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1 cin (7 + 3 or equivalent) or hypomethylation agent).
2 t-suppressed T2-weighted images (no contrast agent).
3 ource of free radicals and a dehydrogenating agent.
4 f a linear vinyl ether as the chain transfer agent.
5 y varying the ratio of olefin/chain-transfer agent.
6 -targeted peptide conjugate as a theranostic agent.
7 o the bovine spongiform encephalopathy (BSE) agent.
8 ted with developing this type of therapeutic agent.
9 to master its potential use as a therapeutic agent.
10 o cisplatin, a DNA-damaging chemotherapeutic agent.
11 -vinylpyrrolidone) (PVP) the shape-directing agent.
12 y of alkali metal salts as a charge-reducing agent.
13 ing the microbiome to develop an efficacious agent.
14 sence of a catalyst to activate the reducing agent.
15 that CC extract is a potential antibacterial agent.
16 ing capability of the current antiangiogenic agents.
17 er sensitivity or resistance to DNA-damaging agents.
18 uated in combination with other antilymphoma agents.
19 ionizing radiation, among other DNA damaging agents.
20 et for the development of new anti-infective agents.
21 c genes and putative causative environmental agents.
22 disease therapy using available therapeutic agents.
23 y reactivated by different latency reversing agents.
24 ity for polymyxins compared with alternative agents.
25 DPP-4) which limits their use as therapeutic agents.
26 pid-lowering mediations, and cardiometabolic agents.
27 nd modulate extracellular spaces via osmotic agents.
28 of diltiazem and tiazesim, both therapeutic agents.
29 f repeated administration of pharmacological agents.
30 tionships (SARs) for prospective therapeutic agents.
31 ve had previous therapy with hypomethylating agents.
32 use of EP2 antagonists as anti-inflammatory agents.
33 VOC biomarkers from two potential biowarfare agents.
34 m heart failure outcomes observed with these agents.
35 poration, even in the presence of templating agents.
36 ty ultrasound and microbubbles or cavitation agents.
37 ncer cells with increased levels of reducing agents.
38 roader utility for PARP-targeted therapeutic agents.
39 noglobulin replacement and immunosuppressive agents.
40 ove the efficacy of conventional therapeutic agents.
41 d alternative methods of detecting biothreat agents.
42 xposure to various gadolinium-based contrast agents.
43 WSPM and multiple prototypical ERS-inducing agents.
44 mplex surface chemistries acting as blocking agents.
45 her combinations of nanocrystals and capping agents.
46 e or from the extrinsic administration of IS agents.
47 ternal cognitive processes across individual agents.
48 of countless natural stimuli and therapeutic agents.
49 mmatory therapies, and novel immunometabolic agents.
50 3' U and G nucleotides become gene-silencing agents.
51 with Gd(III) complexes as T(1) MRI contrast agents.
52 targets for the design of novel antimalarial agents.
53 es, and are considered potential therapeutic agents.
54 with anti-vascular endothelial growth factor agents.
55 de compatible with several external trapping agents.
56 are widely used as fertilizer and oxidizing agents.
57 ecules, nanoparticles, and other therapeutic agents.
58 in anticancer therapies involving DNA damage agents.
61 ethotrexate); (2) anti-tumor necrosis factor agents; (3) combination therapy; and (4) no treatment wi
62 were largely due to a lack of MMP-selective agents; accordingly, it has become important to identify
64 tibody that has shown preclinical and single-agent activity in patients with relapsed or refractory B
65 ails the current landscape of antithrombotic agents, addresses challenges with preventing thromboembo
69 (VSV)-based oncolytic viruses are promising agents against pancreatic ductal adenocarcinoma (PDAC).
73 activation, however, may be detrimental, and agents amenable to tissue targeting for therapeutic appl
74 (ethylene glycol) is considered the reducing agent and poly(N-vinylpyrrolidone) (PVP) the shape-direc
75 unomodulatory effects of targeted anticancer agents and explore potential avenues to harness them in
77 ch as anti-hypertensive drugs, anti-platelet agents and statins) seem to have little or no effect on
78 in particular, has leveraged advances in MI agents and technology to improve the accuracy of tumor d
79 th populations is the need for new antiviral agents and the necessity for combination therapies as ha
80 ges and limitations of current T(1) contrast agents and the potential of IONPs to serve as safe and i
81 oil matrix using sonication and a dispersing agent, and (iii) separating the dissolved and nanopartic
82 patients, those receiving immunosuppressive agents, and especially those receiving combination thera
84 p for designing fluorophores, photoswitching agents, and triplet excited state quenchers for single-m
85 n and inhibition by covalent and noncovalent agents; and finally, the potential value of NAAA-targeti
86 The objective response rate (ORR) for single-agent anti-programmed death receptor 1 (anti-PD-1) thera
87 -trans-RA or previous RA metabolism blocking agents, appears to protect epidermal barrier integrity.
89 , the fundamental principles of MRI contrast agents are discussed, and the current status of MRI cont
91 ctive clinical trials involving (177)Lu-PSMA agents are under way that will likely pave the way for F
94 nstrated that SimCells can be used as a safe agent (as they cannot replicate) for bacterial therapy.
95 ur mathematical analysis with the results of agent-based computation and, making use of approximate B
96 Here, we present results of a stochastic agent-based microsimulation model of the COVID-19 epidem
99 re the differential equation version with an agent-based version of the model run on the empirical ne
100 we interpret behavioral data by assuming an agent behaves rationally-that is, it takes actions that
108 ophoblastic tumors (GTT) resistant to single-agent chemotherapy receive alternative chemotherapy regi
110 lood pressure lowering with antihypertensive agents compared with control was significantly associate
112 ee drugs, non-targeted liposomes, and single-agent controls and reduces severe BTZ-associated side ef
113 may include discontinuation of the specific agent, corticosteroids, and other immune suppressing age
114 the combination of cytotoxic and cytostatic agents could represent an important modality in those tu
115 ion with the catalyst, protic chain transfer agents (CTAs) initiate polymerization and facilitate rap
117 s with diabetes; conventional renoprotective agents did not therapeutically target this elevation.
119 affected independent from the pharmacologic agent, drug concentration, and direction of change in th
120 f action: VEGF inhibitors or anti-angiogenic agents, EGFR inhibitors, mTOR inhibitors, CTLA-4 inhibit
121 n This study indicated that dynamic contrast agent-enhanced perfusion MRI parameter, fractional plasm
124 es that can be protective against infectious agents exhibiting the same carbohydrate modification on
125 s utilizing iron pentacarbonyl as a reducing agent followed by subsequent oxidation leads to a great
126 ctrode (SPCE) using chitosan as cross-linked agent for 5-HT sensing studies; conducted through cyclic
128 nolin-3-yl)methanimine oxide (17) is a novel agent for cerebral ischemia therapy as it is able to sca
129 -associated herpesvirus (KSHV) is the causal agent for Kaposi's sarcoma (KS), the most common maligna
130 as been considered as a possible therapeutic agent for patients with coronavirus disease 2019 (COVID-
133 SARS-CoV-2 has been identified as the causal agent for the pandemic viral pneumonia disease, COVID-19
134 s, may represent a new class of psychotropic agent for the treatment of psychosis in schizophrenia.
135 xposed to standard-of-care chemotherapeutics agents for 2 weeks, attesting the ability of the platfor
139 um-based chelates are a mainstay of contrast agents for magnetic resonance imaging (MRI) in the clini
141 orticosteroids, and other immune suppressing agents for severe (grade 3 or 4) immune-related adverse
142 the potential to be developed as therapeutic agents for the treatment and control of Ebola virus infe
143 using metal complexes as ER stress-inducing agents for the treatment of cancer is provided, along wi
144 n, and Zn turns Li(2) S into a prelithiation agent, forming metal sulfides rather than S(8) after the
145 ation of a uniquely reactive Bi(V) arylating agent from a bench-stable Bi(III) precursor via telescop
146 000 experimental records for anti-retroviral agents from ChEMBL database were extracted for creating
147 ogy as a group III gadolinium-based contrast agent (GBCA), which indicates that there are limited dat
148 te the wide use of gadolinium-based contrast agents (GBCAs) for enhanced MRI, their neurochemical and
149 and bovine serum albumin (BSA) as a blocking agent generated a moderate sensitivity of 0.0164 OD.mL/n
150 that the capacity to compute models of other agents has deep roots in the strategic social behavior o
156 Studies in developing IONPs as T(1) contrast agents have generated promising results, but the complex
162 phylococci are a highly prominent infectious agent in peritonitis, and suggest caution against antico
163 to determine that rigosertib, an anti-cancer agent in phase III clinical trials, kills cancer cells b
164 of nucleobases are accessible to alkylating agents in canonical dsDNA and that Hoogsteen base pairs
166 y of anti-vascular endothelial growth factor agents in the treatment of DME as well as the difference
168 pecific membrane antigen (PSMA)-targeted PET agent, in patients with biochemically relapsed prostate
172 n one cancer-related pathway by multi-target agents is an emerging approach in modern anticancer drug
173 ssed, and the current status of MRI contrast agents is reviewed with a focus on the advantages and li
174 nolate mofetil (MMF) is an immunosuppressive agent (IS) which is widely prescribed in neuromyelitis o
176 etable machine learning for quantifying both agent-level features and global pattern attributes on a
177 this approach does not depend on the use of agents like luciferin, which can cause variability due t
178 he radiopaque drug-carrier and micro-embolic agent Lipiodol, which has been previously established as
180 in value-based decision-making tasks is that agents make decisions based on the feature dimension tha
181 quently, this pH-activatable optical imaging agent may be clinically beneficial in differentiating pr
182 clonal antibodies against infectious disease agents may be debatable, the functional characterization
183 been tacitly believed that the use of these agents may facilitate viral disease; thus, they should n
184 , but available evidence suggests that these agents may have therapeutic effects in specific psychiat
187 vide a balance of accessibility to reductive agents necessary to ensure stability in transit, but rap
188 potent greenhouse gas and an ozone-depleting agent, nitrous oxide (N(2)O) plays a critical role in th
189 anti-programmed cell death protein 1 (PD-1) agents (nivolumab or pembrolizumab) was conducted to ass
190 Upon exposure of human cells to DNA-damaging agents, NUCKS1 controls the resolution of RAD54 foci.
191 o 80% of the population and is the causative agent of a fatal demyelinating disease of the central ne
192 us pleuropneumoniae (App) is the etiological agent of acute porcine pneumonia and responsible for sev
194 ory to infection by Dirofilaria immitis, the agent of canine heartworm disease, mounts a stronger imm
196 me coronavirus 2 (SARS-CoV-2), the causative agent of coronavirus disease 2019 (COVID-19), uses the v
197 coronavirus 2 (SARS-CoV-2), the etiological agent of COVID-19, has been found closely related to the
198 coronavirus 2 (SARS-CoV-2), the etiological agent of COVID-19, is considered a zoonotic pathogen mai
200 Phytophthora capsici Leonian, the causal agent of foliar blight, root rot, fruit rot and crown ro
201 ae was thought to be the exclusive causative agent of leprosy until Mycobacterium lepromatosis was id
202 an intracellular bacterium and the causative agent of melioidosis, a severe disease in tropical regio
203 o challenge with ectromelia virus (ECTV; the agent of mousepox) and that natural killer (NK) cells in
204 propose that social resistance can act as an agent of selection on key life-history strategies and pr
205 oronavirus 2 (SARS-CoV-2) is the etiological agent of the currently uncontrolled coronavirus disease
206 discover lysis inhibition in the etiological agent of the diarrheal disease cholera, Vibrio cholerae,
207 mpen the spread of SARS-CoV-2, the causative agent of the diseases, through restrictive interventions
208 ogen Francisella tularensis is the etiologic agent of tularemia, a potentially fatal disease if untre
209 al pathogen Sclerotinia sclerotiorum, causal agent of white mold diseases on hundreds of plant specie
212 es of the protozoan Leishmania are causative agents of human leishmaniasis, a disease that results in
213 tains a plethora of biomarkers and causative agents of various diseases, some of which are endogenous
216 by either combining different HER2-targeted agents or extending the duration of HER2-targeted therap
220 his heterogeneous redistribution of contrast agent paralleled the gradients and regional variations i
222 anotubes, which are wrapped by encapsulation agent (phospholipid-polyethylene glycol), is demonstrate
227 ding cause of death from a single infectious agent, requiring at least 6 months of multidrug treatmen
228 Bats are also major hosts for biological agents responsible for zoonoses, such as coronaviruses (
229 s release of the chemoattractant and killing agents result in long-range chemotactic attraction, trap
230 le for factor XII and XI as targets for such agents, reviews the data on the factor XII- and factor X
231 dults' reaction times reliably reflected the agent's beliefs only when the agent was free to act on t
234 excluded if they focused solely on contrast agents, served as commentaries/overviews on NIRAF or wer
240 Experiments in the presence of an osmoticant agent suggest that channel gating involves a change in s
242 05089771 and suggesting that combinations of agents targeted to the pore-region binding site of lidoc
247 s indicate that, in the presence of crowding agents, tau can undergo liquid-liquid phase separation (
249 ytotoxicity of treatment with the alkylating agent temozolomide in combination with the PARP inhibito
251 Ivosidenib (AG-120) is an oral, targeted agent that suppresses production of the oncometabolite 2
252 eleasing molecules (photoCORMs) are chemical agents that allow for precise spatial and temporal contr
253 a large body of preclinical work, promising agents that are entering into early clinical evaluation
254 nstead was induced by membrane-intercalating agents that are prevalent in the host gastrointestinal t
255 c chemotherapies as well as targeted therapy agents that are used to treat breast cancer, pancreatic
256 We propose to identify HIV-1-suppressing agents that can inhibit HIV-1 reactivation and reduce HI
257 uncovered many new paramyxoviruses, airborne agents that cause epidemic diseases in animals including
259 2 and Gcn2 are activated by a similar set of agents that cause ribosome stalling, with maximal activa
260 udy was to develop improved radiotherapeutic agents that combine an optimized affinity-modifying grou
261 lso for the development of new pharmacologic agents that exploit or target TMPRSS6 to treat anemias a
262 apies.Significance: These findings highlight agents that target transcriptional addiction in cancer c
263 treatment (more intensive BP goal or active agent) that involved more than 500 adults with hypertens
264 ns, from biosensors to therapeutic treatment agents, their toxicity and their utility in chemical sen
265 syndromes in whom erythropoiesis-stimulating agent therapy is not effective generally become dependen
266 dence that acalabrutinib is active as single-agent therapy with a manageable safety profile in patien
267 trategy using proteins as structure-directed agents to direct the formation of new ZMOFs that can act
268 for use in humans and can act as anti-cancer agents to inhibit chemotherapy-resistant tumor growth by
270 urther inform the development of therapeutic agents to modulate pro-inflammatory immune reactions.
271 uch as autologous transfusion techniques and agents to optimize hemostasis are used during surgery an
273 se should not be treated with bone-modifying agents to prevent recurrence, but could still receive th
274 he (64)Cu-labeled PSMA ligands are promising agents to target PSMA and visualize PSMA-positive tumor
275 iagnostic biosensing devices and therapeutic agents to the target tissues, organs, or cells is an imp
276 oxicology Paracelsus (1493-1541) on chemical agents used as therapeutics, "the dose makes the poison,
277 y have tradeoffs that depend on the specific agents used as well as their dosing levels and schedule.
278 , solvent, substituent, and type of reducing agent using a synergistic experimental-computational app
279 reflected the agent's beliefs only when the agent was free to act on the ball and not when the agent
282 s were indicated, and a guideline-concordant agent was prescribed for guideline-concordant duration)
283 tly demonstrated that bioengineered miR-1291 agent was selectively processed to high levels of target
285 DDR function and sensitivity to DDR-directed agents, we created a series of ATM-deficient preclinical
287 in brain, various preblocking or displacing agents were evaluated for their impact on the PET brain
288 a to inhibit angiogenic stimuli to anti-VEGF agents, which inhibit pathologic angiogenesis but also e
290 (CC-122) is a novel oral cereblon-modulating agent with promising activity in non-Hodgkin lymphoma.
291 Cisplatin is a commonly used chemotherapy agent with significant dose-limiting neurotoxicity resul
294 provides comparative data on two biological agents with different mechanisms of action, which could
295 ompound is more effective in vivo than other agents with equal tumor uptake due to improved tissue pe
296 We believe that by combining new targeted agents with immune regulators and chimeric antigen recep
297 ch complemented by a hydrodynamic theory for agents with mixed alignment symmetries, which captures t
298 loyed as nonhazardous and greener alkylating agents with the formation of environmentally benign wate
299 utions, which afforded new anti-C. difficile agents with ultrapotent activities [MICs as low as 0.003
300 94B, reversibly bound to native and venomous agent X (VX)-inhibited human AChE, here we created seven