ライフサイエンスコーパス: be less sensitive to

1 es of the HPIV3 variant ZM1 HN (T193I/I567V) are less sensitive to 4-GU-DANA's effects.

2 cultures, suggesting that mature osteoclasts are less sensitive to 5-FC.

3 The upper gastrointestinal tract may be less sensitive to (90)Y radioembolization than previo

4 In contrast, sigma is less sensitive to a decrease in nanostructure size, a

5 equired for release of mature growth factor, is less sensitive to a panel of hydroxamates than TNF-al

6 iar4 is less sensitive to a synthetic auxin and low concentra

7 e degree of insulitis in the same animal and was less sensitive to a T1D-reducing diet, but it was si

8 tivity to ABA, while tap46 knockdown mutants are less sensitive to ABA during seed germination, sugge

9 oot growth are well-known ABA responses that were less sensitive to ABA in NPX1-overexpressing plants

10 n addition, the proposed calculus of revenge is less sensitive to absolute magnitudes of revenge than

11 the unfolding free energy barrier for NAPase is less sensitive to acid than that of alphaLP, thereby

12 of TRPM5 currents, and mutant channels that were less sensitive to acid block were also less sensiti

13 Tumor cells overexpressing MDMX are less sensitive to actinomycin D-induced growth arres

14 Human thrombomodulin transgenic PAECs are less sensitive to activation by either HMGB1 or hTNF

15 idity clones (as defined by TMr-GAD binding) were less sensitive to activation as well as less suscep

16 DNA and CBFbeta with higher affinity, but it is less sensitive to allosteric regulation by CBFbeta.

17 Adhesion to the type 2 repeats is less sensitive to alpha-subunit antagonists, but a be

18 Behaviorally, adolescents were less sensitive to amphetamine but more sensitive to

19 Furthermore, HZ mice were less sensitive to an amphetamine disruption of prep

20 cts with RT/WM or WM/WM genotypes as a group were less sensitive to androstenone and androstadienone

21 Src, and TNF pathway activation and in turn were less sensitive to anthracycline compared with patie

22 In contrast, tumors that were less sensitive to anti-VEGF therapy showed an incre

23 contained this new HVR495 glycosylation site were less sensitive to antibody neutralization.

24 standard methods, electron lambda-tomography is less sensitive to artifacts that come from structures

25 Results were less sensitive to assumptions about fitness costs a

26 Moreover, sunlight-illuminated PR+ cells are less sensitive to azide than PR- cells, consistent w

27 Thus, cortical GABA(B) circuits may be less sensitive to baclofen than spinal GABAB circuits

28 rophils during sterile lung inflammation and were less sensitive to bacterial superinfection after in

29 the DNA unwinding activity of HCV helicases is less sensitive to base pair stability.

30 Wild-type mature follicular B cells were less sensitive to BCR stimulation than were immatur

31 locally shifting annotations; this approach is less sensitive to biases arising from local genomic s

32 In control animals, the fovea was less sensitive to blue-light-induced damage than the

33 ylyl cyclase activity in the hippocampus and is less sensitive to Ca2+ than AC1, AC8-/- mice exhibite

34 eNOS behaved similarly to wild-type eNOS and was less sensitive to calcium-dependent activation and h

35 g CD28 harboring a key tyrosine-170 mutation were less sensitive to CD80 elongation.

36 neutrophils and phosphorylation at this site was less sensitive to cell stimulation than at other res

37 gulated in G(0)/G(1)while DNMT3a mRNA levels were less sensitive to cell cycle alterations and were m

38 of cGKIalpha versus cGKIbeta, since cGKIbeta is less sensitive to cGMP activators than cGKIalpha.

39 e mathematically that heterodimer levels can be less sensitive to changes in gene dosage than homodim

40 We show the accession Cape Verde Islands is less sensitive to changes in ambient temperature, and

41 e show that because the Rescorla-Wagner rule is less sensitive to changes in its parameters than the

42 APD is less sensitive to changes in other IKr gating paramet

43 The mutant was less sensitive to changes in free Ca2+, resulting in

44 cer cells that overexpress HER2/neu may also be less sensitive to chemotherapy.

45 conveyed by thinly myelinated Adelta fibers were less sensitive to chemotherapy.

46 development of a more responsive probe that was less sensitive to chloride ion interference.

47 Desialylated PrP(C) was less sensitive to cholesterol depletion than PrP(C)

48 ning transmission electron microscope, which is less sensitive to chromatic aberration.

49 ne and have normal levels of fosB expression are less sensitive to chronic (10-day) administration of

50 ding the cortex, cerebellum, and hippocampus were less sensitive to chronic E(2) treatment.

51 ld-type u-PAR-expressing cells, and cr-u-PAR was less sensitive to chymotrypsin cleavage as compared

52 T7 was less sensitive to chymotryptic regulation, which inv

53 orter (DAT) levels were reduced, and the DAT was less sensitive to cocaine.

54 EG3A, which travels to the intestinal lumen, are less sensitive to colitis than control mice.

55 Gal-3(-/-) mice were less sensitive to Con A-induced hepatitis and had a

56 tomized female rats, suggesting that females are less sensitive to concentrated NaCl solutions during

57 More robust features that are less sensitive to concentration, sampling, and drift

58 Since 6ByJ mice are less sensitive to convulsions despite the fact that

59 glutamate, serotonin) and body muscle cells were less sensitive to CoQ depletion.

60 We hypothesized that DMD myoblasts are less sensitive to cues in the extracellular matrix d

61 ay be transferred to a terminal oxidase that is less sensitive to cyanide.

62 Compared with genotype 1a, genotype 3a was less sensitive to daclatasvir, ledipasvir, and elbas

63 It was previously reported that A422V is less sensitive to dark pulse-induced phase resetting

64 B1 plants, while surprisingly, the knockouts were less sensitive to DCA.

65 mpared with the adult, neonatal heart muscle is less sensitive to deactivation by acidic pH.

66 and mouse alpha2C-AR plasma membrane levels are less sensitive to decrease in temperature, whereas t

67 ally, HIV-1(BORI-15) env-pseudotyped viruses were less sensitive to decreases in the levels of CD4 on

68 As expected, aged rats were less sensitive to delays, and this change was assoc

69 ral genotypes with low fitness were found to be less sensitive to deleterious mutations.

70 ardiac isoform (NCX1.1) expressed in oocytes was less sensitive to depolarizing voltages and to activ

71 Screening laboratory data appears to be less sensitive to detect these injuries, but is usefu

72 naptic currents recorded from epileptic DGCs were less sensitive to diazepam and had altered sensitiv

73 The lysis time models show that the optimum is less sensitive to differences in host density than su

74 We further demonstrate that Th17 cells are less sensitive to direct suppression by 3-HAA than a

75 urring hepatitis C virus (HCV) variants that are less sensitive to direct-acting antiviral (DAA) inhi

76 QOLS, a measure of current QoL, is less sensitive to disease status changes but might be

77 monstrate that polyadenylation sites tend to be less sensitive to DNase I.

78 es alters the polymerase activity so that it is less sensitive to drug inhibition.

79 ltidrug resistance may explain why the virus is less sensitive to drug treatments in prolonged chroni

80 tein-protein interactions, i2-depleted cells were less sensitive to drug-induced cell death (IC50 of

81 scriptase mutations K65R, L74V, and/or Q151M were less sensitive to DXG, whereas the mutation K103N r

82 Dyssynchrony assessed by longitudinal motion is less sensitive to dyssynchrony, follows different tim

83 hat HNSCC cells with reduced p400 expression were less sensitive to E1A-induced suppression of EGFR a

84 However, zebrafish were less sensitive to effects on hepatic gene expressio

85 The flavivirus group epitope (A1) was less sensitive to elimination of SS3 and SS6.

86 However, the prepared state is less sensitive to environmental decoherence because o

87 de range of actA expression levels, and many were less sensitive to environmental signals that normal

88 not greater; and stomata in epidermal strips were less sensitive to exogenous ABA.

89 Flowers from IPT plants were less sensitive to exogenous ethylene and required l

90 lower endogenous NAE content, and seedlings were less sensitive to exogenous NAE.

91 d viscous regime the NP synthesis parameters are less sensitive to experimental variability and there

92 Xanthophylls (lutein and zeaxanthin) were less sensitive to extrusion than carotenes (alpha-c

93 Although HCT116 0-1 cells were less sensitive to FdUrd (IC(50) = 3.5 microM) versu

94 Finally, arrestin2(-/-) mice are less sensitive to ferric chloride-induced thrombosis

95 HtFaNaC expressed in oocytes was less sensitive to FMRFamide (EC(50) = 70 microM) tha

96 The null mutants of GCR1 are less sensitive to GA and BR in seed germination.

97 PDAC xenografts were less sensitive to gemcitabine in hypoglycemic mice

98 uire matched diploid samples for comparison, is less sensitive to global expression changes caused by

99 F mutant receptors, in which agonist binding was less sensitive to guanosine 5'-gamma-thiotriphosphat

100 onses in patients infected for several years were less sensitive to HAART.

101 Structural MRI and FDG-PET were less sensitive to head movement and had superior di

102 cultivars lacking this trait and, therefore, being less sensitive to high temperatures during plantin

103 yperphosphorylated light-activated rhodopsin is less sensitive to high salt and appears to release re

104 Spine Ca(2+) signals were less sensitive to hyperpolarization than shaft syna

105 s, TASK-like currents were reduced and cells were less sensitive to hyperpolarizing effects of haloth

106 Cancer cells containing the K709A mutant are less sensitive to hypoxia-induced growth arrest than

107 roach for identifying a robust gene set that is less sensitive to idiosyncratic results and for quant

108 y chain of kinesin-1) in hematopoietic cells are less sensitive to IgE-mediated, passive, systemic an

109 hese data indicate that distal airways might be less sensitive to IL-13-induced GC metaplasia and muc

110 r the first time an energetic cocrystal that is less sensitive to impact than either of its pure comp

111 , which suggests that this amphibian species is less sensitive to in ovo Se exposure than most of the

112 gher affinity than PLC-zeta, but its binding is less sensitive to incorporating PIP2.

113 Data suggest that males will generally be less sensitive to increased aridity than co-occurring

114 In contrast, adult B6 mice were less sensitive to increasing delays than were adult

115 In addition to IAA, dfl1-D was less sensitive to indole-3-butyric acid and naphthal

116 ROCKII(-/-) dorsal root ganglion neurons are less sensitive to inhibition by Nogo protein or by c

117 duced in late endosomes but their production is less sensitive to inhibition of lysosomal proteases.

118 tive M-MuLV has a lower cholesterol content, is less sensitive to inhibition of release by the choles

119 Phase 2 was less sensitive to inhibition by NBQX but more sensit

120 ctivity in the erythrocytes of diabetic rats was less sensitive to inhibition by NO donors or by AR i

121 GCAP-activated native RetGC1 and RetGC2 were less sensitive to inhibition by Ca(2+) in the prese

122 +-activated nonselective cation channel that is less sensitive to intracellular Ca2+.

123 of the enzyme, whereas responses to menthol were less sensitive to iPLA2 inhibition.

124 The pfsR deletion mutants were found to be less sensitive to iron limitation under low light con

125 oligodendrocytes (O4(-)/GC(+)) were found to be less sensitive to ischemic injury than were the immat

126 electron transfer processes will in general be less sensitive to isotopic substitution.

127 at during SN DA-like neuronal activity LTCCs are less sensitive to isradipine than Cav1.2 LTCCs in re

128 Moreover, these mutants were less sensitive to JAK2 and HSP90 inhibitors than JA

129 Synaptoneurosomes prepared from cerebellum were less sensitive to L-T3 than those from cerebral cor

130 Two HER2 insertional variants found in NSCLC were less sensitive to lapatinib inhibition than two HER

131 e findings may relate to reports that humans are less sensitive to light stimuli in the scotopic rang

132 rod responses rise and decay more slowly and are less sensitive to light than wild-type (WT).

133 NZW Tregs were less sensitive to limiting doses of trophic cytokin

134 jection intraventricular pressure difference was less sensitive to load, whereas ejection fraction an

135 althy subjects, substance-dependent patients were less sensitive to loss compared with gain, made les

136 te and consecutive fragmentation and, hence, are less sensitive to low-abundance peptides.

137 AK activity in Oh545o2 is less sensitive to Lys inhibition than that in Oh51Ao2

138 Wnt5A(high) cells were less sensitive to Lys05 and could be reverted by in

139 -art methods, such as Samtools and GATK, and is less sensitive to mapping parameter settings than the

140 ld initiate a mating response; however, they were less sensitive to mating pheromone than were young

141 ional kinetic analysis of untransformed data is less sensitive to mean zero noise than is graphic ana

142 rmal thermal and visceral pain responses but were less sensitive to mechanical stimuli and exhibited

143 soconstrictor, angiotensin II (AngII), would be less sensitive to metabolic inhibition than an alpha1

144 G1 was found to be less sensitive to meteorological deviations between c

145 licensing of Ly49A(+) NK cells was found to be less sensitive to MHC class I engagement than Ly49A-m

146 jet separator is lower, but its performance is less sensitive to misalignments.

147 r genes FANCC, FANCG and BRCA2 respectively, were less sensitive to MK-1775 as compared to two out of

148 spines and the elimination of existing ones were less sensitive to modulation by sensory experience

149 e abnormally high levels of PKA activity and were less sensitive to modulation of PKA by glucose avai

150 her, it appears that the PDZ domain of PICK1 is less sensitive to mutations for PKCalpha when compare

151 ome this restriction by harboring an NP that is less sensitive to Mx-mediated host defense.

152 ush border, uptake is sodium independent, it is less sensitive to N-ethylmaleimide.

153 06 (serogroup O11), and PA14 (serogroup 010) were less sensitive to NET capture.

154 scale measuring negative symptoms appear to be less sensitive to neurobiological correlates than is

155 Other parental and chimeric viruses were less sensitive to neutralization with this same pan

156 ults demonstrated that cell-associated virus was less sensitive to neutralizing antibodies and inhibi

157 tion in the lss mutant is more extensive and is less sensitive to nitrate and ethylene, resembling th

158 However, SIV-RT-YY was less sensitive to NNRTIs than HIV-1 or RT-SHIV(mne).

159 treatment, whereas oxygen consumption by AOX is less sensitive to NO.

160 v4 deletions, specifically in keratinocytes, are less sensitive to noxious thermal and mechanical sti

161 he same level as mesothelioma cell lines but were less sensitive to NS398 inhibition.

162 whereas PP_3233 and PP_3287 have evolved to be less sensitive to O2.

163 Nasal inspiratory peak flow monitoring was less sensitive to obstruction caused by aspirin than

164 tanal and blocked by citral, other receptors were less sensitive to octanal and not blocked by citral

165 PVP neurons were less sensitive to on-direction head movements durin

166 ured by NMR suggest that the DOPS headgroups are less sensitive to osmotic pressure than DOPC headgro

167 ody formation and that posterior development is less sensitive to overall Lfng levels.

168 Recombinant M295D A. fulgidus Rubisco was less sensitive to oxygen compared with the wild-type

169 hospholipase C-beta(3) (PLC-beta(3)) isoform was less sensitive to PA, requiring greater than 15 mol

170 the betaIII-tubulin-overexpressing cell line was less sensitive to paclitaxel, docetaxel, epothilone

171 We conclude that vascular tissues are less sensitive to pathological disruption of diurnal

172 ts and regulators, whereas mnd2Delta mutants are less sensitive to perturbation of the APC/C. swm1Del

173 th and leaflet formation but leaf initiation is less sensitive to perturbation of SIL3 activity.

174 with control by overall feedback inhibition is less sensitive to perturbations in the values of the

175 We found that rat ENaC is less sensitive to pH than human ENaC, an effect media

176 DNA unwinding was less sensitive to pH changes than RNA unwinding.

177 We show device performance to be less sensitive to phase variations in the circuit tha

178 tivity is abolished by vanadate (10 mM), but is less sensitive to phosphate (IC(50) 50 mM) or chlorid

179 Binding of Kix and IBiD was less sensitive to phosphorylation.

180 BK channels in WKY and SHR cells were less sensitive to physiological changes in intracel

181 g route, as well as by a slower pathway that is less sensitive to PI 3-kinase inhibitors.

182 els of the ER-Golgi SNARE proteins and Sly1p were less sensitive to PI(4)P inhibitors.

183 hen this site is phosphorylated, the channel is less sensitive to PKC inhibition.

184 mmary-level data, we demonstrate that HAPRAP is less sensitive to poor LD estimates.

185 onents less than 2 emphasize that the moduli are less sensitive to porosity than those of natural cel

186 f-life of less than 30 min to about 8 h) and was less sensitive to proteasome-mediated degradation.

187 test the hypothesis that shorter loops would be less sensitive to proteolysis.

188 regates of lymphoma cells were also found to be less sensitive to purified natural killer cells.

189 Mammalian voltage-gated Na(+) channels were less sensitive to pyrethroids than their insect cou

190 populate the tumor and have been reported to be less sensitive to radiation-induced damage through pr

191 T cells demonstrated that Env bearing Asp324 was less sensitive to RANTES, suggesting that Asp or Asn

192 Weaker glomerular responses, however, were less sensitive to raphe stimulation than strong res

193 Gag mutants deficient in nuclear trafficking were less sensitive to reduction of intracellular PI(4,5

194 The mode fidelity is also shown to be less sensitive to reflectivity and phase errors than

195 omb is less sensitive to repression by Brk than sal and is c

196 n pools in tropical montane wet forests will be less sensitive to rising MAT than predicted by ecosys

197 Hybrids formed with Me-S-ODN sequences were less sensitive to RNase H degradation than those fo

198 Na(+) treatments, but the Ca(2+) treatments were less sensitive to SDS concentration changes.

199 Root elongation in these mutants is less sensitive to selenate than in wild-type plants.

200 Primary cells were less sensitive to serum depletion processes.

201 ct; in particular, kainate receptor currents are less sensitive to short- and long-term increases in

202 ctive signals such as draining artifacts and is less sensitive to signal fluctuations.

203 p methylation in vitro, yet their methylases were less sensitive to SIN inhibition than those of the

204 6st1-/- mutants and that Hs6st1-/- RGC axons are less sensitive to Slit2 repulsion than their wild-ty

205 The community ANPP was less sensitive to soil ammonium at lower frequency o

206 roperties of Gln-rich and Ala-rich sequences are less sensitive to solvent quality in denaturing solu

207 Hypoxic cells containing VDAC1-DeltaC were less sensitive to staurosporine- and etoposide-indu

208 The use of lithium carbenoids, which are less sensitive to steric hindrance, allows stericall

209 The affinity of GTP is less sensitive to substitutions at the gamma-phosphor

210 id tumor cells and nontransformed cell types are less sensitive to such treatments.

211 Theory predicts that genetic diversity may be less sensitive to such disruptions in the short term,

212 Importantly, NBM CD34(+) cells were less sensitive to TAK1 inhibition compared with AML

213 e isotopic composition of East Antarctic ice is less sensitive to temperature changes during warmer c

214 Slow life histories are less sensitive to temporal autocorrelation, but thei

215 that oval cells, both in vivo and in vitro, are less sensitive to TGF-beta-induced growth inhibition

216 , we demonstrate that Teffs deficient in p21 are less sensitive to the antiproliferative effects of A

217 These polymers are less sensitive to the conformational disorder of the

218 lysis, it would appear that VPT measurements are less sensitive to the development of peripheral neur

219 with the parent background (P), ceh1 mutants are less sensitive to the ER-stress-inducing agent tunic

220 Tumor cells are less sensitive to the induction of apoptosis and are

221 Cells with reduced Sir2 levels are less sensitive to the inhibition imposed by an eleva

222 STAT3-deficient fibroblasts are less sensitive to the pro-fibrotic effects of TGFbet

223 m of Gsalpha in neurons within the forebrain are less sensitive to the sedative effects of ethanol.

224 reover, heart rates of KO(alphaMHC-Cre) mice are less sensitive to the selective I(f) blocker ivabrad

225 apeutic toxins with improved efficacy.Humans are less sensitive to the therapeutic effects of botulin

226 y more easily applicable in practice as they are less sensitive to the value of the excess absenteeis

227 gesting that BRAF-mutant colonic cells might be less sensitive to the antitumor effects of aspirin th

228 ggest that BRAF-mutant colon tumor cells may be less sensitive to the effect of aspirin.

229 that the carriers of the 7R allele appear to be less sensitive to the effects of age on brain glucose

230 as 5.9, indicating that coastal strains may be less sensitive to the ongoing reduction in ocean pH.

231 S-tetherin is also reported to be less sensitive to the prototypic viral antagonist hum

232 1(+/+) mice, male Y1(-/-) mice were found to be less sensitive to the sedative effects of 3.5 and 4.0

233 type mice, the RIIbeta-/- mice were found to be less sensitive to the sedative effects of ethanol as

234 Rod-shaped particles were found to be less sensitive to the surface charge heterogeneity ch

235 Furthermore, REPPS is less sensitive to the completeness of the metabolic n

236 but that the rate of benzylic C-H borylation is less sensitive to the degree of electron density at t

237 It is less sensitive to the ethylene response inhibitor 1-m

238 The CFHR4-C3bBb convertase is less sensitive to the factor H-mediated decay compare

239 As a result, the bimolecular step is less sensitive to the increased salt concentration, a

240 least 12 h post-induction, and this activity is less sensitive to the MEK inhibitors.

241 The stereochemistry (E vs Z) is less sensitive to the nucleophile and is relatively c

242 A 4-repeat tau isoform is less sensitive to the oxidative potential of the envi

243 atic fields, whereas the electrostatic field is less sensitive to the particular set of the adopted c

244 ith few partners, we found that the epidemic is less sensitive to the partner acquisition rate than o

245 LsAA9A activity is less sensitive to the reducing agent potential when c

246 sizes of oligosaccharide revealed that KfiA is less sensitive to the size of the acceptor substrates

247 tive pathway, with respect to the gas phase, is less sensitive to the surrounding dielectric.

248 ntrast, bcl-2 expression of plasmacytoid DCs was less sensitive to the effects of IL-10.

249 e 2a JFH1 replicon and infectious JFH1 virus was less sensitive to the inhibitory effect of cGAMP tha

250 on CA3-CA1 synapse, neurotransmitter release was less sensitive to the N-type Ca(2+) channel blocker

251 ronate, homorisedronate, and risedronate but was less sensitive to the non-nitrogen-containing bispho

252 The rhamnose-regulated promoter PrhaBAD was less sensitive to the presence of its cognate sugar

253 an NTPase, its helix-destabilizing activity was less sensitive to the presence of Mg2+, suggesting t

254 For Ni(OEP), the E1 degrees values were less sensitive to the %RTIL than were observed for

255 extinction than adults, suggesting that they were less sensitive to the abolishment of the reinforcem

256 Genes in the Kcnq1 domain were less sensitive to the absence of DNMT1.

257 xenografted in macrophage-depleted nude mice were less sensitive to the antitumor effect of IL-13 cyt

258 hospholipids containing docosahexaenoic acid were less sensitive to the applied surface tension than

259 d response shifting and that their decisions were less sensitive to the available evidence, suggestin

260 higher chitin content than the wild-type and were less sensitive to the cell wall-targeting compounds

261 Estimates of gamma were less sensitive to the distance between the electrod

262 tabolites, because cells overexpressing MRP1 were less sensitive to the drug and had reduced levels o

263 nd females and OVX+E but not OVX+Veh females were less sensitive to the effects of D1-receptor antago

264 inants (e.g., PCB-153 and PCB-180), the TMFs were less sensitive to the food web composition, and a b

265 nce at the PM and clathrin-deficient mutants were less sensitive to the impact of SA on the auxin dis

266 fective in auxin influx and efflux proteins, were less sensitive to the inhibition of lateral root fo

267 Nigral neurons lacking DJ-1 were less sensitive to the inhibitory effects of D2 auto

268 rats were broader, decayed more slowly, and were less sensitive to the K(+) channel blocker 4-aminop

269 Measures of type-I performance were less sensitive to the subjects' specific attentiona

270 The nicotine-treated rats were less sensitive to the threshold elevating effects o

271 hermal applications because their absorption is less sensitive to their orientation, which is random

272 However, patients with advanced CML have been less sensitive to therapy and responses have been s

273 quently it has been considered a region that is less sensitive to thermal anomalies.

274 Interestingly, Ago loading of siRNAs is less sensitive to thermostability than that of their

275 TPMT+ cells were less sensitive to thioguanine than MOCK cells (IC(5

276 sing miR396-resistant copies of several GRFs are less sensitive to this inhibition.

277 vation of p(E), the p(I) and p(aQ) promoters are less sensitive to this substitution, suggesting that

278 owning development and that astringent fruit is less sensitive to this disorder than fruit submitted

279 However, the septal rats were less sensitive to this contingency shift, compared

280 population transfer, protocols based on LZT are less sensitive to timing errors.

281 All 3 strains avoided TMT, but Wistar rats were less sensitive to TMT.

282 Toso(-/-) dendritic cells were less sensitive to Toll-like receptor stimulation an

283 , we report that mice lacking IL-1R or MyD88 are less sensitive to topical skin carcinogenesis than t

284 of MFB-1 appear to cause the PLM neurons to be less sensitive to touch than the ALM neurons.

285 y, under glucose-free conditions, Z138 cells were less sensitive to TRAIL with reduced TRAIL-R1/R2 su

286 rminal sequences of the transgene insert, it is less sensitive to transgene duplication, rearrangemen

287 bility that tumors with COX2 methylation may be less sensitive to treatment using specific COX2 inhib

288 Root growth of pPLAIIIbeta-KO plants is less sensitive to treatment with free fatty acids, th

289 -subunit protein and AS enzyme activity that was less sensitive to Trp-feedback inhibition, leading t

290 the Mlh1 linker are removed, whereas repair is less sensitive to truncation of the Pms1 linker arm.

291 Importantly, transgenic mouse skin was less sensitive to tumor promoter-induced inflammatio

292 ur results indicate that Bax-deficient cells are less sensitive to undergo apoptosis following TG tre

293 Earlier evidence suggested that rho is less sensitive to variations in marker allele frequen

294 MAF2 expression is less sensitive to vernalization than that of FLC, and

295 +80 mV, P. aeruginosa and S. coelicolor SoxR are less sensitive to viologens, which have redox potent

296 reviously documented, NR2D-containing NMDARs are less sensitive to voltage-dependent Mg(2+) block tha

297 Furthermore, we show that rolling is less sensitive to wall shear stress and ICAM-1 substr

298 the application of alternative methods that are less sensitive to weak instrument restrictions.

299 s expressing the dominant negative-caspase 9 were less sensitive to XK469.

300 ate (K(i)(app) = approximately 6 micrometer) was less sensitive to Zn(2+), indicating the existence o