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1 ount of insoluble monomeric alpha-syn or its phosphorylation status.
2 ism by which SAUR19 modulates PM H(+)-ATPase phosphorylation status.
3 M in adult rat ventricular myocytes based on phosphorylation status.
4 ength of the interaction depends on the ABI5 phosphorylation status.
5 triction of HSV-1 was not affected by SAMHD1 phosphorylation status.
6 thin the cell is closely associated with its phosphorylation status.
7 h mRNA levels and was largely independent of phosphorylation status.
8 FkappaB signaling and the regulation of Cdk9 phosphorylation status.
9 rength of the interaction depends on the PIN phosphorylation status.
10 tation assay to study dynamic changes in Tau phosphorylation status.
11 D-95 expression depends on miR-125a and FMRP phosphorylation status.
12 ed Rac dynamics at contacts depending on its phosphorylation status.
13 d in TG mouse islets, without changes in Akt phosphorylation status.
14 ivotal roles in N-DRC function through their phosphorylation status.
15 in, prevents tau clearance and regulates its phosphorylation status.
16 raction, which can occur independent of YAP1 phosphorylation status.
17 ese interactions are regulated by the ChREBP phosphorylation status.
18 its its nuclear export, independently of its phosphorylation status.
19 h leads to p53 activation independent of its phosphorylation status.
20 oteins, in particular phospholamban, and its phosphorylation status.
21 ion loop conformation that is independent of phosphorylation status.
22 fect its activity state without changing its phosphorylation status.
23  ITK, and LCK are dynamically altered by ITK phosphorylation status.
24 with the modulation of p53/Mdm2, Erk and Akt phosphorylation status.
25 a, PLN, and ryanodine receptor or in the PLN phosphorylation status.
26 plexes of distinct molecular composition and phosphorylation status.
27 , depending on the degree of aromaticity and phosphorylation status.
28  microtubules dynamics, are dependent on its phosphorylation status.
29 y RNA polymerase II carboxyl-terminal domain phosphorylation status.
30 d that the mobility is tightly linked to its phosphorylation status.
31 surements, and regulatory myosin light chain phosphorylation status.
32 nd phosphatase activities influence the CovR phosphorylation status.
33 -suppressing antinatriuretic hormones to NCC phosphorylation status.
34 -bridge cycling rates via alterations in its phosphorylation status.
35  which was unrelated to the substrate domain phosphorylation status.
36 vated linking chemistry to detect changes in phosphorylation status.
37 ation, cooperativity, and sarcomeric protein phosphorylation status.
38  middle-aged animals, ischemia increased the phosphorylation status/activity of Akt and STAT3, and de
39 ereas estradiol did not detectably alter the phosphorylation status/activity of Akt or STAT3, it prev
40 activity of Akt and STAT3, and decreased the phosphorylation status/activity of CREB in the hippocamp
41 contributes differentially to Tau stability, phosphorylation status, aggregation propensity, resistan
42 ersus 2,3-diamino-2,3-dideoxy-d-glucose, and phosphorylation status all correlated with TLR4 activati
43 ases provides a means to locally control the phosphorylation status and action of proteins on the sur
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        No differences were identified in JNK phosphorylation status and DNA methylation in the evalua
48                           Studies of VEGFR-2 phosphorylation status and down-regulation of neuropilin
49  binding by cMyBPC is independent of protein phosphorylation status and is not significantly affected
50 actor WAPL and show that this regulates WAPL phosphorylation status and is required for efficient coh
51 -SUPPRESSOR 1 (BES1), largely depends on its phosphorylation status and its protein stability, but th
52 ole for neuronal cyclin E1 in regulating the phosphorylation status and localization of Kv2.1 channel
53 idence revealed that the alterations in eNOS phosphorylation status and NO generation were mediated b
54     In turn, electrical activity affects the phosphorylation status and nuclear level of activated Sm
55 ltimately, toxicity, may be modulated by the phosphorylation status and nuclear presence of different
56 y sildenafil (Viagra) is dependent on STEVOR phosphorylation status and on another independent mechan
57 ar mass complexes and hypothesized that PTEN phosphorylation status and PDZ binding domain may be req
58 ort of the phytohormone auxin depends on the phosphorylation status and polar localization of PIN-FOR
59  Diamond and SYPRO Ruby dyes to quantify the phosphorylation status and protein levels, respectively,
60 ta clarify the influence of CovS on the CovR phosphorylation status and provide insight into why sero
61 occurs concomitantly with changes in RNAP II phosphorylation status and recruitment of the elongation
62 elation between increased FAK expression and phosphorylation status and the invasive phenotype of agg
63 QP2 abundance associated with alterations in phosphorylation status and ubiquitination as well as inh
64    Therefore, our findings suggest that eEF2 phosphorylation status (and, as a consequence, translati
65 yl-coenzyme A carboxylase (ACC), reduced ACC phosphorylation status, and dramatically increased hepat
66 1 can directly ubiquitinate IRF7, affect its phosphorylation status, and interfere with the ubiquitin
67 e interactions are essential to regulate the phosphorylation status, and thus the activity, of the do
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 E1 osteoblastic cells and observed that NACA phosphorylation status at PP1A-sensitive sites is import
74 t AMPARs scale differentially based on their phosphorylation status at S845.
75 eo-cytoplasmic shuttling is dependent on the phosphorylation status at Ser-174 and Ser-175 of eIF6.
76 however, prevent cAMP-induced changes to the phosphorylation status at serines 261 or 269.
77                      Surprisingly, while the phosphorylation status at these two sites directly impin
78    This localization was independent of MtrB phosphorylation status but dependent upon the assembly o
79 lokin is not through modulation of the MYPT1 phosphorylation status but rather it contributes to cycl
80 al responses are believed to be regulated by phosphorylation status, but the precise mechanisms by wh
81                       Furthermore, mimicking phosphorylation status by mutating S-->E at S300 and/or
82                                         T101 phosphorylation status can act as an on/off switch to co
83 in components, and subsequent alterations in phosphorylation status can release transcripts for trans
84 protein kinases and three phosphatases whose phosphorylation status changed upon SII treatment.
85        Further, we show that RelB serine 472 phosphorylation status controls MMP3 expression and prom
86 nsor of lipid toxicity and its GSK3-mediated phosphorylation status controls outer mitochondrial memb
87 gulated gene 1 protein (NDRG1) and that Cx43 phosphorylation status controls this interaction and dra
88                       We show that IRE1alpha phosphorylation status correlates with an increased prop
89 tion of PTEN activity through changes in its phosphorylation status could uniquely regulate the conti
90 NA translational control, mediated via eIF4B phosphorylation status, couples neuronal activity to tra
91                                    The HDA15 phosphorylation status determines its subnuclear localiz
92 ed mitochondrial dysfunction, and DRP1(S616) phosphorylation status dichotomizes BRAF(WT) from BRAF(V
93 d expression of UCP3, AAC1, or AAC2, and PDH phosphorylation status did not differ between the nitrit
94 ions causing these phenotypes, and that S149 phosphorylation status does not change upon stress.
95 otic testicular germ cells and its increased phosphorylation status during capacitation suggested mul
96 , old and new histones are distinct in their phosphorylation status during early mitosis in the follo
97 serine 260, a JNK phosphoacceptor site whose phosphorylation status had an unknown role in RXRalpha f
98                      On the other hand, PTEN phosphorylation status has a significant impact on its c
99                   In conclusion, the Ser-637 phosphorylation status in Drp1 is not a determinant that
100 icates that successful prediction of protein phosphorylation status in human based on rat phosphoryla
101 ction (n = 7) was measured by pp185 tyrosine phosphorylation status in insulin-sensitive tissues usin
102 3 in the mitotic cells, correlating with its phosphorylation status in mitosis.
103 lagen and MMP-1 expression, as well as Smad3 phosphorylation status in SSc fibroblasts.
104 JNK, ERK 1/2, NF-kappaBp65, and NF-kappaBp50 phosphorylation status in the GM by western blotting; DN
105  results suggest that modification of the Tm phosphorylation status in the heart, depending upon the
106 based method that provides protein level and phosphorylation status information from nanogram quantit
107 Here, we show that MtrB, irrespective of its phosphorylation status, interacts with Wag31, whereas on
108                 Here we demonstrate that Orm phosphorylation status is highly responsive to sphingoid
109 uppression of HAS2 transcription, with FOXO1 phosphorylation status maintained by operation of the po
110 n analysis data suggests that changes in Bad phosphorylation status may be caused by a coordinated sh
111 rm1, based on the new structures suggests LM phosphorylation status may mediate Ran's selection of ex
112 monly used chemotherapy agents and that Chk1 phosphorylation status may not offer a reliable marker f
113                                 However, the phosphorylation status of a kinase does not always refle
114 obilized alkaline phosphatase to monitor the phosphorylation status of a mixture of peptides.
115 ective activation of the two channels is the phosphorylation status of a single threonine residue (T3
116     By quantitatively assessing the tyrosine phosphorylation status of activated kinases in xenograft
117    These responses were not dependent on the phosphorylation status of Akt and FOXO1.
118 tle cell lymphoma (MCL), we investigated the phosphorylation status of Akt and multiple downstream ta
119 gnalling pathway; therefore, we measured the phosphorylation status of Akt and p70(s6k) in the WT and
120 itch in substrate specificity coupled to the phosphorylation status of Akt may lead to alternative ce
121 nd AMPKalpha activity was ascertained by the phosphorylation status of AMPKalpha Thr(172) in human kn
122  complex signaling pathway that controls the phosphorylation status of an SR-related protein that fun
123 lls with P. gingivalis did not influence the phosphorylation status of beta-catenin but resulted in p
124              We propose a model in which the phosphorylation status of Bid determines the apoptotic t
125 e conclude that anabolic nutrients alter the phosphorylation status of both AMPK- and mTOR-associated
126  Furthermore, in vitro data suggest that the phosphorylation status of BubR1 is important for checkpo
127 tion, and oxidation and by investigating the phosphorylation status of CaMKII downstream targets.
128 ypical target gene of CAR) by modulating the phosphorylation status of CAR.
129 re-forming Cavalpha1.2 and the Akt-dependent phosphorylation status of Cavbeta2 both in a mouse model
130                                          The phosphorylation status of CBLs does not appear to influe
131  in the propionylation, glycosylation and/or phosphorylation status of cell proteins.
132  sign were accompanied by alterations in the phosphorylation status of ChR1.
133       In the present study, we show that the phosphorylation status of CITED1 changes during the cell
134 as suggested by altered transcription and/or phosphorylation status of components of the NF-kappaB sy
135 A pathway as indicated by a reduction in the phosphorylation status of CREB (pCREB).
136 odifier (SUMO) and further controlled by the phosphorylation status of CRMP2.
137 we postulated that PKA evokes changes in the phosphorylation status of CtBP1 that control the ability
138 rimentally observed spatial distribution and phosphorylation status of CtrA in wild-type and mutant c
139 on of this complex (DHIC) is affected by the phosphorylation status of DDL-1.
140 ring, and (iii) the spatial distribution and phosphorylation status of DDR1b and DDR2 after collagen
141 le inhibiting NHEJ, and we conclude that the phosphorylation status of DNA-PK impacts how a cell choo
142 us to determine that the kinase activity and phosphorylation status of DNA-PK(CS) influence the stabi
143 and that neither the kinase activity nor the phosphorylation status of DNA-PK(CS) influences its init
144 n coordination with kinases may regulate the phosphorylation status of downstream targets to accompli
145          Western blot analysis evaluated the phosphorylation status of EGFR, ERK, p38 MAPK, and nucle
146   This mode of regulation is governed by the phosphorylation status of eIF2alpha and controlled by ce
147 nine methylation by PRMT7 and stress-induced phosphorylation status of eIF2alpha at serine 51.
148 13D telokin, without changing the inhibitory phosphorylation status of endogenous MYPT1 (the regulato
149  exercise are mediated by alterations in the phosphorylation status of eNOS (increase in serine 1177
150 creases were accompanied by increases in the phosphorylation status of epidermal growth factor recept
151 imen of CAF with ErbB-2 was not dependent on phosphorylation status of ErbB-2.
152                          PTPRO regulated the phosphorylation status of ERBB2 at Y1248.
153 n larger and more prolonged increases in the phosphorylation status of Erk1/2 and p38.
154          Western blot analysis evaluated the phosphorylation status of Erk1/2 and phosphoinositide 3-
155 tern blot analysis was used to determine the phosphorylation status of Erk1/2, p38, and the mitogen-a
156 % in virus titer), which correlated with the phosphorylation status of ERK1/2.
157  ROCK 1 expression through inhibition of the phosphorylation status of ERK1/2.
158                                          The phosphorylation status of ERK2 did not affect interactio
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 ylation status of histones by regulating the phosphorylation status of histone demethylase enzymes in
163 drial dysfunctioning and perturbation in the phosphorylation status of histones in the nucleus.
164              These data demonstrate that the phosphorylation status of hnRNP A1 serine 199 regulates
165 uld now be possible to routinely monitor the phosphorylation status of hundreds of nodes across multi
166 Na(+)/K(+)-ATPase inhibitor, ouabain, on the phosphorylation status of Jnk, p38, and Src.
167                                          The phosphorylation status of KaiC is thought to mediate glo
168 Interactions between Kai proteins change the phosphorylation status of KaiC, defining the phase of ci
169 es insight into how KaiB might influence the phosphorylation status of KaiC.
170 ta support a role for Srx in controlling the phosphorylation status of key regulatory kinases through
171                                   Hence, the phosphorylation status of KHT-1-MPS-1 seems to be linked
172 de the first evidence that YM155 changes the phosphorylation status of known mTOR-target proteins inv
173   In this study, we investigated the mannose phosphorylation status of leukemia inhibitory factor (LI
174 ealed multiple PtpA-dependent changes to the phosphorylation status of macrophage proteins upon M. tu
175 nhibited autophagy induction by altering the phosphorylation status of mammalian target of rapamycin
176                                          The phosphorylation status of MDF-1 affects its binding to a
177                               Therefore, the phosphorylation status of Mdm2 Ser394 governs p53 protei
178                   The precise control of the phosphorylation status of MeCP2 in neurons is critical f
179                              We assessed the phosphorylation status of Mga in GAS cell lysates with P
180                                              Phosphorylation status of mitogen-activated protein kina
181 -strand break, a process that impacts on the phosphorylation status of multiple factors involved in t
182     Our data indicate that Htt regulates the phosphorylation status of myosin II during chemotaxis an
183                       Here, we show that the phosphorylation status of NBS1 determines the repair pat
184                                    Thus, the phosphorylation status of NCC may not necessarily equate
185 tiparameter phosflow approach to analyze the phosphorylation status of NF-kappaB and three major MAPK
186 led receptor kinase 6A controls the Ser(290) phosphorylation status of NHERF1 and regulates PTH-sensi
187                                 Although the phosphorylation status of NS5A is considered to have a s
188 nases that add a layer of regulation via the phosphorylation status of nucleoporins.
189 ffect was mediated by changes in the protein phosphorylation status of occludin via the action of FAK
190 egulate the assembly of TJ by modulating the phosphorylation status of occludin.
191  Ca(2+) and selective to Ser-635 because the phosphorylation status of other eNOS sites, including Se
192  No differences in the relative abundance or phosphorylation status of other myofilament proteins wer
193 blot analysis was performed to determine the phosphorylation status of p42/44 and Akt/protein kinase
194 rmore, increased GRK5 expression induced the phosphorylation status of p65, increased the activity of
195 tivity depends on the enzymatic activity and phosphorylation status of PHF8, which can be pharmacolog
196 ndling and coupled to its regulation via the phosphorylation status of phospholamban.
197                        In addition, both the phosphorylation status of phospholipase Cgamma-1 at the
198 activation can thereby impact on the Ser-473 phosphorylation status of PKB/Akt and the repair of etop
199               In addition, assessment of the phosphorylation status of PP in these cells reveals that
200 ndent protein kinase signaling modulates the phosphorylation status of pregnane x receptor.
201 ive phosphoproteomics to identify changes in phosphorylation status of presynaptic proteins in restin
202 tern blot analysis identified changes in the phosphorylation status of prospective intracellular sign
203 However, current technologies to monitor the phosphorylation status of proteins are inefficient at de
204    Taken together, the transcript abundance, phosphorylation status of proteins at the fiber initiati
205                              We compared the phosphorylation status of proteins in multiple signaling
206          Together, our findings show how the phosphorylation status of pSTAT1 determines its function
207 re is a paucity of information regarding the phosphorylation status of RASSF1A and its regulation dur
208                             In contrast, the phosphorylation status of retinoblastoma protein (pRB) w
209 controlling the subcellular localization and phosphorylation status of Rho GDP dissociation inhibitor
210 ilings in mRNA splicing and changes with the phosphorylation status of RNA Pol II across the gene.
211 mply that anchored PKC locally modulates the phosphorylation status of Robo3.1 in brain regions gover
212 ineurin, PKC regulates TRESK by changing the phosphorylation status of S264.
213 h unattached kinetochores by controlling the phosphorylation status of S281 in the kinetochore-bindin
214 namically regulated in the cell and that the phosphorylation status of S58 is a critical factor regul
215 rtant for NIS protein stability and that the phosphorylation status of Ser-227 is functionally silent
216  iodide transport of NIS is modulated by the phosphorylation status of Ser-43 and Ser-581.
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                                          The phosphorylation status of several important signaling pr
220                                          The phosphorylation status of Sfi1, a structural component o
221 logical substrates for PP2A, the LPS-induced phosphorylation status of signaling MAPK and Akt kinase
222 conjugates, precluding the evaluation of the phosphorylation status of signaling proteins across diff
223 more, Utp7 can regulate the localization and phosphorylation status of Sli15 independent of its effec
224       Alterations in the Cdk/Cdc14-dependent phosphorylation status of Spc110, or its inactivation du
225 luence pre-mRNA processing by regulating the phosphorylation status of specific regulatory factors, w
226            A dose-dependent reduction in the phosphorylation status of specific SR proteins was detec
227  DNA in DU145 cell lysates without affecting phosphorylation status of STAT3.
228 ied by changes in MT dynamics as measured by phosphorylation status of stathmin and microtubule-assoc
229              We further demonstrate that the phosphorylation status of Synaptojanin at S1029 differen
230 han in interphase cells, as evidenced by the phosphorylation status of T359/S363 in RSK.
231 s in arrestin2 to initially discriminate the phosphorylation status of target receptors.
232 eletal muscle suggest that regulation of the phosphorylation status of TBC1D4 may relay this insulin
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 alpha action by altering both the levels and phosphorylation status of the receptor.
257 the interaction of MDFIC with GR altered the 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 reveals the molecular mechanism by which the phosphorylation status of Thr55 modulates DNA binding an
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          Thus, our results suggest that S318 phosphorylation status, rather than a predominantly shoo
281                           Depending upon its phosphorylation status, RSK1 switched interactions betwe
282 ir individual protein levels or solely their phosphorylation status, should be considered as a paramo
283 53, Akt and c-Src expression levels or their phosphorylation status, suggesting that PRL-2 knockdown
284  GRB2 can bind to BCAP independently of BCAP phosphorylation status, suggesting that the SH2 domains
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

 
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