ライフサイエンスコーパス: gamma-irradiation

1 eloping the GI syndrome after sub-total-body gamma irradiation.

2 ls and mice were screened for sensitivity to gamma irradiation.

3 bioactivity following a sterilizing dose of gamma irradiation.

4 cells were resistant to apoptosis induced by gamma irradiation.

5 ted with sensitivity to apoptosis induced by gamma irradiation.

6 d when cells were arrested at G(2) following gamma irradiation.

7 into adult recipient animals conditioned by gamma irradiation.

8 perates with p53 in the cellular response to gamma irradiation.

9 rved with cells induced to undergo apoptosis gamma irradiation.

10 l p53 downstream target genes on exposure to gamma irradiation.

11 ield in such cells closely resembles that of gamma irradiation.

12 n growth arrest and increased sensitivity to gamma irradiation.

13 ed from C57BL/6 mice and decellularized with gamma irradiation.

14 ans, is dramatically stimulated upon massive gamma irradiation.

15 ockout mouse prostate was also sensitized to gamma-irradiation.

16 a lines and could be further up-regulated by gamma-irradiation.

17 NA-transfected cells were subjected to 12 Gy gamma-irradiation.

18 and atm mutants display hypersensitivity to gamma-irradiation.

19 interferon beta (IFN-beta), IFN-alpha2, and gamma-irradiation.

20 ved 53BP1-/- deficient fibroblasts following gamma-irradiation.

21 within the murine small intestine following gamma-irradiation.

22 modulating the apoptotic response following gamma-irradiation.

23 eloped disseminated varicella 105 days after gamma-irradiation.

24 ction, particularly virus reactivation after gamma-irradiation.

25 their peripheral blood mononuclear cells to gamma-irradiation.

26 ocyte apoptosis induced by dexamethasone and gamma-irradiation.

27 amplification following DNA damage caused by gamma-irradiation.

28 isplayed stable centrosome numbers following gamma-irradiation.

29 d with Nbs1 to sites of DNA damage following gamma-irradiation.

30 ollected at 1, 3, 6, 9, and 24 h after 10 Gy gamma-irradiation.

31 associate with one another in vivo following gamma-irradiation.

32 g agents such as doxorubicin, etoposide, and gamma-irradiation.

33 the Mre11 complex after cellular exposure to gamma-irradiation.

34 significantly enhance HDMEC survival against gamma-irradiation.

35 ated protection of endothelial cells against gamma-irradiation.

36 reaks created by treatment with etoposide or gamma-irradiation.

37 ngiectasia- and RAD3-related) in response to gamma-irradiation.

38 tion between menin and FANCD2 is enhanced by gamma-irradiation.

39 sociation with nuclear matrix is enhanced by gamma-irradiation.

40 at various time points within 24 h following gamma-irradiation.

41 d-type mice when exposed to a single dose of gamma-irradiation.

42 of the IG20 can render cells susceptible to gamma-irradiation.

43 ceptibility, respectively, to the effects of gamma-irradiation.

44 uated p53-mediated cell death in response to gamma-irradiation.

45 rwent sustained G2 arrest up to 4 days after gamma-irradiation.

46 s exposed to a single dose of 30 to 50 Gy of gamma-irradiation.

47 ired for RB-mediated DU-145 cell death after gamma-irradiation.

48 ells sensitizes them to apoptosis induced by gamma-irradiation.

49 ring the cell cycle than on those induced by gamma-irradiation.

50 cted their hypersensitivity to high doses of gamma-irradiation.

51 E. coli cells and their responses to 10 kGy gamma-irradiation.

52 creased at early time points after 2 gray of gamma-irradiation.

53 hypersensitive to DNA damage, epirubicin and gamma-irradiation.

54 oils were not significantly affected by the gamma-irradiation.

55 e demonstrated in MLNs of mice 10-35 d after gamma-irradiation.

56 m G1 arrest and promotes cell survival after gamma-irradiation.

57 s from one fish to another without sublethal gamma-irradiation.

58 ective G(0)/G(1) cell cycle checkpoint after gamma-irradiation.

59 exhibited significant hypersensitivity after gamma-irradiation.

60 orylated in cells in response to UV (but not gamma) irradiation.

61 The suitability of gamma irradiation (1, 2 and 5kGy) for preserving quality

62 P-1-/- and control mice following whole-body gamma-irradiation (1 Gy).

63 'Seedless Kishu' mandarins were treated with gamma irradiation (150, 400, and 1000Gy) and stored for

64 gamma-irradiation (2 kGy) resulted in inhibition of brow

65 nd elicit radioresistant DNA synthesis after gamma-irradiation(2).

66 Gamma irradiation (30 and 6 0kGy) reduced pasting viscos

67 ere transcriptionally altered in response to gamma-irradiation (45.9% upregulated, 54.1% downregulate

68 In combination with a single dose of gamma irradiation 50 at 42 mumol/kg eliminated detectabl

69 ults show that following in vivo exposure to gamma-irradiation, 53BP1 is dispensable for signalling a

70 To evaluate effect of gamma irradiation, A. platensis was exposed to different

71 Here, we show that high-dose gamma-irradiation accompanied with syngeneic bone marrow

72 ly, we found that UM1 cells are sensitive to gamma irradiation and deficient in DNA damage repairs, a

73 tioning of the host with a sublethal dose of gamma irradiation and was associated with complete tumor

74 ance the antitumor efficacy of external-beam gamma-irradiation and (131)I-metaiodobenzylguanidine ((1

75 We have evaluated the effects of sequential gamma-irradiation and arsenite treatment of melanoma cel

76 ential in preventing mitotic entry following gamma-irradiation and does so by inhibiting cyclin B1 ex

77 or for the checkpoint functions of p53 after gamma-irradiation and does so by inhibiting the transiti

78 NT6 was required for cell survival following gamma-irradiation and G(2)-M checkpoint control.

79 everal candidate miRNA-deletion mutants post gamma-irradiation and identified cel-mir-237 as a miRNA

80 SD1 resulted in moderate hypersensitivity to gamma-irradiation and increased homologous recombination

81 P6-transgenic line, A7, were mutagenized by gamma-irradiation and M2 seedlings were screened for mut

82 from undergoing efficient arrest in G1 after gamma-irradiation and markedly increases sensitivity to

83 tivate the G(2)/M cell cycle checkpoint upon gamma-irradiation and to stabilize p53 following N-methy

84 method for treating germ-free (GF) mice with gamma-irradiation and transplanting them with normal or

85 also in mammary glands of mice subjected to gamma-irradiation and was significantly enhanced in tran

86 and after irradiation with 3, 6 and 9 kGy of gamma irradiation, and after 6 and 12 months of storage.

87 such as tumor necrosis factor alpha, UV and gamma irradiation, and different categories of anticance

88 deficient fibroblasts were hypersensitive to gamma irradiation, and gammaH2AX foci, a marker of DSBs,

89 aporation technique, sterilized by 25 kGy of gamma-irradiation, and characterized for size, zeta pote

90 h and without hTERT to stress induced by UV, gamma-irradiation, and H(2)O(2).

91 t levels increased in wild-type animals post gamma-irradiation, and loss of cel-mir-237 also resulted

92 in the cell or be induced experimentally by gamma-irradiation, and represent one of the most serious

93 ote death following Sindbis virus infection, gamma-irradiation, and staurosporine treatment is not co

94 reds of genes are upregulated in response to gamma-irradiation, and that the induction of virtually a

95 synthetic uraninite (UO2(s)), sterilized by gamma-irradiation, and then subjected to a sequential ox

96 accumulation of nuclear forms of ASV DNA in gamma-irradiation-arrested cells.

97 This study suggests the possible use of gamma irradiation as a stimulatory agent to raise the nu

98 Corneal cells were devitalized by gamma irradiation as evidenced by widespread cellular ap

99 xposure and facilitates DNA repair following gamma-irradiation as assessed by the comet assay.

100 We show in the present study that gamma-irradiation, as well as alpha-particle exposure, d

101 pronounced in IL-17Ra(-/-) animals, with the gamma irradiation-associated LD(50) being reduced by 150

102 These results suggest that gamma-irradiation at 1-5kGy, might be recommended as a s

103 Gamma-irradiation at 2 Gray similarly resulted in 74.7 +

104 tochrome P450cam one-electron cryoreduced by gamma-irradiation at 77 K in the absence of substrate an

105 yoreduction of the EPR-silent Compound II by gamma-irradiation at 77 K produces Fe(III) species retai

106 sure of frozen solutions of oxyhemoglobin to gamma-irradiation at 77 K yields EPR- and ENDOR-active,

107 Following gamma-irradiation, ATM phosphorylates ELF4, leading to i

108 provide a framework to assess the safety of gamma-irradiation attenuation and promising targets for

109 lls were treated at four dose levels each of gamma-irradiation, benzo(a)pyrene diol epoxide, N-methyl

110 Gamma irradiation, but not IFN-beta, induced DR4 mRNA.

111 anced sensitivity to oxidising agents, UV or gamma-irradiation, but was hypersensitive to the alkylat

112 osomal integrity and function in response to gamma-irradiation by regulating their DNA-damage respons

113 TP was more efficacious than LPA in reducing gamma irradiation-, camptothecin-, or tumor necrosis fac

114 Gamma irradiation caused the alteration of fatty acids o

115 t with a range of cytotoxic agents including gamma-irradiation, cisplatin, temozolomide and 5-fluorou

116 Ku86(-/-) fibroblasts were hypersensitive to gamma irradiation compared to single mutants and accumul

117 he p53 alleles (-/-) was abolished following gamma irradiation compared with cells with wild-type p53

118 number of cells in the G(1) phase following gamma irradiation compared with the untreated control or

119 s preferentially increased after exposure to gamma-irradiation compared to controls.

120 xhibited an attenuated apoptotic response to gamma-irradiation compared with ASPP2(+/+) thymocytes.

121 etion results in an increased sensitivity to gamma-irradiation, consistent with an increased level of

122 Cell death after gamma-irradiation correlated with an impaired capacity t

123 MEFs in low oxygen and administering 0.5 G y gamma-irradiation daily or 150 muM hydroxyurea, a replic

124 s of platelets while ultraviolet B (UV-B) or gamma irradiation decreased platelet responses.

125 be phosphorylated by ATM persists following gamma-irradiation, delaying the resolution of gammaH2AX

126 In contrast, gamma irradiation did not affect SphK1 activity in prost

127 We found that MYC inhibited the repair of gamma irradiation DNA breaks in normal human cells and b

128 urviving doses (D) of three damaging agents: gamma irradiation, DNase I, and UV radiation.

129 significantly increased with the increase of gamma irradiation doses up to 2.0kGy, above which a redu

130 cell line, KLF4 was not activated following gamma-irradiation due to the absence of p53.

131 Herein, it was aimed to evaluate gamma irradiation effects on processed samples.

132 The gamma-irradiation effects on polyphenolic content and an

133 s and is downregulated by iron depletion and gamma-irradiation, explaining Snail1 stabilization in th

134 The SRD-14 cells were produced by gamma-irradiation, followed by selection with the 1,1-bi

135 Therefore, the suitability of gamma irradiation for preserving fresh-cut watercress qu

136 The direct consequence of gamma-irradiation for most melanoma cells is growth arre

137 evidence that, in contrast to doxorubicin or gamma-irradiation, fulvestrant induction of BIK mRNA is

138 ts arrested by aphidicolin (G(1)/S phase) or gamma-irradiation (G(2) phase), and a partial cell cycle

139 p53 coordinates the response to gamma irradiation (gamma-IR) by either triggering apopto

140 red in 6 of 13 recipients (46%), but neither gamma-irradiation (gamma-I; 0 of 5) nor Mirasol pathogen

141 mperature-sensitive mutant p53 protein or by gamma-irradiation (gamma-irradiation), increases hunting

142 ormal mitochondrial function is required for gamma-irradiation (gammaIR)-induced cell death, which is

143 Gamma-irradiation generally decreased monoterpenes and i

144 The results showed that gamma irradiation had no significant (p>0.05) effect on

145 However, when challenged with gamma irradiation, hemopoietic toxicity is significantly

146 sovers and gene conversion events induced by gamma irradiation in G1- and G2-arrested diploid yeast c

147 HT-29 cells were subjected to 12 Gy gamma-irradiation in a cesium irradiator.

148 ntrols were treated with 12 Gy of whole-body gamma-irradiation in a cesium irradiator.

149 g, hsa-miR-125b, functions as sensitizers to gamma-irradiation in both a nematode in vivo model and b

150 us of H2Av was phosphorylated in response to gamma-irradiation in both tissue culture cells and larva

151 G2 arrest was observed in response to gamma-irradiation in both wild-type and atr plants, albe

152 In short, after gamma-irradiation in dose of 5 kGy, most compounds were

153 ) itself, frozen solutions were subjected to gamma-irradiation in the frozen solution state at 77 K,

154 Furthermore, gamma-irradiation in the presence of KU-55933 rendered T

155 By using gamma-irradiation in the presence of thiocyanate ions, w

156 We show that gamma-irradiation in vivo results in a robust induction

157 incubation of Mphi and DC with live, but not gamma irradiation-inactivated, viruses appeared to bette

158 elial cells show comparable p53 responses to gamma-irradiation, including expression of nuclear p53 a

159 PC-3, to genotoxic treatment (cisplatin and gamma-irradiation) increased several folds when cells we

160 mutant p53 protein or by gamma-irradiation (gamma-irradiation), increases huntingtin mRNA and protei

161 We report that etoposide and gamma irradiation induce apoptosis of salivary acinar ce

162 Both IFN-beta and gamma-irradiation induce apoptosis through the extrinsic

163 nism, we demonstrate that both cisplatin and gamma-irradiation induce the colocalization of coilin wi

164 Whereas gamma-irradiation induced both BIK and PUMA mRNA, only B

165 hRNA) designed to specifically inhibit KLF4, gamma-irradiation induced centrosome amplification.

166 IFN-beta, but not gamma-irradiation, induced TRAIL in NIH-OVCAR-3 cells.

167 repair by non-homologous end joining and of gamma irradiation-induced cellular senescence in human c

168 Knockdown of DDX41 increases basal and gamma irradiation-induced p21 protein levels without aff

169 n and upon a variety of stresses such as UV, gamma irradiation-induced senescence, loss of substrate

170 Etoposide and gamma-irradiation-induced activation of p53 is similar i

171 of PKCdelta protects salivary glands against gamma-irradiation-induced apoptosis in vivo and to explo

172 gamma-Irradiation-induced apoptosis of human dermal micr

173 ast, VEGF-treated HDMECs were protected from gamma-irradiation-induced apoptosis predominantly throug

174 transfection and TUNEL assay, we found that gamma-irradiation-induced apoptosis was decreased in 293

175 hat JNK signaling plays an important role in gamma-irradiation-induced apoptosis, and examine how JNK

176 , 60 provided significant protection against gamma-irradiation-induced apoptosis, as expected.

177 t increases genetic instability and triggers gamma-irradiation-induced apoptosis.

178 t nuclear foci in human cells in response to gamma-irradiation-induced DNA damage, similar to human R

179 ation-mediated DNA repair and also repair of gamma-irradiation-induced DNA damage.

180 ever, mutant seedlings are hypersensitive to gamma-irradiation-induced double-strand breaks.

181 m4 proteins did not measurably accumulate at gamma-irradiation-induced gammaH2AX foci.

182 ermore, Parkin deficiency sensitizes mice to gamma-irradiation-induced tumorigenesis, which provides

183 also less susceptible than wild-type mice to gamma-irradiation-induced tumorigenesis.

184 ice heterozygous for Csn6 were sensitized to gamma-irradiation-induced, p53-dependent apoptosis in bo

185 In spleen-derived T cells, gamma irradiation induces significant murine IL-17A expr

186 Taken together our results suggest that gamma-irradiation induces endothelial cell apoptosis pre

187 that inactivation of Brucella melitensis by gamma-irradiation inhibited its replication capability a

188 The data show that after gamma-irradiation, intact RB mediates transcriptional ac

189 mice treated with lipopolysaccharide before gamma-irradiation, intestinal stem cells were protected

190 ld-type and Ptk6(-/-) mice were subjected to gamma-irradiation; intestinal tissues were collected, pr

191 sults presented in this report indicate that gamma-irradiation (IR) exposure of MCF-7 cells resulted

192 in G2/M checkpoint activation in response to gamma-irradiation (IR) exposure.

193 ion of Cdc25A and G(2) arrest in response to gamma-irradiation (IR) in a dose-dependent manner in viv

194 Repeated low-dose gamma-irradiation (IR) induces thymic lymphoma in mice b

195 ter exposure of MCF-7 breast cancer cells to gamma-irradiation (IR) is dependent on the activation of

196 effects were secondary to cell cycle arrest, gamma-irradiation (IR) was utilized to examine effects o

197 In response to gamma-irradiation (IR)-induced DNA damage, activation of

198 130 patients to double-blinded therapy with gamma irradiation (iridium-192 [(192)Ir]) versus placebo

199 y from oxidative stress but also from UV and gamma irradiation, iron and copper toxicity, thermal str

200 gamma-irradiation is commonly used to create attenuation

201 sappearance of gammaH2AX foci in response to gamma-irradiation, leading to a radio-resistant phenotyp

202 d by treatment with actinomycin D but not by gamma-irradiation, leading to p53 activation.

203 gamma-Irradiation led to a decrease in the concentration

204 gamma-irradiation may be potentially applied to numerous

205 n/repression profile in comparison to pulsed gamma-irradiation may lead to new insights into the ways

206 a key regulator of both HIV type 1 Vpr- and gamma irradiation-mediated apoptosis and possibly serve

207 PI3K and MAPK pathways markedly up-regulated gamma-irradiation-mediated p38 MAPK activation resulting

208 f DNA double-strand breakage associated with gamma-irradiation, meiotic recombination, DNA replicatio

209 Rather than a conservation methodology, gamma irradiation might act as a useful adjuvant to othe

210 r infection of cells that were arrested with gamma-irradiation, mitomycin C, nocodazole, or aphidicol

211 We recently identified, from the gamma-irradiation mixture of duplex DNA, a new intrastra

212 , following exposure of cells to UV, but not gamma-irradiation, MTBP is destabilized as part of the c

213 Five minutes after gamma-irradiation, NFBD1 formed nuclear foci that coloca

214 /MS and demonstrated for the first time that gamma irradiation of a synthetic duplex oligodeoxyribonu

215 Gamma irradiation of B cells selectively abrogates their

216 p21(WAF1) or Bax mRNA following etoposide or gamma irradiation of primary salivary acinar cells.

217 Here we find that gamma irradiation of uvh1 plants specifically triggers a

218 oxidizing agent (SCN)(2)(*)(-) (generated by gamma-irradiation of aqueous thiocyanate) to produce gua

219 Chromosomes were segmented by gamma-irradiation of G. hirsutum (n = 26) pollen, and se

220 Following gamma-irradiation of HeLa cells the uniform nuclear dist

221 The SRD-15 cells were produced by gamma-irradiation of Insig-1-deficient SRD-14 cells, fol

222 After gamma-irradiation of MCF7 cells, BRCA1 protein dispersed

223 port that its efficiency can be increased by gamma-irradiation of recipient cells at the time of tran

224 Gamma-irradiation of the cells caused increases of 0.045

225 In addition, gamma-irradiation of U87 cells increased YKL-40 expressi

226 The effects of stearic acid and gamma irradiation on pasting properties of high amylose

227 In this study, the effects of gamma irradiation on the DNA of fish (Oncorhynchus mykis

228 This is the first report on the effect of gamma irradiation on the expression of glucosinolate bio

229 The effect of external gamma irradiation on the kidneys is well described.

230 The effects of high-dose gamma irradiation on the nutritional quality and sensory

231 the combined apoptotic effects of TRAIL and gamma-irradiation on HeLa cells.

232 The influence of whole-body gamma-irradiation on the antibacterial host defense agai

233 The effect of gamma-irradiation on the growth of asexual Plasmodium fa

234 y adenovirus-mediated delivery of p53 and by gamma irradiation or doxorubicin both in the presence an

235 dent apoptotic pathways after treatment with gamma irradiation or doxorubicin, whereas p53-independen

236 p53 response to treatment with gamma irradiation or etoposide is lost due to a mutation

237 R), relocalizes to the S phase nucleus after gamma irradiation or hydroxyurea treatment.

238 Mice were subjected to gamma irradiation or intravenous etoposide administratio

239 fter tumor cell death by bortezomib, but not gamma irradiation or steroids, leads to the induction of

240 its activity toward p53 after DNA damage by gamma irradiation or the radiomimetic agent neocarzinost

241 HDM2 in high passage cells exposed to either gamma irradiation or ultraviolet C irradiation.

242 ate within the nucleus in response to either gamma-irradiation or mitomycin C exposure, two DNA-damag

243 In response to gamma-irradiation or mitomycin C, WRN leaves the nucleol

244 d convergence of WRN and Nbs1 in response to gamma-irradiation or mitomycin C.

245 Following exposure to sublethal gamma-irradiation or N-ethyl-N-nitrosourea (ENU), MLL-CB

246 suppressor p53 is stabilized in response to gamma-irradiation or treatment with DNA-damaging agents,

247 DNA damage: 4-nitroquinoline-1-oxide (4NQO), gamma-irradiation, or UV-irradiation.

248 /6 and LPA(1) knockout mice exposed to 15 Gy gamma irradiation, orally applied OTP reduced the number

249 to evaluate the effects of electron-beam and gamma irradiation over the phenolic profiles of two plan

250 Upon exposure to sublethal doses of gamma-irradiation, Parp-2-/- mice exhibited bone marrow

251 and VEGF protects endothelial cells against gamma-irradiation predominantly via the PI3K-Akt-Bcl-2 s

252 uided cancer photothermal therapy and UV and gamma-irradiation protection.

253 ng murine penetrating keratoplasty; however, gamma irradiation reduced the allogenicity of these corn

254 Gamma irradiation reduced the microorganisms of sesame s

255 r BIK proapoptotic protein by doxorubicin or gamma-irradiation requires the DNA-binding transcription

256 d cell cycle arrest induced by cisplatin and gamma-irradiation, respectively.

257 Exposure of Bad-null mice to sublethal gamma-irradiation resulted in an increased incidence of

258 We find that DNA damage induced by gamma-irradiation results in increased FBXO31 levels, wh

259 estradiol, or exposure to sublethal dose of gamma irradiation served as prototype thymus-ablating th

260 osition, hypersensitivity to mitomycin C and gamma-irradiation, shortened telomeres, and cell cycle d

261 Finally, gamma-irradiation stimulated an increase in Wnt-activate

262 vent possible toxic effects of external-beam gamma irradiation, strategies for targeted radiation the

263 Pkd1 mRNA levels than wild-type littermates; gamma-irradiation suppressed PKD1 gene expression in p53

264 Sublethal total body gamma irradiation (TBI) of mammals causes generalized im

265 ith the replication inhibitor hydroxyurea or gamma-irradiation that introduces DNA strand breaks.

266 For gamma irradiation, the results were consistent with a si

267 following DNA damage induced by cisplatin or gamma-irradiation, the G2 (but not S) arrest response wa

268 After gamma-irradiation, the survival of intestinal stem cells

269 However, 48 h post-gamma-irradiation there was a significant accumulation o

270 er DNA damage, and when damage is induced by gamma irradiation, this increase requires ATM.

271 dent induction of programmed cell death upon gamma-irradiation through PML-nuclear body (NB)-mediated

272 Moreover, a gamma-irradiation treatment that restores crossovers in

273 Sam68 deletion diminishes gamma-irradiation-triggered PAR synthesis and NF-kappaB

274 oss-link lesion can also form in d(mCG) from gamma irradiation under anaerobic conditions.

275 ere formed in mC-containing duplex ODNs upon gamma irradiation under both aerobic and anaerobic condi

276 Gamma irradiation (up to 20 kGy) did not induce formatio

277 on swabs appear to be a direct result of the gamma irradiation used to sterilize the swabs.

278 hough there may be large dose heterogeneity, gamma irradiation (using a fixed dose prescription) appe

279 xidants, we showed that the damage caused by gamma irradiation was mechanistically different than tha

280 It was previously demonstrated that gamma irradiation was the processing technology with the

281 inal Wnt signaling, the reporter response to gamma-irradiation was examined.

282 The efficiency of the p53 response to gamma-irradiation was found to decline significantly in

283 gamma-Irradiation was used to cryoreduce Rbr at 77 K, th

284 to undergo apoptosis in mice post whole-body gamma-irradiation (WBIR).

285 Using gamma-irradiation, we created opaque QPM variants to ide

286 ples treated with 0, 1, 2 and 3 kGy doses of gamma irradiation were determined.

287 B. pertussis killed by gentamicin or gamma irradiation were unable to intoxicate, illustratin

288 Apoptotic effects of IFN-beta or gamma-irradiation were blocked by expression of a domina

289 into S phase and mitosis after DNA damage by gamma-irradiation were consistent with impaired p53 chec

290 ing growth factor-alpha and p53 responses to gamma-irradiation were measured.

291 on in miRNA expression in cells treated with gamma-irradiation, whereas exposure to sodium arsenite l

292 nd delayed the formation of Rad51 foci after gamma-irradiation, whereas overexpression of TRF2 stimul

293 Subsequent exposure of the cells to gamma irradiation, which causes DNA double-strand breaks

294 Moreover, gamma-irradiation, which activates p53, increases huntin

295 Cisplatin and gamma-irradiation, which cause distinct types of DNA dam

296 -dependent apoptosis, but not in response to gamma-irradiation, which causes cell cycle arrest.

297 gamma-Irradiation, which endogenously generates ceramide

298 lso reduced the normal apoptotic response to gamma-irradiation, which we show is independent of Mlh1

299 cy does not affect the immediate response to gamma-irradiation with normal levels of apoptosis, proli

300 atment of several melanoma lines just before gamma-irradiation with the inhibitor of ATM kinase KU-55