ライフサイエンスコーパス: unaltered

1 Alveolar macrophage TNFalpha production was unaltered.

2 s; however, the capture specificity remained unaltered.

3 of mEPSCs and amplitudes of evoked EPSCs are unaltered.

4 ission, and paired-pulse facilitation remain unaltered.

5 non-mGluR-mediated long-term potentiation is unaltered.

6 e dorsal portion of the hippocampus remained unaltered.

7 lidation, whereas short-term memory remained unaltered.

8 Bone marker levels in HCs remained unaltered.

9 decreased while carotenoid content remained unaltered.

10 ugh both positive and negative selection are unaltered.

11 the presynaptic residual calcium signals are unaltered.

12 formation is altered yet disease outcome is unaltered.

13 ific protein, proteolipid protein (PLP), was unaltered.

14 lls, whereas cell cycle progression remained unaltered.

15 tal number of membrane-proximal vesicles was unaltered.

16 rations, cardiovascular risk biomarkers were unaltered.

17 f endothelial aquaporin-1 water channels was unaltered.

18 fatty acid oxidation, and VLDL secretion was unaltered.

19 solic PKC increased, PKC activity itself was unaltered.

20 +/- 16 and 43 +/- 30%), but OXPHOS remained unaltered.

21 levels of dopamine and its metabolites were unaltered.

22 rons, whereas other synaptic proteins remain unaltered.

23 eeping transpiration (EC) and, hence, runoff unaltered.

24 sm, while leaving transport activity of MCT2 unaltered.

25 ility at the macromolecular level is largely unaltered.

26 enous regulatory elements of mouse Nod2 were unaltered.

27 the essential character of the response was unaltered.

28 DRiPs, and total MHC class I levels remained unaltered.

29 embrane association of the two variants were unaltered.

30 boundaries of PPS, but leaving IPS distance unaltered.

31 pment of vestibular efferent innervation was unaltered.

32 however, TRPC1 and TRPC5 mRNA expression was unaltered.

33 endocytosis, and surface receptor levels are unaltered.

34 iation, despite nonspecific uptake remaining unaltered.

35 cin-induced mEPSCs from C-fiber synapses was unaltered.

36 3(R225Q) mice, whereas glucose tolerance was unaltered.

37 ctivation, sEPSCs in these same neurons were unaltered.

38 egulation of CD25 and CD69, remained largely unaltered.

39 rter components MCU, MCUR1, and MICU1 remain unaltered.

40 the affinity for the substrate (KM) remained unaltered.

41 g technique, whereas APP mRNA level remained unaltered.

42 evels, whereas other coagulation factors are unaltered.

43 he strengths of extant connections were left unaltered.

44 t the aromatic/nonaromatic character remains unaltered.

45 ndothelial capacity to engage leukocytes) is unaltered.

46 whereas in H1299 cells the level of ATP was unaltered.

47 Ca2+ leak, and SR Ca2+ content were largely unaltered.

48 , the strength of the remaining synapses was unaltered.

49 whereas neuronal presynaptic boutons remain unaltered.

50 pacity, while leaving cellular proliferation unaltered.

51 teps in the internalization of the drug were unaltered.

52 fonate (PFOS) found that linear (L)-PFOS was unaltered.

53 bed by PAC spectroscopy, remains essentially unaltered.

54 pped, and their spatial information remained unaltered.

55 t were immunopositive for activin A remained unaltered.

56 n, whereas FRET with other tested SNAREs was unaltered.

57 al health, although lung fibrosis is visibly unaltered.

58 ability of insulin to suppress lipolysis was unaltered.

59 lls, but the surface expression of Ly49A was unaltered.

60 eaving orientation and direction selectivity unaltered.

61 idal cells, whereas D2 receptor function was unaltered.

62 tate global O-GlcNAc levels remained grossly unaltered.

63 an collecting duct cell line, while SPAK was unaltered.

64 ng the overall cellular copper concentration unaltered.

65 ight, litter size and crown rump length were unaltered.

66 ent the target haplotypes over short regions unaltered.

67 cells, those of both AP- and betaE-sites are unaltered.

68 , while maintaining their healthy properties unaltered.

69 vation, leaving synaptic vesicle recruitment unaltered.

70 , although non-oxidative metabolism remained unaltered.

71 velopment of B lymphocytes in bone marrow is unaltered.

72 ile and duration of the SWRs were relatively unaltered.

73 ra littoralis, leaving the midgut microbiota unaltered.

74 tress while FoxP3(+) T-regulatory cells were unaltered.

75 evealed a decrease in [4-(13)C]glutamate but unaltered [4-(13)C]glutamine concentrations in the VMH o

76 Left ventricular ejection fraction remained unaltered (48% +/- 7% to 49% +/- 5%, p = 0.4) as did car

77 The percent peristalsis remained unaltered (94% vs 87%; P = 0.71).Overall, patients with

78 tter sizes and number of fetal loss remained unaltered, a reduced fetal weight and a lower frequency

79 ate-adenosine monophosphate synthase exhibit unaltered ability to control infection in an adenovirus-

80 mTOR complex [mTORC]2)-deficient Treg showed unaltered ability to express CCR9, whereas Raptor (mTORC

81 oth zinc atoms remain bound in an apparently unaltered active site, and the protein displays a well o

82 formation, and long-lived IgG1 responses of unaltered affinity developed in mice lacking cDCs at the

83 6.1%) compared with controls, which remained unaltered after abstinence (-17.0%).

84 roposterior nucleus to area 3b also remained unaltered after injury.

85 hing step of the refining process and remain unaltered after the final deodorizing step.

86 9B expression levels in stable patients were unaltered after transplantation in PBMC but showed an in

87 Moreover, despite unaltered Ag presentation and costimulatory capabilities

88 t, while core clock components remain nearly unaltered, aging is associated with tissue-specific rewi

89 nd Thr(642) phosphorylation concomitant with unaltered Akt phosphorylation.

90 llele used remained basally silent, like the unaltered allele, and it was activated only by drug trea

91 sing wild-type or P-loop mutant RagC exhibit unaltered amino acid regulation of mTORC1.

92 It was found that THC left firing rate unaltered and only slightly reduced theta oscillations.

93 ancreatic lymph node T cell populations were unaltered and T cell proliferation was unaffected by pio

94 of vasopressin on mean arterial pressure was unaltered and that on renal vascular perfusion pressure

95 ite, the phosphorylation state of RNAPII was unaltered, and the transcription bubbles remained open.

96 ough volatilized Aroclors (gaseous PCBs) and unaltered Aroclors (dissolved PCBs) dominate in some sam

97 Hearing acuity in treated animals is unaltered at postnatal day 30.

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

99 re of the double mutant further indicates an unaltered backbone conformation, almost identical side-c

100 evere necrotizing rejection early despite an unaltered baseline immunosuppression.

101 60) preferentially recruited arrestin 3 with unaltered behavioral effects in arrestin 2 KOs.

102 .0005), while total white matter volume was unaltered (beta = -10.10; 95% CI, -20.73 to 0.53; P = .0

103 Unexpectedly, platelets from these mice show unaltered beta3- and beta1-integrin activation and conse

104 al beta-adrenergic signaling components were unaltered between control and DCM iPSC-CMs, we found tha

105 homeostasis maintained throughout growth and unaltered between division and maturation zones.

106 cy of electrospray ionization (ESI) remained unaltered between sample extracts and calibration standa

107 n multilamellar vesicles at equilibrium with unaltered bilayer thicknesses.

108 g, and secondary resistance, associated with unaltered binding.

109 When reacted with unaltered biotite and chlorite, significant sorption of

110 e and real-time discrimination of tumor from unaltered brain tissue offers the possibility for the im

111 eurones excited by cholecystokinin (CCK) was unaltered but the proportion of neurones in which CCK in

112 ammasome activation in mature macrophages is unaltered, but IL-18 production from monocytes is greatl

113 regulatory genes including lmo2 and scl are unaltered, but levels of gata1 transcripts, encoding a k

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

115 duced antibody production and pathology were unaltered by 11beta-HSD1 deficiency though plasma levels

116 61), similar for Alzheimer disease only, and unaltered by accounting for stroke.

117 in the VTA of ClockDelta19 and WT mice were unaltered by acute AUT1 treatment.

118 bit constitutive [(32)P]GTP charging that is unaltered by amino acid withdrawal.

119 In V1, FF excitatory inputs were unaltered by DE, whereas lateral intracortical connectio

120 the singing-related output of HVCX cells is unaltered by distorted auditory feedback (DAF), deafenin

121 Symptoms were minimal and unaltered by either diet among controls.

122 and aggregation in response to agonists was unaltered by JAK2V617F expression.

123 crine cell mass and proliferation rates were unaltered by liraglutide treatment.

124 d blood at the end of the imaging period was unaltered by lung inflammation.

125 ting the genotype variable as irreducible or unaltered by other colocalizing forms of genetic (e.g.,

126 latory partner, phospholamban (PLB) and were unaltered by PLB phosphorylation or changes in calcium o

127 horylation on both phosphorylation sites was unaltered by PP2B or PP2C inhibitors.

128 netration and nonspecific binding, which was unaltered by preadministration of the unlabeled agonist.

129 Sphingosine metabolism kinetics were also unaltered by SERINC5 expression.

130 hereas glucose incorporation to glycogen was unaltered by small interfering RNA against DAPK3, palmit

131 EK cells revealed that Nav1.7 activation was unaltered by the A1632T mutation but that steady-state f

132 positive effects of F19A on NSC growth were unaltered by the addition of a functional blocking antib

133 st natural enemies) are enhanced, reduced or unaltered by the presence of a co-infecting symbiont.

134 viour of non-declining C. septempunctata was unaltered by the presence of H. axyridis.

135 the P2X receptors were fully functional and unaltered by the receptor interaction for P2X2-alpha6bet

136 A variance as a function of the mean remains unaltered by their presence.

137 CXCR5(+)Th17 cell frequencies were unaltered by TNF blockade and in fact remained remarkabl

138 Locomotor activity was unaltered by vector administration to either region.

139 lteration status into somatic gain, loss and unaltered categories, each displaying distinct epigeneti

140 ed with Seahorse XF24 flux analyzer revealed unaltered cellular respiration in neurons derived from R

141 on was also observed for N-tail mutants with unaltered centromeric DNA sequences.

142 (Topo IIalpha) ensures genomic integrity and unaltered chromosome inheritance and serves as a major t

143 These mice, however, showed unaltered cocaine-induced conditioned place preference.

144 Replication of r129 in fibroblasts appeared unaltered compared to that of N13R10.

145 ss, cell walls in fra1-5 have an essentially unaltered composition and ultrastructure.

146 s from Foxp3(Cre)xT-bet(fl/fl) mice revealed unaltered cytokine production and suppressive capacity.

147 which is a membrane-selective ER ligand, was unaltered, demonstrating integrity of MISS actions.

148 transiently increased systolic function and unaltered diastolic function 1 day after single ISO inje

149 integrity of the retinal organization and an unaltered distribution of the different cone photorecept

150 ogies there is a growing demand for removing unaltered DNA over large pools-of-sequences.

151 ing to further electrophilic substitution of unaltered DOM sites and chlorinated DOM moieties.

152 that the isotopic composition of NOx remains unaltered during collection.

153 eased during Valsalva manoeuvre but remained unaltered during handgrip exercise.

154 , a previous study showed that the SCN CC is unaltered during RF, which creates a misalignment betwee

155 nation of the left and right forepaws remain unaltered during the execution of distinct grooming epis

156 d based on our analyses are transcribed with unaltered efficiency but translated with higher efficien

157 oluminescence quantum yields and essentially unaltered emission spectra are maintained.

158 G-based passivation layer, results in nearly unaltered enzymatic activity toward immobilized heterodu

159 ltered kinase activity, resulting in largely unaltered ERK activation but in AKT that was hyperactiva

160 Also correlating with the unaltered expression of BAFF receptor, BAFF stimulation

161 , the aggregated proteins remain active with unaltered fidelity.

162 dback excitation within CA1, thus leading to unaltered firing rates.

163 lure, RyR2 shows decreased CaM affinity, but unaltered FKBP 12.6 affinity.

164 Conversely, at high altitude, FMD was unaltered following moderate-intensity exercise, and adm

165 PSMB5 and STAT3 protein levels remained unaltered following the inhibition of proteasome activit

166 cryopreservation procedure kept sensitivity unaltered for 30 days and possibly longer.

167 ensity of the aluminum-DEMAX complex remains unaltered for over 24h at room temperature and is a line

168 herens junction in TOCA-1-knockout cells but unaltered freeze-fracture fibril morphology.

169 e lead exposure and CpG methylation remained unaltered from 30 to 78 months.

170 show a pattern of NF-kappaB dynamics that is unaltered from wild-type cells, but activation of the TN

171 other combinations result in synergistic or unaltered growth relative to bacteria experiencing a sin

172 ed that unlike in TorA[KQ]-30aa-MalE with an unaltered h-region, the mutated reporters moved deep int

173 sion of key target genes such as Myc remains unaltered, highlighting the existence of alternative mec

174 2+) release events and the rate of DADs were unaltered; however, DADs had lower amplitude in hetKO.

175 Compared with transgenic mice expressing unaltered human PrP, mice expressing the human-elk chime

176 itutive proteasome subunits, while retaining unaltered immunoproteasome subunit expression.

177 ng of APP and other neuronal substrates, was unaltered in 4CA mice despite the lack of BACE1 S-palmit

178 g GABA concentration decreased in V1 but was unaltered in a control parietal area.

179 Megalin expression remained unaltered in adult WT and KO mouse brain, SC, and kidney

180 rm of balanced binocular suppression that is unaltered in amblyopia.

181 Protein and ash proportions were unaltered in any of the treatments.

182 ontrol mice, whereas lactate levels remained unaltered in APP/PS1 mice from 3 to 12 months of age.

183 ound that the cytokine and Ab responses were unaltered in CDG/Ag-immunized IFNAR(-/-) mice.

184 an littermate controls, whereas basal BP was unaltered in Cdh5-CreERT2 Nox2KO mice (in which Nox2 is

185 Slc6a15 protein was unaltered in ChAT interneurons.

186 Given that beta2AR expression is unaltered in CHF, a beta-arrestin-biased agonist that op

187 Although the total AMPK activity was unaltered in cKO hearts because of upregulation of gamma

188 -Ldgp63 in GFP-LdRab1:WT-expressing cells is unaltered in comparison with control cells.

189 tivity ex vivo and hemodynamics in vivo were unaltered in DDAH1(En-/-) mice.

190 tegrin alphaIIbbeta3 affinity regulation was unaltered in Dok-2(-/-) platelets, Dok-2 deficiency was

191 s inhibitory effect on IL-12 production were unaltered in Dusp16tp/tp macrophages.

192 acturonide (OG)-induced immune signaling was unaltered in gae1 gae6 mutant plants, immune signaling i

193 and diacylglycerol and ceramide content were unaltered in gastrocnemius muscle from ob/ob-gamma3(R225

194 regulatory cells, and T-helper 17 cells were unaltered in HIV+ men, CD8 T-cell production of tumor ne

195 kout mice with endothelial GC-A deletion and unaltered in knockout mice with endothelial cGKI deletio

196 , two major hepatic alpha-glucosidases, were unaltered in L-G6pc(-/-) mice, pharmacological inhibitio

197 ssion compared with limb muscles, which were unaltered in microgravity.

198 ss of miR-29a, because miR-29b expression is unaltered in miR-29a/b-1-null HSCs, and only ectopic exp

199 The genomic H3K27me3 landscape was unaltered in mutant tissue, and support for a demethylas

200 Moreover, Foxa2 levels remained unaltered in Myostatin(-/-) mice, while levels of p63/RE

201 port, NLRP3 inflammasome activation remained unaltered in NLRP10-deficient DCs even after restoring D

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

203 to avoid CTL recognition while leaving HLA-C unaltered in order to prevent NK cell activation by enga

204 urrent, and Na+ /Ca2+ -exchange current were unaltered in pAF, indicating the absence of AF-induced e

205 dine receptor fractional phosphorylation was unaltered in pAF, whereas ryanodine receptor expression

206 aso-obliteration and neovascularization were unaltered in Par2 knockout mice, suggesting compensatory

207 n onto parvalbumin-positive interneurons was unaltered in PSD-95 KO mice.

208 Other biophysical channel properties were unaltered in R1389H channels including ion selectivity,

209 protein of mammalian target of rapamycin was unaltered in response to both resistance exercise and am

210 rientation of cortical microtubule arrays is unaltered in rhm1 mutants.

211 nd stimulation of glucose disappearance were unaltered in RYGB subjects.

212 in of GODZ KO versus wild-type (WT) mice but unaltered in SERZ-beta KO mice.

213 Basal synaptic transmission is also unaltered in SPNs of LRRK2 overexpressing mice, but they

214 evelopment and rate of relaxation (tau) were unaltered in TG(S282A) mice.

215 erties of Abeta, including this turn, remain unaltered in the central fragment Abeta18-35.

216 lated tau levels and ubiquitin staining were unaltered in the IFN-gamma cohorts.

217 tent with findings that vGAT mRNA levels are unaltered in the illness and confirming that the number

218 Even though basal synaptic transmission was unaltered in the neuromuscular synapses in IM-AA mice, w

219 de (LPS) surface charge and aggregation were unaltered in the presence of OligoG CF-5/20.

220 and abscisic acid levels and sensitivity are unaltered in the rdo5 mutant.

221 Although apoptosis is unaltered in these mice, they recover more rapidly from

222 RNA replication and viral titre were unaltered in viruses possessing only one mutated structu

223 as, whereas many cells remain phenotypically unaltered in younger mice.

224 he propagation velocity of the CSD waves was unaltered indicating stable neuronal excitability.

225 s and GODZ or SERZ-beta KO brain slices were unaltered, indicating that GODZ-mediated palmitoylation

226 pression of Sost encoding for sclerostin was unaltered, indicating that osteoblastic Lrp4 retains scl

227 cholinergic dendrites was, however, largely unaltered, indicating that the reduction in the areal st

228 found to display reduced binding to LRP1 and unaltered inhibitory activity against prototypic metallo

229 Although total JPH2 levels were unaltered, JPH2 phosphorylation levels were found to be

230 bolic and root growth characteristics albeit unaltered leaf morphology under optimal growth condition

231 The unaltered level of total PrP during phase 1, when prion

232 s containing the base modification exhibited unaltered levels of enhanced GFP reporter gene expressio

233 viously that ADAM17 hypomorphic mice exhibit unaltered levels of serum sIL-6R.

234 These animals displayed unaltered lung Th2 and eosinophilic responses after intr

235 e current focus is on studying the pristine, unaltered materials.

236 ed conjunctival inflammation than birds with unaltered microbiomes, even after accounting for differe

237 The unaltered minerals could not remove Cr(VI) from solution

238 oved and, in the absence of reduction by the unaltered minerals, suggest that only the microbially re

239 olutions, gels, and solids) to be studied in unaltered natural samples.

240 NDPK-B knockout mice had unaltered NDPK-C expression but showed contractile dysfu

241 These Icam1(tm1Jcgr)NOD mice exhibit unaltered numbers of regulatory T cells, but increased I

242 L-ACY-1 expression remained low/unaltered on balanced (P50:C50 and P53:C47) or protein-b

243 We show that glutamate transmission is unaltered onto striatal projection neurons (SPNs) of adu

244 ly enter leaf epidermal cells were seemingly unaltered or showed even enhanced microbial growth or sy

245 In contrast, these transcripts were unaltered, or only modestly changed, in parvalbumin inte

246 Because bone resorption is largely unaltered, OSM could represent a new anabolic treatment

247 HSA-AuNCs against bilirubin was practically unaltered over a wide pH (6-9) and temperature (25-50 de

248 l care for more than 6 hours than those with unaltered oximetry readings.

249 ted in defective Akt phosphorylation despite unaltered phosphatidylinositol 3,4,5-trisphosphate level

250 ion of indomethacin (INDO; 1.2 mg kg(-1)) or unaltered (placebo) followed by LBNP to pre-syncope.

251 ion of ADMA and lower NO concentrations, but unaltered plasma ADMA concentrations.

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

253 The unaltered PPARGC1A gene expression in muscle of O-T1D su

254 yed reduced transcriptional activity despite unaltered protein interactions with co-activators and -r

255 round position 213 in AAT, far away from the unaltered reactive center loop (357-360).

256 ated remote memories (>50 days) while having unaltered recent memories (<24 h).

257 Schwann cell-specific Pex5 mutant mice were unaltered regarding axon numbers, axonal calibers, and m

258 resistant to Pseudomonas syringae but retain unaltered resistance against necrotrophs.

259 of the thin planetary surface layer between unaltered rock and the atmospheric boundary.

260 was significantly less than trapping in the unaltered rock.

261 1 nmol/L; approximately 3-fold increase) and unaltered RyR2 affinity for the FK506-binding protein FK

262 In unaltered samples, the trapping of CO2 and N2 were indis

263 rily probes foreign, modified-self, and also unaltered self-structures.

264 ed angiogenic invasion of fibrin matrix with unaltered sensitivity to proapoptotic stress compared wi

265 D4 with markedly greater efficiency than did unaltered SIVmac239 Env.

266 However, the unaltered SNCA levels observed following ZSCAN21 down-re

267 Although fetal weight is unaltered, specific Rtl1 transcripts and protein levels

268 The majority of target genes are in an unaltered state and cannot be further activated.

269 -/-) strains exhibited increased (strain A), unaltered (strain B) or decreased (strain C) mean arteri

270 An intact bimetallic center and unaltered substrate binding indicate that proper positio

271 REG3G, DEFB4A, S100A9, MUC1, and MUC13) were unaltered, suggesting an adequate production of antimicr

272 ecay of caffeine-induced Ca2+ transients was unaltered, suggesting increased SERCA2a function.

273 Synaptic sound encoding was largely unaltered, suggesting that excess exocytosis occurs extr

274 tion during spontaneous exploration remained unaltered, suggesting that PKMzeta may not affect the ne

275 However, IL-17A and IL-17C expression was unaltered, suggesting that the increased inflammation in

276 median survival of 22 wk, despite otherwise unaltered systemic iron status.

277 he P/Q channel depleted layer VI neurons was unaltered, T-type calcium currents in the postsynaptic t

278 rst adult mice described that lack TFPI with unaltered TF.

279 pe, exacerbated generation of Th2 cells, and unaltered Th17 differentiation.

280 AI (ApoAI) from Si NP hard coronas, leaving unaltered the dispersion physicochemical properties.

281 embrane integrity, maintaining substantially unaltered the vibrational contributions of the other cel

282 Whereas the static spin response remains unaltered, the quantum spin dynamics and associated sele

283 leasable SV pool size, and quantal size were unaltered, the reduced synaptic strength in the absence

284 y in the peripheral blood of T1D patients is unaltered, their suppressive abilities are diminished co

285 urvature and tortuosity of the bile duct are unaltered, this enlargement of the biliary tree is cause

286 (18.3-54.5%) while As and Cd levels remained unaltered throughout the experiments.

287 ed by its retained excellent performance and unaltered TMR ratio after over 1000 bending cycles.

288 e electrode rise potential from 46 +/- 2 mV (unaltered) to -6 +/- 0.5 mV (oxidized), producing a whol

289 Quantitative electron microscopy revealed unaltered ultrastructural parameters.

290 ined increasing popularity, as they offer an unaltered view on the architecture of biological specime

291 ogether or touching, whereas judgements were unaltered when adjacent fingers were stimulated.

292 Connectivity is unaltered when blue cone transmission is suppressed.

293 nd 6.4 g/100 g after production and remained unaltered when stored at 6 degrees C for a shelf life of

294 l-length 2N4R tau protein is 0.03pM, a value unaltered when the assay was processed in bovine serum a

295 uced activation of sympathetic signaling was unaltered, whereas AMPK was enhanced, in AdKO IWAT.

296 maker, the suprachiasmatic nucleus (SCN), is unaltered while the molecular clock in the hippocampus i

297 In this unpaired setting, ApoE levels were unaltered, while ApoA1 was reduced in the anaphylactic g

298 Presence of excess unaltered, wild-type (WT) DNA providing no information o

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

300 f the major amino acids, e.g., Gly, remained unaltered with respect to parity.