ライフサイエンスコーパス: phosphorylation level

1 lysis even though these agents increased its phosphorylation level.

2 d MHC II ligation increases overall tyrosine phosphorylation level.

3 al regulation between ACR4 and PP2A-3 at the phosphorylation level.

4 terized by pronounced changes in the protein phosphorylation level.

5 ve HCC1954 cells showing a particularly high phosphorylation level.

6 AR activity in the PVN by reducing the NMDAR phosphorylation level.

7 hatase, which concomitantly restores protein phosphorylation levels.

8 r stage of mitosis, without changing overall phosphorylation levels.

9 was used to determine protein expression and phosphorylation levels.

10 blots revealed no differences in AKT or ERK phosphorylation levels.

11 rylation state of the CTD, reducing its Ser2 phosphorylation levels.

12 ABA were found to have significantly altered phosphorylation levels.

13 ed with a global repression of histone H3S10 phosphorylation levels.

14 0M mutation confers increased Y992 and Y1068 phosphorylation levels.

15 d Bcl-X(L) protein levels, as well as in Bad phosphorylation levels.

16 e to generate high levels of stress with low phosphorylation levels.

17 N4-OH, N7, and N7-OH had substantially lower phosphorylation levels.

18 -type virus substantially reduced eIF2 alpha phosphorylation levels.

19 ere positively correlated with p53 serine 15 phosphorylation levels.

20 , BK stimulates a reduction of PMCA tyrosine phosphorylation levels.

21 ges in metal selectivity, ATP dependence, or phosphorylation levels.

22 ons in the Glc7 phosphatase that increase H3 phosphorylation levels.

23 TCR-CD3 clusters, which scaled with overall phosphorylation levels.

24 m Fam20C-knockout (KO) mice and analyzed the phosphorylation levels.

25 contrast, estradiol but not G1 increased Akt phosphorylation levels.

26 ces global RNA polymerase II (Pol II) Ser(2) phosphorylation levels.

27 acetylation resulted in increases of Ser-294 phosphorylation levels.

28 abling large-scale determination of relative phosphorylation levels.

29 ally overexpress CD30v exhibit increased ERK phosphorylation levels, activation of the canonical NFka

30 but it is restored to nearly half of the pre-phosphorylation level after dissociation and reconstitut

31 quickly elevates CREB Ser133 and ATF-1 Ser63 phosphorylation levels, although the CREB Ser133 phospho

32 noted modification of both eIF4E and 4E-BP1 phosphorylation levels among viruses that produce capped

33 carbon source utilization independent of its phosphorylation level and 2) in cell wall biosynthesis a

34 In addition, activation of MOR elevates the phosphorylation level and kinase activity of PKCzeta.

35 al functions of resetting response regulator phosphorylation level and suppressing cross-talk.

36 n kinase CK2 normalized the GluN2B Ser(1480) phosphorylation level and the contribution of GluN2A to

37 Furthermore, the GluN2B Ser(1480) phosphorylation level and the synaptosomal GluN2A protei

38 ts in receptor variants that display reduced phosphorylation levels and are more labile as compared w

39 a GSK3 activity-dependent ability to enhance phosphorylation levels and DNA binding of NF-kappaB p65.

40 unoblot analysis to examine phot2 endogenous phosphorylation levels and in vitro phosphorylation assa

41 al intracellular calcium and resting tyrosyl phosphorylation levels and is highlighted by a marked ab

42 mutant flies showed relatively high S936-TRP phosphorylation levels and light-dark phosphorylation dy

43 otein phosphatase I abolished differences in phosphorylation levels and normalized titin-based passiv

44 cetylation levels correlate with Beclin1 S30 phosphorylation levels and poor prognosis in glioblastom

45 levels correlate with PDH S293 inactivating phosphorylation levels and poor prognosis in glioblastom

46 The aberrantly high Smad3 phosphorylation levels and SBE activity in TGF-beta-indu

47 yperresponsive to IL-4 and show higher Stat6 phosphorylation levels and signaling coupled to downstre

48 ed activation of c-Src and elevated tyrosine phosphorylation levels and subsequent formation of podos

49 ssociated with a normalization of both basal phosphorylation levels and T cell signaling.

50 zation, which has consequences on overall H1 phosphorylation levels and the stability of H1 binding t

51 eatures, correlating with changes in protein phosphorylation levels and the subsequent development of

52 verexpression of IKK2 increased cellular MLC phosphorylation level, and pharmacological inhibition of

53 e-related changes in Abeta oligomers and tau phosphorylation levels are correlated with decreases in

54 d intracellular Gln3-Myc13 localization, the phosphorylation levels are markedly influenced by severa

55 Gln3-Myc13 phosphorylation levels are regulated by at least three m

56 Although EGFR phosphorylation levels are ultimately determined by the

57 tumor growth, associated with enhanced Tie2 phosphorylation levels, as compared with low levels in c

58 schizophrenia, a significant decrease in the phosphorylation level at serine 897 (S897) of the NMDA r

59 ng of cells was used to measure the relative phosphorylation levels at the two sites.

60 rostate cancer cell lines, unexpectedly high phosphorylation levels at the Tyr-527 inhibitory site ar

61 trate phosphorylation gradient, with highest phosphorylation levels between the two spindle poles, em

62 eins showing changes in either abundance, or phosphorylation levels, between wild-type and pig-1 muta

63 rporated mutant and WT cTnI, and their basal phosphorylation levels by top-down mass spectrometry dem

64 CPC activity, suggesting that high substrate phosphorylation levels can mask persistent CPC-dependent

65 Mediator phosphorylation levels change upon an external stimulus

66 LC-MS/MS analyses revealed phosphorylation level changes of a number of phosphosite

67 -like cells exhibited increased Syk tyrosine phosphorylation levels compared with WT cells.

68 The S727STAT3 phosphorylation levels correlate with collagen 17 expres

69 Furthermore, PGK1 S203 and PDHK1 T338 phosphorylation levels correlate with PDH S293 inactivat

70 Notably, VDAC phosphorylation level correlated with steatosis severity

71 signature analyses, quantification of STAT5 phosphorylation levels, cytokine neutralization experime

72 n of androgens, Her-2/neu mRNA, protein, and phosphorylation levels decreased linearly with increasin

73 Our data indicate that: (i) observable Gln3 phosphorylation levels do not correlate in a consistent

74 Higher phosphorylation levels do not increase the stability of

75 itosis, HDAC2 and, to a lesser extent, HDAC1 phosphorylation levels dramatically increase.

76 lf-life and is co-regulated, with RNAPII CTD phosphorylation levels, during logarithmic growth in yea

77 myofibrils did not depend on the troponin I phosphorylation level (EC50 P/unP = 0.88 +/- 0.17, p = 0

78 nd long-lasting increase in GSK-3alpha Ser21 phosphorylation levels, followed by a delayed increase i

79 nd extracellular-signal-related kinase (ERK) phosphorylation levels following CLP.

80 on of responding cells, and amplification of phosphorylation levels for at least one phosphoprotein.

81 and rapamycin combination revealed decreased phosphorylation levels for proteins in both upstream and

82 6 conditions, resulting in 18,816 quantified phosphorylation levels from each multiplexed sample.

83 but not gamma-H2AX foci, and suppressed ATM phosphorylation levels >85% throughout the cell cycle.

84 Abnormally high phosphorylation levels (hyperphosphorylation) at Ser-284

85 ylated in 100% confluent BAEC and HUVEC, its phosphorylation level in 50% confluent BAECs or HUVEC wa

86 ucer and activator of transcription (STAT)-6 phosphorylation level in murine heart fibroblasts, and t

87 As the phosphorylation level in the CII domain rises, the relea

88 The global phosphorylation level in the group with a fast pH declin

89 The NCP phosphorylation level in the KO mice was lower than that

90 ric SR protein-phosphatase platform balances phosphorylation levels in a "goldilocks" region for the

91 es was elevated by HU but not Akti XII, AKT2 phosphorylation levels in activated neutrophils and plat

92 r results in significantly elevated receptor phosphorylation levels in cells, both in the absence of

93 Pases) play key roles in regulating tyrosine phosphorylation levels in cells, yet the identity of the

94 NF, and tropomyosin receptor kinase B (TrkB) phosphorylation levels in dorsal CA1, while blocking BDN

95 , exogenous HGF significantly increased ERK2 phosphorylation levels in esophageal mucosa.

96 for a close correlation between AKT and TSC2 phosphorylation levels in glioblastoma.

97 lin partner CCNK did not affect the bulk CTD phosphorylation levels in HCT116 cells, transcriptome se

98 protein levels, p38 MAP kinase isoforms, and phosphorylation levels in human and porcine TM cells.

99 between SENP3 protein levels and STAT3 Y705 phosphorylation levels in human laryngeal carcinoma spec

100 Specifically, IL-6 and p65 phosphorylation levels in mesenteric fat of NT KO mice a

101 lasting reversal of the increased GluA1 S831 phosphorylation levels in NAcc shell and persistently bl

102 APK signaling as observed by elevated ERK1/2 phosphorylation levels in progressive lesions and the ap

103 AT-2, STAT-3, STAT-4, and STAT-5 protein and phosphorylation levels in purified T cells, global trans

104 Assessment of Akt1 phosphorylation levels in response to C5a shows rapid an

105 owed these four proteins had higher tyrosine phosphorylation levels in response to CRP in platelets f

106 ng components also exhibited higher tyrosine phosphorylation levels in response to exogenous addition

107 ns in vivo revealed that PTHrP elevated Y418 phosphorylation levels in Src family kinases in CD11b(+)

108 rectly that the most recent estimates of the phosphorylation levels in this system are reasonably acc

109 nta, and that BRI1 positively regulates BAK1 phosphorylation levels in vivo.

110 obal transcription defects and increased CTD phosphorylation levels in vivo.

111 Although gross Gln3-Myc13 phosphorylation levels in wild type cells do not correla

112 three drugs increased global cellular kinase phosphorylation levels, including the angiogenesis-relev

113 JNK1/2, MKK4, c-Jun, and ATF-2 phosphorylation levels increase in response to TNFalpha

114 in (Shc) and phosphoinositol 3-kinase (PI3K) phosphorylation levels increase rapidly, but equilibrate

115 MKK6 phosphorylation levels increased immediately after H(2)O

116 in 4 binding to Munc18c decreased as Munc18c phosphorylation levels increased in pervanadate-treated

117 d7, Trx-SARA had no effect on the Smad2 or 3 phosphorylation levels induced by TGF-beta1.

118 gene expression to infer changes in protein phosphorylation levels induced in cells by various stimu

119 , is multiply phosphorylated in vivo and the phosphorylation level is dependent on ripening stage and

120 Moreover, we observed that the ATAD3As phosphorylation level is regulated by insulin and serum.

121 phorylation levels, although the CREB Ser133 phosphorylation level is substantial at baseline.

122 ated in vivo at the basal level and that the phosphorylation level is substantially decreased upon st

123 phosphorylation status in human based on rat phosphorylation levels is feasible.

124 hypertension, and reducing the NMDA receptor phosphorylation level may be effective for treating neur

125 vourable growth conditions, reduction in FDH phosphorylation levels may prohibit turnover allowing th

126 ceptor-coupled kinase is used to control the phosphorylation level of a response regulator, are commo

127 s both HER2 and HER3 appear to have a higher phosphorylation level of Akt (activated Akt).

128 INS 832/13 cells produced a reduction in the phosphorylation level of Akt, and phosphorylation was re

129 API-2 suppressed the kinase activity and phosphorylation level of Akt.

130 The phosphorylation level of beta-catenin at Thr(41)/Ser(45)

131 ch effects were associated with an increased phosphorylation level of both Src and extracellular sign

132 l of extracellular signal-regulated kinases, phosphorylation level of c-jun N-terminal kinases, and a

133 astrocytes suggests TSC1/2 and mTOR tune the phosphorylation level of catenin delta-1 by controlling

134 A decrease in the phosphorylation level of cofilin was detected upon v-Src

135 ransformed cells, there is a decrease in the phosphorylation level of cofilin, which is indicative of

136 evated CRMP2 expression accompanies a higher phosphorylation level of CRMP2 and its more pronounced a

137 s, we examined TGFBR2 expression (n=252) and phosphorylation level of downstream target SMAD2 (pSMAD2

138 cessfully been used for measuring changes in phosphorylation level of drug targets and downstream sub

139 along the signaling cascade and parsing the phosphorylation level of each node as a function of its

140 Sorafenib also reduced the phosphorylation level of eIF4E and down-regulated the an

141 In this report, our data show that the phosphorylation level of ErbB-2 primarily at Tyr(1221/2)

142 IGF-I dose-dependently increased the phosphorylation level of Erk1/2 by 1.2-5.3-fold and that

143 Brain tissue nitrites, phosphorylation level of extracellular signal-regulated

144 uced upregulation of nitric oxide synthesis, phosphorylation level of extracellular signal-regulated

145 CaMKII-mediated phosphorylation level of GluN2B serine 1303 (S1303) in t

146 he increased expression of Wnt4 elevated the phosphorylation level of its downstream protein GSK-3 th

147 tase activity and consequent increase in the phosphorylation level of its main substrate Syk.

148 The total phosphorylation level of KaiC oscillates with a circadia

149 The phosphorylation level of MA in defective mutant viruses

150 ux pump, increases due to a reduction in the phosphorylation level of MgrA, which in turn leads to a

151 hange technique, which avoids changes in the phosphorylation level of other proteins.

152 not result in a significant increase in the phosphorylation level of p12.

153 The tyrosine phosphorylation level of PECAM-1 immunoprecipitated from

154 r differentiation of mESCs by modulating the phosphorylation level of pRb.

155 Finally, the phosphorylation level of sarcomeric proteins was reduced

156 The protein phosphorylation level of seven individual protein bands

157 The heat shock-induced phosphorylation level of Slt2 was elevated in an sdp1Del

158 The phosphorylation level of Spo0A in the cell is determined

159 the TULA-2 gene significantly increased the phosphorylation level of Syk at Tyr-323 and Tyr-352 site

160 n cultured endothelial cells showed that the phosphorylation level of syndecan-4 was significantly re

161 l thereby shows inverse correlation with the phosphorylation level of TAK1 and subsequent reduction i

162 ng ethanol sensitivity, and suggest that the phosphorylation level of the downstream effector ERK is

163 LHCII complexes, coinciding with an elevated phosphorylation level of the LHCII under normal growth l

164 nal sensor both at amplifying changes in the phosphorylation level of the regulator caused by signals

165 The phosphorylation level of the regulatory proteins is also

166 pression of titin M-band binding proteins or phosphorylation level of the thin-filament regulatory pr

167 There were no significant changes in phosphorylation level of troponin-T3 and troponin-T4, or

168 ll spreading, interaction with c-Src, or the phosphorylation level of Tyr-402, Tyr-579/580, and Tyr-8

169 ibody Array analysis, measuring the relative phosphorylation levels of 39 intracellular proteins in u

170 decreased PTEN expression and increased the phosphorylation levels of Akt and downstream targets Fox

171 ere we show that perifosine strongly reduces phosphorylation levels of Akt and extracellular signal-r

172 We found that the basal phosphorylation levels of AKT isoforms were markedly inc

173 s FLNA, whereas in the absence of FLNA, high phosphorylation levels of Akt were maintained, enabling

174 Changes in phosphorylation levels of Akt, as measured by Western bl

175 Autophagy activation and phosphorylation levels of Akt, FoxO3, and ribosomal prot

176 ed in increased heart/body weight ratios and phosphorylation levels of Akt, p38, and Erk1/2.

177 milarly, we observe a 30-70% decrease in the phosphorylation levels of all PKA and PKC phospho-sites

178 ed Akt phosphorylation but does not decrease phosphorylation levels of AMP kinase alpha (AMPKalpha).

179 Analysis of the expression and phosphorylation levels of AMPAR subunits (GluA1/2/3/4) i

180 Pim deficiency decreases the phosphorylation levels of BAD, whereas ectopic expressio

181 of RBC CR1 causes a significant increase in phosphorylation levels of beta-spectrin that is inhibite

182 ecules (p38, JNK, and ERK) demonstrated that phosphorylation levels of both p38 and JNK were diminish

183 In these cells, tyrosine phosphorylation levels of both p52(Shc) and ErbB-2 were

184 mad7 within the NCC significantly suppressed phosphorylation levels of both Smad1/5/8 and Smad2/3 in

185 Basal phosphorylation levels of C-protein and troponin I were

186 kably reduced Ca(2+) leakage and lower basal phosphorylation levels of Ca(2+)-cycling proteins includ

187 ated arginine methylation of SRSF5 and lower phosphorylation levels of cobound SRSF2 enhance shuttlin

188 hosphorylation and contraction to changes in phosphorylation levels of CPI-17 at Thr38, RhoA at Ser18

189 Moreover, EC rats had lower basal phosphorylation levels of CREB at serine 133 in PFC and

190 onsiveness to TCR stimulation as assessed by phosphorylation levels of downstream signaling molecules

191 imer mouse model effected an increase in the phosphorylation levels of downstream STEP substrates and

192 Western blotting showed that the phosphorylation levels of ERK, c-Jun-NH(2) kinase, and p

193 AnxA1(-/-) mice also presented higher phosphorylation levels of ERK-1/2 and p65/RelA (NF-kappa

194 pathway as Gsk3beta phosphorylation elevates phosphorylation levels of Erk.

195 ta did not affect either serine or threonine phosphorylation levels of Ets1.

196 in synaptic efficacy correlates with reduced phosphorylation levels of eukaryotic elongation factor 2

197 The phosphorylation levels of FAK Tyr(397) were lower in FN-

198 a RhoA-Rock-PTEN pathway that decreases the phosphorylation levels of GABAAR, thus affecting recepto

199 omotor responding to NAcc AMPA and increased phosphorylation levels of GluR1 (Ser831), a CaMKII site,

200 ctivity as measured by the inhibition of the phosphorylation levels of GSK3beta.

201 raction with Her2, Beclin-1 up-regulates the phosphorylation levels of Her2 and Akt.

202 In addition, the phosphorylation levels of Hsf1 correlate with both trans

203 ion-Western blotting experiments showed that phosphorylation levels of IL-4Ralpha, Janus kinase 1, in

204 reated with CB2 agonists exhibited increased phosphorylation levels of inhibitory sites of the actin-

205 HepG2(SOCS3) show lower phosphorylation levels of insulin receptor substrate 1 (

206 ith concomitant augmentation of the tyrosine phosphorylation levels of insulin-signaling molecules.

207 Moreover, the phosphorylation levels of Itk and a downstream substrate

208 there was a marked elevation in GSK3beta and phosphorylation levels of its cognate phosphorylation si

209 at a single-cell resolution and studied the phosphorylation levels of key proximal human TCR activat

210 s of the TCR signaling pathway, the tyrosine phosphorylation levels of LAT and SLP-76 are the most af

211 mediate various cellular events and modulate phosphorylation levels of many downstream factors in the

212 ession of SND1-BRAF in H1299 cells increased phosphorylation levels of MEK/ERK, cell proliferation, a

213 at rhMIF induces time-dependent increases in phosphorylation levels of MEK1/2, Erk1/2, and Elk-1, as

214 arge B-cell lymphoma patients had high basal phosphorylation levels of most measured signaling nodes,

215 verexpression of Lyp caused reduction in the phosphorylation levels of multiple proteins in KCL22 chr

216 ivity of these kinases and thus the tyrosine phosphorylation levels of NMDA receptors.

217 Phosphorylation levels of OLE3 during seed germination w

218 cin complex 1 (mTORC1) inhibition, since the phosphorylation levels of p70S6 kinase and 4E-BP1 were d

219 in, while echistatin significantly decreased phosphorylation levels of paxillin.

220 Phosphorylation levels of protein kinase A substrates we

221 ith wild-type H. ducreyi had greatly reduced phosphorylation levels of proteins in the 50-to-60-kDa r

222 Phosphorylation levels of PTEN, Akt, and Akt substrate d

223 uR1, but not PKC, reduced the basal tyrosine phosphorylation levels of Pyk2 and Src, suggesting that

224 183A, and R1S183/201A, demonstrated that the phosphorylation levels of R1S4/201A were significantly l

225 The phosphorylation levels of RB at serine residues 780 and

226 exhibited markedly decreased S(8)/T(1)(7)(0) phosphorylation levels of RIG-I and resistance to infect

227 er analog in vitro, had little effect on the phosphorylation levels of ROCK substrates, migration, in

228 Here we show that TICs exhibit increased phosphorylation levels of S727STAT3 because of PP2A inac

229 noted a 10-40% and a 25-35% reduction in the phosphorylation levels of select sites in old wild type

230 We report a 7-35% reduction in the phosphorylation levels of select sites in old wild type

231 ctivated by protein kinase A even though the phosphorylation levels of Ser2844 are similar to control

232 pe I interferon (IFN)-induced expression and phosphorylation levels of signal transducer and activato

233 Leptin also normalized alcohol-reduced phosphorylation levels of signal transducer Stat3 and ad

234 ibition is associated with modulation in the phosphorylation levels of signal transducers and activat

235 rresponding potentially with higher tyrosine phosphorylation levels of SKAP-Hom.

236 bserved a 5-10% and a 20-25% increase in the phosphorylation levels of specific sites in young fatigu

237 red livers of rats exhibited increased basal phosphorylation levels of Src, Shc, and ERK, as well as

238 ed IFN-dependent signaling by decreasing the phosphorylation levels of STAT1 while having little effe

239 responsiveness to IL-12 as indicated by the phosphorylation levels of STAT4.

240 levels of phosphorylation of JAKs and STAT3, phosphorylation levels of the Akt and mitogen-activated

241 human cancer cells, but had no effect on the phosphorylation levels of the AKT, MEK, and S6 kinase at

242 n, but did not alter the cellular protein or phosphorylation levels of the focal adhesion proteins.

243 ations, 30 was able to increase tyrosine the phosphorylation levels of the IR in the absence of insul

244 Western blotting analysis of the phosphorylation levels of the key signaling molecules (p

245 Phosphorylation levels of the kinase p38 (P-p38), the mi

246 An investigation of tyrosine phosphorylation levels of the plasma membrane Ca(2+)-ATP

247 both on Ca(2+) pump activity and on tyrosine phosphorylation levels of the PMCA.

248 The phosphorylation levels of the TAB1-TAK1 complex and its

249 s in inhibition of the kinase activities and phosphorylation levels of the three members of the Akt f

250 s were associated with restoration of normal phosphorylation levels of the transcription factor CREB

251 The phosphorylation levels of Thr-38 of CAR decreased in U01

252 observed dynamic, in vivo alterations in the phosphorylation levels of three key proteins (Akt, FOXO1

253 pocket residues significantly decreased the phosphorylation levels of three p38alpha substrates (ATF

254 h isoproterenol, only the alterations in the phosphorylation levels of troponin I and NADH-ubiquinone

255 lysis demonstrated that PRL increased (>50%) phosphorylation levels of TRPV1 in TG.

256 Phosphorylation levels of two known ATM substrates, Rad1

257 sis and metastasis, likely by increasing the phosphorylation levels of various PP1 substrates.

258 nge, we find prolonged elevation in tyrosine phosphorylation levels of VE-cadherin-associated beta-ca

259 Increased phosphorylation levels of VR1 were also observed in DRG

260 1(-/-) CD4 T cells results in enhanced basal phosphorylation levels of ZAP70 and ERK1/2.

261 Coincident with changes in mTOR phosphorylation, levels of activated protein kinase B (A

262 rhodopsin species to elucidate the impact of phosphorylation level on arrestin interaction with three

263 p proteins in Bacillus subtilis regulate the phosphorylation level or the DNA-binding activity of res

264 localizes with Cdc5p exclusively when Sec4p phosphorylation levels peak during the cell cycle, indic

265 neither Cps2B phosphatase activity nor Cps2D phosphorylation levels per se are determinants of capsul

266 endent on EGFR activation, as STAT3 tyrosine phosphorylation levels persisted after treatment with AG

267 ignal-regulated kinases1/2 in vitro, and its phosphorylation levels positively correlate with Twist1

268 In the wild-type strain, MpkA phosphorylation levels progressively increased in both t

269 Therefore, we propose that Src42A phosphorylation levels provide a link for the ECM enviro

270 al isoenzyme thymidine kinase-2, the highest phosphorylation levels relative to thymidine were seen w

271 ly, Hog1 returns to the cytoplasm, where its phosphorylation levels remain high.

272 es gradient formation, but overall substrate phosphorylation levels remain unchanged.

273 treatment, TRAIL induces a reduction in MADD phosphorylation levels resulting in MADD dissociation fr

274 of the prpC allele, gliding frequencies and phosphorylation levels returned to the wild-type standar

275 Comparing protein abundances and phosphorylation levels revealed specialized, interconnec

276 an active conformational state in which its phosphorylation level tends to rise and an inactive one

277 gh all forms induced similar VEGF receptor 2 phosphorylation levels, the angiogenic outcomes were dis

278 ccompanied with a dramatic reduction in T286 phosphorylation levels throughout the neuron.

279 P, and vasodilator-stimulated phosphoprotein phosphorylation levels to measure P2Y12 receptor inhibit

280 s was not associated with an increase in AKT phosphorylation levels, underlining the existence of an

281 ysates were analyzed for p38/ERK protein and phosphorylation levels using specific Abs and Western bl

282 Ex vivo Stat5 phosphorylation levels varied among HIV-1+ donors but di

283 oughout the day, while in the C3 species the phosphorylation level was maintained during the entire 2

284 ase, tLIN, was increased when the troponin I phosphorylation level was reduced from 1.02 to 0.3 molPi

285 High phosphorylation levels were associated with poor overall

286 o wild-type levels, although Btk protein and phosphorylation levels were comparable to controls.

287 Basal phosphorylation levels were compared with those formed a

288 otal tyrosine FAK phosphorylation and Tyr397 phosphorylation levels were continuously elevated in PRL

289 Stat1 phosphorylation levels were determined by flow cytometry

290 hough total JPH2 levels were unaltered, JPH2 phosphorylation levels were found to be reduced in MCM-S

291 K-3beta) association and beta-catenin serine phosphorylation levels were increased and beta-catenin e

292 AMPK phosphorylation levels were increased by FGF21 treatment

293 In the CP/CPPS group, ERK1/2 phosphorylation levels were increased in the amygdala an

294 o TNF, and ErbB4 messenger RNA, protein, and phosphorylation levels were measured.

295 ted with 52 stimuli, and gene expression and phosphorylation levels were measured.

296 ascular endothelial growth factor receptor-2 phosphorylation levels were observed in Ang1-expressing

297 Protein phosphorylation levels were quantified by Western blotti

298 a and ischemia-associated changes in protein phosphorylation levels, which can misguide the examinati

299 that CCh stimulates an increase in tyrosine phosphorylation levels, which has been reported to inhib

300 or Dullard knockdown leads to increased Mad phosphorylation levels, while Dullard overexpression res