ライフサイエンスコーパス: nuclear

1 GLS2 expression and nuclear accrual notably increased by treatment of SH-SY5

2 solute reliance developing myofibers have on nuclear accrual to establish size, and the limits of ada

3 ith the NFAT blocker A-285222 reduced NFATc3 nuclear accumulation and NFAT-luciferase transcriptional

4 These include the nuclear accumulation of mRNAs encoding components of the

5 1 is not only positively correlated with the nuclear accumulation of SREBP1 in samples from patients

6 substitutions at these sites enhanced ICAP1 nuclear accumulation.

7 moter through a dynamic network of polymeric nuclear actin.

8 ocesses including protein quality control of nuclear aggregates.

9 Further mechanistic dissection suggests that nuclear Akt activity mediates growth factor-induced nucl

10 dicted survival time for selectively neutral nuclear alleles.

11 chromosome arms, yet how the cell regulates nuclear and chromatin-associated RNAs after chromosome c

12 To characterize the nuclear and cytoplasmic transcriptomes during brain deve

13 olyP could nonphysiologically cause K-PPn of nuclear and cytosolic targets.

14 Mitochondrial disorders are the result of nuclear and mitochondrial DNA mutations that affect mult

15 evisiae, the Pif1 helicase functions in both nuclear and mitochondrial DNA replication and repair pro

16 f a multitude of membranous, cytoplasmic and nuclear antigens in whole mouse organs and embryos, huma

17 Model approaches to nuclear architecture have traditionally ignored the biop

18 Here, we describe an approach to large-scale nuclear architecture in metazoans that incorporates cell

19 filament protein critical for the interphase nuclear architecture, was reduced.

20 ENRI-1/2 prevent misloading of the nuclear Argonaute NRDE-3 with small RNAs that normally e

21 nderground at the Laboratory for Underground Nuclear Astrophysics (LUNA) of the Laboratori Nazionali

22 Here, we used the nuclear Auxin Response Circuit recapitulated in yeast (S

23 the range of transcriptional return on a per nuclear basis in myofibers diminishes, which accounts fo

24 In cells, MORC4 mediates formation of nuclear bodies in the nucleus and has a role in the prog

25 ligomerization promote the assembly of large nuclear bodies, which sequester SRSF7 transcripts at the

26 Furthermore, decreases in nuclear but not cytoplasmic Pten levels associated with

27 nuclear translocation of a CaM shuttle, and nuclear CaMKIV activation.

28 Srrt interacts with the nuclear cap-binding complex and facilitates recruitment

29 e has recently been challenged by studies of nuclear cap-binding protein 3 (NCBP3).

30 al GABAergic interneurons in the basolateral nuclear complex (BNC) of the amygdala are critical for t

31 e cochlear nuclear complex, superior olivary nuclear complex, lateral lemniscus, inferior colliculus,

32 We observed the cochlear nuclear complex, superior olivary nuclear complex, later

33 BRD4S nuclear condensation is mediated by its intrinsically di

34 ned, which were modified into the definitive nuclear configuration through the metamorphic climax.

35 ironment and suffers more mutations than its nuclear counterpart.

36 ally, we observed an altered distribution of nuclear cyclic guanosine monophosphate-adenosine monopho

37 Compared to FF, FFPE transcripts coding for nuclear/cytoplasmic proteins involved in DNA packaging,

38 aracterized by neutrophilic inflammation and nuclear debris in post capillary venules.

39 perones for cytoskeletal maintenance in post-nuclear degradation lens fiber cells, perturbation of wh

40 Glucose conjugation nevertheless increases nuclear delivery ca 2.5-fold, and a non-destructive inte

41 chromosomal abnormalities and the release of nuclear DNA into the cytoplasm, activating the cGAS-STIN

42 ries of rNMPs derived from mitochondrial and nuclear DNA of budding and fission yeast.

43 to independently follow both electronic and nuclear dynamics at the same time.

44 rovide insights into both the electronic and nuclear dynamics of this fundamental class of reactions.

45 Both nuclear effectors are secreted via the biotrophic interf

46 The nuclear magnetic dipole and nuclear electric quadrupole hyperfine structure constant

47 e impact of transcriptional reprogramming of nuclear-encoded chloroplast genes during disease and def

48 In addition, expression of lung nuclear-encoded genes changed specifically with mt-SNP.

49 synthetic riboswitches for the regulation of nuclear-encoded genes in planta remains to be explored.

50 of 72 chloroplast genes and 7621 homologous nuclear-encoded proteins, for 157 and 76 taxa, respectiv

51 contrast, the protein abundance of specific nuclear-encoded subunits in oxidative phosphorylation co

52 lly diverse organelles that are dependent on nuclear-encoded, plastid-targeted proteins for all bioch

53 The levels of expression of nuclear-encoded, TIM23-transported mitochondrial protein

54 ox and TF, cytotoxicity of CDT resulted from nuclear entry by Dox, promoting double-stranded DNA brea

55 ch the cytosol, where it disassembles before nuclear entry to promote infection.

56 r permeability barrier depends on closure of nuclear envelope (NE) holes.

57 lines are induced by stretch stimulation and nuclear envelope (NE) proteins including nesprins, SUN2,

58 Comparisons of shape and integrity of the nuclear envelope and its resistance to stresses found th

59 cytoplasmic components are displaced before nuclear envelope assembly by the movement of chromosomes

60 iated RNAs after chromosome condensation and nuclear envelope breakdown is unknown.

61 Since nuclear envelope breakdown occurs during mitosis in meta

62 We therefore isolated nuclear envelope lipids from human kidney cells, analyze

63 alculations support the possibility that the nuclear envelope may balance significant mechanical stre

64 found that both mutations result in similar nuclear envelope perturbations that were reversed in the

65 indle microtubules that traverse the nascent nuclear envelope.

66 ive protein network that underlies the inner nuclear envelope.

67 Poly(ADP-ribose) polymerase 1 (PARP-1) is a nuclear enzyme involved in DNA repair and transcription

68 gical activation of the transcription factor nuclear erythroid 2-related factor 2 (Nrf2) enables ideb

69 Transgenic reporter fish demonstrated nuclear ESR activity in the developing liver.

70 Despite the emerging importance of nuclear events in autophagy regulation, epigenetic contr

71 osphatase activation leading to Akt-mediated nuclear exclusion of FoxO1 and concomitant beta-catenin

72 factor that is specifically required for the nuclear export of intronless and intron-poor mRNAs and l

73 localization (NLS1 to -3) and two potential nuclear export signals (NES1 and -2) within MSH3.

74 Mutations in nuclear export stabilized substrates, and caused accumul

75 kinase C (aPKC) at the contact-free domain, nuclear expression of Hippo signalling pathway effectors

76 Unexpectedly, nuclear expression of the EMT-TF ZEB2 in human primary m

77 the presence of polyadenylation factors from nuclear extracts.

78 ive androstane receptor (CAR) and hepatocyte nuclear factor 4 alpha (HNF4alpha).

79 entified that aging alters Sirtuin-1-hepatic nuclear factor 4alpha circuit in hepatocytes to downregu

80 imary cultures of rat enteric neurons and in nuclear factor erythroid 2-related factor (Nrf2) knockou

81 the master regulator of antioxidant defense nuclear factor erythroid 2-related factor 2 (Nrf2).

82 alyses across technologies demonstrated that nuclear factor kappa B (NF-kappaB) and cholesterol biosy

83 Serum receptor activator of nuclear factor kappa B ligand (RANKL) and its antagonist

84 tivated protein kinases as well as NFkappaB (nuclear factor kappa B).

85 insulin receptor, which in turn activates a nuclear factor kappa B-dependent metabolic pathway, lead

86 dly induces co-occupancy of KDM7A and UTX at nuclear factor kappa-B (NF-kappaB)-associated elements i

87 nducible expression of receptor-activator of nuclear factor kappa-Beta ligand (Rankl) leads to ectopi

88 ntrols whether the cell undergoes NF-kappaB (nuclear factor kappa-light-chain-enhancer of activated B

89 e (MAPK), Jun NH2-terminal kinase (JNK), and nuclear factor kappa-light-chain-enhancer of activated B

90 antagonist; or parthenolide, a caspase-1 and nuclear factor kappa-light-chain-enhancer of activated B

91 tion of EGLN3, a known negative regulator of nuclear factor kappaB (NF-kappaB), as a direct target of

92 Nuclear Factor of Activated T cells 5 (NFAT5) is a trans

93 elated with serum zonulin and phosphorylated nuclear factor-kappaB expression.

94 Genetic faults in several components of the nuclear factor-kappaB pathway cause immunodeficiency.

95 This was associated with blockade of nuclear factor-kappaB pathway signaling, resulting in ab

96 e that SETD6 is necessary for memory-related nuclear factor-kappaB RELA methylation at lysine 310 and

97 ypothesis, we resequenced two 3-4 generation nuclear families (totaling 29 individuals) of olive babo

98 a expression, especially for CaMKIIdeltaC in nuclear fractions.

99 nuclides that result from processing of used nuclear fuel is a major challenge.

100 CRM1 inhibition rescued p53-dependent nuclear functions and sensitized NBAT1-depleted cells to

101 A single nuclear gene can be translated into a dual localized pro

102 onses, including transcriptional rewiring of nuclear gene expression, return to levels, such as, or e

103 us to retrieve the plastome, 57 single copy nuclear genes, and the nuclear ribosomal ITS from 29 spe

104 In primary transcripts of eukaryotic nuclear genes, coding sequences are often interrupted by

105 ity is uncultivated, under-studied and lacks nuclear genome data.

106 mitochondrial DNA are also reflected in the nuclear genome or, alternatively, are the product of lim

107 s local pool at each cell division modulates nuclear growth kinetics and dictates size scaling throug

108 st known as a scaffolding protein within the nuclear hetero-hexameric transcriptional Elongator prote

109 interactions with the LINC complex regulate nuclear homeostasis in the cardiomyocyte.

110 -bundling events instituted by Medicare (CT, nuclear imaging, echocardiography).

111 in aggregate followed by modality (CT, MRI, nuclear imaging, echocardiography, US, radiography).

112 ex blockade to monitor the kinetics of HIV-1 nuclear import and define the biochemical staging of the

113 , we show that the MA region is required for nuclear import of Gag through the TNPO3 pathway.

114 IMPalpha-1, -2 and -3 are necessary for the nuclear import of LHP1.

115 on between PB1 and RanBP5, which impeded the nuclear import of vRNP.

116 ggest that the C9orf72-HRE impairs Mitf/TFEB nuclear import, thereby disrupting autophagy and exacerb

117 ng, RNA processing, translation, metabolism, nuclear integrity, protein trafficking, and cytoskeletal

118 his vital intracellular barrier to enter the nuclear interior.

119 Src family kinase biosensors showed that the nuclear kinase activities are much suppressed compared t

120 The nuclear lamina (NL) is an extensive protein network that

121 ndent downregulation of lamin B1, one of the nuclear lamins in adult neural stem/progenitor cells (AN

122 ly the GCL, inner plexiform layer, and inner nuclear layer thickness with rates of -0.11 mum/year, -0

123 or resolved PAMM lesion was defined as inner nuclear layer thinning with outer plexiform layer (OPL)

124 ression model showed that SSPiM in the inner nuclear layer was related to treatment response (P = 0.0

125 tive EYS secretory vesicles within the outer nuclear layer, and diminished EYS protein near the conne

126 s, and thinned the outer plexiform and inner nuclear layers of both WT and hWtEPOR 8-week-old mice.

127 Human Nuclear Lipid Membranes were at least two orders of magn

128 We applied CARPID to the nuclear lncRNA XIST, and it captured a list of known int

129 Overall, our data suggest that nuclear localised OsPIP5K1 acts with DWT1 and/or DWL2 to

130 In this study, we manipulated three putative nuclear localization (NLS1 to -3) and two potential nucl

131 d that the ring component anillin contains a nuclear localization signal (NLS) that binds to importin

132 at CRWN4 is coimported into the nucleus with nuclear localization signal (NLS)-bearing paralogues in

133 These features include enhancement of the nuclear localization signals in the nucleocapsid protein

134 These interactions regulate nuclear localization, phase separation, and stress granu

135 TAL effectors nuclear-localize in plants, where they bind and activate

136 re, we show that an AT-hook motif-containing nuclear localized (AHL) protein regulates lipid mobiliza

137 ataset consisting of hundreds of single-copy nuclear loci.

138 The nuclear magnetic dipole and nuclear electric quadrupole

139 Quantum mechanical/nuclear magnetic resonance (NMR) approaches are widely u

140 iology techniques are X-ray crystallography, nuclear magnetic resonance (NMR) imaging, and cryogenic

141 Nuclear magnetic resonance (NMR) spectroscopy and mass s

142 Sera were analysed using (1)H nuclear magnetic resonance (NMR) spectroscopy and mass s

143 Here we show by circular dichroism and nuclear magnetic resonance (NMR) spectroscopy that Spp2

144 ando synchrotron X-ray diffraction (XRD) and nuclear magnetic resonance (NMR) spectroscopy to demonst

145 on reaction mechanism was examined employing nuclear magnetic resonance (NMR) spectroscopy to determi

146 and analysis of its glycan interactions via nuclear magnetic resonance (NMR) spectroscopy.

147 Here, solution nuclear magnetic resonance (NMR), neutron reflectometry

148 (1)H quantitative Nuclear Magnetic Resonance (qNMR) spectroscopy technique

149 2D proton nuclear magnetic resonance and SAXS data provided constr

150 Mass spectrometry and nuclear magnetic resonance are the most commonly reporte

151 A proton nuclear magnetic resonance metabolomics platform provide

152 1D (1)H nuclear magnetic resonance spectra were acquired in plas

153 ctures elucidated by one and two-dimensional nuclear magnetic resonance spectroscopy (1D and 2D NMR)

154 17 wines of Czech origin were analysed using nuclear magnetic resonance spectroscopy (NMR) with the a

155 anic molecules is typically determined using nuclear magnetic resonance spectroscopy (NMR).

156 d de-N-acetylated by mono- and bidimensional Nuclear Magnetic Resonance spectroscopy and mass spectro

157 e spectroscopic analysis performed by proton-nuclear magnetic resonance spectroscopy showed that the

158 ng circular dichroism, thermal denaturation, nuclear magnetic resonance spectroscopy, analytical ultr

159 , electrospray ionization mass spectrometry, nuclear magnetic resonance spectroscopy, and density fun

160 omplex at polymer chain ends is evidenced by nuclear magnetic resonance spectroscopy, end group analy

161 hydrogen/deuterium fractionation factors by nuclear magnetic resonance spectroscopy.

162 tal analysis, thermogravimetric analysis and nuclear magnetic resonance spectroscopy.

163 gh spectroscopic resolution using zero-field nuclear magnetic resonance spectroscopy.

164 Nuclear magnetic resonance studies and density functiona

165 ty classes has been evaluated by time domain Nuclear Magnetic Resonance, Thermogravimetric analysis a

166 We analyzed nuclear magnetic resonance-derived lipoprotein and metab

167 Comparison of nuclear magnetic resonance-derived structures revealed s

168 y stable isotope-labeled GPCR for studies by nuclear magnetic resonance.

169 ting, localizing, and characterizing special nuclear material (e.g. highly-enriched uranium, plutoniu

170 y, American College of Radiology, Society of Nuclear Medicine and Molecular Imaging, American Urologi

171 ey was to evaluate the impact of COVID-19 on nuclear medicine departments.

172 onstructed images were blindly reviewed by 3 nuclear medicine physicians and scored (using a Likert s

173 Conclusion: Both diagnostic and therapeutic nuclear medicine procedures declined precipitously, with

174 f the predicted PET images was assessed by 2 nuclear medicine specialists using a 5-point grading sch

175 Nuclear medicine studies are often performed in patients

176 a physical explanation for the formation of nuclear membrane invaginations.

177 ne encompassing the acentrics fuses with the nuclear membrane, facilitating integration of the acentr

178 rfaces of neuroepithelia during interkinetic nuclear migration.

179 both necessary and sufficient to orient both nuclear migrations.

180 cues that pattern cortical Galphai, LGN, and nuclear mitotic apparatus protein (NuMA) [3, 7-18].

181 he list of epigenetic regulators that impact nuclear morphology.

182 ural development is the origin of stochastic nuclear movement between apical and basal surfaces of ne

183 lization of Raptor to the nucleus results in nuclear mTORC1 activity in the absence of growth factor

184 We previously identified a nuclear myocardin-related transcription factor (nMRTF) r

185 nd presents dynamic crowding within the bulk nuclear nanoenvironment as a novel regulatory framework

186 ving force for the effort is in the realm of nuclear nonproliferation efforts, the ubiquitous use of

187 r the assembly of paraspeckles, membraneless nuclear organelles involved in gene regulation.

188 ery in the field of chromosome structure and nuclear organization.

189 ility, nucleosome positioning/occupancy, and nuclear organization.

190 emonstrated that A2AR ligation increased the nuclear P-SMAD2/3/P-SMAD1/5/8 ratio, a change associated

191 ive uptake, and those that measure cytosolic/nuclear penetration, which represents only productive up

192 apex of chromosome loops protruding from the nuclear periphery into the interior.

193 The nuclear permeability barrier depends on closure of nucle

194 growth of rice shoots, likely to be through nuclear phosphoinositide signals, and provides insights

195 perimental results settle the most uncertain nuclear physics input to BBN calculations and substantia

196 of important systems in condensed matter and nuclear physics, as well as the study of many-body state

197 e ambitious room temperature in situ dynamic nuclear polarisation studies of batteries and the select

198 The Nuclear Pore Complex (NPC) has emerged as an important h

199 Here, we use an inducible nuclear pore complex blockade to monitor the kinetics of

200 is activity is also important for interphase nuclear pore complex insertion into growing germline nuc

201 subset of 8, including key components of the nuclear pore complex scaffold and the transmembrane nucl

202 cleus, including several constituents of the nuclear pore complex.

203 Nuclear pore complexes (NPCs) are important for cellular

204 intuiting which molecular forces govern the nuclear positioning; we therefore used computational scr

205 does not rely on a physical rearrangement of nuclear positions, material constraints are lifted, thus

206 on in freshwater systems after the Chernobyl Nuclear Power Plant (NPP) accident in 1986 and in freshw

207 ntamination caused by the Fukushima Dai-ichi Nuclear Power Plant accident has aroused great concern r

208 ding yeast Hsp70 chaperones Ssa1 and Ssa2 in nuclear PQC degradation varies with the substrate.

209 leukemia protein (PML) bodies, sites of many nuclear processes including protein quality control of n

210 Nuclear processes, such as V(D)J recombination, are orch

211 y found in light-water reactors and in other nuclear processes.

212 ification, chromatin forms the nexus of most nuclear processes.

213 poptotic markers and increased expression of nuclear protein 1 and tribbles related protein-3 compare

214 syltransferase that modifies cytoplasmic and nuclear protein by transfer of N-acetylglucosamine (O-Gl

215 TEX15 is predominantly a nuclear protein that is not required for piRNA biogenesi

216 Regulated transport of nuclear proteins (e.g., transcription factors) between m

217 EBV nuclear proteins usurp normal transcriptional programs t

218 used to predict the spatial distributions of nuclear proteins within a myotube.

219 correlates with increased ubiquitination of nuclear proteins.

220 e by-product of mechanical work, chemical or nuclear reactions, or information processing.

221 R4A3 is a transcription factor of the orphan nuclear receptor family.

222 tein activator receptor gamma (PPARgamma), a nuclear receptor involved in inflammatory responses.

223 t directs the biodistribution of parent drug nuclear receptor modulators into the CNS while masking t

224 Nuclear receptor modulators, which often feature carboxy

225 cells, PD-L1 expression was regulated by the nuclear receptor NR4A1/Sp1 complex bound to the proximal

226 Here we identify the nuclear receptor peroxisome proliferator-activated recep

227 These lipids are endogenous ligands for the nuclear receptor PPARalpha, and we demonstrate that Ppar

228 The nuclear receptor small heterodimer partner (Shp) plays a

229 The nuclear receptors (NRs), NR2F2 and NR2C2, can bind to (T

230 how that liver X receptors (LXRs)-a class of nuclear receptors and transcription factors with diverse

231 ol metabolism and energy balance via several nuclear receptors and/or G-protein-coupled receptors(3,4

232 Nuclear receptors have a broad spectrum of biological fu

233 roperties of druggability and actionability, nuclear receptors have demonstrated much promise as nove

234 liminarily been identified as a modulator of nuclear receptors involved in beta-amyloid (Abeta) metab

235 Consequently, EP300 is redirected away from nuclear receptors that promote differentiation towards b

236 ndrome, as RXR heterodimerizes with multiple nuclear receptors that regulate genes involved in metabo

237 ted together with associated genes to silent nuclear regions.

238 XO3a and further expand the role of CARM1 in nuclear regulation of autophagy.

239 ing the circumstances of the undeclared 2017 nuclear release of ruthenium that led to widespread dete

240 d heterochromatin-lamina interactions during nuclear remodeling.

241 example, they describe how long interspersed nuclear repeat (LINE1) transcripts are recruited togethe

242 uggest that the initial clustering is due to nuclear repulsion from the cell poles, while the third,

243 e mutants can rescue iMEF survival and small nuclear ribonucleoprotein (snRNP) assembly, demonstratin

244 The U2 small nuclear ribonucleoprotein (snRNP) has an essential role

245 -type spliceosomes, large complexes of small nuclear ribonucleoprotein particles and associated prote

246 o the mRNA processing protein, heterogeneous nuclear ribonucleoprotein-L (hnRNPL).

247 interacting with nucleolin and heterogeneous-nuclear-ribonucleoprotein-A1.

248 stome, 57 single copy nuclear genes, and the nuclear ribosomal ITS from 29 species representing all b

249 tin-beta1, nucleoporin 98 and nucleoporin 62 nuclear rim staining are observed in Purkinje cells of A

250 ding sites of TRAMP components with multiple nuclear RNA binding proteins, revealing preferential col

251 ost abundant non-coding (spliceosomal) small nuclear RNA, silences proximal PASs and its inhibition w

252 dditionally, they are negative regulators of nuclear RNAi triggered from exogenous sources.

253 NPR1 nuclear roles include pathogenesis response (PR) gene re

254 Site is highly desirable for the purpose of nuclear safety and environmental protection, but current

255 tance for society and future improvements in nuclear safety.

256 relamin A, the farnesylated precursor of the nuclear scaffold protein lamin A.

257 Despite the correlation between abnormal nuclear shape and human pathologies, the mechanism by wh

258 eographing proper chromatin decompaction and nuclear shape by directly associating with the DNA.

259 atin decondensation at the mitotic exit, and nuclear shape in interphase.

260 y fusing the enzyme with the light-activated nuclear shuttle (LANS) domain.

261 ependent signaling cascade that controls YAP nuclear shuttling.

262 relocation were connected by a novel synapto-nuclear signaling pathway that surprisingly invoked mech

263 ce uniformity via a largely unexplored plant nuclear signalling pathway.

264 se TOE1 in distinguishing the fates of small nuclear (sn)RNAs of the spliceosome from unstable genome

265 Spatial repositioning of genes in nuclear space has been extensively linked to regulation

266 nerated from short transcripts accumulate in nuclear speckles and are bound to Nxf1.

267 ession correlates inversely with distance to nuclear speckles, with chromosome regions of unusually h

268 fficient splicing of the IAV M transcript in nuclear speckles.

269 anging the coherent superposition of initial nuclear spin states with an external magnetic field.

270 action with the nanoscale ensemble of atomic nuclear spins, which is particularly problematic in stra

271 arkably, after this cytoplasmic passage, the nuclear stability of telomerase RNA no longer depends on

272 or 2 (RTF2) restricts influenza virus at the nuclear stage (and perhaps other stages) of the viral li

273 Nuclear staining percentage has a fair diagnostic abilit

274 il to capture the viscoelastic modulation of nuclear stress-strain relationships by the physiological

275 We show that transmembrane actin nuclear (TAN) lines are induced by stretch stimulation a

276 Removal of (99)TcO(4)(-) from legacy defense nuclear tank waste at Savannah River Site is highly desi

277 osphorylated N-terminus that interacted with nuclear TCF-4 resulting in luciferase reporter activity

278 lly, these data bring a new dimension to the nuclear theranostic model by showing a requirement for i

279 It undergoes nuclear transit before accumulating at the plasma membra

280 rylation of PHB1 at Thr258, resulting in its nuclear translocation and binding to the Axin1 promoter.

281 RT1) repression and stimulates NF-kappaB p65 nuclear translocation and transactivation of NF-kappaB t

282 ctivation, enhanced spine Ca(2+) transients, nuclear translocation of a CaM shuttle, and nuclear CaMK

283 ular activation of c-Jun was demonstrated by nuclear translocation of c-Jun, enhanced phosphorylation

284 between CLOCK and BMAL1 and interferes with nuclear translocation of CLOCK both in vivo and in vitro

285 Loss of WASp impedes nuclear translocation of GOLPH3 and its colocalization w

286 STING-mediated IFN production is mediated by nuclear translocation of IRF3 whereas TLR9-mediated acti

287 t maternal piRNAs, which prevents precocious nuclear translocation of NRDE-3 in the early embryo.

288 Akt activity mediates growth factor-induced nuclear translocation of Raptor, a regulatory scaffoldin

289 c study showed the inhibition of EGFR caused nuclear translocation of S6K1 for binding with MDM2 in r

290 Additional factors, including nuclear translocation of UBQLN2, may facilitate its acti

291 FFSS signaling drives class IIa HDAC nuclear translocation through a signaling pathway involv

292 esenchymal transition (EMT) and beta-catenin nuclear translocation to promote cell migration and inva

293 on 6 to 9 (ARM6-9) of KAP3, required for its nuclear translocation, is also necessary and sufficient

294 -activating group P65 by phosphorylation and nuclear translocation.

295 Nuclear war, beyond its devastating direct impacts, is e

296 ble to host a geological repository in every nuclear waste-generating country, but carbonate rocks ma

297 The path of a nuclear wavepacket in the vicinity of the conical inters

298 is it that someone would approve of using a nuclear weapon to kill millions of enemy civilians in th

299 cility to confirm the absence or presence of nuclear weapons and fissile materials.

300 mics, we show that a cycle of fast exodus of nuclear YAP to the cytoplasm followed by fast reentry to