ライフサイエンスコーパス: intranuclear

1 ed to chromosomes, and in interphase, it was intranuclear.

2 ow macrophage precursors and that osteoclast intranuclear abundance is specifically increased by RANK

3 ytoplasmic transport (Gle1 and RanGAP1), and intranuclear accumulation of mRNA.

4 egion-specific aggregate pathology marked by intranuclear accumulation of the mutant Atxn3 protein, a

5 tion of Wnt coreceptor LRP6 and beta-catenin intranuclear accumulation.

6 ve enabled the visualization of a variety of intranuclear activities, from chromosome dynamics to gen

7 s progressive muscle weakness accompanied by intranuclear aggregates and TUNEL-stained nuclei in skel

8 ated PABPN1 proteins accumulate as insoluble intranuclear aggregates in muscles of OPMD patients.

9 The formation of intranuclear aggregates is not necessary for in vitro ce

10 ppUL69 localized to intranuclear aggregates that did not overlap with viral

11 solubility in the lens and forms substantial intranuclear aggregates that disrupt the denucleation pr

12 hanges are observed without the formation of intranuclear aggregates.

13 Doxy was shown to attenuate aberrant intranuclear aggregation and toxicity of misfolded prote

14 We thus propose that intranuclear aggregation of FUS triggered by a subset of

15 ytoplasmic and nuclear ubiquitin levels, and intranuclear and cytoplasmic aggregates that were immuno

16 tingtin protein (htt), formation of neuronal intranuclear and cytoplasmic inclusions, and neuronal dy

17 bles from its partners and localizes to both intranuclear and cytoplasmic protein quality control (PQ

18 variants deficient in IPO5 binding remained intranuclear and exhibited decreased levels, which were

19 with insoluble neuronal inclusions, usually intranuclear, and neuronal death.

20 In ES cells, Chk2 kinase is not intranuclear as in somatic cells but is sequestered at c

21 The goal of this review is to outline these intranuclear assembly steps and illustrate potential and

22 t was possible to infer the targets of their intranuclear axons (projection cells vs inhibitory inter

23 Both forms were associated with intranuclear B and C capsids, yet only the 58-kDa polype

24 These intracellular and intranuclear bacteria reside in specialized cells in sev

25 t of isoform NFATc3) and formation of NFATc1 intranuclear bodies independent of calcineurin.

26 rodlets of Roncoroni, are poorly understood intranuclear bodies originally identified within neurona

27 olonged nuclear Ca(2+) transients and slowed intranuclear Ca(2+) diffusion.

28 revented nuclear mGlu5-mediated increases in intranuclear Ca2+.

29 2+)]i release was followed by an increase in intranuclear calcium and the depolarization of both the

30 During their progression from intranuclear capsids to mature trilaminar virions, herpe

31 .5 kDa, is transported to the nucleus, binds intranuclear capsids, and is converted to 58 kDa at some

32 ed that this DNA was in fact packaged within intranuclear capsids, but these capsids failed to egress

33 oscopy and Western blot analysis of purified intranuclear capsids.

34 120-kDa MCP fragment; and reduced numbers of intranuclear capsids.

35 ression of NHERF2 in sympathetic neurons (by intranuclear cDNA injections) does not affect the extent

36 ence of the ORF66 kinase, matrin 3 displayed intranuclear changes, while matrin 3 showed a pronounced

37 ral anchoring points contributing locally to intranuclear chromosome organization.

38 e mutant, RIIbeta(S114A), did not form these intranuclear clusters as well as wild-type RIIbeta, and

39 4 (pRIIbeta) and localization of pRIIbeta in intranuclear clusters.

40 comparative analyses of the internuclear and intranuclear coherence between bipolar derivations of LF

41 local field potentials in the basal ganglia, intranuclear coherence, and, thus, lateral functional co

42 storage in the nuclear envelope (NE) to the intranuclear compartment (INC), the mechanisms of Ca(2+)

43 n founder cells, Aret accumulates in a novel intranuclear compartment that we termed the Bruno body,

44 ylation of the triple serine motif regulates intranuclear compartmentalization of murine Olig2.

45 lear retention of Ctn RNA, they modulate its intranuclear compartmentalization.

46 ll nucleus and differentially associate with intranuclear compartments.

47 aled the general behavior of the nucleus and intranuclear components, direct visualization and estima

48 Intranuclear delivery of a specific antisense oligonucle

49 potential as a mediator of intracellular and intranuclear delivery of p53 for prevention and treatmen

50 suggest that peptide conjugation may enhance intranuclear delivery of reagents designed to bind to ch

51 le because of the need for intracellular and intranuclear delivery of targeting and therapeutic moiet

52 The identification of an effective intranuclear delivery vehicle and pathway for the transp

53 elivery system could boost intracellular and intranuclear delivery, thereby circumventing drug efflux

54 The disease is characterized by intranuclear deposits consisting primarily of PABPN1.

55 Intranuclear diffusion of a functional c-Myc-eGFP, expre

56 as9-sgRNAs, it was possible to determine the intranuclear distance between loci on different chromoso

57 o acid substitution (Cys19Gly) alters ORF61p intranuclear distribution and abolishes ORF61p-mediated

58 as no detectable effect on nuclear import or intranuclear distribution of hsTAF5 and hsTAF12.

59 challenged with 100-200 mm sorbitol, and the intranuclear distribution of nucleolin was monitored by

60 thesis centered on nucleoli: the specialized intranuclear domains within which ribosomes are assemble

61 nd performed a comprehensive analysis on the intranuclear dwell times of four steroid receptors and a

62 ase has indicated an unanticipated degree of intranuclear dynamics of both its RNA and protein subuni

63 the mechanism of this resistance, we studied intranuclear dynamics of hVDR and hRXRalpha-tagged const

64 ng protein-5 (IGFBP-5) has IGF-1-independent intranuclear effects that are poorly defined.

65 he mechanisms whereby IGFBP-5 and FLNa exert intranuclear effects.

66 used as a biophysical strategy to probe the intranuclear environment.

67 s of estrogens are mediated via two distinct intranuclear estrogen receptor (ER) proteins, ERalpha an

68 eviously showed that apoB mRNA editing is an intranuclear event.

69 r regulation of gene transcription and other intranuclear events.

70 Intranuclear expression of SOX2 marks the clonogenic CD1

71 ely, activate cell surface FGF receptors and intranuclear FGFR1, to determine the roles of membrane F

72 ncoding full-length NSs completely abrogated intranuclear filament formation in infected cells.

73 t virus encoding the NSs core domain induced intranuclear filaments, suggesting it contains all essen

74 nvolved in retaining cellular transcripts in intranuclear foci and can regulate the export of mRNA to

75 rts differential effects on the formation of intranuclear foci by ATR and replication protein A, impl

76 We have found that hTR accumulates within intranuclear foci called Cajal bodies in all typical tum

77 e abnormalities and induced the formation of intranuclear foci in the primary keratinocytes expressin

78 at ATRIP is required for ATR accumulation at intranuclear foci induced by DNA damage.

79 demonstrated abnormal nuclear envelopes with intranuclear foci of lamins in cardiac cells expressing

80 lamina at prophase, and also transiently to intranuclear foci.

81 ng to ATR and localization to damage-induced intranuclear foci.

82 erinucleolar sites associated with lamin A/C intranuclear foci.

83 linked and unlinked, coalesce into discrete intranuclear foci.

84 us Nup98 that lead to mislocalization of the intranuclear fraction of Nup98, but do not alter the lev

85 Intranuclear free Zn(2+) sparks caused by reactive oxyge

86 transfer, and we found that the formation of intranuclear Gag complexes was dependent on the NC domai

87 In FIV-infected feline cells, some intranuclear Gag was detected in the steady state withou

88 entation allowed the direct visualization of intranuclear Gag-Gag dimers.

89 Intranuclear gamma-crystallin aggregates, incomplete den

90 SMN protein levels and intranuclear gems also were significantly increased in t

91 Most occur in conjunction with intranuclear genomic rearrangements, and the features of

92 2 ALS patients revealed disease-specific (1) intranuclear GGGGCCexp RNA foci, (2) dysregulated gene e

93 nuclear O(2)(.-) production, suggesting that intranuclear glucose-6-phosphate dehydrogenase (G6PD) ca

94 earts was essential for targeting RyR2 to an intranuclear Golgi apparatus and promoted the intracellu

95 matin in mouse cells and sites of DAPI-dense intranuclear heterochromatin in human and hamster cells

96 Mitotic cells have a distinctive intranuclear heterochromatin-free "spindle tunnel" with

97 Restoration of intranuclear HIF-1alpha to these areas was achieved by h

98 al DNA, which would obscure the detection of intranuclear HIV-1 genomes.

99 inucleotide binding permits CtBP1 to form an intranuclear homodimer through a Trp(318) switch, creati

100 ntage of htt-positive nuclei and the size of intranuclear htt aggregates were reduced by the CaM-frag

101 n-containing interneurons, inflammation, and intranuclear huntingtin aggregates.

102 Hand2 is developmentally regulated and is intranuclear in precursors but cytoplasmic in neurons.

103 lly leading to deposition of cytoplasmic and intranuclear inclusion bodies containing htt.

104 duct A or 1 (cp-A/1), form intracellular and intranuclear inclusion bodies in the brains of patients

105 c of pan-cellular HD mouse models, including intranuclear inclusion bodies, motor impairment, and cha

106 Striatal neuronal intranuclear inclusion burden was similar between HD kno

107 , nuclear mutant huntingtin accumulation and intranuclear inclusion formation.

108 hallmark of FXTAS is the ubiquitin-positive intranuclear inclusion found in neurons and astrocytes i

109 he neuropathological hallmark of FXTAS is an intranuclear inclusion, present in both neurons and astr

110 colytic fibres, containing a large number of intranuclear inclusions (INIs).

111 arly as 9 weeks of age and striatal neuronal intranuclear inclusions (NIIs) by 20 weeks.

112 Neuronal intranuclear inclusions (NIIs) characteristically occur.

113 other than widespread ubiquitinated neuronal intranuclear inclusions (NIIs).

114 l dysregulation and accumulation of neuronal intranuclear inclusions (NIIs).

115 ed extensively convoluted nuclear envelopes, intranuclear inclusions and chromatin clumps in cardiomy

116 Striatal and cortical intranuclear inclusions and cytoplasmic aggregates of mu

117 ve neuronal cytoplasmic inclusions, neuronal intranuclear inclusions and neurites were recorded and f

118 hole mount immunohistochemistry, to identify intranuclear inclusions and quantify subsets of enteric

119 Formation of fibrillar intranuclear inclusions and related neuropathologies of

120 hich is found in the neuronal and astrocytic intranuclear inclusions associated with the disorder.

121 ation) CGG repeat, we have demonstrated that intranuclear inclusions can be formed in both primary ne

122 ure death that are characterized by abnormal intranuclear inclusions composed of TDP-43 and fused in

123 Whether intranuclear inclusions containing DNA damage response (

124 Ubiquitin-positive intranuclear inclusions have also been found in the neur

125 Intranuclear inclusions have also been reported in the n

126 FTLD with ubiquitin-positive cytoplasmic and intranuclear inclusions in all PGRN mutation carriers.

127 ds to determine the pathological features of intranuclear inclusions in astroglia and neurons.

128 ebral white matter and (iii) the presence of intranuclear inclusions in both brain and spinal cord.

129 the number of CGG repeats and the numbers of intranuclear inclusions in both neurons and astrocytes,

130 1C2-positive intranuclear inclusions in cerebellar Purkinje and brain

131 The morphology of intranuclear inclusions in CGG KI mice was compared to t

132 st time, de novo formation of ChHV5-positive intranuclear inclusions in cultured green turtle cells,

133 complete striatal degeneration and rarity of intranuclear inclusions in HD, and the fact that mice ex

134 rectly relevant to the formation of neuronal intranuclear inclusions in Huntington's disease.

135 a syndrome typically have cerebellar ataxia, intranuclear inclusions in neurons and astrocytes, as we

136 allmark of the disease is ubiquitin-positive intranuclear inclusions in neurons and astrocytes.

137 isease is the presence of ubiquitin-positive intranuclear inclusions in neurons and in astrocytes.

138 FXTAS is the presence of ubiquitin-positive intranuclear inclusions in neurons and in astroglia.

139 The models exhibit the presence of intranuclear inclusions in Purkinje neurons, Purkinje ne

140 tion of FUS but facilitated the formation of intranuclear inclusions in rat hippocampal neurons with

141 logy and by the late development of neuronal intranuclear inclusions in spinal neurons.

142 que pathological feature - appearance of the intranuclear inclusions in the neurons and astrocytes, i

143 , and in some familial cases UBQ-ir neuronal intranuclear inclusions of a lentiform appearance.

144 Ubiquitin-positive intranuclear inclusions were also present in protoplasmi

145 clear mutant huntingtin and the formation of intranuclear inclusions were fastest in the C57BL/6 back

146 In CGG KI mice, ubiquitin-positive intranuclear inclusions were found in neurons (e.g., pyr

147 In female CGG KI mice, ubiquitin-positive intranuclear inclusions were found in neurons and astrog

148 in sarcoma-positive neuronal cytoplasmic and intranuclear inclusions were found in the hippocampal gr

149 axia, weight loss, premature death, neuronal intranuclear inclusions, and decreased tyrosine hydroxyl

150 ere distinct and temporally dissociated from intranuclear inclusions, and disappeared rapidly after c

151 mmunolocalized to both nuclear membranes and intranuclear inclusions, fluorescent detection of NADPH-

152 o induce the formation of ubiquitin-positive intranuclear inclusions, which also stain positive for t

153 both grey and white matter and also neuronal intranuclear inclusions.

154 icularly visceral neuropathies with neuronal intranuclear inclusions.

155 rs, including some characterized by neuronal intranuclear inclusions.

156 ith alterations in the formation of neuronal intranuclear inclusions.

157 eristic lentiform ub-immunoreactive neuronal intranuclear inclusions.

158 e, particularly in those cases with neuronal intranuclear inclusions.

159 gender-specific motor deficits, and neuronal intranuclear inclusions.

160 transglutaminase 2 and with huntingtin in HD intranuclear inclusions.

161 the proteasome after it is incorporated into intranuclear inclusions.

162 r neuron loss, with polyQ-AR accumulation in intranuclear inclusions.

163 l neurons contained ubiquitin-immunoreactive intranuclear inclusions.

164 athway by which this occurs involves direct, intranuclear interaction of the photoactivated phy molec

165 ved N-terminal region of pUL50 determine its intranuclear interaction with pUL53.

166 During interphase, the lamins form an intranuclear intermediate filament network that must be

167 canceri's adaptation to intranuclear life is underpinned by the expansion of tra

168 hibition of poly(ADP-ribosylation) prevented intranuclear localization of apoptosis-inducing factor a

169 The lack of SUMOylation did not affect the intranuclear localization of IE1-72 kDa, including its a

170 ered that mutant Nna1 dramatically increases intranuclear localization of lysyl oxidase propeptide, w

171 on of oxidative stress markers, and enhanced intranuclear localization of pancreatic and duodenal hom

172 ic evidence demonstrates the requirement for intranuclear localization of regulatory complexes that f

173 RXR alpha C terminus may play a role in the intranuclear localization of RXR alpha.

174 Because the intranuclear localization of the UL9 protein, along with

175 we show an explicit relationship between the intranuclear localization of various chromosome segments

176 an aberrant Ad E2 DNA-binding protein (DBP) intranuclear localization pattern and an apparent failur

177 This intranuclear localization remains throughout adulthood a

178 shown in cells by coimmunoprecipitation, and intranuclear localization studies using confocal microsc

179 ingle amino acid substitution that abrogates intranuclear localization was introduced in the AML1 sub

180 It controls the intranuclear localization, stability, and DNA repair fun

181 Thus, C/EBPalpha conformation varies with intranuclear location and with cellular environment.

182 The intranuclear location of genomic loci and the dynamics o

183 of this segregation by modulating either the intranuclear location of the MyoD gene or TAF3 protein l

184 The intranuclear mechanisms that signal apoptosis after DNA

185 ogenesis, composition, and function of these intranuclear membrane cisternae are unknown.

186 are sufficient to traffic fusion proteins to intranuclear membranes and the ODV envelope during infec

187 ects in cell division and a proliferation of intranuclear membranes derived from the nuclear envelope

188 then is incorporated into the virus-induced intranuclear membranes.

189 um to the nuclear envelope and viral-induced intranuclear membranes.

190 action of cells with diffuse, perinuclear or intranuclear mHTT changed in parallel with decreasing mo

191 receptor that registers BMP signaling as the intranuclear migration of Smad2, and as the transcriptio

192 Mod20p is not required for intranuclear mitotic spindle assembly, although it is re

193 tubule nucleation ceases simultaneously with intranuclear mitotic spindle assembly.

194 n of AML1 with ETO or MTG16 exhibits reduced intranuclear mobility compared with wild-type AML1 or ei

195 own that PAX5-PML fusion protein has reduced intranuclear mobility compared with wild-type PAX5.

196 ting prolonged nuclear retention and reduced intranuclear mobility especially following ligand stimul

197 By measuring the abundance and intranuclear mobility of an upstream transcription facto

198 Using FRAP, we demonstrated that the intranuclear mobility of each X-RAR alpha was reduced co

199 Furthermore, although the intranuclear mobility of GFP-Stat3alpha was rapid and in

200 and increased with cytokine stimulation, the intranuclear mobility of GFP-Stat3beta in unstimulated c

201 (CC) of PML was responsible for the reduced intranuclear mobility of PAX5-PML.

202 Prolonged nuclear retention, but not reduced intranuclear mobility, mapped to the CT7 domain of Stat3

203 nged nuclear retention but did not alter its intranuclear mobility.

204 s U1-small nuclear RNA is a highly conserved intranuclear molecular complex involved in splicing pre-

205 d at NaCl concentrations within the reported intranuclear monovalent cation concentration range, and

206 l stimulation: an initial event of increased intranuclear movement followed by a regime of intranucle

207 The role of the intranuclear movement of chromatin in gene expression is

208 ntranuclear movement followed by a regime of intranuclear movements that reflect the dose of applied

209 Thus, applied extracellular forces stimulate intranuclear movements, resulting in repositioning of nu

210 cytoplasmic MTs arise from spindle or other intranuclear MTs that exit the nucleus.

211 e 85 years; microscopic examination revealed intranuclear neuronal and astrocytic inclusions, in acco

212 FXTAS is characterized by ubiquitin-positive intranuclear neuronal inclusions, raising the possibilit

213 a proinflammatory state with an increase in intranuclear NF-kappaB binding, a decrease in IkappaB-be

214 e T cells lacking CCR5 had reduced levels of intranuclear NFAT following activation.

215 Intranuclear nuclear factor kappaB (NF-kappaB) binding a

216 ntake has been shown to cause an increase in intranuclear nuclear factor-kappa B and a decrease in in

217 mutant-infected cells showed the presence of intranuclear nucleocapsids and the absence of cytoplasmi

218 cation of the DExH/D-box helicase DHX9 as an intranuclear Nup98 binding partner.

219 We found that the intranuclear organization and nucleosome interactions of

220 Our findings suggest that fidelity of Runx2 intranuclear organization is necessary for expression of

221 Correct intranuclear organization of chromosomes is crucial for

222 e nucleolus, possibly to avoid disruption of intranuclear organization.

223 Intranuclear p21 accumulates in Pttg-null aneuploid GH-s

224 crosporidium saccamoebae [Rozellomycota], an intranuclear parasite of amoebae.

225 y immunoblotting and increased the number of intranuclear particles called gems.

226 ese data suggest that an initial step in the intranuclear path of some mRNAs is passage from the gene

227 eby ebselen prevents apoptosis and preserves intranuclear Pdx-1 and MafA, which, in turn, is a likely

228 mRNA editing by shuttling apobec-1 from the intranuclear perinucleolar compartment to the cytoplasm.

229 with GIRK1+GIRK2 (Kir3.1 + 3.2) channels by intranuclear plasmid injections into cultured rat sympat

230 posite strand, ATXN8OS) and the discovery of intranuclear polyglutamine inclusions suggests SCA8 path

231 ection is established by the formation of an intranuclear pool of covalently closed circular DNA (ccc

232 ther our data uncover a previously neglected intranuclear pool of the Y-complex that may underscore a

233 The intranuclear position of many genes has been correlated

234 pendent transcription was independent of the intranuclear position of the gene, but the nucleolar rec

235 summary, TFIIIC and Mps3 together direct the intranuclear positioning of a new class of S. cerevisiae

236 onferred by the HD is critical for the final intranuclear positioning of the metastable complex.

237 ot recruit RNA polymerase III, show specific intranuclear positioning.

238 We used live-cell imaging to determine the intranuclear positions of 13 Pol III-transcribed genes.

239 We determined intranuclear positions of 15 loci distributed every ~100

240 Accordingly, we examined whether the intranuclear positions of Bdnf and Trkb genes, encoding

241 Considering that perturbed intranuclear pre-tRNA metabolism and apparent deficiency

242 anization, rupture because of an increase in intranuclear pressure from actin-based nucleus confineme

243 These findings suggest that MLL5 forms intranuclear protein complexes that may play an importan

244 , full-length interleukin-33 (FLIL33), is an intranuclear protein in many cell types, including fibro

245 g et al. now show that it is organized by an intranuclear protein, UAP56.

246 (CCT) and 25 other proteins--define a novel intranuclear quality control compartment (INQ) that sequ

247 of glomeromycotan genomes could accommodate intranuclear rDNA polymorphism and buffer these apparent

248 a framework of how different signals affect intranuclear redistribution, posttranslational modificat

249 r and checkpoint proteins undergo a dramatic intranuclear relocalization, translocating to nuclear fo

250 anges occur coincident with ICP8 assembly at intranuclear replication structures.

251 ORF72 ALS/FTD, including sense and antisense intranuclear RNA foci and poly(glycine-proline) dipeptid

252 Arg mutation, which resulted in reduction of intranuclear RNA-binding proteins.

253 Intranuclear rod myopathy is a subtype of NM in which ro

254 iated with NM, only ACTA1 is associated with intranuclear rod myopathy.

255 Intranuclear rodlets (INRs), also known as rodlets of Ro

256 mild NM, especially when cardiac problems or intranuclear rods are present.

257 spiratory function, cardiac involvement, and intranuclear rods in biopsied muscle were observed in tw

258 his study suggests that nesprin-2 is a novel intranuclear scaffold, essential for nuclear ERK1/2 sign

259 Strikingly, RNAi-mediated knockdown of intranuclear Sec13 and Nup98 specifically inhibits trans

260 We suggest that intranuclear sequestration of core transcription compone

261 cccDNA probe set was confirmed by its strict intranuclear signal and by a series of Southern blot ana

262 These results suggest mGlu5 may mediate intranuclear signaling pathways.

263 Intranuclear single-chain uPA binds directly to and inte

264 hat the two proteins partially colocalize at intranuclear sites in iEBHX1S-4 cells.

265 -encoded COX subunit genes all occupy common intranuclear sites in the murine neuronal nuclei.

266 ntial components of telomerase accumulate at intranuclear sites separate from telomeres.

267 rget green fluorescent protein and emerin to intranuclear sites that contained the UL31 protein.

268 perhaps differentially regulated at various intranuclear sites, may be a major determinant of nuclea

269 ocalized to the nuclear rim and occupies the intranuclear space surrounding the chromosomes.

270 pon light exposure, PIF7 rapidly migrates to intranuclear speckles, where it colocalizes with phyB.

271 h pAPP epitopes and with expressed Cgamma at intranuclear speckles.

272 Z(K178D) localized to the periphery of large intranuclear spheres, to discrete nuclear aggregates, an

273 ebp1c, Chrebp, Lpk, Dgat, Fasn and Scd1, and intranuclear SREBP1c and ChREBP.

274 turation was also delayed, evident as strong intranuclear staining and little virus at the mucosa.

275 Autoantibody function was assessed by intranuclear staining for GM-CSF-induced STAT5 phosphory

276 XP3(-) ex-Treg by applying a newly developed intranuclear staining protocol that permits the isolatio

277 ng for intracellular cytokine production and intranuclear STAT5 phosphorylation.

278 in the cleavage bodies, which are a kind of intranuclear structure.

279 ies revealed its dynamic localization within intranuclear structures known as GLFG bodies.

280 type-specific expression of these enigmatic intranuclear structures.

281 d electron microscopic studies that revealed intranuclear sun-shaped capsid factories, tubules, vario

282 alamocortical system is regulated in part by intranuclear synaptic inhibition within the reticular nu

283 The compromised intranuclear targeting of regulatory proteins under path

284 une receptors across the nuclear envelope to intranuclear targets.

285 peckles but is also present in long branched intranuclear tracks connecting splicing speckles with si

286 sue, Jady et al. place the Cajal body on the intranuclear traffic route of telomerase RNA.

287 t the trans-acting factors important for the intranuclear trafficking and nucleolar localization of s

288 that telomerase activity may be regulated by intranuclear trafficking of the key components of the en

289 viral NS1 protein and cellular factors to an intranuclear trafficking pathway that targets the viral

290 viral NS1 protein and cellular factors to an intranuclear trafficking pathway that targets the viral

291 d connects HIV-1 preintegration complexes to intranuclear trafficking pathways that link integration

292 Regulation of gene expression by intranuclear transduction of macromolecules such as tran

293 icroscopy of VZV-infected cells demonstrated intranuclear translocation of the Mediator complex to vi

294 uctural features of FANCD2 required for this intranuclear translocation.

295 is inconsistent with a role in micron-scale intranuclear transport, and their localization suggests

296 ing transcription, chromatin remodeling, and intranuclear transport.

297 for immunohistochemistry had cytoplasmic and intranuclear ubiquitin positive, tau negative inclusions

298 Intranuclear uPA modulates gene transcription by binding

299 litis in control and knockout mice; however, intranuclear viral inclusions were seen only in Il1r1(-/

300 Virtually all FIV Gag rapidly became intranuclear when the CRM1 export pathway was blocked, i