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 transmission, and paired-pulse facilitation remain unaltered.

3 nzyme complex is formed where the substrates remain unaltered.

4 ing neurons, whereas other synaptic proteins remain unaltered.

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

6 usters, whereas neuronal presynaptic boutons remain unaltered.

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

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

9 4 months of age, neurofascin 155 low levels remain unaltered.

10 rylation of the cytoplasmic substrate p90RSK remains unaltered.

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

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

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

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

15 d etoposide-stabilized DNA cleavage activity remains unaltered.

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

17 integrin coupling with intracellular motors remains unaltered.

18 hnique involving dual fluorescence labeling, remains unaltered.

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

20 evated Cdk5 activity, whereas p35 expression remains unaltered.

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

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

23 l structure that induces anomalous diffusion remains unaltered.

24 ternalization; the activation state of Cdc42 remains unaltered.

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

26 ells remapped, and their spatial information remained unaltered.

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

28 damental nature of the temporal pattern code remained unaltered.

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

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

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

32 baseline, although non-oxidative metabolism remained unaltered.

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

34 reduced and shortened, PI3 kinase activation remained unaltered.

35 odestly increased, and sphingomyelin content remained unaltered.

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

37 se activation, whereas Erk kinase activation remained unaltered.

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

39 electrodes; however, the capture specificity remained unaltered.

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

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

42 ase and glucosylceramide synthase activities remained unaltered.

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

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

45 UC alone from equivalently treated seedlings remained unaltered.

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

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

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

49 transcriptional activation of chromogranin A remained unaltered.

50 capsaicin, although the unitary conductance remained unaltered.

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

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

53 the mechanical properties of the sarcolemma remained unaltered.

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

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

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

57 Bone marker levels in HCs remained unaltered.

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

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

60 contents decreased while carotenoid content remained unaltered.

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

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

63 precursor protein proopiomelanocortin (POMC) remained unaltered.

64 associated with many key metabolic processes remained unaltered.

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

66 ary conductance and nucleotide sensitivities remained unaltered.

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

68 cytes that were immunopositive for activin A remained unaltered.

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

70 RKO mice while regional brain glucose uptake remained unaltered.

71 The time course of the evoked signals remained unaltered.

72 expression of other death effector proteins remained unaltered.

73 dritic cells and resident tissue macrophages remained unaltered.

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

75 lthough classical estrogen receptor function remained unaltered.

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

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

78 umor irradiation, despite nonspecific uptake remaining unaltered.

79 1 versus control), whereas arterial dilation remained unaltered (-19.3+/-5%).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

115 The ATP binding capacity remains unaltered by the modifications.

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

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

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

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

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

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

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

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

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

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

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

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

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

129 0 to 95% following infection with 8-DR.R but remained unaltered following infection with delta8-DR, s

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

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

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

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

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

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

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

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

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

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

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

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

142 64%) sites, decreased in 19 (18%) sites, and remained unaltered in 19 (18%) sites (P < .01).

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

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

145 Lymphocyte subsets remained unaltered in all monkeys.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

181 (18:2n-6) and alpha-linolenic acid (18:3n-3) remained unaltered, there was a decrease in arachidonic

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

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

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

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

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

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

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

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

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

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

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

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

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

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