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1 cytotoxic chemotherapy, ionizing radiation).
2 serious adverse events (SAE) and exposure to ionizing radiation.
3 bility, and cellular response to therapeutic ionizing radiation.
4 potential risks associated with exposure to ionizing radiation.
5 hromosome instability, which was enhanced by ionizing radiation.
6 roliferation, tumor growth and resistance to ionizing radiation.
7 vivo and enhanced the cytotoxic response to ionizing radiation.
8 erm cellular responses of human GBM cells to ionizing radiation.
9 pathogens and, as shown here, in response to ionizing radiation.
10 r resistance to cytotoxic chemotherapies and ionizing radiation.
11 ic species are known for their resistance to ionizing radiation.
12 e, significantly sensitizing cancer cells to ionizing radiation.
13 /CT-as it requires exposure to high doses of ionizing radiation.
14 ention of gammaH2AX and Rad51 foci following ionizing radiation.
15 effects arising from environmental gases and ionizing radiation.
16 ( 1.40 eV) on samples previously exposed to ionizing radiation.
17 nic RAS and reduced tissue inflammation upon ionizing radiation.
18 n measure bone properties without the use of ionizing radiation.
19 ection of the direct and indirect effects of ionizing radiation.
20 1 associates with gamma-H2A.X in response to ionizing radiation.
21 repair pathways and increases sensitivity to ionizing radiation.
22 tors of GSC quiescence following exposure to ionizing radiation.
23 y, with high diagnostic accuracy and without ionizing radiation.
24 hibitor hydroxyurea, but not the DSB inducer ionizing radiation.
25 hought to be responsible for the bulk of the ionizing radiation.
26 ds from plants exposed to elevated levels of ionizing radiation.
27 or to drive cell cycle progression following ionizing radiation.
28 ess and a major cause of oxidative stress is ionizing radiation.
29 ge compared to control in cells treated with ionizing radiation.
30 as well as increases sensitivity of cells to ionizing radiation.
31 s that occur after exposure to high doses of ionizing radiation.
32 l role in modulating biological responses to ionizing radiation.
33 ulated but later is strongly up-regulated by ionizing radiation.
34 ch recombination (CSR) and DSBs generated by ionizing radiation.
35 to STT-MRAM applications are robust against ionizing radiation.
36 are occupationally exposed to high doses of ionizing radiation.
37 of colonic epithelium is highly sensitive to ionizing radiation.
38 ely impact skeletal health: microgravity and ionizing radiation.
39 ve assessment of myocardial ischemia without ionizing radiation.
40 ildlife resulting from its field exposure to ionizing radiation.
41 ould be avoided whenever possible because of ionizing radiation.
42 rand breaks induced by either doxorubicin or ionizing radiation.
43 an disease and responses to stresses such as ionizing radiation.
44 sensitive to external toxic agents, such as ionizing radiation.
45 for dosimetry, including high sensitivity to ionizing radiation (20 times that of Al2O3:C, under the
46 We exposed male fish to sublethal low-dose ionizing radiation, a genotoxic stress affecting the som
48 exposed to 11 genotoxins, including UV-B and ionizing radiation, alkylating compounds, aristolochic a
50 ng the highest exposed to elevated levels of ionizing radiation, although their occupational doses ar
51 result of the indirect and direct effects of ionizing radiation, among other DNA damaging agents.
52 o exhibit significantly enhanced survival of ionizing radiation and bleomycin treatment, agents that
54 caspase-3 in oral cancer cells treated with ionizing radiation and chemotherapeutic drug, paclitaxel
56 essed in cancer cells, confers resistance to ionizing radiation and chemotherapy agents, and promotes
58 the diversity of tumour cellular response to ionizing radiation and establish multiple lines of evide
59 diomycete fungus that is highly resistant to ionizing radiation and has been identified in highly rad
60 Thymidine radical cation (1) is produced by ionizing radiation and has been invoked as an intermedia
61 ession of abscopal tumours in the context of ionizing radiation and immune checkpoint blockade in viv
64 hypersensitivity of BRCA1-depleted cells to ionizing radiation and PARP inhibition, highlighting the
65 letion leads to the increased sensitivity to ionizing radiation and poly (ADP-ribose) polymerase inhi
68 ool to map the amount of the body exposed to ionizing radiation and the location of exposure, which a
69 that radiation shielding reduces the flux of ionizing radiation and thereby increases the energy-rela
70 this patient showed increased sensitivity to ionizing radiations and phleomycin, attesting to a proba
71 ological tissue, as compared to UVB, UVC and ionizing radiation, and cause longlasting deep tissue da
72 es, including reactive oxygen species (ROS), ionizing radiation, and chemotherapies, activate acid sp
73 ection, increases HR and cell survival after ionizing radiation, and prevents cellular senescence.
74 IR imaging has relatively low cost, uses non-ionizing radiation, and provides minimally invasive spat
75 ization and activation in cells treated with ionizing radiation, and that loss of Mdm2 Ser394 phospho
77 ygen species generated by exposure to UV and ionizing radiation are characterized by clusters of lesi
78 adiation absorption of tumors, high doses of ionizing radiations are often needed during RT, leading
79 vant exposures to chemotherapeutic drugs and ionizing radiation, as well as BM recovery after drug-in
82 cores are known to emit very high levels of ionizing radiation, becoming visible over intergalactic
83 mbers of the Acidobacteria), or resistant to ionizing radiation (Brevundimonas and Truepera); elucida
85 hat could only be formed through exposure to ionizing radiation, but not by any other means of physic
86 induction by chemotherapeutic agents such as ionizing radiation caused SNP-dependent synergistic incr
89 on, splicing, and translation in response to ionizing radiation. Changes at the transcriptional level
90 e knowledge and better inform the effects of ionizing radiation chronic exposure on nonhuman species,
93 lling and faster DNA repair upon exposure to ionizing radiations compared to vehicle-only treated cel
94 irectly from a human population, that MF non-ionizing radiation could have adverse biological impacts
95 to identify minimally invasive biomarkers of ionizing radiation damage to the CNS that are predictors
96 ted that melanin may also protect cells from ionizing radiation damage, against which C. neoformans i
98 rved to exhibit resistance to high levels of ionizing radiation despite sharing most DNA repair mecha
99 of material properties for high performance ionizing radiation detection based on direct detection m
100 ted increasing attention in recent years for ionizing radiation detection due to their strong stoppin
101 tion detectors with current state-of-the-art ionizing radiation detectors, we show the promising feat
103 al importance in understanding the effect of ionizing radiation, developing DNA biosensors and design
105 ial and temporal resolution and reduction in ionizing radiation dose with new generation scanners.
106 es were subjected, for a week, to cumulative ionizing radiation doses, as used during cancer treatmen
108 allows for precise and instant detection of ionizing radiations down to the level of 10(-4) Gy, repr
109 f cell cycle checkpoint activation following ionizing radiation drives increased production of immuno
110 pecies, we investigated the transposition to ionizing radiation ecotoxicity of one method proposed fo
111 nvironments (e.g., elevated temperatures and ionizing radiation environments) found in many engineeri
112 This study uncovers mechanisms by which ionizing radiation, especially particle radiation, promo
113 n this article, we show that DSBs induced by ionizing radiation, etoposide, or bleomycin suppress Rag
114 on whether the linear no-threshold model of ionizing radiation exposure accurately predicts the subs
115 he chromatin factors H2AX and KAP1 following ionizing radiation exposure and drives local chromatin d
117 signatures of somatic mutation characterize ionizing radiation exposure irrespective of tumour type.
119 raphy may have harms resulting from low-dose ionizing radiation exposure or identification of extraco
124 by accelerating cosmic rays that can deliver ionizing radiation for up to [Formula: see text] ky.
127 imaging of both radionuclide- and beam-based ionizing radiation from high-energy photons and charged
128 Individuals are exposed to air pollution and ionizing radiation from natural sources through inhalati
131 ugh transgenerational effects of exposure to ionizing radiation have long been a concern, human resea
133 date novel epigenetic rheostats that promote ionizing radiation hypersensitivity in various normal st
136 er, DYRK1A knock out conferred resistance to ionizing radiation in colony formation assays, suggestin
137 iciently high energy to produce ionization." Ionizing radiation in cosmic chemistry includes high-ene
138 ~100 mSv is lacking; however, concerns about ionizing radiation in medical imaging remain and can aff
141 e for type I interferon signaling induced by ionizing radiation in the presence or absence of ATR inh
146 ficient to repress the apoptotic response to ionizing radiation independent of developmental signalin
148 induced DNA damage, and RAD51 recruitment to ionizing radiation induced foci (IRIF), which requires e
150 1 overexpression suppresses the formation of ionizing radiation-induced 53BP1 and BRCA1 but not RNF16
153 ofluorescent detection of repair proteins at ionizing radiation-induced DNA damage foci that Wwox exp
155 ese two proteins and variably contributes to ionizing radiation-induced DSB repair in human and chick
157 (TIRR) that specifically associates with the ionizing radiation-induced foci formation region of 53BP
159 tem cells exhibit reduced ATM activation and ionizing radiation-induced foci, they display apoptotic
160 onse kinase ATR can significantly potentiate ionizing radiation-induced innate immune responses.
161 nucleosome (50-500 bp) scale, obtained using ionizing radiation-induced spatially correlated cleavage
164 itigates RIGS lethality in vivo after lethal ionizing radiation injury-induced intestinal epithelial
165 mutants demonstrate increased sensitivity to ionizing radiation (IR) and a decrease in DNA double-str
167 rference sensitizes prostate cancer cells to ionizing radiation (IR) and etoposide treatment, as asse
168 we challenged Plk1-overexpressing mice with ionizing radiation (IR) and found that Plk1-overexpressi
169 -negative breast cancer cells in response to ionizing radiation (IR) and localizes to rDNA sequences
170 ivation and repression events in response to ionizing radiation (IR) and synthetic p53 activation.
171 s (GSCs) to survive exposure to low doses of ionizing radiation (IR) as a model of adult stem cell in
172 in these cells, we exposed pregnant mice to ionizing radiation (IR) at specific gestational time poi
174 sponse to a combination of PDI knockdown and ionizing radiation (IR) compared with either modality al
175 mal thyroid function is disturbed because of ionizing radiation (IR) exposure, deleterious effects ca
176 reported that cells exposed to low doses of ionizing radiation (IR) in the G(2)-phase of the cell cy
177 that the AR directly interacts with CHK2 and ionizing radiation (IR) increases this interaction.
179 Exposure of murine and human tissues to ionizing radiation (IR) induces the expression of p16(IN
185 l of cancer cells mediated by high levels of ionizing radiation (IR) reduces the effectiveness of rad
186 forts to understand the complex phenotype of ionizing radiation (IR) resistance, a genome sequence ca
187 melanogaster larvae irradiated with doses of ionizing radiation (IR) that kill about half of the cell
188 ak worker subjects occupationally exposed to ionizing radiation (IR) to investigate the contribution
190 lved in sensitizing radioresistant tumors to ionizing radiation (IR) treatments while minimizing inju
191 ity and its combination with DDR inhibitors, ionizing radiation (IR), and chemotherapy can be exploit
194 ses of HuR in oral cancer cells treated with ionizing radiation (IR), determined that HuR cleavage pr
195 n growth under 36 Gy/h) and acute (10 kGy/h) ionizing radiation (IR), heavy metals (chromium, mercury
196 es mediating the response of glioblastoma to ionizing radiation (IR), we used polysome profiling to d
198 ibed mechanism promoting cell survival after ionizing radiation (IR)-induced DNA damage involves frag
202 RC5A contributes significantly to preventing ionizing radiation (IR)-induced lung tumorigenesis.
203 scarce and the mutational processes defining ionizing radiation (IR)-induced mutagenesis in vivo are
219 Using data generated with cells exposed to ionizing-radiation (IR) in G(2)-phase of the cell cycle,
223 ortance of nontargeted (systemic) effects of ionizing radiation is attracting increasing attention.
224 f competing risk methods, suggesting that if ionizing radiation is impacting the risk of death due to
229 ren may be more vulnerable to the effects of ionizing radiation, it is necessary to develop methods t
230 vailability, its noninvasiveness and lack of ionizing radiation, its low cost, and its good reproduci
234 the effect of oxidative stress from low-dose ionizing radiation (LDIR) on wild-type and p53 mutant ce
236 eas around Chernobyl differing in background ionizing radiation levels and one control study site in
237 pathology is suspected, but the presence of ionizing radiation makes it harder to construct database
239 factor XLF result in extreme sensitivity for ionizing radiation, microcephaly, and growth retardation
240 the cellular response of tumours exposed to ionizing radiation, modelling the alteration of oxygen p
241 main clinical mainstays, optical readouts of ionizing radiation offer numerous benefits and complemen
242 nding that cancer chemotherapeutic drugs and ionizing radiation often promote autophagy has provided
247 d field data concerning potential effects of ionizing radiation on the abundance of mammals collected
250 d that independently assessed the effects of ionizing radiation on transcription and post-transcripti
252 ts normal cells from DNA damage induction by ionizing radiation or chemotherapeutics, whereas cancer
255 HAEC) by replicative exhaustion, exposure to ionizing radiation or doxorubicin, and expression of the
256 ells to DNA damage under conditions, such as ionizing radiation or hydrogen peroxide treatment, that
257 inflammatory challenges, such as exposure to ionizing radiation or to bacterial lipopolysaccharides.
258 e induced by a variety of stimuli, including ionizing radiation, oxidative stress, and inflammation.
259 which are the likely sources of the elevated ionizing radiation powering the observed Lyman-alpha emi
260 molecular probes sensitive to byproducts of ionizing radiation (primarily reactive oxygen species, o
261 benefits of metastasis-directed therapy with ionizing radiation (primarily stereotactic ablative radi
263 exists in nature, where it provides superior ionizing radiation protection to organisms compared to k
264 ouse B-cell line, and dispensable for normal ionizing radiation resistance in both G1-arrested and cy
267 dividuals with PPM1D truncating mutations to ionizing radiation resulted in normal p53 activation, su
268 e variation induced by chemical treatment or ionizing radiation results in higher mutation rates.
272 r studying biological effects under low-dose ionizing radiation, safety control in medical radiation
275 of melanized fungi to cosmic and terrestrial ionizing radiation suggests that melanin also plays a pi
276 ace travelers are exposed to unique forms of ionizing radiation that pose potentially serious health
277 damage caused by exogenous sources, such as ionizing radiation, the tumour suppressor p53 mediates c
281 nction and show that SNP309G cooperates with ionizing radiation to exacerbate tumor development.
282 as more recently been realized and relies on ionizing radiation to induce irreversible DNA damage, re
283 dy to E-cadherin, works synergistically with ionizing radiation to promote the epidermal damage.
284 therapy and precisely deliver high doses of ionizing radiation to small deep-seated target volumes.
286 t to conventional radiotherapy, TRT delivers ionizing radiation to tumors in a targeted manner, reduc
289 ed the function of miR-24 in NPC cells after ionizing radiation treatment, resulting in increased apo
290 harmful biological effects from exposure to ionizing radiation, understanding the mechanisms by whic
291 ice and non-human primates (NHPs) exposed to ionizing radiation up to 8 days after radiation exposure
292 BSGI on the basis of the Biologic Effects of Ionizing Radiation VII report, the benefit-to-radiation
293 udy, stimulation by doxorubicin, hypoxia and ionizing radiation was used to induce MDR in HCC cells.
295 N109D) mutant RUNX1 conferred resistance to ionizing radiation when overexpressed in Ba/F3 cells und
296 , PDE12 or AKAP7 (which degrade 2-5A), or by ionizing radiation (which induces IFN-dependent signalin
297 qubits, reducing or mitigating the impact of ionizing radiation will be critical for realizing fault-