ライフサイエンスコーパス: cytotoxicity

1 LKB1 by ATM was involved in AZD1775-mediated cytotoxicity.

2 h an agonistic antibody enhanced CD4+ T cell cytotoxicity.

3 y, and increased antibody-dependent cellular cytotoxicity.

4 ll models, and can ameliorate FUS-associated cytotoxicity.

5 X with R1 and R2 significantly prolonged its cytotoxicity.

6 sed on the mechanisms underlying mutant SOD1 cytotoxicity.

7 DA-MB-468 TNBC cells without any significant cytotoxicity.

8 annels (Pico145) strongly inhibited Icat and cytotoxicity.

9 ntributes to the molecular basis of graphene cytotoxicity.

10 is efficiently internalized by cells without cytotoxicity.

11 cessfully decaged in live cells to reinstate cytotoxicity.

12 nd is even more intriguing in the absence of cytotoxicity.

13 to be the principle mechanism of IFN-induced cytotoxicity.

14 lasmic antibiotic concentration for enhanced cytotoxicity.

15 MMR-deficient cells, resulting in selective cytotoxicity.

16 g ThCTL that mediate MHC class II-restricted cytotoxicity.

17 gs with increased anti-clot activity and low cytotoxicity.

18 ells to investigate both cellular uptake and cytotoxicity.

19 o Jurkat T-cells and severely impaired their cytotoxicity.

20 re prepared, characterized and evaluated for cytotoxicity.

21 an increase antibody-dependent cell-mediated cytotoxicity.

22 anscriptional, including NK localization and cytotoxicity.

23 It is anticancer because of its cytotoxicity.

24 fected mice were polyfunctional and mediated cytotoxicity.

25 h phenotypic data on cellular cytostasis and cytotoxicity.

26 imal doses active in depleting DNMT1 without cytotoxicity.

27 HCV RNA replication through antigen-specific cytotoxicity.

28 increased inflammatory monocytes and reduced cytotoxicity.

29 rther sphingosine accumulation and, thereby, cytotoxicity.

30 edical applications by reducing the possible cytotoxicity.

31 including oligomerization, fibrillation, and cytotoxicity.

32 ability and confer resistance to indisulam's cytotoxicity.

33 ts is an effective strategy to enhance Taxol cytotoxicity.

34 of sAML cell growth, and enhancement of DNR cytotoxicity.

35 ducing mTORC1 signaling, thus evoking little cytotoxicity.

36 beta oligomerization, amyloid formation, and cytotoxicity.

37 ide-induced H2O2 accumulation and associated cytotoxicity.

38 ing was achieved in vitro with no detectable cytotoxicity.

39 1 depletion abrogates PARP-inhibitor-induced cytotoxicity.

40 secretion of effector proteins and HeLa cell cytotoxicity.

41 de the most accurate quantification of honey cytotoxicity.

42 vitro as well as apoE4 potentiation of Abeta cytotoxicity.

43 target cells, including complement-dependent cytotoxicity, Ab-dependent cellular cytotoxicity, and Ab

44 The boron compounds 3 and 4 have shown low cytotoxicity activity in cell line A-431 and low green s

45 cells, and had minimal complement-dependent cytotoxicity activity similar to that of the negative co

46 d moderate antibody-dependent, cell-mediated cytotoxicity activity was demonstrated.

47 gp120 with high antibody-dependent cellular cytotoxicity (ADCC) activity.

48 ies that mediate antibody-dependent cellular cytotoxicity (ADCC) against avian influenza virus subtyp

49 riments and antibody-dependent cell-mediated cytotoxicity (ADCC) assays indicate that this protection

50 Moreover, antibody-dependent cell-mediated cytotoxicity (ADCC) assays revealed that the cell surfac

51 eatment via antibody-dependent cell-mediated cytotoxicity (ADCC) has been little studied.

52 Antibody-dependent cellular cytotoxicity (ADCC) may be an important component of pro

53 Ab-dependent cellular cytotoxicity (ADCC) responses are of growing interest in

54 est in utilizing antibody-dependent cellular cytotoxicity (ADCC) to eliminate infected cells followin

55 V1V2 responses, antibody-dependent cellular cytotoxicity (ADCC), and low-titer tier 1B and tier 2 ne

56 cantly decreases antibody-dependent cellular cytotoxicity (ADCC), whereas terminal alpha2,6-sialylati

57 uces HA-specific antibody-dependent cellular cytotoxicity (ADCC)-mediating antibodies.

58 eted by antibody-dependent cellular-mediated cytotoxicity (ADCC).

59 ility to mediate antibody-dependent cellular cytotoxicity (ADCC).

60 ted, PTX+TET/iRGD LPNs presented the highest cytotoxicity against A2780/PTX cells and effectively pro

61 drugs, explaining their better 24 h in vitro cytotoxicity against human glioblastoma U87 cell line.

62 n, help for CD8(+) T and B cells, and direct cytotoxicity against infected cells.

63 ies towards Hsp70 and Abl, and display lower cytotoxicity against leukemia cells compared to those of

64 CD7 CAR T cells produced robust cytotoxicity against malignant T-cell lines and primary

65 cid LpxC inhibitors, exemplified by 1, where cytotoxicity against mammalian cell lines was reduced, s

66 gainst murine erythrocytes, as well as their cytotoxicity against mammalian cells.

67 60 cell line screen and relatively selective cytotoxicity against melanoma cells.

68 bacterial activity against MRSA and MSSA and cytotoxicity against NCI-H460, MCF-7 and HeLa.

69 ipt 1 (LLT1) interaction in NK cell-mediated cytotoxicity against normal human articular chondrocytes

70 ancer cell lines, while demonstrating little cytotoxicity against normal mobilized peripheral blood p

71 illoma virus (HPV) 16 E7 oncoprotein induces cytotoxicity against peptide-expressing targets in vivo,

72 (Pr20M) directed antibody-dependent cellular cytotoxicity against PRAME+HLA-A2+ leukemia cells and wa

73 has garnered attention due to their natural cytotoxicity against tumor cells and safety upon adoptiv

74 These cells have reduced cytotoxicity against tumor cells, and mice with NFATc1-d

75 Rosemary has shown selective cytotoxicity against V-C8 cells (IC50 17 microg/ml) comp

76 ule compounds called G4 ligands often causes cytotoxicity, although the potential medicinal impact of

77 containing ChR2 or YFP gene and subjected to cytotoxicity analysis.

78 It was shown that complement-dependent cytotoxicity and Ab-dependent cellular cytotoxicity favo

79 in 21 (IL-21), which induces direct lymphoma cytotoxicity and activates immune effector cells, to the

80 drug concentrations, and biological effects (cytotoxicity and anti-migration) on drug-naive recipient

81 we demonstrate that DOCK8 regulates NK cell cytotoxicity and cytokine production in response to targ

82 tin-like receptor (CTLR) triggering cellular cytotoxicity and cytokine secretion upon high-affinity i

83 sed tumor-infiltrating T-cell activation and cytotoxicity and decreased the frequency of immunosuppre

84 e inhibitor (ouabain) potentiated EA-induced cytotoxicity and direct Na(+) loading by gramicidin-A ca

85 drug delivery nanocarriers due to their low cytotoxicity and facile surface functionalization.

86 The films were then studied for cytotoxicity and found to have high cell viability befor

87 Moreover, gladiolin displayed low mammalian cytotoxicity and good activity against several M. tuberc

88 expose underlying mechanisms of nanomaterial cytotoxicity and guide the design of safer nanomedical t

89 h treatment with 100-1000nM PTX), and caused cytotoxicity and inhibited migration of Recipient cells.

90 regulates gene expression and stress-induced cytotoxicity and is required in early embryogenesis thro

91 Here the authors show NFATc1 controls the cytotoxicity and metabolic switching of activated CD8(+)

92 HSPCs produced T cells with antigen-specific cytotoxicity and near-complete lack of endogenous TCR Vb

93 Rpn11 upstream of 20S proteasome to enhance cytotoxicity and overcome proteasome inhibitor resistanc

94 that they mediate graft rejection via direct cytotoxicity and priming of alloreactive T cells.

95 lla meneghiniana as a test subject to assess cytotoxicity and pro-inflammatory reactions to diatom-bi

96 y escape from macrophages uptake, and reduce cytotoxicity and proinflammation.

97 We herein assess the cytotoxicity and radiation dosimetry for (68)Ga-NOTA-UBI

98 at replicated efficiently but exhibited less cytotoxicity and reduced antitranscriptional activities,

99 e, NK92mi, resulted in inhibition of NK cell cytotoxicity and reproduced other aspects of the CHS cel

100 n dispersed in phosphate-buffered saline for cytotoxicity and senescence-associated beta-galactosidas

101 Histones released during influenza induced cytotoxicity and showed strong binding to platelets with

102 Compounds 1 and 2 exhibited moderate to weak cytotoxicity and significant inhibitory activity against

103 e evidence that poly GA is a key mediator of cytotoxicity and that cross-talk between DPR proteins li

104 rginine availability is a determinant of GBS cytotoxicity and that the pathway between stringent resp

105 ted cells showed a protective effect against cytotoxicity and viral replication in HIV-1-infected mac

106 ependent cytotoxicity, Ab-dependent cellular cytotoxicity, and Ab-dependent cellular phagocytosis.

107 re assessed for their size, charge, in vitro cytotoxicity, and capacity to transfect human bone marro

108 These particles show no cytotoxicity, and in vitro nanomolar irreversible activi

109 uction of TNF and IFNgamma, elevated natural cytotoxicity, and increased antibody-dependent cellular

110 er inflammation and MAIT cell activation and cytotoxicity, and increased the MAIT cell frequency amon

111 dies mediate functions such as phagocytosis, cytotoxicity, and maintenance of immune homeostasis.

112 rrelations were observed among genotoxicity, cytotoxicity, and NAC thiol reactivity for all disinfect

113 nd proliferation, induction of apoptosis and cytotoxicity, and up-regulation of the type 1 interferon

114 CD4(+) T cells restrains Runx3 functions and cytotoxicity; and STAT3 restrained cytotoxic gene expres

115 PAC cytotoxicity appears somewhat less than RAC, the standar

116 Our findings establish reduced cytotoxicity as a key mechanism by which tumor PD-L1 sup

117 Fluids containing nicotine exerted cytotoxicity as demonstrated by increased levels of LDH,

118 e cell and to the lungs, as evidenced by the cytotoxicity assay and analyses of the injury markers in

119 iazol-2-yl]-2,5-diphenyltetrazolium bromide) cytotoxicity assay revealed that Sf9 cells expressing CY

120 Enzyme-linked immunospots, cytotoxicity assays as well as adoptive transfer in NOD/

121 Natural killer (NK)-cell cytotoxicity assays can quickly screen for all of these

122 ate drug safety in a regime that the current cytotoxicity assays cannot cover and be generally applie

123 Viability/cytotoxicity assays indicate dose-dependent cytotoxic ef

124 Cytotoxicity assays suggest that toxicity is a property

125 Safety of drugs is regularly evaluated using cytotoxicity assays that measure cell death.

126 Using NK cell activation and NK cytotoxicity assays, we compared ADCC-mediating antibodi

127 ive to CMV peptides in IFN-gamma release and cytotoxicity assays.

128 bolished the inhibitory function of Ly49A in cytotoxicity assays.

129 ThCTL also express more cytotoxicity-associated genes including perforin and gra

130 The absence of cytotoxicity at physiologic expression levels suggests v

131 Cytotoxicity at the early stage was investigated on twen

132 er RNA or pharmacologic interference induced cytotoxicity both in vitro and in vivo.

133 No changes were produced in cytotoxicity, but the anti-inflammatory activity slightl

134 constituent chemicals were tested for their cytotoxicity by colony formation assay in cells of diffe

135 hocytes and demonstrate that T1-IFN augments cytotoxicity by inducing rapid phosphorylation of STAT4,

136 senescent, but not dividing, fibroblasts to cytotoxicity by natural killer cells.

137 LA2G16 as a host factor that is required for cytotoxicity by rhinoviruses, which cause the common col

138 luded those that investigated mammalian cell cytotoxicity, C. parvum proliferation inhibition in vitr

139 lates (EC50: 0.0014-0.0028 muM) with minimal cytotoxicity (CC50: 39.0 muM).

140 es tumor cell lysis via complement-dependent cytotoxicity (CDC) and attracts and activates cytotoxic

141 tibodies, complement-dependent cell-mediated cytotoxicity (CDCC) and complement-dependent cell-mediat

142 f DNA repair enzymes in trimethoprim-induced cytotoxicity clearly indicates that different amounts an

143 LCPM from PU-CNT shows significantly higher cytotoxicity compared to PU which could be attributed to

144 cells use different signaling mechanisms for cytotoxicity compared with other cytotoxic lymphocytes.

145 Finally, we showed that this cytotoxicity could be abrogated using CME inhibitors or

146 NK/CD8+ T-cell cytotoxicity could play a role in determining Chagas dis

147 Their in-house cytotoxicity data convey an important message that both

148 Thus, mandelalide cytotoxicity depends on basal metabolic phenotype; cells

149 Transactivator-mediated cytotoxicity depends on DNA binding, but can be overcome

150 We hypothesize that the enhanced cytotoxicity derives from RF-facilitated drug transport

151 ariant-dependent intracellular K(+) loss and cytotoxicity does not drive kidney disease progression.

152 We report here the synthesis, assembly and cytotoxicity evaluation of self-assembling hybrid prodru

153 ndent cytotoxicity and Ab-dependent cellular cytotoxicity favored a membrane-proximal epitope, wherea

154 While the primary mechanism of cytotoxicity for 1 was consistent with ion leakage, we f

155 The cytotoxicity for human peripheral blood lymphocytes is e

156 Compound 1 exhibited potent in vitro cytotoxicity (GI50 0.55 +/- 0.04 microM) and in vivo ant

157 profile (including CCR2 and CCR5), profound cytotoxicity (Granzyme B and CD107A), resistance to apop

158 l linkers have shown a significant effect on cytotoxicity, growth and cytokine response, thus warrant

159 h high Top1 inhibitory activities and potent cytotoxicities in human cancer cell cultures and reduced

160 tion, oxidative phosphorylation, and induced cytotoxicity in a panel of AML cell lines.

161 The role of cytotoxicity in accumulating autophagosomes (representin

162 ulation and pharmacologic inhibition induced cytotoxicity in all MCL models.

163 PF-06747143 also induced cytotoxicity in AML cells via Fc-effector function.

164 NTPs, we show here that SAMHD1 reduces Ara-C cytotoxicity in AML cells.

165 ar. (BVr) roots were combined and tested for cytotoxicity in CaCo-2 colon cancer cells.

166 50 nm SiNPs did not induce acute significant cytotoxicity in corneal endothelial cells at concentrati

167 The enhanced cisplatin cytotoxicity in histone H4 knockdown cells was associate

168 showed that all pectic samples reduced Stx2 cytotoxicity in HT29 cells, as measured by the reduction

169 d cellular impermeability but did not impact cytotoxicity in macrophages.

170 T) FAM46C overexpression induces substantial cytotoxicity in multiple myeloma cells.

171 ral-mediated ChR2 overexpression might cause cytotoxicity in NRVM cultures, which could be alleviated

172 activity of APOL1 and drives APOL1-mediated cytotoxicity in overexpression systems.

173 We observe enhanced cytotoxicity in oxidizing-agent treated pol beta express

174 ide/siRNA complexes did not show significant cytotoxicity in selected cell lines.

175 s via heteromeric TRPC4/C1 channels to cause cytotoxicity in some types of cancer cell but not normal

176 ing by gramicidin-A caused Pico145-resistant cytotoxicity in the absence of EA.

177 Moreover, they did not show any significant cytotoxicity in the dark or under irradiation on nontumo

178 iferation, decreased apoptosis and increased cytotoxicity in the presence of immunosuppressive ascite

179 Acute cytotoxicity in uroepithelial cells triggered by covR-de

180 nstrated no antibody-dependent cell-mediated cytotoxicity in vitro against Daudi cells with cynomolgu

181 and accessible assays for measuring honey's cytotoxicity in vitro, we found honey is cytotoxic towar

182 l diabetogenicity or beta cell resistance to cytotoxicity in vitro.

183 less polar analogues of curcumin have potent cytotoxicity in vitro.

184 ) T cells also resisted chemotherapy-induced cytotoxicity in vivo and underwent significant expansion

185 Cellular cytotoxicity is essential for the elimination of virus-i

186 nding how decidual CD8(+) T cell (CD8(+) dT) cytotoxicity is regulated and how these cells integrate

187 y with thermal ablation or thermally-induced cytotoxicity, limited access of the drug to tumor loci i

188 memory maturation subtype and expressed the cytotoxicity marker CD107a.

189 Eighteen of the new compounds had cytotoxicity mean-graph midpoint (MGM) GI50 values in th

190 to treat cancer and its subsequent impact on cytotoxicity measurements and assays have not been inves

191 lication on macrophage function, we assessed cytotoxicity, nitric oxide or reactive oxygen species pr

192 The in vitro determination of reactivity, cytotoxicity, NLRP3 ATPase inhibition, and antipyroptoti

193 n of nonprotein sulfhydryl and occurrence of cytotoxicity (observable by routine histology) in the OM

194 This implies that the cytotoxicity observed comes from the entire complex and

195 PX), which reduces ER stress, alleviated the cytotoxicity of 5-aza.

196 of both alloforms and also to the increased cytotoxicity of Abeta42.

197 The newly created nATC retains the cytotoxicity of ABX and CD20 affinity of rituximab in vi

198 have been proposed to play a key role in the cytotoxicity of amyloid fibrils and the pathogenesis of

199 alized, virus-like particles-potentiates the cytotoxicity of Ara-C in AML cells.

200 Thus, despite the known cytotoxicity of cobalt and zinc ions, these results sugg

201 ction is dominated by signal blocking or the cytotoxicity of Fc-driven innate immune effector functio

202 bination of factors crucial for the enhanced cytotoxicity of GAELs opens new avenues to develop poten

203 Although the cytotoxicity of HU may significantly contribute to its t

204 gamma exposure during activation reduced the cytotoxicity of human-origin type 1 diabetes-relevant au

205 chemical profile, antioxidant activity, and cytotoxicity of hydroethanolic extracts of green Coffea

206 lar carcinoma), were used to investigate the cytotoxicity of indospicine and its metabolite 2-aminopi

207 sometimes physical targeting with the potent cytotoxicity of ionising radiation.

208 the transcription factor NFATc1 controls the cytotoxicity of mouse cytotoxic T lymphocytes.

209 s essential for efficient activation and for cytotoxicity of NK cells because it initiates the assemb

210 Exposure to IL12 rescued the cytotoxicity of NK cells but also led to the emergence o

211 underlying biochemical cause of the impaired cytotoxicity of NK cells in patients with CHS.

212 ptive NK-92 cell therapy block anti-leukemia cytotoxicity of NK-92 cells and other NK-92 cell functio

213 cancer therapy, as well as understanding the cytotoxicity of pathogenic assemblies.

214 vated by this issue, we focused on screening cytotoxicity of polymers widely used for the layer-by-la

215 s, leading us to determine the structure and cytotoxicity of protein segments composing the amyloid s

216 of exosomes on intercellular drug transfer, cytotoxicity of PTX on Donor cells and cytotoxicity of P

217 sfer, cytotoxicity of PTX on Donor cells and cytotoxicity of PTX-containing exosomes on Recipient cel

218 ent nitrotyrosine formation and abrogate the cytotoxicity of RNS against phoQ Salmonella, presumably

219 echin gallate (EGCG) effectively reduces the cytotoxicity of the Alzheimer's disease beta-amyloid pep

220 ular targeting selectivity and p53-dependent cytotoxicity of the clinical prototype ATSP-7041.

221 structure changes during stability test and cytotoxicity of the extracts against Vero cells were eva

222 However, the inherent cytotoxicity of the rabies largely prevents its implemen

223 The results suggest that cytotoxicity of these peptides stems from their (moderat

224 The synergistic cytotoxicity of tyramine and histamine should be taken i

225 Moreover, the cytotoxicity of XWL-1-48 is more potent than its congene

226 cells, which allowed prolonged and elevated cytotoxicity of YM155.

227 Cytotoxicity of zinc- and copper-chlorophylls extracts w

228 t the potential genotoxicity, as well as the cytotoxicity, of toxic species generated in cell culture

229 not fully known, there is evidence of their cytotoxicity on cells belonging to the oral cavity.

230 particles are investigated in terms of their cytotoxicity on suspension and adherent cells to prove t

231 ment of cancer, having the ability to impart cytotoxicity only to specific tumor types.

232 Although all 3 mAbs potently neutralized cytotoxicity, only SA-15 and SA-17 significantly inhibit

233 vitro characteristics of growth, adherence, cytotoxicity, or serum resistance, though it profoundly

234 neutralization, antibody-dependent cellular cytotoxicity, phagocytosis, and virion capture).

235 Cytotoxicity profiling was performed by using a colorime

236 terial metabolism underpins fluoropyrimidine cytotoxicity, providing a paradigm for unraveling bacter

237 associated with antibody-dependent cellular cytotoxicity rather than EGFR pathway inhibition.

238 bserved that inducible IFN-gamma and natural cytotoxicity receptor (NCR) expression in a specific sub

239 es, and robustly fits data with outliers and cytotoxicity-related signal loss.

240 neered bNAb variants, antibody-mediated cell cytotoxicity reporter assays, and Fcgamma receptor-defic

241 While a cytotoxicity response from a polyfunctional T cell activ

242 ted to tier 1 viruses and antibody-dependent cytotoxicity responses (ADCC) after DC-targeting boosts.

243 d high levels of antibody-dependent cellular cytotoxicity responses and HIV-1-neutralizing antibodies

244 growing evidence that an important aspect of cytotoxicity results from treatment-induced metabolic pe

245 Inducing differentiation of myeloblasts, not cytotoxicity, seems to drive the clinical efficacy of en

246 e related to natural killer (NK)/CD8+ T-cell cytotoxicity, separated the 2 groups.

247 hus making them more prone to Ca(2+)-induced cytotoxicity.SIGNIFICANCE STATEMENT In the inner ear, se

248 matory (absent in S. bellinii mycelia) and a cytotoxicity similar (sometimes superior) to its fruitin

249 In vitro cytotoxicity studies demonstrated that (19)F-FCP has an

250 osomes (t-L) was assessed by cell uptake and cytotoxicity studies in the alphavbeta6 positive cells l

251 Cytotoxicity studies reveal that the alt-PASs are nontox

252 -alpha fibrillation of PSMalpha3 facilitated cytotoxicity, suggesting that this assembly mode underli

253 and spatial correlation between PrP(Sc) and cytotoxicity suggests the contribution of host factors.

254 In vitro cytotoxicity test of the Mg extract via human vascular e

255 sitive and no less specific compared with NK cytotoxicity testing for screening for genetic HLH and s

256 assay is suitable for cell proliferation and cytotoxicity testing.

257 Electrical and cytotoxicity tests showed no negative impact on human he

258 he liver had higher levels of activation and cytotoxicity than MAIT cells from blood (P < .0001).

259 pecific fractions showed reproducibly higher cytotoxicity than other fractions as well as the unsepar

260 in-resistant cells more resistant to NK cell cytotoxicity than parental cells.

261 wn to be selective for Cys181 and have lower cytotoxicity than the approved NNRTI drugs efavirenz and

262 Vgamma9Vdelta2 cells displayed potent cytotoxicity through TCR-dependent and independent mecha

263 notypic changes enhancing drug transport and cytotoxicity, thus providing a potential baseline for cl

264 were evaluated for transfection efficacy and cytotoxicity to a range of human HCC cells as well as he

265 over other anti-apoptotic proteins, possess cytotoxicity to cancer cell lines, and induce hallmarks

266 ced the PD-L1 Ab effect in enhancing NK cell cytotoxicity to cisplatin-resistant cells.

267 ted similarly effective complement-dependent cytotoxicity to GM2-expressing cancer cell line MCF-7.

268 c cancer cells (HGC27 and SGC7901), but less cytotoxicity to non-malignant gastric epithelial cells G

269 utively activated STAT3 cancer cells without cytotoxicity to normal cells with dormant STAT3.

270 le formulation, while maintaining comparable cytotoxicity to those of Abraxane and solvent-dissolved

271 l effects on Candida albicans ATCC90028, the cytotoxicity toward human dental pulp cells (HDPCs), and

272 e show that Y3 exhibits selective and potent cytotoxicity toward human T-cell leukemia Jurkat cells c

273 ivity against several lymphoma types and low cytotoxicity toward normal cells.

274 le in many diseases, primarily through their cytotoxicity toward nucleated cells and their ability to

275 icity in living cells, exhibited substantial cytotoxicity towards HeLa cells, and was a highly sensit

276 Cytotoxicity, transepithelial electrical resistance (TEE

277 iched for diverse immune functions including cytotoxicity, viral response, B cell, platelet, neutroph

278 Cytotoxicity was evaluated in green monkey kidney epithe

279 otected fibroblasts from 5-aza only when the cytotoxicity was examined cell autonomously.

280 Cytotoxicity was mediated by the intrinsic apoptotic pat

281 Fecal water cytotoxicity was not modified by HPDs, but was associate

282 viability tests (0.1 mug/mL), at which acute cytotoxicity was not observed.

283 osic acid and gallic acid, but the selective cytotoxicity was not observed.

284 conventional, but with the addition of DDP, cytotoxicity was similar and considerably less than expe

285 Cytotoxicity was the result of ionic and nonionic Cu fra

286 oteins such as PD-1 to evade immune-mediated cytotoxicity, we did a trial of the anti-PD-1 antibody n

287 rescribed to hybrubin A except for a lack of cytotoxicity, we further profiled this unique alkaloid a

288 To explore molecular mechanism of their cytotoxicity, we have designed and tested a number of ne

289 ch the stringent response leads to increased cytotoxicity, we performed transcriptome sequencing (RNA

290 f autophagy, rapamycin-induced apoptosis and cytotoxicity were blocked in STAT1-deficient cells but r

291 which bind the oligomers and neutralize the cytotoxicity were exclusively identified in the serum of

292 on viability, proliferation, apoptosis, and cytotoxicity were monitored.

293 and NK cell-mediated antibody-dependent cell cytotoxicity were present in aleumtuzumab-treated CMV se

294 lity of cisplatin-resistant cells to NK cell cytotoxicity when neutralizing antibody of PD-1 or PD-L1

295 e weak inhibitors of the Icat and EA-induced cytotoxicity whereas a potent inhibitor of TRPC4/C1 chan

296 Both BioRoot and MTA Fillapex showed cytotoxicity which reduced at higher dilutions.

297 unction of IL-17A in promoting CD8(+) T cell cytotoxicity, which may have broad implications in other

298 ated over the last two decades express their cytotoxicity with a mechanism of action involving, among

299 mpounds induce tumour cell death and enhance cytotoxicity with chemotherapeutic agents and targeted c

300 promise in cancer treatment by coupling drug cytotoxicity with thermal ablation or thermally-induced