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1 cytotoxic chemotherapy, ionizing radiation).
2 hought to be responsible for the bulk of the ionizing radiation.
3 ds from plants exposed to elevated levels of ionizing radiation.
4 ess and a major cause of oxidative stress is ionizing radiation.
5 ge compared to control in cells treated with ionizing radiation.
6 r resistance to cytotoxic chemotherapies and ionizing radiation.
7 as well as increases sensitivity of cells to ionizing radiation.
8 l role in modulating biological responses to ionizing radiation.
9 ic species are known for their resistance to ionizing radiation.
10 ulated but later is strongly up-regulated by ionizing radiation.
11 ch recombination (CSR) and DSBs generated by ionizing radiation.
12 rnatives to current agents that emit harmful ionizing radiation.
13 s normal tissues while sensitizing tumors to ionizing radiation.
14 treatment with the ATR inhibitor AZD6738 and ionizing radiation.
15 gents that increase oxidative damage such as ionizing radiation.
16 tize prostate cancer cells to the effects of ionizing radiation.
17 ect strand break formation in RNA exposed to ionizing radiation.
18 -electrophiles, reactive oxygen species, and ionizing radiation.
19 ent stays, and increased patient exposure to ionizing radiation.
20 to develop molecules that sensitize cells to ionizing radiation.
21 n, and phosphorylation in response to UV and ionizing radiation.
22 of gammaH2AX accumulation was studied after ionizing radiation.
23 ically induced double strand breaks, UVB and ionizing radiation.
24 d negates PIDDosome-mediated apoptosis after ionizing radiation.
25 efined substrates and cellular resistance to ionizing radiation.
26 genomic instability and hypersensitivity to ionizing radiation.
27 aging of body without the use of any harmful ionizing radiation.
28 on of H2AX and cell viability in response to ionizing radiation.
29 ensitivity of the developing embryo/fetus to ionizing radiation.
30 HR and an increased cellular sensitivity to ionizing radiation.
31 tly exposed to imaging examinations that use ionizing radiation.
32 ur center are exposed to very high levels of ionizing radiation.
33 egative consequences of repeated exposure to ionizing radiation.
34 telangiectasia are exquisitely sensitive to ionizing radiation.
35 s and environmental oxidative stress such as ionizing radiation.
36 e, significantly sensitizing cancer cells to ionizing radiation.
37 ions because it does not involve exposure to ionizing radiation.
38 es at relatively low cost without the use of ionizing radiation.
39 ogenitors also are more resistant to H2O2 or ionizing radiation.
40 endoplasmic reticulum stress and exposure to ionizing radiation.
41 (IGF-1R) enhances tumor cell sensitivity to ionizing radiation.
42 s such as that caused by exposure to chronic ionizing radiation.
43 /CT-as it requires exposure to high doses of ionizing radiation.
44 ention of gammaH2AX and Rad51 foci following ionizing radiation.
45 effects arising from environmental gases and ionizing radiation.
46 ( 1.40 eV) on samples previously exposed to ionizing radiation.
47 nic RAS and reduced tissue inflammation upon ionizing radiation.
48 ection of the direct and indirect effects of ionizing radiation.
49 1 associates with gamma-H2A.X in response to ionizing radiation.
50 repair pathways and increases sensitivity to ionizing radiation.
51 tors of GSC quiescence following exposure to ionizing radiation.
52 y, with high diagnostic accuracy and without ionizing radiation.
53 hibitor hydroxyurea, but not the DSB inducer ionizing radiation.
54 for dosimetry, including high sensitivity to ionizing radiation (20 times that of Al2O3:C, under the
57 o exhibit significantly enhanced survival of ionizing radiation and bleomycin treatment, agents that
59 caspase-3 in oral cancer cells treated with ionizing radiation and chemotherapeutic drug, paclitaxel
60 essed in cancer cells, confers resistance to ionizing radiation and chemotherapy agents, and promotes
61 the diversity of tumour cellular response to ionizing radiation and establish multiple lines of evide
63 Thymidine radical cation (1) is produced by ionizing radiation and has been invoked as an intermedia
65 ession of abscopal tumours in the context of ionizing radiation and immune checkpoint blockade in viv
66 ely formed when triglycerides are exposed to ionizing radiation and is being widely used as marker si
67 s the advantages of real-time imaging and no ionizing radiation and may obviate the need for the pati
68 letion leads to the increased sensitivity to ionizing radiation and poly (ADP-ribose) polymerase inhi
70 n laboratory mice after parental exposure to ionizing radiation and show irradiation markedly alters
71 own to differ for exposures like smoking and ionizing radiation and simple cumulative exposure does n
72 ool to map the amount of the body exposed to ionizing radiation and the location of exposure, which a
73 ed, of which 408 (22%) involved considerable ionizing radiation and were the focus of investigation.
74 this patient showed increased sensitivity to ionizing radiations and phleomycin, attesting to a proba
75 mutants however display hypersensitivity to ionizing radiation, and combination of rpa1c and rpa1e r
76 ection, increases HR and cell survival after ionizing radiation, and prevents cellular senescence.
77 ization and activation in cells treated with ionizing radiation, and that loss of Mdm2 Ser394 phospho
78 Oxidative and genotoxic stresses caused by ionizing radiation are detrimental to healthy tissues bu
80 adiation absorption of tumors, high doses of ionizing radiations are often needed during RT, leading
82 ascorbate enhances the cytotoxic effects of ionizing radiation as seen by decreased cell viability a
83 the knowledge of the effects of exposure to ionizing radiation as well as questions related to respo
85 es alters patterns of DNA damage repair from ionizing radiation at a gene locus-specific and genome-w
88 cores are known to emit very high levels of ionizing radiation, becoming visible over intergalactic
90 hat could only be formed through exposure to ionizing radiation, but not by any other means of physic
92 ant fraction of mammalian cells treated with ionizing radiation can survive despite caspase-3 activat
94 irectly from a human population, that MF non-ionizing radiation could have adverse biological impacts
95 ) and 5,6-dihydrothymidine (dHT), formed via ionizing radiation damage to 2'-deoxycytidine and thymid
96 6-dihydro-2'-deoxyuridine (dHdU), formed via ionizing radiation damage to cytosine under anoxic condi
97 rafts, pharmacologic ascorbate combined with ionizing radiation decreased tumor growth and increased
98 with the combination of an AKT inhibitor and ionizing radiation decreased tumor size in a p53-deficie
100 ganic materials have been mainly proposed as ionizing radiation detectors in the indirect conversion
103 the notion that survival after high doses of ionizing radiation does not depend on a single mechanism
104 es were subjected, for a week, to cumulative ionizing radiation doses, as used during cancer treatmen
106 allows for precise and instant detection of ionizing radiations down to the level of 10(-4) Gy, repr
107 n this article, we show that DSBs induced by ionizing radiation, etoposide, or bleomycin suppress Rag
109 on whether the linear no-threshold model of ionizing radiation exposure accurately predicts the subs
113 signatures of somatic mutation characterize ionizing radiation exposure irrespective of tumour type.
114 raphy may have harms resulting from low-dose ionizing radiation exposure or identification of extraco
125 man lymphocytes proportional to TP53 status (ionizing radiation exposure: patients with LFS, 2.71% [9
127 galaxies probably facilitated the escape of ionizing radiation from galaxies when the Universe was a
128 imaging of both radionuclide- and beam-based ionizing radiation from high-energy photons and charged
130 he genetic consequences of human exposure to ionizing radiation has been a long-standing goal of huma
134 date novel epigenetic rheostats that promote ionizing radiation hypersensitivity in various normal st
137 eptible to cataract induction by exposure to ionizing radiation in early postnatal age, when lens epi
139 methanol-based - interstellar model ices to ionizing radiation in the form of energetic electrons.
140 ssociated gene (ATDC) mediated resistance to ionizing radiation in vitro and in vivo in mouse xenogra
141 ions about its role in DNA damage induced by ionizing radiation, in which low-energy electrons are kn
142 llow (Hirundo rustica) nestlings to low dose ionizing radiation increased genetic damage to their per
145 ficient to repress the apoptotic response to ionizing radiation independent of developmental signalin
146 and persistence of gammaH2AX foci following ionizing radiation, indicating a defect in DNA double-st
148 induced DNA damage, and RAD51 recruitment to ionizing radiation induced foci (IRIF), which requires e
151 1 overexpression suppresses the formation of ionizing radiation-induced 53BP1 and BRCA1 but not RNF16
154 Bs, which in normal cells is responsible for ionizing radiation-induced cell senescence and protectio
155 X functions together with XLF in response to ionizing radiation-induced complex DSBs, whereas they fu
157 ofluorescent detection of repair proteins at ionizing radiation-induced DNA damage foci that Wwox exp
159 ese two proteins and variably contributes to ionizing radiation-induced DSB repair in human and chick
160 sensitive technique to monitor external-beam ionizing radiation-induced DSBs in peripheral blood lymp
161 (TIRR) that specifically associates with the ionizing radiation-induced foci formation region of 53BP
162 tem cells exhibit reduced ATM activation and ionizing radiation-induced foci, they display apoptotic
163 opment of therapeutics capable of mitigating ionizing radiation-induced hematopoietic toxicity could
164 nucleosome (50-500 bp) scale, obtained using ionizing radiation-induced spatially correlated cleavage
165 irst, Plk3 and CtIP enhance the formation of ionizing radiation-induced translocations; second, they
169 ocyst perturbation resulted in resistance to ionizing radiation (IR) and accelerated resolution of DN
170 eaks are the major lethal lesions induced by ionizing radiation (IR) and can be efficiently repaired
171 mediate ATM kinase signaling in response to ionizing radiation (IR) and chromatin changes, respectiv
172 we challenged Plk1-overexpressing mice with ionizing radiation (IR) and found that Plk1-overexpressi
173 ency enhances accumulation of p53 induced by ionizing radiation (IR) and sensitizes mice to IR-induce
174 ivation and repression events in response to ionizing radiation (IR) and synthetic p53 activation.
175 r responses to genotoxic stresses, including ionizing radiation (IR) and topoisomerase inhibitors.
177 s (GSCs) to survive exposure to low doses of ionizing radiation (IR) as a model of adult stem cell in
180 mal thyroid function is disturbed because of ionizing radiation (IR) exposure, deleterious effects ca
182 Exposure of murine and human tissues to ionizing radiation (IR) induces the expression of p16(IN
188 ogaster germline and midgut are resistant to ionizing radiation (IR) or chemically induced apoptosis
190 discrete foci in response to DSBs induced by ionizing radiation (IR) or radiomimetic drugs, including
191 l of cancer cells mediated by high levels of ionizing radiation (IR) reduces the effectiveness of rad
192 forts to understand the complex phenotype of ionizing radiation (IR) resistance, a genome sequence ca
193 melanogaster larvae irradiated with doses of ionizing radiation (IR) that kill about half of the cell
194 s typically insulted during chemotherapy and ionizing radiation (IR) therapy and disposed to mucositi
196 lved in sensitizing radioresistant tumors to ionizing radiation (IR) treatments while minimizing inju
197 isite sensitivity of mitotic cancer cells to ionizing radiation (IR) underlies an important rationale
200 ses of HuR in oral cancer cells treated with ionizing radiation (IR), determined that HuR cleavage pr
201 ed cell survival after DNA damage induced by ionizing radiation (IR), expression of BRCA1 K898E prove
202 uction of NADPH, such that after exposure to ionizing radiation (IR), there were higher levels of rea
203 cterial cells to survive extreme exposure to ionizing radiation (IR), we broadly screened nonessentia
204 es mediating the response of glioblastoma to ionizing radiation (IR), we used polysome profiling to d
205 e, we show that clinically relevant doses of ionizing radiation (IR)-induce cellular invasion of ErbB
206 g pharmacological strategies for controlling ionizing radiation (IR)-induced cell death is important
209 broblasts (MEFs) showed defects in repairing ionizing radiation (IR)-induced DNA double-strand breaks
210 religate transformed linear plasmids, repair ionizing radiation (IR)-induced DSBs in nonreplicating c
211 RC5A contributes significantly to preventing ionizing radiation (IR)-induced lung tumorigenesis.
212 ent study, we report for the first time that ionizing radiation (IR)-induced MMP-9 enhances SDC1 shed
213 scarce and the mutational processes defining ionizing radiation (IR)-induced mutagenesis in vivo are
214 s accumulate more alkylator-induced, but not ionizing radiation (IR)-induced, mutations than similarl
234 ing the consequences of exposure to low dose ionizing radiation is an important public health concern
235 ortance of nontargeted (systemic) effects of ionizing radiation is attracting increasing attention.
237 minimizing exposure to alkylating agents and ionizing radiation is important for optimizing survival
241 ren may be more vulnerable to the effects of ionizing radiation, it is necessary to develop methods t
242 llographic and Raman analysis indicates that ionizing radiation kick-starts both peroxide decompositi
245 eas around Chernobyl differing in background ionizing radiation levels and one control study site in
246 ormation and an increase of metal depletion, ionizing radiations, marine eutrophication, and particul
247 stem cells (HSCs) are highly susceptible to ionizing radiation-mediated death via induction of ROS,
249 factor XLF result in extreme sensitivity for ionizing radiation, microcephaly, and growth retardation
250 the cellular response of tumours exposed to ionizing radiation, modelling the alteration of oxygen p
251 he long-term risk of cancer from exposure to ionizing radiation, most participants reported that thei
252 main clinical mainstays, optical readouts of ionizing radiation offer numerous benefits and complemen
253 nding that cancer chemotherapeutic drugs and ionizing radiation often promote autophagy has provided
256 d that independently assessed the effects of ionizing radiation on transcription and post-transcripti
257 ts normal cells from DNA damage induction by ionizing radiation or chemotherapeutics, whereas cancer
260 ere we report that treatment of tumours with ionizing radiation or genotoxic drugs drives p21-activat
262 inflammatory challenges, such as exposure to ionizing radiation or to bacterial lipopolysaccharides.
263 e induced by a variety of stimuli, including ionizing radiation, oxidative stress, and inflammation.
264 is concerning owing to the cancer risk from ionizing radiation, particularly in children younger tha
265 molecular probes sensitive to byproducts of ionizing radiation (primarily reactive oxygen species, o
268 lpha-imaging systems: an alpha-camera and an ionizing-radiation quantum imaging detector (iQID) camer
269 he common access to imaging methods based on ionizing radiation requires also radiation protection.
270 ouse B-cell line, and dispensable for normal ionizing radiation resistance in both G1-arrested and cy
271 dividuals with PPM1D truncating mutations to ionizing radiation resulted in normal p53 activation, su
272 r studying biological effects under low-dose ionizing radiation, safety control in medical radiation
273 NHEJ and sensitizes nonreplicating cells to ionizing radiation, selective ablation of the ligase act
277 of melanized fungi to cosmic and terrestrial ionizing radiation suggests that melanin also plays a pi
278 lasts from these pigs were more sensitive to ionizing radiation than non-SCID piglets, eliminating th
280 damage caused by exogenous sources, such as ionizing radiation, the tumour suppressor p53 mediates c
284 nction and show that SNP309G cooperates with ionizing radiation to exacerbate tumor development.
285 dy to E-cadherin, works synergistically with ionizing radiation to promote the epidermal damage.
286 therapy and precisely deliver high doses of ionizing radiation to small deep-seated target volumes.
288 ed the function of miR-24 in NPC cells after ionizing radiation treatment, resulting in increased apo
290 h yejH and radA hypersensitized the cells to ionizing radiation, UV and ciprofloxacin damage, indicat
292 BSGI on the basis of the Biologic Effects of Ionizing Radiation VII report, the benefit-to-radiation
295 udy, stimulation by doxorubicin, hypoxia and ionizing radiation was used to induce MDR in HCC cells.
297 N109D) mutant RUNX1 conferred resistance to ionizing radiation when overexpressed in Ba/F3 cells und
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