ライフサイエンスコーパス: gamma-irradiation

1 ans, is dramatically stimulated upon massive gamma irradiation.

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

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

4 cells were resistant to apoptosis induced by gamma irradiation.

5 xposure to desiccation, heavy metals, UV and Gamma irradiation.

6 ted with sensitivity to apoptosis induced by gamma irradiation.

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

8 into adult recipient animals conditioned by gamma irradiation.

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

10 rved with cells induced to undergo apoptosis gamma irradiation.

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

12 bioactivity following a sterilizing dose of gamma irradiation.

13 o give rise to regenerating crypts following gamma irradiation.

14 n growth arrest and increased sensitivity to gamma irradiation.

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

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

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

18 exhibited significant hypersensitivity after gamma-irradiation.

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

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

21 and atm mutants display hypersensitivity to gamma-irradiation.

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

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

24 within the murine small intestine following gamma-irradiation.

25 modulating the apoptotic response following gamma-irradiation.

26 eloped disseminated varicella 105 days after gamma-irradiation.

27 ction, particularly virus reactivation after gamma-irradiation.

28 their peripheral blood mononuclear cells to gamma-irradiation.

29 ocyte apoptosis induced by dexamethasone and gamma-irradiation.

30 amplification following DNA damage caused by gamma-irradiation.

31 isplayed stable centrosome numbers following gamma-irradiation.

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

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

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

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

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

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

38 significantly enhance HDMEC survival against gamma-irradiation.

39 ated protection of endothelial cells against gamma-irradiation.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

62 Combined effects of gamma irradiation (0, 3, 6 and 9 kGy) and aging (1 and 1

63 onths) in the male CD2F1 strain using (60)Co gamma irradiation (~0.6 Gy/min, 7.5-12.5 Gy).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

92 stics, collection method, additive solution, gamma irradiation, and storage duration.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

108 iosensitivity was tested in combination with gamma-irradiation at doses of 0, 2, 4, or 6 Gy by colony

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

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

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

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

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

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

115 Gamma irradiation caused the alteration of fatty acids o

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

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

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

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

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

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

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

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

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

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

126 bine, 5-fluorouracil (5-FU), doxorubicin and gamma-irradiation directly or indirectly target nucleoti

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 bittered bitter gourd juice was subjected to gamma irradiation doses of 0, 0.25, 0.5, 0.75, 1, 1.5 an

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

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

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

133 The gamma-irradiation effects on polyphenolic content and an

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

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

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

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

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

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

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

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

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

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

144 Gamma-irradiation generally decreased monoterpenes and i

145 cles and its subsequent modification through gamma irradiation (GI) and electrochemical immobilizatio

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

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

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

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

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

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

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

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

154 lve properties determining protein damage by gamma-irradiation in Escherichia coli and D. radiodurans

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

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

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

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

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

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

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

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

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

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

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

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

170 gamma-Irradiation-induced apoptosis of human dermal micr

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

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

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

174 , 60 provided significant protection against gamma-irradiation-induced apoptosis, as expected.

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

176 2 receptor activation prevents and mitigates gamma-irradiation-induced colonic mucosal barrier dysfun

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

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

179 prophase-arrested oocytes rapidly respond to gamma-irradiation-induced DNA double-strand breaks by ac

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

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

190 agents doxorubicin, cisplatin, olaparib, and gamma-irradiation (IR) enhances the antiproliferative ef

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

199 gamma-irradiation is commonly used to create attenuation

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

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

202 gamma-Irradiation led to a decrease in the concentration

203 gamma-irradiation may be potentially applied to numerous

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

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

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

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

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

209 of the following scenarios: (A) Homogeneous gamma-irradiation, mimicking total-body exposures, vs. m

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 signed to receive VZV vaccine inactivated by gamma irradiation (n=2637) or placebo (n=2649).

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

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

216 Gamma irradiation of B cells selectively abrogates their

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

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

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

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

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 Gamma-irradiation of the cells caused increases of 0.045

224 gamma-irradiation of TOF-16 to an unprecedented 4 MGy do

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

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

237 Mice were subjected to gamma irradiation or intravenous etoposide administratio

238 ive four doses of VZV vaccine inactivated by gamma irradiation or placebo approximately 30 days apart

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 inactivated metabolic-active bacteria using gamma-irradiation or sodium azide, respectively.

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

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

249 /6 and LPA(1) knockout mice exposed to 15 Gy gamma irradiation, orally applied OTP reduced the number

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

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

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

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

254 cipient sex, Rh-D status, collection method, gamma irradiation, recipient age and body mass index, an

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

256 Gamma irradiation reduced the microorganisms of sesame s

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

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

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

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

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

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

263 Gamma irradiation showed >98% active structures of melat

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

279 Gamma irradiation was associated with higher contents in

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

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

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

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

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

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

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

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

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

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

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

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