ライフサイエンスコーパス: phosphorylation status

1 h mRNA levels and was largely independent of phosphorylation status.

2 FkappaB signaling and the regulation of Cdk9 phosphorylation status.

3 rength of the interaction depends on the PIN phosphorylation status.

4 tation assay to study dynamic changes in Tau phosphorylation status.

5 , depending on the degree of aromaticity and phosphorylation status.

6 D-95 expression depends on miR-125a and FMRP phosphorylation status.

7 ed Rac dynamics at contacts depending on its phosphorylation status.

8 d in TG mouse islets, without changes in Akt phosphorylation status.

9 ivotal roles in N-DRC function through their phosphorylation status.

10 in, prevents tau clearance and regulates its phosphorylation status.

11 raction, which can occur independent of YAP1 phosphorylation status.

12 ese interactions are regulated by the ChREBP phosphorylation status.

13 microtubules dynamics, are dependent on its phosphorylation status.

14 its its nuclear export, independently of its phosphorylation status.

15 h leads to p53 activation independent of its phosphorylation status.

16 oteins, in particular phospholamban, and its phosphorylation status.

17 ion loop conformation that is independent of phosphorylation status.

18 ions that preserve the physiological in vivo phosphorylation status.

19 y RNA polymerase II carboxyl-terminal domain phosphorylation status.

20 LB levels, monomer to pentamer ratio, or its phosphorylation status.

21 3-3 and Cdc25C independently of the latter's phosphorylation status.

22 monomerization of PLB or by a change in PLB phosphorylation status.

23 protein Cdc25C, independent of the latter's phosphorylation status.

24 d that the mobility is tightly linked to its phosphorylation status.

25 surements, and regulatory myosin light chain phosphorylation status.

26 with the modulation of p53/Mdm2, Erk and Akt phosphorylation status.

27 nd phosphatase activities influence the CovR phosphorylation status.

28 -suppressing antinatriuretic hormones to NCC phosphorylation status.

29 -bridge cycling rates via alterations in its phosphorylation status.

30 which was unrelated to the substrate domain phosphorylation status.

31 vated linking chemistry to detect changes in phosphorylation status.

32 ation, cooperativity, and sarcomeric protein phosphorylation status.

33 a, PLN, and ryanodine receptor or in the PLN phosphorylation status.

34 ism by which SAUR19 modulates PM H(+)-ATPase phosphorylation status.

35 plexes of distinct molecular composition and phosphorylation status.

36 M in adult rat ventricular myocytes based on phosphorylation status.

37 ength of the interaction depends on the ABI5 phosphorylation status.

38 triction of HSV-1 was not affected by SAMHD1 phosphorylation status.

39 thin the cell is closely associated with its phosphorylation status.

40 middle-aged animals, ischemia increased the phosphorylation status/activity of Akt and STAT3, and de

41 ereas estradiol did not detectably alter the phosphorylation status/activity of Akt or STAT3, it prev

42 activity of Akt and STAT3, and decreased the phosphorylation status/activity of CREB in the hippocamp

43 ersus 2,3-diamino-2,3-dideoxy-d-glucose, and phosphorylation status all correlated with TLR4 activati

44 rmine whether long term estradiol alters the phosphorylation status and activity of Akt, STAT3 and CR

45 quent effects of RvE1 to induce increases in phosphorylation status and cell migration.

46 dance of active Ypt11 forms is controlled by phosphorylation status and degradation.

47 Studies of VEGFR-2 phosphorylation status and down-regulation of neuropilin

48 binding by cMyBPC is independent of protein phosphorylation status and is not significantly affected

49 -SUPPRESSOR 1 (BES1), largely depends on its phosphorylation status and its protein stability, but th

50 nitored survival signaling by evaluating the phosphorylation status and localization of Forkhead box

51 ole for neuronal cyclin E1 in regulating the phosphorylation status and localization of Kv2.1 channel

52 idence revealed that the alterations in eNOS phosphorylation status and NO generation were mediated b

53 In turn, electrical activity affects the phosphorylation status and nuclear level of activated Sm

54 y sildenafil (Viagra) is dependent on STEVOR phosphorylation status and on another independent mechan

55 ar mass complexes and hypothesized that PTEN phosphorylation status and PDZ binding domain may be req

56 ort of the phytohormone auxin depends on the phosphorylation status and polar localization of PIN-FOR

57 Diamond and SYPRO Ruby dyes to quantify the phosphorylation status and protein levels, respectively,

58 ties mediated by DAPK are controlled both by phosphorylation status and protein stability.

59 ta clarify the influence of CovS on the CovR phosphorylation status and provide insight into why sero

60 occurs concomitantly with changes in RNAP II phosphorylation status and recruitment of the elongation

61 elation between increased FAK expression and phosphorylation status and the invasive phenotype of agg

62 Therefore, our findings suggest that eEF2 phosphorylation status (and, as a consequence, translati

63 yl-coenzyme A carboxylase (ACC), reduced ACC phosphorylation status, and dramatically increased hepat

64 1 can directly ubiquitinate IRF7, affect its phosphorylation status, and interfere with the ubiquitin

65 bition of CDK1 kinase activity, altered CDK1 phosphorylation status, and interference with downstream

66 e interactions are essential to regulate the phosphorylation status, and thus the activity, of the do

67 at Thr389 (but not at Thr421/Ser424), 4E-BP1 phosphorylation status, and total eEF2 accretion were al

68 The expression, phosphorylation status, and/or kinase activity of the in

69 EGF-induced changes in Erk1/2 and p38 phosphorylation status are dependent on PP-mediated cros

70 Our findings suggest YAP and its phosphorylation status as candidate prognostic markers i

71 o GTPase is involved in regulating cofilin's phosphorylation status at invadopodia.

72 roteome, impacting ERK signaling by reducing phosphorylation status at multiple levels of the kinase

73 t AMPARs scale differentially based on their phosphorylation status at S845.

74 eo-cytoplasmic shuttling is dependent on the phosphorylation status at Ser-174 and Ser-175 of eIF6.

75 however, prevent cAMP-induced changes to the phosphorylation status at serines 261 or 269.

76 Surprisingly, while the phosphorylation status at these two sites directly impin

77 ession, no differences were observed in cTnI phosphorylation status between wild type and cardiac-spe

78 ity primarily by maintaining proper receptor phosphorylation status but also serves a previously unap

79 This localization was independent of MtrB phosphorylation status but dependent upon the assembly o

80 lokin is not through modulation of the MYPT1 phosphorylation status but rather it contributes to cycl

81 al responses are believed to be regulated by phosphorylation status, but the precise mechanisms by wh

82 Furthermore, mimicking phosphorylation status by mutating S-->E at S300 and/or

83 protein kinases and three phosphatases whose phosphorylation status changed upon SII treatment.

84 Further, we show that RelB serine 472 phosphorylation status controls MMP3 expression and prom

85 nsor of lipid toxicity and its GSK3-mediated phosphorylation status controls outer mitochondrial memb

86 maintaining genome integrity, whereby BRCA1 phosphorylation status controls the selectivity of repai

87 We show that IRE1alpha phosphorylation status correlates with an increased prop

88 tion of PTEN activity through changes in its phosphorylation status could uniquely regulate the conti

89 NA translational control, mediated via eIF4B phosphorylation status, couples neuronal activity to tra

90 ed mitochondrial dysfunction, and DRP1(S616) phosphorylation status dichotomizes BRAF(WT) from BRAF(V

91 otic testicular germ cells and its increased phosphorylation status during capacitation suggested mul

92 , old and new histones are distinct in their phosphorylation status during early mitosis in the follo

93 serine 260, a JNK phosphoacceptor site whose phosphorylation status had an unknown role in RXRalpha f

94 On the other hand, PTEN phosphorylation status has a significant impact on its c

95 etyltransferase activity is dependent on its phosphorylation status in cells, and p300 phosphorylatio

96 induced a similar pattern of changes in the phosphorylation status in Erk1/2 and p38 following PP in

97 icates that successful prediction of protein phosphorylation status in human based on rat phosphoryla

98 ction (n = 7) was measured by pp185 tyrosine phosphorylation status in insulin-sensitive tissues usin

99 3 in the mitotic cells, correlating with its phosphorylation status in mitosis.

100 lagen and MMP-1 expression, as well as Smad3 phosphorylation status in SSc fibroblasts.

101 results suggest that modification of the Tm phosphorylation status in the heart, depending upon the

102 based method that provides protein level and phosphorylation status information from nanogram quantit

103 Here, we show that MtrB, irrespective of its phosphorylation status, interacts with Wag31, whereas on

104 Thus Ser129 phosphorylation status is crucial in mediating alpha-syn

105 Here we demonstrate that Orm phosphorylation status is highly responsive to sphingoid

106 AMPK activity, as assessed by phosphorylation status, is increased following both midd

107 uppression of HAS2 transcription, with FOXO1 phosphorylation status maintained by operation of the po

108 n analysis data suggests that changes in Bad phosphorylation status may be caused by a coordinated sh

109 rm1, based on the new structures suggests LM phosphorylation status may mediate Ran's selection of ex

110 monly used chemotherapy agents and that Chk1 phosphorylation status may not offer a reliable marker f

111 obilized alkaline phosphatase to monitor the phosphorylation status of a mixture of peptides.

112 ective activation of the two channels is the phosphorylation status of a single threonine residue (T3

113 By quantitatively assessing the tyrosine phosphorylation status of activated kinases in xenograft

114 These responses were not dependent on the phosphorylation status of Akt and FOXO1.

115 tle cell lymphoma (MCL), we investigated the phosphorylation status of Akt and multiple downstream ta

116 gnalling pathway; therefore, we measured the phosphorylation status of Akt and p70(s6k) in the WT and

117 itch in substrate specificity coupled to the phosphorylation status of Akt may lead to alternative ce

118 nd AMPKalpha activity was ascertained by the phosphorylation status of AMPKalpha Thr(172) in human kn

119 complex signaling pathway that controls the phosphorylation status of an SR-related protein that fun

120 lls with P. gingivalis did not influence the phosphorylation status of beta-catenin but resulted in p

121 We propose a model in which the phosphorylation status of Bid determines the apoptotic t

122 e conclude that anabolic nutrients alter the phosphorylation status of both AMPK- and mTOR-associated

123 Furthermore, in vitro data suggest that the phosphorylation status of BubR1 is important for checkpo

124 were consistent with the observed changes in phosphorylation status of c-Jun and Bim.

125 iption is independent of the sumoylation and phosphorylation status of c-Jun but is critically depend

126 tion, and oxidation and by investigating the phosphorylation status of CaMKII downstream targets.

127 ypical target gene of CAR) by modulating the phosphorylation status of CAR.

128 re-forming Cavalpha1.2 and the Akt-dependent phosphorylation status of Cavbeta2 both in a mouse model

129 The phosphorylation status of CBLs does not appear to influe

130 in the propionylation, glycosylation and/or phosphorylation status of cell proteins.

131 In the present study, we show that the phosphorylation status of CITED1 changes during the cell

132 as suggested by altered transcription and/or phosphorylation status of components of the NF-kappaB sy

133 A pathway as indicated by a reduction in the phosphorylation status of CREB (pCREB).

134 odifier (SUMO) and further controlled by the phosphorylation status of CRMP2.

135 we postulated that PKA evokes changes in the phosphorylation status of CtBP1 that control the ability

136 rimentally observed spatial distribution and phosphorylation status of CtrA in wild-type and mutant c

137 s of CXCR4 phosphorylation and evaluated the phosphorylation status of CXCR4 in human astrocytomas.

138 on of this complex (DHIC) is affected by the phosphorylation status of DDL-1.

139 le inhibiting NHEJ, and we conclude that the phosphorylation status of DNA-PK impacts how a cell choo

140 us to determine that the kinase activity and phosphorylation status of DNA-PK(CS) influence the stabi

141 and that neither the kinase activity nor the phosphorylation status of DNA-PK(CS) influences its init

142 n coordination with kinases may regulate the phosphorylation status of downstream targets to accompli

143 Western blot analysis evaluated the phosphorylation status of EGFR, ERK, p38 MAPK, and nucle

144 nslational ternary complex, regulated by the phosphorylation status of eIF2 alpha.

145 This mode of regulation is governed by the phosphorylation status of eIF2alpha and controlled by ce

146 t Sub1 influences and/or is sensitive to the phosphorylation status of elongating RNAP II.

147 13D telokin, without changing the inhibitory phosphorylation status of endogenous MYPT1 (the regulato

148 exercise are mediated by alterations in the phosphorylation status of eNOS (increase in serine 1177

149 creases were accompanied by increases in the phosphorylation status of epidermal growth factor recept

150 imen of CAF with ErbB-2 was not dependent on phosphorylation status of ErbB-2.

151 PTPRO regulated the phosphorylation status of ERBB2 at Y1248.

152 n larger and more prolonged increases in the phosphorylation status of Erk1/2 and p38.

153 Western blot analysis evaluated the phosphorylation status of Erk1/2 and phosphoinositide 3-

154 tern blot analysis was used to determine the phosphorylation status of Erk1/2, p38, and the mitogen-a

155 ROCK 1 expression through inhibition of the phosphorylation status of ERK1/2.

156 % in virus titer), which correlated with the phosphorylation status of ERK1/2.

157 The phosphorylation status of ERK2 did not affect interactio

158 ning the phosphatase Pph3 that regulates the phosphorylation status of gammaH2AX in vivo and efficien

159 ostsynaptic density-and are regulated by the phosphorylation status of gephyrin.

160 This sorting decision is related to the phosphorylation status of GluA1 Ser845, the dephosphoryl

161 The dynamic phosphorylation status of H5 influences this structure a

162 drial dysfunctioning and perturbation in the phosphorylation status of histones in the nucleus.

163 These data demonstrate that the phosphorylation status of hnRNP A1 serine 199 regulates

164 Furthermore, the phosphorylation status of hsp27 may influence its abilit

165 uld now be possible to routinely monitor the phosphorylation status of hundreds of nodes across multi

166 nearby Lys-163, which in turn modulates the phosphorylation status of IKKbeta at select C-terminal s

167 ctly regulates Ca2+ handling by altering the phosphorylation status of inhibitor-1, which in turn sup

168 orrelia burgdorferi is strictly dependent on phosphorylation status of its input receiver domain.

169 Na(+)/K(+)-ATPase inhibitor, ouabain, on the phosphorylation status of Jnk, p38, and Src.

170 The phosphorylation status of KaiC is thought to mediate glo

171 Because the phosphorylation status of KaiC oscillates over the daily

172 Interactions between Kai proteins change the phosphorylation status of KaiC, defining the phase of ci

173 es insight into how KaiB might influence the phosphorylation status of KaiC.

174 Here we assessed expression and phosphorylation status of key Ca handling proteins and m

175 ta support a role for Srx in controlling the phosphorylation status of key regulatory kinases through

176 Hence, the phosphorylation status of KHT-1-MPS-1 seems to be linked

177 In this study, we investigated the mannose phosphorylation status of leukemia inhibitory factor (LI

178 ealed multiple PtpA-dependent changes to the phosphorylation status of macrophage proteins upon M. tu

179 nhibited autophagy induction by altering the phosphorylation status of mammalian target of rapamycin

180 The phosphorylation status of MDF-1 affects its binding to a

181 Therefore, the phosphorylation status of Mdm2 Ser394 governs p53 protei

182 The precise control of the phosphorylation status of MeCP2 in neurons is critical f

183 We assessed the phosphorylation status of Mga in GAS cell lysates with P

184 Phosphorylation status of mitogen-activated protein kina

185 Our data indicate that Htt regulates the phosphorylation status of myosin II during chemotaxis an

186 Here, we show that the phosphorylation status of NBS1 determines the repair pat

187 Thus, the phosphorylation status of NCC may not necessarily equate

188 tiparameter phosflow approach to analyze the phosphorylation status of NF-kappaB and three major MAPK

189 Although the phosphorylation status of NS5A is considered to have a s

190 nases that add a layer of regulation via the phosphorylation status of nucleoporins.

191 ffect was mediated by changes in the protein phosphorylation status of occludin via the action of FAK

192 egulate the assembly of TJ by modulating the phosphorylation status of occludin.

193 Ca(2+) and selective to Ser-635 because the phosphorylation status of other eNOS sites, including Se

194 No differences in the relative abundance or phosphorylation status of other myofilament proteins wer

195 blot analysis was performed to determine the phosphorylation status of p42/44 and Akt/protein kinase

196 rmore, increased GRK5 expression induced the phosphorylation status of p65, increased the activity of

197 tivity depends on the enzymatic activity and phosphorylation status of PHF8, which can be pharmacolog

198 In addition, both the phosphorylation status of phospholipase Cgamma-1 at the

199 o the OS is determined by the amount and the phosphorylation status of photolyzed rhodopsin.

200 activation can thereby impact on the Ser-473 phosphorylation status of PKB/Akt and the repair of etop

201 In addition, assessment of the phosphorylation status of PP in these cells reveals that

202 ndent protein kinase signaling modulates the phosphorylation status of pregnane x receptor.

203 ive phosphoproteomics to identify changes in phosphorylation status of presynaptic proteins in restin

204 tern blot analysis identified changes in the phosphorylation status of prospective intracellular sign

205 However, current technologies to monitor the phosphorylation status of proteins are inefficient at de

206 Taken together, the transcript abundance, phosphorylation status of proteins at the fiber initiati

207 Together, our findings show how the phosphorylation status of pSTAT1 determines its function

208 re is a paucity of information regarding the phosphorylation status of RASSF1A and its regulation dur

209 In contrast, the phosphorylation status of retinoblastoma protein (pRB) w

210 controlling the subcellular localization and phosphorylation status of Rho GDP dissociation inhibitor

211 ilings in mRNA splicing and changes with the phosphorylation status of RNA Pol II across the gene.

212 mply that anchored PKC locally modulates the phosphorylation status of Robo3.1 in brain regions gover

213 namically regulated in the cell and that the phosphorylation status of S58 is a critical factor regul

214 rtant for NIS protein stability and that the phosphorylation status of Ser-227 is functionally silent

215 iodide transport of NIS is modulated by the phosphorylation status of Ser-43 and Ser-581.

216 The phosphorylation status of Ser-53 significantly affects s

217 e proteins is thought to be regulated by the phosphorylation status of Ser-776.

218 hat transactivation is not influenced by the phosphorylation status of serine 78 in the UR1 domain.

219 Hence, the phosphorylation status of serine-162 in the alphaI coil

220 The phosphorylation status of several important signaling pr

221 trastructural analysis and by monitoring the phosphorylation status of several viral proteins that un

222 The phosphorylation status of Sfi1, a structural component o

223 logical substrates for PP2A, the LPS-induced phosphorylation status of signaling MAPK and Akt kinase

224 more, Utp7 can regulate the localization and phosphorylation status of Sli15 independent of its effec

225 Alterations in the Cdk/Cdc14-dependent phosphorylation status of Spc110, or its inactivation du

226 luence pre-mRNA processing by regulating the phosphorylation status of specific regulatory factors, w

227 A dose-dependent reduction in the phosphorylation status of specific SR proteins was detec

228 DNA in DU145 cell lysates without affecting phosphorylation status of STAT3.

229 We further demonstrate that the phosphorylation status of Synaptojanin at S1029 differen

230 ore, ECT2 activity might be regulated by the phosphorylation status of T341.

231 han in interphase cells, as evidenced by the phosphorylation status of T359/S363 in RSK.

232 s in arrestin2 to initially discriminate the phosphorylation status of target receptors.

233 ctin cytoskeleton network and changes in the phosphorylation status of the actin regulatory protein c

234 e findings indicate a connection between the phosphorylation status of the activation loop and phosph

235 ion on the kinase that was influenced by the phosphorylation status of the activation loop.

236 to tyrosine kinase inhibitors (TKIs) in the phosphorylation status of the adaptor protein CrkL, a ma

237 Thus the protein kinase A phosphorylation status of the beta(2) adrenoceptor and,

238 ption cycle is accompanied by changes in the phosphorylation status of the C-terminal domain (CTD), a

239 yV ST induces this process by regulating the phosphorylation status of the cellular microtubule-assoc

240 Loss of Pdp1epsilon also alters the phosphorylation status of the CLK protein and disrupts c

241 tion mechanism that specifically detects the phosphorylation status of the CTD.

242 sf-CD levels are also modulated by the phosphorylation status of the cytosolic domain and by th

243 Activity and phosphorylation status of the downstream molecules casei

244 ion of mTORC1 was monitored by measuring the phosphorylation status of the downstream substrate prote

245 N23 may increase the activity of SRC and the phosphorylation status of the E-cadherin/beta-catenin si

246 report that IFT is regulated in part by the phosphorylation status of the kinesin-II subunit FLA8/KI

247 Thus, determining the phosphorylation status of the M1 mAChR at Ser(228) not o

248 d activity of NPFF, we have investigated the phosphorylation status of the MOP receptor using phospho

249 telomere end protection and reveals how the phosphorylation status of the NBS1(S432) dictates repair

250 during S-phase and may be controlled by the phosphorylation status of the p150 subunit of CAF-1.

251 n the NF-kappaB activation mechanism and the phosphorylation status of the p65 NF-kappaB subunit requ

252 promotes or inhibits growth depending on the phosphorylation status of the p65 NF-kappaB subunit.

253 ed for wild-type circadian period and normal phosphorylation status of the protein.

254 t b(6)/f supercomplex was dependent upon the phosphorylation status of the PsbP-like protein and the

255 conformation of the extracellular domain and phosphorylation status of the receptor are involved in m

256 the interaction of MDFIC with GR altered the phosphorylation status of the receptor.

257 alpha action by altering both the levels and phosphorylation status of the receptor.

258 ges is gene specific and depends on the S536 phosphorylation status of the recruited p65 NF-kappaB.

259 ruption of RRM1-PP1 interactions reduces the phosphorylation status of the RS domain in vitro and in

260 ide and RhoA signaling pathways dictates the phosphorylation status of the Ser(696)-Thr(697) and Ser(

261 layed a significant increase in the Ser(473) phosphorylation status of the Ser/Thr kinase protein kin

262 hat the ODC IRES element is regulated by the phosphorylation status of the translation factor eIF4E.

263 adjacent to the dimer interface, linking the phosphorylation status of the transporter to its oligome

264 The effects of the absence of TIMP-3 on the phosphorylation status of the VEGF-receptor-2 (VEGFR-2)

265 NCS)/Rapgef2] was examined by monitoring the phosphorylation status of their respective targets, cAMP

266 air bundle may be actively maintained by the phosphorylation status of these proteins.

267 Together, these findings indicate that the phosphorylation status of this single residue in STIM1 r

268 munity resource cataloging the abundance and phosphorylation status of thousands of maize proteins at

269 We also found that the phosphorylation status of Thr-577 may be important for N

270 idue that is phosphorylated by JNKs, and the phosphorylation status of Thr450 regulates reactivation

271 findings demonstrate that modulation of the phosphorylation status of tristetraprolin is an importan

272 Furthermore, the differential phosphorylation status of TTP results in its sequestrati

273 ibitor sensitivity correlated with the STAT3 phosphorylation status of tumor cells.

274 Notably, in LMW-PTPs, the phosphorylation status of two well conserved tyrosine re

275 The phosphorylation status of Tyr-142 in H2A.X has been show

276 The phosphorylation status of various components of the mTOR

277 e of the phenotypes observed were due to the phosphorylation status of VieA.

278 se directly and diametrically controlled the phosphorylation status of Y36 and subsequent ERbeta func

279 Regardless of its phosphorylation status or following co-expression of con

280 ized either the target protein regardless of phosphorylation status (pan protein) or a housekeeping p

281 Thus, our results suggest that S318 phosphorylation status, rather than a predominantly shoo

282 Depending upon its phosphorylation status, RSK1 switched interactions betwe

283 ir individual protein levels or solely their phosphorylation status, should be considered as a paramo

284 53, Akt and c-Src expression levels or their phosphorylation status, suggesting that PRL-2 knockdown

285 n contrast, Akt activity, as assessed by Akt phosphorylation status (T308 and S473), phosphorylation

286 ists in many different isoforms differing in phosphorylation status that are likely to interact diffe

287 Our work identifies a novel regulator of phosphorylation status that provides an additional layer

288 We found that irrespective of eIF2alpha phosphorylation status, the presence of SGs in cells cor

289 e activity of S6K1 is tightly coupled to its phosphorylation status, the regulation of S6K1 activity

290 ude that in addition to receptor subtype and phosphorylation status, the stereochemistry of a given a

291 l cycle of spermatogenesis, depending on its phosphorylation status, to facilitate the transit of pre

292 Studies indicate that tropomyosin (Tm) phosphorylation status varies in different mouse models

293 Finally, we found that ERK5 phosphorylation status was not significantly affected by

294 n addition, a decrease in the pp185 tyrosine phosphorylation status was observed after insulin stimul

295 e 1 (S6K1) and 4E-binding protein 1 (4E-BP1) phosphorylation status) was also increased (P<0.05).

296 Protein synthesis and cell signalling (phosphorylation status) was unchanged in the control gro

297 to BiP, an ER chaperone protein, and sigmaR1 phosphorylation status were examined by immunoprecipitat

298 The changes in AQP2 phosphorylation status were paralleled by increases in c

299 Tau proline-rich region independently of the phosphorylation status, whereas the second, ADx215, dete

300 A positive correlation of TOB1 phosphorylation status with proliferation marker Ki67 su