ライフサイエンスコーパス: increased sensitivity

1 h extended interrogation times and therefore increased sensitivity.

2 r signal-to-noise ratios that translate into increased sensitivity.

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

4 predicted patient benefit from therapy with increased sensitivity.

5 agent showed the strongest association with increased sensitivity.

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

7 cted with phenylephrine, with HA-UtA showing increased sensitivity.

8 nce of the light and heavy chains of mAbs at increased sensitivity.

9 owever, newer technologies are emerging with increased sensitivities.

10 We can quantify ALT with increased sensitivity (1.53 nA/(U/L*mm(2)) and over a wi

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

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 Aged APP/PS1 mice reveal an increased sensitivity also to LPS of Escherichia coli, w

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

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

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

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

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

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

21 The MAM method, by virtue of the increased sensitivity and selectivity provided with LC-M

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

23 s associated with cancer antigen 125 such as increased sensitivity and specificity especially in the

24 the lateral flow assay (LFA) having reported increased sensitivity and specificity, but with minimal

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

26 dium mass resolution offering the benefit of increased sensitivity and versatility of this method.

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

28 Exploiting the increased sensitivity at ultra-high field, we performed

29 ed substrates allows PIERS sensor to achieve increased sensitivity beyond the normal SERS effect upon

30 atization resulted in stable derivatives and increased sensitivity by a factor of 4-30 compared with

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

32 Low-dose whole-body CT has increased sensitivity compared with conventional skeleta

33 stream biomarkers, such as STAT5, and showed increased sensitivity compared with diastereomeric contr

34 have shown higher signal-to-noise ratios and increased sensitivity compared with fluorescent beacon s

35 FMMS also has increased sensitivity, compared to UC separation, to mea

36 ongitudinal sectioning of hairs dramatically increased sensitivity; even single-dose administrations

37 Contemporary imaging modalities with increased sensitivity for detecting subclinical lymph no

38 MRSI at ultra-high field (>= 7 T) provides increased sensitivity for fast high-resolution metabolic

39 the field ionization technique demonstrates increased sensitivity for isotope separation and measure

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

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

42 ative by clinical diagnostics, demonstrating increased sensitivity for missed pulmonary pathogens (P

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

44 Finally, we determined an increased sensitivity (>=10-fold) compared to observed m

45 f our decision support algorithm, we show an increased sensitivity in a subset of 87 cases that under

46 Our results show increased sensitivity in A. thaliana when using the PARE

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

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

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

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

51 day 0, 2, 4, and 6 to rats did not result in increased sensitivity in response to mechanical or therm

52 ase from adaptation to unique identities and increased sensitivity in the adaptation response to phys

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

54 nce, excellent retention time stability, and increased sensitivity in the analysis of low-input prote

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

56 troduces a translated search mode, providing increased sensitivity in viral metagenomics analysis.

57 For example, many groups appear to show increased "sensitivity" in the presence of perceived thr

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

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

60 This increased sensitivity may be due to surface-dependent la

61 The increased sensitivity of (68)Ga-PSMA-11 PET/MRI for the

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

63 Increased sensitivity of anionic trypsinogen to CTRC-med

64 kine genes POSTN and IL33; and (3) a 10-fold increased sensitivity of basophils to profilin.

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

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

67 cases could reflect changes in incidence or increased sensitivity of case detection with rt-PCR.

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

69 irect detection of magnetization, exploiting increased sensitivity of cryogenically cooled probes.

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

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

72 y, severely allergic patients presented with increased sensitivity of effector cells.

73 This notion is further supported by increased sensitivity of endotube mutants to oxidative a

74 aracterized by reduced energy production and increased sensitivity of ESCC cells to combined treatmen

75 ) doubled [Formula: see text], indicating an increased sensitivity of k to the choice of anion, while

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

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

78 gh separation powers in combination with the increased sensitivity of MALDI-2 available in one instru

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

80 The increased sensitivity of NIR readouts for colon permeabi

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

82 9; 0.25 mumol/L) significantly mitigated the increased sensitivity of old fibroblasts to IR and chemo

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

84 the cancer biomarker KRAS G12D and ~100-fold increased sensitivity of Peptide Nucleic Acid (PNA) and

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

86 acids and C. acnes culture supernatant also increased sensitivity of S. epidermidis to antibiotic ki

87 proposed to reconcile this discrepancy is an increased sensitivity of smaller size classes of organis

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

89 The increased sensitivity of surface-associated cells to QS

90 p55-deficient leukemic cells correlated with increased sensitivity of the cells to glucose deprivatio

91 st seeking in An. coluzzii coincides with an increased sensitivity of the CO(2)-sensitive neurons and

92 ound treatment or protein knockdown leads to increased sensitivity of the parasite plasma membrane (P

93 redible interval [CI]: -80.71 to -42.83) and increased sensitivity of the QT interval to heart rate c

94 y provides a mechanistic explanation for the increased sensitivity of TNBC to Hsp90 inhibition.

95 ra (Xpert Ultra) for TBM diagnosis suggested increased sensitivity of Xpert Ultra.

96 e root surface and size of calculus deposits increased, sensitivity of detection also increased.

97 f PTP1B, which, because of its substantially increased sensitivity, provides a comprehensive understa

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

99 In addition to increased sensitivity, the perpendicular arrangement off

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

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

102 Combining one NPA and one IS increased sensitivity to 80%.

103 The addition of total NCP volume increased sensitivity to 82.4% while maintaining 100% sp

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

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

106 ticity, whereas LCMT-1 gene-trap mice showed increased sensitivity to Abeta-induced impairments.

107 Increased sensitivity to AF-induced airway disease was n

108 basal (constitutive) activity and displayed increased sensitivity to agonist activation, as assessed

109 ng reflex assessment, knockout mice revealed increased sensitivity to alcohol-induced sedation and de

110 ate cancer cells leads to reduced migration, increased sensitivity to anoikis and reduced tumor growt

111 may come at a cost of decreased fecundity or increased sensitivity to another drug.

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

113 s further enhanced by radiation and leads to increased sensitivity to anti-PD-L1 therapy.See related

114 ingly, the DIDS-resistant virus demonstrated increased sensitivity to antibody neutralization, which

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

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

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

118 on-mediated SGC-SGC and neuron-SGC coupling, increased sensitivity to ATP, downregulation of Kir4.1 p

119 nt of MGMT-deficient cells with temozolomide increased sensitivity to ATR inhibitors both in vitro an

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

121 Increased sensitivity to aversive conditioned cues in co

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

123 Slower neurite outgrowth and increased sensitivity to axonal stress are also evident

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

125 BMP7-LCs exhibit proliferative activity and increased sensitivity to bacterial stimulation.

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

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

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

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

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

131 pid emergence of resistance to docetaxel and increased sensitivity to carboplatin, therefore sequenti

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

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

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

135 multi-polarity mixing ratio combined with an increased sensitivity to certain changes in the hyperfin

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

137 /-), also known as Lgals9(-/-)) animals show increased sensitivity to chemically induced colitis and

138 educed anti-microbial peptide production and increased sensitivity to chemically induced colitis asso

139 s in HNSCC as well as possible mechanisms of increased sensitivity to chemoradiation in HPV-positive

140 sired epigenetic alterations consistent with increased sensitivity to chemotherapeutic agents or with

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

142 pression of IHH, decreased self-renewal, and increased sensitivity to chemotherapy in vivo.

143 beta-catenin levels, prolonged survival, and increased sensitivity to chemotherapy than controls.

144 ity, loss of tumor-initiating potential, and increased sensitivity to chemotherapy.

145 trations, reduced cellular proliferation and increased sensitivity to cisplatin in a SASH1-dependent

146 rthermore, knockdown of BRCA1/2 dramatically increased sensitivity to cisplatin in ESCC cells.

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

148 -/-) mice phenocopy Fam3D-deficiency showing increased sensitivity to colitis and skewed composition

149 asing the ratio of public to private benefit increased sensitivity to collapse.

150 disease during a pig challenge study and had increased sensitivity to complement killing and phagocyt

151 s metacyclic-enriched transcripts, displayed increased sensitivity to complement lysis and a signific

152 nd nuclease-dead MRE11D20A/- mutants display increased sensitivity to CTNAs, accumulate more DNA dama

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

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

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

156 SWN tumors, sensitized DRG neurons, causing increased sensitivity to depolarization by KCl, increase

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

158 DNA content, changes in cell morphology, and increased sensitivity to DNA damaging agents.

159 following subsequent radiation exposure but increased sensitivity to Docetaxel.

160 NO66 resulted in decreased cell survival and increased sensitivity to docetaxel.

161 nificantly reduced background expression and increased sensitivity to doxycycline.

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

163 IST1 in EGFR TKI-resistant EGFR-mutant cells increased sensitivity to EGFR TKIs.

164 nished proliferative ability of these cells, increased sensitivity to endoplasmic reticulum (ER) stre

165 Increased sensitivity to endotoxins in cirrhosis is asso

166 ronger higher-order beliefs about others and increased sensitivity to environments.

167 Consequently, Slc39a8 A391T mice exhibit increased sensitivity to epithelial injury and pathologi

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

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

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

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

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

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

174 ild-type mice, but they displayed a markedly increased sensitivity to flurothyl-, kainic acid-, and h

175 both banana leaves and pseudostems exhibited increased sensitivity to Foc TR4 invasion.

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

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

178 molecule inhibitor gefitinib synergistically increased sensitivity to gefitinib.

179 ZEB1-knockdown cells had increased sensitivity to gemcitabine.

180 ; spheroids established from these cells had increased sensitivity to gemcitabine.

181 UBQLN4 deficiency leads to increased sensitivity to genotoxic stress and delayed DN

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

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

184 ate/cystine antiporter (xCT) is required for increased sensitivity to glucose deprivation.

185 genes is suppressed upon PQ exposure causing increased sensitivity to Gram-negative bacterial infecti

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

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

188 ng PI(4,5)P(2) levels.SIGNIFICANCE STATEMENT Increased sensitivity to heat in inflammation is partial

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

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

191 independently of HSPGs and the generation of increased sensitivity to humoral immunity.

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

193 Additionally, the FA796-defective mutant had increased sensitivity to hydrogen peroxide-induced stres

194 ith deletion of Ubp10, but not Ubp8, confers increased sensitivity to hydroxyurea and activates a cry

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

196 ng that certain genetic mutations may confer increased sensitivity to immune checkpoint blockade.

197 This resulted in increased sensitivity to important lipid molecules in th

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

199 Deletion of SPF1 resulted in increased sensitivity to inhibitors of sterol production

200 growth and repair, Gal9(-/-) animals showed increased sensitivity to intestinal challenge in multipl

201 s to human BLM (hBLM) as mutants demonstrate increased sensitivity to ionizing radiation (IR) and a d

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

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

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

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

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

207 Behaviorally, the mutants have increased sensitivity to itch, but acute sensitivity to

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

209 aureus strain backgrounds also displayed an increased sensitivity to LA.

210 These mice demonstrated increased sensitivity to light touch, pinprick, and ther

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

212 d increased lipid accumulation, resulting in increased sensitivity to lipid-induced cell death.

213 Although the loss of ATP7A increased sensitivity to low Cu concentrations, the abse

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

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

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

217 on, reduced brood size, altered survival and increased sensitivity to microbial toxin, osmotic and ox

218 This disease progression is accompanied by increased sensitivity to microenvironmental TGF-beta.

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

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

221 differentiated tumors were predicted to have increased sensitivity to multiple Rho kinase (ROCK) inhi

222 tyrosine aminotransferase activity displayed increased sensitivity to multiple sources of oxidative s

223 he PKDs increased guanylyl cyclase activity, increased sensitivity to natriuretic peptide, or reduced

224 , including expression of neural markers and increased sensitivity to neurotransmitters.

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

226 d that rovers have higher pr1 expression and increased sensitivity to nociception relative to sitters

227 These mutations cause increased sensitivity to NRTIs, such as AZT.

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

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

230 sion and mitochondrial fusion mutants showed increased sensitivity to osmotic stress and anoxia, surp

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

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

233 S1 in Columbia-0 delayed leaf senescence and increased sensitivity to oxidative stress, suggesting th

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

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

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

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

238 n a fusion positive ovarian cancer cell line increased sensitivity to paclitaxel more than 50-fold.

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

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

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

242 a range of behavioral phenotypes, including increased sensitivity to pentylenetetrazole-induced seiz

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 Double PIK3CA mutations predict increased sensitivity to PI3Kalpha inhibitors compared w

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

248 own to phosphorylate BAD protein resulted in increased sensitivity to platinum agents in TNBC cell li

249 cancers, overall survival is associated with increased sensitivity to platinum chemotherapy due to lo

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

251 lls with high CXorf67 expression levels show increased sensitivity to poly(ADP-ribose) polymerase (PA

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

253 nd leads to physiological changes, including increased sensitivity to reactive oxygen species, reduce

254 Strains with inactivated hsmR or hsmA have increased sensitivity to redox-active compounds and redu

255 mouse embryonic fibroblasts confers not only increased sensitivity to RIPK1 activation-mediated apopt

256 ith DNA double-strand break repair genes and increased sensitivity to select cytotoxic chemotherapeut

257 viable and replicative in culture but showed increased sensitivity to sphingolipid synthesis inhibiti

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

259 pared to control spindles also indicating an increased sensitivity to stretch.

260 revealed that this could be explained by an increased sensitivity to subjective values of choice alt

261 tarvation conditions, flies normally have an increased sensitivity to sugar; however, loss of CCAP, o

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

263 Increased sensitivity to susceptibility-enhanced iron im

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

265 to proliferate and form colonies, as well as increased sensitivity to the BRAF inhibitor vemurafenib.

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

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

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

269 t of tamoxifen-resistance is associated with increased sensitivity to the OGT small molecule inhibito

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

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

272 in more consistent and efficient choices and increased sensitivity to the price of giving.

273 evated in TAZ-KO cells, which also exhibited increased sensitivity to the pyruvate carboxylase inhibi

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

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

276 whereas AsPC-1 cells with ZIP4 knockdown had increased sensitivity to these drugs.

277 led to a decrease in MGMT expression and an increased sensitivity to TMZ.

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

279 encounters (i.e., quaternary memory) showed increased sensitivity to tumor-derived inflammation that

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

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

282 se loss of ENG in endothelial cells leads to increased sensitivity to VEGF and a hyperproliferative r

283 In the absence of endothelial ENG, increased sensitivity to VEGF drives abnormal endothelia

284 Moreover, silencing COMET markedly increased sensitivity to vemurafenib, a common inhibitor

285 enhanced neurosphere formation in vitro, and increased sensitivity to Vismodegib.

286 p53-dependent cytotoxic drugs, also display increased sensitivity to XL177A.

287 2(C134W) including SLC35F2, whose expression increased sensitivity to YM155.

288 As thresholds increased, sensitivity to detect incident TB waned for a

289 mania-like qualities: locomotor activity was increased; sensitivity to D-amphetamine was heightened;

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

291 In addition, the loss of ppiB leads to increased sensitivity toward multiple antibiotics, inclu

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

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

294 nd firmness (F) of the oils while exhibiting increased sensitivity towards processing conditions.

295 8/31/33-genotyping also showed significantly increased sensitivity versus cytology, comparing regress

296 8/31/33 genotyping also showed significantly increased sensitivity vs cytology when comparing regress

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