ライフサイエンスコーパス: nuclei

1 biculum projections to the anterior thalamic nuclei.

2 masks and assigning boundaries for touching nuclei.

3 ns in the ipsilateral medial-dorsal thalamic nuclei.

4 e development of zebrafish ocular motor (sub)nuclei.

5 y of different types of muscle and nonmuscle nuclei.

6 oked potentials from midbrain electrosensory nuclei.

7 tial neuronal loss, particularly in its deep nuclei.

8 including well-delineated vocal and auditory nuclei.

9 l (DMH), and ventromedial (VMH) hypothalamic nuclei.

10 nd the endoplasmic reticulum but also to the nuclei.

11 t sensor was transferred efficiently to cell nuclei.

12 d HVC showed the slowest myelination of song nuclei.

13 pore complex insertion into growing germline nuclei.

14 stically, alter the NMR shifts of the nearby nuclei.

15 racil, based on a quantum description of the nuclei.

16 beta dynamics differed across basal ganglia nuclei.

17 connectivity of the DCN and their associated nuclei.

18 metaphase progression and ploidy of daughter nuclei.

19 gs for structural deficits specific to these nuclei.

20 he vocal pattern generator and cranial motor nuclei.

21 to DNAJB6 inhibits the formation of amyloid nuclei.

22 rotein translocated to both mitochondria and nuclei.

23 f the striatum is preserved in all BG output nuclei.

24 ge-symmetry-breaking forces acting in atomic nuclei.

25 pain, such as ventral posteromedial thalamic nuclei.

26 behavioral states via its output to midbrain nuclei.

27 ver encapsulated payloads directly into cell nuclei.

28 tegration of the acentrics into newly formed nuclei.

29 cally different from a random positioning of nuclei.

30 of the protein and an increase in misshapen nuclei.

31 tides, helped the identification of thalamic nuclei.

32 are mitigated by these cells having multiple nuclei.

33 stream brain regions as well as hypothalamic nuclei.

34 s transcriptional reprogramming of syncytial nuclei.

35 mors and the size and heterogeneity of their nuclei.

36 ntense innervation of all these hypothalamic nuclei.

37 and high natural abundance of several halide nuclei ((79/81)Br and (127)I) combined with the enhanced

38 ermassive black hole in some active galactic nuclei (AGN) drives relativistic jets of plasma, which d

39 ral nerves ramify within the dermis, all the nuclei along their course belong to glial cells.

40 to dissolve any potential tiny crystals and nuclei already present in the raisins.

41 poptosis, via nuclear condensation (87.5% of nuclei analyzed) and plasma membrane damage (in 100% of

42 Both altered mechanical properties of nuclei and abnormal nuclear morphologies are hallmarks o

43 ed, validated method for segmenting thalamic nuclei and complementary voxel-based morphometry.

44 g (QPI) data, we measured the growth of both nuclei and cytoplasm independently, over many days, with

45 (2-3 times, P < .01) specific NIR FI in the nuclei and cytoplasm of islets cells than in non-treated

46 idopsis cell suspensions to sort replicating nuclei and determine genome-wide cytosine methylation dy

47 r by DA neurons within multiple hypothalamic nuclei and elucidate a novel functional mechanism for th

48 this tool, we identified and classified cell nuclei and extracted 48 cell spatial organization-relate

49 neuroimaging research into small subcortical nuclei and help to chart terra incognita.

50 w-level concentrations of cloud condensation nuclei and ice nucleating particles.

51 ionships are maintained across the BG output nuclei and in downstream targets is unclear.

52 study the mechanical properties of isolated nuclei and in living cells.

53 notably in the striatum/pallidum, amygdaloid nuclei and in the hippocampus it was more diverse than i

54 ntegrates information from numerous auditory nuclei and is an important hub for sound processing.

55 e in the dorsal tegmentum, medial vestibular nuclei and lateral parabrachial nucleus, and in brainste

56 r, paraventricular, and arcuate hypothalamic nuclei and locus ceruleus of mice exhibited STAT5 phosph

57 leus accessible chromatin profiles of 90,980 nuclei and matched single-nucleus transcriptomes of 46,5

58 of outer limiting membrane by photoreceptor nuclei and Muller cell microvilli could minimize the lig

59 cells, scaling is set at the level of single nuclei and not the entire cell, making the nucleus a det

60 g the response to applied forces of isolated nuclei and nuclei within intact cells.

61 Our work provides insight into how nuclei and spatial system dimensions can control local c

62 osis was commonly initiated at sperm-derived nuclei and their accompanying centrosomes.

63 affecting nucleoporin levels within neuronal nuclei and ultimately downstream neuronal survival.

64 and posterior vermis through the cerebellar nuclei and ventromedial thalamus and culminating in the

65 /81)Br, (87)Rb, (127)I, (133)Cs, and (207)Pb nuclei) and locally and shedding light onto the connecti

66 s mechanical force that acts on cells, their nuclei, and chromatin, but how the genome is protected a

67 , reduced neuronal density in some amygdalar nuclei, and decreased calbindin-positive neuron density

68 at DLM showed earlier myelination than other nuclei, and HVC showed the slowest myelination of song n

69 mation (RF), pontine and midbrain vestibular nuclei, and medullary raphe.

70 , suprachiasmatic nuclei, anterior olfactory nuclei, and spinal cord gray matter.

71 A), suprachiasmatic (SCN), and arcuate (ARC) nuclei, and that RFRP-3 neurons are present in the parav

72 rtex, hippocampus, amygdala, suprachiasmatic nuclei, anterior olfactory nuclei, and spinal cord gray

73 ween distinct cortical networks and thalamic nuclei are among the most consistent large-scale brain i

74 ic chromosome fragments that rejoin daughter nuclei are associated with nuclear membrane but devoid o

75 e species-specific vocal patterns, how vocal nuclei are connected to generate vocal patterns, as well

76 Intriguingly, brain DA nuclei are differentially affected in Parkinson's diseas

77 aptic circuits between TRN and sensory relay nuclei are known to underlie the generation of sleep spi

78 hod, defined ratios of mouse and human fixed nuclei are mixed and subjected to endonuclease digestion

79 other exception is denervation-atrophy where nuclei are not eliminated.

80 Some novel nuclei are proposed, and some instances of potential tan

81 In pseudostratified epithelia, where nuclei are staggered across the tissue, each nucleus mig

82 of nuclei, the formation and early growth of nuclei are very difficult to observe.

83 way to analyze mixtures by considering (31)P nuclei as chemical shift markers.

84 lass was established to be from pre-existing nuclei as confirmed by Avrami exponents of 0.25 +/- 0.01

85 ypothalamus increase SNA, highlighting these nuclei as likely targets.

86 riple-alpha reaction, and eventually heavier nuclei as the material expands and cools.

87 cing nuclei optimally and randomly using the nuclei as the origin of a transportation network.

88 ensively connected with both local amygdalar nuclei as well as long-range circuits, is involved in a

89 s and heterogeneity associated with myofiber nuclei, as well as other mononucleated cell types that c

90 influence of the chemical environment on the nuclei being probed.

91 fine the establishment of the homology of DA nuclei between vertebrate species.

92 amus also receives inputs from basal ganglia nuclei (BG) involved in value-based decision making, sug

93 voked dopamine release in all four reticular nuclei, but not in the spinal cord.

94 halamus have mostly focused on sensory relay nuclei, but the organization of pathways associated with

95 Direct epoxidation of aromatic nuclei by cytochrome P450 monooxygenases is one of the m

96 sregulation of homeostatic and hedonic brain nuclei can lead to pathological feeding behaviors, namel

97 n, building a de novo path along which their nuclei can return to the basal side.

98 atorubrothalamic tract, and other deep brain nuclei cannot be clearly identified.

99 e differentially expressed in specific brain nuclei causing aggressive behavior in the white-throated

100 articles form most of the cloud condensation nuclei (CCN) that influence the indirect radiative effec

101 ve to the availability of cloud condensation nuclei (CCN).

102 ters the activity of their target cerebellar nuclei cells.

103 n the dorsomedial/ventrolateral and pulvinar nuclei compared with the 14 subjects with the greatest t

104 In contrast, the nearest-neighbor nuclei, coupled to the methyl carbons, resonate in disti

105 xtracts of Xenopus laevis eggs, we find that nuclei define such pacemakers by concentrating cell cycl

106 Nuclei deformed nonmonotonically under constant load.

107 We further observe that the multilobulated nuclei, despite continuous absence of cohesin, pass thro

108 , but purified centrosomes in the absence of nuclei did not.

109 entional RGCs across ipsi- and contralateral nuclei differ.

110 gether, our findings reveal how two thalamic nuclei differentially communicate with the PFC through d

111 We find that developing ocular motor (sub)nuclei differentially express classical cadherins.

112 ding to the reviewed data, neurotransmitters nuclei diffusively project to subcortical and cortical r

113 except the hypothalamus and two hypothalamic nuclei display sexually dimorphic OTR expression.

114 e essential for the apical migration of cone nuclei during development.

115 namic localization of HPR3 between axons and nuclei during myelination was consistent with its axonal

116 d abnormal positioning of photoreceptor cell nuclei early in development.

117 on transfer (DEPT) and refocused insensitive nuclei enhanced by polarization transfer (RINEPT) are ex

118 r landscape of molecules where electrons and nuclei evolve on comparable timescales and thus become s

119 kines in their brainstem respiratory control nuclei, exhibit a higher respiratory frequency (fR) and

120 hanced electric field gradients around these nuclei existing in LHPs as well as the instrumental simp

121 lon cancer images with pathologist-annotated nuclei, finding that both cellular and intercellular reg

122 d: hunchback genes decide in minutes whether nuclei follow the anterior/posterior developmental bluep

123 In the songbird brain, discrete nuclei form interconnected myelinated circuits that cont

124 ogenesis and the largest structures in human nuclei, form around nucleolar organizer regions (NORs) c

125 nd the existence of an energy barrier before nuclei formation.

126 ventral posterior lateral and posterior (PO) nuclei, forming a pair of recurrent cortico-thalamo-cort

127 onstrate automated segmentation of cells and nuclei from brightfield images with a mean average preci

128 number profiling on mixtures of cell lines, nuclei from frozen prostate tumors, and biopsy washes.

129 generated by sequencing approximately 17,000 nuclei from matched cortical and SN samples.

130 ped chromatin accessibility in 19,453 single nuclei from mouse embryos at 8.25 days post-fertilizatio

131 ession patterns of cell lines and individual nuclei from neurons dissected from the mouse brain.

132 minally differentiated, postmitotic myofiber nuclei from obese individuals had elevated gammaH2AX abu

133 e apparent mechanical properties of isolated nuclei from patients of acute lymphoblastic leukemia.

134 connected basal ganglia output and thalamic nuclei (globus pallidus-internus [GPi] and ventrolateral

135 e of myelin development across discrete song nuclei has not been systematically studied in a quantita

136 amygdala (lateral [LA] and basolateral [BL] nuclei) have closely related functions and similar extri

137 8 to adult (up to 147 d) in five major song nuclei: HVC (proper name), robust nucleus of the arcopal

138 er dataset with more than 30 000 IHC stained nuclei in 88 images were prepared.

139 those in U*G or U:A pairs, and localizes to nuclei in a dispersed form.

140 Here we report finding haploid vegetative nuclei in A. gallica at multiple sites in southeastern M

141 e frequency of dual positive gammaH2AX & p16 nuclei in adipose tissue of OSA patients receiving stati

142 B nucleus is smaller than both the La and Ba nuclei in both morphometric and stereological estimators

143 The chemical shifts of the (1)H nuclei in CH(3) and NH(3) remained constant with increas

144 ablation, YAP accumulated in supporting cell nuclei in chicken utricles and promoted regenerative pro

145 pal1 mutant was normal in meiosis with eight nuclei in developing asci but most asci were aborted.

146 al nets differentiates these intercollicular nuclei in guinea pigs.

147 scale nuclear architecture across human cell nuclei in interphase.

148 rydendroid neurons (ENs) in fish (cerebellar nuclei in mammals).

149 ched single-nucleus transcriptomes of 46,500 nuclei in non-diseased lungs from donors of ~30 weeks ge

150 sed isoLG adducts in gastric epithelial cell nuclei in patients with gastritis and intestinal metapla

151 mediate-early gene (IEG) expression in brain nuclei in response to an experience is necessary for the

152 s new insights into the organization of 5-HT nuclei in teleosts and provides neuroanatomical evidence

153 We measured the spin dynamics of nuclei in the CTT backbone by NMR spectroscopy to explor

154 number of minor variations across a range of nuclei in the density of structures expressing the calci

155 s well as the lateral posterior and pulvinar nuclei in the domestic ferret compared to the banded mon

156 nstrate that the apical localization of cone nuclei in the ONL is required for the timely dark adapta

157 a change in the surroundings of the (207)Pb nuclei in the PbBr(6) octahedra and of the C-N groups in

158 itory output to principal sound-localization nuclei in the superior olive (SOC) as well as other comp

159 restingly, we observed a tenfold increase of nuclei in thin myocardial sections stained positive for

160 suppresses activity in both visual thalamic nuclei in vivo, moderate-frequency (10 Hz) stimulation p

161 typically associated with hypothalamic brain nuclei, including the paraventricular nucleus of the hyp

162 vLGN) projects subcortically to sensorimotor nuclei, including the superior colliculus (SC), via long

163 T(1rho) values for (1)H, (13)C, and (207)Pb nuclei increased with increasing temperature and did not

164 Observations of comet nuclei indicate that the main constituent is a mix of ic

165 -seq) measures gene expression in individual nuclei instead of cells, allowing for unbiased cell type

166 d coalescence of pre-existing monomeric IgG1 nuclei into a dead-end aggregate, rather than through ma

167 tage would be preceded by segregation of the nuclei into a large number of clusters, proportional to

168 compaction of heterochromatin converts these nuclei into microlenses that focus light and facilitate

169 d non-Born-Oppenheimer effects for specified nuclei into quantum chemistry calculations in an accessi

170 Thus, our study identified a number of nuclei involved in parental care in birds and suggests s

171 cy and Kv3.3 dominance between the brainstem nuclei involved in sound localization.

172 One of the brainstem nuclei involved in the regulation of anxiety is the dors

173 r of active replication origins in embryonic nuclei is higher than in somatic ones, ensuring rapid ge

174 volutionarily conserved localization of cone nuclei is unknown.

175 chanism by which nucleoporins are altered in nuclei isolated from C9orf72 induced pluripotent stem-ce

176 f central GLP-1, with midbrain and forebrain nuclei known to regulate cocaine-seeking behavior.

177 stimators in the whole AC and its three main nuclei (lateral [La], basal [Ba], and accessory basal [A

178 rsal tegmental and sublaterodorsal tegmental nuclei (LDT/SubLDT) using male and female transgenic mic

179 s recombine in auditory and vestibular brain nuclei, making it difficult to ascribe resulting phenoty

180 s of the mouse medial (fastigial) cerebellar nuclei (mCbN), which fire spontaneously with wide dynami

181 been conjectured that the anterior thalamic nuclei might be key partners with the hippocampal format

182 appeared that an equidistant positioning of nuclei minimizes transport distances along the surface f

183 s controls, including larger basal cells and nuclei, more persistent basal and ectopic lumenal KRT14(

184 Single-cell or single-nuclei mRNA sequencing of dissociated mouse kidneys and

185 ucing fungi typically contain paired haploid nuclei (n + n), most Armillaria gallica vegetative cells

186 med to detect the neuronal-markers; neuronal nuclei (NeuN), microtubule-associated protein-2 (MAP-2)

187 tigated the Purkinje cell to deep cerebellar nuclei neuron synapses (PC_DCNs), which display frequenc

188 the Purkinje cells, on identified cerebellar nuclei neurons in vivo in male mice.

189 Using tegmental hindbrain nuclei neurons in zebrafish embryos together with subcel

190 itter release in projections from cerebellar nuclei neurons onto gigantocellular reticular nucleus ne

191 discharges depends on the type of cerebellar nuclei neurons targeted.SIGNIFICANCE STATEMENT Motor coo

192 The fused macrophage morphologies, the nuclei number in the fused macrophage, and the fusion ra

193 lts revealed an inverse relationship between nuclei numbers and reserve capacity.

194 H bilayers, stable 2H domains dominate, with nuclei of a second metastable phase.

195 quitous, because MNESmut was retained in the nuclei of all cell types tested.

196 of 8 to 14 min, which corresponds to droplet nuclei of ca. 4 mum diameter, or 12- to 21-mum droplets

197 gnalling cascade recruits nucleolin from the nuclei of cells to the plasma membrane, where it also bi

198 s: maintaining the herpesvirus genome in the nuclei of cells; partitioning the viral genome to daught

199 mbers (FYCO1, WDFY3, Hrs) also distribute to nuclei of different cells in the brain cortex, which rai

200 SIRT2 accumulated in the nuclei of dorsal root ganglion sensory neurons and preve

201 ds determined by sub-tomogram averaging from nuclei of eukaryotic cells, achieved by cryo-electron to

202 idinone derivatives are widely recognized as nuclei of great value for obtaining molecules with vario

203 c interfacial complex, translocated into the nuclei of initially penetrated and surrounding cells, an

204 reticulospinal neurons in the four reticular nuclei of lampreys.

205 and cerebrospinal fluid directed against the nuclei of Purkinje cells, striatal neurons, and hippocam

206 We propose that KIN-29/SIK acts in nuclei of sensory neuroendocrine cells to transduce low

207 IN-Seq uses immunohistochemical isolation of nuclei of specific cell types from frozen human tissue,

208 sal forebrain (BF) receives inputs from many nuclei of the ascending arousal system, including the br

209 NPNs were scattered throughout all nuclei of the BNC and had aspiny or spine-sparse dendrit

210 ity in populations of the serotonergic raphe nuclei of the brainstem reticular formation, with three

211 suggest that the anteroventral region of bed nuclei of the stria terminalis (avBST) regulates glucoco

212 al area (VTA) and ventrolateral-ventromedial nuclei of the thalamus (VL-VM).

213 rahippocampal gyri, the dorsomedial/pulvinar nuclei of the thalamus, and the fusiform gyri, as well a

214 ry with metastatic tumors and found that the nuclei of tumor cells were significantly larger in metas

215 tic transformants consisting of two types of nuclei, one with the wild-type CpRbp1 allele and another

216 We modeled the effect of placing nuclei optimally and randomly using the nuclei as the or

217 otube length, with a small average number of nuclei per cluster.

218 t produced conidia with fewer septa and more nuclei per compartment than the wild type.

219 ion, our findings indicate that within human nuclei, positioning of all 10 acrocentric chromosomes is

220 soleus muscle, however, which were richer in nuclei, positioning of nuclei to reduce transport distan

221 east cancer samples with 1% to 100% of tumor nuclei positive should be interpreted as ER positive.

222 eus praeeminentialis (nP) arise from isthmic nuclei, possibly including the nucleus lateralis valvula

223 ture during long-term storage, cryopreserved nuclei preparations from chicken lung were used to optim

224 ytochemistry to Iba1 in samples of free cell nuclei prepared with the isotropic fractionator from bra

225 Nuclei produced from phage DNA, which did not possess ce

226 profiles show clear evidence of crowding as nuclei reach close-packing and are quantitatively descri

227 e-segregating chromosomes to rejoin daughter nuclei remain underexplored.

228 l level(13) means that precisely how and why nuclei reorganize remains an area of intense investigati

229 emonstrate that smaller thalamic association nuclei represent a neurodevelopmental abnormality associ

230 hree-dimensional reconstructions of isolated nuclei revealed that NI type1 are completely enclosed wi

231 the transcriptomes of 287 269 single cardiac nuclei, revealing 9 major cell types and 20 subclusters

232 rojection of the neural image onto brainstem nuclei reveals features of the neural image in a percept

233 ons control sleep via the serotonergic raphe nuclei (RN), a hindbrain structure that is critical for

234 tween high-throughput single-cell and single-nuclei RNA-seq approaches, we compared Drop-seq and DroN

235 Single-nuclei RNA-sequencing revealed that SCN(VIP) neurons com

236 The serotonergic raphe nuclei (RNi) connections involve regions of the SMN and

237 ters in both, the AC, and the La, Ba, and AB nuclei separately.

238 Comparison of the bulk tissue and single-nuclei sequencing revealed that conventional RNA sequenc

239 We combine genetic approaches and single-nuclei sequencing to demonstrate that muscle-derived Pvf

240 nated transcriptional activity of individual nuclei shapes complex developmental patterns.

241 Multiple nuclei sharing a common cytoplasm are found in diverse t

242 ers of neutrons and protons, known as mirror nuclei, should have an identical set of states(7), inclu

243 All of these nuclei showed an increase in the density of myelination

244 All vocal midbrain nuclei showed considerable 5-HT-ir innervation, as did t

245 low diffusivity at hyphal tips and near some nuclei, showing that the physical state of the cytosol v

246 Herein, we report a 78-nuclei silver nanocluster (NC) [Ag(78) ((i) PrPhS)(30) (

247 innervate the interpeduncular nucleus, raphe nuclei, substantia nigra pars compacta and ventral tegme

248 pedunculopontine and laterodorsal tegmental nuclei synapse with striatal cholinergic interneurons an

249 Within this pseudostratified epithelium, nuclei synthesize DNA near the basal surface and move ap

250 gnaling capacity within microdissected brain nuclei that are important for social behaviors.

251 ng a characteristic horseshoe-shaped ring of nuclei that are present within granulomas of infectious

252 ent discharge of neurons from the cerebellar nuclei that communicate cerebellar computation to other

253 ers of the amygdaloid complex and their main nuclei that could help us to detect small changes in neu

254 he flow of information through basal ganglia nuclei that eventually project back to the mPFC to compl

255 Furthermore, we explore brain nuclei that express Brn3c or receive input from Brn3c(+)

256 complex behavior regulated by discrete brain nuclei that integrate homeostatic nutritional requiremen

257 Among the brainstem raphe nuclei, the dorsal raphe nucleus (DR) contains the great

258 se of the scale and highly dynamic nature of nuclei, the formation and early growth of nuclei are ver

259 er mammalian myotubes with a large number of nuclei, the spreading stage would be preceded by segrega

260 nsduction defects in cones with mislocalized nuclei, their dark adaptation was impaired, consistent w

261 ter wave of growth: these neurons had larger nuclei, thicker dendrites, and more dendritic filopodia

262 n of particular functional groups, inserting nuclei to act as reporters on their surrounding chemical

263 stinct first-order and higher-order thalamic nuclei to form molecularly defined TRN-thalamus subnetwo

264 nal RGCs (non-ipRGCs) target ipRGC-recipient nuclei to influence subconscious visual behavior.

265 ight the importance of spatially distributed nuclei to minimize transport distances to the surface wh

266 which were richer in nuclei, positioning of nuclei to reduce transport distances to the cytoplasm we

267 omplexes resulted in mislocalization of cone nuclei to the basal side of ONL in mouse retina.

268 irect projections from the anterior thalamic nuclei to the dorsal hippocampal formation were inhibite

269 We describe a human single-nuclei transcriptomic atlas for the substantia nigra (SN

270 -mortem studies indicates that monoaminergic nuclei undergo degeneration at the pre-symptomatic stage

271 s in early sea urchin embryos, we found that nuclei undergo substantial growth in each interphase, re

272 proton-induced nuclear reactions on titanium nuclei using a 24-MeV cyclotron.

273 of DFT theory, solvent model, and NMR-active nuclei, using both user-selected reference compounds and

274 ture, whereas those of the (13)C and (207)Pb nuclei varied near the phase transition temperature (T(C

275 lfactory bulb, basal telencephalon, preoptic nuclei, ventral thalamus, posterior tuberculum, and locu

276 However, the need to address the nuclei via oscillating magnetic fields complicates their

277 combine to form alpha particles, then (12)C nuclei via the triple-alpha reaction, and eventually hea

278 Thalamic nuclei volumes were tested in a cross-sectional sample o

279 ypomethylation in exon 3 of IRX2 in neuronal nuclei was associated with cocaine dependence.

280 accumulation of multiple kinetoplasts and/or nuclei was detected.

281 By UV cross-linking of isolated nuclei we determined the cross-linking sites of several

282 labeled with 5-ethynyl-2'-deoxy-uridine, and nuclei were subjected to two-parameter flow sorting.

283 ion assays reveal subcellular sites, such as nuclei, where puromycylated peptides accumulate post-rel

284 uch concepts requires controlling individual nuclei, which can be detected when coupled to an electro

285 regions, such as the thalamus and brainstem nuclei, which mediate complex interactions with the brai

286 source using tracer injections in reticular nuclei, which retrogradely labeled dopaminergic neurons

287 sensitivity ensures rapid repair at primary nuclei while causing unrestrained activity at ruptured m

288 pyrolyzed at high temperatures, resulting in nuclei with a small size.

289 y emerges from this isobaric-spin formalism: nuclei with exchanged numbers of neutrons and protons, k

290 Integrating electrically controllable nuclei with quantum dots(11,12) could pave the way to sc

291 olution: RAISIN RNA-seq for profiling intact nuclei with ribosome-bound mRNA and MIRACL-seq for label

292 DDX21 was detected mostly in the tumor cell nuclei, with high expression in some mitotic cells.

293 scriptional diversity and whether individual nuclei within a multinucleated myofiber might respond di

294 ular dimensions and the positions of all the nuclei within fiber segments.

295 nse to applied forces of isolated nuclei and nuclei within intact cells.

296 ured the dry mass content of individual cell nuclei within spheroids.

297 The positioning of nuclei within the cell is a dynamic process that depends

298 The extent to which different nuclei within the shared cytoplasm of a myofiber may dis

299 retinogenesis to track entire populations of nuclei within the tissue.

300 hesised that the MRI signal of monoaminergic nuclei would be a statistically significant predictor of