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 terized by pronounced changes in the protein phosphorylation level.

4 al regulation between ACR4 and PP2A-3 at the 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 acetylation resulted in increases of Ser-294 phosphorylation levels.

8 abling large-scale determination of relative phosphorylation levels.

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

10 was used to determine protein expression and phosphorylation levels.

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

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

13 ABA were found to have significantly altered phosphorylation levels.

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

15 0M mutation confers increased Y992 and Y1068 phosphorylation levels.

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

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

18 ely Il1b and TNFa mRNA and IKB-alpha protein phosphorylation levels.

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

20 -type virus substantially reduced eIF2 alpha phosphorylation levels.

21 ere positively correlated with p53 serine 15 phosphorylation levels.

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

23 hatase, which concomitantly restores protein phosphorylation levels.

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

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

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

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

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

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

30 ction coupling displayed significantly lower phosphorylation levels after TAC and significantly reduc

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

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

33 allow recovery of viable virus, and the NS2 phosphorylation level and assembly of viral inclusion bo

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

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

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

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

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

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

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

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

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

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

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

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

53 the abundances of signaling partners, while phosphorylation levels are dependent on dimer lifetimes.

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 ed such algorithms to data measuring protein phosphorylation levels, assuming that the phosphorylatio

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 Here, osteopontin phosphorylation level declined in hypo- and hyper- phosp

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

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

75 Higher phosphorylation levels do not increase the stability of

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

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

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

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

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

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

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

83 6 conditions, resulting in 18,816 quantified phosphorylation levels from each multiplexed sample.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

105 ic SSL-induced skin carcinogenesis and c-Jun phosphorylation levels in SKH1 hairless mice.

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

107 rotein kinase C (PKC)-mediated NMDA receptor phosphorylation levels in the hypothalamus are increased

108 Disrupting GSK activity diminishes Gpa2 phosphorylation levels in vivo, and the purified GSK iso

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 lioblastoma specimens reveals that PGK1 Y324 phosphorylation levels inversely correlate with PTEN exp

120 However, its phosphorylation level is decreased in individuals with h

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 y rescue the cop1 stomatal phenotype and the phosphorylation level of OST1, a crucial SnRK2-type kina

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

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

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

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

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

161 t the calcium binding preferentially affects phosphorylation level of the NS2 and has a role in regul

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

163 The phosphorylation level of the regulatory proteins is also

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

182 , in agreement with increased expression and phosphorylation levels of both proteins.

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

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

185 hand, sodium-calcium exchanger function and phosphorylation levels of calcium-handling proteins were

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

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

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

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

190 different basal and BCR stimulation-induced phosphorylation levels of downstream signaling proteins.

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 nfection may cause an indirect effect on the phosphorylation levels of essential proteins involved in

196 nfection may cause an indirect effect on the phosphorylation levels of essential proteins involving i

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

198 (FAK) phosphorylation at Ser910, whereas the phosphorylation levels of FAK at Tyr397 and Tyr861 were

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

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

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

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

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

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 yonic fibroblasts (MEFs) exhibited decreased phosphorylation levels of IRF3 and TBK1 when challenged

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

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

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

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

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

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

213 Phosphorylation levels of OLE3 during seed germination w

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

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

216 Phosphorylation levels of protein kinase A substrates we

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

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

219 The phosphorylation levels of RB at serine residues 780 and

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

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

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

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

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

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

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

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

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

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

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

231 and, hypoxia and reoxygenation increased the phosphorylation levels of Src and VE-cadherin and reduce

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

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

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

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

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

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

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

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

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

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

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

243 REAM Proteogenomics Challenge for predicting phosphorylation levels of the proteome across cancer pat

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

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

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

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

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

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

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

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

252 Phosphorylation levels of two known ATM substrates, Rad1

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

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

255 Increased phosphorylation levels of VR1 were also observed in DRG

256 1(-/-) CD4 T cells results in enhanced basal phosphorylation levels of ZAP70 and ERK1/2.

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

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

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

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

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

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

263 , which allows us to incorporate the protein phosphorylation level, pharmacological interventions and

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

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

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

267 on IRF8 gene that were associated with MP2K1 phosphorylation levels, providing a first clue on how th

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

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

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

271 in phosphorylation levels, assuming that the phosphorylation levels represent protein activity states

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

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

274 Comparing protein abundances and phosphorylation levels revealed specialized, interconnec

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

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

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

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

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

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

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

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

283 In osteopontin-deficient mice, global matrix phosphorylation level was not associated with toughness.

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 Protein phosphorylation levels were quantified by Western blotti

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

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

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

300 increasing p38MAPK and decreasing JAK1-STAT1 phosphorylation levels, while osteogenic induction was e