ライフサイエンスコーパス: protein phosphatase 2A

1 se 3beta, cyclin-dependent kinase 5, and tau protein phosphatase 2A.

2 up a CAR surface, allowing interaction with protein phosphatase 2A.

3 olase 15 family members and the A subunit of protein phosphatase 2A.

4 d somatic mutations in PPP2R1A, a subunit of protein phosphatase 2A.

5 that then recruits the catalytic subunit of protein phosphatase 2A.

6 f phosphorylated Akt to dephosphorylation by protein phosphatase 2A.

7 ear region as well as from the inhibition of protein phosphatase 2A.

8 The dephosphorylation is mediated by protein phosphatase 2A.

9 m downregulation of both O-GlcNAcylation and protein phosphatase 2A.

10 omplex composed of Akt, beta-arrestin 2, and protein phosphatase 2A.

11 otubule star (mts) that encodes a subunit of protein phosphatase 2A.

12 are mediated by protein kinase C but not by protein phosphatase 2A.

13 ed for NF-kappaB activation by regulation of protein phosphatase 2A.

14 YAP, small t antigen brings it together with protein phosphatase 2A.

15 e 406 in a rapid process that is mediated by protein phosphatase 2A.

16 We identified PROTEIN PHOSPHATASE 2A-3 (PP2A-3), a catalytic subunit o

17 ase signaling (eg, protein kinase A R1alpha, protein phosphatase 2A A R1-alpha).

18 ase-mediated restriction of synthesis of the protein phosphatase 2A-A (PP2A-A), a key factor that fac

19 We conclude that protein phosphatase 2A accounts for enhanced SP-1 dephos

20 s inhibition was not due to H(2)S release or protein phosphatase 2A activation, which are key propert

21 s [B56alpha, B56gamma, PR72/PR130, and PTPA (protein phosphatase 2A activator)], which when suppresse

22 tion is regulated depending on the sites and protein phosphatase 2A, active in mitosis, is essential

23 restoration of brain tau O-GlcNAcylation and protein phosphatase 2A activity may offer promising ther

24 Rts1 constitutively directs protein phosphatase 2A activity toward the prodomain, ef

25 ynthase (nNOS) down-regulation and decreased protein phosphatase 2A activity.

26 (ATM) activation by a mechanism dependent on protein phosphatase 2A activity.

27 to protein kinase C activation and increased protein phosphatase- 2A activity, thereby suppressing HG

28 by DIM may be due, in part, to inhibition of protein phosphatase 2A, an upstream regulator of ATM.

29 l effect of inhibiting Akt, calcineurin, and protein phosphatase 2A and established that inhibition o

30 re known to bind to the catalytic subunit of protein phosphatase 2A and inhibit its activity.

31 In vitro, FAM13A interacts with protein phosphatase 2A and recruits protein phosphatase

32 chemical analysis showed increased levels of protein phosphatase 2A and reduced levels of activated A

33 results from protein kinase A activation of protein phosphatase 2A and subsequent dephosphorylation

34 y was associated with reduced Tau binding to protein phosphatase 2A and was dependent on Cdk5 but not

35 uced the cleavage of I2(PP2A), inhibition of protein phosphatase 2A, and hyperphosphorylation of Tau,

36 at Rts1, a regulatory subunit of the general protein phosphatase 2A, and Ptr3 have opposing roles in

37 clin-dependent kinase, the mediator complex, protein phosphatase 2A, and ribosomal proteins L13B and

38 Mutations in PPM1, which methylates protein phosphatase 2A, and target of rapamycin (TOR1) w

39 (armadillo/huntingtin, elongation factor 3, protein phosphatase 2A, and the yeast kinase TOR1) or BE

40 in to HEAT (Huntingtin, elongation factor 3, protein phosphatase 2A, and the yeast kinase TOR1) repea

41 named after Huntingtin, elongation factor 3, protein phosphatase 2A, and yeast kinase TOR1) repeat.

42 identify CIP2A (cancerous inhibitor of PP2A [protein phosphatase 2A]) as a key modulator of mTORC1 an

43 yeasts to be mediated by recruitment of the protein phosphatase 2A B' (PP2A B').

44 nd related proteins that bind to and inhibit protein phosphatase 2A/B55, the principal phosphatase fo

45 r-suppressive functions of B56gamma-specific protein phosphatase 2A (B56gamma-PP2A).

46 kinase-3 (GSK-3), and a beta-arrestin-2/AKT/protein phosphatase 2A (beta-arrestin-2/AKT/PP2A) comple

47 t, Cdr2-T166 phosphorylation is regulated by protein phosphatase 2A but not by the Sds23-PP6 pathway.

48 hase kinase 3beta, protein phosphatase 1, or protein phosphatase 2A, but reduces p35 subunit of Cdk5.

49 showed that Len inhibits the haplodeficient protein phosphatase 2A catalytic domain alpha (PP2Acalph

50 e for KPNA1, the mTOR-associated phosphatase protein phosphatase 2A catalytic interacted directly wit

51 dose-dependent increase in the levels of the protein phosphatase 2A catalytic subunit (PP2Ac) but not

52 e show that RSK1, PKA subunits, D-AKAP1, and protein phosphatase 2A catalytic subunit (PP2Ac) exist i

53 -155-mediated suppression of the phosphatase protein phosphatase 2A catalytic subunit alpha (PPP2CA).

54 phosphatase catalytic subunit, Sit4, and the protein phosphatase 2A catalytic subunits, Pph21/Pph22.

55 at low mitogen or nutrient levels, mTOR and protein phosphatase 2A catalytically control the constit

56 Cancerous inhibitor of protein phosphatase 2A (CIP2A) is overexpressed in most

57 berrant expression of cancerous inhibitor of protein phosphatase 2A (CIP2A), a recently identified en

58 Among these, the protein phosphatase 2A-dependent dephosphorylation of Ak

59 Protein phosphatase 2A dephosphorylates JAM-A at S285, s

60 ostulated to target the catalytic subunit of protein phosphatase 2A for degradation.

61 catalytic subunit) demonstrated that PP1 and protein phosphatase 2A had opposite effects on AR protei

62 Here we discovered that the protein phosphatase 2A heterotrimer, PP2A(Ppp2r2d), regu

63 s, of which three (two peptide inhibitors of protein phosphatase 2A (I1PP2A and I2PP2A) and prostagla

64 In this study, the inhibitor 2 of protein phosphatase 2A (I2PP2A) was identified in vitro

65 this is mediated by metabolic activation of protein phosphatase 2A in complex with the B55beta targe

66 PKC activation and protein phosphatase 2a inhibition increased the open pro

67 e important structural features required for protein phosphatase 2A inhibition, the mechanism of acti

68 Induction of transport was abolished by the protein phosphatase 2A inhibitor, OA.

69 ties of tau kinases and phosphatases such as protein phosphatase 2A, irrespective of fisetin treatmen

70 Protein phosphatase 2A is known to activate SP-1 through

71 more, we show that a novel host cell factor, protein phosphatase 2A, is involved in NS2 dephosphoryla

72 whereas dephosphorylation by a mitochondrial protein phosphatase 2A isoform and the calcium-calmoduli

73 tion of a beta-arrestin 2-associated pool of protein phosphatase 2A, leading to activation of Akt and

74 related with reduced Akt activity, increased protein phosphatase 2A levels, derepression of FoxO3a, a

75 ulated kinase pathways, and independently of protein phosphatase 2A, liver kinase B1/AMP-activated pr

76 Protein phosphatase 2A mediated the reduction in NF-kapp

77 a (alpha isoform of the catalytic subunit of protein phosphatase 2A) negatively regulate the adhesion

78 BR1) interacted with the B'' subunit of rice protein phosphatase 2A (OsPP2A B'') and underwent revers

79 untingtin, elongation factor 3, a subunit of protein phosphatase 2A, PI3 kinase target of rapamycin 1

80 We discovered that a specific form of protein phosphatase 2A (PP2A(Cdc55)) opposes the initial

81 d sphingolipids are required to activate the protein phosphatase 2A (PP2A(Cdc55)) to attenuate Swe1 p

82 tein kinase C (Pkc1), and a specific form of protein phosphatase 2A (PP2A(Cdc55)).

83 Somatic missense mutations in the Ser/Thr protein phosphatase 2A (PP2A) Aalpha scaffold subunit ge

84 that a small molecule inhibitor, LB-1.2, of protein phosphatase 2A (PP2A) activates Plk-1 and Akt-1

85 dding yeast, protein phosphatase 1 (PP1) and protein phosphatase 2A (PP2A) activities have each been

86 We found a decrease in protein phosphatase 2A (PP2A) activity associated with a

87 Here we find that specific disruption of protein phosphatase 2A (PP2A) activity by either express

88 Here we analyzed an endogenous inhibitor of protein phosphatase 2A (PP2A) activity called SET, and i

89 Protein phosphatase 2A (PP2A) activity can be enhanced p

90 ral human malignancies via the inhibition of protein phosphatase 2A (PP2A) activity toward c-Myc.

91 , also called SET, in rat brain, decrease in protein phosphatase 2A (PP2A) activity, abnormal hyperph

92 phorylation correlated with an inhibition of protein phosphatase 2A (PP2A) activity.

93 etaphase entry or progression by suppressing protein phosphatase 2A (PP2A) activity.

94 Here, we show that protein phosphatase 2A (PP2A) acts as opsin phosphatase

95 ells was associated with a lower activity of protein phosphatase 2A (PP2A) and augmented activity of

96 requires inhibition of the tumor suppressor protein phosphatase 2A (PP2A) and expression--but not ac

97 regulates the methylesterification state of protein phosphatase 2A (PP2A) and has been implicated in

98 associated with decreased phosphorylation of protein phosphatase 2A (PP2A) and increased phosphorylat

99 /ERK and its subsequent dephosphorylation by protein phosphatase 2A (PP2A) and inhibition of focal ad

100 regulates the methylesterification state of protein phosphatase 2A (PP2A) and is implicated in cance

101 Non-canonically activated ERK activates protein phosphatase 2A (PP2A) and lengthens cell cycle d

102 Alpha4 (alpha4) is a key regulator of protein phosphatase 2A (PP2A) and mTOR in steps essentia

103 tion of beta-catenin is highly vulnerable to protein phosphatase 2A (PP2A) and must be protected by t

104 It has been reported that protein phosphatase 2A (PP2A) and the Far3-7-8-9-10-11 c

105 dynamics of PIN proteins are affected by the protein phosphatase 2A (PP2A) and the PINOID kinase, whi

106 r translocation of HDAC4 was reversed by the protein phosphatase 2A (PP2A) antagonist, okadaic acid.

107 eres, the cohesin protector shugoshin (Sgo1)-protein phosphatase 2A (PP2A) antagonizes Aurora B and C

108 several biochemical analyses and identified protein phosphatase 2A (PP2A) as a candidate.

109 per in Immunity, Long et al. (2014) identify protein phosphatase 2A (PP2A) as a deactivator of phosph

110 phosphoprotein-32A (ANP32A), an inhibitor of protein phosphatase 2A (PP2A) as a direct target of sphi

111 We identified Cdc55-protein phosphatase 2A (PP2A) as a key phosphatase that

112 In this study, we identify serine/threonine protein phosphatase 2A (PP2A) as a key regulator of Bcl-

113 oupled with mass spectrometry, we identified protein phosphatase 2A (PP2A) as a perphenazine target.

114 We identified the A1 subunit of Ser/Thr protein phosphatase 2A (PP2A) as interacting with full-l

115 We now show that protein phosphatase 2A (PP2A) associated with mAKAP comp

116 l that de novo ceramide biosynthesis induced protein phosphatase 2A (PP2A) association directly with

117 We show here that PI3Kgamma inhibits protein phosphatase 2A (PP2A) at the beta-adrenergic rec

118 Interaction with the protein phosphatase 2A (PP2A) B regulatory subunit is re

119 Here we show that cytoplasm-localized protein phosphatase 2A (PP2A) B' regulatory subunits int

120 Protein phosphatase 2A (PP2A) became more eNOS-associate

121 of the general serine-threonine phosphatase protein phosphatase 2A (PP2A) can replace ST in this par

122 Protein phosphatase 2A (PP2A) complexes counteract many

123 Protein phosphatase 2A (PP2A) complexes function as tumo

124 un with chromatin is positively regulated by protein phosphatase 2A (PP2A) complexes targeted to c-Ju

125 A particular form of protein phosphatase 2A (PP2A) containing a B55delta subu

126 Together with protein phosphatase 1, protein phosphatase 2A (PP2A) contributes the bulk of Se

127 kinase 1 (RACK1) as the regulatory subunit, protein phosphatase 2A (PP2A) dephosphorylates threonine

128 Protein phosphatase 2A (PP2A) enzyme consists of a heter

129 endent PKA activity but specifically reduced protein phosphatase 2A (PP2A) expression and activity in

130 In this study, we found that protein phosphatase 2A (PP2A) expression is high in neur

131 The adenovirus E4orf4 protein must bind protein phosphatase 2A (PP2A) for its functions.

132 Observed deficits in protein phosphatase 2A (PP2A) function in a variety of h

133 ly conserved serine (Ser)/threonine-specific protein phosphatase 2A (PP2A) functions as a heterotrime

134 eport show that serine (Ser)/threonine (Thr) protein phosphatase 2A (PP2A) has an important role in G

135 a direct interaction between formoterol and protein phosphatase 2A (PP2A) has been described in vitr

136 lation of AM colonization via ABA requires a PROTEIN PHOSPHATASE 2A (PP2A) holoenzyme subunit, PP2AB'

137 reviously reported that PP2A/Balpha, a major protein phosphatase 2A (PP2A) holoenzyme, binds to and d

138 Proper formation of protein phosphatase 2A (PP2A) holoenzymes is essential f

139 ivation chaperones control the biogenesis of protein phosphatase 2A (PP2A) holoenzymes that contain a

140 otential role and functional significance of protein phosphatase 2A (PP2A) in CaBP4 dephosphorylation

141 Here we report a role for protein phosphatase 2A (PP2A) in centriole duplication.

142 Here, we identify the protein phosphatase 2A (PP2A) in complex with the regula

143 23 but not IL-12 was negatively regulated by protein phosphatase 2A (PP2A) in dendritic cells (DC).

144 s, and that serine 59 is dephosphorylated by protein phosphatase 2A (PP2A) in mitosis.

145 t of increased expression of the phosphatase protein phosphatase 2A (PP2A) in T cells, as recorded in

146 lst8Delta bypass mutants reveals a role for protein phosphatase 2A (PP2A) in the regulation of TORC2

147 We show that Pin1 can act along with protein phosphatase 2A (PP2A) in vitro to dephosphorylat

148 t of rapamycin (mTOR), whereas inhibition of protein phosphatase 2A (PP2A) induced phosphorylation of

149 Protein phosphatase 2A (PP2A) inhibition rescued S6K act

150 These effects did not involve protein phosphatase 2A (PP2A) inhibition.

151 enyl-4H-1-benzopyran-4-one (Ly294002) or the protein phosphatase 2A (PP2A) inhibitor okadaic acid rev

152 Here, we show that overexpression of the protein phosphatase 2A (PP2A) inhibitor protein PME-1 dr

153 Protein phosphatase 2A (PP2A) is a critical negative reg

154 Protein phosphatase 2A (PP2A) is a family of heterotrime

155 Protein phosphatase 2A (PP2A) is a family of multifuncti

156 Protein phosphatase 2A (PP2A) is a heterotrimeric Ser/Th

157 Protein phosphatase 2A (PP2A) is a heterotrimeric serine

158 Protein phosphatase 2A (PP2A) is a highly conserved and

159 Protein phosphatase 2A (PP2A) is a major serine/threonin

160 Protein phosphatase 2A (PP2A) is a member of the intrace

161 We provide evidence that protein phosphatase 2A (PP2A) is a negative regulator of

162 Strong evidence has indicated that protein phosphatase 2A (PP2A) is a tumor suppressor, but

163 Herein, cellular serine/threonine protein phosphatase 2A (PP2A) is identified as a functio

164 Protein phosphatase 2A (PP2A) is involved in many cellul

165 Protein phosphatase 2A (PP2A) is one of the most abundan

166 In KO synapses, protein phosphatase 2A (PP2A) is overactivated after mGl

167 Protein phosphatase 2A (PP2A) is regulated through a var

168 Here, we show that protein phosphatase 2A (PP2A) is required for the develo

169 Protein phosphatase 2A (PP2A) is the major MAP phosphata

170 erine 3 by interfering with serine/threonine protein phosphatase 2A (PP2A) leads to decreased class s

171 Down-regulation of protein phosphatase 2A (PP2A) methylation occurs in Alzh

172 Protein phosphatase 2A (PP2A) negatively regulates tumor

173 inhibited mTORC1 signaling independently of protein phosphatase 2A (PP2A) or AMP-activated protein k

174 We found that deletion of protein phosphatase 2A (PP2A) or of protein phosphatase

175 Protein phosphatase 2A (PP2A) participates in multiple m

176 Here we demonstrate that protein phosphatase 2A (PP2A) plays a pivotal role as a

177 Protein phosphatase 2A (PP2A) plays important roles in c

178 Protein phosphatase 2A (PP2A) presents unique opportunit

179 Here we show that protein phosphatase 2A (PP2A) promotes SREBP-2 LDLR prom

180 Protein phosphatase 2A (PP2A) regulates almost all cell

181 Protein phosphatase 2A (PP2A) regulates many essential a

182 blished, far less is known regarding cardiac protein phosphatase 2A (PP2A) regulation.

183 de novo mutations revealed four mutations in protein phosphatase 2A (PP2A) regulatory subunit B famil

184 We identify Drosophila protein phosphatase 2A (PP2A) regulatory subunit B' [Wrd

185 orylation and activation of serine/threonine protein phosphatase 2A (PP2A) regulatory subunit, B56bet

186 beta-arrestin2/protein kinase B (PKB or Akt)/protein phosphatase 2A (PP2A) signaling complex regulate

187 The protein phosphatase 2A (PP2A) subfamily of phosphatases,

188 lternative splice mutation in the regulatory protein phosphatase 2A (PP2A) subunit PPP2R2A.

189 plex in vivo with Twins, a Drosophila B-type protein phosphatase 2A (PP2A) subunit, and that Twins an

190 terase-4D3 (PDE4D3), ryanodine receptor, and protein phosphatase 2A (PP2A) to the sarcoplasmic reticu

191 e SET oncoprotein, a potent inhibitor of the protein phosphatase 2A (PP2A) tumor suppressor, is overe

192 in 2 subunits of serine/threonine (Ser/Thr) protein phosphatase 2A (PP2A) were identified in 16 indi

193 Like A1AT, protein phosphatase 2A (PP2A), a major serine-threonine

194 sferase that specifically methylates Ser/Thr protein phosphatase 2A (PP2A), a major Tau phosphatase.

195 ated that activation of the tumor suppressor protein phosphatase 2A (PP2A), a negative regulator of m

196 iquitination and blocking the recruitment of protein phosphatase 2A (PP2A), a phosphatase that inhibi

197 Protein phosphatase 2A (PP2A), a ubiquitous and pleiotro

198 oblastoma protein (Rb) family member p107 by protein phosphatase 2A (PP2A), a ubiquitously expressed

199 udies, we identified two holoenzyme forms of protein phosphatase 2A (PP2A), ABalphaC and ABdeltaC, as

200 f key regulators of hepatic gluconeogenesis, protein phosphatase 2A (PP2A), AMP-activated protein kin

201 small t (SV40ST) oncoprotein interacts with protein phosphatase 2A (PP2A), an abundantly expressed f

202 e exchange factor (RasGEF) Aimless, RasGEFH, protein phosphatase 2A (PP2A), and a scaffold designated

203 r processes, inhibiting the tumor suppressor protein phosphatase 2A (PP2A), and inhibiting the metast

204 these pathways, including sprouty2 (SPRY2), protein phosphatase 2A (PP2A), and phosphatase and tensi

205 The MWPyV small T antigen (ST) binds protein phosphatase 2A (PP2A), and the large T antigen (

206 fied a protein serine/threonine phosphatase, protein phosphatase 2A (PP2A), as a MEKK3 phosphatase.

207 blished that Wee1 and Cdc25 are regulated by protein phosphatase 2A (PP2A), but a full understanding

208 xes that appear to act through regulation of protein phosphatase 2A (PP2A), but their functions in ma

209 Mechanistically, PI3Kgamma sequesters protein phosphatase 2A (PP2A), disrupting ERK-PP2A inter

210 we show that a regulatory pathway involving protein phosphatase 2A (PP2A), glycogen synthase kinase

211 Phosphatases, such as protein phosphatase 2A (PP2A), interestingly, also are c

212 The activity of the HDAC4 phosphatase, protein phosphatase 2A (PP2A), is downregulated by ATM-m

213 249-amino acid long endogenous inhibitor of protein phosphatase 2A (PP2A), is increased, the activit

214 PyST enhanced YAP association with protein phosphatase 2A (PP2A), leading to decreased YAP

215 SH-BC-893 activated protein phosphatase 2A (PP2A), leading to mislocalizatio

216 Binding of YAP to MT brings it together with protein phosphatase 2A (PP2A), leading to the dephosphor

217 Exposure of BL41-3 cells to an inhibitor of protein phosphatase 2A (PP2A), okadaic acid, resulted in

218 Protein phosphatase 2A (PP2A), one of the main serine-th

219 his study, we show that the tumor suppressor protein phosphatase 2A (PP2A), one of the major Ser/Thr

220 d that, along with the previously identified protein phosphatase 2A (PP2A), pigment aggregation signa

221 mportant myocardial proteins is regulated by protein phosphatase 2A (PP2A), representing a heterotrim

222 The proto-oncogene and inhibitor of protein phosphatase 2A (PP2A), SET, interacts with the t

223 Protein phosphatase 2A (PP2A), the major serine/threonin

224 discovery of a protein network comprised of protein phosphatase 2A (PP2A), Transducer of Erb-B2 (Tob

225 r suppressor activity of protein phosphatase protein phosphatase 2A (PP2A), which by dephosphorylatin

226 The phosphorylation of Tau is regulated by protein phosphatase 2A (PP2A), which in turn is modulate

227 te require an interaction between E4orf4 and protein phosphatase 2A (PP2A), which is mediated through

228 Protein phosphatase 2A (PP2A), YAP, Src family tyrosine

229 FTY720 is also a potent protein phosphatase 2A (PP2A)-activating drug (PAD).

230 Here, we report that the protein phosphatase 2A (PP2A)-associated protein, alpha4

231 in mammalian tissue culture cells it induces protein phosphatase 2A (PP2A)-B55- and Src-dependent cel

232 signaling mechanism that involves transient, protein phosphatase 2A (PP2A)-dependent dephosphorylatio

233 amycin-induced Akt phosphorylation involving protein phosphatase 2A (PP2A)-dependent DNA protein kina

234 ll death in a number of mammalian cells in a protein phosphatase 2A (PP2A)-dependent manner.

235 Here we report that MEF2 induces a Protein phosphatase 2A (PP2A)-mediated dephosphorylation

236 n be rapidly stimulated by mGluR-induced and protein phosphatase 2a (PP2A)-mediated dephosphorylation

237 R) activity-dependent manner following brief protein phosphatase 2A (PP2A)-mediated dephosphorylation

238 d Bub1 kinase and the Sgo1-bound phosphatase protein phosphatase 2A (PP2A)-Rts1 underlie a tension-de

239 involving the formation of a beta1 integrin-protein phosphatase 2A (PP2A)-tuberous sclerosis complex

240 ephosphorylated by specific heterotrimers of protein phosphatase 2A (PP2A).

241 ependent kinases (CDKs) and serine/threonine protein phosphatase 2A (PP2A).

242 ifications, make it a nanomolar inhibitor of protein phosphatase 2A (PP2A).

243 o depended on Cdc55, a regulatory subunit of protein phosphatase 2A (PP2A).

244 ressed XPO1, followed by the reactivation of protein phosphatase 2A (PP2A).

245 s dependent on receptor dephosphorylation by protein phosphatase 2A (PP2A).

246 t also binds to the Aalpha subunit (PR65) of protein phosphatase 2A (PP2A).

247 which is a potent physiological inhibitor of protein phosphatase 2A (PP2A).

248 n dephosphorylation of myosin II mediated by protein phosphatase 2A (PP2A).

249 een SVST and POLST may lie in utilization of protein phosphatase 2A (PP2A).

250 es with tau, other molecular chaperones, and protein phosphatase 2A (PP2A).

251 its activity, an effect that is reversed by protein phosphatase 2A (PP2A).

252 raction with Cdc55p, a regulatory subunit of protein phosphatase 2A (PP2A).

253 uated eNOS S1179 phosphorylation mediated by protein phosphatase 2A (PP2A).

254 ylation of Jun was dependent on both Akt and protein phosphatase 2A (Pp2a).

255 is dephosphorylated by the serine/threonine protein phosphatase 2A (PP2A).

256 of the SV40 small t antigen known to inhibit protein phosphatase 2A (PP2A).

257 (ST), which interferes with serine/threonine protein phosphatase 2A (PP2A).

258 t translational modification and activity of protein phosphatase 2A (PP2A).

259 activities of a group of phosphatases called protein phosphatase 2A (PP2A).

260 reduced Janus kinase-mediated inhibition of protein phosphatase 2a (PP2A).

261 on group A (XPA), pygopus homolog 2 (PYGO2), protein phosphatase 2A (PP2A)B subunit, Tat-interactive

262 that retraction was triggered by a putative protein phosphatase 2A (PP2A, a Ser/Thr phosphatase acti

263 E3 ligase targeting the catalytic subunit of protein phosphatase 2A (PP2A-C) for ubiquitin-mediated d

264 thylation status of the catalytic subunit of protein phosphatase 2A (PP2A-C), but was not associated

265 Protein phosphatase-2A (PP2A) is an abundant serine/thre

266 in protein kinase A dependent activation of protein phosphatase-2A (PP2A).

267 of a feed forward mechanistic loop involving protein phosphatase 2A [PP2A] and its downstream substra

268 in and zinedin (the regulatory B subunits of protein phosphatase 2A [PP2A]), which interact with CTTN

269 The catalytic subunit of protein phosphatase 2A (PP2Ac) is stabilized in a latent

270 nvestigated whether the catalytic subunit of protein phosphatase 2A (PP2Ac), which is overexpressed i

271 that interact with the catalytic subunit of protein phosphatase 2A (PP2Ac).

272 The catalytic subunit alpha isoform of protein phosphatase 2A (PP2Acalpha) activity, protein, a

273 ), casein kinase 2 (CK2), and B56 containing protein phosphatase 2As (PP2As).

274 on did not require sTAg interaction with the protein phosphatase 2A protein complex, a tumor suppress

275 ic control of the many CaMKII-controlled and protein phosphatase 2A-regulated physiological processes

276 lex containing the ubiquitin ligase MID1 and protein phosphatase 2A regulates the nuclear localizatio

277 have previously shown that the Dictyostelium protein phosphatase 2A regulatory subunit B56, encoded b

278 s paper, we show, in budding yeast, that the protein phosphatase 2A regulatory subunit Cdc55 couples

279 ulation of Hmg1 phosphorylation requires the protein phosphatase 2A-related phosphatase Ppe1 and its

280 which results from the activity of AMPK and protein phosphatase 2A, respectively.

281 The complex between shugoshin and protein phosphatase 2A (Sgo1-PP2A) localizes to centrome

282 ial protease LON1, ribosomal protein RPL24A, protein phosphatase 2A subunit A3, a MADS box protein, a

283 deletion of the catalytic subunits of yeast protein phosphatase 2A, suggesting that lower PKA activi

284 f six (A-F) Huntingtin, elongation factor 3, protein phosphatase 2A, target of rapamycin (HEAT) repea

285 ease, and asparaginyl endopeptidase-I2(PP2A)-protein phosphatase 2A-Tau hyperphosphorylation pathway

286 Furthermore, MIG-7 protein inhibited protein phosphatase 2A to sustain Akt/GSK-3beta phosphor

287 cogene SET, thereby inducing reactivation of protein phosphatase 2A tumor suppressor and inhibition o

288 In this paper, we show that PP2A (Protein Phosphatase 2A(Twins)) counteracts Plk4 autophos

289 by fasting, but not those in rat brains when protein phosphatase 2A was inhibited.

290 encodes a regulatory B subunit of the PP2A (protein phosphatase 2A), which plays important roles in

291 Inhibition of protein phosphatase 2A, which also contributes to sustai

292 the B'alpha1 subunit of the serine/threonine protein phosphatase 2A, which binds to cyclin G1, can st

293 rillar fraction, of the catalytic subunit of protein phosphatase 2A, which corresponded to the loss o

294 The phosphorylation of Tau is regulated by protein phosphatase 2A, which in turn is regulated by in

295 stead, both agents increased the activity of protein phosphatase 2A, which inactivates protein kinase

296 d by the Arabidopsis thaliana B'' subunit of protein phosphatase 2A, which is encoded by the TONNEAU2

297 unit, as well as with protein kinase CK2 and protein phosphatase 2A, which modulate Ca(2+) sensitivit

298 that Pin1 interacted with both PKC-alpha and protein phosphatase 2A, which together control Pin1 isom

299 tion and inactivation of a CDK-counteracting protein phosphatase 2A with a B55delta subunit (PP2A:B55

300 cts with protein phosphatase 2A and recruits protein phosphatase 2A with glycogen synthase kinase 3be