コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 beta-catenin while CHIR99021 increased it in nuclear localization.
2 n Ser207, release of LysRS from the MSC, and nuclear localization.
3 antiviral action to be through inhibiting C nuclear localization.
4 e cells, phosphorylates it, and enhances its nuclear localization.
5 pendent phosphorylation regulate its dynamic nuclear localization.
6 Phosphorylated Runx2 had an exclusively nuclear localization.
7 matrix stiffness perturbations regulate YAP nuclear localization.
8 and or receptor, respectively, inhibited YAP nuclear localization.
9 e of the same class, does not influence NADH nuclear localization.
10 the mitochondria and thereby increasing p53 nuclear localization.
11 induced its cellular protein expression and nuclear localization.
12 increased CAPN6 induction and impaired CWC22 nuclear localization.
13 or contractility-mediated regulation of YAP nuclear localization.
14 appropriate receptor protein expression and nuclear localization.
15 so support that BMAL1 is important for CLOCK nuclear localization.
16 biquitination of SMAD4, which can impair its nuclear localization.
17 hat had the most significant increase in YAP nuclear localization.
18 s key residues for inducing host shutoff and nuclear localization.
19 ibitors promote 14-3-3 dissociation and TFEB nuclear localization.
20 ygenase-2 (COX-2)/PGE2 axis and inducing its nuclear localization.
21 s mRNA and protein expression and favors its nuclear localization.
22 an colorectal cancers and correlate with DVL nuclear localization.
23 e Esrp1 peptide that is sufficient to confer nuclear localization.
24 but one mutant in the cytoplasm, as well as nuclear localization.
25 prevented decorin-evoked TFEB induction and nuclear localization.
26 we confirmed that stauprimide inhibits NME2 nuclear localization.
27 -113 is essential for catalytic activity and nuclear localization.
28 cade to control YAP-S397 phosphorylation and nuclear localization.
29 55 and Baf170 and displayed differential sub-nuclear localization.
30 ased TFEB promoter activity, expression, and nuclear localization.
31 ine residues 421 and 423 as critical for its nuclear localization.
32 and promoted transcription factor EB (TFEB) nuclear localization.
33 X observed in 3 patients led to constitutive nuclear localization and activation of both canonical an
34 via activation of JNK1 and causes increased nuclear localization and activity of androgen receptor.
36 adhesion molecule expression while reducing nuclear localization and activity of NFkappaB, which is
37 Here we report that exercise increases the nuclear localization and activity of p53 by acutely down
38 cologic inhibition of PKCiota decreases YAP1 nuclear localization and blocks OSC tumor growth in vitr
39 dependent regarding their protein stability, nuclear localization and chromatin recruitment and contr
43 B pathway and consequently reduces NF-kappaB nuclear localization and downregulates NF-kappaB targets
44 box deletion of MAF1 leads to increased MAF1 nuclear localization and enhanced repression of ACC1 and
45 ctor 4 alpha (HNF4A) through increased ROCK1 nuclear localization and enhanced ROCK1 association with
46 tuent of ORC but displays S-phase restricted nuclear localization and expression, suggesting it posit
47 t a SUMOylation-mediated mechanism regulates nuclear localization and function of the ICD of ErbB4 re
50 essed STAT3 phosphorylation, decreased STAT3 nuclear localization and inhibited STAT3 transcriptional
51 In HPK1ARas cells, 1alpha,25(OH)2D3-induced nuclear localization and interaction of hRXRalpha are re
52 tance to genotoxic agents by modulating YB-1 nuclear localization and interaction with the splicing f
53 Oylation) in Sox11, which suppresses Sox11's nuclear localization and its ability to promote RGC diff
54 ge tumor suppressor homolog) reduces Yap/Taz nuclear localization and minimizes their cytoplasmic lev
55 SIRT1 at Ser-164 substantially inhibited its nuclear localization and modestly affected its deacetyla
59 hat drug binding to FABP1 and FABP2 promotes nuclear localization and PPARalpha activation in a drug-
60 dings reveal RET as a novel dual kinase with nuclear localization and provide mechanisms by which RET
62 did not affect heat-induced oligomerization, nuclear localization and specific DNA binding but inhibi
66 s provide a mechanism for regulation of Bag6 nuclear localization and the functional integrity of the
67 d DNA binding, transcriptional activity, and nuclear localization and the possible formation of cytop
68 cid, and this binding was required for IP6K1 nuclear localization and the regulation of mIno1 transcr
69 d downstream Akt activation, increased FOXO1 nuclear localization and transcriptional activation, and
71 logical inhibition both decrease expression, nuclear localization and transcriptional activity of YAP
75 ough Erk1/2 and Stat3 leads to upregulation, nuclear localization, and activation of the transcriptio
76 cytoskeletal integrity is essential for YAP nuclear localization, and can override phosphoregulation
77 and OGT led to p53 stabilization, increased nuclear localization, and increased protein and mRNA lev
81 -cell studies demonstrate that mDia2 and its nuclear localization are required to maintain CENP-A lev
82 enced by decreased percent androgen receptor nuclear localization (%ARNL) and increased microtubule b
83 sponsive transcription factor Crz1 undergoes nuclear localization bursts during the pheromone respons
84 he C-terminal region play a critical role in nuclear localization, but additional basic residues were
85 the first 9 amino acids were sufficient for nuclear localization, but an additional 6 residues were
86 d AAP2BR2 play the most influential role for nuclear localization, but either one of the two AAP2BRs
87 lements that contributed multiplicatively to nuclear localization, but the conserved DNA binding resi
89 ncta and the shorter isoform displays higher nuclear localization compared to the longer isoform.
90 Mutant IPMK had reduced kinase activity and nuclear localization, compared with the full-length prot
91 ows that the inability to disrupt Aux/IAA CC nuclear localization correlates with a reduced ability t
92 iously described nuclear functions because a nuclear localization-defective mutant BMI1 rescued sever
96 own cells showed an increase in beta-catenin nuclear localization, enhanced transcriptional activity,
98 expressed de novo in macrophages with early nuclear localization followed by later translocation to
100 ctional nuclear localization signal and that nuclear localization impairs the ability of ICAP1 to sup
102 and FANCD2, phosphorylation of p53 or BRCA1 nuclear localization in response to DNA damage caused by
106 F) whose function was previously ascribed to nuclear localization, instead plays multiple essential r
107 a phosphorylation significantly disrupts its nuclear localization, interaction with VDR, intra-nuclea
109 onine and adenine auxotrophy of Ppmet6 Thus, nuclear localization is essential for the stability and
114 a transcription activation domain but retain nuclear localization motifs and are expressed from genes
117 between the cytoplasm and nucleus due to its nuclear localization (NLS) and export sequences (NES).
122 ted ERK1/2 in all types of liver tumors, but nuclear localization of beta-catenin, a sign of malignan
124 in various cell lines specifically increases nuclear localization of BMP receptor-activated SMADs (R-
125 Mutations in BRCA2, FANCC and NBN decreased nuclear localization of BRCA1 in response to drug treatm
128 ws the timing of muscle relaxation, promotes nuclear localization of calcineurin target Nfatc3, and/o
129 Our results suggest that AMP inhibits the nuclear localization of ChREBP through an allosteric act
136 However, the mechanisms controlling the nuclear localization of FLIL33 or its stability in cells
137 t of the FLIL33 protein, is not required for nuclear localization of FLIL33, and protects FLIL33 from
139 serine 124 to leucine promotes constitutive nuclear localization of Foxc2 and expression of mesenchy
141 rom aberrant PI3K signaling, which decreases nuclear localization of FOXO3A and decreases catalase ex
142 ignant cells in culture and in vivo and that nuclear localization of Gal-1 promotes a transformed phe
145 logical hypertrophy were assessed, including nuclear localization of GRK5, and compared with TAC.
146 d less reactive oxygen species, resulting in nuclear localization of HDAC4 and miR-206 repression.
148 bly, polyinosinic:polycytidylic acid induced nuclear localization of iNOS, and its binding to, and ni
150 Moreover, we find that ICAP1 drives the nuclear localization of KRIT1 in a manner dependent upon
151 function and mechanism for regulation of the nuclear localization of LANA will enhance our understand
154 d function primarily inside the nucleus, but nuclear localization of mRNAs has been considered rare i
158 ive hypertrophic astrocytes showed increased nuclear localization of NF-kappaB and elevated chemokine
159 iously reported that genotoxic agents induce nuclear localization of NF-kappaB essential modulator (N
161 Unlike monocytic THP-1 cells with prominent nuclear localization of NLRP1, melanoma cells expressed
163 w that long term Cn infection induces stable nuclear localization of p65 and IkappaBalpha proteins in
165 cytoplasm and nucleus of the cells, but the nuclear localization of PA-X mediated by its C-terminal
166 atment significantly elevated expression and nuclear localization of PAK4 in correlation with inducti
169 at R742A as well as D113R mutations abrogate nuclear localization of PpMS and its ability to reverse
172 croscopy, we confirmed the mitochondrial and nuclear localization of RIbeta in cultured neurons.
173 lular analysis showed that TCS inhibited the nuclear localization of SKN-1/Nrf2 and the expression of
174 nd this effect was supported by an increased nuclear localization of Skp2, disruption of Skp2 interac
175 beta) pathway, exposure to ligand stimulates nuclear localization of Smad proteins, which then regula
176 effects in our cytological studies, and the nuclear localization of ssDNA-FITC suggest that nano-LDH
177 emia/reperfusion injury in vivo This induced nuclear localization of TAZ and increased expression of
180 te how this setup can be used to control the nuclear localization of the budding yeast transcription
182 tem cell (ESC) differentiation by inhibiting nuclear localization of the MYC transcription factor NME
184 eactive oxygen species production, increased nuclear localization of the NRF2 transcription factor, i
185 OSC cells is regulated by PKCiota-dependent nuclear localization of the oncogenic transcription fact
188 osis and lipid-loaded Huh7 cells had reduced nuclear localization of the pregnane X receptor (PXR), a
190 tream mediator of this response by promoting nuclear localization of the TAZ transcriptional modulato
191 re kinases hippo or warts leads to premature nuclear localization of the transcriptional co-activator
192 ility are paralleled by modifications in the nuclear localization of the transcriptional regulator YA
193 man cancers, and normally the expression and nuclear localization of these proteins is tightly regula
195 tically, we found that DMF treatment reduced nuclear localization of transcriptional coactivator with
196 (IL6) beta2SP(+/-) LSCs not only exhibited nuclear localization of Twist and Slug, markers of epith
197 e demonstrated that both photoactivation and nuclear localization of UVR8 are required for UV-B-induc
199 Bcl-6, c-Myc), reduced proliferation (Ki67), nuclear localization of XPO1 cargos (p53, PTEN), and inc
200 In particular, ARF knockdown reduced non-nuclear localization of YAP which led to an increase in
202 of mouse arteries demonstrated an increased nuclear localization of YAP/TAZ and elevated levels of t
203 kPa) led to a decrease in the cell area and nuclear localization of YAP/TAZ, and subsequent stiffeni
205 interactions caused either AHR constitutive nuclear localization or failure to translocate to nucleu
206 localization of HLD2 with the addition of a nuclear localization or nuclear export sequence demonstr
207 and Sr50 CC domains fused to YFP and either nuclear localization or nuclear export signals in N bent
208 ng early mitosis and then displays different nuclear localization patterns at different times during
209 ourse spanned the onset of mutant huntingtin nuclear localization phenotypes and somatic CAG-length i
211 ower protein expression levels and increased nuclear localization, providing a mechanism for accessin
212 n to be in part due to impaired beta-catenin nuclear localization resulting from alterations in the a
213 with p53 and promotes its mitochondrial and nuclear localization, resulting in transcription of p53-
214 binding of Cdh1 but inactivated a bipartite nuclear localization sequence (NLS) and thereby controll
216 e LSD1 complex through its domain containing nuclear localization sequence and phosphorylation sites.
217 is critical not only for occluding the Bag6 nuclear localization sequence from karyopherin alpha to
218 ation in length of the lysine stretch of the nuclear localization sequence is a determinant for impor
220 fused to a yellow fluorescent protein and a nuclear localization sequence to simplify quantitative n
221 trol, PELP1-wt, or mutant PELP1 in which the nuclear localization sequence was altered, resulting in
222 fluorescent protein), protein translocation (nuclear localization sequence), DNA recombination (Cre)
225 lization of RBM45 is mediated by a bipartite nuclear-localization sequence (NLS) located at the C-ter
226 lypeptide sequences that implicate mammalian nuclear localization sequences and many cell penetrating
227 gineered variants of Cas9 with multiple SV40 nuclear localization sequences enabled a tenfold increas
228 h a kinase substrate is fused to a bipartite nuclear localization signal (bNLS) and nuclear export si
229 mouse overexpressing exogenous FUS without a nuclear localization signal (DeltaNLS-FUS), which develo
230 t at residues 11-27 and an isoleucine-lysine nuclear localization signal (IK-NLS) motif at residues 3
232 N-terminal region of FMDV 3D that acts as a nuclear localization signal (NLS) and in template bindin
234 leasing importin alpha/beta from a bipartite nuclear localization signal (NLS) located in the tail do
235 uctural analysis suggests that a monopartite nuclear localization signal (NLS) may reside in the N-te
236 s simplex virus 1 (HSV-1) mutant lacking the nuclear localization signal (NLS) on the ICP0 gene (0Del
237 e analyzed the structure and conservation of nuclear localization signal (NLS) sequences previously i
238 scent protein (GFP) reporter fusion assays a nuclear localization signal (NLS) that was mapped to a 2
239 ted mutant mouse, nBmp2NLS(tm), in which the nuclear localization signal (NLS) was inactivated to pre
241 he CTD of topo IIalpha, while preserving the nuclear localization signal (NLS), enhances the decatena
243 triphosphate (RanGTP) gradient that imports nuclear localization signal (NLS)-specific cargoes (NLS-
244 amino-terminal residues (1-45) including the nuclear localization signal (NLS1) are dispensable.
247 ivities of both a peptide-encoded N-terminal nuclear localization signal and C-terminal nuclear expor
248 vely spliced Set-beta transcript lacking the nuclear localization signal and demonstrated that the fu
249 One of its isoforms, DNAJB6a, contains a nuclear localization signal and regulates beta-catenin s
250 try to show that ICAP1 contains a functional nuclear localization signal and that nuclear localizatio
251 s to the N-terminal DNA-binding domains, the nuclear localization signal becomes more highly exchangi
254 e these sequences do not correspond to known nuclear localization signal motifs, they represent a new
255 ) phosphorylation at S659, which exposed the nuclear localization signal of ACSS2 for importin alpha5
256 e novo predicted deleterious variants in the nuclear localization signal of Heterogeneous Nuclear Rib
257 BPN1 but not a truncated version lacking the nuclear localization signal protects from pathogenic TDP
258 ed cereals showed that all of them contain a nuclear localization signal sequence flanking to the K1
260 found that residues (20)KY(21) constitute a nuclear localization signal that is not required for the
261 nteracts with importin alpha via a classical nuclear localization signal that recruits importin alpha
262 rions parallels effects of the attachment of nuclear localization signal to Sis1, indicating that Cur
264 e N-terminal 25 amino acids to function as a nuclear localization signal was not required for restric
265 referred to as pUL31, containing a bipartite nuclear localization signal, an intrinsically disordered
266 A longer DCL4 transcript isoform encoding a nuclear localization signal, DCL4(NLS), is present in Ar
268 We fuse the ADAR2 domain, tagged with a nuclear localization signal, to an RNA binding peptide f
275 minal 25 amino acids of MxB to function as a nuclear localization signal; however, the ability of the
277 ycete plant pathogen Phytophthora sojae uses nuclear localization signals (NLSs) for translocation of
278 , unlike their bacterial homologues, possess nuclear localization signals (NLSs) to enter the cell nu
279 l strains of influenza A viruses contain two nuclear localization signals (NLSs): a well-studied mono
280 e splicing, but specific Rbfox isoforms lack nuclear localization signals and accumulate in the cytop
283 the cargo proteins, including the classical nuclear localization signals, recognized by the adaptor
284 ed by the adaptor importin-alpha, and the PY nuclear localization signals, recognized by transportin-
286 to potentiate each other to block NF-kappaB nuclear localization stimulated by inflammatory cytokine
288 ced MET, glandular redifferentiation, and AR nuclear localization that was inhibited by androgen depr
291 f cells have both been shown to regulate YAP nuclear localization to modulate cell proliferation.
293 tus loss-of-function alleles decrease Dorsal nuclear localization ventrally, where Toll signals are h
295 d dipeptides were present in the nucleus and nuclear localization was necessary and sufficient for th
296 Based on Ki67 co-localization studies YAP nuclear localization was not simply a marker of prolifer
297 ed the ability to downregulate Cx43 mRNA, so nuclear localization was required for its function.
299 ppressor activity has been attributed to its nuclear localization, where it helps to maintain genome
300 al effects required combined cytoplasmic and nuclear localization, whereas the effects on cell moveme
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。