ライフサイエンスコーパス: nucleoplasm

1 ceptors located on nuclear membranes and the nucleoplasm.

2 ncluding nucleostemin and nucleolin into the nucleoplasm.

3 positioned at the nuclear periphery into the nucleoplasm.

4 in the nucleus, where it is localized to the nucleoplasm.

5 nsport to the INM in addition to the nucleus/nucleoplasm.

6 tween GNL3L and MDM2 also takes place in the nucleoplasm.

7 ctions as a transcriptional regulator in the nucleoplasm.

8 s but are instead distributed throughout the nucleoplasm.

9 take and distribution into the cytoplasm and nucleoplasm.

10 RdDM effector complex at target sites in the nucleoplasm.

11 speckles and GFP fluorescence throughout the nucleoplasm.

12 in herniations, vesicles that bulge into the nucleoplasm.

13 at the periphery and is interspersed in the nucleoplasm.

14 ibution of both deltaAg and nucleolin to the nucleoplasm.

15 st Imp alpha and cargo molecules entered the nucleoplasm.

16 in the distribution of H3K9me3 in interphase nucleoplasm.

17 the outer nuclear membrane and/or within the nucleoplasm.

18 70-kDa isoform was detected primarily in the nucleoplasm.

19 was observed in the Golgi apparatus (GA) and nucleoplasm.

20 he accumulation of ribosomal proteins in the nucleoplasm.

21 ne barrier separating the cytoplasm from the nucleoplasm.

22 on of nuclear IP(3) receptors are facing the nucleoplasm.

23 s localized within foci in the nucleolus and nucleoplasm.

24 of large proteins between the cytoplasm and nucleoplasm.

25 expression of US17 in both the cytoplasm and nucleoplasm.

26 ensitive and more diffusely localized in the nucleoplasm.

27 icronuclei in mitosis and accumulates in the nucleoplasm.

28 and emerin, were mislocalized throughout the nucleoplasm.

29 in ZPR1 is present in both the cytoplasm and nucleoplasm.

30 , a mammalian SENP/Ulp, localizes within the nucleoplasm.

31 n, and delocalized from the nucleolus to the nucleoplasm.

32 ol of virus replication by p30 occurs in the nucleoplasm.

33 dynamic shuttling between the nucleolus and nucleoplasm.

34 slocation of Trm1-II-GFP from the INM to the nucleoplasm.

35 ervations were initiated in a speckle or the nucleoplasm.

36 lizes mainly to the oocyte cortex and to the nucleoplasm.

37 R membrane, nuclear envelope, cytoplasm, and nucleoplasm.

38 o the RNA foci and depleted elsewhere in the nucleoplasm.

39 o the nuclear membrane and 7.4-fold into the nucleoplasm.

40 edia, where they are no longer surrounded by nucleoplasm.

41 h Myc were more uniformly distributed in the nucleoplasm.

42 ential for ribosome biogenesis, occur in the nucleoplasm.

43 thus in direct contact with the surrounding nucleoplasm.

44 t provides access to macromolecules from the nucleoplasm.

45 lizes the nucleolar Fbw7gamma isoform to the nucleoplasm.

46 as a new phase, separating from cytoplasm or nucleoplasm.

47 lesces to from a nucleating structure in the nucleoplasm.

48 s being diffusely distributed throughout the nucleoplasm.

49 d co-localizes with the Mre11 complex in the nucleoplasm.

50 ughter nuclei occurs after separation of the nucleoplasm.

51 lei, GFP-SR45 was found both in speckles and nucleoplasm.

52 ctivity from potential RNA substrates in the nucleoplasm.

53 ds are not randomly dispersed throughout the nucleoplasm.

54 sion of cytosolically expressed GFP into the nucleoplasm.

55 l kinase-dependent WRN relocalization to the nucleoplasm.

56 portant mitotic proteins into and out of the nucleoplasm.

57 lexes that must ultimately dissociate in the nucleoplasm.

58 ir re-localization from the nucleolus to the nucleoplasm.

59 ups), and dissociation of the complex in the nucleoplasm.

60 lpha redistributing uniformly throughout the nucleoplasm.

61 g in delocalization of TOP1 from nucleoli to nucleoplasm.

62 ation of its components from the surrounding nucleoplasm.

63 istributed across euchromatic regions of the nucleoplasm.

64 ction of lamins also localize throughout the nucleoplasm.

65 d to the nucleus and maximally active in the nucleoplasm.

66 monomeric, whereas PRC2 can dimerize in the nucleoplasm.

67 delocalize from the Xi and disperse into the nucleoplasm.

68 ization of individual chromosomes within the nucleoplasm.

69 s in frequent release of mRNAs back into the nucleoplasm.

70 h AR, and observe these proteins in the cell nucleoplasm.

71 completed upon the release of mRNA into the nucleoplasm.

72 phosphorylated NPM from the nucleolus to the nucleoplasm.

73 nd resulting in complete mixing of cyto- and nucleoplasm.

74 interacts with NPM1 within nucleoli and the nucleoplasm.

75 complexes, some nucleoporins function in the nucleoplasm.

76 macromolecules between the cytoplasm and the nucleoplasm.

77 ondensed liquid-like phases of the cytoplasm/nucleoplasm.

78 nlike yeast, these interactions occur in the nucleoplasm.

79 e of molecules between the cytoplasm and the nucleoplasm.

80 ing, but clustering can be maintained in the nucleoplasm.

81 f fluorescent UTP-labeled transcripts in the nucleoplasm.

82 used to estimate protein concentrations for nucleoplasm (0.106 g/cm3), CBs (0.136 g/cm3), speckles (

83 and (+)-strands of PSTVd RNAs occurs in the nucleoplasm, (2) the (-)-strand RNA is anchored in the n

84 The results suggest that, in the nucleoplasm, a complex interplay of histones, DNA, and p

85 most La is phosphorylated and resides in the nucleoplasm, a fraction is in the nucleolus, the site of

86 Finally, we show that within the nucleoplasm, a fraction of Nup107, a key component of th

87 tinguish three fractions of Rad51 within the nucleoplasm: a relatively mobile fraction, an immobile o

88 In the nucleoplasm, AGO4 displays a strong co-localization with

89 the available delta antigen to sites in the nucleoplasm, almost exclusively colocalized with Pol II

90 g HDV RNA, it was found predominantly in the nucleoplasm along with Pol II.

91 RF increases the localization of XRN2 in the nucleoplasm and a concomitant suppression of pre-rRNA pr

92 , the mRNA export factor NXF1 resides in the nucleoplasm and at nuclear pore complexes.

93 It is widely distributed in cytoplasm and nucleoplasm and bound to chromatin.

94 e the steady-state exchange rate between the nucleoplasm and CBs of three fluorescently tagged molecu

95 ar in most G2/M cells but accumulates in the nucleoplasm and colocalizes with DSBs in rad52Delta cell

96 s with SNF2h, regulates its diffusion in the nucleoplasm and controls its accumulation at DNA breaks.

97 ght protein filaments that protrude into the nucleoplasm and converge in a ring distal to the NPC.

98 a selectively permeable barrier between the nucleoplasm and cytoplasm and an organizational scaffold

99 assumed that the physical barrier separating nucleoplasm and cytoplasm remains intact during the rest

100 mal RNA remodelling events in the nucleolus, nucleoplasm and cytoplasm.

101 in the host cell cytoplasm or the host cell nucleoplasm and did not develop as liver stages.

102 d not interfere with PB2 localization to the nucleoplasm and disrupted the subnuclear transport of vR

103 deltaAg facilitates HDV RNA transport to the nucleoplasm and helps redirect host RNA polymerase II (P

104 containing protein (VCP) were present in the nucleoplasm and in nucleolar foci in mammalian cells and

105 he current study, Ca(2+) changes both in the nucleoplasm and in the cytosol of INS-1 and pancreatic b

106 interaction after stress occurs both in the nucleoplasm and in the nucleolus.

107 ckdown of nucleolin mobilized capsids to the nucleoplasm and increased transduction 10- to 30-fold.

108 dc14B translocates from the nucleolus to the nucleoplasm and induces the activation of the ubiquitin

109 2alpha (LAP2alpha) localizes throughout the nucleoplasm and interacts with the fraction of lamins A/

110 GNL3L binds TRF1 in the nucleoplasm and is capable of promoting the homodimeriza

111 rt of a large, viscoelastic structure in the nucleoplasm and may act as scaffolds that help organize

112 sids of approximately 125 nm assemble in the nucleoplasm and must reach the nuclear membranes for egr

113 us, based on regulation of Ca2+ flux between nucleoplasm and nuclear envelope.

114 showed defects in redistribution between the nucleoplasm and nuclear matrix.

115 of phosphoinositides in the eukaryotic cell nucleoplasm and nuclear membrane prompted us to study th

116 Because the properties of the nucleoplasm and nuclear organelles influence the exchang

117 ear protein that colocalizes with Rev in the nucleoplasm and nuclear periphery of transfected cells.

118 We found that IFI16 was localized in the nucleoplasm and nucleoli.

119 M to provide evidence for translation in the nucleoplasm and nucleolus, which is regulated by infecti

120 recognition motif (RRM) and localizes to the nucleoplasm and nucleolus.

121 olecular fluorescence complementation in the nucleoplasm and nucleolus.

122 ing spatial distribution of XRN2 between the nucleoplasm and nucleolus.

123 to rapidly distribute throughout the entire nucleoplasm and other speckles, regardless of whether th

124 that Firre, a lncRNA highly enriched in the nucleoplasm and previously reported to mediate chromosom

125 PB2 and M1 induced CLUH translocation to the nucleoplasm and SC35-positive speckles, respectively, ev

126 se cells, GFP-TBP distributes throughout the nucleoplasm and shows a FRAP that is 100-fold slower tha

127 Rapid translocation of NS and NPM to the nucleoplasm and suppression of new preribosomal RNA synt

128 We studied the density of the nucleoplasm and the density and permeability of nucleoli

129 us from the nuclear periphery to the central nucleoplasm and to foci of hyperphosphorylated Pol II "t

130 an accumulate in either the cytoplasm or the nucleoplasm and, upon cell stimulation, translocates to

131 m, (2) the (-)-strand RNA is anchored in the nucleoplasm, and (3) the (+)-strand RNA is transported s

132 terphase, Ran-GTP was highly enriched in the nucleoplasm, and a steep concentration difference betwee

133 ematurely released from the nucleolus to the nucleoplasm, and cannot be exported to the cytoplasm.

134 NPM1 and BER components from nucleoli to the nucleoplasm, and cellular experiments targeting APE1 sug

135 enesis occurs successively in the nucleolus, nucleoplasm, and cytoplasm.

136 e of proteins at the plasma membrane, in the nucleoplasm, and in the cytoplasm of living cells.

137 n5 can enter the nucleus, but is left in the nucleoplasm, and not assembled into the nuclear membrane

138 Phosphorylated lamin-A,C localizes to nucleoplasm, and phosphorylation is enriched on lamin-A,

139 s and displays a speckled pattern within the nucleoplasm, and RGH3alpha colocalizes with U2AF(65).

140 P-green fluorescent protein localized to the nucleoplasm, and substrate SL RNA derived from SNIP knoc

141 nce recovery was markedly slower than in the nucleoplasm, and there were at least three kinetic compo

142 P-NS1 localized throughout the nucleolus and nucleoplasm, and to several transcriptionally active int

143 in nucleoli, thus driving it to bind in the nucleoplasm; and camptothecin treatment, which increases

144 s to determine whether tubulin levels in the nucleoplasm are regulated in the fungus Aspergillus nidu

145 s (MSCs) increases DNA breaks throughout the nucleoplasm as assessed by endogenous damage markers and

146 lamina and have different mobilities in the nucleoplasm as determined by fluorescence correlation sp

147 ogerin away from the nuclear envelope to the nucleoplasm, as determined by immunofluoresence microsco

148 exchanged continuously between chromatin and nucleoplasm, as well as between chromatin domains.

149 MBNL1 is depleted from the muscle nucleoplasm because of sequestration in nuclear foci, an

150 el in mitotic nuclei than in the surrounding nucleoplasm before leaving in anaphase/telophase.

151 genesis, are proposed to be assembled in the nucleoplasm before localizing to the nucleolus.

152 ear rDNA positioning, disrupts the nucleolus-nucleoplasm boundary, induces the formation of recombina

153 odel in which ARF interacts with MDM2 in the nucleoplasm but is consequently subject to proteasomal d

154 he initial complex formation with XPC in the nucleoplasm but it enhances the recruitment of XPC to th

155 -containing S6 variant [NLS-S6(Rpt1)] to the nucleoplasm (but not to the nucleolus) resulted in compl

156 n-tagged HvRBK1 appears in the cytoplasm and nucleoplasm, but CA HvRACB or CA HvRAC1 can recruit gree

157 The nucleolin was transferred into the nucleoplasm, but it distributed there non-uniformly; loc

158 ctor that shuttles between the nucleolus and nucleoplasm, but it has no known involvement in ribosome

159 plasmid can be detected in the nucleolus and nucleoplasm, but it largely fails to assemble into ribos

160 onreplicating HDV RNAs, deltaAg moved to the nucleoplasm, but nucleolin was unchanged.

161 e-60S ribosomes initially accumulated in the nucleoplasm, but then strongly concentrated in a subnucl

162 inuous flow of molecules between CBs and the nucleoplasm, but there are few data that directly suppor

163 mice would be strikingly mislocalized to the nucleoplasm, but this was not the case; most was at the

164 ase droplets and appear to condense from the nucleoplasm by concentration-dependent phase separation.

165 INM) where it mediates Ca(2+) changes in the nucleoplasm by coupling with Gq/11 Here, we identified a

166 racter of the nucleus is thus set largely by nucleoplasm/chromatin, whereas the extent of deformation

167 tially delocalized from the nucleolus to the nucleoplasm, consistent with a specific function in cell

168 shifts the distribution of the enzyme to the nucleoplasm constitutively.

169 rotein that can shuttle among the nucleolus, nucleoplasm, cytoplasm, and plasma membrane.

170 In the nucleoplasm, DDX21 binds 7SK RNA and, as a component of

171 that localize to either the NE lumen or the nucleoplasm demonstrates that outer membrane fusion prec

172 The composition of the nucleoplasm determines the behavior of key processes suc

173 nsor translocating from the nucleolus to the nucleoplasm during heat stress; nucleolar pools are repl

174 HKIF4A localizes in the nucleoplasm during interphase and on condensed chromosom

175 ndle begins to form, and is removed from the nucleoplasm during the M-to-G1 transition.

176 ning SDS1 and PEST2 sequences) into the cyto/nucleoplasm enables selective topovectorial processing o

177 enome experience distinctive coupling to the nucleoplasm environment at all scales.

178 lular and nuclear volume following cytoplasm/nucleoplasm expulsion.

179 roteins from nuclear storage speckles to the nucleoplasm for splicing function, dephosphorylation par

180 revealed the presence of CD40 protein in the nucleoplasm fraction of activated B cells, and chromatin

181 ries suggest the compartmentalization of the nucleoplasm from the cytoplasm.

182 or in membrane vesicles that bulged into the nucleoplasm (herniations).

183 after photobleaching at the PNC than in the nucleoplasm, illustrating the different molecular intera

184 leolar droplets" (ENDs) that condense in the nucleoplasm in a transcription-independent manner.

185 its move out from the nucleolus and into the nucleoplasm in all directions, with no evidence of conce

186 able L22 is relocalized from nucleoli to the nucleoplasm in EBV-infected cells.

187 Although TLC1 RNA accumulates in the nucleoplasm in G1/S, Pif1 activity promotes TLC1 RNA loc

188 ed by a C-terminal NLS, TgEB1 resides in the nucleoplasm in interphase and associates with the spindl

189 tructures, which are in equilibrium with the nucleoplasm in interphase and disassemble during mitosis

190 ase II was observed diffusely throughout the nucleoplasm in interphase nuclei, whereas, the nucleolus

191 apidly between ND10 foci and the surrounding nucleoplasm in live cells.

192 pression at the nuclear periphery and in the nucleoplasm in metazoans.

193 ntrating in nucleoli and relocalizing to the nucleoplasm in response to DNA damage.

194 r alpha (RXR alpha) localized throughout the nucleoplasm in retinoid-sensitive normal human mammary e

195 ) fusion was detected in the cytosol and the nucleoplasm in spite of the presence of an N-terminal se

196 e, we show that the retention of RelA in the nucleoplasm inhibits this decrease in NF-kappaB-driven t

197 ltaNp63 by preventing its translocation from nucleoplasm into nucleoli.

198 e was defective, resulting in leakage of the nucleoplasm into the cytoplasm through large gaps in the

199 e documented accumulation in the cytosol and nucleoplasm is because of the bypassing of the transloca

200 In contrast, the behavior of proteins in the nucleoplasm is well explained by the dumbbell shape of t

201 In the nucleoplasm, La binds to and protects from 3' exonucleas

202 anslocation of B23 from the nucleolus to the nucleoplasm, leading to stabilization and activation of

203 sequence of SelH fused to GFP had a diffuse nucleoplasm location.

204 that regulation of protein movement into the nucleoplasm may be important for regulating mitotic onse

205 active transport of the GFP fusion into the nucleoplasm may indicate an as yet undiscovered feature

206 -nucleolus, nucleolus-associated structures, nucleoplasm, nuclear bodies and extra-nuclear-is provide

207 Meq and Meq/vIL8 both localized to the nucleoplasm, nucleoli, and Cajal bodies of transfected c

208 d nucleolin raises new possibilities for the nucleoplasm-nucleolus pathways of these proteins and the

209 at pronounced aggregation of proteins in the nucleoplasm of apoptotic cells coincides with a gradual

210 BAF53 and yeast Arp4 is concentrated in the nucleoplasm of Arabidopsis, Brassica, and tobacco cells.

211 ited to CBs, but is dispersed throughout the nucleoplasm of cells in general.

212 ctively involved in transcription inside the nucleoplasm of Drosophila cells.

213 re transported between the cytoplasm and the nucleoplasm of eukaryotic cells through nuclear pore com

214 embrane that separates the cytoplasm and the nucleoplasm of eukaryotic cells.

215 ructure exists between the cytoplasm and the nucleoplasm of eukaryotic cells.

216 phospho-Ser(211) staining was evident in the nucleoplasm of hormone-treated cells.

217 FANCI is in close proximity to SF3B1 in the nucleoplasm of interphase and mitotic cells.

218 nal antibodies localized ARP5 protein to the nucleoplasm of interphase cells in Arabidopsis and Nicot

219 several different proteins in the cyto- and nucleoplasm of living cells.

220 phila, but they function equally well in the nucleoplasm of mutant flies that lack CBs.

221 ulation of Kap60p.NLS-cargo complexes in the nucleoplasm of yeast.

222 , suggesting that decay occurs either in the nucleoplasm or at the outer nuclear membrane.

223 gene failed to show the presence of N in the nucleoplasm or nucleolus.

224 oplasmic reticula that reach deep within the nucleoplasm, or during somatic and nonsomatic nuclear en

225 s described as a chromatin solution with the nucleoplasm playing the role of the solvent and the chro

226 c61beta expression reduces EGFR level in the nucleoplasm portion and accumulates it in the INM portio

227 This compartmentalization of the nucleoplasm promoted Ace2 asymmetry in anaphase nuclei.

228 ld-type Maf was uniformly distributed in the nucleoplasm, R288P Maf was enriched in nuclear foci.

229 isrupted, being highly dispersed through the nucleoplasm rather than focal.

230 ctivated form of CHK1 for destruction in the nucleoplasm rather than on chromatin and that this occur

231 upon reentry into G(1) and colocalize in the nucleoplasm, RbS795 migrates between nucleoplasmic and s

232 infected cells, B23 undergoes a nucleolus-to-nucleoplasm redistribution, evocative of virus-induced n

233 ggesting that the majority of deltaAg in the nucleoplasm reflects ribonucleoprotein accumulation rath

234 formed, clustering can be maintained in the nucleoplasm, requires distinct nuclear pore proteins, an

235 - and 2.7-fold into the nuclear membrane and nucleoplasm, respectively.

236 representing the nuclear envelope and inner nucleoplasm, respectively.

237 p53-independent translocation of ARF to the nucleoplasm, resulting in a masking of the ARF NH2 termi

238 tributes it from the nuclear speckles to the nucleoplasm, resulting in cyclin A1 but not A2 up-regula

239 f endogenous ADAR2 from the nucleolus to the nucleoplasm results in increased editing of endogenous A

240 sical boundary between the cytoplasm and the nucleoplasm, sandwiched in between two highly active sys

241 very after photobleaching experiments in the nucleoplasm show a decreased mobility of intron-retained

242 ior of poly(A) RNA in either speckles or the nucleoplasm, strongly suggesting that its movement in an

243 the two compartments studied (nucleolus and nucleoplasm), suggesting a direct transcription-dependen

244 sults in translocation of the protein to the nucleoplasm, suggesting that nucleolar association of AD

245 led to accumulation of wild-type Nmd3 in the nucleoplasm, suggesting that the interaction of mutant N

246 ses transduction, mobilized virions into the nucleoplasm, suggesting that two separate pathways influ

247 NC-84 also recruits FA nuclease FAN-1 to the nucleoplasm, suggesting that UNC-84 both alters the exte

248 ed very similar distributions throughout the nucleoplasm, SUMO-1 was uniquely distributed to the nucl

249 promoter and exhibits higher mobility in the nucleoplasm than the agonist-bound receptor.

250 ustained calcium (Ca2+) responses within the nucleoplasm that can be blocked by receptor-specific ant

251 onounced presence both at the NPC and in the nucleoplasm that can move between these different locali

252 es or other entities within the cytoplasm or nucleoplasm that collectively we term "assemblage." Intr

253 In the nucleoplasm, the apparent diffusion coefficients for the

254 that ARF can bind and inactivate Mdm2 in the nucleoplasm, the prevailing view is that ARF exerts its

255 ion of unassembled ribosomal proteins in the nucleoplasm, thereby providing a mechanism for mammalian

256 lus, facilitates translocation of L11 to the nucleoplasm, thus activating p53 through inhibiting HDM2

257 Importantly, NMD does not occur within the nucleoplasm, thus countering the long-debated idea of nu

258 tes PRC2 binding by sequestering PRC2 in the nucleoplasm, thus reducing PRC2 binding to many targets

259 leus before heat shock and translocates from nucleoplasm to chromosomal loci after heat shock.

260 NA-binding protein that must localize to the nucleoplasm to exert its antiangiogenic and tumor suppre

261 pletion results in the release of L11 to the nucleoplasm to inhibit MDM2, leading to p53 activation.

262 argeted to NE/endoplasmic reticulum (ER) and nucleoplasm to monitor [Ca(2+)](ne/er) and [Ca(2+)](n) r

263 tion of SIRT1 reduces WRN translocation from nucleoplasm to nucleoli after DNA damage.

264 In addition, ARF relocalizes E2F1 from the nucleoplasm to nucleolus and inhibits E2F1-activated tra

265 cific redistribution of Sm proteins from the nucleoplasm to the cytoplasmic periphery of the nucleus

266 3T3-L1 cells, CCTalpha translocated from the nucleoplasm to the nuclear envelope and cytosol but did

267 activates cPla2 by translocating it from the nucleoplasm to the nuclear envelope.

268 ange in localization of the protein from the nucleoplasm to the nucleolus.

269 inhibits the translocation of RelA from the nucleoplasm to the nucleolus.

270 Consequently, ARF relocalizes c-Myc from the nucleoplasm to the nucleolus.

271 f ARF causes a relocalization of E7 from the nucleoplasm to the nucleolus.

272 phorylates Maf1 in vitro, and regulates Maf1 nucleoplasm-to-nucleolus translocation.

273 ed by TORC1, indicating that TORC1 regulates nucleoplasm-to-nucleolus transport of Maf1.

274 ress conditions, NKRF directs XRN2 nucleolus/nucleoplasm trafficking, controlling 5'-to-3' exoribonuc

275 It forms a stable complex with XPC in the nucleoplasm under steady-state conditions before irradia

276 tially distributed fluorescent VLC-PUFA into nucleoplasm versus nuclear envelope, especially for the

277 Inasmuch as Ca2+ can enter the nucleoplasm via the nuclear pore complex or from the nuc

278 d NS5A is able to transduce signals into the nucleoplasm via UBF hyperphosphorylation leading to rRNA

279 At this stage, the nucleoplasm was highly compartmentalized; little exchang

280 defective in GTP binding and exported to the nucleoplasm was much less stable than wild-type NS.

281 Moreover, accumulation in the nucleoplasm was shown to be microtubule dependent unlike

282 signals, a portion of RPS27L shuttled to the nucleoplasm where it colocalizes with MDM2.

283 by way of the nuclear pore complex into the nucleoplasm where it is transcribed and replicated.

284 and small subunit precursors at site 2; the nucleoplasm, where it co-localizes with the RNA/DNA heli

285 anslocates through the nuclear pore into the nucleoplasm, where it is transcribed and replicated to p

286 phorylated Akt is found primarily inside the nucleoplasm, where it partially colocalizes with the Rho

287 anslocation of L11 from the nucleolus to the nucleoplasm, where it participates in a complex with HDM

288 The E2F1/DP1 complex localizes in the nucleoplasm, whereas ARF is detected in the nucleolus, s

289 pathway, as p53 and mdm2 are located in the nucleoplasm, whereas ARF is largely nucleolar in tumor c

290 ncentrated more in the nucleolus than in the nucleoplasm, whereas on rich medium, it was more evenly

291 af formed complexes with Sox proteins in the nucleoplasm, whereas R288P Maf recruited Sox proteins as

292 inuclear regions of the cell, but not in the nucleoplasm, whereas strong phospho-Ser(211) staining wa

293 nts, the (-)-strand RNA was localized in the nucleoplasm, whereas the (+)-strand RNA was localized in

294 olin to relocalize from the nucleolus to the nucleoplasm, whereupon it binds replication protein A an

295 imarily in a punctate pattern throughout the nucleoplasm, while nonmetabolizable fluorescent LCFAs (B

296 localized in the nucleolus as well as in the nucleoplasm with distinct spatial patterns.

297 hat an increase in buffering capacity in the nucleoplasm would cause a period of rapid oscillations.

298 of both proteins, rings move throughout the nucleoplasm yet remain silent.

299 Sim3 is distributed throughout the nucleoplasm, yet it associates with CENP-A(Cnp1) and als

300 e checkpoint signals can be amplified in the nucleoplasm, yet kinetochore localization of spindle che