cathepsin K, or treatment with calcineurin inhibitor rescued cells from
74 and (3) T-cell ablation with rituximab after treatment with CD20-coexpressing CART123 (CART123-CD20).
75 reveals the potential for using combination treatment with CDK4/6 inhibitors and PD-1-PD-L1 immune c
76 served reduction in (18)F-FMISO uptake after treatment with cediranib may be mistakenly interpreted a
78 linked by isopeptide bonds, are dispersed by treatment with chemical denaturants or soluble competing
79 preterm birth and low birth weight included treatment with chemotherapy and a diagnosis of breast ca
80 cognitive difficulties up to 6 months after treatment with chemotherapy than do age-matched noncance
81 tients should have access to multiple cancer treatments with close monitoring while receiving regimen
83 e levels were measured using LC-MS following treatment with colistin (2 mg/L) or doripenem (25 mg/L)
89 of a small number of genes, whereas combined treatment with DAC enhanced the effects of the latter fo
92 upon inflammatory stimulation and subsequent treatment with dexamethasone, a powerful antiphlogistic
94 transcriptional regulation of SNCA following treatment with different drugs known to regulate alpha-S
95 -intact SOAT1-/SOAT2-CHO cells prepared by a treatment with digitonin (plasma membrane permeabilized)
96 to up-regulate IFN-beta and TNF-alpha after treatment with DMXAA or the natural STING ligand cyclic
97 3 subjecting to DNA-damaging stimuli such as treatment with doxorubicin, was also significantly inhib
99 tion rates and reduces PHH symptoms, as does treatment with drugs that antagonize TLR4-NF-kappaB sign
103 r growth but render tumor cells sensitive to treatment with EGFR tyrosine kinase inhibitors (TKI).
107 x human fecal microbial communities, whereas treatment with either glycerol or L. reuteri alone was i
111 In multivariable Cox regression analysis, treatment with either regimen (hazard ratio [HR], 0.43;
112 and a left ventricular EF of 40% or less to treatment with enalapril 10 mg twice daily or sacubitril
113 F, severe hyperkalemia is more likely during treatment with enalapril than with sacubitril/valsartan.
115 ssigned with equal likelihood to 12 weeks of treatment with escitalopram (10-20 mg/day), duloxetine (
116 raction was observed with placebo treatment, treatment with estradiol attenuated the effects of ACE a
118 cardiovascular effects of adding once-weekly treatment with exenatide to usual care in patients with
121 n-KO pups, the genetic deletion of Slc6a4 or treatment with Fluoxetine, a 5-HT reuptake inhibitor, re
127 T-risk (4Ts score >/=4 points), and received treatment with >/=1 dose of the aforementioned anticoagu
131 e combination of a propidium monoazide (PMA) treatment with haRPA, the so-called viability haRPA, is
133 f PKM2 activity with TEPP-46 and shikonin or treatment with histone deacetylase inhibitors produced s
135 ls maintained elevated BCR signaling despite treatment with ibrutinib, a Bruton's tyrosine kinase inh
136 pain reduction at 2 hours among single-dose treatment with ibuprofen and acetaminophen or with 3 dif
137 ple HPV types, including oncogenic types, by treatment with IFN-gamma, an antiviral cytokine that is
138 rs IRF1 and BATF were induced early on after treatment with IL-27 and were required for the different
142 une cell infiltration in claudin-low tumors, treatment with immune checkpoint inhibitory antibodies a
143 l terminal pathway activity under eculizumab treatment with important implications for anti-C5 therap
145 st 1 risk factor for hypoglycemia, 32 weeks' treatment with insulin degludec vs insulin glargine U100
146 ents developing depression in the context of treatment with interferon-alpha, a widely used model to
149 (8.6) (VIVID) letters from the initiation of treatment with intravitreal aflibercept injection throug
159 ; (2) T-cell ablation with alemtuzumab after treatment with lentivirally transduced anti-CD123-4-1BB-
162 mab did not confer a survival advantage over treatment with lomustine alone in patients with progress
163 omewhat prolonged progression-free survival, treatment with lomustine plus bevacizumab did not confer
164 s whose asthma remained uncontrolled despite treatment with long-acting beta-agonists and medium-to-h
165 ts were randomly assigned (1:1:1) to receive treatment with long-acting pasireotide (60 mg intramuscu
166 However, high concentrations or prolonged treatment with low doses of HU can cause cell lethality.
170 Assessments also gathered information on treatment with medications and confounding factors, such
171 carcinoma cells to apoptosis in response to treatment with microtubule-disrupting drugs, identifying
172 Transcriptional analysis showed that after treatment with miRYR2-U10, the ratio between wild-type a
173 were 129 patients with psoriasis undergoing treatment with MTX, while 107 patients (57 women and 50
175 nced NSCLC, 27.7% (33/119) were suitable for treatment with National Comprehensive Cancer Network (NC
177 1 decreased already after a short (3 hours) treatment with necrostatin-1 during renal ischemia-reper
178 oethite occurred in the zero and low PO4(3-) treatments, with negligible transformation in higher PO4
180 d histological damage are all ameliorated by treatment with NitroSynapsin, a new dual-action compound
181 red responses could be corrected in vitro by treatment with NKH-477, a compound discovered as protect
183 inutes of exposure to CLCA1 or after a short treatment with nocodazole, consistent with the hypothesi
188 ssed in normal mouse organs before and after treatment with olaparib (n = 14), a PARP inhibitor, or i
190 cquiring mutations in response to vaccine or treatment with one or a cocktail of monoclonal antibodie
192 rcinoma tumors were allocated to RFA or sham treatment with or without a STAT3 inhibitor (S3I-201 or
193 nimals were allocated to hepatic RFA or sham treatment with or without STAT3 (signal transducer and a
196 ent and shorter length of hospital stay than treatment with oral morphine, with similar rates of adve
197 s on doxycycline is non-inferior to standard treatment with oral prednisolone for short-term blister
202 was significantly affected (p < 0.05) after treatment with paclitaxel or nocodazole due to changes i
204 in patients develop anti-PEG antibody during treatment with PEGylated medicines, suggesting that gene
205 ast cancer were randomly assigned to receive treatment with perindopril, bisoprolol, or placebo (1:1:
206 thio phenolate species with a boronic ester, treatment with Ph3 BiF2 or Martin's sulfurane gave the c
208 were randomized to receive 12 weeks of blind treatment with placebo or MABp1, a true human antibody t
209 otic or occlusive lesions were randomized to treatment with plain balloon angioplasty (BA) followed b
210 ividuals with bacterial keratitis to topical treatment with povidone-iodine or antibiotics (neomycin-
211 onSG and 12 RD-SG patients were subjected to treatment with prednisone and/or glucocorticoid-sparing
213 in patients with FH at 3 and 6 months after treatment with probucol, a cholesterol-lowering agent.
214 S were measured in healthy neutrophils after treatment with purified albumin from the study groups.
216 notypes have been observed following chronic treatment with R-baclofen, a selective agonist of GABAB
218 mice, which could be suppressed by combined treatment with rapamycin and an extracellular signal-reg
219 ompared to patients submitted to orthodontic treatment with rapid maxillary expansion and facemask th
224 ot have a sustained virologic response after treatment with regimens containing direct-acting antivir
230 this study, we assessed the effect of 2-year treatment with rosuvastatin on carotid IMT in children w
232 oximately 30% in cystic cholangiocytes after treatment with SBI-115 alone and by approximately 50% wh
238 ificant predictors of improved survival were treatment with sorafenib (hazard ratio [HR], 0.66; 95% c
240 tudy was to examine the associations between treatment with statins, renin-angiotensin system blocker
242 fants with the neonatal abstinence syndrome, treatment with sublingual buprenorphine resulted in a sh
243 (SC) expressing ENb-TRAIL, we show that the treatment with synthetic extracellular matrix (sECM) enc
246 rm that both exemestane alone and sequential treatment with tamoxifen followed by exemestane are reas
247 dine and a platinum agent, followed by later treatment with taxanes and irinotecan, provides some ben
249 terone and age-associated memory impairment, treatment with testosterone for 1 year compared with pla
250 formed to combine direct comparisons between treatments with that of indirect simulated evidence.
251 levels of overexpressed FLIL33, reversed by treatment with the 20S proteasome inhibitor bortezomib.
257 l lines with acquired resistance to combined treatment with the BRAF inhibitor vemurafenib and the mi
258 pVHL), a negative regulator of HIF, and that treatment with the c-src inhibitor PP2 rescued this effe
259 ctivation of leukocytes with LPS followed by treatment with the calcium ionophore A23187 resulted in
260 n multiple cohorts of AML patients receiving treatment with the cytidine nucleoside analogue cytarabi
262 he hydrogel, as well as cell viability after treatment with the hydrogel containing naringin, were ev
264 titutive activation was abrogated by ex vivo treatment with the janus kinase 1/2 inhibitor ruxolitini
266 helix peptide, the present study showed that treatment with the Kalpha2 peptide fused with the TAT pe
268 cation following infection with FHV, whereas treatment with the KATP channel antagonist tolbutamide d
272 timulated gene (ISG) transcription following treatment with the noncanonical cyclic dinucleotide 2',3
275 WT vs. CD-WT mice, which was prevented by co-treatment with the reactive oxygen species scavenger Tem
277 r epithelial cells in vitro and in vivo, and treatment with the small molecule TNFR inhibitor R-7050
281 d EG7-OVA tumor growth in mice, however only treatment with the thioether linked vaccine construct re
282 mplementary in vivo studies demonstrate that treatment with the TLR7 ligand imiquimod can inhibit Th1
285 ring the intracellular zinc concentration by treatment with the zinc chelator N,N,N'-tetrakis-(2'-pyr
286 psychotic medications were the pharmacologic treatments with the highest rates of prevention of relap
298 icant differences of the NOACs compared with treatment with warfarin across strata were evident.
299 re Brain Bank criteria, were on dopaminergic treatment with wearing-off effects, and were at Hoehn an
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。