ライフサイエンスコーパス: nuclei

1 s system is discrete clusters of neurons or 'nuclei'.

2 ltiple effectors that target chloroplasts or nuclei.

3 mainly within the medio-dorsal and pulvinar nuclei.

4 nipulation experiments stretching individual nuclei.

5 racting features from fluorescently labelled nuclei.

6 mus (pulvinar) and the medio-dorsal thalamic nuclei.

7 tion via its receptor in the ARC and/or AVPV nuclei.

8 nce to cancers, which often exhibit enlarged nuclei.

9 s to visualize mouse muscle fibers and their nuclei.

10 enerate three lines of mice cloned from iNKT nuclei.

11 echanisms by which NR can form in interphase nuclei.

12 ight lead to the splitting of bilobate comet nuclei.

13 Drosophila and evaluated the position of the nuclei.

14 ds forebrain targets and away from hindbrain nuclei.

15 ed to maximize the distance between adjacent nuclei.

16 and pontine reticular formation and pontine nuclei.

17 mitotic metaphase chromosomes and interphase nuclei.

18 but not in the relatively spared extraocular nuclei.

19 ventral medial and ventral anterior-lateral nuclei.

20 cross two BLA regions, the lateral and basal nuclei.

21 ends on those of the other electrons and the nuclei.

22 he claustrum proper and related endopiriform nuclei.

23 nje cells and neurons of the deep cerebellar nuclei.

24 halamic supraoptic (SON) and paraventricular nuclei.

25 ulate signal reception processed by afferent nuclei.

26 ntacts in organizing the genome in mammalian nuclei.

27 ns that supply serotonin to the hypothalamic nuclei.

28 in reduced nuclear blebbing in lamin B1 null nuclei.

29 and area of each telomere within individual nuclei.

30 gulate genetic information within eukaryotic nuclei.

31 and cognitive function via numerous distinct nuclei.

32 Dense bilateral connections were to caudate nuclei.

33 CNM were each necessary to properly position nuclei.

34 tion of chloroplasts closely associated with nuclei.

35 rest at S phase with increased cell size and nuclei.

36 trong feedback from stars or active galactic nuclei.

37 predominance of type 1 fibre and centralized nuclei.

38 y is NSs filament formation in infected cell nuclei.

39 at the plasma membrane, in cytosol and cell nuclei.

40 limiting factor in the minimal volume of the nuclei.

41 and innervating major midbrain monoaminergic nuclei.

42 orsal gray commissural and intermediolateral nuclei.

43 le pollen and embryo sacs with unfused polar nuclei.

44 ng and separations of the highly radioactive nuclei.

45 iations of the net magnetic anisotropy of FM nuclei.

46 on of mergers originate from active galactic nuclei.

47 istent with the neurobiology of the amygdala nuclei.

48 s resulted in syncytia with only 2-fold more nuclei, a -0.5-log10 reduction in titers, and pOka-like

49 ly interpreted as originating from brainstem nuclei, a recent study using MEG suggested that there is

50 oxymethyltransferase (SHMT), was enriched in nuclei, accounting for 35% of folate cofactors, explaini

51 x-ray scattering, we show that isolated bull nuclei achieve slightly lower DNA packing densities comp

52 ns was assessed by direct sequencing, locked nuclei acid (LNA)-based PCR, and immunohistochemistry.

53 rst-order and higher-order sensory and motor nuclei across different modalities are largely segregate

54 We found that in mouse liver nuclei all three PERs, both CRYs, and Casein Kinase-1del

55 known neurobiology of individual amygdaloid nuclei, allowing for human imaging studies to accurately

56 thought to provide an essential link between nuclei and actin.

57 apses from Purkinje cells to deep cerebellar nuclei and at vestibular synapses in mice.

58 pipeline on the selected regions to extract nuclei and compute shape, size, intensity, and texture f

59 the pattern of connectivity between thalamic nuclei and cortical areas or deep nuclei), which indepen

60 nt of ERK activity by analysis of individual nuclei and faithfully reports ERK activity during develo

61 N-terminal mHtt accumulates in the nuclei and forms aggregates, causing decreased secretion

62 in brain tissue, most notably in the dentate nuclei and globus pallidus.

63 pts expressed in neurons of the dorsal raphe nuclei and lateral hypothalamus that project to the meso

64 portion of mediodorsal nucleus, intralaminar nuclei and magnocellular portion of ventral anterior nuc

65 between bands 3 and 4 corresponds to the RPE nuclei and melanosomes zone.

66 Secondary analyses examined the parabrachial nuclei and other brain regions involved in food intake a

67 he nuclear scaffold protein lamin A distorts nuclei and sequesters nuclear proteins.

68 ssible co-evolution of the inferior pulvinar nuclei and temporal cortical visual areas within the MT

69 in vivo significantly reduced the number of nuclei and the number of Lgr5EGFP-positive stem cells pe

70 he pathway that connects the brainstem vagal nuclei and the SNpc, and to determine whether this pathw

71 erated >6000 methylomes from single neuronal nuclei and used them to identify 16 mouse and 21 human n

72 ifts the master clock in the suprachiasmatic nuclei and/or slows down the photic entrainment in noctu

73 l RBCs, such as those of mammals (which lack nuclei) and birds, contribute to shorter diffusion dista

74 cP (spiriformis lateral and lateral terminal nuclei), and PcP (anterior pretectal nucleus) to those d

75 s of the cerebellum, habenula, preglomerular nuclei, and several other diencephalic, mesencephalic, a

76 g cells are prominent in motor cranial nerve nuclei, and some scattered cells lie in the preoptic are

77 le myofibrillar apparatus with mitochondria, nuclei, and the sarcolemma.

78 in pretectal output is to the reticulospinal nuclei, and thus the pretectum indirectly affects the co

79 ynert, basolateral and basomedial amygdaloid nuclei, anterior pretectal and interpeduncular nuclei, a

80 The habenular nuclei are a conserved integrating center in the vertebr

81 Thus, even when not moving, nuclei are actively maintained in position by engaging t

82 at MET+ neurons in the brainstem vagal motor nuclei are anatomically positioned to regulate distinct

83 scle cells are a syncytium in which the many nuclei are positioned to maximize the distance between a

84 he arcuate and anteroventral periventricular nuclei are postulated to mediate negative and positive f

85 Expelled nuclei are smaller thus could be removed by size-based s

86 Their nuclei are uniquely structured as multiple lobes that es

87 the spreading of cells and the stiffening of nuclei as both actomyosin assembly and nucleoskeletal la

88 hanical properties of single cells and their nuclei as critical drivers for the onset of cancer.

89 inary black hole mergers and active galactic nuclei as hosts, even if only a sub-population of merger

90 of the literature focuses on the mesolimbic nuclei as the core of reward behavior regulation.

91 raventricular, ventromedial, and dorsomedial nuclei as well as in the lateral area of the hypothalamu

92 tinct changes, with a loss of multilobulated nuclei, as well as nuclear decondensation followed by me

93 clei, anterior pretectal and interpeduncular nuclei, as well as select laminae of the superior collic

94 ignificant decline occurred in photoreceptor nuclei at 240 days of age ( approximately 36.8% rods and

95 hors visualize the birth and growth of metal nuclei at electrode surfaces in real time via high-speed

96 e, direct H2O2 transfer from chloroplasts to nuclei, avoiding the cytosol, enables photosynthetic con

97 of neurons in lateral nuclei (LAT) and basal nuclei (BA) of the BLA that were associated with greater

98 At constant temperature, isolated nuclei behaved like passive, elastic and incompressible

99 teral sclerosis-affected cranial nerve motor nuclei but not in the relatively spared extraocular nucl

100 C) receives dopaminergic input from midbrain nuclei, but the role of dopamine in the OFC is still unc

101 sitive for acrosomal markers and attached to nuclei, but these vesicles failed to form large acrosoma

102 this end, we have measured the compliance of nuclei by applying oscillatory strains between 1 and 700

103 itin-conjugating enzyme 9 (Ubc9) in HCC cell nuclei by cell fractionation and confocal microscopy; ph

104 accurate mitotic NPC segregation to daughter nuclei by linking mitotic DNA and NPC segregation via th

105 re host galaxy types-such as active galactic nuclei-can nevertheless be identified statistically thro

106 TS: Large premotor neurons of the cerebellar nuclei (CbN cells) integrate synaptic inhibition from Pu

107 : Large projection neurons of the cerebellar nuclei (CbN cells), whose activity generates movement, a

108 rge premotor neurons of the mouse cerebellar nuclei (CbN cells).

109 en pack ice increased the cloud condensation nuclei concentration background by at least ca. 20%, sup

110 ed for nucleated cells, enucleated cells and nuclei (day 14) of 1.04 +/- 0.47 kPa, 0.53 +/- 0.12 kPa

111 We observed that FTO is expressed in the nuclei, dendrites and near dendritic spines of mouse dor

112 ons are focally located in specific thalamic nuclei depending on the initial infarct location; and (i

113 hown that the assembly of motor neurons into nuclei depends on cadherin-mediated adhesion.

114 e analyzed at later developmental stages the nuclei derived from these areas, attending to their gene

115 wer DNA packing densities compared to salmon nuclei despite salmon protamine lacking cysteine residue

116 It is found that nuclei develop at sites of high stored energy and they h

117 Nuclei displaced by centrifugation rapidly recentered by

118 We report for a number of cell types that nuclei display auxetic properties.

119 We report that nuclei display spontaneous calcium transients, and that

120 eased suddenly by even a few degrees Kelvin, nuclei displayed a repeatable and reversible temperature

121 Nuclei divide asynchronously through schizogony, with on

122 KEY POINTS: A cerebellar dentate nuclei (DN) contribution to volitional oculomotor contro

123 rebellum (cerebellar hemispheres and dentate nuclei, DN) is less well understood.

124 In higher eukaryotic nuclei, DNA is periodically anchored to an extraction-re

125 c resonance (MR) imaging, cerebellar dentate nuclei (DNs) functional connectivity abnormalities in mu

126 egenerating muscle fibers, increased central nuclei, elevated creatine kinase activity and endomysial

127 hin the mitochondrial organelle suggest that nuclei-encoded spliceosome can mediate splicing of mtRNA

128 mtRNA introns and of core components of the nuclei-encoded spliceosome machinery within the mitochon

129 ed a fast adiabatic (13)C-INEPT (Insensitive Nuclei Enhanced by Polarization Transfer) experiment for

130 sting that assembled aggregates can serve as nuclei for aggregation in bulk solution.

131 with electrodes implanted in the subthalamic nuclei for deep brain stimulation.

132 otentially may act as nanosized condensation nuclei for the condensation of atmospheric low-volatile

133 tromeres were observed to aggregate in sperm nuclei, forming an average of 20 and 7 clusters, respect

134 ower changes were analyzed in 22 subthalamic nuclei from 13 Parkinson disease patients (57.5 +/- 5.9

135 We also analyze 416 nuclei from a frozen breast tumor sample and 380 nuclei

136 We enriched nuclei from infected and noninfected tissues and quantit

137 ei from a frozen breast tumor sample and 380 nuclei from normal breast tissue.

138 te that sparse DNA sequencing of single-cell nuclei from prostate core biopsies is a rich source of q

139 re, we describe transfer of the isolation of nuclei from tagged specific cell types (INTACT) to the m

140 vglut2.1 is widely expressed in many nuclei from the olfactory bulbs to the hindbrain, while

141 nome mapping in the neuronal and nonneuronal nuclei from the postmortem brain.

142 n of nuclei, two-dimensional aggregation and nuclei growth.Electrochemical deposition is important fo

143 The organization of chromosomes in sperm nuclei has been proposed to possess a unique "hairpin-lo

144 coherent elastic scattering of neutrinos off nuclei has eluded detection for four decades, even thoug

145 onsible for organelle DNA incorporation into nuclei has not been performed until the present analysis

146 at actin cytoskeletal regulatory pathways in nuclei have a direct role in the regulation of gene tran

147 l anterior cingulate cortex with subcortical nuclei have been the target of neurosurgical lesions as

148 enetic framework to show that dinoflagellate nuclei have recruited DNA-binding proteins in three dist

149 onal parameters, CQ and eta, for quadrupolar nuclei, I > (1)/2) to 2D correlations, to analysis of ch

150 Application of ATAC-seq to sorted nuclei identifies accessible regions genome-wide.

151 eurosecretory arcuate nucleus, cranial motor nuclei III and IV, Edinger-Westphal nucleus, parabigemin

152 t article, we show that the lesions of these nuclei impair the spatial representations encoded by CA1

153 in many precerebellar neurons and in several nuclei implicated in the control of autonomic functions.

154 sitioning, we developed a method to displace nuclei in adherent cells using centrifugal force.

155 portant resource for identification of brain nuclei in other fishes, as well as future comparative st

156 ell selection to sequence up to 1800 single nuclei in parallel.

157 eyond, it has been limited to 50-65% for the nuclei in quantum dots.

158 studies had implicated the dorsal habenular nuclei in regulating fear responses and boldness in zebr

159 l distribution among excitatory SNc afferent nuclei in response to cocaine, and suggest a compelling

160 during meiosis II to sequester the dividing nuclei in sporulating yeast.

161 studied the material properties of isolated nuclei in suspension using an optical stretcher.

162 L5B cells target six nuclei in the anterior midbrain and thalamus, including

163 MNTB is one of the primary inhibitory nuclei in the auditory brainstem and participates in the

164 ury it was suggested that a complex group of nuclei in the avian posterior ventral telencephalon is c

165 all mice, and infection of CNS visual system nuclei in the brain was common.

166 cal implantation of electrodes into specific nuclei in the brain.

167 ypothalamic neurons that project directly to nuclei in the brainstem and spinal cord that regulate pa

168 ajor central source of GLP-1, with the other nuclei in the midbrain and forebrain, we tested the hypo

169 ibiting the erratic output of the cerebellar nuclei in the mutant mice improved movement.

170 ongation and possibly mispositioning of cone nuclei in the retina.

171 nctional connectivity of the visual thalamic nuclei in the various populations of subjects under inve

172 lls and suppresses deformations of xenograft nuclei in vivo.

173 ARAS nuclei included: cuneiform/subcuneiform, dorsal raphe, l

174 Nuclei including the lateral habenula (LHb), the lateral

175 le is known about homeostatic positioning of nuclei, including whether it is an active process.

176 structures of the cerebellum, the cerebellar nuclei, integrate their inputs and influence downstream

177 ory behaviours driven by the brainstem raphe nuclei into these parallel systems.

178 Common to all target nuclei investigated here is the maintenance of projectio

179 e emergence of mature topography among motor nuclei involves a novel interplay between spontaneous ac

180 the global chromatin organization of zygote nuclei is fundamentally different from that of other int

181 e electron spin accumulation and the lattice nuclei is observed.

182 vironment prior to the formation of critical nuclei is unveiled, featuring formation/re-dissolution o

183 projects strongly to midbrain monoaminergic nuclei, is believed to underlie the transient inhibition

184 cing (ATAC-seq) to neuronal and non-neuronal nuclei isolated from frozen postmortem human brain by fl

185 A binding of RelB and NFkappaB2, detected in nuclei isolated from the kidneys.

186 ar posterior commissure and lateral terminal nuclei), JcP (spiriformis lateral and lateral terminal n

187 interpretations for both image-labeling and nuclei-labeling tasks (83% and 87%), as compared to the

188 rences in the activity of neurons in lateral nuclei (LAT) and basal nuclei (BA) of the BLA that were

189 inked polyglutamine initially accumulates in nuclei, leading to disruption of nuclear envelope archit

190 licystronic molecules, but also processed as nuclei-like transcripts that are differentially spliced

191 lls and to frozen post-mortem human cortical nuclei, matching the performance of a previous lower-thr

192 dex of the 95th percentile within individual nuclei (medio-dorsal, pulvinar, lateral group) were comp

193 Growing evidence suggests that these nuclei might play a crucial role in cognitive processes

194 rough which 5-HT neurons in the dorsal raphe nuclei modulate amygdala circuits.

195 ly and axonal projections to brainstem motor nuclei most prominently, and, when silenced, observed bl

196 cond time scale within inhibitory vestibular nuclei networks contributes to ensuring a relatively rob

197 certa, lateral posterior and medial pulvinar nuclei, nucleus limitans, pretectal area, nucleus of Dar

198 whole-genome copy-number profiling of single nuclei obtained from formalin-fixed paraffin-embedded cl

199 SIRT1 co-localizes with BCL6 in the nuclei of affected individuals and both proteins bind to

200 ing of the hippocampus detected nBMP2 in the nuclei of CA1 neurons in wild type but not mutant mice,

201 omologous chromosomal loci in the interphase nuclei of Caenorhabditis elegans embryos.

202 ndant TRIM family member and is localized in nuclei of ECs.

203 s unknown, its ability to translocate to the nuclei of host cells and bind DNA suggests a possible ro

204 f covalently closed circular DNA (cccDNA) in nuclei of infected cells.

205 hat lives exclusively inside epithelial cell nuclei of its crab host.

206 ragranular location, can be found within the nuclei of mast cells where it truncates core histones at

207 y, we showed that T-oligo can form G4 in the nuclei of melanoma cells.

208 y strains between 1 and 700 Hz to individual nuclei of multiple mammalian cell-lines that were compre

209 umulation of the murf1 regulator FoxO in the nuclei of ncx1-deficient cardiomyocytes.

210 MUC4beta forms a complex with GRalpha in the nuclei of NP epithelial cells from corticosteroid-resist

211 s revealed strong expression of NUPR1 in the nuclei of renal proximal tubules of injured human kidney

212 ich were confirmed as highly enriched in the nuclei of specific cell types using anatomic methods.

213 , the ACo projects moderately to the central nuclei of the amygdala and anterior bed nucleus of the s

214 ion of the central, basolateral, and lateral nuclei of the amygdala nonetheless strongly suppressed o

215 vating the central, basolateral, and lateral nuclei of the amygdala selectively strengthened the weak

216 lar, Co-like neurons participate in specific nuclei of the bed nucleus of the stria terminalis, which

217 stribution and function in one of the output nuclei of the BG of the rodent, the entopeduncular nucle

218 Exploiting the NMR-active nuclei of the ChB-donor chalcogen atoms, heteronuclear (

219 complex, which includes both the PrV and the nuclei of the descending trigeminal tract (nTTD), have o

220 ve repeatedly been found within dopaminergic nuclei of the midbrain and dopaminoceptive areas of the

221 how that MANF is highly enriched in distinct nuclei of the mouse hypothalamus, and that MANF expressi

222 on, while glutamatergic expression dominates nuclei of the pallial dorsal telencephalon.

223 GABAergic expression dominates nuclei of the subpallial ventral telencephalon, while gl

224 The reuniens (Re) and rhomboid (Rh) nuclei of the ventral midline thalamus are reciprocally

225 s redistribution across healthy rodent brain nuclei over a 2-week timeframe, whereas in rodents follo

226 ted mostly the basolateral and CeM amygdalar nuclei, poised to activate CeM for autonomic arousal.

227 80% of its thalamic input from multisensory nuclei (primarily medial pulvinar).

228 Both the AR- and the AR+ nuclei project to the intercollicular nucleus of the mid

229 roventral periventricular (AVPV) and arcuate nuclei, providing homeostatic feedback on episodic GnRH/

230 lation directed to the interposed cerebellar nuclei reduced dystonia-like postures in these mice.

231 We demonstrate that isolated nuclei regulate their volume in a highly temperature-sen

232 lopment and organization of diverse thalamic nuclei remain largely unknown.

233 ific role of progesterone receptors in these nuclei remains unknown.

234 However, how cell nuclei respond to external cues such as heat is not well

235 Accumulation of HDAC4 in the nuclei results in an attenuation of HIF-1alpha acetylati

236 itates freezing by favoring the formation of nuclei rich in cubic ice, which, as demonstrated by us e

237 e activation of rod/cone and suprachiasmatic nuclei (SCN) by light was paradoxically greatly reduced,

238 Suprachiasmatic nuclei (SCN) neurons contain an intracellular molecular

239 dian clock is located in the suprachiasmatic nuclei (SCN) of the hypothalamus and it regulates circad

240 aster circadian clock in the suprachiasmatic nuclei (SCN) of the hypothalamus regulates physiology an

241 in mammals is located in the suprachiasmatic nuclei (SCN) which regulate physiology and behaviour, as

242 ltered networking within the suprachiasmatic nuclei (SCN), the circadian "master clock," which is DNA

243 ter circadian pacemaker, the suprachiasmatic nuclei (SCN).

244 central circadian pacemaker (Suprachiasmatic Nuclei, SCN) maintains the phase relationship with the e

245 hift the master clock in the suprachiasmatic nuclei (SCNs) and/or reduce the synchronizing effects of

246 Alterations in the nuclei shape and expression of nuclear envelope-associat

247 as conserved among different cell-lines: all nuclei showed a softer and more viscous response towards

248 mbining ATAC-seq with fluorescence-activated nuclei sorting (FANS) to identify and map open chromatin

249 ere, mesenchymal stem cells (MSCs) and their nuclei spread in response to thickness-corrected matrix

250 (6) to 4.0(4) A, indicating that spin-active nuclei sufficiently close to the electronic spin center

251 rain sites in adult, including major sensory nuclei, suggesting that sensory transmission may also be

252 The ability to image nuclei tagged with MR/Optical gene markers may also find

253 to cortical areas as well as to subcortical nuclei that are under the direct control of corticofugal

254 send a dense feedback projection to thalamic nuclei that provide input to sensory neocortex.

255 oson transcripts must identify the subset of nuclei that will be transmitted to offspring.

256 and/or modulated by a group of five afferent nuclei (the Medial Magnocellular nucleus of the Anterior

257 sal, anteroventral, and parateanial thalamic nuclei, the fasciculus retroflexus of Meynert, basolater

258 ce leukaemia-targeting CAR genes into T-cell nuclei, thereby bringing about long-term disease remissi

259 is push-pull shift between lateral and basal nuclei, these results help to explain disparate findings

260 whereas the newly nucleated secondary small nuclei through a concentration change have relatively hi

261 otonin (5-HT) neurons project from the raphe nuclei throughout the brain where they act to maintain h

262 We compare the transcriptomes of 485 single nuclei to 424 single cells in a breast cancer cell line,

263 on reorganization, and rapid displacement of nuclei to dense central structures compared to pOka usin

264 roposed, but none have been shown to move to nuclei to modulate gene expression.

265 uggested to channel signals from distinct BG nuclei to target regions involved in diverse functions.

266 How LINC complexes are regulated to connect nuclei to the cytoskeleton during nuclear migration is u

267 forms linear structures in meiotic prophase nuclei to which Zhp3 localizes.

268 ional regulator Ikaros into mouse pre-B cell nuclei triggered immediate binding to target gene promot

269 eiled, featuring formation/re-dissolution of nuclei, two-dimensional aggregation and nuclei growth.El

270 o and whether the newly introduced nonmuscle nuclei undergoes nuclear reprogramming has not been inve

271 at propagate among sensory-modality thalamic nuclei up to the cortex and that provide a means of comm

272 remaining chromatin-bound in the individual nuclei using histone type- or posttranslational modifica

273 f kinetochore capture in small fission-yeast nuclei using hybrid Brownian dynamics/kinetic Monte Carl

274 of proton and carbon (1', 2', 2, 5, 6 and 8) nuclei using only one sample and <24 h of NMR instrument

275 a and is transmitted to the ventral cochlear nuclei (VCN).

276 quantify the electron-spin density at ligand nuclei (via the weak hyperfine interactions) in molecula

277 ral recruitment of ventral spinal projecting nuclei (vSPNs) implicated in turning.

278 atory factor 7(IRF7) from the cytosol to the nuclei was effectively blocked in the presence of PI3K i

279 The purification of biotinylated nuclei was redesigned by replacing the outer nuclear-env

280 , H3K27me3, and H2AK119ub1 from transplanted nuclei, we reveal the basis for resistance of genes to t

281 icant signal enhancement for slowly relaxing nuclei, we show that it enables more precise and frequen

282 ith wounds oriented orthogonal to the force, nuclei were displaced toward the front and back of the c

283 tal muscle fibres were hypotrophic and their nuclei were morphologically abnormal with a wider perinu

284 ial fibrillary acidic protein), and neuronal nuclei were performed.

285 sal raphe, pedunculopontine, and subthalamic nuclei were tested for synaptic modifications following

286 s evidence that PDC localizes to cancer cell nuclei where it plays a role in histone acetylation.

287 entriolar material to the surface of myotube nuclei, where it nucleates microtubules to ensure even s

288 ely throughout the nucleoplasm in interphase nuclei, whereas, the nucleolus region exhibited a more p

289 s their ability to act as cloud condensation nuclei, whereby they impact cloud coverage and precipita

290 This single cell has myriad of nuclei which contribute to a network of bio-chemical osc

291 n thalamic nuclei and cortical areas or deep nuclei), which independently contributes to functional,

292 Blazars are active galactic nuclei, which are powerful sources of radiation whose ce

293 se found a limiting factor for the volume of nuclei, which averages 41.9% and 49.2% of the cell body

294 ral periventricular (AVPV) and arcuate (ARC) nuclei, while the region-specific role of progesterone r

295 te sucrose-gradient-assisted purification of nuclei with droplet microfluidics to develop a highly sc

296 Using mouse embryonic fibroblast nuclei with normal or reduced DNA methylation in combina

297 and soma are partitioned into two different nuclei within a single cell.

298 reproduction, similarity or dissimilarity of nuclei within an individual, and species boundaries need

299 ice and is distinct in paternal and maternal nuclei within single-cell zygotes.

300 eates microtubules to ensure even spacing of nuclei within the developing myotube.