ライフサイエンスコーパス: nuclear

1 DAF-16 (in the daf-16 (mu86); muIs61 strain) nuclear accumulation and high expression of the SOD-3 ge

2 e induces the rapid induction of Arc and its nuclear accumulation in striatal neurons.

3 evealed differences in their cytoplasmic and nuclear accumulation, and data from quantitative PCR ana

4 epeat containing E3 ubiquitin protein ligase nuclear accumulation, and iii) Fyn phosphorylation.

5 olyphosphate multikinase (IPMK) and promotes nuclear actin assembly that is required for ATR recruitm

6 ring early Xenopus laevis embryogenesis both nuclear and cell volumes decrease with the nuclear-to-cy

7 es (psaI and csos4A) are encoded by both the nuclear and chromatophore genomes, suggesting that EGT i

8 ions demonstrate that the production of both nuclear and cytoplasmic Esrp1 isoforms through alternati

9 identified splice variants encoding distinct nuclear and cytoplasmic isoforms of fusilli, the D.

10 world sand dollar genus Encope, based on one nuclear and four mitochondrial genes, calibrated with fo

11 (OxPhos) are caused by mutations in both the nuclear and mitochondrial genomes.

12 profiles in previous studies, depending upon nuclear and mtDNA haplotype, the magnitude and direction

13 Here, we have characterized nuclear and whole cell transcriptomes in mouse single ne

14 We confirmed a high concordance between nuclear and whole cell transcriptomes in the expression

15 bly, ARv5es was free from HSP90, exclusively nuclear, and constitutively active similarly as previous

16 omitant presence of sputum anti-EPX and anti-nuclear antibodies of the IgG subtype.

17 Latency-associated nuclear antigen (LANA) is a conserved Rhadinovirus prote

18 teins such as herpesvirus latency-associated nuclear antigen (LANA).

19 study, we identified the proliferating cell nuclear antigen (PCNA) as a nIGF-1R-binding partner.

20 beta-SiC, preferred for nuclear applications, is metastable and undergoes a phas

21 karyotic genomes that has essential roles in nuclear architecture, DNA repair and genome stability, a

22 ia is distinct from that in the well-studied nuclear, bacterial, or bacteriophage transcription syste

23 modification state is a major determinant of nuclear blebbing and morphology via its contribution to

24 ML) protein is an essential component of PML nuclear bodies (PML NBs) frequently lost in cancer.

25 treatment also led to elevated cytosolic and nuclear Ca(2+) levels.

26 al axis of human eye lenses with age-related nuclear cataract showed increasing concentration of fluo

27 pecific inputs to the NAc that mediate these nuclear changes are investigated.

28 ctive NCD layers may prolong the lifetime of nuclear cladding and consequently enhance nuclear fuel b

29 This value is still not limited by nuclear coherence effects.

30 olic roles and a distinct biotin-independent nuclear coregulatory function.

31 nteractions, supporting the role of XRCC1 in nuclear cotransport of APLF.

32 signaling pathway that ultimately increases nuclear CREB phosphorylation and, in most cases, express

33 provides critical biophysical insights into nuclear crowding, nucleic acid based pharmaceutical deve

34 with increased pigmentation, cell volume and nuclear cyclin D1 levels.

35 al profiling (SHAPE-MaP) to probe PAN in its nuclear, cytoplasmic or viral environments or following

36 The proteasome is a nuclear-cytoplasmic proteolytic complex involved in near

37 inus (AAs 176-192) that contributes to CASZ1 nuclear-cytoplasmic shuttling in a chromosomal maintenan

38 ctive nuclear uptake allows development of a nuclear/cytosolic concentration gradient against a backg

39 Difficulties in generating nuclear data for polyploids have impeded phylogenetic st

40 essing cells can form an actin cap to resist nuclear deformation in response to physiological mechani

41 ebellar cellular pathology, characterized by nuclear degeneration through nucleophagy-based LaminB1 d

42 pathological feature in most cases of ALS is nuclear depletion and cytoplasmic accumulation of the pr

43 with multiple rounds of DNA replication and nuclear division without cytokinesis, resulting in a mul

44 ell explored in central Europe using ancient nuclear DNA [1, 2], its genetic impact on northern and e

45 Nuclear DNA indicated Neanderthals as a sister group of

46 e were bred to female MNX mice having FVB/NJ nuclear DNA with either FVB/NJ, C57BL/6J, or BALB/cJ mtD

47 Here we report that the inducible nuclear dual-specificity MAP kinase phosphatase (MKP) DU

48 CRT-I components) are required for efficient nuclear egress of progeny nucleocapsids.

49 itochondria, TOM and TIM complexes transport nuclear-encoded proteins, whereas the Oxa1 is required f

50 ressed pah1Delta effects on lipid synthesis, nuclear/endoplasmic reticulum membrane morphology, and l

51 TNF-alpha, but not IL-1beta or LPS, promoted nuclear enrichment of TonEBP protein.

52 The p.H67R variant reduced nuclear entry of p50 and showed decreased transcriptiona

53 al how relaxation of external tethers to the nuclear envelope and internal chromatin-chromatin tether

54 ribution of the mRNAs to the cytoplasm after nuclear envelope breakdown (NEBD) at prometaphase.

55 on of the retinoblastoma protein and lamins, nuclear envelope breakdown, and duplication of centrosom

56 ed a heterozygous splice site variant in the nuclear envelope gene SYNE1 in a child with severe dilat

57 oted through chromosome movement mediated by nuclear envelope proteins, microtubules, and dynein.

58 Morphology of the nuclear envelope was assessed with immunofluorescence on

59 DDR) which the virus exploits to prepare the nuclear environment for effective takeover.

60 he mitochondrial genome is placed in a novel nuclear environment using this technique.

61 ocytosis and activation of cytosolic PKC and nuclear ERK, which derive from endosomal CLR.

62 e and rapidly degraded in the nucleus by the nuclear exosome.

63 Here, we show that depletion of the nuclear export adaptor SRSF1 prevents neurodegeneration

64 Striking behaviors include "burst" RNA nuclear export dynamics regulated by HIV-1's Rev respons

65 ation by increasing the interaction with the nuclear export factor CRM1.

66 ion and acetylation of FOXO3a results in its nuclear export for degradation and consequent down-regul

67 As tRNA nuclear export is essential, we previously interrogated

68 Gastrin-induced nuclear export of menin via cholecystokinin B receptor (

69 he coordination of synthesis, processing and nuclear export of mRNAs.

70 Furthermore, we identified a nuclear export signal (NES) at the N terminus (AAs 176-1

71 l nuclear localization signal and C-terminal nuclear export signal (NES).

72 characterized for its essential role in mRNA nuclear export, cofunctions with Los1 in tRNA nuclear ex

73 to identify candidates that function in tRNA nuclear export.

74 uclear export, cofunctions with Los1 in tRNA nuclear export.

75 utating phosphorylation sites to enhance its nuclear expression induces profound autophagy in culture

76 Using the Xenopus nuclear extract system, here we show that the Dna2 nucle

77 he basic leucine zipper transcription factor nuclear factor (erythroid-derived 2)-like 2 (NRF2) plays

78 The hepatocyte nuclear factor (HNF) family regulates complex networks o

79 Variants in HNF1A encoding hepatocyte nuclear factor 1alpha (HNF-1A) are associated with matur

80 which was down-regulated in mouse hepatocyte nuclear factor 4A knockout mice; were early-stage tumors

81 nted 29% of all HCCs; expressed a hepatocyte nuclear factor 4A-driven gene network, which was down-re

82 ated with impaired glutathione synthesis and nuclear factor erythroid-derived 2 related factor 2 (NRF

83 d with a decreased GSH/GSSG ratio, augmented nuclear factor erythroid-related factor 2, and increased

84 /Notch-like EGF repeat containing (Dner) and nuclear factor I/A (Nfia), that are each heavily express

85 IkappaBalpha enhances the rate of release of nuclear factor kappa B (NFkappaB) from DNA target sites

86 nate attenuated the HS-induced activation of nuclear factor kappa B and reduced the expression of pro

87 ted T cells to produce receptor activator of nuclear factor kappa-B ligand (RANKL), which, in turn, p

88 atients were less capable in phosphorylating nuclear factor kappa-light-chain-enhancer of activated B

89 of p38 mitogen activated protein kinase and nuclear factor kappa-light-chain-enhancer of activated B

90 aining adapter-inducing IFN-alpha (TRIF) and nuclear factor kappaB (NF-kappaB) causes the apoptosis o

91 ed the pro-inflammatory transcription factor nuclear factor kappaB (NF-kappaB), whereas stable, non-o

92 g to caspase-8-mediated apoptosis as well as nuclear factor kappaB (NF-kappaB)-dependent cell surviva

93 Nuclear Factor Y (NF-Y) is a heterotrimeric transcriptio

94 , the repressor of the receptor activator of nuclear factor-kappaB ligand-mediated osteoclastogenesis

95 Mechanistically, Nrp1 deletion activates the nuclear factor-kappaB pathway, which in turn accentuates

96 rrest through inhibiting the activity of the nuclear factor-kappaB pathway.

97 opathy, characterized by elevated NF-kappaB (nuclear factor-kappaB) activation and TNF (tumor necrosi

98 at infection with HCV leads to activation of nuclear factor-kappaB, resulting in increased expression

99 Nuclear foci corresponding to epigenetic marks as well a

100 in, for example, international safeguards or nuclear forensics.

101 ice, resulting in quadrupolar satellites for nuclear [Formula: see text] isotopes, whereas NMR of the

102 ines of diverse tissue origin by blockade of nuclear FOXO4 degradation and induction of caspase-depen

103 scale proteomics analysis of cytoplasmic and nuclear fractions from normal versus regenerating mouse

104 zation, but endogenous C3G is a component of nuclear fractions in a variety of cell types.

105 of nuclear cladding and consequently enhance nuclear fuel burnup.

106 The nuclear function of PHYs, however, has so far been inves

107 siological stimuli and provide insights into nuclear functions for C3G.

108 omatin domains in general regulate essential nuclear functions.

109 The endosymbiont nuclear genome is 9.5 Mbp in size, the smallest of a ki

110 chromosome, a finding that helps to resolve nuclear genome organization and indicates monocentric re

111 sconnect, we analyzed 41 mitochondrial and 4 nuclear genomes from passenger pigeons and 2 genomes fro

112 rather than ILS, explains most of the shared nuclear genomic variation between these two species and

113 ediated by p38 MAPK specifically inactivates nuclear GSK3beta in the cortex and hippocampus.

114 ropose a model whereby RAPGEF5 activates the nuclear GTPases, Rap1a/b, to facilitate the nuclear tran

115 We found that dephosphorylated, nuclear histone deacetylase 5 (HDAC5) in the nucleus acc

116 r prior studies with the bile acid-activated nuclear hormone receptor farnesoid X receptor (FXR) and

117 Nuclear hormone receptors (NRs) regulate physiology by s

118 timicrobial peptide with great potential for nuclear imaging of infectious diseases, as its cationic-

119 ey role in HIV infection by facilitating the nuclear import of the pre-integration complex (PIC) that

120 ypically ascribed to roles in either histone nuclear import or deposition.

121 n infected cells during cytoplasmic transit, nuclear import, and mRNA synthesis.IMPORTANCE The fates

122 of the precursor and cleavage, resulting in nuclear import.

123 L4 biochemical activities by RPS3 along with nuclear interaction during UV and oxidative stress may s

124 Here, I review the evidence of whether mito-nuclear interactions are likely to pose a problem for MR

125 theory, which predicts that deleterious mito-nuclear interactions are unlikely to be much more preval

126 protein, the tumour suppressor protein Niam (Nuclear Interactor of ARF and Mdm2).

127 enhancer repositioned from the lamina to the nuclear interior.

128 kinase dependent, unforeseen function of the nuclear isoform of the Receptor for Advanced Glycation E

129 upporting the conclusion that RIMA-dependent nuclear IYO accumulation triggers cell differentiation i

130 in Henle's fiber layer (HFL) than the inner nuclear layer (INL) and was highly associated with hyper

131 Microcystoid macular changes in the inner nuclear layer were diagnosed in 52 out of 264 eyes with

132 ells) have their soma displaced to the inner nuclear layer.

133 via regulation of gene transcription at the nuclear level.

134 Indeed, RIMA knockdown reduces the nuclear levels of IYO and prevents its prodifferentiatio

135 B pathway and consequently reduces NF-kappaB nuclear localization and downregulates NF-kappaB targets

136 Moreover, ACOT1 exhibited partial nuclear localization during fasting and cAMP/cAMP-depend

137 ctional nuclear localization signal and that nuclear localization impairs the ability of ICAP1 to sup

138 on at the molecular level to regulate YAP1's nuclear localization is still puzzling.

139 Heat inactivation of HIV-1 blocks nuclear localization of LysRS, but treatment with a reve

140 We conclude that nuclear localization of MS is a unique feature of respir

141 Moreover, the nuclear localization of PINN-1 is altered in dapk-1 muta

142 tically, we found that DMF treatment reduced nuclear localization of transcriptional coactivator with

143 In particular, ARF knockdown reduced non-nuclear localization of YAP which led to an increase in

144 ely accrues from a phosphorylation-sensitive nuclear localization sequence located in the PLD.

145 triphosphate (RanGTP) gradient that imports nuclear localization signal (NLS)-specific cargoes (NLS-

146 ivities of both a peptide-encoded N-terminal nuclear localization signal and C-terminal nuclear expor

147 try to show that ICAP1 contains a functional nuclear localization signal and that nuclear localizatio

148 e these sequences do not correspond to known nuclear localization signal motifs, they represent a new

149 rions parallels effects of the attachment of nuclear localization signal to Sis1, indicating that Cur

150 were full length, containing the N-terminal nuclear localization signal.

151 Mutations lacking nuclear localization uncover a novel mechanism whereby l

152 lation cycle by promoting TDG function, TET1 nuclear localization, and TET/TDG association.

153 appropriate receptor protein expression and nuclear localization.

154 e Esrp1 peptide that is sufficient to confer nuclear localization.

155 prevented decorin-evoked TFEB induction and nuclear localization.

156 beta-catenin while CHIR99021 increased it in nuclear localization.

157 iometry and proteasome-dependent turnover of nuclear MAF1.

158 Proton Nuclear Magnetic Resonance ((1)H NMR) was employed to st

159 Nuclear magnetic resonance (NMR) profiles were analyzed

160 he exceptionally rich information content of nuclear magnetic resonance (NMR) spectra is routinely us

161 lts of a two-dimensional solid-state (77) Se nuclear magnetic resonance (NMR) spectroscopic study of

162 nolic extract and structurally elucidated by Nuclear Magnetic Resonance (NMR) spectroscopy and mass s

163 In this study, nuclear magnetic resonance (NMR) spectroscopy-based meta

164 cal calculations, in combination with (7) Li nuclear magnetic resonance (NMR) spectroscopy.

165 on MS (LC-HRMS), LC-tandem MS (LC-MS/MS) and nuclear magnetic resonance (NMR) spectroscopy.

166 Nuclear magnetic resonance (NMR) titrations, potentiomet

167 We demonstrate using nuclear magnetic resonance (NMR)-based relaxation disper

168 The proton nuclear magnetic resonance analysis indicated that all o

169 ray diffraction, solid fat content by pulsed nuclear magnetic resonance and thermal behaviour by diff

170 Here, using high-accuracy (75)As and (51)V nuclear magnetic resonance measurements, we investigate

171 ur was investigated using time-domain proton nuclear magnetic resonance relaxometry, and related to t

172 Using (1)H Nuclear Magnetic Resonance spectroscopy (NMR) and Gas Ch

173 Here we show, using nuclear magnetic resonance spectroscopy and density func

174 Nuclear magnetic resonance spectroscopy demonstrated tha

175 While X-ray crystallography and nuclear magnetic resonance spectroscopy have revealed th

176 metabolic content measured in lymphocytes by nuclear magnetic resonance spectroscopy was altered in s

177 determined using (1)H and (7)Li solid-state nuclear magnetic resonance spectroscopy.

178 ake rats as measured by ex vivo (1)H-[(13)C]-nuclear magnetic resonance spectroscopy.

179 y, and sequential (2)H and (31)P solid-state nuclear magnetic resonance spectroscopy.

180 Nuclear magnetic resonance structural studies reveal tha

181 Here, we describe crystal and nuclear magnetic resonance structures of KaiB-KaiC,KaiA-

182 Freeze-trapping x-ray crystallography, nuclear magnetic resonance, and computational techniques

183 ble-isotope tracer experiments combined with nuclear magnetic resonance-based metabolic analysis demo

184 lation of SIRPalpha and the mechanosensitive nuclear marker lamin-A.

185 ial DNA (mtDNA) survey and sequencing of two nuclear markers (AME and RAG-1) from P. theobaldi, from

186 c process in which neutrophils release their nuclear material in the form of neutrophil extracellular

187 malignant transformation compromises the DNA-nuclear matrix interface.

188 ombination, so-called "FLI medium," improves nuclear maturation of oocytes in cumulus-oocyte complexe

189 we review some of the emerging mechanisms of nuclear mechanosensing, which range from changes in prot

190 The Society of Nuclear Medicine and Molecular Imaging and the American

191 ics, is among the most promising concepts in nuclear medicine for optimizing and individualizing trea

192 olecular Imaging and the American College of Nuclear Medicine should choose the membership of a radio

193 ges in the separation of the inner and outer nuclear membrane are responsible for the additional fluc

194 Strikingly, we also find that the inner nuclear membrane protein Sun1 antagonizes Sun2 LINC comp

195 ns of RNAs into discrete foci at or near the nuclear membrane triggered by multiple elements; and a n

196 uggested by results obtained for luminal and nuclear membrane-associated EGFP-tagged proteins.

197 Spartan, the protein encoded by SPRTN, is a nuclear metalloprotease that is involved in the repair o

198 ension, apical constriction and interkinetic nuclear migration, as well as precise molecular control

199 gh-resolution confocal microscopy to analyze nuclear morphology and F-actin rearrangements during the

200 ell measurements of size and cytoplasmic and nuclear morphology in high throughput, but only the fina

201 present a method to detect subtle changes in nuclear morphometrics at single-cell resolution by combi

202 Nuclear movement is critical for developmental events, c

203 ics and the regulatory mechanisms underlying nuclear movements in root epidermal cells remains limite

204 The 3.3 A structure of a twelve-subunit nuclear Mpp6 exosome bound to RNA shows the central regi

205 TGFbeta did not act by promoting nuclear MRTF translocation; instead, it triggered p38- a

206 ensing applications in diverse ares, such as nuclear nonproliferation, environmental monitoring, geop

207 axiom of choice (ZFC) that there is a simple nuclear nonseparable [Formula: see text]-algebra, which

208 Using nuclear notch filtering, we demonstrate a spin coherence

209 e identify Insensible (Insb), another neural nuclear Notch pathway inhibitor, as a critical direct mi

210 The reduction in nuclear NRF2 leads to reduced ferroportin 1 (FPN1) expre

211 Our work sheds light on how nuclear organization and Polycomb group (PcG) proteins c

212 n to the membrane determines the dynamics of nuclear oscillations and, in essence, dynein activity.

213 measure these interactions through both (1)H nuclear Overhauser enhancement (NOE) and paramagnetic re

214 ring is accompanied by relocalization to the nuclear periphery and requires Nup2, suggesting a role f

215 Transport of incoming viral capsids to the nuclear periphery was unaffected by the cholesterol redu

216 the greatest outstanding problems in modern nuclear physics.

217 In addition, this activation of the nuclear piston mechanism slowed the 3D movement of HT108

218 eloped to increase the efficiency of dynamic nuclear polarization (DNP) in solid-state NMR studies.

219 ental isotopic labeling schemes with dynamic nuclear polarization (DNP) NMR.

220 Rucaparib is an inhibitor of nuclear poly (ADP-ribose) polymerases (inhibition of PAR

221 Binding of the capsid to the nuclear pore complex (NPC) is mediated by the capsid pro

222 ery and requires Nup2, suggesting a role for nuclear pore complexes.

223 to the cytoplasm, docking of the capsid at a nuclear pore, and release of the viral genome into the n

224 Both activities were necessary to maintain nuclear position in uncentrifuged cells.

225 vel function for Nesprin-1alpha/Nesprin-1 in nuclear positioning through recruitment of Akap450-media

226 (CsMPs) released from the Fukushima Daiichi Nuclear Power Plant (FDNPP) provide nano-scale chemical

227 Transcription factors are essential nuclear proteins that trigger the expression of gene pro

228 otein lamin A distorts nuclei and sequesters nuclear proteins.

229 changes in the tomato (Solanum lycopersicum) nuclear proteome during infection by the oomycete pathog

230 We found that nuclear PTEN alone is sufficient to regulate soma size.

231 a promising fuel for the next generation of nuclear reactors.

232 to function as a physiological ligand for a nuclear receptor and direct environmental sensing as a n

233 irectly facilitates its interaction with the nuclear receptor co-repressor (NCoR1), resulting in repr

234 ting mutation (c.279delG, p.Trp93fs*) of the nuclear receptor interacting protein 1 gene (NRIP1) in a

235 One such nuclear receptor is DAF-12, which is required for normal

236 this study, we report overexpression of the nuclear receptor NR4A1 in rhabdomyosarcomas that is suff

237 Accumulation of PIP3 in complex with the nuclear receptor protein, SF1, at damage sites requires

238 e of dietary vitamin A, acts as a ligand for nuclear receptor transcription factors with more than 50

239 Inhibiting the nuclear receptor's activity using a chemical antagonist

240 We previously showed that Nur77, an orphan nuclear receptor, induces apoptosis by targeting mitocho

241 es suggested that differential expression of nuclear receptors involved in adipogenesis underlie the

242 e effects of SUMOylation on other classes of nuclear receptors, dexamethasone (Dex)-induced trans-rep

243 ption as part of a heterodimer with 14 other nuclear receptors, including the peroxisome proliferator

244 environmental sensing as a novel function of nuclear receptors.

245 which competitive recruitment of DNA-binding nuclear receptors/transcription factors in trans to hot

246 newly introduced nonmuscle nuclei undergoes nuclear reprogramming has not been investigated.

247 t the partition of the receptor in different nuclear reservoirs ultimately regulates the concentratio

248 ing the flow of genetic information from the nuclear residence of genes to the disparate, cytoplasmic

249 ciation, PABP1 deacetylation, and poly(A)RNA nuclear retention.

250 er successful DNA extraction fragment of the nuclear rhodopsin gene (RH1) and 9 microsatellite region

251 MicroRNAs (miRNAs) and heterogeneous nuclear ribonucleoproteins (hnRNPs) are families of sequ

252 Using seven chloroplast and nuclear ribosomal genes, we constructed a phylogeny of 5

253 D1 and D2 domains of the large subunit (LSU) nuclear ribosomal RNA (nrRNA) gene and by morphological

254 bbing and morphology via its contribution to nuclear rigidity.

255 Differential expression analysis following nuclear RNA-seq of neutrophil active transcriptomes reve

256 but instead requires both maternal germline nuclear RNAi and chromatin-modifying activity.

257 Further analysis of nuclear RNAi and morc-1(-) mutants revealed a progressiv

258 Somatic silencing does not require somatic nuclear RNAi but instead requires both maternal germline

259 find that silencing is dependent on germline nuclear RNAi factors and post-transcriptional mechanisms

260 ity requires repression of MET-1 activity at nuclear RNAi targets.

261 Taken together, our results support a novel nuclear role for SmgGDS in protecting malignant cells fr

262 ogeria syndrome (HGPS), a mutant form of the nuclear scaffold protein lamin A distorts nuclei and seq

263 In this work, we study nuclear shape fluctuations at short time scales of secon

264 t the airway wall with marked cytoplasmic to nuclear shift in COPD (P < 0.01).

265 cortical blebbing is tightly coupled to MRTF nuclear shuttling to promote the SRF transcriptional act

266 2(KI)), which exhibits aberrant beta-catenin nuclear signaling, beta-catenin haploinsufficiency induc

267 n conventional cultures as determined by the nuclear Smad2/3 localization.

268 Although the level of nuclear Smad3 varied across cells, the fold change in th

269 cross cells, the fold change in the level of nuclear Smad3 was a more precise outcome of ligand stimu

270 ap resonators, we drive Rabi oscillations on nuclear spins exclusively using electric fields by emplo

271 nanoscale ensembles down to approximately 30 nuclear spins in atomically thin hexagonal boron nitride

272 erence times or T2, due to interactions with nuclear spins in the local environment.

273 derstanding of precisely how the position of nuclear spins relative to the electronic spin center aff

274 g of the electrons and robust storage in the nuclear spins.

275 yzed, 73% were positive for KLF5 (defined as nuclear staining in more than 5% of tumor cells).

276 nal testing (exercise electrocardiography or nuclear stress testing) from 2009 to 2015.

277 ional testing (exercise electrocardiography, nuclear stress, or stress echocardiography) or coronary

278 To test the role of nuclear surveillance in reprogramming gene expression, w

279 C is considered for applications in advanced nuclear systems, as well as for electronic or spintronic

280 h nuclear and cell volumes decrease with the nuclear-to-cytoplasmic (N/C) volume ratio reaching a max

281 find upregulated extracellular Wg ligand and nuclear trans-synaptic signal transduction, as well as d

282 biogenesis, and regulation of apoptosis and nuclear transcription.

283 gulation of biotin utilization and acts as a nuclear transcriptional coregulator of gene expression.

284 rtion mapping, and profiling of the complete nuclear transcriptome, including a ribosomal RNA degrada

285 production and its ability to induce GRalpha nuclear translocation and GRE-dependent GILZ expression.

286 n of glioblastoma stem-like cells drives the nuclear translocation of an intracellular fragment of OD

287 ERK, CREB, and Ser-727 of STAT3 and induced nuclear translocation of pCaMKII.

288 ification in RPE cells, which coincides with nuclear translocation of the lysosomal stress-sensing tr

289 father's lymphocytes showed reduced pSTAT4, nuclear translocation, and impaired IFN-gamma production

290 ivity, which stimulates SMAD3 expression and nuclear translocation.

291 s IkappaBalpha phosphorylation and NF-kappaB nuclear translocation.

292 se element (XRE) in partnership with the AhR nuclear translocator (Arnt).

293 nuclear GTPases, Rap1a/b, to facilitate the nuclear transport of beta-catenin, defining a parallel n

294 ansport of beta-catenin, defining a parallel nuclear transport pathway to Ran.

295 n (C) by the host importin (IMP) alpha/beta1 nuclear transport proteins.

296 ster) and from specific tRNA loci (e.g., the nuclear tRNA(Gly) and tRNA(Leu), the mitochondrial tRNA(

297 Active nuclear uptake allows development of a nuclear/cytosolic

298 hnetium-99 ((99)Tc) contained in reprocessed nuclear waste and present in contaminated subsurface sys

299 re deuterium and the removal of tritium from nuclear waste are the key challenges in separation of li

300 e shear zone under conditions relevant for a nuclear waste repository in crystalline rock.