ライフサイエンスコーパス: irradiate

1 he chemotherapy-alone groups (all previously irradiated).

2 ng 100 mum may therefore not be sufficiently irradiated.

3 of the radiotherapy dose and volume of brain irradiated.

4 A to knock down expression of HDAC4 and then irradiated (2.5-10.0 Gy).

5 )Ra, in high yield and purity, from a proton irradiated (232)Th matrix.

6 cluded fluorescence EEMs from 291 untreated, irradiated (253.7 nm, 310-410 nm), and oxidized (UV-H2O2

7 ing products were obtained when santonin was irradiated (365 nm) in the presence of methylamine.

8 ects were observed without irradiation; when irradiated (520 nm, 100 J/cm(2), 160 mW/cm(2)) to produc

9 ells from Fx-/- or control mice (Ly5.2) into irradiated 8-week-old Fx-/- or control mice (Ly5.1).

10 ed by x-rays, produced by a long pulse laser irradiating a copper foil placed at one end of the tube.

11 represent increasing clinician comfort with irradiating a new breast reconstruction and may have cos

12 HSCs have reduced repopulation potential in irradiated adult transplant recipients but mechanisms un

13 ssed more intracellular IFNgamma in both the irradiated and contralateral tumors.

14 din-rich extracts prevented oxidation in non-irradiated and gamma-irradiated fish model system.

15 Some mice were irradiated and given transplants of bone marrow cells fr

16 he assumption that constituent phases in ion-irradiated and heat-treated films are identical and that

17 vered intraoperatively (IORT), by collecting irradiated and non-irradiated breast tissues from BC pat

18 ein and sugar contents were recorded between irradiated and non-irradiated samples.

19 d by SRFA in calcium-containing waters under irradiated and nonirradiated conditions.

20 men induced immune infiltrate changes in the irradiated and nonirradiated lesions featured by reducti

21 to be unaffected by reuse of the previously irradiated and processed uranyl sulfate solution.

22 f CXCL10 responsible for these processes, we irradiated and reconstituted wild-type (WT) and CXCL10(-

23 ells, Tie2-Cre/LoxP-PTP1B mice were lethally irradiated and reconstituted with bone marrow from wild-

24 pr2(R899X) mutant or controls, were lethally irradiated and transplanted with either control or Bmpr2

25 ts with subtotal nephrectomies were lethally irradiated and underwent salvage transplantation with ei

26 lease soluble protein from these depots when irradiated, and leave behind only small easily absorbed

27 Recombinant ANG protein improves survival of irradiated animals and enhances hematopoietic regenerati

28 tal muscle and adipose progenitor cells from irradiated animals revealed substantial DNA methylation

29 Out of 7 irradiated animals, complete atrioventricular block was

30 re significantly increased in blood cells of irradiated animals, covering three types of genotoxic ac

31 'M26' roots cultivated in ARD soil or gamma-irradiated ARD soil suggests that typical defense reacti

32 he number of osteoblasts and activity in the irradiated area and suppressed the number and activity o

33 nfigurations and variations in peak dose and irradiated area in the response of normal tissues outsid

34 esulted from even short exposures of a small irradiated area.

35 diation leads to oxygen penetration into the irradiated areas, and diffuses along the Cu-rich domains

36 %, 1.5%, and 5%) was added to HAMS, and then irradiated at 0, 30, and 60 kGy before pasting.

37 study defect interaction dynamics in 3C-SiC irradiated at 100 degrees C with ions of different masse

38 tion of 2-alkylcyclobutanones in cashew nuts irradiated at 100 Gray and in nutmeg irradiated at 400 G

39 ew nuts irradiated at 100 Gray and in nutmeg irradiated at 400 Gray.

40 Animals were x-ray-irradiated at a dose of 7.5 Gy with 1 of 3 radiation sch

41 eous solutions of these compounds were gamma-irradiated at doses of 0.5, 0.7 and 1kGy, with a dose ra

42 port radioactive decay signatures in targets irradiated at the Elfie laser facility by laser-accelera

43 ve employed a single wavelength laser, which irradiates at 266 nm.

44 , transfer of sortilin-deficient BM cells to irradiated atherosclerotic mice did not affect vascular

45 es with intense X-ray pulses have shown that irradiated atoms reach a very high degree of ionization,

46 The dominant DNA photolesion found in UV-irradiated bacterial endospores is a thymine dimer, 5-th

47 eated splenocytes were infused into lethally irradiated BALB/c (same-party) or C3H/HeJ (third-party)

48 L/6 splenocytes were cocultured for 5 d with irradiated BALB/c splenocytes and then photodepleted (PD

49 ional and structural changes that affect the irradiated brain and cognition.

50 pothesize that depletion of microglia in the irradiated brain would have a neuroprotective effect.

51 uman neural stem cell (hNSC) grafting in the irradiated brain, where intrahippocampal transplantation

52 socenter was placed at the center of the pre-irradiated brainstem (BS)/spinal cord (SC) and the jaws

53 n recur more rapidly in a xenograft model of irradiated breast cancer cells; Wwox-deficient cells exh

54 ely (IORT), by collecting irradiated and non-irradiated breast tissues from BC patients, after tumor

55 or alpha (TNFalpha) was elevated in directly irradiated but not bystander cells; while TNFalpha recep

56 Starch samples were irradiated by (60)Co in doses 1, 2 and 5kGy, on a rate o

57 he (148)Gd and (154)Dy content in Pb targets irradiated by 220-2600 MeV protons.

58 results obtained from a similar coil target irradiated by a fs class laser at an order of magnitude

59 ear-critical density hydrogen gas jet target irradiated by a high intensity (10(18) W/cm(2)), short-p

60 t the rear of a 50-mum thick plastic target, irradiated by a multi-picosecond petawatt laser pulse at

61 ium atomic vapours from bulk strontium oxide irradiated by a simple low power diode laser.

62 s for H3(+) formation from organic molecules irradiated by a strong-field laser.

63 large-scale gradients, low-density targets, irradiated by an intense near-infrared laser is observed

64 the transient self-charging of solid targets irradiated by intense laser pulses.

65 stellar to the substellar regime, it is also irradiated by the primary (compact accretor).

66 adrupole ion trap mass spectrometer and then irradiated by the tunable infrared output of a free elec

67 nolate induction was, however, unaffected in irradiated cabbage suggesting their non-involvement in g

68 In gamma-irradiated cabbage, enhanced sinigrin, a major glucosino

69 T74B1, CYP79F1 and SUR1 were up-regulated in irradiated cabbage.

70 myostatin were significantly changed in the irradiated cachectic NHP compared to the non-irradiated

71 response to paracrine signals emerging from irradiated CAF.

72 as an "on-target effect" originating within irradiated cancer cells, but also as an "off-target effe

73 the immune system to recognize and eliminate irradiated cancer cells, either as an "on-target" or as

74 Irradiated CD73(-/-) mice showed an altered regulation o

75 ism to minimize the risk of mutagenesis, UVB-irradiated cells also activate a checkpoint signaling ca

76 nome-wide profiling of repair activity in UV irradiated cells has revealed significant variations in

77 unique process in which factors released by irradiated cells or tissues exert effects on other parts

78 The population doubling times (DT) of sham-irradiated cells varied from 18.9 to 28.7 hours for diff

79 ered and grew with the same rate as the sham-irradiated cells.

80 rmation of distinctive super enhancers in UV-irradiated cells.

81 idone (6-4) photoproducts [(6-4)PPs] from UV-irradiated cellular and naked DNA revealed that the effe

82 y, PC-reactive B-1 cells expressed PD-L2 and irradiated chimeras demonstrated that B cell-intrinsic P

83 d PC-specific IgM, naive PD-L2(-/-) mice and irradiated chimeras reconstituted with PD-L2(-/-) B cell

84 tail length and mean tail moment% levels of irradiated citrus fruits at all doses are significantly

85 Irradiated citrus fruits showed the separated tails from

86 be a practical quarantine control method for irradiated citrus fruits since it has been possible to e

87 on of applied dose for quarantine control in irradiated citrus fruits.

88 lear non-haem [(13-TMC)Co(IV)(O)](2+) (2) by irradiating [Co(II)(13-TMC)(CF3SO3)](+) (1) in the prese

89 ss-induced NF-kappaB activation in the gamma-irradiated colon and animal and that Sam68-dependent NF-

90 The mortality of irradiated combination formulation on second-instar larv

91 with increased Fe(III) reduction rates under irradiated conditions and decreased Fe(II) oxidation rat

92 m via which the Fe(III) reduction rate under irradiated conditions is impacted by calcium addition is

93 leached from the sand patties under dark and irradiated conditions were substantially different, but

94 abiotic transformations under both dark and irradiated conditions.

95 In contrast, in H2 treated irradiated corneas oxidative stress was suppressed and m

96 Some irradiated corneas remained untreated or buffer treated.

97 n of oxidative and nitrosative stress in UVB irradiated corneas, which may represent a novel prophyla

98 smaller colonies in soft agar than their 2D-irradiated counterparts (gamma P = 0.0004; (+)H P = 0.04

99 Application of the model to data from irradiated crypts after an extended recovery period perm

100 ypts before adenoma formation, also found in irradiated crypts.

101 The buildup of radiation damage in ion-irradiated crystals often depends on the spatial distrib

102 From 24 compounds, irradiated CSP retained 23 volatile compounds, while the

103 the discovery of autophagy induced by X-ray irradiated Cu-Cy nanoparticles sheds a good insight to t

104 oth light-irradiated primary tumours and non-irradiated distant tumours by inducing a strong tumour-s

105 ven by H2(g) at a pressure of 1 atm in a non-irradiated dry system.

106 tions measured under flow conditions between irradiated endothelial cells and monocytes.

107 urgically excised human carcinomas that were irradiated ex vivo These mechanisms involving crossprimi

108 sted that stratospheres could form in highly irradiated exoplanets, but the extent to which this occu

109 anges related to carbon contamination in ion irradiated F/M steels are also presented and briefly dis

110 ormation of 2-ACBs was also observed in UV-C irradiated fatty acids, triglycerides, corn oil, and por

111 aggregates are then dispersed and plated on irradiated feeder cells to propagate and isolate individ

112 n the response of normal tissues outside the irradiated field at 1 and 4 days after irradiation, we m

113 lts indicated that the microstructure of the irradiated films consisted of carbon clusters within a s

114 major shortcoming in previous studies of ion-irradiated films is the assumption that constituent phas

115 vented oxidation in non-irradiated and gamma-irradiated fish model system.

116 Wild-type (WT) mice were irradiated followed by isoform-specific betaAR knockout

117 imated by the ORIGEN code and lower than non-irradiated fuel, suggesting non-uniform volatilization o

118 Endometriotic lesions were induced in irradiated FVB/N mice, which were reconstituted with bon

119 metriotic lesions were surgically induced in irradiated FVB/N mice, which were reconstituted with bon

120 damage thresholds in nanosecond pulsed laser-irradiated gold nanospheres, and compared our results wi

121 erior when compared with the 0.5 W and 0.7 W irradiated groups immediately after treatment (P < 0.001

122 EDS results of the irradiated groups showed an increase in the proportion o

123 ed Dex responsiveness to inflammation in UVB-irradiated HaCaT cells.

124 ric acid increased the paste viscosity of un-irradiated HAMS from 420 mPas to 557 and 652 mPas for 1.

125 Pasting of gamma irradiated HAMS resulted in the formation of type I amyl

126 0(7) particles at 10 +/- 0.5 MeV obtained by irradiating helical coil targets with a few joules, sub-

127 Remarkably, mandibular HSCs reconstituted irradiated hematopoietic bone marrow in vivo, just as ap

128 Phenotypic modifications of irradiated, Hey2 siRNA- and Hey2 vector plasmid-transfec

129 ved MCs (CBMCs) were infected with HRV or UV-irradiated HRV at increasing multiplicities of infection

130 Treatment of irradiated HSCs with Dkk1 in vitro increased the recover

131 cant changes in paired samples of normal and irradiated human skin.

132 We found that EndoMT occurs in irradiated HUVECs with concomitant Hey2 mRNA and protein

133 Cells irradiated in 3D produced significantly fewer and smalle

134 OTA was irradiated in its dry form, in aqueous and in methanolic

135 When irradiated in paddy-field water, propanil (PRP) undergoe

136 Additionally, the toxicity of OTA irradiated in water was tested.

137 Control or Bcl3(-/-) mice were irradiated, injected with bone marrow from Bcl3(-/-) or

138 ice were imaged with Cone-Beam CT (CBCT) and irradiated (IR) to the marked area using the Small Anima

139 Ultraviolet (UV)-irradiated keratinocytes secrete the lipid mediator of i

140 hibition of chromosomal DNA synthesis in UVB-irradiated keratinocytes.

141 l line J774 to infection with live and gamma-irradiated (killed) M. tuberculosis.

142 hological NK-cell overactivation, we treated irradiated Ldlr(-/-) mice reconstituted with either wild

143 ld-type mice were transplanted into lethally irradiated Ldlr(-/-) mice.

144 ate that the decrease in leaf growth in UV-B-irradiated leaves is a consequence of a reduction in cel

145 In UV-irradiated lens tissues, fibers are not observed with TE

146 nal photon radiotherapy, proton radiotherapy irradiates less normal tissue and might improve health o

147 his challenge, a Plasmodium falciparum gamma-irradiated long-lived merozoite (LLM) line was developed

148 y promotes accumulation of M2 macrophages in irradiated lung tissues.

149 ease in the mean number of detected cells in irradiated lungs compared to control, although the latte

150 Irradiated lungs from wild-type c57BL/6NcR mice accumula

151 mation of prefibrotic macrophage clusters in irradiated lungs.

152 Importantly, irradiated macrophages promoted cancer cell-invasion and

153 Irradiated macrophages remained viable and metabolically

154 hylium cations were also detected in the pre-irradiated malic acid solution.

155 elemental composition and the morphology of irradiated MAPbI3 thin films as a function of the electr

156 he single-crystal structure of the gamma-ray irradiated material, and subsequently leads to a very ef

157 These mechanisms are available in the irradiated material, but not in the as-deposited films.

158 lume ratio may alleviate radiation damage in irradiated metallic materials as free surface are defect

159 DT-deficient HSCs in reconstituting lethally irradiated mice and a strong competitive disadvantage wh

160 and adipose progenitor cells collected from irradiated mice and differentiated in culture.

161 When BM cells were harvested from UV-irradiated mice and transplanted into naive mice, the re

162 nt and enhanced overall survival in lethally irradiated mice by mitigating damage to the BM vascular

163 of Fubp1(-/-) hematopoietic stem cells into irradiated mice entirely failed to reconstitute hematopo

164 ferentiating from the bone marrow (BM) of UV-irradiated mice had a reduced ability to migrate toward

165 ells, and systemic administration of Dkk1 to irradiated mice increased hematopoietic recovery and imp

166 the BM of nonirradiated mice, those from UV-irradiated mice produced more lactate, consumed more glu

167 significant increase in crypt progenitors in irradiated mice treated with AA-ORS for six days (8.8 +/

168 In cognitively impaired irradiated mice we observed increased 5-methylcytosine a

169 mice (ie, mice transplanted with BM from UV-irradiated mice) after injection of an inflammatory stim

170 fferentiated from the bone marrow (BM) of UV-irradiated mice, even after activation with LPS, migrate

171 igand 21 by DCs differentiated from BM of UV-irradiated mice.

172 ctionally similar to those from the BM of UV-irradiated mice.

173 ility to initiate new immune responses in UV-irradiated mice.

174 eletal muscle satellite cells collected from irradiated mice.

175 roved electrolyte and nutrient absorption in irradiated mice.

176 A-ORS) improved gastrointestinal function in irradiated mice.

177 number of HSPCs required to rescue lethally irradiated mice.

178 nd preserves the structural integrity of the irradiated microenvironment.

179 s of (90)Y, (177)Lu, (111)In, and (161)Tb at irradiating micrometastases.

180 In addition, vaccination of mice with irradiated Mobilan-transduced prostate tumor cells prote

181 Glyoxylic acid produced in the irradiated model wine was present in free and hydrogen s

182 rogramming (CR), which involves coculture of irradiated mouse fibroblast feeder cells with normal and

183 the anti-inflammatory effects of Dex in UVB-irradiated mouse skin.

184 oretical heat transfer model of pulsed laser-irradiated nanoparticles and found to be in reasonably g

185 In vivo, the heat generation of irradiated nanoparticles was evaluated in human tumor xe

186 ation and absorption cross-section of single irradiated nanoparticles were quantified using a tempera

187 nmelanoma skin cancer was not observed among irradiated NHBs, and the risk was lower among Hispanic s

188 irradiated cachectic NHP compared to the non-irradiated NHP.

189 nies when cultured on plates pre-seeded with irradiated NIH3T3 fibroblasts, and were also capable of

190 Irradiated nitrophenols can produce nitrite and nitrous

191 cells (HSCs) were injected into sublethally-irradiated NOD-scid-IL2Rg-/- (NSI) mice.

192 stine treatment supports DSB repair in gamma-irradiated normal NHDF fibroblasts but alters it in MCF7

193 n the irradiated samples to that of the sham-irradiated ones varied from 0.6 to 0.8 after 0.2 Gy, and

194 bility to radiation damage was determined by irradiating operators' blood in vitro.

195 ministration of ABT263 to either sublethally irradiated or normally aged mice effectively depleted SC

196 Reconstitution of irradiated Panx1 knockout mice with hematopoietic Panx1(

197 At acute time points (30 min to 2 h), irradiated parotid glands had significantly decreased le

198 ta suggest that IGF-1 promotes DNA repair in irradiated parotid glands through the maintenance and ac

199 ene expression profiles derived from ex vivo-irradiated patient lymphocytes.

200 little is known about complication rates in irradiated patients treated in the broader community.

201 The numbers needed to irradiate per IBE prevented were 10.5, 9.1, 7.5, and 13.

202 s and examined the number of women needed to irradiate per IBE prevented.

203 s and hydrogen peroxide, act in synergy with irradiated perchlorates to cause a 10.8-fold increase in

204 ion of aseptic, purified, cryopreserved, non-irradiated PfSPZ ('PfSPZ Challenge') to malaria-naive, h

205 Morphologically, irradiated podocytes demonstrated loss of filopodia and

206 ti-PD-L1 results in the eradication of light-irradiated primary tumors and the complete inhibition of

207 @pyrolipid mediates regression of both light-irradiated primary tumours and non-irradiated distant tu

208 ntly, their repopulation occurs rapidly from irradiated progenitors rather than via qNSC activation.

209 t-IR derive from activated qNSCs rather than irradiated progenitors, minimising damage compounded by

210 We show here that irradiating prostate cancer cells stimulates a durable u

211 oliferative neoplasms, we engrafted lethally irradiated recipient mice with bone marrow cells transdu

212 and forskolin, enhanced survival of lethally irradiated recipient mice.

213 to reconstitute the bone marrow in lethally irradiated recipient mice.

214 c controls and used to reconstitute lethally irradiated recipients for analysis of long-term self-ren

215 coding the human RAG2 gene and injected into irradiated recipients with OS.

216 n vitro and to reconstitute hematopoiesis in irradiated recipients, consistent with a hematopoietic p

217 ctable by direct transplantations into adult irradiated recipients, the size and growth of this popul

218 ts fast, large, and reversible strain in the irradiated region, which causes a synergistically couple

219 nd apoptosis or necrosis was not observed in irradiated regions.

220 In the current study, we used lethally irradiated S. aureus as a model multicomponent vaccine a

221 ical properties of oils extracted from gamma-irradiated Sacha Inchi (Plukenetia volubilis L.) seeds (

222 Irradiated samples showed a general increase in individu

223 e ratio of normalized cell population in the irradiated samples to that of the sham-irradiated ones v

224 Lastly, NMR spectroscopy using in situ LED-irradiated samples was utilized to monitor the kinetics

225 ores for taste, flavor, color and texture of irradiated samples were higher, but not significantly (p

226 ids that can differentiate between naive and irradiated samples, as well as providing potential marke

227 not significantly (p>0.05) than those of non-irradiated samples.

228 nts were recorded between irradiated and non-irradiated samples.

229 ble or void formation, or segregation in all irradiated samples.

230 EIEIO involves irradiating singly charged lipid ions with electrons hav

231 nd to significantly improve wound healing in irradiated skin and was associated with decreased inflam

232 nt resection of all or nearly all previously irradiated skin plus mastectomy ("radical").

233 Wound healing is significantly delayed in irradiated skin.

234 The pre-irradiated solutions containing tartaric acid exhibited

235 absorption for furans during the storage of irradiated solutions.

236 ormation is proposed based on NMR studies of irradiated solutions.

237 MRI of irradiated spines detected radiation-induced BM vascular

238 sterile protection afforded by injection of irradiated sporozoites, CD8(+) T cells have been shown t

239 from pre-erythrocytic vaccine candidates and irradiated sporozoites, has shown that CD8(+) T cells pl

240 idation rate in nonirradiated and previously irradiated SRFA solutions with the addition of calcium c

241 Although placement of gamma-irradiated sterile cornea (GISC) as a patch graft over t

242 Gamma-irradiated sterile corneal patch grafts do not always re

243 oscopic detection and characterization of an irradiated substellar donor in an accreting white-dwarf

244 ovide a natural laboratory in which to study irradiated substellar objects.

245 t when the snowpack surface was artificially irradiated, suggesting a photochemical production mechan

246 of tungsten polycrystalline samples with ion-irradiated surfaces.

247 transformations in acidic nonirradiated and irradiated Suwannee River Fulvic Acid (SRFA) solutions a

248 SEM studies show that irradiated Ta surfaces undergo significant morphology ch

249 d XRD both show significant oxidation of the irradiated Ta surfaces, giving further qualitative infor

250 namics of hot electron escape from the laser irradiated target was studied numerically for these two

251 The encoded excitation light is used to irradiate the liquid sample and its fluorescence is disp

252 emical reactions using an unfocused laser to irradiate the precursor solution.

253 beams generated by a gas field ion source to irradiate the sample.

254 We gamma irradiated the cells to prevent their productive infecti

255 n-5-phosphate solution with enhancers and by irradiating the cornea with a 10 mW/cm(2) ultraviolet A

256 Irradiating the o-nitrobenzyl phosphate-functionalized m

257 Here, by irradiating the parent TeDB-DiPhOBz (solution 1) with na

258 hing, the captured RNA target is released by irradiating the photocleavable DNA capture probe with ul

259 s responses at unexposed sites distal to the irradiated tissue.

260 We observed that beta-SiC, neutron irradiated to 9 dpa (displacements per atom) at approxim

261 ction of wild-type (WT) marrow into lethally irradiated TSP2 KO mice did not rescue the bleeding diat

262 the assembly of cell-particle hybrids where irradiated tumor cells were surface engineered with adju

263 d with immunostimulatory mAbs to act both on irradiated tumor lesions and on distant, nonirradiated t

264 nally, FGFR1 silencing delayed the growth of irradiated tumor xenografts, in a manner that was associ

265 hilic-CpG revealed increased accumulation in irradiated tumors along with decreased off-target accumu

266 However, radioresistance in irradiated tumors can also develop, resulting in relapse

267 By irradiating two colliding elliptically-polarized lasers

268 The aligned ZnO NR arrays were irradiated using 150 MeV Ag ions with different fluences

269 rapy plus bevacizumab groups (all previously irradiated) versus three (1%) of 220 in the chemotherapy

270 A control not irradiated was used for comparison.

271 It is well-known that vaccines comprising of irradiated whole tumor cells or tumor-derived heat shock

272 Sema3e(-/-) bone marrow progenitor cells to irradiated wild-type (WT) recipients exacerbates airway

273 Furthermore, plasma from irradiated wild-type mice showed a transient increase in

274 Reconstituting irradiated wild-type mice with Rora(-/-) or Il17rb(-/-)

275 n, the tumors are serially transplantable in irradiated wild-type mice, underlying the tumoral origin

276 MiRNA from normal and irradiated Wistar rat lungs and whole blood were analyze

277 the miR-193b-3p promoter in the HepG2 cells irradiated with 0.01 Gy.

278 Ta samples were irradiated with 100 eV He(+) ions at various fluences up

279 is was evident in the microbeam path of rats irradiated with 150 Gy, whereas no increase was observed

280 Gy, whereas no increase was observed in rats irradiated with 360 Gy.

281 D setup the sample is coated with Au-NPs and irradiated with 532 nm laser radiation to induce thermop

282 We show that when irradiated with a simulated Martian UV flux, perchlorate

283 Mice were locally irradiated with a synchrotron X-ray broad beam and a mul

284 In the current study, AL cells were irradiated with alpha particles and responses of bystand

285 c surfaces and renders them fluorescent when irradiated with blue light.

286 Drosophila melanogaster larvae irradiated with doses of ionizing radiation (IR) that ki

287 sorption spectroscopy at the P K-edge on DNA irradiated with either UVA light or protons.

288 Standardization to be used to identify foods irradiated with ionizing irradiation.

289 n membrane were exposed to papain based gel, irradiated with laser and analyzed about their integrity

290 148)Gd, (150)Gd, and (146)Sm from Ta targets irradiated with protons up to 2.6 GeV to determine their

291 Methylene blue (4 muM) irradiated with red light (660 nm) catalyzes the rapid o

292 A mean volume of 2.5+/-0.5 mL was irradiated with target dose.

293 CPR-4 is secreted from animals irradiated with ultraviolet or ionizing gamma rays, and

294 Pre-organized gemini monomers were irradiated with UV light and monitored by FT-IR.

295 In brief, cells are irradiated with UV light to induce protein-RNA cross-lin

296 factor of 35 at 1 V when the closed form is irradiated with UV light to induce the ring-opening reac

297 After irradiating with an NIR laser, a good anti-tumor effect

298 Using this catalyst and irradiating with white LEDs resulted in the production o

299 In irradiated WT mice treated with the A2AR antagonist, the

300 marrow cells from Id cDKO mice into lethally irradiated WT mice.