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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.
35                Surprisingly, MML-1 regulates nuclear localization and activity of HLH-30/TFEB, a conv
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
40 e that TAZ-CAMTA1 (TC) fusion results in its nuclear localization and constitutive activation.
41      BR treatment promotes the accumulation, nuclear localization and dephosphorylation/phosphorylati
42 mbled the unliganded AR (apo-AR), precluding nuclear localization and DNA binding.
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
48 h mature HMR rescues both its plastidial and nuclear localization and functions.
49           Two proteins involved in NF-kappaB nuclear localization and IL-6 expression, IkappaBalpha a
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
56                                              Nuclear localization and nucleosome remodeling and histo
57 erminus (AAs 23-40) that mediates the CASZ1b nuclear localization and NuRD interaction.
58 , and NUP43 transcripts is uncorrelated with nuclear localization and paraspeckle association.
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
61                          Here we show unique nuclear localization and regulation of gene transcriptio
62 did not affect heat-induced oligomerization, nuclear localization and specific DNA binding but inhibi
63 M2 are dispensable for the exclusive protein nuclear localization and speckle-like distribution.
64 tion to K63 ubiquitination and thus promotes nuclear localization and stabilization of Bcl3.
65                        ABL also enhanced TAZ nuclear localization and the formation of the TAZ-TEAD c
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
70  posttranslational modification controls its nuclear localization and transcriptional activation.
71 logical inhibition both decrease expression, nuclear localization and transcriptional activity of YAP
72  region (UTR) plays dual roles in CDC20 mRNA nuclear localization and translation.
73                 Yes-associated protein (YAP) nuclear localization and up-regulation of canonical targ
74               Pyruvate is essential for this nuclear localization, and a failure of TCA cycle enzymes
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
78                   Endogenous FUS expression, nuclear localization, and splicing activity were not alt
79 lation cycle by promoting TDG function, TET1 nuclear localization, and TET/TDG association.
80                     ACLY phosphorylation and nuclear localization are necessary for its role in promo
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
88  activity through phosphorylation of general nuclear localization clusters.
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
93                 Moreover, TH increased FOXO1 nuclear localization, DNA binding, and target gene trans
94            Moreover, ACOT1 exhibited partial nuclear localization during fasting and cAMP/cAMP-depend
95                  Sequences within two of the nuclear localization elements defined a new form of bipa
96 own cells showed an increase in beta-catenin nuclear localization, enhanced transcriptional activity,
97 mous NLS activity and the fourth served as a nuclear localization enhancer.
98  expressed de novo in macrophages with early nuclear localization followed by later translocation to
99  a cis-acting role, we showed a preferential nuclear localization for two selected candidates.
100 ctional nuclear localization signal and that nuclear localization impairs the ability of ICAP1 to sup
101  a statistically significant increase in YAP nuclear localization in 100% of tumors.
102  and FANCD2, phosphorylation of p53 or BRCA1 nuclear localization in response to DNA damage caused by
103                                         AIRE nuclear localization in the human thymic epithelial cell
104 keletal integrity-mediated regulation of YAP nuclear localization independent of contractility.
105                               Blocking AURKA nuclear localization inhibits this newly discovered tran
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
108                      Furthermore, CC Aux/IAA nuclear localization is disrupted upon infection with an
109 onine and adenine auxotrophy of Ppmet6 Thus, nuclear localization is essential for the stability and
110       Mutational analyses reveal that cFLIPL nuclear localization is necessary and sufficient for inh
111                                          Its nuclear localization is required for enhanced P. infesta
112 on at the molecular level to regulate YAP1's nuclear localization is still puzzling.
113      Our results also demonstrate that ErbB3 nuclear localization is transient as it is exported out
114 a transcription activation domain but retain nuclear localization motifs and are expressed from genes
115 f the virus life cycle thus rely on distinct nuclear localization motifs of NP.
116           An ORF2 stop codon mutant, an ORF2 nuclear localization mutant, or a mutant lacking the 5 p
117 between the cytoplasm and nucleus due to its nuclear localization (NLS) and export sequences (NES).
118                            IFN-alpha-induced nuclear localization of activated STAT1 is markedly redu
119 , and promoted protein expression as well as nuclear localization of AHRR.
120                                          The nuclear localization of beta-catenin is the defining ste
121                            Stabilization and nuclear localization of beta-catenin result in the expre
122 ted ERK1/2 in all types of liver tumors, but nuclear localization of beta-catenin, a sign of malignan
123  in transfected cells, which resulted in the nuclear localization of beta-catenin.
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
126                 Mutations in BRCA1 decreased nuclear localization of BRCA1 in response to individual
127 port by leptomycin B resulted in predominant nuclear localization of C3G.
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
130                                              Nuclear localization of ChREBP was rapidly inhibited whe
131 ating that SPA proteins are not required for nuclear localization of COP1 in darkness.
132                This association disturbs the nuclear localization of CWC22, thereby suppressing the s
133            Consistent with this possibility, nuclear localization of cyclin B1 was increased.
134 al TDP-43 and restores normal solubility and nuclear localization of endogenous TDP-43.
135  dephosphorylate phospho-Ser-322 and promote nuclear localization of Fam13a.
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
138 PO5 knockdown in cell culture did not affect nuclear localization of FLIL33.
139  serine 124 to leucine promotes constitutive nuclear localization of Foxc2 and expression of mesenchy
140                          We also report that nuclear localization of FOXO1 correlated with PTEN mutat
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
143                                          The nuclear localization of Gene 33 also provides a spatial
144                       We also found that the nuclear localization of Gene 33 is regulated by its 14-3
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.
147            Notch1, Notch2, Notch4, DLL-1 and nuclear localization of Hes1 were significantly elevated
148 bly, polyinosinic:polycytidylic acid induced nuclear localization of iNOS, and its binding to, and ni
149 P inhibits IRF7 function by antagonizing the nuclear localization of IRF7.
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
152            Heat inactivation of HIV-1 blocks nuclear localization of LysRS, but treatment with a reve
153                    Here, we demonstrate that nuclear localization of Mre11 (Mre11-NLS) is able to byp
154 d function primarily inside the nucleus, but nuclear localization of mRNAs has been considered rare i
155                             We conclude that nuclear localization of MS is a unique feature of respir
156 iquitination increases protein stability and nuclear localization of mutant PTEN.
157              We further discovered increased nuclear localization of mutant TNNT2 and epigenetic modi
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
160                                              Nuclear localization of NF-kappaB, a major downstream ta
161  Unlike monocytic THP-1 cells with prominent nuclear localization of NLRP1, melanoma cells expressed
162                                              Nuclear localization of P. pastoris MS (PpMS) was abroga
163 w that long term Cn infection induces stable nuclear localization of p65 and IkappaBalpha proteins in
164                                In this case, nuclear localization of p65 is not accompanied by TNFalp
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
167              NF-kappaB reporter activity and nuclear localization of phosphorylated NF-kappaB subunit
168                                Moreover, the nuclear localization of PINN-1 is altered in dapk-1 muta
169 at R742A as well as D113R mutations abrogate nuclear localization of PpMS and its ability to reverse
170                                              Nuclear localization of PsbZIP1 was determined by a cent
171                                              Nuclear localization of RBM45 is mediated by a bipartite
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
178                       Finally, a predominant nuclear localization of TFEB is unveiled in fully fed pa
179                                              Nuclear localization of TFPI-2 contributed to inhibition
180 te how this setup can be used to control the nuclear localization of the budding yeast transcription
181                                          The nuclear localization of the MEF2 corepressor HDAC4 is im
182 tem cell (ESC) differentiation by inhibiting nuclear localization of the MYC transcription factor NME
183                    However, there was strong nuclear localization of the NFkappaB subunit p65 in the
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
186                          Importantly, forced nuclear localization of the PA-X C-terminal deletion mut
187 itant with decreased aggregation and reduced nuclear localization of the pathogenic protein.
188 osis and lipid-loaded Huh7 cells had reduced nuclear localization of the pregnane X receptor (PXR), a
189                          We demonstrate that nuclear localization of the Repressor Element 1-Silencin
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
194                         Finally, an impaired nuclear localization of TRADD triggers cell death throug
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
198                                 Altering the nuclear localization of villin affects the expression an
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
201  in nucleus that may further lead to the non-nuclear localization of YAP.
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
204 . 3.5 to 28 kPa) increased the cell area and nuclear localization of YAP/TAZ.
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
210           A subset of these mutations lacked nuclear localization, prompting us to examine the role o
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
215                       Monopartite C-terminal nuclear localization sequence (NLS) motifs conserved in
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
219 ely accrues from a phosphorylation-sensitive nuclear localization sequence located in the PLD.
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)
223 umulate in the cytoplasm because they lack a nuclear localization sequence.
224 he fusion protein required that it contain a nuclear localization sequence.
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
231                         In these proteins, a nuclear localization signal (NLS) and an intrinsically d
232  N-terminal region of FMDV 3D that acts as a nuclear localization signal (NLS) and in template bindin
233                 Anillin contains a conserved nuclear localization signal (NLS) at its C-terminus that
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
240                         Both HDAgs contain a nuclear localization signal (NLS), but only HDAg-L conta
241 he CTD of topo IIalpha, while preserving the nuclear localization signal (NLS), enhances the decatena
242                             Notably, the PB2 nuclear localization signal (NLS)-containing domain tran
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.
245               Here, we show that the PY-type nuclear localization signal (PY-NLS)/karyopherinbeta2 (K
246 n of a TDP-43 variant with a mutation in the nuclear localization signal (TDP-43-NLS).
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
252                              Mutation of the nuclear localization signal in CELF1 abolished the abili
253 nt manner through an atypical basic patch PY nuclear localization signal motif.
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
259              The C terminus encompassing the nuclear localization signal sequesters the enzyme in the
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
263 xpression, which could be reversed after the nuclear localization signal was deleted.
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
267               One isoform loses the putative nuclear localization signal, generating c-Drosha.
268      We fuse the ADAR2 domain, tagged with a nuclear localization signal, to an RNA binding peptide f
269  were full length, containing the N-terminal nuclear localization signal.
270 calize TRAF3 to the nucleus via a functional nuclear localization signal.
271 es its C-terminal transmembrane domain and a nuclear localization signal.
272 MRKTKLAPT (residues 16 to 24) that acts as a nuclear localization signal.
273 way for mediating ligand-induced exposure of nuclear localization signal.
274  both the C-terminal basic stretch and basic nuclear localization signal.
275 minal 25 amino acids of MxB to function as a nuclear localization signal; however, the ability of the
276 urn (HT), proline/serine (PS) domain and two nuclear localization signals (NLS).
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
281                This is because the predicted nuclear localization signals of HMR are nonfunctional, a
282 karyopherins for Rrp6 nuclear import and the nuclear localization signals recognized by them.
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-
285 e the nuclear import of viral genome via its nuclear localization signals.
286  to potentiate each other to block NF-kappaB nuclear localization stimulated by inflammatory cytokine
287                       Furthermore, the GRP88 nuclear localization suggests nonclassical GPCR modes of
288 ced MET, glandular redifferentiation, and AR nuclear localization that was inhibited by androgen depr
289                           In addition to its nuclear localization, the protein unexpectedly localizes
290      DNA polymerase beta (pol beta) requires nuclear localization to fulfil its DNA repair function.
291 f cells have both been shown to regulate YAP nuclear localization to modulate cell proliferation.
292                            Mutations lacking nuclear localization uncover a novel mechanism whereby l
293 tus loss-of-function alleles decrease Dorsal nuclear localization ventrally, where Toll signals are h
294                   In addition, enhanced Yap1 nuclear localization was also evident in 7,12-dimethylbe
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.
298       To show the functional significance of nuclear localization, we demonstrated that downregulatio
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

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