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1  enhanced STAT1-mediated gene expression via serine phosphorylation.
2  the addition of a negative charge mimicking serine phosphorylation.
3 tivation, which followed the onset of RhoGDI serine phosphorylation.
4  specifically localized to the ER on its own serine phosphorylation.
5  (PKA) activity and increases beta3 integrin serine phosphorylation.
6               Instead PTP1B was activated by serine phosphorylation.
7 ession, GRK-2 sequestration, and D1 receptor serine phosphorylation.
8 2) membranous translocation, and D1 receptor serine phosphorylation.
9  both direct and indirect regulation of IRS1 serine phosphorylation.
10 d in wild-type, metastatic mammary tumors by serine phosphorylation.
11 h key protein interactions are controlled by serine phosphorylation.
12 cking antibodies and involved beta1 integrin serine phosphorylation.
13 cent subunits and regulating factors such as serine phosphorylation.
14 ttle is known about the significance of Spry serine phosphorylation.
15 egulated by EGFR through modulation of STAT3 serine phosphorylation.
16 ine phosphorylation, while stimulating c-Met serine phosphorylation.
17 lipase C (PLC) activity was required for PKD serine phosphorylation.
18 ne/threonine kinase responsible for alphaPIX serine phosphorylation.
19 stimulate HBV replication by increasing core serine phosphorylation.
20 ion by ERBB4 is also mediated through STAT5A serine phosphorylation.
21 y through a detailed study of the role of MA serine phosphorylation.
22 ich key protein interactions are governed by serine phosphorylation.
23 nd NF-kappaB signaling through modulation of serine phosphorylation.
24 Exposure to E2 significantly decreased STIM1 serine phosphorylation.
25 in in a ternary complex that is regulated by serine phosphorylation.
26 dation, consistent with GRK isoform-specific serine phosphorylation.
27 ivation of Stat5b requires both tyrosine and serine phosphorylation.
28  lysine methylation, lysine acetylation, and serine phosphorylation.
29 tochemistry showed decreases in beta-catenin serine phosphorylation (33/37) and ubiquitinylation in t
30                               Increased IRS2 serine phosphorylation, a marker of insulin resistance,
31  interaction is regulated by topoisomerase I serine phosphorylation, a modification that regulates to
32 ding domain or mutating two newly discovered serine phosphorylation acceptor sites, Ser106 and Ser110
33 t posttranslational modifications, including serine phosphorylation, acetylation, methylation, and su
34                   Conversely, enhancement of serine phosphorylation achieved through either the inhib
35 BDNF stimulated m-calpain but not mu-calpain serine phosphorylation, an effect also blocked by MAPK i
36 horylation as well as an enhancement of KCC2 serine phosphorylation and activity.
37 activates GSK3beta, thereby preventing PDX-1 serine phosphorylation and alleviating GSK3beta-mediated
38        Unusually, activation is regulated by serine phosphorylation and consequent inhibition of a ty
39 tion of this kinase as well as for efficient serine phosphorylation and degradation of IFNAR1 and ens
40  3-kinase (PI3K)/Akt pathway, which involves serine phosphorylation and degradation of IkappaB alpha.
41 d Ser523 as the first-described site of Jak2 serine phosphorylation and demonstrated that this site i
42 nction-blocking antibodies on beta3 integrin serine phosphorylation and EC-ralpha4LN fragment binding
43 cient mice fail to exhibit LPS-induced Stat3 serine phosphorylation and IL-10 gene expression yet sti
44  because of protein kinase A (PKA)-dependent serine phosphorylation and inactivation of RhoA.
45                                              Serine phosphorylation and inhibition of AMPK activity w
46 der various pathological conditions, through serine phosphorylation and inhibition of insulin recepto
47 vation of p70S6K, which in turn promotes the serine phosphorylation and inhibition of IRS-1.
48 titutively active Src expression resulted in serine phosphorylation and inhibition of WASP-associated
49  a transcription factor that is regulated by serine phosphorylation and is critical for the developme
50                           G-CSF induced both serine phosphorylation and membrane translocation of p47
51 ergoes conformational changes in response to serine phosphorylation and proline isomerization.
52 e isomerisation can be inhibited by adjacent serine phosphorylation and requires a prolyl isomerise,
53 direct-detect experiments and show that both serine phosphorylation and RNA binding are necessary for
54 cer and activator of transcription 1 (Stat1) serine phosphorylation and Stat1 nuclear translocation t
55  (-/-) animals, OPN was necessary for PDLIM2 serine phosphorylation and STAT1 ubiquitination in bone
56  induces Egr-1 nuclear accumulation and CREB serine phosphorylation and that both are markedly attenu
57  glucose induces a decrease in overall PDX-1 serine phosphorylation and that overexpression of WT PAS
58 e we show that Ins(1,3,4,5,6)P5 inhibits the serine phosphorylation and the kinase activity of Akt/PK
59                            Moreover, loss of serine phosphorylation and the resulting enhanced degrad
60                       The relative levels of serine phosphorylation and tyrosine phosphorylation are
61 etagamma subunits were required for both PKD serine phosphorylation and tyrosine phosphorylation, int
62 anslocation and subsequent D1 receptor hyper-serine phosphorylation and uncoupling.
63 lated Akt phosphorylation and higher Irs-1/2 serine phosphorylation, and all of these events were dep
64 alpha, PKA, PKG, and CaMKII, which catalyzed serine phosphorylation, and ERK1, JNK, and p38, which ca
65 d partial inhibition of IkappaB and RelA/p65 serine phosphorylation, and p50 and p65 nuclear transloc
66 r export, is associated with increased HDAC7 serine phosphorylation, and requires conserved serines i
67 we demonstrated that both Stat3 tyrosine and serine phosphorylations are required for optimal binding
68 mplex phosphosignaling network with kindlin2 serine phosphorylation as a key regulatory element.
69 ythrocytes undergoes increased PKA-dependent serine phosphorylation as a result of activation.
70 aling promotes AQP4 expression by decreasing serine phosphorylation associated with the water channel
71           Activation of up-regulated AKT2 by serine phosphorylation associates with high-grade tumors
72 e findings suggested that the requirement of serine phosphorylation at residue 536 and the distance b
73 nscriptional activity by a process involving serine phosphorylation at serine (Ser) residue 276.
74 utational analysis showed that PMA increased serine phosphorylation at three sites on IRS2 (positions
75                                 In addition, serine phosphorylation at various sites of the p65 subun
76 coexpressed with ERBB4, we identified STAT5A serine phosphorylations at the previously described Ser-
77 ivities of GSK-3 are regulated negatively by serine phosphorylation but positively by tyrosine phosph
78 whose activities are negatively regulated by serine phosphorylation but positively controlled by tyro
79 rotein, reduction in efflux, and increase in serine phosphorylation by 12S-hydroxyeicosatetranoic aci
80 singly, full Paxillin activity also requires serine phosphorylation by a kinase downstream of MOS and
81 ite motifs, which is mutually exclusive with serine phosphorylation by Akt.
82 nding motif, dramatically increased endoglin serine phosphorylation by all three receptors, suggestin
83 uman PDC is subject to inactivation at E1 by serine phosphorylation by four kinases, an inactivation
84       Activity of TFEB is inhibited upon its serine phosphorylation by mTOR The overall mechanisms by
85 sits to the Golgi complex where it undergoes serine phosphorylation by PKD.
86       We found that laminar flow induced SP1 serine phosphorylation by protein kinase CK2 and thereby
87 ple tyrosine phosphorylation events and also serine phosphorylation by protein kinase D.
88  mechanisms, including regulation of cofilin serine phosphorylation by Rho GTPases.
89                                   C-terminal serine phosphorylation by TGF-beta and BMP membrane rece
90                                              Serine phosphorylation, calcium, and calmodulin binding
91 F2 factors and that alternative splicing and serine phosphorylation converge to provide complex combi
92  and that coincident AKT2 activation through serine phosphorylation correlates with malignancy.
93                               Thus, ARF is a serine phosphorylation-dependent coregulator of topoisom
94 including the ligand-stimulated and specific serine phosphorylation-dependent degradation of the IFNA
95      A mutant of hSpry2 that is deficient in serine phosphorylation displays enhanced tyrosine phosph
96 importance of threonine phosphorylation than serine phosphorylation due to larger induced structural
97                              Concurrently, a serine phosphorylation event in the transcription activa
98  appeared to be a likely site for regulatory serine phosphorylation events.
99 ike that of H358 cells, is largely devoid of serine phosphorylation, has low activity, and complexes
100 tion was associated with enhanced N-terminal serine phosphorylation in both GSK-3 isoforms.
101 t analyses indicated that BDNF increases SK2 serine phosphorylation in hippocampal slices.
102               To directly assess the role of serine phosphorylation in mediating fat-induced insulin
103 inhibitor, resulted in an opposite effect on serine phosphorylation in N2A cells and primary hippocam
104 r, these results highlight the importance of serine phosphorylation in regulating type II hemidesmoso
105 eins have been shown to undergo tyrosine and serine phosphorylation in response to growth factor stim
106 s expressed ubiquitously and is activated by serine phosphorylation in response to viral infection or
107 f binding to EloC is negatively regulated by serine phosphorylation in the BC-box motif of the SOCS-b
108            Here we investigate the effect of serine phosphorylation in the interior of an alpha-helix
109  N2A neuroblastoma cell line along with p35, serine phosphorylation in their Cdk5 motifs was found to
110 ted erbB2/4 tryosine phosphorylation and Akt serine phosphorylation in ventricular myocytes, whereas
111  activation and insulin receptor substrate 1 serine phosphorylation in vitro and in vivo.
112       Glycogen synthase kinase 3 (GSK-3beta) serine phosphorylation (inactivation) was blunted in PEC
113 ersed inflammatory cytokine-stimulated IRS-1 serine phosphorylation, increased insulin signaling to A
114      Rapamycin inhibits S6K1-dependent IRS-1 serine phosphorylation, increases IRS-1 protein levels,
115 hypothesis that PKA regulates beta3 integrin serine phosphorylation indirectly through phosphorylatio
116 at antagonism between lysine methylation and serine phosphorylation is a fundamental mechanism for co
117                                   Inhibitory serine phosphorylation is a potential molecular mechanis
118 nolytic vascular surveillance by blockade of serine phosphorylation is A2-dependent.
119                                         This serine phosphorylation is essential for the maximal tran
120                                         This serine phosphorylation is necessary for SRF activity and
121                                The amount of serine phosphorylation is regulated by agents that affec
122 ortance of sequential modification of FAK-by serine phosphorylation, isomerization, and tyrosine deph
123 phosphorylation, resulting in blocking Stat1 serine phosphorylation, its subsequent nuclear transloca
124 e 3 (GSK-3beta) association and beta-catenin serine phosphorylation levels were increased and beta-ca
125  insulin/glucose-dependent Ser/Thr-Pro motif serine phosphorylation mediated by the mTOR pathway.
126 inhibited IL-2-induced Stat5a/b tyrosine and serine phosphorylation, nuclear translocation, and DNA b
127 ore serine mutants demonstrate that multiple serine phosphorylations occur on the same core protein.
128          Our previous studies indicated that serine phosphorylation of a single tryptic peptide inhib
129 Treatment of myeloma cells with IL-6 induced serine phosphorylation of A1 and increased its binding t
130 y, to reduce protein levels, and to increase serine phosphorylation of ABCA1.
131 rated that 12/15LO enhances the turnover and serine phosphorylation of ABCG1.
132 ne phosphorylation transiently, and enhanced serine phosphorylation of Akt and ERK.
133  actions, including erbB2/4 phosphorylation, serine phosphorylation of Akt, and negative inotropy.
134                                              Serine phosphorylation of AMPA receptor (AMPAR) subunits
135 cetylglucosamine modifications and maximized serine phosphorylation of ankyrin(G) and p85 binding to
136  to alanine abolished the insulin-stimulated serine phosphorylation of APS and prevented the localiza
137                       The insulin-stimulated serine phosphorylation of APS was inhibited by a PI3-kin
138 oocyte permeability assays, we conclude that serine phosphorylation of AQP0 does not inhibit CaM bind
139 nged PTEN expression results in the enhanced serine phosphorylation of Bdp1.
140 ity of GSK-3beta, which in turn affected the serine phosphorylation of beta-catenin and its proteosom
141 assic isoforms of protein kinase C mediating serine phosphorylation of beta-catenin and Src-tyrosine
142                       ERK activation-induced serine phosphorylation of both STAT1 and p65 mediated th
143  We recently revealed that p38 MAPK-mediated serine phosphorylation of both Stat1 and Stat3 is requir
144 hat PTEN initially induces a decrease in the serine phosphorylation of Brf1, leading to a selective r
145  is accompanied by PKC-dependent increase in serine phosphorylation of c-Cbl in cells expressing elev
146 ibitors of protein kinase C activity reduced serine phosphorylation of caveolin-1 and increased stero
147          MIF binding was associated with the serine phosphorylation of CD74 and CD44.
148 inase assays show that EGFRvIII induction of serine phosphorylation of Dock180 is PKA-dependent.
149         We demonstrate that EGFRvIII induces serine phosphorylation of Dock180, stimulates Rac1 activ
150 SK1 phosphorylation at Serine-966, decreased serine phosphorylation of FAK, and decreased association
151 on of 18 kDa subunit of complex I, decreased serine phosphorylation of FeS protein in complex III, in
152                      GRP blockade diminished serine phosphorylation of GRPR with ozone or OVA.
153 d treatment with lithium and VPA potentiated serine phosphorylation of GSK-3 alpha and beta isoforms
154 otein kinase IV (CaMKIV), through inhibitory serine phosphorylation of GSK-3beta and inhibition of FB
155                                    Increased serine phosphorylation of hepatic IRS-1 may contribute t
156   Similarly, whereas CaMKIV(+/+) Mphi showed serine phosphorylation of HMGB1 in response to LPS, this
157                                     Although serine phosphorylation of HMGB1 is necessary for nucleoc
158                    Additionally, LPS induced serine phosphorylation of HMGB1, which correlated with a
159 ess may be mediated through CaMKIV-dependent serine phosphorylation of HMGB1.
160         Our results imply that Mnk1-mediated serine phosphorylation of hSpry2 constitutes a regulator
161 tutive activation of NF-kappaB signalling by serine phosphorylation of IkappaBalpha and constitutive
162        In this study, we examine the role of serine phosphorylation of insulin receptor substrate (IR
163 mammalian target of rapamycin (mTOR)-induced serine phosphorylation of insulin receptor substrate (IR
164              Furthermore, resistin increased serine phosphorylation of insulin receptor substrate (IR
165 nied by increased phosphorylation of JNK and serine phosphorylation of insulin receptor substrate 1 (
166               Consistent with these changes, serine phosphorylation of insulin receptor substrate 1 w
167 kt and insulin receptor was reduced, whereas serine phosphorylation of insulin receptor substrate 1 w
168                                              Serine phosphorylation of insulin receptor substrate-1 (
169 c-Jun N-terminal kinase (JNK) and subsequent serine phosphorylation of insulin receptor substrate-1 (
170   Quercetin prevented the TNF-alpha-mediated serine phosphorylation of insulin receptor substrate-1 a
171 togen-activated protein kinase, enhances the serine phosphorylation of insulin receptor substrate-1,
172 ns-RSV prevented only the TNF-alpha-mediated serine phosphorylation of insulin receptor substrate-1.
173         TLR4 signaling also led to increased serine phosphorylation of intestinal focal adhesion kina
174 osine kinase (IRK) activity and a kinase for serine phosphorylation of IR substrate 1 (IRS-1).
175               First, it became apparent that serine phosphorylation of IRS proteins can reduce their
176                           Here, we show that serine phosphorylation of IRS-1 (IRS-1pSer) is common to
177                                Concurrently, serine phosphorylation of IRS-1 at serine 632/635, which
178  activates the insulin signaling pathway and serine phosphorylation of IRS-1 blocks insulin action, o
179 creased expression of p85alpha and increased serine phosphorylation of IRS-1 is needed to induce clin
180                  These data demonstrate that serine phosphorylation of IRS-1 plays an important role
181 n of the PI3K/Akt pathway via the inhibitory serine phosphorylation of IRS-1, notably on serine 1101
182 d insulin signaling as well as a decrease in serine phosphorylation of IRS-1.
183 tivation of protein kinase p70S6K and to the serine phosphorylation of IRS-1.
184 tion of several serine kinases, leading to a serine phosphorylation of IRS-1.
185 ity after IL-4 stimulation is dependent upon serine phosphorylation of IRS-2.
186 ylation of IRS1/2, while slightly increasing serine phosphorylation of IRS.
187 n by activating protein kinases that enhance serine phosphorylation of IRS1 and have been thus associ
188 lin-induced akt phosphorylation by increased serine phosphorylation of IRS1 and increased expression
189 uced (siRNA or a pharmacological inhibitor), serine phosphorylation of IRS1 is reduced, and insulin-i
190 cells resulted in a significant induction of serine phosphorylation of JAK3 and STAT5, and serine/thr
191  that Fsk-treated cells resulted in elevated serine phosphorylation of Jak3 but not Stat5, suggesting
192                            IL-6 also induced serine phosphorylation of K8.
193 0 null junctions supported this pathway, and serine phosphorylation of KENESKA was critical.
194     Specifically, AMPA stimulation triggered serine phosphorylation of KLC2 and, subsequently, the di
195 s attain additional negative charges through serine phosphorylation of Lys-Ser-Pro (KSP) repeat motif
196                    Further, AT1002 increased serine phosphorylation of myosin 1C and, at the same tim
197 ng [(3)H]tetraphenylphosphonium), as well as serine phosphorylation of NOS-3 (by Western blotting and
198            This disruption was the result of serine phosphorylation of Notch.
199                           We have shown that serine phosphorylation of P450c17 and the allosteric act
200  neutrophil NADPH oxidase involves extensive serine phosphorylation of p47(phox), the role of tyrosin
201                    In addition, Ron inhibits serine phosphorylation of p65 and NF-kappaB transcriptio
202                    Importantly, Erk-mediated serine phosphorylation of paxillin is also required for
203 resent study, we show that palmitate-induced serine phosphorylation of phosphoinositide-dependent pro
204 -linking of VCAM-1 stimulated an increase in serine phosphorylation of PTP1B, the active form of PTP1
205 in oxidative activation of PKCalpha and then serine phosphorylation of PTP1B.
206 respectively, leading to enhanced inhibitory serine phosphorylation of pyruvate dehydrogenase (PDH) a
207 anding of PDC regulation involves inhibitory serine phosphorylation of pyruvate dehydrogenase (PDH) b
208 otensin II or 1 microm serotonin resulted in serine phosphorylation of Rb that was equal in magnitude
209 r 15 min of ligand stimulation, but only the serine phosphorylation of signal transducer and activato
210 tide agonist suppressed the TGF-beta-induced serine phosphorylation of Smad2, a critical mediator of
211 s remain relatively constant while levels of serine phosphorylation of Smad6 increase.
212      LC-MS/MS analysis further revealed that serine phosphorylation of Sort1 protein was required for
213 r, Ly294002 and H7 blocked IFN-gamma-induced serine phosphorylation of STAT1alpha.
214 n of MAPK activity blocked IFN-gamma-induced serine phosphorylation of STAT1alpha; but its tyrosine p
215  As well, OSM and IL-6/R induce tyrosine and serine phosphorylation of STAT3 in primary cortical neur
216 es such as interleukin-6 induce tyrosine and serine phosphorylation of Stat3 that results in activati
217 e kinase responsible for LMP1-CTAR1-mediated serine phosphorylation of STAT3 was identified to be PKC
218 ion of STAT3((Tyr705)), while increasing the serine phosphorylation of STAT3((Ser727)).
219 gulated kinases, which caused an increase in serine phosphorylation of STAT3(Ser727).
220 a serum-independent manner with constitutive serine phosphorylation of STAT3.
221 m DARPP-32-depleted mice, basal tyrosine and serine phosphorylation of striatal NMDA receptor subunit
222 nase- (ERK) dependent pathways and increases serine phosphorylation of the alpha(1)-subunit.
223 one (PTH) inhibits Na+-K+-ATPase activity by serine phosphorylation of the alpha1 subunit through pro
224 d adhesion via a protein kinase A-dependent, serine phosphorylation of the alpha4 cytoplasmic domain.
225 ome disassembly by a mechanism that involves serine phosphorylation of the beta 4 integrin subunit.
226       Concomitantly, there is an increase in serine phosphorylation of the beta3 integrin cytoplasmic
227 ide additional support for the idea that the serine phosphorylation of the C-terminal domain (CTD) se
228            Here, we provide NMR evidence for serine phosphorylation of the C-terminus using (31)P dir
229                                     Although serine phosphorylation of the hinge of SF-1 (NR5A1), the
230 a double-strand break (DSB) in eukaryotes is serine phosphorylation of the histone variant H2AX at th
231                  In addition, PRL stimulated serine phosphorylation of the HRPAP20 protein with a sim
232 ds to a significant decrease in the level of serine phosphorylation of the insulin receptor substrate
233 ha inhibitory peptide blocked PTH-stimulated serine phosphorylation of the Na+-K+-ATPase alpha1 subun
234 sphoinositide 3-kinase and PKB/Akt-dependent serine phosphorylation of the precursor SREBP-1c protein
235  of gene expression by Sall1 is modulated by serine phosphorylation of the Sall1 repression motif.
236 2A and NR2B was drastically reduced, whereas serine phosphorylation of these NMDA subunits was unchan
237 orrelated with the ability of IL-6 to induce serine phosphorylation of this domain.
238   Lipopolysaccharide (LPS) treatment induced serine phosphorylation of USP14 as well as further reduc
239                                              Serine phosphorylation of WASP enhanced the ability of W
240 Src diminished the SGK1-mediated increase in serine phosphorylation of WNK4, suggesting that c-Src en
241 KNgamma in turn increases threonine (but not serine) phosphorylation of phospholipase C (PLC) gamma1
242 de (AICAR) and used to assess the following: serine-phosphorylation of Akt (P-Akt), immunoreactivity
243                                   LPS caused serine-phosphorylation of ANXA1 (ANXA1-S27-PO4) and tran
244 us of FX mice displayed decreased inhibitory serine-phosphorylation of GSK3beta compared with wild-ty
245                To investigate the effects of serine phosphorylation on CaM-mediated Ca(2+) regulation
246 orylation on residue Y705 but have increased serine phosphorylation on residue S727, consistent with
247 l peptides were synthesized with and without serine phosphorylation on S231 and S235, and the ability
248 ased STAT1 tyrosine phosphorylation, whereas serine phosphorylation on the protein was unchanged.
249  SIN-1, which also blocked tyrosine, but not serine phosphorylation, on STAT1.
250 p50 but did not affect basal levels of STAT3 serine phosphorylation or induce EGFR expression.
251 ynamic remodeling of the CTD, especially its serine phosphorylation pattern, conveys informational cu
252 hat PKD plays a key role in copper-dependent serine phosphorylation, permitting high levels of ATP7B
253                   These results suggest that serine phosphorylation plays an important role in at lea
254 oprecipitate with IGF-1R and increase IGF-1R serine phosphorylation, promoting beta-arrestin1 associa
255                           On the other hand, serine phosphorylation protected WT ATP7B from degradati
256 ) and phosphorylation of Akt while enhancing serine phosphorylation (pS(307)) of IRS1.
257 uced rapid, sustained, and site-specific k-8 serine phosphorylation (pSer73) dependent on signaling b
258          These studies suggest that, through serine phosphorylation, Raptor-mTOR and S6K1 cell autono
259 b have been extensively studied, the role of serine phosphorylation remains to be fully elucidated.
260 ct tyrosine kinase activity to regulate GAT1 serine phosphorylation requires a change in its tyrosine
261 fails to share a positionally conserved Stat serine phosphorylation sequence; however, known phosphoa
262 etween tyrosine phosphorylation (Tyr(P)) and serine phosphorylation (Ser(P)) of IRS-2 after IL-4 stim
263    To investigate these issues, we mutated a serine phosphorylation site (S408) in the cytoplasmic ta
264  analysis, Ser-164 was identified as a major serine phosphorylation site in SIRT1 in obese, but not l
265 to acquire full transcriptional activity, no serine phosphorylation site in STAT2 has been reported.
266 ence of c-Src, and by mutation of a putative serine phosphorylation site in the actin-binding domain
267 hysiological substrate for PKB and the first serine phosphorylation site on APS.
268              Previously identified potential serine phosphorylation sites at Ser-10, Ser-77, and Ser-
269 ectrometry analyses of DP revealed six novel serine phosphorylation sites dependent on GSK3 signaling
270 f 14-3-3 required 2 previously unappreciated serine phosphorylation sites in LNK, and we found that t
271  binding focal adhesion protein with several serine phosphorylation sites in the amino terminus that
272                                              Serine phosphorylation sites mutant, cortactin(S405A/S41
273 dentified serines 1248 and 1291 as the major serine phosphorylation sites of the IGF-1R, and subseque
274                     Mutagenesis of potential serine phosphorylation sites on Sox9 was used to demonst
275 the alpha-parvin N-terminal proline-directed serine phosphorylation sites reduced its complex formati
276 YK phoshorylates Ikaros at unique C-terminal serine phosphorylation sites S358 and S361, thereby augm
277                                     Multiple serine phosphorylation sites were identified in the secr
278       We have identified more than six novel serine phosphorylation sites within Htt, one of which li
279 arkedly increased upon mutation of two GSK-3 serine phosphorylation sites within the carboxyl-termina
280                To determine whether specific serine phosphorylation sites within the Na(+),K(+)-ATPas
281 reen of human TRPC6 identified several novel serine phosphorylation sites.
282 post-translationally regulated by these five serine phosphorylation sites.
283 orylation and c-Cbl binding, indicating that serine phosphorylation stabilizes hSpry2 by exerting an
284 1 and 2A and activation of PKC increased the serine phosphorylation state of the HCN1 protein.
285 ted threonine phosphorylation required prior serine phosphorylation, suggesting a sequential mechanis
286 ot all, MAPK agonists induced the regulatory serine phosphorylation, suggesting an involvement of dif
287    Tyr(641) was dispensable for IL4-mediated serine phosphorylation, suggesting that dimerization is
288 duced ABCA1 protein levels and increased its serine phosphorylation, suggesting that PLD2-generated d
289 l growth in response to EGF by site-specific serine phosphorylation that regulates nuclear-cytoplasmi
290                        LPS induces cortactin serine phosphorylation, ubiquitination, and degradation
291                An additive increase in GSK-3 serine phosphorylation was also observed in mice chronic
292                              IL-2-stimulated serine phosphorylation was corroborated in Kit 225 T cel
293                            We found that the serine phosphorylation was crucial for TLR-induced inter
294                           Stat3 tyrosine and serine phosphorylation was still detected in these mice
295 axillin and significantly increased paxillin serine phosphorylation, whereas Nek3 siRNA-transfected c
296  is also inhibited, thereby preventing Stats serine phosphorylation, which is essential for downstrea
297          STATs are activated by tyrosine and serine phosphorylation, which normally occurs as a tight
298          Moreover, TNFalpha enhanced FLIP(L) serine phosphorylation, which was increased by activated
299                              We propose that serine phosphorylation within LCS I may regulate the ass
300 owed that Grb10 underwent insulin-stimulated serine phosphorylation, yet the kinase(s) responsible fo

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