ライフサイエンスコーパス: nucleoli

1 y, although slower diffusion was observed in nucleoli.

2 in vitro exhibit smaller and more elongated nucleoli.

3 distribution of MageB2 protein includes the nucleoli.

4 reduces alpha-satellite DNA association with nucleoli.

5 sed in mammalian cells, these variants bound nucleoli.

6 lear membrane; they exhibited small punctate nucleoli.

7 pheries of both replication compartments and nucleoli.

8 ting its translocation from nucleoplasm into nucleoli.

9 of MDM2 and translocation of DeltaNp63 into nucleoli.

10 ould not confirm localization of midnolin in nucleoli.

11 meric clusters, chromosomal territory 3, and nucleoli.

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

13 , and lipids in the molecular composition of nucleoli.

14 NA-containing NORs that are dissociated from nucleoli.

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

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

17 eudosubstrate that directly recruits Fbw7 to nucleoli.

18 y to pericentric heterochromatin-surrounding nucleoli.

19 istributed throughout nuclei and enriched in nucleoli.

20 in large nuclear aggregates that often ring nucleoli.

21 sors, and fibrillarin does not accumulate in nucleoli.

22 repeats of rDNA coding sequences within the nucleoli.

23 bserved accumulation of SUMO proteins within nucleoli.

24 e only phosphorylation site, retains FEN1 in nucleoli.

25 es in late mitosis before the reformation of nucleoli.

26 Pes1 was typically restricted to nuclei and nucleoli.

27 e with its targeting and localization to the nucleoli.

28 o a lesser extent PP1beta concentrate in the nucleoli.

29 endogenous proteins appear within mammalian nucleoli.

30 ther lack an organized nucleolus or have two nucleoli.

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

32 s but also necessary for localizing ADAR2 to nucleoli.

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

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

35 id not localize bulk sumoylated molecules to nucleoli.

36 plicing positioned at varying distances from nucleoli.

37 asmic locations, Lsm proteins are present in nucleoli.

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

39 rotein nucleostemin, and enlarged, malformed nucleoli.

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

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

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

43 t IFI16 was localized in the nucleoplasm and nucleoli.

44 pair in human cells colocalize with Mus81 in nucleoli.

45 lization of RGS6 proteins from such sites to nucleoli.

46 encing of chromatin associated with purified nucleoli.

47 ormation of membrane-less organelles such as nucleoli.

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

49 ion coupled with exercise also display small nucleoli.

50 vitro and for localization within mammalian nucleoli.

51 ssociation of Pol III-transcribed genes with nucleoli.

52 ~60% of which were detected in the H1 mutant nucleoli.

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

54 led within major nuclear compartments called nucleoli(1,2).

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

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

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

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

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

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

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

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

63 logical features, such as prominent/abundant nucleoli and a colony with a tightly packed appearance a

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

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

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

67 We also show that EloA localizes to the nucleoli and associates with RNA polymerase I transcribe

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

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

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

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

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

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

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

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

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

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

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

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

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

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

82 In cells, poly(PR) DPRs disperse NPM1 from nucleoli and entrap rRNA in static condensates in a DPR-

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

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

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

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

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

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

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

90 an emerging body of evidence suggesting that nucleoli and NF-kappaB signalling converge at multiple l

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

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

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

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

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

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

97 s dominate endogenous LLPS, and give rise to nucleoli and other condensates that do not exhibit a fix

98 les and stress granules in the cytoplasm and nucleoli and paraspeckles in the nucleus.

99 tury from both animal and plant cells, human nucleoli and particularly the five human nucleolus organ

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

101 tes DDX21, an RNA helicase that localizes to nucleoli and promotes rDNA transcription when ADP-ribosy

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

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

104 umerous genomic regions with nuclear lamina, nucleoli and surface of chromosomes in the same, single

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

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

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

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

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

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

111 ng viral replication and its localization to nucleoli and viral replication centers provide further i

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

128 The nucleoli are abundant with autoantigens.

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

130 Nucleoli are prominent nuclear structures assembled and

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

132 Nucleoli are rich in nucleolin, a potent transcription f

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

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

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

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

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

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

139 In contrast, Type II NADs associate with nucleoli but do not overlap with LADs.

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

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

142 s, identify disease-associated disruption of nucleoli by noncoding RNAs, and establish locus-targeted

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

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

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

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

147 Intracellular bodies such as nucleoli, Cajal bodies and various signalling assemblies

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

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

150 number of membraneless organelles, including nucleoli, Cajal bodies, P-bodies, and stress granules, e

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

152 oly(GR) and poly(PR), infiltrate liquid-like nucleoli, co-localize with the nucleolar protein nucleop

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

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

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

156 Nucleoli continued to diminish in postmitotic cells foll

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

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

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

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

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

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

163 Ds allow time-lapse imaging of chromatin and nucleoli during cell division and Caenorhabditis elegans

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

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

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

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

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

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

170 At the same time, nucleoli exhibited a significantly higher mass density t

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

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

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

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

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

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

177 -PK, but not other cNHEJ factors, resides in nucleoli in an rRNA-dependent manner and is co-purified

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

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

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

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

182 the impact of the surrounding nucleoplasm on nucleoli in living cells.

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

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

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

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

187 Furthermore, while FAM111A localized to nucleoli in uninfected cells in a cell cycle-dependent m

188 Here, we study the motion of human nucleoli in vivo, while monitoring the shape of the nucl

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

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

191 nt delocalization of paraspeckle proteins to nucleoli is an early event in PS-ASO toxicity, followed

192 on of heterodimer proteins P54nrb and PSF to nucleoli is an early event in the pathway that explains

193 NBS1-dependent recruitment of TOPBP1 in the nucleoli is required for inhibition of ribosomal RNA syn

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

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

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

197 These nucleoli lacked significant autoproteolysis, but many nu

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

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

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

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

202 Gelled nucleoli no longer coalesce and relax into spheres but n

203 oteins in major nuclear organelles including nucleoli, nuclear speckles, Cajal bodies, as well as in

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

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

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

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

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

209 -1 (IRS-1) can translocate to the nuclei and nucleoli of cells and bind UBF1.

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

211 Nucleoli of cells depleted of NF45 and NF90 have altered

212 1 protein (which localizes to the nuclei and nucleoli of cells) interacts with both IRS-1 and the SV4

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

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

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

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

217 ion in the cytoplasm, and elevated levels in nucleoli of germlings.

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

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

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

221 ass densities of cytoplasm, nucleoplasm, and nucleoli of human cell lines, challenged by various pert

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

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

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

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

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

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

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

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

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

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

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

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

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

235 ccumulation of Ran-GTP, which accumulates at nucleoli of transfected or infected cells, thus perturbi

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

237 that RNA polymerase II (Pol II) inside human nucleoli operates near genes encoding rRNAs to drive the

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

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

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

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

242 l a strong correlation between disruption of nucleoli, reduced association of RAG1 with a nucleolar m

243 of RAG1, required for efficient egress from nucleoli, reduces recombination activity.

244 Proteins within nucleoli regulate ribosome biosynthesis and p53-dependen

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

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

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

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

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

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

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

252 consistent with phase separation, including nucleoli, stress granules, Cajal bodies, and numerous ad

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

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

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

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

257 rules of engagement between these p-arms and nucleoli takes on added significance as describing the t

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

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

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

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

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

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

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

265 Nucleoli, the sites of ribosome biogenesis and the large

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

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

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

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

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

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

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

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

274 While unprocessed POLGARF localizes to the nucleoli together with its interacting partner C1QBP, se

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

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

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

278 The isolated nucleoli were broadly reactive with SLE patient autoanti

279 Although nucleoli were found to behave like liquid droplets, many

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

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

282 Nucleoli were isolated to homogeneity and structurally d

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

284 is reduced in the cytoplasm and increased in nucleoli when Y RNAs are absent.

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

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

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

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

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

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

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

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

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

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

295 53 by release of ribosomal proteins from the nucleoli, which bind to MDM2 and inhibit p53 degradation

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

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

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

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

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