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1 f KIBRA on Ser(539), probably via regulating protein phosphatase 1.
2 1epsilon (CK1epsilon) and was antagonized by protein phosphatase 1.
3 hereas the carboxyl-terminal domain binds to protein phosphatase 1.
4 is effect is exacerbated by pretreating with protein phosphatase 1.
5 ssive tension, an effect that is reversed by protein phosphatase 1.
6 ty but modulated the binding and activity of protein phosphatase 1.
7 M phase with the mitotic kinase Aurora B and protein phosphatase 1.
8  other proteins such as protein kinase A and protein phosphatase 1.
9 rough the activation of specific isoforms of protein phosphatase 1.
10  okadaic acid, suggesting the involvement of protein phosphatase 1.
11 resistant to serine 133 dephosphorylation by protein phosphatase 1.
12 rmones or by dephosphorylation of lipin with protein phosphatase 1.
13  induced Ser(847)-PO(4) dephosphorylation by protein phosphatase 1.
14 acting proteins such as protein kinase A and protein phosphatase 1.
15 rora B, Mps1, and Plx1) and is suppressed by protein phosphatase 1.
16 ethod was expanded to detect the activity of protein phosphatase 1.
17 inactivation of CaMKII bound to caspase 2 by protein phosphatase 1.
18 kinase-3 and the glycogen-associated form of protein phosphatase 1.
19 n phospho-protein kinase A and a decrease in protein phosphatase-1.
20 e derivative of the protein kinase inhibitor protein phosphatase 1 (1NM-PP1), it is possible to produ
21 at could be achieved in vitro by recombinant protein phosphatase 1 (230 +/- 30%) was significantly gr
22 lular signal activated kinase 1/2), p38MAPK, protein phosphatase 1/2A (PP1/2A), and reactive oxygen s
23  (CaMKII) but was augmented by inhibition of protein phosphatase 1/2A (PP1/2A).
24 T840 dephosphorylation could be blocked by a protein phosphatase 1/2A (PP1/PP2A) inhibitor and was pa
25 brain slices of WKY rats pretreated with the protein phosphatase 1/2A, calcineurin, or casein kinase-
26 cAMP-regulated phosphoprotein-32--> increase protein phosphatase 1/2A--> decrease GABA(A).
27  in hippocampal slices induces a calcium and protein phosphatase 1/2A-dependent dephosphorylation of
28 as mediated through Src tyrosine kinases and protein phosphatase-1/2A.
29 ttributed to the intracellular inhibition of protein phosphatases 1/2A due to lack of specific transm
30 A) versus agents that act on microtubules or protein phosphatases 1/2A.
31                                          The protein phosphatase 1 a (PP1a)-specific phosphatase inhi
32                                Inhibition of protein phosphatase 1 action on phospho-eIF2alpha by kno
33                                The increased protein phosphatase 1 activity is partially due to depho
34                                              Protein phosphatase 1 activity negatively regulates this
35 also show that pharmacological inhibition of protein phosphatase 1 activity, which will result in pRb
36 and cardiomyocytes, related to inhibition of protein phosphatase 1 activity.
37                       Finally, inhibition of protein phosphatase-1 activity by calyculin A or knockdo
38 tus of inhibitor-1, which in turn suppresses protein phosphatase-1 activity, thus modulating phosphol
39               These results demonstrate that protein phosphatase 1 acts as a major phosphatase to dep
40 d a direct association between InsP(3)R1 and protein phosphatase 1 alpha (PP1 alpha).
41   In addition, dephosphorylation of BRCA1 by protein phosphatase 1 alpha enhances the E3 ubiquitin li
42  ligase is controlled by Aurora-A kinase and protein phosphatase 1 alpha-mediated phosphoregulation t
43 ed by PC1 binding through the recruitment of protein phosphatase-1 alpha (PP1alpha).
44 erature upon incubation with okadaic acid, a protein phosphatase 1 and 2A inhibitor.
45      Neurabin and spinophilin are homologous protein phosphatase 1 and actin binding proteins that re
46 n of glycogen synthase due to codigestion by protein phosphatase 1 and beta-d-N-acetylglucosaminidase
47                      Moreover, inhibition of protein phosphatase 1 and glycogen synthase kinase 3beta
48 ciated protein Doublecortin is controlled by protein phosphatase 1 and its regulator spinophilin.
49           We further show that the Reg1-Glc7 protein phosphatase 1 and Sit4 type 2A-like phosphatase
50 accharomyces cerevisiae SNF1/AMPK, Reg1-Glc7 protein phosphatase 1 and Sit4 type 2A-related phosphata
51 strate that Myosin phosphatase, a complex of Protein phosphatase 1 and the scaffolding protein Mypt1,
52 ted by 2 phosphoproteins, the inhibitor-1 of protein phosphatase 1 and the small heat shock protein 2
53 m that involves activation by this kinase of protein phosphatase 1 and/or 2A and resultant increased
54       Spinophilin is a protein that binds to protein phosphatase-1 and actin and modulates excitatory
55 g complex promoted Axin dephosphorylation by protein phosphatase-1 and inactivated ("closed") Axin th
56                                Inhibition of protein phosphatases 1 and 2A and activation of PKC incr
57                                Inhibition of protein phosphatases 1 and 2A blocked ITM when animals w
58 yrosine phosphatases or the serine/threonine protein phosphatases 1 and 2A decreased Ih at maximal ac
59               Inhibition of serine/threonine protein phosphatases 1 and 2A decreased maximal Ih and H
60 nd okadaic acid indicated that inhibition of protein phosphatases 1 and 2A dramatically enhanced ERK2
61 dent of Ca2+ and independent of calcineurin, protein phosphatase 1, and/or protein phosphatase 2A act
62  containing substrates for protein kinase A, protein phosphatase-1, and matrix metalloproteinases 2 a
63 , bath application of NMDA induced a strong, protein phosphatase 1- and/or 2A-mediated decrease in T8
64  regulators identified different kinases and protein phosphatase 1 as the molecules that control reve
65 at involves the phosphatases calcineurin and protein phosphatase-1, as well the serine/threonine kina
66                         The interaction with protein phosphatase 1 beta/Mypt1 resulted in exclusion o
67   Here, we show that the neuronal actin- and protein phosphatase-1-binding protein, neurabin-I, promo
68 h forms of LTD were blocked by inhibitors of protein phosphatase 1, but only LTD of AMPAR EPSCs was a
69 MDARs was independent of protein kinase A or protein phosphatase 1, but was abolished by incubation o
70            Pi04314 interacts with three host protein phosphatase 1 catalytic (PP1c) isoforms, causing
71 eurabin II may induce the association of the protein phosphatase 1 catalytic subunit (PP1) with neura
72 oduct of which recruits the alpha-isoform of protein phosphatase 1 catalytic subunit (PP1alpha) and e
73                 Through interaction with the protein phosphatase 1 catalytic subunit (PP1c), Gadd34 r
74                         The serine/threonine protein phosphatase-1 catalytic subunit (PP-1c) is a maj
75 in phosphatase (MP) holoenzyme consisting of protein phosphatase-1 catalytic subunit (PP1c) and MP ta
76        Dephosphorylation studies showed that protein phosphatase 1 catalyzed near-complete in vitro d
77               Exposure of these CCM cells to protein phosphatase 1 caused a transitory increase in Ca
78      Therefore, Sgo1, Ipl1 kinase, Dam1, and protein phosphatase 1 comprise the SAC silencing network
79                        Finally, we show that protein phosphatase 1 counteracts Aurora B activity to e
80 neurons, NMDA receptor stimulation induces a protein phosphatase 1-dependent dephosphorylation of CDK
81 lated by A20/glycogen synthesis kinase-3 and protein phosphatase 1-dependent mechanisms.
82                              First, purified protein phosphatase-1 directly dephosphorylates Pax-6 in
83 Perturbation of both microtubule binding and protein phosphatase 1 docking at the KNL-1 N terminus ad
84        A reg1Delta mutant, lacking Reg1-Glc7 protein phosphatase 1, exhibits elevated glycogen accumu
85                           The involvement of protein phosphatase 1 explains why second messengers lik
86 RK-1/2 via increased DUSP1 (dual-specificity protein phosphatase 1) expression.
87 Ser-518/Thr-514/Thr-509) is carried out by a protein phosphatase 1 family member in vitro, in neurobl
88 gamma(1)34.5 recruits both IKKalpha/beta and protein phosphatase 1, forming a complex that dephosphor
89 ated with a parallel depletion of G beta and protein phosphatase 1 from the oligomeric GIRK1 complexe
90             Dephosphorylation of channels by protein phosphatase 1 (from 75% to near 0% at serine-280
91                             Repo-Man targets protein phosphatase 1 gamma (PP1gamma) to chromatin at a
92 e phosphorylation of Rpt6 were reversible by protein phosphatase 1 gamma.
93 effect of activating the inhibitor (I-1c) of protein phosphatase 1 (I-1) through gene transfer on car
94  insulin intolerance and inactivated adipose protein phosphatase 1 in association with the up-regulat
95 o-Ser(65) inhibitor-1 is dephosphorylated by protein phosphatase 1 in the striatum.
96 er(65) inhibitor-1 from dephosphorylation by protein phosphatase 1 in vivo.
97 electively inhibited a regulatory subunit of protein phosphatase 1 in vivo.
98                                    Increased protein phosphatase-1 in heart failure (HF) induces mole
99                     Third, overexpression of protein phosphatase-1 in human lens epithelial cells lea
100                       Phosphorylation of the protein phosphatase 1 inhibitor 1 (I-1), a direct calcin
101 athway using PKC-alpha and the PKC-regulated protein phosphatase 1 inhibitor 14D that is required for
102 MBS85), paxillin and CPI-17 (PKC-potentiated protein phosphatase 1 inhibitor protein of 17 kDa) phosp
103                               Calyculin A, a protein phosphatase 1 inhibitor, blocked the hypertonici
104                     This approach identified protein phosphatase 1 inhibitor-1 (I-1) as a DCT-enriche
105 r Ser(67) did not convert inhibitor-1 into a protein phosphatase 1 inhibitor.
106        PHLPP1 (PH domain leucine-rich repeat protein phosphatase 1) is a protein-serine/threonine pho
107 clude that PDE4D3, like protein kinase A and protein phosphatase 1, is recruited to the I(Ks) channel
108 ein lipase (Lpl), lactamase beta (Lactb) and protein phosphatase 1-like (Ppm1l), are validated as pre
109 ade of RCAN1-CaN interaction reduced CaN and protein phosphatase-1 localization to nuclear-enriched p
110                                              Protein phosphatase 1 mediated the dephosphorylation eve
111 increase in GIRK surface expression requires protein phosphatase-1-mediated dephosphorylation of a se
112 A (PP2A) is responsible for DHEA action, and protein phosphatase 1 might be involved in nafenopin ind
113 by protein kinase A and dephosphorylation by protein phosphatase 1 modulate the inhibitory activity o
114 n is an actin binding protein that positions protein phosphatase 1 next to its substrates in dendriti
115 s alpha or beta of the catalytic subunits of protein phosphatase 1 not only increased phosphorylation
116             In this study, we identified the protein phosphatase-1 nuclear targeting subunit PNUTS (P
117                                              Protein phosphatase 1 occurs in all tissues and regulate
118                     Here we show that either protein phosphatase 1 or 2A is sufficient to suppress ac
119 se 5 (Cdk5), glycogen synthase kinase 3beta, protein phosphatase 1, or protein phosphatase 2A, but re
120 RPP-32), a potent and selective inhibitor of protein phosphatase-1, or the protein tyrosine kinase Fy
121 trin homology domain and leucine-rich repeat protein phosphatase 1 (PHLPP1) as a regulatory phosphata
122 eckstrin homology domain leucine-rich repeat protein phosphatase 1 (PHLPP1) differentially attenuates
123 trin homology domain and leucine rich repeat protein phosphatase 1 (PHLPP1) is a member of the serine
124 ariants of PH domain and Leucine-rich repeat Protein Phosphatase 1 (PHLPP1), PHLPP1alpha and PHLPP1be
125 ion of the PH domain and leucine-rich repeat protein phosphatases 1 (PHLPP1), a phosphatase of Akt.
126 eckstrin-homology domain leucine-rich repeat protein phosphatases 1 (PHLPP1).
127 ications implicated an indirect role of PP1 (protein phosphatase 1), potentially via its interphase r
128 ase 1I (PP-1I) is a major endogenous form of protein phosphatase 1 (PP-1) that consists of the core c
129 the first identified endogenous inhibitor of protein phosphatase 1 (PP-1), was previously reported to
130 ously demonstrated that the serine/threonine protein phosphatase-1 (PP-1) plays an important role in
131  inhibitor-1 (I-1), altering the activity of protein phosphatase-1 (PP-1), which may account for the
132 require the kinetochore-localized isoform of protein phosphatase 1 (PP1(Dis2)).
133 icates that the protein regulators governing protein phosphatase 1 (PP1) activity have crucial functi
134 receptors through a dominant coupling to the protein phosphatase 1 (PP1) activity in postsynaptic neu
135 h similarity to Sds22p, a regulator of yeast protein phosphatase 1 (PP1) activity in the nucleus.
136 have studied Sds22, a conserved regulator of protein phosphatase 1 (PP1) activity, and determined its
137 t long-lasting tolerance, was facilitated by protein phosphatase 1 (PP1) activity.
138 rora B inhibition, is rescued by restraining protein phosphatase 1 (PP1) activity.
139 sphorylation in IL-2 signaling, the roles of protein phosphatase 1 (PP1) and 2A (PP2A) were examined.
140 utation disrupts Phactr4, an uncharacterized protein phosphatase 1 (PP1) and actin regulator family m
141  spindle MTs in vivo, Mars binds directly to protein phosphatase 1 (PP1) and coimmunoprecipitates fro
142  axonal transport (FAT) by activating axonal protein phosphatase 1 (PP1) and glycogen synthase kinase
143 ivities of cyclin-dependent kinase 5 (CDK5), protein phosphatase 1 (PP1) and glycogen synthase kinase
144 disrupt protein-protein interactions between protein phosphatase 1 (PP1) and its regulator CPI-17, re
145 nhibits many protein phosphatases, including protein phosphatase 1 (PP1) and PP2A, that can reverse P
146 atase drives this reversal in budding yeast, protein phosphatase 1 (PP1) and protein phosphatase 2A (
147 e (MP), which includes the catalytic subunit protein phosphatase 1 (PP1) and the regulatory targeting
148                   Additionally, we show that protein phosphatase 1 (PP1) antagonizes rpS6 C terminus
149 t wild-type, but not catalytically inactive, protein phosphatase 1 (PP1) associates with KIBRA.
150 d amino acid within the domain important for protein phosphatase 1 (PP1) binding.
151                       SAMe and MTA increased protein phosphatase 1 (PP1) catalytic subunit mRNA and p
152                                              Protein phosphatase 1 (PP1) catalytic subunits dephospho
153 rmed, and it was observed that knock-down of protein phosphatase 1 (PP1) catalytic subunits significa
154 C-3 prostate cancer cells by disrupting HDAC-protein phosphatase 1 (PP1) complexes.
155                  We also show that host cell protein phosphatase 1 (PP1) controls VP30 dephosphorylat
156                         The serine-threonine protein phosphatase 1 (PP1) deactivates this pathway whe
157                         The serine/threonine protein phosphatase 1 (PP1) dephosphorylates hundreds of
158                    Cut12 harbors a bipartite protein phosphatase 1 (PP1) docking domain.
159         Opposing roles of Aurora kinases and protein phosphatase 1 (PP1) during mitosis have long bee
160               In one approach, a recombinant protein phosphatase 1 (PP1) has been conjugated to MPs v
161                                    Recently, protein phosphatase 1 (PP1) has been shown to interact w
162 t the catalytic subunit of the budding yeast protein phosphatase 1 (PP1) homolog, Glc7, regulates exi
163 acid, implicating PDGF-induced activation of protein phosphatase 1 (PP1) in CRMP2 regulation.
164     Dephosphorylation of CDK9 on Thr(186) by protein phosphatase 1 (PP1) in stress-induced cells or b
165               Here we demonstrate a role for protein phosphatase 1 (PP1) in the regulation of the maj
166 Here we show in vitro and in Drosophila that Protein Phosphatase 1 (PP1) inactivates Mps1 by dephosph
167        However, pretreatment of GCs with the protein phosphatase 1 (PP1) inhibitor tautomycin increas
168  regulatory subunit 1A (PPP1R1A) is a potent protein phosphatase 1 (PP1) inhibitor; however, its role
169 strated that NKCC1 activity is stimulated by protein phosphatase 1 (PP1) inhibitors.
170                                              Protein phosphatase 1 (PP1) is a ubiquitous serine/threo
171                      We recently showed that protein phosphatase 1 (PP1) is activated by ATM.
172                                              Protein phosphatase 1 (PP1) is an essential and ubiquito
173     The serine/threonine protein phosphatase protein phosphatase 1 (PP1) is known to play an importan
174                               In particular, protein phosphatase 1 (PP1) is recruited to a DSB-mimick
175  6983 prevents the dephosphorylation by pure protein phosphatase 1 (PP1) or the hydrophobic motif pho
176 hosphorylation was blocked by treatment with protein phosphatase 1 (PP1) pharmacological inhibitors a
177 ly, pharmacological or genetic inhibition of protein phosphatase 1 (PP1) prevented HTTex1 aggregation
178 biquitously expressed and highly promiscuous protein phosphatase 1 (PP1) regulates many cellular proc
179 We show that PKA directly phosphorylates the protein phosphatase 1 (PP1) regulatory subunit myosin ph
180 IF2alpha phosphatases comprising a catalytic protein phosphatase 1 (PP1) subunit in complex with a PP
181                        Overexpression of the protein phosphatase 1 (PP1) subunit protein targeting to
182                                Repo-Man is a protein phosphatase 1 (PP1) targeting subunit that regul
183 e targeting subunit Repo-Man from recruiting protein phosphatase 1 (PP1) to chromatin at anaphase ons
184 he mitotic chromosome periphery and recruits protein phosphatase 1 (PP1) to chromatin at anaphase ons
185 transmission through their ability to target protein phosphatase 1 (PP1) to dendritic spines where PP
186 tes with the broadly acting serine/threonine protein phosphatase 1 (PP1) to dephosphorylate eIF2alpha
187    The Ska1 C-terminal domain (CTD) recruits protein phosphatase 1 (PP1) to kinetochores to promote t
188      Here, we show that Ska complex recruits protein phosphatase 1 (PP1) to kinetochores.
189  kinase activity of the IGF-1R by activating protein phosphatase 1 (PP1) to promote dephosphorylation
190 ein KNL1 directly interacts with and targets protein phosphatase 1 (PP1) to the outer kinetochore.
191 her, Sp3 was shown to promote the binding of protein phosphatase 1 (PP1) to the p21(CIP1) promoter, l
192         We report that Ikaros interacts with protein phosphatase 1 (PP1) via a conserved PP1 binding
193 We also demonstrated that functional CK2 and protein phosphatase 1 (PP1) were selectively tethered to
194 through the RHO/ROCK pathway and coordinates protein phosphatase 1 (PP1) with cofilin activity to reg
195 ew study, we investigated the interaction of protein phosphatase 1 (PP1) with the SR protein splicing
196                                              Protein phosphatase 1 (PP1), a major protein phosphatase
197    Using a directed RNAi screen we find that protein phosphatase 1 (PP1), a ubiquitous serine/threoni
198  of p38 MAPK, phosphatidylinositol 3-kinase, protein phosphatase 1 (PP1), and dynamin GTPase.
199 by protein kinase A results in inhibition of protein phosphatase 1 (PP1), and phosphorylation at Thr-
200 s, we have found novel links among ERK, JNK, protein phosphatase 1 (PP1), and the eukaryotic initiati
201 /2 as a positive regulator, whereas purified protein phosphatase 1 (PP1), dephosphorylated Thr-450 in
202 es involved in glycogen synthesis, including protein phosphatase 1 (PP1), glycogen synthase, phosphor
203 amily serine/threonine phosphatases PP2A and protein phosphatase 1 (PP1), had cell type-dependent eff
204               Sds22, a regulatory subunit of protein phosphatase 1 (PP1), has recently been linked to
205                                              Protein phosphatase 1 (PP1), in particular, is ubiquitou
206  this study we show that Gwl associates with protein phosphatase 1 (PP1), particularly PP1gamma, whic
207 R cytoplasmic domain (cd) and the associated protein phosphatase 1 (PP1), requiring NMDARcd movement,
208 eins that are glycogen-targeting subunits of protein phosphatase 1 (PP1), the muscle-specific regulat
209 the largely uncharacterized Phactr family of protein phosphatase 1 (PP1)-and actin-binding proteins.
210 stone H3-Lys(4) methyltransferase complexes, protein phosphatase 1 (PP1)-associated proteins, a chape
211 e how Rif1 opposes DDK function by directing Protein Phosphatase 1 (PP1)-mediated dephosphorylation o
212  phosphorylated glycogen synthase at a GSK-3/protein phosphatase 1 (PP1)-regulated site in rictor kno
213 ed predominantly by an Src kinase inhibitor, protein phosphatase 1 (PP1)-sensitive but Src/Yes/Fyn-in
214  by the balance between CK1delta/epsilon and protein phosphatase 1 (PP1).
215 ased with IP(3) (IRBIT) and by inhibition of protein phosphatase 1 (PP1).
216  inhibition of the serine-threonine-specific protein phosphatase 1 (PP1).
217 itor-1, which, when phosphorylated, inhibits protein phosphatase 1 (PP1).
218 omitantly with dephosphorylation of PDE3A by protein phosphatase 1 (PP1).
219 d from Cdc25 and S287 is dephosphorylated by protein phosphatase 1 (PP1).
220 ctions in the checkpoint through controlling protein phosphatase 1 (PP1).
221  this phosphorylation is rapidly reversed by protein phosphatase 1 (PP1).
222 gulation, pSer-68-PLM is dephosphorylated by protein phosphatase 1 (PP1).
223 ed levels of GADD34, a regulatory subunit of protein phosphatase 1 (PP1).
224 d calcineurin (CaN)-deactivated inhibitor of protein phosphatase 1 (PP1).
225 lated by the broadly acting serine/threonine protein phosphatase 1 (PP1).
226  a master regulator of mitosis by modulating protein phosphatase 1 (PP1).
227  yeast [6], we show here that the binding of protein phosphatase 1 (PP1/Glc7) to the evolutionarily c
228  (TTN) is highly selective for a single PPP, protein phosphatase 1 (PP1/PPP1C).
229                                              Protein phosphatase-1 (PP1) activity is important for ma
230 sphorylation-dependent mechanism mediated by protein phosphatase-1 (PP1) and dual specificity phospha
231 nhibitor-1 (I-1) is a selective inhibitor of protein phosphatase-1 (PP1) and regulates several PP1-de
232 uires activity of NMDA receptors (NMDAR) and protein phosphatase-1 (PP1) and takes place within 15 mi
233                                              Protein phosphatase-1 (PP1) catalytic subunit isoforms i
234                                              Protein phosphatase-1 (PP1) controls many processes in e
235                     PTG and G(L) are hepatic protein phosphatase-1 (PP1) glycogen-targeting subunits,
236                The reaction catalyzed by the protein phosphatase-1 (PP1) has been examined by linear
237 ively inhibit myosin phosphatase among other protein phosphatase-1 (PP1) holoenzymes.
238 ation as a targeting subunit for the Ser/Thr protein phosphatase-1 (PP1) in yeast.
239                                              Protein phosphatase-1 (PP1) is a major Ser/Thr phosphata
240                                              Protein phosphatase-1 (PP1) is a Ser/Thr protein phospha
241                                              Protein phosphatase-1 (PP1) is an essential protein Ser/
242 in kinase A by 8-bromo-cAMP or inhibition of protein phosphatase-1 (PP1) or calcineurin (PP2B) result
243       Our data further show that PKA targets protein phosphatase-1 (PP1) through the phosphorylation
244 in binding protein neurabin I (NrbI) targets protein phosphatase-1 (PP1) to specific postsynaptic mic
245 minal coiled-coil domains and association of protein phosphatase-1 (PP1) with neurabin-I through a ca
246                        Cellular functions of protein phosphatase-1 (PP1), a major eukaryotic serine/t
247  The regulatory circuit controlling cellular protein phosphatase-1 (PP1), an abundant group of Ser/Th
248 defects did not involve changes in levels of protein phosphatase-1 (PP1), and the multinuclear phenot
249  that S135 dephosphorylation is catalyzed by protein phosphatase-1 (PP1), which directly binds C2.
250 ase SR-protein phosphorylation by activating protein phosphatase-1 (PP1).
251 -induced HIV-1 transcription is regulated by protein phosphatase-1 (PP1).
252                  We find that Spinophilin, a Protein-phosphatase 1 (PP1) targeting protein, is respon
253 chemical compound that specifically inhibits protein phosphatase 1(PP1)-GADD34 phosphatase activity,
254 glycogen synthase kinase 3beta (GSK3beta) by protein phosphatase 1(PP1)-mediated dephosphorylation of
255  of Shoc2/Sur-8 and the catalytic subunit of protein phosphatase 1 (PP1c) as a highly specific M-Ras
256      We report that the catalytic subunit of protein phosphatase 1 (PP1c) constitutively associates w
257 rate specificity of the catalytic subunit of protein phosphatase 1 (PP1c) is dictated by PP1c-interac
258 n MEL-28/ELYS docks the catalytic subunit of protein phosphatase 1 (PP1c) to direct kinetochore disas
259 P)/PPP1r15B targets the catalytic subunit of protein phosphatase 1 (PP1c) to phosphorylated eIF2alpha
260  1 (MYPT1) binds to the catalytic subunit of protein phosphatase 1 (PP1C).
261  of the catalytic subunit (gamma isoform) of protein phosphatase-1 (PP1c gamma) in vitro.
262 s mediated at least in part by inhibition of protein phosphatase-1 (PP1c) via persulfidation at Cys-1
263 abenz, that bound to a regulatory subunit of protein phosphatase 1, PPP1R15A/GADD34, selectively disr
264  identified a membrane-associated subunit of protein phosphatase 1 (PPP1R16A, or abbreviated as R16A)
265                                Together with protein phosphatase 1, protein phosphatase 2A (PP2A) con
266                        Furthermore, both the protein phosphatase 1/protein phosphatase 2A inhibitor o
267 nhibitors, but not okadaic acid (a selective protein phosphatase 1/protein phosphatase 2A inhibitor),
268 itogen-activated protein kinase pathway, and protein phosphatase 1, regulate activation of Msn2 in di
269 etermined the expression and localization of protein phosphatase 1 regulatory inhibitor subunit 11 (P
270 MPK in vivo in several substrates, including protein phosphatase 1 regulatory subunit 12C (PPP1R12C)
271                                              Protein phosphatase 1 regulatory subunit 1A (PPP1R1A) is
272                                              Protein phosphatase 1 regulatory subunit 1B(+) BLA pyram
273 , glucokinase regulatory protein (GCKR), and protein phosphatase 1 regulatory subunit 3b (PPP1R3B) th
274 ction closest to the mapped region, PPP1R3B (protein phosphatase 1 regulatory subunit 3B), encodes a
275 nophilin (abbreviated spn; gene name Ppp1r9b protein phosphatase 1 regulatory subunit 9b) and the cla
276                    In this study, we propose protein phosphatase 1, regulatory (inhibitor) subunit 1A
277  line resulted in the isolation of a mutated protein phosphatase 1, regulatory (inhibitor) subunit 3B
278 131, which affects the expression of ORMDL3, protein phosphatase 1, regulatory inhibitor subunit 1B (
279 between TIBC and a variant near the gene for protein phosphatase 1, regulatory subunit 3B (PPP1R3B; r
280 in-dependent protein kinase II, calcineurin, protein phosphatase 1, Rho GTPase, mitogen-activated pro
281                    Therefore the role of the protein phosphatase 1 should be considered as an additio
282                           The Src homology-2 protein phosphatase-1 (SHP-1) coprecipitated with integr
283 monstrate that dephosphorylation of Pax-6 by protein phosphatase-1 significantly modulates its functi
284  Inh3 (inhibitor-3) is a potent inhibitor of protein phosphatase-1 that selectively associates with P
285 nt triggers the dephosphorylation of Dam1 by protein phosphatase 1, this dephosphorylation likely coo
286                                   Inhibiting protein phosphatase-1 through the overexpression of a co
287 homeostasis regulator GADD34, which recruits protein phosphatase 1 to dephosphorylate eIF2alpha durin
288  factor of herpes simplex viruses, redirects protein phosphatase 1 to dephosphorylate the alpha subun
289 ss, the gamma(1)34.5 protein associates with protein phosphatase 1 to form a large complex that depho
290  protein kinase (protein kinase A (PKA)) and protein phosphatase 1 to the carboxyl terminus of the I(
291 KAP-9), which recruits protein kinase A) and protein phosphatase 1 to the channel.
292 o-mediated targeting of protein kinase A and protein phosphatase-1 to the I(Ks) channel.
293       Expression of the catalytic subunit of protein phosphatase 1 was increased in all mutant hearts
294 NA encoding PP1cgamma1 (catalytic subunit of protein phosphatase 1) was present in several independen
295    Inhibitor-1 becomes a potent inhibitor of protein phosphatase 1 when phosphorylated by cAMP-depend
296 s dephosphorylation by kinetochore-localized protein phosphatase 1, which allows Cdc20 to activate th
297 del systems parallel the observation that in protein phosphatase-1, which has an active site that res
298 ons in PPM1D, encoding wild-type p53-induced protein phosphatase 1D (WIP1), in 37.5% of the BSGs that
299 tact has a direct parallel in the contact of protein phosphatase 1 with its regulatory proteins, sugg
300 c were determined to be potent inhibitors of protein phosphatase-1 with similar activity.

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