ライフサイエンスコーパス: nucleus

1 hibitory output to the projections from this nucleus.

2 e for UL21 in preventing their exit from the nucleus.

3 ity to relocalize Sis1 from the cytoplasm to nucleus.

4 may have novel moonlighting functions in the nucleus.

5 lso distributed throughout the cytoplasm and nucleus.

6 itatively measure 3D protein dynamics in the nucleus.

7 nucleus, septum, and laterodorsal tegmental nucleus.

8 protein showed that MybA is localized to the nucleus.

9 d entry, after the arrival of capsids at the nucleus.

10 e transiently and partially localized to the nucleus.

11 egulates replication of viral DNA within the nucleus.

12 ar rigidity on the diffusive behavior of the nucleus.

13 and function with TET1 relocating out of the nucleus.

14 NLS)-specific cargoes (NLS-cargoes) into the nucleus.

15 is observed and partially relocalized to the nucleus.

16 tion sequence (NLS) and is trafficked to the nucleus.

17 als from the disturbed organelles toward the nucleus.

18 ptation Hog1 pathway, which signals from the nucleus.

19 al regulated kinase (ERK) in the cytosol and nucleus.

20 traffics to its therapeutic destination-the nucleus.

21 1 in global DNA replication in the mammalian nucleus.

22 foundation of these opposing effects in the nucleus.

23 e EPR spectra arising from the I=7/2 (45) Sc nucleus.

24 and posterior subregions of the subthalamic nucleus.

25 -eGFP was localized in the cytoplasm and the nucleus.

26 tion and the structure of the reverse-domain nucleus.

27 po-mediated inhibition and drove YAP1 to the nucleus.

28 ocytic organelles but also the flagellum and nucleus.

29 within the anterior and ventral subthalamic nucleus.

30 was correlated with their orientation in the nucleus.

31 has functional roles in both the ER and the nucleus.

32 -activity-linked genomic interactions in the nucleus.

33 jections originating from beyond the arcuate nucleus.

34 oRNA and lncRNA interactions enriched in the nucleus.

35 ) to pro-inflammatory gene expression in the nucleus.

36 econd messenger, Smad2/3, accumulated in the nucleus.

37 mplete and distorted versions of the folding nucleus.

38 cts in the accumulation of viral cDNA in the nucleus.

39 re, and release of the viral genome into the nucleus.

40 but brainstem structures can influence this nucleus.

41 riggers release of the viral genome into the nucleus.

42 ite at the ventral border of the dorsomedial nucleus.

43 material from the organellar genomes to the nucleus.

44 he putative homolog of the mammalian arcuate nucleus.

45 the kinetoplast (mitochondrial nucleoid) and nucleus.

46 L-18-containing axons to the interpeduncular nucleus.

47 nd magnocellular portion of ventral anterior nucleus.

48 la (BLA) sends excitatory projections to the nucleus accumbens (NAc) and regulates motivated behavior

49 ated dopamine receptor (DRD)-1 and -2 in the nucleus accumbens (NAc) and with down-regulated Lepr in

50 ions in global DNA hydroxymethylation in the nucleus accumbens (NAc) because neuroplastic changes in

51 The nucleus accumbens (NAc) gates motivated behaviors throug

52 sed in C57BL/6J mice to confirm the role for nucleus accumbens (NAC) glutamate/Homer2 expression in M

53 lc6a15, a neutral amino acid transporter, in nucleus accumbens (NAc) in depression and stress suscept

54 nvestigated the role of AMPK activity in the nucleus accumbens (NAc) in relapse to cocaine seeking.

55 The nucleus accumbens (NAc) is a primary brain reward region

56 lar mechanisms of GLP-1R signaling on PVT-to-nucleus accumbens (NAc) projecting neurons.

57 nuclear histone deacetylase 5 (HDAC5) in the nucleus accumbens (NAc) reduced cocaine reward-context a

58 cue-activated orbitofrontal cortex (OFC) and nucleus accumbens (NAc) shell ensembles using wild-type

59 creased dopamine release and reuptake in the nucleus accumbens (NAc) shell, a major target region.

60 stone posttranslational modifications in the nucleus accumbens (NAc), a brain reward region.

61 s DA release in terminal regions such as the nucleus accumbens (NAc).

62 ject to the ventral tegmental area (VTA) and nucleus accumbens (NAc); however, direct neuroanatomical

63 dy examined Slc6a15 in the ventral striatum [nucleus accumbens (NAc)] in depression.

64 the medial orbitofrontal cortex (P=0.01) and nucleus accumbens (P=0.08).

65 thic care was preferentially associated with nucleus accumbens and medial orbitofrontal cortex activi

66 porter 1 (GLT-1) and system xC- (Sxc) in the nucleus accumbens core (NAc).

67 echanism for use-dependent inhibition in the nucleus accumbens core and dorsal striatum, is also mini

68 (t-SP) of cortical glutamatergic synapses on nucleus accumbens core medium spiny neurons, but it is u

69 nset, long-lasting increase in extracellular nucleus accumbens DA, locomotion, and brain-stimulation

70 orking model that synaptic plasticity in the nucleus accumbens is central to age-related changes in v

71 circuit from the medial prefrontal cortex to nucleus accumbens is dynamically modulated to enhance fe

72 thway from the prelimbic (PrL) cortex to the nucleus accumbens is implicated in reinstatement.

73 ssion was also upregulated postmortem in the nucleus accumbens of male human cocaine addicts.

74 d miR-181b in human brain and blood, greater nucleus accumbens reactivity to positive emotional stimu

75 ubstantia nigra, entopeduncular nucleus, and nucleus accumbens shell measured using brain mapping ana

76 of D1-like dopamine receptors (D1DRs) in the nucleus accumbens shell promoted cocaine seeking through

77 repressor of gene expression, acting in the nucleus accumbens, a brain reward region, is capable of

78 gression within the caudate, ventral caudate/nucleus accumbens, and anterior and posterior insula, 2)

79 e recruited a more excitable ensemble in the nucleus accumbens, but not orbitofrontal cortex, compare

80 gions (cortex, hippocampus, caudate-putamen, nucleus accumbens, thalamus, and hypothalamus) of BAC al

81 involve common brain regions afferent to the nucleus accumbens, within the mesolimbic pathway.

82 rter assays and in vivo microdialysis in rat nucleus accumbens.

83 rexcitability of medium spiny neurons of the nucleus accumbens.

84 al response to anticipation of reward in the nucleus accumbens.

85 age and was modulated by D1 availability in nucleus accumbens.

86 trength at prefrontal cortex synapses in the nucleus accumbens.

87 e respective change of the RPE signal in the nucleus accumbens.

88 The anterior cortical amygdaloid nucleus (ACo) is a chemosensory area of the cortical amy

89 This dorsomedial nucleus also showed substantial innervation by trigemina

90 millo-thalamic tract (MTT)/anterior thalamic nucleus (AN) complex would be critical for recollection

91 can enter L. bicolor hyphae, localize to the nucleus and affect hyphal growth and morphology.

92 ts modulate the mechanical properties of the nucleus and also chromatin condensation.

93 oinositide lipids (PPIs) are enriched in the nucleus and are accumulated at DNA damage sites.

94 e subcomplexes of vRNA are exported from the nucleus and assembled en route to the plasma membrane.

95 On mitotic entry, NuMA is released from the nucleus and competes LGN from E-cadherin to locally form

96 titioning of cellular components between the nucleus and cytoplasm is the defining feature of eukaryo

97 by a maternal effect gene, is present in the nucleus and cytoplasm of zygotes and has been associated

98 man cells contain five topoisomerases in the nucleus and cytoplasm, but which one is the major topois

99 the selective degradation of proteins in the nucleus and cytosol and is an established target for ant

100 ATP citrate-lyase produces acetyl-CoA in the nucleus and cytosol and regulates histone acetylation le

101 om the lateral hypothalamus and dorsal raphe nucleus and defined a discrete subset of transcripts exp

102 responses from inhibitory thalamic reticular nucleus and excitatory tectothalamic terminals.

103 PR1 oligomers into monomers, which enter the nucleus and function as transcriptional coactivators of

104 peduncular nucleus (EP) is a major BG output nucleus and has been suggested to channel signals from d

105 anding of how the genome folds inside the 3D nucleus and how these folding patterns are miswired duri

106 traffics the tumor suppressor PTEN into the nucleus and in so doing protects it from cytoplasmic pro

107 ord dorsal horn and caudal spinal trigeminal nucleus and in the nucleus of the solitary tract express

108 ith SSc reduces T-bet translocation into the nucleus and its ability to associate with GATA-3, allowi

109 the viral DNA replication centers within the nucleus and likely plays a direct role in replication of

110 decrease heterochromatin results in a softer nucleus and nuclear blebbing, without perturbing lamins.

111 wever, the mechanism of targeting HMR to the nucleus and plastids is still poorly understood.

112 ltipolar ChAT-ir interneurons in the caudate nucleus and putamen, whereas monkeys have a more heterog

113 with anterior associative-limbic subthalamic nucleus and right dorsolateral prefrontal functional con

114 STAiRs 1, 2 and 6 remain unprocessed in the nucleus and show myeloma-specific expression, STAiRs 15

115 lateral projections to the olivary pretectal nucleus and the LGN.

116 eurons per case were selected in the lateral nucleus and traced using Neurolucida software in their e

117 dogenous opioid release in thalamus, caudate nucleus, and anterior insula.

118 GAPDH bound Ape1 in the SMC nucleus, and blocking (or oxidation) of GAPDH active sit

119 e, apical vesicle-rich inverted cone region, nucleus, and cytoplasm.

120 d by Akt, was activated, translocated to the nucleus, and induced the pro-apoptotic gene BCL2-like 11

121 NM in which rod-like bodies are seen in the nucleus, and it often manifests as a severe phenotype.

122 cluding the substantia nigra, entopeduncular nucleus, and nucleus accumbens shell measured using brai

123 TCP20-NLP6&7 heterodimers accumulate in the nucleus, and this coincides with TCP20 and NLP6&7-depend

124 ecs beyond the galactic disks-host an active nucleus, and two of them also have galactic-scale ioniza

125 Arcuate nucleus (ARC) neurons sense the fed or fasted state and

126 resence of RFRP-3 cell bodies in the arcuate nucleus (Arc).

127 HPV replication factories formed in the nucleus are locations where viral DNA is copied to suppo

128 However, protein dynamics within the 3D nucleus are poorly understood.

129 Cav1.2 current density and signaling to the nucleus, are reduced in neurons from densin KO mice.

130 While it functions in the nucleus as a transcriptional coactivator in phytochrome

131 As herpesvirus genomes enter the nucleus as naked DNA, we asked whether the HIRA chaperon

132 ex partitioned to a peripheral region of the nucleus, as shown by super-resolution microscopy.

133 , CDC20 and CCS52B mRNAs are confined to the nucleus at prophase, and the cognate proteins are not tr

134 ral RNA-dependent RNA polymerase in the cell nucleus before being exported to the cytoplasm for trans

135 ne ATP signalling, as shown for the cochlear nucleus bushy cells and principal neurons in the medial

136 ted in the claustrum and dorsal endopiriform nucleus, but not in cortical regions.

137 notoxic stress drives damaged DNA out of the nucleus by forming micronuclei.

138 As) are unstable and rapidly degraded in the nucleus by the nuclear exosome.

139 sm whereby lipid phosphatase activity in the nucleus can regulate mammalian target of rapamycin signa

140 DNA viruses replicating in the nucleus challenge the resident genome and must overcome

141 The mitochondria and the nucleus communicate to coordinate energy production and

142 thalamic nucleus uvaeformis, a multi-sensory nucleus connected to the song system.

143 er carnivores, the dorsal lateral geniculate nucleus consisted of three main layers, A, A1, and C, wh

144 asma membrane, while NFIA is confined to the nucleus, consistent with known functions of each of thes

145 The dorsal cochlear nucleus (DCN) integrates auditory nerve input with a div

146 aBalpha-mediated export of NFkappaB from the nucleus decreased markedly.

147 trin 3 led to its re-distribution within the nucleus, decreased co-localization with endogenous Matri

148 patial organization within the budding yeast nucleus, demonstrates the conserved role of genome archi

149 topography involving bed nucleus vs central nucleus divisions; (2) CRF content of the CEA-DA path; a

150 onses in the mouse dorsal lateral geniculate nucleus (dLGN; thalamic relay for cortical vision).

151 on the signal intensity (SI) of the dentate nucleus (DN) of the pediatric brain on nonenhanced T1-we

152 on the signal intensity (SI) of the dentate nucleus (DN) on unenhanced T1-weighted magnetic resonanc

153 siding in the brainstem's dorsal vagal motor nucleus dramatically impairs exercise capacity, while op

154 The dorsal raphe nucleus (DRN) is an important brain area for body-weight

155 improved high-throughput methods for single-nucleus droplet-based sequencing (snDrop-seq) and single

156 een shown to cycle between the cytoplasm and nucleus due to its nuclear localization (NLS) and export

157 ovo dTMP biosynthesis and translocate to the nucleus during S-phase, where they form a multienzyme co

158 n conformational requirements for fibril and nucleus elongation.

159 ng can be bypassed through the expression of nucleus-encoded, edited forms of plastid genes.

160 The entopeduncular nucleus (EP) is a major BG output nucleus and has been s

161 of the BG of the rodent, the entopeduncular nucleus (EP).

162 ev's trafficking to and retention within the nucleus even prior to RNA binding.

163 hy cells in the mouse anteroventral cochlear nucleus following occlusion of the ear canal.

164 dimers that monomerise and accumulate in the nucleus following UV-B exposure, similar to Arabidopsis

165 lated in the cytoplasm and imported into the nucleus for assembly with the rRNAs.

166 as signal molecules to communicate with the nucleus for maintaining their viability remain unclear.

167 s been scored from energy deposits in a cell nucleus; for very low-energy ions, it has been defined l

168 urons, we show dependence of paraventricular nucleus GLP-1 signaling in the coordination of neuroendo

169 junction and interface coherency affect the nucleus growth, shape and kinetic pathways.

170 its often-observed position in front of the nucleus, has been challenged by contradictory observatio

171 ells, chromosomes are packed inside the cell nucleus in an organised fashion.

172 ily members p100 and RelB translocate to the nucleus in response to CO2 A cohort of RelB protein-prot

173 sources, Msn2 is constantly localized to the nucleus in wild-type cells.

174 h midline structures, including the MnR/DRC, nucleus incertus, supramammillary nucleus, septum, and l

175 mplitude of beta activity in the subthalamic nucleus increases in proportion to burst duration, consi

176 by its degree of C-C bond equalization and a nucleus-independent chemical shift value lower than that

177 t and complementary roles in integrating the nucleus into its environment and influencing its mechani

178 with the paralamellar portion of mediodorsal nucleus, intralaminar nuclei and magnocellular portion o

179 Spatial chromatin interactions in the nucleus involving gene promoters and distal regulatory e

180 ssociated with a reduced dentate and caudate nucleus iron content compared to placebo.

181 similar magnitude to those observed when the nucleus is altered intrinsically, inducing chromatin dec

182 The dynamic organization of genes inside the nucleus is an important determinant for their function.

183 nstrated that neural activity in the caudate nucleus is modulated by task-relevant action values [6,

184 Rev's shuttling into and out of the nucleus is regulated by the antagonistic activities of b

185 afficking route by which beta-DG reaches the nucleus is unknown.

186 USP5 both inactivates and anchors ERK in the nucleus, it paradoxically increases and prolongs cytopla

187 d hence the associated kinetically effective nucleus (KEN), for nanoparticle formation for the first

188 ing mice to evaluate the role of the arcuate nucleus kisspeptin (ARN(KISS)) neurons in LH pulse gener

189 nergic neurons in the laterodorsal tegmental nucleus; lateral noradrenergic neurons in the LC; medial

190 e tonotopic representation in the IC central nucleus leads to the multiple tonotopic representations

191 es in the firing of mouse lateral geniculate nucleus (LGN) neurons, leading to increased firing-rate

192 on of fine details in cell shape, cytoplasm, nucleus, lipid bodies and cytoskeletal structures in 3D

193 eocortex are connected with the claustrum, a nucleus located between the neocortex and the striatum,

194 tical for recollection while the Mediodorsal nucleus (MD) of the thalamus would support familiarity a

195 tical projections from the medial geniculate nucleus (MGN).

196 lamina terminalis (OVLT) and median preoptic nucleus (MnPO).

197 included localization to the lateral tuberal nucleus (NLT), the putative homolog of the mammalian arc

198 alized with 5-methylcytosine in the prophase nucleus of a subset of KIT(+) progenitors during mitosis

199 rin-9-yl pendant to the quinazolin-4(3H)-one nucleus of both aS and aR isomers of 1 had a critical ef

200 eotactically administered to the hypoglossal nucleus of C57BL/6J mice.

201 vagal nerve also projects to the commissural nucleus of Cajal, a general visceral sensory center.

202 otentials were recorded from the subthalamic nucleus of eight Parkinson's disease patients during tem

203 n of CRTC1 from the cytosol/dendrites to the nucleus of hippocampal neurons in the mouse brain.

204 eptor-expressing neurons in the parabrachial nucleus of mice (Oxtr(PBN) neurons) are key regulators o

205 (123)I-FP-CIT binding ratios in the caudate nucleus of PSP patients than in that of both PD and MSA-

206 lecular complex between FAK and Runx1 in the nucleus of SCC cells and showed that FAK interacted with

207 face-centered-cubic stacking, to serve as a nucleus of stacking fault.

208 Because GABAergic neurons of the central nucleus of the amygdala (CeA) target brainstem regions k

209 of locally projecting neurons in the central nucleus of the amygdala (CeA) that produce the neuropept

210 etrogradely transported dye from the central nucleus of the amygdala (CeA) to identify CeA-projecting

211 avian analog of primary motor cortex (robust nucleus of the arcopallium, RA) in Bengalese Finches.

212 We show that the paraventricular thalamus, a nucleus of the dorsal midline thalamus, is integral to t

213 lizes to the centromeres/kinetochores in the nucleus of the host cells by its interaction with the co

214 mulates the growth of axons from the arcuate nucleus of the hypothalamus (ARH) to other regions that

215 neurons densely populate the paraventricular nucleus of the hypothalamus (PVN).

216 r type 1 receptor within the paraventricular nucleus of the hypothalamus is an important central comp

217 or-containing neurons of the paraventricular nucleus of the hypothalamus, the goal being to determine

218 nd glycine for the first time in the central nucleus of the inferior colliculus of the auditory midbr

219 d protein (AgRP) is expressed in the arcuate nucleus of the mammalian hypothalamus and plays a key ro

220 he AR+ nuclei project to the intercollicular nucleus of the midbrain.

221 he amygdala (CeA) to identify CeA-projecting nucleus of the solitary tract (NTS) neurons for synaptic

222 a restricted central-lateral portion of the nucleus of the solitary tract (nTS)-the same area that s

223 caudal spinal trigeminal nucleus and in the nucleus of the solitary tract express aromatase.

224 moderate projections from the posterior bed nucleus of the stria terminalis, mesocortical structures

225 alyx of Held synapse in the mammalian medial nucleus of the trapezoid body (MNTB) plays an important

226 connections in the mammalian CNS: the medial nucleus of the trapezoid body to lateral superior olive

227 hy cells and principal neurons in the medial nucleus of the trapezoid body.

228 T) is a type IB topoisomerase encoded in the nucleus of vertebrate cells.

229 t gamma1 or gamma3 subunit translocated into nucleus on AMPK activation.

230 ocated with a low-luminosity active galactic nucleus or a previously unknown type of extragalactic so

231 From crystallization to embryogenesis, a nucleus or seed is formed and built upon.

232 hways in their subsequent projections to the nucleus ovoidalis (Ov) in the thalamus.

233 ated previously that parafascicular thalamic nucleus (PF)-controlled neurons in the posterior dorsome

234 ee-dimensional (3D) architecture of the cell nucleus plays an important role in protein dynamics and

235 variety of mammals, with the medial preoptic nucleus (POM) and the ventromedial hypothalamic nucleus

236 The pedunculopontine nucleus (PPN) has long been considered an interface betw

237 tergic synapses arising from pedunculopotine nucleus (PPN) neurons were characterized using optical a

238 upregulation in a neighbouring somatosensory nucleus preluding the enlargement of the barrel-field.

239 nucleus interpolaris, subnucleus oralis, and nucleus principalis.

240 mus (the equivalent of the mammalian arcuate nucleus), projecting throughout the hypothalamus and tow

241 The nucleus pulposus (NP) of the intervertebral disc (IVD) d

242 rning and afternoon imaging results for both nucleus pulposus (R = 0.92) and annulus fibrosus (R = 0.

243 inate the notochord from the surrounding the nucleus pulposus, especially in murine models.

244 ts of SK channel subunits mRNA in supraoptic nucleus punches revealed a diminished expression of SK2/

245 rate via projections to the paraventricular nucleus (PVN) and dorsomedial hypothalamus (DMH).

246 NPS within the hypothalamic paraventricular nucleus (PVN) are mediated via actions on local OXT neur

247 Preautonomic neurons in the paraventricular nucleus (PVN) of the hypothalamus play a large role in t

248 Neurones in the principal olivary nucleus receive monosynaptic extra-somatic glutamatergic

249 nsus sequence relocalizes mutant SOD1 to the nucleus, resulting in higher toxicity in cells, and seve

250 ulation exerted by the cytoskeleton onto the nucleus results in changes that are of similar magnitude

251 anscriptomic analysis of the paraventricular nucleus revealed widespread changes in expression of imm

252 tegmental area (VTA)/rostromedial tegmental nucleus (RMTg) regions were activated by peripheral stim

253 Aergic neurons in the rostromedial tegmental nucleus (RMTg), a region that receives dense projections

254 ger complex (preBotC) and the retrotrapezoid nucleus (RTN), but the specific ion channels essential t

255 The suprachiasmatic nucleus (SCN) of the hypothalamus orchestrates daily rhy

256 s arrhythmic hamsters in the suprachiasmatic nucleus (SCN) that paralleled changes in the medial sept

257 e MnR/DRC, nucleus incertus, supramammillary nucleus, septum, and laterodorsal tegmental nucleus.

258 uggesting that topological structures in the nucleus shape local gene activities by a sequestering me

259 ed by neuronal activity, in which synapse to nucleus signalling, mediated via NMDAR and L-type calciu

260 igh-frequency stimulation of the subthalamic nucleus (STN HFS) for heroin addiction.

261 The neuronal population of the subthalamic nucleus (STN) has the ability to prolong incoming cortic

262 cross species has shown that the subthalamic nucleus (STN) is activated by scenarios involving stoppi

263 erent activity in the cortex and subthalamic nucleus (STN).

264 ed in striatal projections to entopeduncular nucleus/substantia nigra, preferentially expressing D1 r

265 aster circadian clock of the suprachiasmatic nucleus synchronizes to light, while environmental cues

266 ound that the residues making up the folding nucleus tend to interact in the denatured state in a tra

267 NLSs) for translocation of proteins into the nucleus that differ from conventional well-characterized

268 derived carbon dots can interact with ARF in nucleus that may further lead to the non-nuclear localiz

269 Thus, the MNTB works as a relay nucleus that preserves the temporal pattern of firing at

270 Accordingly we suggest that for each nucleus the embryonic volume arises from a structural el

271 ysically-based model of a binaural brainstem nucleus, the medial superior olive (MSO), that accounts

272 ylation of and loss of beta-catenin from the nucleus, thereby reducing expression of microphthalmia-a

273 targeting hepatitis B virus (HBV) DNA in the nucleus thus affecting its persistence.

274 anied by a rapid translocation of 5-LOX from nucleus to cytoplasm in both ECs and VSMCs, potentially

275 cytoskeleton (LINC) complexes connecting the nucleus to cytoskeletal elements.

276 ciated nuclear (TAN) lines, which couple the nucleus to dorsal perinuclear actin cables undergoing re

277 astrol promotes Nur77 translocation from the nucleus to mitochondria, where it interacts with tumor n

278 ed from the ER membrane, and then enters the nucleus to participate in transcription regulation of th

279 e been proposed but not shown to move to the nucleus to promote plant acclimation to fluctuating ligh

280 Cactus complex, allowing Dorsal to enter the nucleus to regulate target genes.

281 Remarkably, PSPC1 relocates from the nucleus to the cytoplasm during differentiation, coincid

282 the bond connecting the quinazolin-4(3H)-one nucleus to the o-tolyl is sterically hampered, which lea

283 minal fragment from the ER, which enters the nucleus to work as a transcription factor.

284 rmacological studies highlight the hindbrain nucleus tractus solitarius (NTS) as a brain region impor

285 calized exclusively in the area postrema and nucleus tractus solitarius of the mouse brainstem.

286 tion from nTTD to the contralateral thalamic nucleus uvaeformis, a multi-sensory nucleus connected to

287 intracellular trafficking from the PM to the nucleus via the endosome-ER network.

288 oronate motif are actively trafficked to the nucleus via the importin alpha/beta pathway.

289 leus (POM) and the ventromedial hypothalamic nucleus (VMH) mediating control of male and female sexua

290 n, or a more direct topography involving bed nucleus vs central nucleus divisions; (2) CRF content of

291 The nucleus was the most sensitive cellular compartment to 5

292 ial lobe projections to the medial funicular nucleus were also noted.

293 GSK3beta and protein expression of GATA4 in nucleus were detected with Western blot experiment.

294 rocessed and translocated from the ER to the nucleus, where interaction with the WRKY29 transcription

295 ot shifts localization of the complex to the nucleus, where it facilitates the association of YAP and

296 he single-stranded DNA (ssDNA) genome to the nucleus, where viral replication occurs.

297 us, result from phase separations within the nucleus, which are driven by the enrichment of protein-m

298 and subsequent accumulation of puncta in the nucleus, which remained stable through 5 days.

299 easing factor neurons in the paraventricular nucleus, which when activated result in elevated plasma

300 Cs) are multiprotein channels connecting the nucleus with the cytoplasm.