ライフサイエンスコーパス: nucleus

1 enetic information is sequestered within the nucleus.

2 rkinG430D, are selectively excluded from the nucleus.

3 e used for monitoring proton dynamics in the nucleus.

4 cleoprotein particle assembly throughout the nucleus.

5 d substrates, and caused accumulation in the nucleus.

6 roteins, are predominantly trafficked to the nucleus.

7 e of CasRx, and redirected the editor to the nucleus.

8 r cytoplasmic molecules are cleared from the nucleus.

9 tion of capsid protein-encoding mRNAs in the nucleus.

10 and remyelination, to drag Sox10 out of the nucleus.

11 ogenesis or the localization of MIWI2 to the nucleus.

12 hat cohesin is its primary interactor in the nucleus.

13 he DBS device bilaterally in the subthalamic nucleus.

14 d its localization from the cytoplasm to the nucleus.

15 mpartment, and more specifically, within the nucleus.

16 NLS and lowers the abundance of CRWN4 in the nucleus.

17 y of three-dimensional structures within the nucleus.

18 and upregulate the biosensor signals in the nucleus.

19 and liquid-like condensates in vitro and in nucleus.

20 educed the binding of RelA/p65 to DNA in the nucleus.

21 sient activity observed in the cytoplasm and nucleus.

22 gue Msp300 at the cytoplasmic surface of the nucleus.

23 ng their largest and stiffest organelle, the nucleus.

24 nocortin neurons in the hypothalamic arcuate nucleus.

25 ualised in cellular vacuoles and in the cell nucleus.

26 protein platform tethering the Golgi to the nucleus.

27 to both package and organize DNA within the nucleus.

28 ade transport pathway for trafficking to the nucleus.

29 rticular NPY and POMC neurons in the arcuate nucleus.

30 -STAT3) and enables it to translocate to the nucleus.

31 re to reflect "transcriptional niche" in the nucleus.

32 nd facilitate HIV-1 viral replication in the nucleus.

33 f these proteins from the cytoplasm into the nucleus.

34 ell, such as endosomes, the cytosol, and the nucleus.

35 eir small genome (mitochondrial DNA) and the nucleus.

36 excitatory synapse arising from the cochlear nucleus.

37 factor that activates gene expression in the nucleus.

38 populations including the dorsal raphe (DR) nucleus.

39 esence of NE axons projections in this brain nucleus [6], we assessed the effects of NE activity in t

40 oking in human postmortem brain, focusing on nucleus accumbens (NAc) as a key brain region in develop

41 pression was increased in D1+ neurons in the nucleus accumbens (NAc) core and dorsolateral (DLS) stri

42 Here we studied the role of the nucleus accumbens (NAc) in this model.

43 The nucleus accumbens (NAc) is a reward processing hub sensi

44 nvestigated whether GSK3beta activity in the nucleus accumbens (NAc) is associated with depression-li

45 ectivity (FC) of reward neurocircuitry using nucleus accumbens (NAc) seed regions of interest, and th

46 The nucleus accumbens (NAc), a central component of the midb

47 In the nucleus accumbens (NAc), structural and physiological pl

48 and decreases AMPAR-mediated currents in the nucleus accumbens (NAc).

49 Finally, patch recordings in nucleus accumbens (NAcc) medium spiny neurons (MSNs) rev

50 er problems on adolescent depression through nucleus accumbens (NAcc) volume alteration, but not thro

51 PAR/GluR composition both in the PFC and the nucleus accumbens (NAcc).

52 t fMRI experiment, we show that learning and nucleus accumbens activation in a simple unidimensional

53 vivo dopamine and glutamate microdialysis in nucleus accumbens and medial prefrontal cortex, and ex v

54 nding does not elicit differences in overall nucleus accumbens Ca(2+) activity.

55 tween the basolateral amygdala (BLA) and the nucleus accumbens core (NAcC).

56 The nucleus accumbens core (NAcore) contains two predominate

57 for differences in dopamine signaling in the nucleus accumbens core at baseline, in response to a sin

58 of cocaine to inhibit dopamine uptake in the nucleus accumbens core using fast scan cyclic voltammetr

59 shRNA-mediated knockdown of Lmo4 in the nucleus accumbens enhanced alcohol consumption, whereas

60 ometry revealed that dopamine release in the nucleus accumbens evoked by reward-predictive cues is ac

61 rojections from the prefrontal cortex to the nucleus accumbens has been argued to underlie motivation

62 Substantial evidence implicates the nucleus accumbens in motivated performance, but very lit

63 These results may be relevant to roles of nucleus accumbens mechanisms in pathological motivations

64 ect was seen specifically on the inputs from nucleus accumbens medium spiny neurons expressing either

65 activity in spiny projection neurons in the nucleus accumbens of mice during learning.

66 ow this family regulates activity within the nucleus accumbens or behavioral responses to drugs of ab

67 against acute oxycodone-induced decreases in nucleus accumbens oxygen levels.

68 Is neuronal inhibition in nucleus accumbens required for such pharmacologically-in

69 ifically, prediction-error activation in the nucleus accumbens was similar across age groups, and num

70 weeks, and transcriptomic regulations in the nucleus accumbens were measured by RNA sequencing.

71 coded RPEs and did so more robustly than the nucleus accumbens, an input to the VP.

72 mo in most areas except for the hippocampus, nucleus accumbens, and thalamus.

73 The latest research demonstrates that in the nucleus accumbens, opioid-induced excitatory synaptic pl

74 involved in the pair-bonding process in the nucleus accumbens, our work illustrates the vast extent

75 ated within DS synapses, but enhanced in the nucleus accumbens, suggesting a dichotomous role of BDNF

76 erging of the parental genomes into a single nucleus after mitosis.

77 l and structural organization of the olivary nucleus and a novel experimental and theoretical approac

78 a mice; CAR spontaneously accumulates in the nucleus and activates the Sult1e1 promoter by recruiting

79 area, and lamina I of the spinal trigeminal nucleus and all levels of the spinal cord.

80 ssigned voxels were localised to the caudate nucleus and anterior putamen, overlapping with executive

81 pon activation, YAP/TAZ translocate into the nucleus and bind to TEAD transcription factors to promot

82 GFP:EXO70A2 was localized to the nucleus and cytoplasm in developing pollen grains and la

83 hat resolve transcript subpopulations in the nucleus and cytoplasm indicate post-transcriptional proc

84 nucleolar localization that shuttles between nucleus and cytoplasm.

85 mediates formation of nuclear bodies in the nucleus and has a role in the progression of S-phase of

86 e shown that cGAS is localized mostly in the nucleus and has low activity as a result of tight nuclea

87 ese kinases are regulated differently in the nucleus and in the cytosol.

88 pid increase in refractive index in the lens nucleus and increased expression of a particular crystal

89 ne transcripts associated with growth in the nucleus and macromolecular RNA-protein complexes contrib

90 ed with affective pain, such as parabrachial nucleus and medial thalamic nucleus, as well as sensory-

91 ipir correlated with tau lesion score in red nucleus and midbrain tegmentum across patients, but not

92 brain cell types from the anterior pretectal nucleus and periaqueductal gray (p<1.2x10(-4)).

93 ulted from directly binding of AMPKalpha2 in nucleus and phosphorylating it at Thr172 residue.

94 nths after injection, the anterior olfactory nucleus and piriform cortex displayed a high alpha-synuc

95 cognition-action separation between caudate nucleus and putamen-a striatal sub-division unique to pr

96 It largely localizes in the cell nucleus and regulates CD39 by interacting with nucleolin

97 rds a unique opportunity to record from this nucleus and stimulate it in a controlled manner.

98 ntrality values in OCD for volume of caudate nucleus and thalamus, and surface area of paracentral co

99 demonstrate that Parkin has functions in the nucleus and that Parkinson's disease-associated Parkin m

100 in regions of interest placed in the dentate nucleus and the pons, and we calculated the dentate nucl

101 put from the substantia nigra to the caudate nucleus and the putamen.

102 the behavior of matter denser than an atomic nucleus and to measure the expansion rate of the Univers

103 psule, the ventral striatum, the subthalamic nucleus, and a midbrain target.

104 enza virus transcription, likely acts in the nucleus, and contributes to the upregulation of antivira

105 e cell cycle, and in interphase cells to the nucleus, and in both a diffuse and punctate pattern in t

106 ral RNA transcription and replication in the nucleus, and its functions rely on host factors.

107 ed miRNAs, partial retention of miRNA in the nucleus, and reduced levels of AGO1.

108 ing an Ugi reaction, building of the pyrrolo nucleus, and reduction-cyclization to the corresponding

109 RPS2B binds directly to pre-rRNAs in the nucleus, and such binding is enhanced in atprmt3-2.

110 perior colliculus, dorsal lateral geniculate nucleus, and the posterior nucleus of the pulvinar are w

111 w that the neurons of the anterior olfactory nucleus (AON), which form abundant synaptic projections

112 the homologous chromosomes to the center of nucleus are almost the same.

113 ase in the mitochondria and functions in the nucleus as a transcriptional activator for hundreds of g

114 , it stimulates lysosome clustering near the nucleus as seen in TMEM106B-deficient cells.

115 as parabrachial nucleus and medial thalamic nucleus, as well as sensory-discriminative pain, such as

116 l inversion of the dorsal lateral geniculate nucleus, as well as the lateral posterior and pulvinar n

117 , the centrosome is positioned away from the nucleus at the apical surface of the ventricular zone of

118 uate hypothalamic nucleus -> paraventricular nucleus axonal fiber outgrowth.

119 thologies, the mechanism by which the cancer nucleus becomes misshapen is not fully understood.

120 H domain of YTHDC1 (known to localize in the nucleus) binds ssDNA containing N6mA, with a 10 nM disso

121 terial in a manner distinct from that of the nucleus but that requires organized mito-nuclear communi

122 ort that it not only localizes mainly to the nucleus, but is concentrated in the nucleolus, where the

123 Nucleus centering in mouse oocytes results from a gradie

124 hose various components are localized in the nucleus, centrosome, and cytoplasm.

125 285 x 10(-3) mm(2)/s, p = 0.031) and caudate nucleus (CN) (1.319 vs. 1.394 x 10(-3) mm(2)/s, p = 0.04

126 oncomitant beta-catenin translocation to the nucleus, collectively leading to cMyc transcription.

127 Exquisitely regulated plastid-to-nucleus communication by retrograde signaling pathways i

128 l particles were unevenly distributed in the nucleus, cytoplasm of the cell body, and axon.

129 I sequences is that the ventral intermediate nucleus, dentatorubrothalamic tract, and other deep brai

130 serotonergic neuron enriched embryonic raphe nucleus-derived neural stem cells/progenitors into the l

131 ve deep brain stimulation of the subthalamic nucleus differentially modifies different oscillatory ac

132 the brainstem raphe nuclei, the dorsal raphe nucleus (DR) contains the greatest number of Pet1-lineag

133 n the ventral subnucleus of the dorsal raphe nucleus (DRv).

134 oteins (RNPs) to shuttle the template to the nucleus, enhancing HDR efficiency approximately two- to

135 We validated the single-nucleus findings using RNA fluorescence in situ hybridiz

136 visual cortex to the dorsolateral geniculate nucleus (first-order) and pulvinar (higher-order) using

137 cts with NP1 to escort NP1 imported into the nucleus for its function in the modulation of viral mRNA

138 erefore, the vRNPs must be imported into the nucleus for viral transcription and replication, which r

139 the solitary tract and arcuate hypothalamic nucleus -> paraventricular nucleus axonal fiber outgrowt

140 The basal ganglia, especially the caudate nucleus 'head' (CDh) of the striatum, receive indirect a

141 Thousands of proteins localize to the nucleus; however, it remains unclear which contain trans

142 ents rifted from the Congo/Tanzania cratonic nucleus in a manner very similar to the development of t

143 chidonic acid in the cerebellar interpositus nucleus in males only; (2) decreased 2-arachidonoyl glyc

144 Further, Parkin translocates to the nucleus in response to hypoxia which correlates with inc

145 y chemosensory neurons of the retrotrapezoid nucleus in the brainstem(4-6) and pH homeostasis by kidn

146 fusion of Fyn kinase between the cytosol and nucleus in the cells, which is important for the mainten

147 VTA (also called the rostromedial tegmental nucleus) in male rats.

148 es in numerous proteins that function in the nucleus, including several constituents of the nuclear p

149 In this sense, nucleus-independent chemical shift (NICS) and anisotropy

150 onic oscillator model of aromaticity), NICS (nucleus-independent chemical shift), ACID (anisotropy of

151 ct almost exclusively to the interpeduncular nucleus (IPn) and are known to regulate nicotine avoidan

152 anscripts in the habenula or interpeduncular nucleus (IPn) increases nicotine intake in rats.

153 p brain stimulation (DBS) of the subthalamic nucleus is a symptomatic treatment of Parkinson's diseas

154 about the protein copy number of TFs in the nucleus is limited.

155 on, egress of nascent viral capsids from the nucleus is mediated by the viral nuclear egress complex

156 tions from these neurons to the parabrachial nucleus is reinforcing, and increases ethanol drinking a

157 e found that the octavolateral efferent (OE) nucleus is the likely source of cholinergic fibers inner

158 from isthmic nuclei, possibly including the nucleus lateralis valvulae (nLV) and the isthmic nucleus

159 The laterodorsal tegmental nucleus (LDTg) expresses GLP-1Rs and functions as a neur

160 activity in subcortical (lateral geniculate nucleus, LGN) and cortical (area MT) visual areas in ana

161 aeruginosa, by constructing a proteinaceous nucleus-like compartment.

162 he cytoplasm followed by fast reentry to the nucleus ("localization-resets") activates YAP target gen

163 icial mamillary area, laterodorsal tegmental nucleus, locus coeruleus, inferior and superior collicul

164 Lateral posterior nucleus (LP) of thalamus, the rodent homologue of primat

165 iaqueductal gray (PAG), lateral parabrachial nucleus (LPB), caudal pressor area, and lamina I of the

166 pressing neurons in the lateral parabrachial nucleus (LPBN(Htr2c) neurons) inhibit sodium appetite.

167 The lateral parabrachial nucleus (lPBN) is a major target of spinal projection ne

168 this information to the mediodorsal thalamic nucleus, magnocellular part (MDmc).

169 In the nucleus, more than half of P-TEFb are sequestered in the

170 requires asymmetric cell division, where the nucleus moves to the division site based on cellular pol

171 d with opioid markers in the medial preoptic nucleus (mPOA).

172 multichannel spike trains of dorsal cochlear nucleus neurons to disentangle reciprocal and feedforwar

173 Moreover, in thalamic reticular nucleus neurons, burst firing is impaired accompanied by

174 uclei neurons onto gigantocellular reticular nucleus neurons, which might produce an action tremor by

175 MN targets of glucose-elevating parabrachial nucleus neurons.

176 eus lateralis valvulae (nLV) and the isthmic nucleus (nI).

177 Transport into and out of the nucleus occurs through the nuclear pore complex (NPC).

178 xo1 (SD-Foxo1) was largely excluded from the nucleus of CD8 T cells and failed to transactivate these

179 population of ERalpha neurons in the arcuate nucleus of female mice undergoes a shift in phenotype, f

180 ve synapses onto bushy cells in the cochlear nucleus of mice of both sexes.

181 ted eEF1A1 (Ac-eEF1A1) translocates into the nucleus of myelinating cells where it binds to Sox10, a

182 Given the role of the central nucleus of the amygdala (CeA) in the expression of such

183 ectrophysiological recordings in the central nucleus of the amygdala (CeA), we found that rats with h

184 The central nucleus of the amygdala plays a significant role in alco

185 ous analgesia neural ensemble in the central nucleus of the amygdala.

186 in PACAP levels were observed in the central nucleus of the amygdala.

187 t, we show that the zebra finch vocal robust nucleus of the arcopallium (RA) shares numerous markers

188 mologs, hypothalamus, preoptic area, septum, nucleus of the diagonal band of Broca, and main olfactor

189 tin (PNOC)-expressing neurons in the arcuate nucleus of the hypothalamus (ARC).

190 ke, POMC and NPY/AgRP neurons in the arcuate nucleus of the hypothalamus (ARH) are derived from the s

191 Neurons within the paraventricular nucleus of the hypothalamus (PVH) are a key component of

192 and send projections to the paraventricular nucleus of the hypothalamus (PVN) that appear to synapse

193 ateral geniculate nucleus, and the posterior nucleus of the pulvinar are well-developed by birth.

194 The nucleus of the solitary tract (NTS) is activated by vaga

195 control the development of area postrema -> nucleus of the solitary tract and arcuate hypothalamic n

196 parison, CeL/C neurons projecting to the bed nucleus of the stria terminalis (BNST) are also frequent

197 The bed nucleus of the stria terminalis (BNST) is a sexually dim

198 e investigated the effects of CRF in the bed nucleus of the stria terminalis (BNST) of lactating mice

199 Even though the lateral geniculate nucleus of the thalamus (LGN) is associated with form vi

200 perior colliculus (SC) through medial-dorsal nucleus of the thalamus (MD) to frontal eye field (FEF)

201 neurons which span the area postrema and the nucleus of the tractus solitarius of the mouse.

202 c sound localization pathway from the medial nucleus of the trapezoid body (MNTB) to the lateral supe

203 at the trophic effects of one forebrain song nucleus on its target are mediated transsynaptically by

204 ensity of the globus pallidus and/or dentate nucleus on unenhanced T1-weighted magnetic resonance (MR

205 g new microtubules at distances far from the nucleus or cell body.

206 equence, therefore, self-DNA leaked from the nucleus or mitochondria can also serve as a cGAS ligand

207 hree sub-regions: the parabrachial pigmented nucleus (PBP), parainterfascicular nucleus (PIF), and pa

208 pigmented nucleus (PBP), parainterfascicular nucleus (PIF), and paranigral nucleus (PN).

209 ic organization of chromatin inside the cell nucleus plays a key role in gene regulation and genome r

210 nterfascicular nucleus (PIF), and paranigral nucleus (PN).

211 The difference in the dentate nucleus-pons signal intensity ratio between the first an

212 Projections to the nucleus praeeminentialis (nP) arise from isthmic nuclei,

213 (i.e., the lateral dorsal nucleus, submedial nucleus) previously unidentified as L5 targets.

214 3 protein is constitutively localized in the nucleus prior to DNA damage.

215 t that this central amygdala to parabrachial nucleus projection influences the expression of reward-r

216 drugs to reach their target cells inside the nucleus pulposus (NP), the central gelatinous region of

217 owing areas: level of basal ganglia (caudate nucleus, putamen, corpus callosum, posterior limb of int

218 ignaling in the hypothalamic paraventricular nucleus (PVN) is necessary for the expression of binge-e

219 differentially innervate the interpeduncular nucleus, raphe nuclei, substantia nigra pars compacta an

220 loss, its precise function in the interphase nucleus remains elusive.

221 restriction factor, RTF2, which acts in the nucleus, restricts influenza virus transcription, and co

222 ported muscleblind-like-1 (MBNL1) out of the nucleus, resulting in significant inhibition of MBNL1 ac

223 are reactivated in the companion vegetative nucleus, resulting in siRNA production and the intercell

224 in mTORC1, and localization of Raptor to the nucleus results in nuclear mTORC1 activity in the absenc

225 The nucleus reuniens (NR) is an important anatomic and funct

226 anized cells assemblies are recruited in the nucleus reuniens at the UP state onset during slow oscil

227 Reconstruction of the 3D nucleus revealed that distances of the homologous chromo

228 rovided unprecedented access to this elusive nucleus, revealing new levels of organization and functi

229 nputs to the VTA, the rostromedial tegmental nucleus (RMTg), and the periaqueductal gray (PAG).

230 this, we characterized neural signals in red nucleus (RN), a brain region linked to motor control, as

231 Single cell and single nucleus RNA profiling provide one avenue to decipher thi

232 Single-nucleus RNA sequencing (snRNA-seq) measures gene express

233 Single-nucleus RNA sequencing provides an alternative way to ob

234 t an area postrema cell atlas through single-nucleus RNA sequencing, revealing a few neuron types.

235 es single-cell RNA-seq (scRNA-seq) or single-nucleus RNA-seq (snRNA-seq) data to generate a reference

236 cells dissociated from fresh tumors, single-nucleus RNA-Seq (snRNA-Seq) is needed to profile frozen

237 In this study, we performed single-nucleus RNA-Seq on the adult mouse SV in conjunction wit

238 paring 13 commonly used scRNA-seq and single-nucleus RNA-seq protocols applied to a heterogeneous ref

239 We innovated single-nucleus RNA-sequencing protocols and profiled more than

240 respiratory group (pFRG) and retrotrapezoid nucleus (RTN) region are capable of rapidly responding t

241 /H(+)-vasoconstriction in the retrotrapezoid nucleus (RTN) supports chemoreception by a purinergic-de

242 is a fast, accurate, and persistent mark of nucleus rupture whose kinetics are partially dictated by

243 The suprachiasmatic nucleus (SCN) is a complex structure dependent upon mult

244 tion potential firing in the suprachiasmatic nucleus (SCN) translate time-of-day throughout the mamma

245 l horn laminae II-IV, and dorsal commissural nucleus (SDCom).

246 The comparison with neonatal single-nucleus sequencing data showed a different cellular comp

247 Here, we show in the mouse that raphe nucleus serotonin neurons activate ventral tegmental are

248 e concentrated in the sacral parasympathetic nucleus (SPN), dorsal horn laminae II-IV, and dorsal com

249 athway from the isocortex to the subthalamic nucleus (STN) adjacent to the PSTN.

250 stimulation (DBS), targeting the subthalamic nucleus (STN) and globus pallidus interna, is a surgical

251 CANCE STATEMENT It is known that subthalamic nucleus (STN) beta activity is linked to symptom severit

252 p brain stimulation (DBS) of the subthalamic nucleus (STN).

253 s specifically attributed to the subthalamic nucleus (STN).

254 reas activation of lPBN efferents to the bed nucleus stria terminalis (BNST) or central amygdala (CEA

255 rticofugal targets (i.e., the lateral dorsal nucleus, submedial nucleus) previously unidentified as L

256 NI type1 are completely enclosed within the nucleus, suggesting that NI, although probably derived f

257 A receptors at plasma membrane, cytosol, and nucleus, targeting them for degradation via the endosoma

258 ervated by motoneurons within the protractor nucleus that also has a motoneuron afferent population.

259 of the central amygdala, a stress-sensitive nucleus that forms a major input to the DR.

260 phically and functionally organized thalamic nucleus that is largely dedicated to visual processing.

261 his set constitutes an archetypal cerebellar nucleus that was repeatedly duplicated to form new regio

262 anterior insula and one in the dorsal raphe nucleus, that track global reward state as well as speci

263 drenergic receptors in the midbrain auditory nucleus, the inferior colliculus (IC), but have not exam

264 opeptide galanin from the main noradrenergic nucleus, the locus coeruleus (LC).

265 Apart from the presence of the perireticular nucleus, the most notable difference between the species

266 les can easily enter cells and even the cell nucleus, these data provide evidence that ultrasmall nan

267 lear transfer (SCNT) can reprogram a somatic nucleus to a totipotent state.

268 changes in epigenetic marks, allow a somatic nucleus to become totipotent after transfer into an oocy

269 Synapses from the posterior medial thalamic nucleus to edge TRN cells evoke slower, less depressing

270 d, allowing the protein to accumulate in the nucleus to enhance its transcription function.

271 enges chromosome folding architecture in the nucleus to establish functional structures.

272 otein stabilization and translocation to the nucleus to regulate context-specific transcriptional pro

273 ufonamides featuring a diazaspiro[4,4]nonane nucleus to target the guanine nucleotide exchange activi

274 pan the nuclear envelope, which connects the nucleus to the cytoplasm.

275 complex process involving transport from the nucleus to the plasma membrane.

276 ministrations and an increase in the dentate nucleus-to-middle cerebral peduncle signal intensity rat

277 and the pons, and we calculated the dentate nucleus-to-pons signal intensity ratios and the differen

278 0.23 +/- 0.09; P < .001) and thalamus to red nucleus tract (mean number of tracts at baseline, 1663,

279 Interleukin (IL)-1beta microinjected in the nucleus tractus solitarii increases fR and the predictab

280 rain [regions involved in autonomic control: nucleus tractus solitarius (NTS) and rostral ventrolater

281 ions as a neuroanatomical hub connecting the nucleus tractus solitarius (NTS), the primary source of

282 d activated gustatory neurons in the rostral nucleus tractus solitarius.

283 ontrol of the window of time over which each nucleus transcribes even-skipped plays a critical role i

284 alyses of large-scale single-cell and single-nucleus transcriptomes, we characterize six anatomical a

285 ing sleep, neurons in the thalamic reticular nucleus (TRN) participate in distinct types of oscillato

286 kinase can be actively transported into the nucleus upon light activation and upregulate the biosens

287 These interorganelle nucleus-vacuole junctions (NVJs) cooperate with lipid dr

288 us-internus [GPi] and ventrolateral anterior nucleus [VLa]) in monkeys performing a reaching task.

289 e the sleep-promoting ventrolateral preoptic nucleus (VLPO) is lesioned (male Sprague-Dawley rats).

290 ns were also observed within the vocal motor nucleus (VMN), forming putative contacts on those cells.

291 cell types in the ventromedial hypothalamic nucleus (VMN), we studied the cholecystokinin receptor B

292 The lateral geniculate nucleus was only modulated by 3 to 9% luminance contrast

293 s in the mouse fastigial (medial cerebellar) nucleus, we identify five major classes of glutamatergic

294 ed that KDR is translocated primarily to the nucleus when coexpressed with these interactors.

295 glutamine protein expressed primarily in the nucleus where it binds chromatin and functions as a tran

296 re we report that LOXL1-AS1 localizes to the nucleus where it selectively binds to the mRNA processin

297 s glutamate release in an auditory brainstem nucleus, while suppressing evoked release.

298 ion of chromosome-autonomous signaling and a nucleus-wide crossover-counting mechanism partitions hol

299 ossibility that CRWN4 is coimported into the nucleus with nuclear localization signal (NLS)-bearing p

300 , here we review the roles of the CBC in the nucleus, with a focus on protein-coding genes.