ライフサイエンスコーパス: nucleoli

1 , and lipids in the molecular composition of nucleoli.

2 ing occur in regions of the nucleus known as nucleoli.

3 ion coupled with exercise also display small nucleoli.

4 mordia, and its protein was localized to the nucleoli.

5 eudosubstrate that directly recruits Fbw7 to nucleoli.

6 y to pericentric heterochromatin-surrounding nucleoli.

7 istributed throughout nuclei and enriched in nucleoli.

8 in large nuclear aggregates that often ring nucleoli.

9 sors, and fibrillarin does not accumulate in nucleoli.

10 bserved accumulation of SUMO proteins within nucleoli.

11 e only phosphorylation site, retains FEN1 in nucleoli.

12 es in late mitosis before the reformation of nucleoli.

13 Pes1 was typically restricted to nuclei and nucleoli.

14 o a lesser extent PP1beta concentrate in the nucleoli.

15 endogenous proteins appear within mammalian nucleoli.

16 ther lack an organized nucleolus or have two nucleoli.

17 yield mature H/ACA RNPs in Cajal bodies and nucleoli.

18 s but also necessary for localizing ADAR2 to nucleoli.

19 also observed miR-206 to be concentrated in nucleoli.

20 calization of the marker protein, coilin, to nucleoli.

21 id not localize bulk sumoylated molecules to nucleoli.

22 asmic locations, Lsm proteins are present in nucleoli.

23 ver, La lacking the SBM does not localize to nucleoli.

24 ha-actinin and exhibited a nucleus with many nucleoli.

25 n the cytosol and in other cells also in the nucleoli.

26 RNp and p97/VCP physically interacted in the nucleoli.

27 t IFI16 was localized in the nucleoplasm and nucleoli.

28 pair in human cells colocalize with Mus81 in nucleoli.

29 lization of RGS6 proteins from such sites to nucleoli.

30 nuclear protein, with super accumulation in nucleoli.

31 d increased intense speckled staining in the nucleoli.

32 he U6 base-pairing region still localizes to nucleoli.

33 import of chimeric proteins into nuclei and nucleoli.

34 Drosophila variants colocalize to HeLa cell nucleoli.

35 e analysis revealed that it was localized to nucleoli.

36 s of the nucleus and was also present in the nucleoli.

37 , promyelocytic leukemia protein bodies, and nucleoli.

38 nucleolar R-loops recruited RNase H1 to the nucleoli.

39 vitro and for localization within mammalian nucleoli.

40 ssociation of Pol III-transcribed genes with nucleoli.

41 ~60% of which were detected in the H1 mutant nucleoli.

42 in vitro exhibit smaller and more elongated nucleoli.

43 distribution of MageB2 protein includes the nucleoli.

44 reduces alpha-satellite DNA association with nucleoli.

45 sed in mammalian cells, these variants bound nucleoli.

46 lear membrane; they exhibited small punctate nucleoli.

47 pheries of both replication compartments and nucleoli.

48 ting its translocation from nucleoplasm into nucleoli.

49 of MDM2 and translocation of DeltaNp63 into nucleoli.

50 ould not confirm localization of midnolin in nucleoli.

51 meric clusters, chromosomal territory 3, and nucleoli.

52 d in specific, robust accumulation of Gag in nucleoli.

53 62 g/cm3), and the dense fibrillar region of nucleoli (0.215 g/cm3).

54 alized to distinct nuclear bodies, including nucleoli (148), promyelocytic leukemia nuclear bodies (3

55 h a single nucleolus and those with multiple nucleoli; (2) the percentage of each phenotype is sex sp

56 ndent sequestration of the telomerase RNA in nucleoli, a process that excludes telomerase from DNA re

57 However, nucleoli actively consume chemical energy, and it is unc

58 olar stress and establish the postulate that nucleoli acts as sensors of stress, regulating the cellu

59 We show that NBS1 relocalizes to nucleoli after DNA damage in a manner dependent on TCOF1

60 educes WRN translocation from nucleoplasm to nucleoli after DNA damage.

61 increased protein synthesis, and report that nucleoli also expand as aging progresses in cells derive

62 eolar transcription units directly in intact nucleoli, although highly spread preparations in the ele

63 er cells depleted of NPM1 displayed deformed nucleoli and a striking rearrangement of perinucleolar h

64 luorescence that ubiquitin is present within nucleoli and also demonstrate by immunoprecipitation tha

65 regulatory events are directly regulated by nucleoli and are dependent on intact nucleolar structure

66 s associate with the fibrillar components of nucleoli and bind pre-rRNA during transcription, trigger

67 BEN domain-containing protein, localizes in nucleoli and binds to ribosomal RNA gene promoters to he

68 ACA11 localized to nucleoli and bound what we believe to be a novel small n

69 hat NHPX is specifically accumulated in both nucleoli and Cajal bodies (CBs) in vivo.

70 plex associations of both hTR and hTERT with nucleoli and Cajal bodies during S phase, implicating bo

71 is a nuclear protein localized primarily in nucleoli and Cajal bodies that was identified as a downs

72 , form the [U4/U6] di-snRNP, and localize to nucleoli and Cajal bodies.

73 Crosstalk between nucleoli and CBs is also discussed in the context of str

74 e report that mammalian RNase H1 enriches in nucleoli and co-localizes with R-loops in cultured human

75 a-irradiation or mitomycin C, WRN leaves the nucleoli and co-localizes with the Mre11 complex in the

76 NF45 and NF90 are enriched in nucleoli and cosediment with pre-60S ribosomal particles

77 at RBS was associated with highly fragmented nucleoli and defects in both ribosome biogenesis and pro

78 We show that growth of nucleoli and ENDs is consistent with a first-order phase

79 is is elevated as a consequence of activated nucleoli and enhanced ribosome biogenesis in HGPS-derive

80 uded the following: (1) increased numbers of nucleoli and enlarged nuclei, (2) narrower spaces betwee

81 d insulin-like-peptide mutants exhibit small nucleoli and fibrillarin expression, as do long-lived di

82 protein colocalized with fibrillarin in the nucleoli and formed punctate structures associated with

83 's p53-dependent activity by targeting it to nucleoli and impairing ARF-Mdm2 association.

84 nocarcinomas, leads to formation of enlarged nucleoli and increased nucleolar number in prostate lumi

85 cells from patients with HGPS have expanded nucleoli and increased protein synthesis, and report tha

86 stinfection, UXP is strongly associated with nucleoli and is found throughout the nucleus; later, UXP

87 mic reticulum membranes, capsid localizes in nucleoli and lipid droplets.

88 ) is a DEAD-box enzyme that localizes to the nucleoli and may be involved in ribosomal RNA synthesis

89 yses in purified subnuclear fractions (e.g., nucleoli and nuclear matrix).

90 ouble-labeling showed colocalization in both nucleoli and nucleoplasmic foci in breast tumor cells an

91 of MCF7 cells, BRCA1 protein dispersed from nucleoli and nucleoplasmic foci to other nucleoplasmic s

92 cell lines revealed BRCA1 expression in both nucleoli and nucleoplasmic foci.

93 SmD1b resides in nucleoli and nucleoplasmic speckles, colocalizing with t

94 and BAX were induced and exported out of the nucleoli and nucleus, respectively.

95 These data suggest a role for nucleoli and pericentromeric heterochromatin clusters as

96 the cytoplasm and nucleus, concentrating in nucleoli and relocalizing to the nucleoplasm in response

97 found localization of UL84 with nucleolin in nucleoli and showed that the presence of nucleolin is in

98 has large, pleomorphic nuclei with prominent nucleoli and the cells tend to involve the entire lumen

99 protein chaperone that shuttles between the nucleoli and the cytoplasm and has been associated with

100 onjugate was observed to localize within the nucleoli and the cytosol of treated cancer cells.

101 t signals, allowing its accumulation in both nucleoli and the cytosol.

102 ons, specifically interacts with NPM1 within nucleoli and the nucleoplasm.

103 h binds to Mdm2 and NPM but is excluded from nucleoli and the other of which enters nucleoli but is h

104 stores, and protects ribosomal protein S9 in nucleoli and therefore could facilitate ribosome biogene

105 nocytes with oval vesicular nuclei, distinct nucleoli, and abundant cytoplasm.

106 Meq/vIL8 both localized to the nucleoplasm, nucleoli, and Cajal bodies of transfected cells.

107 dilational capacity of the nuclear envelope, nucleoli, and chromatin.

108 ng distinct longevity pathways exhibit small nucleoli, and decreased expression of rRNA, ribosomal pr

109 omatically identify lipid droplets, nucleus, nucleoli, and endoplasmic reticulum in datasets that are

110 mislocalization of telomerase and scaRNAs to nucleoli, and failure of telomere elongation.

111 at brat mutant cells are larger, have larger nucleoli, and have more ribosomal RNA than wild-type cel

112 ote are retained in the nucleus, localize to nucleoli, and interact with the X. laevis Box C/D RNA bi

113 , and mitochondria-rich cytoplasm, prominent nucleoli, and markers of hepatocytes and cholangiocytes.

114 calization to the nucleus and exclusion from nucleoli, and no surface staining was detected.

115 lear organelles, such as Cajal bodies (CBs), nucleoli, and other nuclear bodies, is dynamic and can c

116 granular components, respectively, in active nucleoli, and partition separately into the two componen

117 ntered cells, migrated to the nucleus, bound nucleoli, and poisoned RNA biogenesis, which caused cell

118 eome, enzymatically active PP1 is present in nucleoli, and PP1gamma is highly concentrated in nucleol

119 We show that SmgGDS localizes in nucleoli, and that RNAi-mediated depletion of SmgGDS in

120 upstream binding factor UBF-1 at interphase nucleoli, and this interaction is epigenetically retaine

121 Other CMV proteins associate with nucleoli, and we demonstrate that pUL31 specifically int

122 We suggest that small nucleoli are a cellular hallmark of longevity and metabo

123 The nucleoli are abundant with autoantigens.

124 In addition to ribosome biogenesis, nucleoli are critical for control of cell proliferation

125 Nucleoli are prominent nuclear structures assembled and

126 egrity and organization of repeated DNAs and nucleoli are regulated by the H3K9 methylation and RNAi

127 Nucleoli are rich in nucleolin, a potent transcription f

128 autoantibodies, which frequently target the nucleoli, are pathogenic hallmarks of systemic lupus ery

129 biquitin-like modifier (SUMO) 1 localized to nucleoli as p19(Arf) accumulated there.

130 used by steps in p53 regulation occurring in nucleoli, as suggested by some biochemical evidence.

131 [U4/U6.U5] tri-snRNP localize transiently to nucleoli, as visualized by microscopy after injection of

132 ion factor UBF1, and undergo transition into nucleoli at sites of rRNA synthesis during interphase.

133 hey have rounded cell bodies, have prominent nucleoli, attach poorly to the culture dish, and are sen

134 from nucleoli and the other of which enters nucleoli but is handicapped in binding to Mdm2 and NPM,

135 and dense fibrillar components of PtK2 cell nucleoli by immunoelectron microscopy.

136 We propose that FRGY2a and YB1 disassemble nucleoli by sequestering B23, which is associated with p

137 ceous and membraneless organelles, including nucleoli, Cajal and PML bodies, and stress granules.

138 leoplasm and the density and permeability of nucleoli, Cajal bodies (CBs), and speckles in the Xenopu

139 nuclear compartments including chromosomes, nucleoli, Cajal bodies and histone locus bodies.

140 ction of the endogenous FRG1 is localized in nucleoli, Cajal bodies, and actively transcribed chromat

141 Nuclear bodies including nucleoli, Cajal bodies, nuclear speckles, Polycomb bodie

142 t AgNOR-stained nucleoli, unlike H&E-stained nucleoli, can be captured and measured by an automated i

143 ing nucleocytoplasmic transport) and also in nucleoli, clearly visible against the less concentrated

144 asing nucleolar proteins to the cytoplasm as nucleoli concomitantly reform in daughter nuclei.

145 d similar high mobility, with exclusion from nucleoli, consistent with high rates of association and

146 tion signals traffic through CBs en route to nucleoli, consistent with the role of CBs in small RNP a

147 It was recently discovered that the nucleoli contain cell cycle machinery in close proximity

148 Nucleoli continued to diminish in postmitotic cells foll

149 that an Lsm2-Lsm7 protein complex resides in nucleoli, contributing to the biogenesis or function of

150 Retargeting a NET39 fragment to nucleoli correspondingly repositioned a target gene, ind

151 tumors revealed hypercelluarity, pleomorphic nucleoli, cytological atypia and necrosis, and positive

152 their neurotoxicity included aggregation in nucleoli, decreased number of processing bodies, and str

153 Analysis of purified nucleoli demonstrated that human and mouse NORs are equa

154 RNAs of the [U4/U6.U5] tri-snRNP localize to nucleoli, demonstrated by fluorescence microscopy of nuc

155 3R-GFP-TOP1 was markedly concentrated within nucleoli, depleted from the remainder of nucleus, and fa

156 Rev/CRM1 colocalization in nucleoli dropped exponentially after addition of leptomy

157 the nucleolar-organizing regions (NORs) from nucleoli during Aspergillus nidulans mitosis.

158 ogy and contributes to the reorganization of nucleoli during infection.IMPORTANCE Nucleolar biology i

159 R-loops accumulate in nucleoli during RNA polymerase I (RNAP I) transcription.

160 ificant interaction of ZO-1 with proteins in nucleoli during the healing process.

161 Intracellular localization (cytosol, nucleoli, endosomes) is independent of the substrate and

162 ized L5 and L11 continue to be imported into nucleoli even after nucleolar disruption and colocalize

163 with DNMT1 on heterochromatic regions of the nucleoli exclusively before cell division.

164 ikingly, assessment of the morphology of the nucleoli exposed an abnormal nucleolar structure in Pf1-

165 arrest at morula stages of development, the nucleoli fail to differentiate and accumulation of ribos

166 come hypersensitive to micrococcal nuclease, nucleoli fail to form, and transcript levels of the copi

167 On exit from mitosis, nucleoli form around individual active NORs.

168 uncapped small RNAs using RNA from isolated nucleoli from Arabidopsis cell cultures.

169 Nucleoli from Arf(-/)(-) cells displayed increased nucle

170 nalyse highly purified preparations of human nucleoli from different cell lines.

171 oteomic profiling of purified wild-type mESC nucleoli identified a total of 613 proteins, only ~60% o

172 eckled pattern and colocalized with ORF2p in nucleoli in a subset of cells.

173 distributed to the ribosomal RNA (rRNA)-rich nucleoli in cells treated with the DNA-damaging agents c

174 Both Drosophila variants localize to nucleoli in Drosophila Schneider II cells and Xenopus oo

175 ize the assembly and disassembly dynamics of nucleoli in early Caenorhabditis elegans embryos.

176 nalogies to liquid-like compartments such as nucleoli in eukaryotes.

177 Adenovirus protein V associates with nucleoli in infected cells.

178 demonstrate that Misu translocates from the nucleoli in interphase to the spindle in mitosis as an R

179 ylated histone H3 that normally circumscribe nucleoli in oocytes and early embryos, respectively.

180 er of nucleus, and failed to be cleared from nucleoli in response to camptothecin treatment.

181 that is required for NBS1 relocalization to nucleoli in response to DNA damage.

182 xhibited trafficking from subnuclear dots to nucleoli in response to heat-, proteotoxic- or transcrip

183 espectively, and traffic from these sites to nucleoli in response to stress signaling.

184 ive analysis of the molecular composition of nucleoli in skin fibroblasts and iPSC derived from them.

185 escing phases that are remarkably similar to nucleoli in vivo.

186 Alterations in nucleoli, including increased numbers, increased size, a

187 e, we demonstrate that these RNAs traffic to nucleoli independently of one another, because U4 snRNA

188 nucleoli, whereas DmNopp140 partitions HeLa nucleoli into phase-light and phase-dark regions.

189 Sequestration of MDM2 by ARF in the nucleoli is not essential for a p53 response in REF52 ce

190 oteins identified in a proteomic analysis of nucleoli isolated from Arabidopsis cell culture.

191 dation/alkylation in mammalian cells; within nucleoli it interacts with nucleophosmin and rRNA throug

192 nternalization and decrease in the number of nucleoli; (iv) increase in the number of pericentromeric

193 These nucleoli lacked significant autoproteolysis, but many nu

194 The broad autoantigenicity of the nucleoli may attribute to their poor autoproteolysis, ca

195 Conversely, the presence of active nucleoli may determine the potential for neurorepair.

196 This suggests that the disrupted nucleoli may provide a platform for L5- and L11-dependen

197 tumor, the mean of the 10 longest and widest nucleoli (MLN) was calculated.

198 ynthesized ribosomal proteins accumulated in nucleoli more quickly than other nucleolar components.

199 for anti-RNAP I/III antibodies clearly stain nucleoli, nucleolar staining is inconsistent and cannot

200 ins, DNA, RNA, and lipids were determined in nucleoli, nucleoplasmic transcription sites, nuclear spe

201 Nucleostemin (NS) is expressed in the nucleoli of adult and embryonic stem cells and in many t

202 lysis to identify protein changes within the nucleoli of Arf-deficient mouse cells.

203 d corneal fibroblasts, ZO-1 was localized to nucleoli of both serum-starved and serum-treated cells.

204 -1 (IRS-1) can translocate to the nuclei and nucleoli of cells and bind UBF1.

205 The Raman maps show the nucleus and the nucleoli of cells as well as subcellular organization in

206 Nucleoli of cells depleted of NF45 and NF90 have altered

207 1 protein (which localizes to the nuclei and nucleoli of cells) interacts with both IRS-1 and the SV4

208 a novel protein, nucleostemin, found in the nucleoli of CNS stem cells, embryonic stem cells, and se

209 Localization of ZO-1 to nucleoli of corneal and 293T fibroblasts under prolifera

210 ntrast, it colocalized with nucleolin in the nucleoli of corneal fibroblasts after serum-starved cell

211 In Xenopus somatic cell nuclear cloning, the nucleoli of donor nuclei rapidly and almost completely d

212 fferent nucleolar proteins assemble into the nucleoli of Drosophila melanogaster embryos.

213 lysis for Raman spectra measured in the same nucleoli of HeLa cells before and after fixation by eith

214 -fluorescein stains the cytosol, nuclei, and nucleoli of HeLa cells under conditions where the Ru-oct

215 MeCP2, are localized both in the nuclei and nucleoli of HepG2 cells.

216 ucleolar RNA-TAR decoy that localizes to the nucleoli of human cells and colocalizes in the nucleolus

217 In the nucleoli of human embryonic stem cells, methylated LIN28

218 (ANG) protein, which entered the nuclei and nucleoli of infected cells and stimulated 45S rRNA gene

219 also observed an accumulation of Gag in the nucleoli of infected cells derived from mammary gland tu

220 Similarly, Us11 does not accumulate in the nucleoli of infected cells that overexpress PAT1.

221 nt upon the interaction of Gag and L9 in the nucleoli of infected cells.

222 NA-encoding units (rDNA units) that form the nucleoli of insects.

223 eoli, and PP1gamma is highly concentrated in nucleoli of interphase cells.

224 romolecules and protein conformations in the nucleoli of iPSC and human embryonic stem cells (hESC) w

225 cleolar disassembly, FRGY2a localized to the nucleoli of isolated nuclei and was capable of disassemb

226 observed a strong Rev-Rev interaction in the nucleoli of living cells.

227 TPase activity and that it is present within nucleoli of most larval and adult cells.

228 Our earlier report that BIG1 concentrated in nucleoli of serum-starved HepG2 cells prompted us to ide

229 ids and protein conformations indicates that nucleoli of skin fibroblasts contain similar subsets of

230 embranes and delivered the antibodies to the nucleoli of the cells.

231 of nucleolar components, which condense into nucleoli only above a threshold concentration.

232 otein but does not affect U6 localization to nucleoli or Cajal bodies.

233 e staining patterns partially overlap in the nucleoli, promotes ATF5 protein degradation through prot

234 interaction of IRS-1, PI3-K, and UBF1 in the nucleoli provides one of the mechanisms for the effects

235 ed in over 4500 human proteins from purified nucleoli, providing enhanced coverage of the nucleolar p

236 al and proteomics approaches to characterize nucleoli purified from cultured human and mouse cells.

237 Proteins within nucleoli regulate ribosome biosynthesis and p53-dependen

238 mbrane, in the cytoplasm, and in the nucleus/nucleoli respectively.

239 associated with heterochromatic regions and nucleoli, respectively, where yeast Sir2 functions; 2) S

240 f POG to the perinuclear localization or the nucleoli, respectively.

241 i) pathway components displayed disorganized nucleoli, ribosomal DNA (rDNA) and satellite DNAs.

242 ymerase III (Pol III)-transcribed genes with nucleoli seems to be an evolutionarily conserved propert

243 Counts of their nucleoli show that about 120,000 globuli cells supply ea

244 umulated multiple kinetoplasts, flagella and nucleoli, similar to the effects of RNAi-dependent knock

245 Recent experiments on nucleoli suggest that their dynamic behavior is liquid-l

246 ei and was capable of disassembling purified nucleoli, suggesting a direct interaction between FRGY2a

247 d promote localization of box C/D snoRNPs to nucleoli, suggesting a role in rRNA maturation.

248 ted TDP-43 was specifically recruited to the nucleoli, suggesting that p-T153/Y155 regulates a previo

249 Distinct localization to the nucleoli supports the evidence that TaxREB107 is a ribos

250 In addition to classical nucleoli that assemble at the transcriptionally active n

251 asmic shuttling protein, mainly localized at nucleoli, that plays a key role in several cellular func

252 asmic shuttling protein, mainly localized at nucleoli, that plays a number of functions in ribosome b

253 l CRs toward both the nuclear border and the nucleoli, the former being enhanced in nonproliferating

254 s from highly purified preparations of human nucleoli, the most prominent nuclear organelle.

255 markers for organelles or regions, including nucleoli, the nuclear envelope, nuclear speckles, centro

256 mponents of membrane-less organelles such as nucleoli, the nuclear pore complex and stress granules.

257 ructures of the interphase nucleus including nucleoli, the site of ribosome biogenesis.

258 t mutually exclusive) hypothesis centered on nucleoli: the specialized intranuclear domains within wh

259 red region prevents TOP1 binding to sites in nucleoli, thus driving it to bind in the nucleoplasm; an

260 e various histologic methodologies for using nucleoli to assess the malignant potential of uveal mela

261 In particular, we found the nucleoli to be stiffer than both the nuclear envelope (p

262 However, C1q targets at these nucleoli to cause C1 protease activation and the cleavag

263 Nevertheless, segregation of nucleoli to daughter cells still occurs, indicating the

264 ing resulting in delocalization of TOP1 from nucleoli to nucleoplasm.

265 Co-migration of RNase H1 and R-loops from nucleoli to perinucleolar ring structures was observed u

266 ction and recruitment of heterochromatin and nucleoli to the nuclear lamina facilitates the folding o

267 raction of available L22 is relocalized from nucleoli to the nucleoplasm in EBV-infected cells.

268 localization of NPM1 and BER components from nucleoli to the nucleoplasm, and cellular experiments ta

269 viously been demonstrated that AgNOR-stained nucleoli, unlike H&E-stained nucleoli, can be captured a

270 In addition, c-Myc accumulates in nucleoli upon inhibition of the proteasome, suggesting n

271 l transcription units in Pisum sativum plant nucleoli using a novel labelling technique.

272 ion of newly expressed NHPX from speckles to nucleoli was dependent on RNA polymerase II transcriptio

273 nt accumulation of NHPX in speckles prior to nucleoli was observed in multiple cell lines, including

274 Fluorescence in nucleoli was used to sort nuclei from D1R- or D2R-expres

275 frame 1 (ORF1) in cell nuclei, especially in nucleoli, was detected by IFA.

276 The isolated nucleoli were broadly reactive with SLE patient autoanti

277 lular fractionation, virions accumulating in nucleoli were found to retain infectivity in secondary i

278 When nucleoli were isolated from non-apoptotic cells, C1q als

279 Nucleoli were isolated to homogeneity and structurally d

280 dering a recent finding that, in dead cells, nucleoli were targeted by C1q and two nucleolar autoanti

281 even samples had to be discarded because the nucleoli were unmeasurable.

282 onal proteasome, and E2F1 was relocalized to nucleoli when coexpressed with p19ARF.

283 These data show that mTORC1 is located in nucleoli where it acts to regulate events involved in ri

284 found in different subcellular compartments-nucleoli, where it associates with ribosomal RNA and is

285 ate 1 (IRS-1) translocates to the nuclei and nucleoli, where it binds to the upstream binding factor

286 mponents raptor and mTOR are both present in nucleoli, where they may regulate rRNA maturation events

287 ary for the localization of c-Myc protein to nucleoli, whereas c-Myc nucleolar localization is indepe

288 eLa cells, DmNopp140-RGG localizes to intact nucleoli, whereas DmNopp140 partitions HeLa nucleoli int

289 primarily nuclear and largely excluded from nucleoli, whereas PP1gamma and to a lesser extent PP1bet

290 abidopsis thaliana are present within sorted nucleoli, whereas silenced rRNA genes are excluded.

291 GFP fusion protein localized specifically to nucleoli, whereas the N-terminal sequence of SelH fused

292 antly increased 18S expression, and enlarged nucleoli which were reduced in number per cell.

293 Nucleolin is a marker of nucleoli, which are membrane-less regions involved in re

294 53 by release of ribosomal proteins from the nucleoli, which bind to MDM2 and inhibit p53 degradation

295 sulting in misdirection of telomerase RNA to nucleoli, which prevents telomerase from elongating telo

296 Incubation of nucleoli with C1 caused degradation of the nucleolar pro

297 Fluorescent labeling of budding yeast nucleoli with CDC14-GFP revealed that a split rDNA locus

298 firmed that nucleolin localizes primarily to nucleoli with RNA polymerase I, we demonstrated that nuc

299 ions, profile counts in paraffin sections of nucleoli within a nucleus were 36% greater in 100-day-ol

300 telomerase mislocalizes from Cajal bodies to nucleoli within the iPSCs.