ライフサイエンスコーパス: remain unaltered

1 y-state NAD(+) levels and NAD(+)/NADH ratios remain unaltered.

2 nzyme complex is formed where the substrates remain unaltered.

3 urgdorferi B31 spirochetes expression levels remain unaltered.

4 adaptation, and tonotopic channel properties remain unaltered.

5 transmission, and paired-pulse facilitation remain unaltered.

6 ing neurons, whereas other synaptic proteins remain unaltered.

7 ) uniporter components MCU, MCUR1, and MICU1 remain unaltered.

8 usters, whereas neuronal presynaptic boutons remain unaltered.

9 old, whereas other components of the cascade remain unaltered.

10 f 'costs per lion.' Our original conclusions remain unaltered.

11 4 months of age, neurofascin 155 low levels remain unaltered.

12 after bending their emissive spectral output remains unaltered.

13 ternalization; the activation state of Cdc42 remains unaltered.

14 lation as CD45R, SHP-1, and SHP-2 expression remains unaltered.

15 rylation of the cytoplasmic substrate p90RSK remains unaltered.

16 nt 'threshold' voltage of current activation remains unaltered.

17 nts, but the response to abscisic acid (ABA) remains unaltered.

18 l under conditions in which 5-methylcytosine remains unaltered.

19 sulfobromophthalein by rat hepatocytes; K(m) remains unaltered.

20 d etoposide-stabilized DNA cleavage activity remains unaltered.

21 for the initiation stage of DNA replication, remains unaltered.

22 integrin coupling with intracellular motors remains unaltered.

23 hnique involving dual fluorescence labeling, remains unaltered.

24 is ablated while the exons encoding p14(ARF) remains unaltered.

25 verall structure and ligand-binding affinity remains unaltered.

26 unds, but the aromatic/nonaromatic character remains unaltered.

27 evated Cdk5 activity, whereas p35 expression remains unaltered.

28 fore, while 2 is reduced by ascorbic acid, 1 remains unaltered.

29 cess, whereas hydroxyl group at C-2 position remains unaltered.

30 l structure that induces anomalous diffusion remains unaltered.

31 RKO mice while regional brain glucose uptake remained unaltered.

32 The time course of the evoked signals remained unaltered.

33 expression of other death effector proteins remained unaltered.

34 dritic cells and resident tissue macrophages remained unaltered.

35 By contrast, responses to painful stimuli remained unaltered.

36 ver, their 5-HT2C pre-mRNA editing phenotype remained unaltered.

37 lthough classical estrogen receptor function remained unaltered.

38 The level of active H-Ras in these cells remained unaltered.

39 onses, signaling, and cell wall biosynthesis remained unaltered.

40 cells, although Th1/Th2 cytokine production remained unaltered.

41 damental nature of the temporal pattern code remained unaltered.

42 s the type 2 cytokines IL-4, IL-5, and IL-10 remained unaltered.

43 re augmented (p < 0.05), yet IGF bioactivity remained unaltered.

44 h (p<0.001), but channel modulator responses remained unaltered.

45 TR; P < 0.001), whereas other ERG components remained unaltered.

46 signaling via protease-activated receptor 2 remained unaltered.

47 levels of IAP proteins, Mcl-11 and Bcl-x(L) remained unaltered.

48 reduced and shortened, PI3 kinase activation remained unaltered.

49 odestly increased, and sphingomyelin content remained unaltered.

50 C) betaII mRNA, whereas PKCbetaI mRNA levels remained unaltered.

51 se activation, whereas Erk kinase activation remained unaltered.

52 Bax, a pro-apoptotic member of Bcl-2 family, remained unaltered.

53 er L. casei CHCC3139, while IL-10 production remained unaltered.

54 yocytes, whereas the level of necrotic cells remained unaltered.

55 ase and glucosylceramide synthase activities remained unaltered.

56 level of mutated and wild type TAO (35 kDa) remained unaltered.

57 ion of mitogen-activated protein kinase WIPK remained unaltered.

58 UC alone from equivalently treated seedlings remained unaltered.

59 d IL-12-induced Janus kinase phosphorylation remained unaltered.

60 ce expression of other markers such as CD62L remained unaltered.

61 whereas the recruitment of Vbeta-3+ T cells remained unaltered.

62 transcriptional activation of chromogranin A remained unaltered.

63 capsaicin, although the unitary conductance remained unaltered.

64 days, both ntcp protein and mRNA expression remained unaltered.

65 ells remapped, and their spatial information remained unaltered.

66 e enzymes II were reduced, but the Km values remained unaltered.

67 the mechanical properties of the sarcolemma remained unaltered.

68 by innate "training"; epithelial stem cells remained unaltered.

69 ed lateral-PMv CART neurons, but CART-levels remained unaltered.

70 Fibroblastic phenotype remained unaltered.

71 Bone marker levels in HCs remained unaltered.

72 striatal reward prediction error signalling remained unaltered.

73 reas the relationship between Q(tw) and [Pi] remained unaltered.

74 FcepsilonRI (gamma chain) and MAPK proteins remained unaltered.

75 contents decreased while carotenoid content remained unaltered.

76 ke phase versus animal position relationship remained unaltered.

77 ficient endothelial cells, while proton leak remained unaltered.

78 Time to therapy remained unaltered.

79 hile the level of transcription factor SOX-2 remained unaltered.

80 cytes that were immunopositive for activin A remained unaltered.

81 Accordingly, glucose metabolism remained unaltered.

82 baseline, although non-oxidative metabolism remained unaltered.

83 electrodes; however, the capture specificity remained unaltered.

84 SCs in the dorsal portion of the hippocampus remained unaltered.

85 ory consolidation, whereas short-term memory remained unaltered.

86 observed only in the spleen, and TPO levels remained unaltered.

87 T-ALL cells, whereas cell cycle progression remained unaltered.

88 ng ET (18 +/- 16 and 43 +/- 30%), but OXPHOS remained unaltered.

89 ucts, or DRiPs, and total MHC class I levels remained unaltered.

90 ertheless, the composition of FAAs and PBAAs remained unaltered.

91 whereas the affinity for the substrate (KM) remained unaltered.

92 c labeling technique, whereas APP mRNA level remained unaltered.

93 precursor protein proopiomelanocortin (POMC) remained unaltered.

94 associated with many key metabolic processes remained unaltered.

95 e contrary, the expression of CXCR1 and CCR7 remained unaltered.

96 ary conductance and nucleotide sensitivities remained unaltered.

97 uramine, the ability of DBS to suppress VCMs remained unaltered.

98 AChR) expression and localization at the NMJ remained unaltered.

99 ls, with total myofilament TM protein levels remaining unaltered.

100 umor irradiation, despite nonspecific uptake remaining unaltered.

101 1 versus control), whereas arterial dilation remained unaltered (-19.3+/-5%).

102 22 bpm, both P < 0.05) while cardiac output remained unaltered (219 +/- 64 vs. 197 +/- 39 ml min(-1)

103 Left ventricular ejection fraction remained unaltered (48% +/- 7% to 49% +/- 5%, p = 0.4) a

104 6) increased significantly in NAFLD, but FFA remained unaltered (5533 versus 5929 versus 6115).

105 nsitivity response, as their gene expression remained unaltered 8 h after nickel exposure.

106 in heat-shocked cells, O(2) consumption rate remained unaltered (8.19 +/- 1.01 mm Hg/min/10 x 10(6) c

107 The percent peristalsis remained unaltered (94% vs 87%; P = 0.71).Overall, patie

108 verall litter sizes and number of fetal loss remained unaltered, a reduced fetal weight and a lower f

109 In contrast, SHM in kappa light chain genes remains unaltered, acquitting for any global SHM defect

110 reas HLA-DRB1*15 frequency in affected males remains unaltered across the two generations (chi(2) = 0

111 e bleaching step of the refining process and remain unaltered after the final deodorizing step.

112 ients (-16.1%) compared with controls, which remained unaltered after abstinence (-17.0%).

113 isk of bias was low to moderate; conclusions remained unaltered after exclusion of four high risk stu

114 interval (CI)]: 1.54 [1.09 to 2.19]), which remained unaltered after further adjustment for CAC scor

115 , acidity, and fatty acid profiles of WG oil remained unaltered after HA and MW treatments.

116 antly, but blood flow in the brain and heart remained unaltered after hemorrhage and resuscitation.

117 the ventroposterior nucleus to area 3b also remained unaltered after injury.

118 resting cells, RyR2 interdomain interaction remained unaltered after introduction of SCD-linked muta

119 However, catalase (CAT) protein expression remained unaltered after p53 induction.

120 ffects because the responses to L-Glu (5 mM) remained unaltered after the microinjection of these ant

121 oked exercise and PECO of the untrained limb remained unaltered after training.

122 The CSF content of PREG and PROG remained unaltered after treatment and failed to correla

123 RNA yield and integrity remained unaltered after treatment with 70% ethanol, eve

124 lysis revealed that the level of PML protein remained unaltered after UV-C treatment.

125 e, the high PR-1 expression observed in hrl1 remains unaltered after avirulent and virulent pathogen

126 ce, we show that although its own expression remains unaltered after cocaine exposure, RXRalpha contr

127 yst stability, as the catalyst's performance remains unaltered after several cycles.

128 The pKa of N6' '' remained unaltered, and resonances of N1 and N3 showed s

129 nd untouched so that its biological activity remained unaltered, and we modified the passenger strand

130 ear-complete GAP/GEF-resistance of KRAS Q61H remains unaltered, and high-affinity RAF interaction is

131 ERalpha depletion whose polysome association remains unaltered are enriched in codons requiring U34-m

132 prisingly, the decay rate of MPO Compound II remained unaltered as NO concentrations were increased.

133 Of note hippocampal GluA1 levels remained unaltered at the PSD, but were reduced near the

134 efficiency of electrospray ionization (ESI) remained unaltered between sample extracts and calibrati

135 polarized potentials, so the spike threshold remained unaltered but the afterhyperpolarization became

136 nsitivity, plasma insulin, and triglycerides remained unaltered, but both male and female 2-Gy groups

137 l progression and cardiac retroviral content remained unaltered, but cardiac toll-like receptor 4 was

138 Steady-state levels of 4E-BP transcript remained unaltered, but the rate of 4E-BP synthesis was

139 The shape of the granules remained unaltered, but there were low levels of surface

140 In this mutant, the level of p60v-src remains unaltered, but the protein is much less active i

141 of refilling of the readily releasable pool remain unaltered by latrunculin treatment.

142 Mucosal 5-HT, 5-HIAA, and KA concentrations remained unaltered by ATD.

143 Neutral memory contextualization remained unaltered by cortisol, irrespective of the timi

144 essing, presentation, and T-cell stimulation remained unaltered by dyslipidemia.

145 SR proteins, but their phosphorylation state remained unaltered by insulin in fibroblasts from Akt2(-

146 Neflamapimod-evoked vasorelaxation remained unaltered by the inhibition of smooth muscle ce

147 lerance to the analgesic effects of morphine remained unaltered by the lack of M5 receptors.

148 s, the distribution of SNAP-25 in MDCK cells remained unaltered by treatment with dibutyryl cAMP or f

149 hibitory-input synapses across RBC terminals remains unaltered by sensory deprivation, although ribbo

150 The ATP binding capacity remains unaltered by the modifications.

151 the mRNA variance as a function of the mean remains unaltered by their presence.

152 dies showed that while the acetyl-CoA levels remain unaltered, CoA levels diminish by more than 50% w

153 inter) approximately 1.7 x 10(4) m(-1)s(-1)) remains unaltered, consistent with the absence of contac

154 phenotypes characteristic of this condition remained unaltered despite the dMSN inhibition.

155 , hepatocyte growth factor receptor (c-Met), remains unaltered despite reduced levels of the signalin

156 Normally, triterpenoid skeletons then remain unaltered during subsequent tailoring steps.

157 Moreover, these responses remain unaltered during the early postnatal stress-nonre

158 coordination of the left and right forepaws remain unaltered during the execution of distinct groomi

159 ic oxides in pellet biomass, which seemed to remain unaltered during the photogranulation process.

160 TBS remained unaltered during CR.

161 ures decreased during Valsalva manoeuvre but remained unaltered during handgrip exercise.

162 The active-site structure of PCu has remained unaltered during the evolutionary process.

163 zide, cell ATP content and glucose transport remained unaltered during the initial 1-h period of expo

164 evealed that the unitary transporter current remained unaltered during the loss of hDAT membrane expr

165 beta-Zearalenol remained unaltered during the process.

166 Ox such that the isotopic composition of NOx remains unaltered during collection.

167 orn Swl/+ mice, whereas motor neuron numbers remain unaltered even in aged animals.

168 E(1/2) and MA remained unaltered even after 50,000 accelerated degrada

169 pain, a chronic pain due to neuronal lesion, remains unaltered even after the injury-induced spinal a

170 ASOs reveals that the ASO-RNA hybridization remains unaltered even for a hypothetical single point m

171 usly developed methods, unbiased selectivity remains unaltered even with the exposure to the primary

172 Surprisingly, repetitive RNA loci expression remained unaltered following histone acetylation-mediate

173 0 to 95% following infection with 8-DR.R but remained unaltered following infection with delta8-DR, s

174 PSMB5 and STAT3 protein levels remained unaltered following the inhibition of proteasom

175 How can species remain unaltered for long periods yet also undergo rapid

176 earing capacity and peak structural strength remained unaltered for ITB tissues.

177 ence intensity of the aluminum-DEMAX complex remains unaltered for over 24h at room temperature and i

178 nce specificity in the DNA cleavage reaction remains unaltered for the mutant proteins.

179 cumulative lead exposure and CpG methylation remained unaltered from 30 to 78 months.

180 iability indices during controlled breathing remained unaltered; heart rate responses during tilt and

181 e expression of key target genes such as Myc remains unaltered, highlighting the existence of alterna

182 Placental expression of the apelinergic axis remained unaltered, however.

183 Procaspase-3 levels remained unaltered if superinfected with Bac-U(S)3 at 3

184 stress, the integrity of the viral episomes remained unaltered.IMPORTANCE DNA viruses have evolved c

185 in stress fibers and the microtubule network remain unaltered in infected cells.

186 modeled in these variants, the exterior lips remain unaltered in position.

187 al properties of Abeta, including this turn, remain unaltered in the central fragment Abeta18-35.

188 sic characteristics of somatic hypermutation remain unaltered in the MMR-deficient mice: a preference

189 m the psaAB operon, encoding these proteins, remain unaltered in the mutant strain.

190 position, and overall body mass constituents remain unaltered in the transgenic mice.

191 64%) sites, decreased in 19 (18%) sites, and remained unaltered in 19 (18%) sites (P < .01).

192 Megalin expression remained unaltered in adult WT and KO mouse brain, SC, a

193 The number of Fos-staining cells remained unaltered in AH and PH in both groups of rats.

194 Lymphocyte subsets remained unaltered in all monkeys.

195 G protein-mediated inhibition remained unaltered in alpha1B subunits containing a poin

196 rtex of control mice, whereas lactate levels remained unaltered in APP/PS1 mice from 3 to 12 months o

197 of cbl and its interaction with p190 BCR/abl remained unaltered in BaF3 cells transformed by p190Y177

198 e protein whose sorting is AP-3 independent, remained unaltered in both AP-3- and vimentin-null cells

199 cases alike, while Pp for peptidyl transfer remained unaltered in cognate but increased 10-fold in n

200 However, the B-family structure of DNA remained unaltered in DNA-methylxanthines complexes or i

201 r results suggested that miR-20a and miR-92a remained unaltered in HCV-infected patients who progress

202 st, the systemic T2 elements of the response remained unaltered in IL-10 KO mice whereas the T2 respo

203 Treg development, because frequency of nTreg remained unaltered in mice lacking NFAT1, NFAT2, or NFAT

204 Moreover, Foxa2 levels remained unaltered in Myostatin(-/-) mice, while levels

205 iginal report, NLRP3 inflammasome activation remained unaltered in NLRP10-deficient DCs even after re

206 on was selective for MNCs because ER-beta-IR remained unaltered in PVN parvocellular neurons.

207 Low levels of serum anti-idiotypic antibody remained unaltered in recipients of T-cell-depleted immu

208 All VibStim variables remained unaltered in RI (n = 20, 10 females).

209 However, Ca2+ current expression levels remained unaltered in several K+ channel mutants, illust

210 V-VOR gain remained unaltered in the 5 children tested.

211 pment and responses to viral infections also remained unaltered in the absence of Pex5 Thus, this stu

212 d methyl triclosan lack a phenolic group and remained unaltered in the cell cultures.

213 of CR1 was significantly reduced, whereas it remained unaltered in the presence of MCP.

214 The data demonstrate that the global shapes remained unaltered in the presence of the aromatic ligan

215 Dopamine levels remained unaltered in the presence of the nonreward SDel

216 s), tactile spatial discriminative capacity remained unaltered in the same subjects when the duratio

217 ription of RNAII and RNAIII of the agr locus remained unaltered in the sigB mutant.

218 The number of NOS positive cells remained unaltered in the SON, MePO and LH in rats with

219 cebo pigs and worsened at Day 42, whereas it remained unaltered in ticagrelor +/- AZD3366-administere

220 The mitotic index remained unaltered in vivo, whereas the apoptotic index

221 acellular release of SP-D/A from A549, which remained unaltered in WI26.

222 ast, the response to strong agonist peptides remains unaltered in Dock2-deficient T cells.

223 ry sensory projections to the olfactory bulb remains unaltered in G(olf) mutants.

224 As the food intake remains unaltered in NPC1L1-knockout (L1-KO) mice, we hy

225 al species, whereby the iron oxidation state remains unaltered in the presence of a highly oxidizing

226 urements that the bis-histidine coordination remains unaltered in the solution phase.

227 stribution of the substituents in the allene remains unaltered in two perpendicular planes (configura

228 However, some protein levels remained unaltered, including cyclin E and keratin 8.

229 The tail bleeding time and blood loss remained unaltered, indicating normal hemostasis.

230 In aging rat aorta, although TG2 expression remains unaltered, its activity increases and S-nitrosyl

231 Nonetheless, the peroxyl scavenging activity remained unaltered, likely, at least partly, due to syne

232 Growth of aminoglycoside-resistant isolates remained unaltered on passage to nonselective media.

233 n of the epithelial marker E-cadherin either remained unaltered or increased.

234 e granule cells to excitatory synaptic input remains unaltered, owing to an increase in a 'leak' cond

235 nts with AS as compared with controls, which remained unaltered post-TAVI.

236 Parasympathetic control remains unaltered post-SCI and does not contribute to re

237 , spermidine-dependent hypusination of eIF5A remained unaltered, suggesting further compensatory mech

238 l orientation during spontaneous exploration remained unaltered, suggesting that PKMzeta may not affe

239 ours decreased by 60%, whereas cdk6 activity remained unaltered, suggesting that the loss of cdk2 act

240 binding and infectivity of the mutant virus remained unaltered, the changes in Env antigenicity were

241 f antibody-functionalized DNA nanostructures remains unaltered, the absolute number of bound surface

242 Whereas the static spin response remains unaltered, the quantum spin dynamics and associa

243 renergic receptor kinase, betaARK1, activity remains unaltered, the unresponsiveness of beta(1)-AR is

244 (18:2n-6) and alpha-linolenic acid (18:3n-3) remained unaltered, there was a decrease in arachidonic

245 levated within the first 5 s of exercise and remained unaltered thereafter, with no differences betwe

246 tained in the absence of these molecules and remains unaltered through the Cl- plasma level.

247 behavioral selectivity of the cocaine SDelta remained unaltered throughout an 8-day test period.

248 content (18.3-54.5%) while As and Cd levels remained unaltered throughout the experiments.

249 ibuted in PAs, and that this proportion will remain unaltered under future climate change.

250 tics, arachidonic acid and internal acidosis remains unaltered under conditions of hypoxia.

251 graphene sheets, where the basal plane sites remain unaltered until the available edge plane like- si

252 However, phosphotaurocyamine concentration remains unaltered until the MbO2 saturation falls below

253 This result remained unaltered upon adding formic acid-d(2) (DCOOD)

254 Conversely, XPC transcription remained unaltered upon Brg1 knockdown indicating that B

255 AnxA8 gene expression, on the other hand, remained unaltered upon manipulating Wnt signalling, sug

256 of sigmaE:RseA:RseB is 2:5:1 and this ratio remains unaltered upon heat shock induction of the sigma

257 benzo[a]pyrene in hydrated magnesium sulfate remain unaltered when exposed to UV radiation comparable

258 However the sensitivity to Sigma1R ligands remained unaltered when co-expressed with the Sigma1R in

259 was 6.5 and 6.4 g/100 g after production and remained unaltered when stored at 6 degrees C for a shel

260 CpG sites adjacent to or within Alu repeats remain unaltered, while a small set of CpG sites gain or

261 Glomerular volume and number remained unaltered with cisplatin exposure, but cortical

262 ynamics of the major amino acids, e.g., Gly, remained unaltered with respect to parity.

263 o which zebrafish NSC potential decreases or remains unaltered with age.