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1 n, and dentine matrix resorption without any cytotoxicity.
2 ase suppresses neutrophil-induced tumor cell cytotoxicity.
3 mune synapse, lytic granule trafficking, and cytotoxicity.
4 macrophage cells, and in some cases, minimal cytotoxicity.
5 HL5, to require hRpn13 Pru and not UCHL5 for cytotoxicity.
6 s were shown to prevent aSyn aggregation and cytotoxicity.
7 ced physicochemical properties and low human cytotoxicity.
8   Among tested species, P. disiens exhibited cytotoxicity.
9 NK-induced necrosome signaling and resultant cytotoxicity.
10 mulation with cytokine production and direct cytotoxicity.
11 cytoskeleton significantly inhibited NK cell cytotoxicity.
12 whereas inhibiting TRPV3 exacerbated ERS and cytotoxicity.
13 anule polarization to the immune synapse and cytotoxicity.
14 olobenzodiazepines toward DNA and thus their cytotoxicity.
15  values in solution, strongly supports their cytotoxicity.
16  with longer alkyl chains enhancing analogue cytotoxicity.
17 g and found out that these peptides mediated cytotoxicity.
18  to be safe, preventing further GAG loss and cytotoxicity.
19 r serine proteases, and do not show relevant cytotoxicity.
20 sphorylation and reduces its aggregation and cytotoxicity.
21 tor functions, such as Ab-dependent cellular cytotoxicity.
22  proresolving mediators to influence NK cell cytotoxicity.
23 spectively, and without measurable host cell cytotoxicity.
24 the composite material does not advocate any cytotoxicity.
25 gative bacteria without inducting observable cytotoxicity.
26 ced the RFP intensity due to lactose-induced cytotoxicity.
27 nd genetic mechanisms influencing CAR T-cell cytotoxicity.
28 l release from hTF as potentially related to cytotoxicity.
29  analyse annexin A5 effects on Abeta-induced cytotoxicity.
30 e tolerance and lower CD8(+) T-cell-mediated cytotoxicity.
31  in deoxyuridine mitigated ER stress-induced cytotoxicity.
32 ) T cells, which mediated antibody-dependent cytotoxicity.
33  cancer cells promotes T cell-induced cancer cytotoxicity.
34 th specific GRNs exacerbating TDP-43-induced cytotoxicity.
35 d its capacity to rescue mitomycin C-induced cytotoxicity, accounting for two infrequent onset-hasten
36 mAbs endowed with Ab-dependent cell-mediated cytotoxicity activity.
37 exhibited strong antibody-dependent cellular cytotoxicity (ADCC) activity in a reporter assay.
38  with measurable antibody-dependent cellular cytotoxicity (ADCC) activity.
39 ivities, such as antibody-dependent cellular cytotoxicity (ADCC) and phagocytosis, are mediated by Fc
40                            Ab-dependent cell cytotoxicity (ADCC) is a common effector function for no
41             Antibody-dependent cell-mediated cytotoxicity (ADCC) is an important mechanism of action
42             Antibody-dependent cell-mediated cytotoxicity (ADCC) is an important pathway responsible
43 and mediate antibody-dependent cell-mediated cytotoxicity (ADCC) may play a dominant role in protecti
44 e impact of the host antibody (AB)-dependent cytotoxicity (ADCC) on HCMV is still unclear.
45  of HIV-specific antibody-dependent cellular cytotoxicity (ADCC) responses with protection from and d
46                  Antibody-dependent cellular cytotoxicity (ADCC) was measured by a bioluminescence re
47 ility of inducing Ab-dependent cell-mediated cytotoxicity (ADCC), complement deposition, and compleme
48  to mediate antibody-dependent cell-mediated cytotoxicity (ADCC), during HCV infection is poorly defi
49 ting in crippled antibody-dependent cellular cytotoxicity (ADCC).
50 ity but enhanced antibody-dependent cellular cytotoxicity (ADCC).
51 ptors to mediate antibody-dependent cellular cytotoxicity (ADCC).
52 e susceptible to antibody-dependent cellular cytotoxicity (ADCC).
53 ers were synthesized and tested for in vitro cytotoxicity against a panel of cancer cell lines.
54 ticles exhibited enhanced ultrasound-induced cytotoxicity against both prostate cancer cell lines.
55        These findings imply that CD8+ T cell cytotoxicity against both tumor and viral antigens as we
56 hocytes yields a pool of cells with enhanced cytotoxicity against cancer cells.
57  Staphylococcus aureus MIC = 5 mg/mL) and no cytotoxicity against carcinogenic and non-tumour primary
58 86, IC(50) 0.7 nM, HDAC1), 25-fold increased cytotoxicity against five human cancer cell lines, and u
59     These novel ADCs displayed sub-nanomolar cytotoxicity against HER2-expressing cancer cells, while
60 protein output assessment (delta-toxin), and cytotoxicity against human keratinocytes (HaCaT).
61 at show enhancements in selective anticancer cytotoxicity against MCF-7 breast cancer cells in vitro.
62 AGT1 inhibitory activity, CPPB does not show cytotoxicity against normal cells and a series of cancer
63 y blasts from AML patients, while showing no cytotoxicity against normal PBMCs, NIH3T3, and HEK293 ce
64 reducible crosslinked MLNPs exhibited higher cytotoxicity against TNBC and breast cancer cells which
65 erase (NAMPT), synergizes with MMS to induce cytotoxicity and Aag(-/-) cells are resistant to this co
66 lyses revealed that these fibrils showed low cytotoxicity and affinity to plasma membrane.
67                          Additionally, their cytotoxicity and anti-inflammatory potential were assess
68  well as biological investigations including cytotoxicity and apoptotic assays, and quantitative poly
69 This leads to substantial levels of cellular cytotoxicity and breakdown of tight junctions between ce
70 ting a link between mechanisms of CAR T-cell cytotoxicity and cancer genetics.
71 large clones overexpress genes implicated in cytotoxicity and characteristic of effector memory T cel
72 protection of neurons from cisplatin-induced cytotoxicity and CIPN in mice.
73 lling to promote antibody-dependent cellular cytotoxicity and complement-dependent cytotoxicity throu
74 ificantly reduced G9Calpha(-/-)CD8(+) T-cell cytotoxicity and dendritic cell-induced proliferation, t
75 ad, soft bread and biscuits), evaluate their cytotoxicity and determine their suitability as function
76                                              Cytotoxicity and haemolysis of the progenitor peptide is
77 exes, we used a series of time-kill studies, cytotoxicity and hemolysis assays, as well as whole-cell
78 ddition, these novel carbons have negligible cytotoxicity and high biocompatibility for human cells,
79 17-30)] through in silico analysis to reduce cytotoxicity and improve the anti-inflammatory activity
80 wed, with their structures, cancer cell line cytotoxicity and in vivo antitumor activity, structure-a
81 ogically cold melanoma to both induce direct cytotoxicity and increase immune responses in the contex
82 pendently of both O(6)-methyl guanine adduct cytotoxicity and MUTYH-dependent glycosylase activity.
83 d in brain plaques are viewed as triggers of cytotoxicity and neuroinflammation in Alzheimer disease
84 formed molecular biology studies revealed no cytotoxicity and no influence of engineered carbon nanom
85 line, RTgill-W1, to investigate pH-dependent cytotoxicity and permeation of IOCs across cultured epit
86 m infused clusters with higher expression of cytotoxicity and proliferation genes.
87 ying tumors and virus-infected cells through cytotoxicity and rapid cytokine production.
88 effect of cottonseed ethanol extracts on the cytotoxicity and regulation of anti-inflammatory tristra
89 erivatives have been studied regarding their cytotoxicity and virus-inhibiting activity against influ
90 block the M2 proton channel and show reduced cytotoxicity and zebrafish-embryo toxicity.
91 ides have continuously cited minimal to zero cytotoxicity and, where tested, sufficient drug release
92 ludes in vitro optimization to maximize drug cytotoxicity and/or synergistic drug interactions.
93  the multidrug-resistant K1 strain, in vitro cytotoxicity, and cardiotoxicity and were addressed thro
94 241, to restore anti-MM immunity, enhance MM cytotoxicity, and improve patient outcome.
95 ased rates of Mn membrane transport, reduced cytotoxicity, and increased selectivity for Mn over calc
96 in vitro activity, a selectivity window over cytotoxicity, and microsomal metabolic stability.
97 ic antibody-dependent phagocytosis, cellular cytotoxicity, and natural killer cell activation were as
98  to determine of nutritional value, in vitro cytotoxicity, and oxidative stress parameters in cells o
99 pairments with increased amyloidogenesis and cytotoxicity, and this dimer was then used in a screenin
100 s against intestinal inflammation, potential cytotoxicity, anti-inciting action, and suppression of a
101  subset of benzodiazepines exacerbated p-tau cytotoxicity apparently via enhancing p-tau aggregation.
102 nse and tumour necrosis factor (TNF)-induced cytotoxicity are dominant sub-phenotypes.
103              While NR-160 displayed only low cytotoxicity as a single agent against leukemia cell lin
104 curate irinotecan drug loadings and the same cytotoxicity as unformulated irinotecan.
105 ap and coat tumor cells and shield them from cytotoxicity, as mediated by CD8(+) T cells and natural
106  analyzed by focal expansion assay and CD107 cytotoxicity assay.
107                                 We have used cytotoxicity assays and a variety of biophysical approac
108  Standard degranulation and chromium release cytotoxicity assays confirm the ability of cryopreserved
109                                  Comparative cytotoxicity assays of 41 MTM(ox) analogues using E-twen
110                                              Cytotoxicity assays on primary clinical DS-ALL samples d
111 sis, with biological activity as assessed by cytotoxicity assays performed in adenocarcinoma human al
112                                              Cytotoxicity assays show good correlation at the outer l
113         Biocompatibility was evaluated using cytotoxicity assays utilising L-929 cell line.
114 he present study, using liposome-leakage and cytotoxicity assays, LC-MS/MS-based proteomics, and CCF-
115                Using protein aggregation and cytotoxicity assays, we found that the dissociation of t
116 lene glycol), is demonstrated using standard cytotoxicity assays.
117  prescription drugs in p-tau aggregation and cytotoxicity assays.
118 ed effector functions as defined by in vitro cytotoxicity assays.
119 s often recommended because of the potential cytotoxicity associated with EdU during longer incubatio
120                           Antibody-dependent cytotoxicity became detectable 3 months posttransplantat
121  cells is associated with diminished natural cytotoxicity but enhanced antibody-dependent cellular cy
122 e of autophagy upregulated radiation-induced cytotoxicity but only modestly affected the levels of ce
123 contributed to both CD8+ and CD4+ CAR T cell cytotoxicity but was not required for in vitro or in viv
124 ne kinase inhibitors that inhibit CAR T-cell cytotoxicity by impairing T-cell signaling transcription
125 pulp fibroblasts (FP6) were used to evaluate cytotoxicity by incorporating MTT dye, and genotoxicity
126 es to the surface of cancer cells and induce cytotoxicity by peripheral blood mononuclear and enginee
127 iew, we discuss how NKDs that affect NK cell cytotoxicity can be approached in the clinic and laborat
128  power for downstream cancer, and assays for cytotoxicity can predict deleterious health effects.
129 atumumab, which, in addition to its inherent cytotoxicity, can be radiolabeled with tracers for imagi
130 lth problem in part as a result of extensive cytotoxicity caused by the infection.
131 (IC(50) = 0.27 muM), significantly decreased cytotoxicity (CC(50) = 156.8 muM), and low in vivo toxic
132 plement deposition, and complement-dependent cytotoxicity (CDC).
133 l cytotoxic effects, thus departing from the cytotoxicity-centric paradigm previously assigned to HDA
134 rable transfection efficacies but much lower cytotoxicities compared to the Lpf2k in vitro.
135    ALDC1 exhibited improved drug release and cytotoxicity compared to ALDC3 in vitro.
136 ternalization, transgene expression, and low cytotoxicity compared to commercial controls for several
137 al due to its reduced removal time and lower cytotoxicity compared to the other treatment options.
138                No significant differences in cytotoxicity comparing lidocaine-containing solutions we
139 f natural sunlight) decreased the calculated cytotoxicity contributed by dihaloacetonitrile-FP in mos
140 s such as high cellular internalization, low cytotoxicity, controllable pharmacokinetics and biodistr
141 efined DSA but negative complement-dependent cytotoxicity crossmatches were enrolled.
142 e water sorption (SOR), solubility (SOL) and cytotoxicity (CYTO) of experimental adhesives containing
143                                              Cytotoxicity data showed that TNBC cell lines are more s
144  PRMT5 activity synergistically enhances Gem cytotoxicity due to the accumulation of excessive DNA da
145 istone deacetylase HDAC3 inhibits CD8 T cell cytotoxicity early during activation and is required for
146                                           No cytotoxicity effect was observed in macrophages treated
147                                     The weak cytotoxicity encountered led us to perform an in vivo ex
148  strain HF_1994 displayed a striking lack of cytotoxicity, even exerting a cytoprotective effect on a
149                        Rather than impairing cytotoxicity, excess IL-18 acted on T lymphocytes to amp
150 tant resistance mechanism to T cell-mediated cytotoxicity for TNBC cells.
151 ncertain significance affecting a lymphocyte cytotoxicity gene or the perforin variant A91V was obser
152            In addition, CD8+ T cell-mediated cytotoxicity has not been linked to parasite killing.
153 especially its capacity for antigen-directed cytotoxicity, has become a central focus for engaging th
154 he assays conducted include, Ag-Phen induced cytotoxicity (IC(50) 4.5 muM at 72 h) and 2-fold ROS gen
155               Apart from its remarkably high cytotoxicity (IC(50) = 0.07-0.7 muM in different cancero
156  that alpha-syn aggregates attenuate NK cell cytotoxicity in a dose-dependent manner and decrease the
157 le in DNA repair, AAG-initiated BER promotes cytotoxicity in a process dependent on poly (ADP-ribose)
158                    aKG esters also conferred cytotoxicity in a variety of cancer types if their cell
159 matic evaluation of natural killer (NK) cell cytotoxicity in adult patients with secondary HLH.
160 ing how DNA damage response inhibitors cause cytotoxicity in cancer cells is crucial to their further
161 erapeutic intervention via increasing T cell cytotoxicity in cancer.
162 imary cells, potentiated gemcitabine and JQ1 cytotoxicity in cell culture, and Gem + TSA + JQ1 inhibi
163 ted alphaS-positive vesicular inclusions and cytotoxicity in cultured human neurons.
164 chemistry's recommendations as well as their cytotoxicity in different cancer models.
165 ains of MRSA and displayed as importantly no cytotoxicity in four mammalian cell lines.
166 A-approved PARP inhibitor, could enhance the cytotoxicity in HCC cells with a lower BRCA1 expression,
167 UV-A dosage decreased the aflatoxins-induced cytotoxicity in HepG2 cells, and no significant aflatoxi
168 CD56 in stimulating exocytosis and promoting cytotoxicity in human NK cells.
169 ility, prolonged drug release and remarkable cytotoxicity in human pancreatic cancer cell lines and K
170        ARGX-117 prevents complement-mediated cytotoxicity in in vitro models for autoimmune hemolytic
171 of aflatoxins in pure water and assesses the cytotoxicity in liver hepatocellular cells.
172 ylosoxidans isolates from CF patients induce cytotoxicity in macrophages, suggestive of a pathogenic
173  Formation of NBs alleviates TDP-43-mediated cytotoxicity in mammalian cells and fly neurons.
174 nfounding bovine serum amine oxidase-induced cytotoxicity in mechanistic studies of the roles of poly
175                        JAs possess selective cytotoxicity in mixed populations of cancer and normal c
176 wed that miR-124 protects against As-induced cytotoxicity in neural cells with concomitant suppressio
177 ressor, in As-induced ER stress response and cytotoxicity in neural cells.
178 strated implicated in blocking Abeta-induced cytotoxicity in neuronal cell cultures.
179 ecies (ROS) inducer, QD394, with significant cytotoxicity in pancreatic cancer cells.
180 P372-1 with PARP inhibition creates enhanced cytotoxicity in pancreatic cancer cells.
181 ical studies suggest that Amiodarone induces cytotoxicity in several types of cancer cells, thus maki
182  the landscape of microRNAs with significant cytotoxicity in the context of glioblastoma (GBM), we pe
183  enhanced both DOX-EDT-IONP permeability and cytotoxicity in the MDCK-MDR1-GBM co-culture model.
184 abolic (microsomal) stability, and promising cytotoxicity in three cancer cell lines (DU145, HeLa, A5
185               Furthermore, we assessed their cytotoxicity in various human tumor cell lines.
186 O4 and CEBPD knockdown improved CDDP-induced cytotoxicity in vitro and in vivo.
187  for bio-applications, we investigated their cytotoxicity in vitro as well as their utilization as su
188             The empty MLNPs did not show any cytotoxicity in vitro in 2D monolayers of MDA-MB-231 (tr
189 /-)) MEFs, but this blockade had no additive cytotoxicity in WT MEFs, suggesting the cytotoxicity is
190 y linked to a cationic polymer induce strong cytotoxicity, including reduced cellular viability and s
191 show that this pathway is required to resist cytotoxicity induced by the cytokines IFNgamma and TNF.
192 study provides mechanistic insights into the cytotoxicity instigated by KP372-1 and lays an essential
193 nsition metals have been employed, but their cytotoxicity is an issue and hence must be reduced, typi
194 ntify DNA damage, DNA repair, mutations, and cytotoxicity is broadly relevant to health.
195 tive cytotoxicity in WT MEFs, suggesting the cytotoxicity is due to MUTYH interactions with MNNG-indu
196                   It remains unclear whether cytotoxicity is RRV-dependent or driven solely by varian
197 lood lifespan, high drug loading and reduced cytotoxicity leading to better drug compliance.
198 Such polymorphism can dramatically influence cytotoxicity, leading to much interest in the conditions
199                                              Cytotoxicity, lytic granule exocytosis, and the phosphor
200 tiple targets, together with its outstanding cytotoxicity, make complex 1 a valuable candidate in the
201 e concentration (EC(50)) against Shiga toxin cytotoxicity measured in a cell protein synthesis assay.
202                                     Possible cytotoxicity mechanisms, such as DNA damage, DNA interca
203 sitive and 100 negative) were tested by cell cytotoxicity neutralization assay (CCNA), C. diff Quik C
204 d then prioritized and guided by cancer cell cytotoxicity, NMR-based SMART 2.0, and MS(2)-based molec
205                             Furthermore, the cytotoxicities of established drugs and other rhenium an
206           The PDT study revealed significant cytotoxicities of porphyrins with IC(50) values between
207                                 The in vitro cytotoxicity of (125)I-KX1 was assessed in 19 neuroblast
208  breaks, contributes strongly to the overall cytotoxicity of anthracyclines, and structures containin
209 ulnerabilities of the tumour, or enhance the cytotoxicity of anti-cancer drugs.
210            Thus, oligomerization reduces the cytotoxicity of arrestin-1 monomer, ensuring long-term p
211 us therapeutics directly linking Dox and TF, cytotoxicity of CDT resulted from nuclear entry by Dox,
212                Studies investigated in vitro cytotoxicity of Dox when combined with either Pgp inhibi
213                               We detected no cytotoxicity of Gd-lip in human liver cells including ca
214 d for the higher anti-proliferative activity/cytotoxicity of HE extracts on Caco-2 and HepG2 cells as
215            Thus, oligomerization reduces the cytotoxicity of high levels of arrestin-1 monomer.
216                     Significant pH-dependent cytotoxicity of individual IOCs, acidic fractions, and r
217 ate defense against pathogens through direct cytotoxicity of infected cells and are the predominant i
218 es that bound to TKO pRBCs, but there was no cytotoxicity of IVIg to TKO pRBCs.
219 metric properties, antioxidant capacity, and cytotoxicity of melanoidins were assessed.
220                                              Cytotoxicity of melatonin was carried out using both liv
221  review assesses, in the first instance, the cytotoxicity of MOFs (particularly those used for variou
222 ng ability, the effect on enamel surface and cytotoxicity of novel tooth-whitening formulations conta
223                              We modified the cytotoxicity of our nanoparticles to cancer cells by cha
224                                              Cytotoxicity of OWM sera to TKO PBMCs was significantly
225 cell culture models are widely used to study cytotoxicity of RRVs, but results have been contradictor
226                                 Finally, the cytotoxicity of so-obtained BRJ to human epithelial colo
227 l inhibition of MLK3 promotes activation and cytotoxicity of T cells.
228 zymes such as granzyme B, thus enhancing the cytotoxicity of T cells.
229 ion of immunosuppressive cells, the improved cytotoxicity of T lymphocytes, decreased inhibitory and
230  accumulation of genomic 8-oxodG and reduced cytotoxicity of TH588, in line with the notion that mito
231 ed genomic 8-oxodG correlated with increased cytotoxicity of TH588.
232 d inhibitor vemurafenib, which decreased the cytotoxicity of the drug in BRAF(V600E) melanoma cells.
233  transcription-blocking agents, and that the cytotoxicity of the G-quadruplex ligand pyridostatin inv
234  proliferation, and improved the synergistic cytotoxicity of treatment with the alkylating agent temo
235 g for predicting antiplasmodial activity and cytotoxicity of untested compounds.
236  temperature, can enhance Temozolomide (TMZ) cytotoxicity on a glioblastoma cell line (U87MG).
237 ve MEIS inhibitors (MEISi) with no predicted cytotoxicity or cardiotoxicity.
238  driven by HLA class I (essential for T-cell cytotoxicity) or class II (important for T-cell helper r
239       Our knowledge of amyloid formation and cytotoxicity originating from self-assembly of alpha-hel
240 class I and/or II >99%, complement-dependent cytotoxicity panel reactive antibody [CDC PRA+], C1q+) h
241 1 (G0, G1, G2, G0G0, G0G1, or G0G2) on known cytotoxicity phenotypes, including reduced viability, in
242 o a new generation with high solubility, low cytotoxicity, potent broad-spectrum sterilizing activity
243  RR aqueous emulsions were examined for cell cytotoxicity, proliferation, redox state and migration u
244 oxins, the structural features important for cytotoxicity remain unknown.
245                                     However, cytotoxicity remained high, and the absorption, distribu
246 nfected chicken cells, accompanied by marked cytotoxicity, requires the full-length protein.
247       Proposed mechanisms of kidney podocyte cytotoxicity resulting from APOL1 variant overexpression
248                                    Regarding cytotoxicity results, loaded particles had a good biocom
249  analysis, and assessment of aggregation and cytotoxicity revealed that the TTR segment inhibits Abet
250 ated with inherited defects in cell-mediated cytotoxicity, serves as a prototypical CSS for which the
251 infection of wastewaters increased mammalian cytotoxicity several orders of magnitude, with chloramin
252 Ss, including impairment of granule-mediated cytotoxicity, specific viral infections, excess IL-18, a
253           In this latter setting, lymphocyte cytotoxicity status is not known.
254                                              Cytotoxicity studies, clonogenic assay, flow cytometry a
255 th mild HT, which correlated well with their cytotoxicity studies.
256                                          The cytotoxicity study has shown that the treated melanin an
257    Thus, complexes 1-4 expressed much higher cytotoxicities than complexes 5 and 6.
258 anostructure architecture exhibits less cell cytotoxicity than conventional SNAs without a decrease i
259 and has greater in vitro complement-mediated cytotoxicity than rituximab.
260          The assembled dGAE shows more acute cytotoxicity than the soluble, non-aggregated form.
261 nable protection while minimizing epithelial cytotoxicity that can often accompany an inflammatory re
262 llular cytotoxicity and complement-dependent cytotoxicity through relief of immunosuppression.
263 ysis of FBIC efficacy included evaluation of cytotoxicity, tissue penetration, foam stability, temper
264 as conducted to evaluate in vitro fibroblast cytotoxicity to a solution of MMC (0.2 mg/ml) and 1% pre
265 -1 micelles were observed to bind and induce cytotoxicity to cancer cells through interaction with CC
266 otericin B doses, while exhibiting much less cytotoxicity to healthy macrophages than amphotericin B.
267                                     However, cytotoxicity to immune cells has accompanied the use of
268 cretion system (T3SS) substrate that induces cytotoxicity to mammalian cells.
269 t-bound complexes and correlate the reported cytotoxicity to the peptide oligomeric structures and th
270 did not reveal anti-inflammatory capacity or cytotoxicity to the tested cell lines.
271 ig IgM/IgG binding, and complement-dependent cytotoxicity to wild-type (WT), alpha1,3-galactosyltrans
272     Moreover, the cryogels showed negligible cytotoxicity toward murine fibroblasts and prevented act
273                         EMD exhibited strong cytotoxicity toward various human lung cancer cell lines
274 -specific TCRs showed IFNgamma secretion and cytotoxicity towards EBV-LMP2-expressing malignant cell-
275 ound that narciclasine displays preferential cytotoxicity towards PEL at low nanomolar concentrations
276 cquired tetracycline resistance and enhanced cytotoxicity towards red blood cells.
277                                              Cytotoxicity, transcriptional, and functional properties
278 id not exert significant oxidative stress or cytotoxicity upon incubating with differentiated SHSY5Y
279 estigated druggable mechanisms of CAR T-cell cytotoxicity using >500 small-molecule drugs and genome-
280                       We assessed CAR-T cell cytotoxicity using a carboxyfluorescein succinimidyl est
281 l-cell lung cancer (NSCLC) cells showed that cytotoxicities varied by more than three orders of magni
282                                      Histone cytotoxicity was also reduced by citrullination by pepti
283                                     GNP-HCIm cytotoxicity was evaluated by MTT assay, apoptosis/necro
284 ed cellular detachment from the surface, and cytotoxicity was monitored using the trypan blue life/de
285  cells, and no significant aflatoxin-induced cytotoxicity was observed at UV-A dose of 1,200 mJ/cm(2)
286                 CCK-8 assay revealed that no cytotoxicity was observed for all tested NP concentratio
287                        Specifically, ERS and cytotoxicity were attenuated by TRPA1 inhibition, wherea
288  normal; and degranulation tests and NK cell cytotoxicity were not different from those in DCs.
289                                Low levels of cytotoxicity were observed in eyesalve-treated cell line
290                           Seven endpoints of cytotoxicity were recorded.
291  drug screen revealed significantly enhanced cytotoxicity when NR-160 was used in combination with ep
292 y was assessed by production of IFNgamma and cytotoxicity when stimulated with EBV-LMP2-expressing ce
293 phosphomimetic) reduces ischemic proteo- and cytotoxicity, whereas a phospho-silenced CHIP-S20A ampli
294  complement- and antibody-dependent cellular cytotoxicity, which are critical mediators of AMR.
295 nhibitors (PI3K/mTORi) showed supra-additive cytotoxicity with CHK1i.
296 phagy for survival and displayed synergistic cytotoxicity with the poly (ADP-ribose) polymerase (PARP
297 BD-14270 (8), showed a marked improvement in cytotoxicity, with 3-fold and 58-fold improvements in se
298 tor of cancer cell sensitivity to CAR T-cell cytotoxicity, with potential for pharmacological targeti
299 target DNA mismatches and selectively induce cytotoxicity within MMR-deficient cells.
300 , we hypothesized that inhibiting CD8 T-cell cytotoxicity would reduce disease severity in patients.

 
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