ライフサイエンスコーパス: increased sensitivity

1 agent showed the strongest association with increased sensitivity.

2 l biotesting, is a promising tool due to its increased sensitivity.

3 NKT cell cytokines ex vivo and in vitro with increased sensitivity.

4 model to classify PSMs using decoy hits with increased sensitivity.

5 faces) of mass spectrometers, thus providing increased sensitivity.

6 e complexes with enhanced photostability and increased sensitivity.

7 r than those of conventional columns, giving increased sensitivity.

8 predicted patient benefit from therapy with increased sensitivity.

9 owever, newer technologies are emerging with increased sensitivities.

10 ide variant calling on the human genome with increased sensitivity (15%) over the next best mapper, p

11 initial findings in most cases, resulting in increased sensitivity (91%) and specificity (99%) when c

12 lera sensor shows excellent reproducibility, increased sensitivities, a very satisfying detection lim

13 ase in GLO1(-/-) cells is associated with an increased sensitivity against MG, elevated intracellular

14 detect NP-binding surfaces on proteins with increased sensitivity, also extending the applicability

15 ules in a noncompetitive format (PHAIA) with increased sensitivity and a positive readout.

16 first- to second-generation MFC resulted in increased sensitivity and allowed us to identify 3 patie

17 The greatly increased sensitivity and amenability to functionalizati

18 DSBCapture shows substantially increased sensitivity and data yield compared with other

19 The reduced complexity increased sensitivity and enabled high-resolution imagin

20 eptamer assays performed with over a 10-fold increased sensitivity and excellent recovery from spiked

21 To measure rare cells with increased sensitivity and improved data managements, we

22 ilable algorithms, BreaKmer detected SV with increased sensitivity and limited calls in non-tumor sam

23 Novel methodologies are providing increased sensitivity and rapid turnaround time to resul

24 RISPR-UMI negative-selection screen provided increased sensitivity and robustness compared with conve

25 eepFinder2, an extension of SweepFinder with increased sensitivity and robustness to the confounding

26 Further increased sensitivity and simplicity of S-Poly(T) Plus,

27 The ensemble machine-learning model showed increased sensitivity and specificity compared with earl

28 rotron radiation) for product detection with increased sensitivity and universal detection power, and

29 ata sets, we demonstrate that our method has increased sensitivity, and thus our pipeline identifies

30 dual (1)H density from exchangeable protons, increased sensitivity at (1)H resonance frequencies arou

31 on nanotubes) above such a film dramatically increased sensitivity by up to 3 orders of magnitude com

32 ctrodynamic dual-funnel interface results in increased sensitivity characterized by a limit of detect

33 CD8(+) T cells develop increased sensitivity following Ag experience, and diffe

34 PET/MR imaging showed increased sensitivity for liver (40 of 40 [100%] for rea

35 annotate long noncoding RNAs (lncRNAs), with increased sensitivity for low-abundance lncRNAs.

36 PET/CT trended toward increased sensitivity for lung metastases (20 of 23 [87%

37 ns, dual-energy CT virtual noncalcium images increased sensitivity for the detection of nondisplaced

38 idual anatomical regions and may demonstrate increased sensitivity in association studies.

39 brid method is able to detect selection with increased sensitivity in both simulated and experimental

40 dition of PET to diagnostic CT significantly increased sensitivity in both the abdomen and pelvis whi

41 ildly responsive to PIM inhibition exhibited increased sensitivity in combination with PIK3CA inhibit

42 scFv fragments show increased sensitivity in comparison to the state-of-the-

43 y and transmitting them to low pressures for increased sensitivity in mass spectrometry (MS) analysis

44 l metabolism is the underlying basis for the increased sensitivity in the aged heart to stress.

45 gnificantly milder conversion conditions and increased sensitivity in the PCR amplification of bisulf

46 The increased sensitivity in using the MAE-DLLME-HPLC-UV has

47 iamond can be used for NMR spectroscopy, but increased sensitivity is needed to avoid long measuremen

48 oscopy for real-time analytics when strongly increased sensitivity is required.

49 r nanoscale sensors is responsible for their increased sensitivity, is incorrect.

50 her rapid diagnostic test detection reflects increased sensitivity, lack of specificity or both, is u

51 te that inhibition of MEK1/2 with trametinib increased sensitivity of ALL cells and primary samples t

52 osphingosine (PHS), and further saw that VPA increased sensitivity of an rsb1Delta mutant to PHS, sug

53 Increased sensitivity of anionic trypsinogen to CTRC-med

54 dating about cue validity (as opposed to the increased sensitivity of behavioral responses to those b

55 Additionally, inactivation of Cdu1 led to increased sensitivity of C. trachomatis for IFNgamma and

56 concurrent reduction of Mcl-1L, resulting in increased sensitivity of cancer cells to apoptotic stimu

57 was to demonstrate a previously hypothesized increased sensitivity of corticostriatal glutamatergic t

58 A potentially increased sensitivity of CT, as compared to radiography,

59 on-based sample might be attributable to the increased sensitivity of current recording techniques an

60 Given the high throughput and increased sensitivity of direct-detect (1)H NMR, this an

61 anxiety during ethanol withdrawal, and that increased sensitivity of DR neurons to subsequent ethano

62 Increased sensitivity of error-detection networks in par

63 In visual cortex, this change coincides with increased sensitivity of excitatory synapses to monocula

64 mia, an increased risk of thrombosis, and an increased sensitivity of JAK2-mutant progenitors to ruxo

65 global reduction of histone acetylation and increased sensitivity of leukemia cells to histone deace

66 Herein, this longevity and increased sensitivity of LLS and LLC lifetime is utilize

67 TREK-1 deficiency resulted in increased sensitivity of lungs to hyperoxia, but this ef

68 However, increased sensitivity of males to environmental conditio

69 Weakened lateral inhibition also produces an increased sensitivity of MSN output to cortical correlat

70 Mechanistic investigations revealed that the increased sensitivity of mutant ERBB2-expressing cells t

71 These mutations lead to an increased sensitivity of neutrophils and lymphocytes to

72 To test whether the increased sensitivity of next-generation sequencing (NGS

73 iated anti-oxidant capacity resulting in the increased sensitivity of offspring to hypertensive damag

74 9; 0.25 mumol/L) significantly mitigated the increased sensitivity of old fibroblasts to IR and chemo

75 ne and fisheries management by demonstrating increased sensitivity of pelagic fish to exploitation du

76 le-tube isothermal signal amplification, has increased sensitivity of plain linear QPA by three order

77 The increased sensitivity of Pten knock-out neurons was due,

78 ned shoot-root sugar gradient in RNAi plants increased sensitivity of root tips to decreasing soil wa

79 electrophysiological remodelling, including increased sensitivity of ryanodine receptors (RyRs) and

80 Important cellular changes include increased sensitivity of ryanodine receptors (RyRs) to C

81 This mechanism may help to explain the increased sensitivity of some stressed individuals to fr

82 ly, deletion of the nmoA gene resulted in an increased sensitivity of the cells to 3-nitropropionic a

83 ed terminal emitter Chl trimer results in an increased sensitivity of the excited state energy landsc

84 N52Y substitution in NP results in increased sensitivity of the H7N9 virus to human Mx, ind

85 t in part, a mechanistic explanation for the increased sensitivity of the mutant parasite lines to ch

86 cted to reach 5-15 W m(-2) by 2050, implying increased sensitivity of the surface to clouds.

87 Mechanistically, the increased sensitivity of the TLR pathway was associated

88 nes, and we correlate the impairment with an increased sensitivity of VP40 to restriction by human bu

89 Therefore, increased sensitivity of YW flies to bacterial infection

90 The MVista Histoplasma antibody EIA offers increased sensitivity over current antibody tests while

91 or long-time assessment in liquid media with increased sensitivity over standard SPR analyses.

92 are with Smart-Seq to demonstrate CEL-Seq2's increased sensitivity relative to other available method

93 ain DA neurons correlated with decreased and increased sensitivity, respectively, to the motor-stimul

94 MEK4 knockdown increased sensitivity specifically to prednisolone by in

95 n recent years have led to reduced costs and increased sensitivity, specificity, and applicability.

96 Due to its increased sensitivity, the detection of CMV DNA in patie

97 duced in growth rate and conidiation but had increased sensitivities to SDS, Congo red, and hyperosmo

98 These changes are indicated by increased sensitivities to SDS-mediated dissociation and

99 g the p38gamma/c-Jun/PTPH1 signaling network increased sensitivities to TKIs in K-Ras mutant cells in

100 diated currents at MF-CA3 synapses exhibited increased sensitivity to a GluN2B-selective antagonist i

101 M imidacloprid leads to a receptor-dependent increased sensitivity to a normally innocuous level of a

102 we find that FUS or TDP43 depletion leads to increased sensitivity to a transcription-arresting agent

103 , whereas etr2 loss-of-function mutants have increased sensitivity to ABA and germinate slower than t

104 n in H2O2 production within the guard cells, increased sensitivity to ABA, and a reduction in stomata

105 Increased sensitivity to AF-induced airway disease was n

106 y cancers lacking fumarate hydratase display increased sensitivity to agents that interfere with thei

107 MEK2 knockdown increased sensitivity to all chemotherapy agents tested

108 hereas cells treated with Th2 cytokines have increased sensitivity to alpha toxin-induced lethality.

109 ology, reduced tumor spheroid outgrowth, and increased sensitivity to anoikis.

110 or gene IRS2 were identified in tumours with increased sensitivity to anti-EGFR therapy.

111 These anomalies are accompanied by increased sensitivity to anti-mitotic agents, a phenotyp

112 umber despite lower ATP levels, resulting in increased sensitivity to apoptosis.

113 ted phenotype of ASFs is characterized by an increased sensitivity to apoptotic stimuli.

114 n arsenic accumulation in shoots, causing an increased sensitivity to arsenate toxicity.

115 T4 led to increased arsenic accumulation and increased sensitivity to arsenite.

116 I) oxidation ability of strain SY and led to increased sensitivity to As(III), suggesting that As(III

117 cation-stress associated subtype that showed increased sensitivity to ataxia telangiectasia inhibitio

118 ung cancer cells depleted of ERCC1 exhibited increased sensitivity to ATR pathway-targeted drugs.

119 co)receptor stabilization and a dramatically increased sensitivity to auto- and paracrine Wnts.

120 Increased sensitivity to aversive conditioned cues in co

121 istered online, corroborated the findings of increased sensitivity to aversive visual stimuli in syna

122 for sesquarterpenoid synthesis, leads to an increased sensitivity to bacitracin, an antibiotic that

123 Drosophila melanogaster Fmr1 mutants exhibit increased sensitivity to bacterial infection and decreas

124 ith either aging and/or high-fat feeding and increased sensitivity to beta cell injury relative to wi

125 y with UCN-01 and its expression with shChk1 increased sensitivity to bleomycin and radiation.

126 knockdown in bone-derived cells resulted in increased sensitivity to both Erk1/2 inhibition and AMPK

127 have defective homologous recombination and increased sensitivity to both platinum and PARP inhibito

128 gesting that relapse may occur at a cost for increased sensitivity to Ca(2+) overload mediated cell d

129 out of Bbmsn2 resulted in reduced growth and increased sensitivity to Calcofluor White, H2 O2 and Con

130 ual myocytes but eventually contribute to an increased sensitivity to cardiovascular stress and to he

131 Most mutations increased sensitivity to CD4bs-directed MAbs without exp

132 It also showed increased sensitivity to cell wall-damaging agents and t

133 This mesR mutant also exhibited increased sensitivity to certain stressors, including po

134 on of TF-dependent genes typically showed an increased sensitivity to changes in binding levels as me

135 ceinamine to the nanoparticles results in an increased sensitivity to changes in pH within a physiolo

136 C2, leading to attenuated Akt activation and increased sensitivity to chemotherapeutic drugs.

137 ed on a consumer camera modified for greatly increased sensitivity to chlorophyll-a fluorescence, and

138 These parasites also have increased sensitivity to chloroquine and some other quin

139 RET knockdown also increased sensitivity to cisplatin-induced apoptosis.

140 cal shocks (39 of 51 patients [76%]), mildly increased sensitivity to cold (38 of 51 patients [75%]),

141 gene (ctpB), and crp-deleted bacteria showed increased sensitivity to copper toxicity.

142 Knockdown of Ubc-E2H and pastrel also led to increased sensitivity to CrPV, whereas knockdown of CG84

143 genotype 2a (JFH1), but not genotype 1b, had increased sensitivity to cyclosporine.

144 ML-DS blast cells ex vivo have increased sensitivity to cytarabine (araC) and daunorubi

145 methylation, leading to impaired DNA repair, increased sensitivity to DD, and reduced HSC self-renewa

146 rown in the presence of adenine demonstrated increased sensitivity to deoxyadenosine.

147 We observed long-lasting, increased sensitivity to differences in reward magnitude

148 romosomal (but not in episomal) contexts and increased sensitivity to DNA cross-linking agents.

149 CSB-deficient neural cells exhibited increased sensitivity to DNA crosslinking agents, partic

150 with impaired Fanconi C and F expression and increased sensitivity to DNA damage in bone marrow myelo

151 in defects in transcriptional silencing and increased sensitivity to DNA damaging agents, and these

152 following subsequent radiation exposure but increased sensitivity to Docetaxel.

153 esponse time of 0.84 +/- 0.19 s, but display increased sensitivity to dopamine, at 46 +/- 13 nA/muM,

154 al cancer cells and tumor models resulted in increased sensitivity to doxorubicin, suggesting that p5

155 ell proliferation in the small intestine and increased sensitivity to doxorubicin-induced acute intes

156 nificantly reduced background expression and increased sensitivity to doxycycline.

157 k changes the efflux pump mechanism, causing increased sensitivity to drugs from several antibiotic c

158 the ddm1-2 inherited epigenotypes caused an increased sensitivity to environmental changes, probably

159 ants pro1, pro2, and pro3 were shown to have increased sensitivity to ER stress relative to wild-type

160 tores, leading to constitutive ER stress and increased sensitivity to ER stressors.

161 C2 deficient EGFR wildtype lung cancer cells increased sensitivity to erlotinib.

162 ctions, and faster relearning, reflecting an increased sensitivity to errors.

163 derexpression of EmbC resulted in reduced or increased sensitivity to ethambutol, respectively.

164 ibited ongoing spontaneous pain behavior and increased sensitivity to evoked pain compared with litte

165 hibition, calbindin-negative neurons exhibit increased sensitivity to excitatory inputs, which can th

166 rimary neurons with silenced PARK9 exhibited increased sensitivity to extracellular zinc (Zn(2+)).

167 This increased sensitivity to eye orientation in upright face

168 CD27(+) memory B-cells in cirrhosis exhibit increased sensitivity to Fas-induced apoptosis in an act

169 ck corrections; indeed, the patients show an increased sensitivity to feedback.

170 ceptibility to cortical spreading depression increased sensitivity to focal cerebral ischaemia, and b

171 cessive consumption of palatable food and an increased sensitivity to food cues.

172 icle stimulant hormone (FSH) dependence] and increased sensitivity to FSH.

173 ression lines of AtORM1 and AtORM2 displayed increased sensitivity to fumonisin B1 and an accompanyin

174 molecule inhibitor gefitinib synergistically increased sensitivity to gefitinib.

175 MYSM1-deficient cells are characterized by increased sensitivity to genotoxic stress associated wit

176 ordial dwarfism, cognitive deficiencies, and increased sensitivity to genotoxic stress.

177 Deletion of nts1 causes increased sensitivity to genotoxins and deregulated expr

178 t ratio of glutamate responses, and strongly increased sensitivity to glutamate toxicity in cell cult

179 -1 and rbm25-2, two Arabidopsis mutants with increased sensitivity to growth inhibition by ABA.

180 utant had no detectable phenotype other than increased sensitivity to H2 O2 and Fgap1 Fgatf1 and Fgap

181 AaGPx3 deletion mutants displayed increased sensitivity to H2 O2 and many ROS-generating c

182 t P. gingivalis FLL366 (DeltaPG_2212) showed increased sensitivity to H2O2 and decreased gingipain ac

183 High expression of MYD88 exhibited increased sensitivity to HDAC inhibitors; conversely, lo

184 Furthermore, lipin-2-deficient mice exhibit increased sensitivity to high lipopolysaccharide doses.

185 embryos from heat-stressed mothers displayed increased sensitivity to high-temperature exposure.

186 S. mutans causes decreased c-di-AMP levels, increased sensitivity to hydrogen peroxide and increased

187 tidial glutathione reductase 3 mutant showed increased sensitivity to Hyg.

188 nhibition of MIF receptor binding results in increased sensitivity to hyperoxia.

189 f functional FoxP3(+) cells, associated with increased sensitivity to IL-2.

190 Furthermore, AT from obese mice exhibits an increased sensitivity to IL-4 stimulation, indicated by

191 F), including primary patient cells, have an increased sensitivity to in vitro sudemycin treatment re

192 Increased sensitivity to infection and a variety of immu

193 leanness, improved glucose homeostasis, and increased sensitivity to insulin and leptin.

194 ptake compared with NCX3-B, together with an increased sensitivity to intracellular Ca(2+).

195 Lastly, RNF126 depletion leads to the increased sensitivity to ionizing radiation and poly (AD

196 Cells from this patient showed increased sensitivity to ionizing radiations and phleomy

197 Inactivation of tlpD resulted in an increased sensitivity to iron limitation and oxidative s

198 Furthermore, a pmtA mutant exhibited increased sensitivity to iron toxicity and oxidative str

199 Cells lacking LKB1 display increased sensitivity to irradiation, accumulates more D

200 alterations in substrate metabolism, and an increased sensitivity to ischemic insults.

201 -ABL tyrosine kinase inhibitor treatment but increased sensitivity to JAK inhibitors.

202 quinine-odor pairings were reliable, we find increased sensitivity to learning the quinine-odor exper

203 ss a panel of MM cell lines and consistently increased sensitivity to lenalidomide.

204 ht compared to wild-type mice, suggesting an increased sensitivity to light.

205 ed oocytes matured to MII; however, they had increased sensitivity to low pH and acetylcholine (ACh),

206 had reduced litter sizes, and their eggs had increased sensitivity to low pH and ACh.

207 ated with resistance to aminoquinolines, but increased sensitivity to lumefantrine (pfcrt 76T; pfmdr1

208 vps or vacJ in Shigella flexneri resulted in increased sensitivity to lysis by the detergent sodium d

209 requent episodes of symptom exacerbation and increased sensitivity to medications are observed in old

210 anization, aberrant T-tubule structures, and increased sensitivity to membrane tension, which was res

211 ry smooth muscle cells and resulted in their increased sensitivity to methoxamine being attenuated (m

212 This heterogeneity is the result of increased sensitivity to Mg(2+)- and Ca(2+)-mediated foc

213 th under basal conditions, but did result in increased sensitivity to microtubule-depolymerizing drug

214 t patients with atopic dermatitis experience increased sensitivity to minimal stimuli inducing sustai

215 Mice lacking beta-arr2 exhibit increased sensitivity to morphine reinforcement; however

216 le region 1 (HVR1) mutation T385P caused (i) increased sensitivity to neutralizing patient IgG and hu

217 in two infection models, in association with increased sensitivity to neutrophil killing, platelet-de

218 aviorally as lower pain thresholds caused by increased sensitivity to NGF.

219 ha4* nAChRs in VTA GABAergic neurons confers increased sensitivity to nicotine reward and points to n

220 old increase in cmr expression, which led to increased sensitivity to nitrosative stress.

221 accharomyces cerevisiae deletion library for increased sensitivity to nonlethal concentrations of tri

222 nt strain (MIG1) showed reduced motility and increased sensitivity to novobiocin.

223 tified an immune-evasion subtype that showed increased sensitivity to nuclear factor-kappaB and mitog

224 Salmonella rod-shaped appearance, exhibited increased sensitivity to osmotic and detergent stress, l

225 The mutant exhibited increased sensitivity to osmotic and oxidative stresses,

226 d FgHog1 null mutant (DeltaFgHog1) exhibited increased sensitivity to osmotic and oxidative stresses.

227 To determine if loss of Dck results in increased sensitivity to other drugs, we conducted a scr

228 otility, reduction of pyoverdine production, increased sensitivity to oxidative stress and antibiotic

229 The increased sensitivity to oxidative stress could be compl

230 onstrate that mitochondrial dysfunction with increased sensitivity to oxidative stress is due to the

231 g impaired growth, decreased ATP production, increased sensitivity to oxidative stress, increased res

232 enotypes that favored attenuation, including increased sensitivity to oxidative stress.

233 ine neurons, while djr-1.1 mutants showed an increased sensitivity to oxidative stress.

234 In addition, trm4b mutants show increased sensitivity to oxidative stress.

235 ssion of ModA2, modA2 ON status, resulted in increased sensitivity to oxidative stress.

236 lls lacking either of these pathways exhibit increased sensitivity to oxidising genotoxins.

237 tial biomarkers for identifying tumours with increased sensitivity to OXPHOS inhibitors.

238 rate that deletion of SerpinB2 abrogates the increased sensitivity to papilloma formation seen on DUS

239 w that the loss of RECQL5 or WRN resulted in increased sensitivity to PARP inhibition.

240 n which Ewing's sarcoma cell lines showed an increased sensitivity to PARP inhibitors (Figure 4C).

241 the absence of DA signaling, nematodes show increased sensitivity to pathogenic bacteria and heat-sh

242 othesis that TEM induce less GVHD because of increased sensitivity to PD-ligands.

243 flammatory cytokines IL-1beta and IL-18, and increased sensitivity to peritonitis.

244 s harbouring spliceosome gene mutations have increased sensitivity to pharmacological perturbation of

245 euroendocrine-associated subtype that showed increased sensitivity to phosphoinositide 3-kinase and f

246 and Pten(G129E/+) cells and tissues exhibit increased sensitivity to PI3-K/Akt activation compared t

247 tion models showed that silencing MAF led to increased sensitivity to PIs, enhanced apoptosis, and ac

248 leads to a channel with reduced activity and increased sensitivity to PKC inhibition.

249 n a pancreatic cancer cell line (MIA PaCa-2) increased sensitivity to platinum-based anticancer agent

250 The rho0 cell lines exhibited increased sensitivity to PLX4720 compared to the respira

251 specific MAPK pathway members MEK2 and MEK4 increased sensitivity to prednisolone through distinct m

252 en with autism spectrum disorder, showing an increased sensitivity to proprioceptive error and a decr

253 duced structural disorder is correlated with increased sensitivity to proteolysis and lower-resolutio

254 ludes multiple steps in which a phenotype of increased sensitivity to sCD4 and enhanced CD4 usage acc

255 Rather, they implicate increased sensitivity to sensory noise and less use of p

256 tions of 25-HC, Ch25h-deficient mice exhibit increased sensitivity to septic shock, exacerbated exper

257 All mutants showed increased sensitivity to serum killing, especially wcaG:

258 , use low-density CD4 more efficiently, have increased sensitivity to soluble CD4 (sCD4), and show tr

259 Conversely, inhibition of tyrosine sulfation increased sensitivity to soluble CD4, 412d, and anti-V3

260 This plasticity reflects increased sensitivity to spectrotemporal features, enhan

261 richment of EMT features was associated with increased sensitivity to statins in a large panel of can

262 Increased sensitivity to stress and dysfunctional reward

263 lacking a squalene hopene cyclase, displays increased sensitivity to stressful conditions and reduce

264 cells to convert to Th1 cells and to acquire increased sensitivity to suppression, leading to control

265 Increased sensitivity to susceptibility-enhanced iron im

266 g tissues, the hypothalamus is wired to have increased sensitivity to T4.

267 RNA resulted in increased proliferation and increased sensitivity to tamoxifen treatment.

268 MYC in MCF10A basal breast cells results in increased sensitivity to TGFbeta-stimulated invasion and

269 Finally, pyl6 T-DNA mutant plants show an increased sensitivity to the addition of JA along with A

270 king the C-terminal PIP motif) results in an increased sensitivity to the DNA damaging agent mitomyci

271 delayed progression from G1 into S phase and increased sensitivity to the DNA synthesis inhibitor hyd

272 his enrichment was an excess of alleles that increased sensitivity to the euphoric effects of d-amphe

273 Notably, these cells exhibited increased sensitivity to the growth inhibitory and proap

274 system operates with less auxin but with an increased sensitivity to the hormonal signal.

275 CP14/15-overexpressing flowers resulted from increased sensitivity to the hormone and not from higher

276 imension and high lacunarity correlates with increased sensitivity to the mitochondrial inhibitor met

277 ted in decreased survival in human blood via increased sensitivity to the oxidative burst.

278 of Ewing's sarcoma family tumors, exhibited increased sensitivity to the PARP inhibitor olaparib as

279 obtained from an affected individual exhibit increased sensitivity to the transcriptional inhibitor a

280 ts in decreased expression of ESRE genes and increased sensitivity to thermal stress.

281 stress-inducing drugs, and knockdown of IFI6 increased sensitivity to these drugs.

282 Conversely, loss of TT8 leads to increased sensitivity to these stresses.

283 system or general inhibition of efflux pumps increased sensitivity to this antibiotic.

284 considers two different approaches to obtain increased sensitivity to transient species for experimen

285 patients and relatives also showed markedly increased sensitivity to two chemotherapeutic drugs, ble

286 be due to decreased viral RNA synthesis and increased sensitivity to type-1-interferon inhibition.

287 -lactalbumin (alpha-La) were associated with increased sensitivity to ultrasonication.

288 and found that dPoleta-derived embryos have increased sensitivity to ultraviolet irradiation and exh

289 y of these three genes results in cells with increased sensitivity to UV light and defective TCR.

290 Moreover, E2f1(S29A/) (S29A) mice display increased sensitivity to UV-induced skin carcinogenesis.

291 xylase (CYP24A1) were described that lead to increased sensitivity to vitamin D due to accumulation o

292 Both czcD and gczA mutants exhibited increased sensitivity to zinc.

293 incomplete granulocytic differentiation and increased sensitivity toward bacterial infections.

294 The knockout mutant Deltamnx showed increased sensitivity toward externally supplied Mn and

295 ion, resulting in less complex pyrograms and increased sensitivity toward the most stable compounds.

296 changes of corresponding metabolites and an increased sensitivity towards glycolysis inhibition.

297 Using acetonitrile as a dopant, an increased sensitivity was observed compared to conventio

298 had little or no impact on SNP calling, but increased sensitivity was observed in INDEL calling for

299 With the increased sensitivity, we investigate the dominant depha

300 ent silica nanoparticles which significantly increased sensitivity without compromising the specifici