ライフサイエンスコーパス: cell nuclei

1 deliver encapsulated payloads directly into cell nuclei.

2 s and viral particles in swollen endothelial cell nuclei.

3 al DNA entered ATM-negative and ATM-positive cell nuclei.

4 t phosphorylation siteswere retained in hair cell nuclei.

5 protocols for the isolation and analysis of cell nuclei.

6 al (NLS) that targets this effector to plant cell nuclei.

7 mpty VZV capsids in Delta54S-infected ARPE19 cell nuclei.

8 were still localized to the somatic support cell nuclei.

9 s capable of inducing totipotency in somatic cell nuclei.

10 leic acid band intensities across individual cell nuclei.

11 ocalized with the EBV genome in LCL and Raji cell nuclei.

12 cted the presence of Pol II and Ell3 in germ cell nuclei.

13 etate and (64)Cu-DOTA-cetuximab to the tumor cell nuclei.

14 e PKD, Snail1 was predominantly localized to cell nuclei.

15 s, mitochondria, and glial cells, as well as cell nuclei.

16 spatial gene repositioning in breast cancer cell nuclei.

17 ion and sequestration of MRN within infected-cell nuclei.

18 asm and that U(S)3 retains PDCD4 in infected cell nuclei.

19 rrored that of vimentin and was localized in cell nuclei.

20 chromosomes to segregate episomes to progeny cell nuclei.

21 imity of cytoplasmic hybridization signal to cell nuclei.

22 visualization of positions and identities of cell nuclei.

23 from concatemers that accumulate in infected cell nuclei.

24 inding protein-alpha in live mouse pituitary cell nuclei.

25 ers of nuclear pore complexes (NPCs) on germ cell nuclei.

26 e, has been thought to be found primarily in cell nuclei.

27 ominant active isoform in corneal epithelial cell nuclei.

28 ient translocation into the proximal tubular cell nuclei.

29 ns of achieving the reprogramming of somatic cell nuclei.

30 gnificantly decreases YAP abundance in HepG2 cell nuclei.

31 sicles, while the second was coisolated with cell nuclei.

32 f a monoallelically expressed gene in single cell nuclei.

33 mmunofluorescence measurements at individual cell nuclei.

34 e U2 snRNP auxiliary factor (U2AF35) in live-cell nuclei.

35 ithout effect on ATF-3 expression in Schwann cell nuclei.

36 ced green fluorescent protein exclusively to cell nuclei.

37 s long as mitotic S phase in C. elegans germ cell nuclei.

38 and delivered the fluorescent label into the cell nuclei.

39 to detect nanoparticles inside fractionated cell nuclei.

40 tein, has also been identified in urothelial cell nuclei.

41 icient cells restores 3E10 Fv transport into cell nuclei.

42 Smad3, Smad4, and hZimp10 co-localize within cell nuclei.

43 of virus, or the trafficking to the infected cell nuclei.

44 hrough the nuclear pores, accumulated in the cell nuclei.

45 d Sf9 cells, five vankyrins were detected in cell nuclei.

46 om the full-length protein and is present in cell nuclei.

47 of the nuclear envelope and causes misshapen cell nuclei.

48 R DNA to segregate virus genomes to daughter cell nuclei.

49 ng mismatch-selective metal complexes inside cell nuclei.

50 0-green fluorescent fusion protein entered B-cell nuclei.

51 requent localization of the enzyme to cancer cell nuclei.

52 n, ORF29p is localized primarily to infected cell nuclei.

53 hibiting GBM specificity and localization to cell nuclei.

54 (primary targets of the Notch pathway) in KS cell nuclei.

55 the subcellular fractions of brain including cell nuclei.

56 ting in elevated mutant huntingtin levels in cell nuclei.

57 chromosomes to segregate genomes to daughter cell nuclei.

58 tin in vivo and depletes eIF5A and eEF2 from cell nuclei.

59 nd (t70)Zn molar fractions close to 1 in the cell nuclei.

60 assembly of filamentous actin within somatic cell nuclei.

61 hology is NSs filament formation in infected cell nuclei.

62 lized at the plasma membrane, in cytosol and cell nuclei.

63 RNA secondary structure in hair and nonhair cell nuclei.

64 tretching and imaging the lamina of isolated cell nuclei.

65 of assembly of this key virulence factor in cell nuclei.

66 referred spatial positions within interphase cell nuclei.

67 nfluency cell cultures with many overlapping cell nuclei.

68 ed RPL4 expression and redistributed RPL4 to cell nuclei.

69 oplasmic vesicles and is present in infected cell nuclei.

70 , that sensor was transferred efficiently to cell nuclei.

71 ) tract, which typically aggregates into the cell nuclei.

72 ells in 3D, without the need to first detect cell nuclei.

73 be the consequences if it also functions in cell nuclei?

74 y to deliver a focused radiation dose to the cell nuclei, (125)I-KX1 remained less effective than its

75 ity to deliver focused radiation dose to the cell nuclei, (125)I-KX1 remained less effective than its

76 aining DNA, ~30% of DNA was localized in the cell nuclei, ~30% was in autophagosomes/autophagolysosom

77 Deformations of cell nuclei accompany a number of essential intracellula

78 g deep-learning-based models that identified cell nuclei across many image types and experimental con

79 and Lmo4 was particularly high in outer hair cell nuclei after cisplatin treatment.

80 tivated ERK and MSK1 were colocalized in SCN cell nuclei after photic stimulation.

81 uscle genes in a range of non-muscle somatic cell nuclei after transplantation to Xenopus oocytes.

82 ubstrates led to the promotion of long-range cell nuclei alignment not seen in the hanging-drop model

83 terized by the choreographed displacement of cells' nuclei along the apicobasal axis according to pha

84 oprecipitated from primary human endothelial cell nuclei also phosphorylated the ACD of hnRNP-C at th

85 the axial direction, while lymphatic muscle cell nuclei and actin fibers are oriented in both circum

86 tions that increase its ability to penetrate cell nuclei and bind DNA causes accumulation of DNA doub

87 e Rta protein is constitutively localized to cell nuclei and contains two putative nuclear localizati

88 detected by electron microscopy in neuronal cell nuclei and cytoplasm but not in satellite cells.

89 were compared with fluorescence staining of cell nuclei and cytoplasm to show that the origin of the

90 s (mRNPs), allow the visualization of intact cell nuclei and enable analyses of where and when differ

91 do bind to the polytene chromosomes in nurse-cell nuclei and enter the oocyte nucleus.

92 sing this tool, we identified and classified cell nuclei and extracted 48 cell spatial organization-r

93 rmline causes F-actin formation in the nurse cell nuclei and germinal vesicle during mid-oogenesis.

94 developmental programming of differentiated cell nuclei and impose pluripotency.

95 owed that these compounds accumulate in live cell nuclei and inhibit PU.1-dependent gene transactivat

96 by decreased NF-kappaB migration to infected cell nuclei and interference in transcription.

97 rizes evidence for mammalian RNAi factors in cell nuclei and mechanisms that might contribute to the

98 vidence for DNA damage is detected in muscle cell nuclei and muscular atrophy is accelerated when one

99 Sustained fiber cell nuclei and nuclear remnants scatter light, whereas

100 The lens capsule was devoid of epithelial cell nuclei and showed excessive thickening with the pre

101 hlea and vestibule and also to cochlear hair cell nuclei and stereocilia.

102 entromeric/pericentromeric positions in germ-cell nuclei and strongly colocalizes with the major hete

103 , they have extensive interactions with host cell nuclei and the proteins and RNAs that normally resi

104 They included 53 specimens, 181,415 detected cell nuclei and the segmentation of 98 gene expression p

105 The model we present here can detect cell nuclei and their morphology even in high-confluency

106 t the lead compound is able to permeate into cell nuclei and trigger a DNA damage response in cancer

107 levels of MM41 are rapidly transported into cell nuclei and were found to accumulate in the tumour.

108 xpressed histone-GFP fusion protein to label cells/nuclei and a confocal microscope, the imaging prot

109 with the orientation of axons, the areas of cell nuclei, and cellular in plane proximity.

110 ntity, delivery of viral DNA to the infected cell nuclei, and expression of KSHV genes suggested that

111 rity of the nuclear lamina, causes misshapen cell nuclei, and leads to multiple aging-like disease ph

112 Select lupus autoantibodies penetrate into cell nuclei, and the potential for application of these

113 Nondividing somatic cell nuclei appeared normal, whereas dividing cells had

114 However, in many biological specimens cell nuclei are densely packed and appear to touch one a

115 Undifferentiated cell nuclei are easily deformable, with an active transc

116 onsidered ER negative if < 1% or 0% of tumor cell nuclei are immunoreactive.

117 to elucidate the mechanism by which somatic-cell nuclei are reprogrammed to have an embryo-like patt

118 arge and euchromatic nuclei, whereas granule cell nuclei are small and have a more typical heterochro

119 s replication compartments (RCs) in infected cell nuclei as sites of viral DNA replication and late g

120 h can robustly segment fluorescent images of cell nuclei as well as phase images of the cytoplasms of

121 ed 1,2-d(GpG) intrastrand cross-links in the cell nuclei, as confirmed by an antibody specific for th

122 eus or cytoplasm, pUL6 localized in infected cell nuclei, as viewed by indirect immunofluorescence.

123 biological significance of DNA packaging in cell nuclei, as well as for gene therapy applications.

124 f a premature aging disorder using images of cell nuclei, as well as the phenotypes of two non-infect

125 real-time images in live cells, visualizing cell nuclei at 10 volumes per second.

126 in parallel to the unc-84 pathway to move P-cell nuclei at 15 degrees .

127 uter border of the ONL, the location of cone cell nuclei, at 1 and 2 days after injection of FeSO(4).

128 The ability to reprogram somatic cell nuclei back into a pluripotent epigenetic state pro

129 complex was purified from activated Jurkat T-cell nuclei based on sequence-specific DNA binding to th

130 ate at early times, forming foci in infected cell nuclei between 3.5 and 5.5 h p.i.

131 mPAM provides histology-like imaging of cell nuclei, blood vessels, axons, and other anatomical

132 exogenous rSPARC was not able to localize to cell nuclei, but instead accumulated as perinuclear clus

133 However, PTEN is also found in cell nuclei, but mechanism, function, and relevance of n

134 bels both wild-type mouse and human Purkinje cell nuclei, but not leaner mouse cerebellum.

135 Ace2 and drives its accumulation in daughter cell nuclei, but the mechanism of this transcription fac

136 omes are highly organized in the 3D space of cell nuclei, but whether this affects gene function is u

137 rmed, CAI administration reduced neovascular cell nuclei by 72% (P < 0.001).

138 nteract with each other predominantly within cell nuclei by an androgen-dependent mechanism in a horm

139 ubiquitin-conjugating enzyme 9 (Ubc9) in HCC cell nuclei by cell fractionation and confocal microscop

140 nd hZimp10 proteins was also observed within cell nuclei by immunostaining.

141 yte maturation, is required for timely nurse cell nuclei clearing from mature egg chambers.

142 Binuclear cell nuclei combine their genomes on a single metaphase

143 ing 33 anatomical regions, as well as 88,047 cell nuclei composing three of these regions.

144 hannel mutation with enlargement of the beta-cell nuclei confined to the focal lesion.

145 Mammalian cell nuclei contain three RNA polymerases (RNAP I, RNAP

146 Stratified squamous cell and goblet cell nuclei contained TrkC.

147 regulatory regions of genes in keratinocyte cell nuclei, demethylating and activating a muscle-speci

148 lularity strongly correlated with numbers of cell nuclei determined using immunohistochemistry.

149 Structural changes in cell nuclei due to subtle environmental stimuli, includi

150 te cortex, actin-mediated tethering of nurse cell nuclei, "dumping" of nurse cell contents into the o

151 caused abnormal positioning of photoreceptor cell nuclei early in development.

152 Targeting the bar-code to cell nuclei enables individual cells expressing distingu

153 SuV2-specific open reading frame 1 (ORF1) in cell nuclei, especially in nucleoli, was detected by IFA

154 hly isolated ganglia, no neuronal or Schwann cell nuclei exhibited ATF-3 immunoreactivity.

155 al space was filled with dense collagen, and cell nuclei expressed hypoxia-inducible factor 1alpha.

156 Within CE cell nuclei, ferritin and ferritoid are coassembled into

157 Practitioners must segment cell membranes or cell nuclei from a tissue and annotate the clones before

158 These studies show that 64Cu localization to cell nuclei from internalizing, receptor-targeted radiop

159 Cell nuclei from old individuals acquire defects similar

160 Observations of cultured cell nuclei from orthogonal perspectives revealed that n

161 nstrate that sparse DNA sequencing of single-cell nuclei from prostate core biopsies is a rich source

162 In WT vegetative cell nuclei, genetically unlinked ribosomal DNA (rDNA) l

163 Defects in the nuclear lamina of animal cell nuclei have dramatic effects on nuclear structure a

164 In metazoan cell nuclei, heterochromatin constitutes large chromatin

165 In mammalian cell nuclei, however, the impact of RNAi has remained mo

166 In cdc48a mutant vegetative cell nuclei, however, these rDNA loci frequently colocal

167 In metazoan cell nuclei, hundreds of large chromatin domains are in

168 TOCA-1 functions to move P-cell nuclei in a cell-autonomous manner.

169 ization of lamin A/C from permeabilized Hep2 cell nuclei in an ATP-dependent manner.

170 0), which we determined is recruited to host cell nuclei in an mLANA-dependent process.

171 ateral ventricle, we observed c-Fos-positive cell nuclei in areas close to the fourth ventricle, indi

172 efflux of protein cargo from preloaded HeLa cell nuclei in cell-free reactions dependent upon Xenopu

173 cell ablation, YAP accumulated in supporting cell nuclei in chicken utricles and promoted regenerativ

174 ear envelope/lamina components into daughter cell nuclei in early G(1) is impaired in cells expressin

175 ed the mean diameter and refractive index of cell nuclei in esophageal epithelium at 172 biopsy sites

176 mage-processing routines to identify stromal cell nuclei in images from the ConfoScan 4 confocal micr

177 arge-scale nuclear architecture across human cell nuclei in interphase.

178 ng (SRS) microscopy for visualization of the cell nuclei in live animals and intact fresh human tissu

179 rogeneity, with alignment of both fibers and cell nuclei in local pockets far exceeding the global av

180 factor PQM-1, which localizes to intestinal cell nuclei in nhr-14 mutants.

181 ncreased isoLG adducts in gastric epithelial cell nuclei in patients with gastritis and intestinal me

182 essfully demonstrated the ability to resolve cell nuclei in situ achieved via SIM, which allowed segm

183 ization of functional sites in intact single-cell nuclei in the 20-250 nm range.

184 Although SRC-1 concentrates in Sertoli cell nuclei in the absence of TIF2, nuclear SRC-1 is not

185 Syto 16 revealed a decrease in viable muscle cell nuclei in the anterior tibial muscle on day 10 in a

186 ive genes and the number of phospho-STAT1(+) cell nuclei in the brain were substantially higher with

187 Progenitor cell nuclei in the rapidly expanding epithelium of the e

188 observed strong staining for FoxM1b in tumor cell nuclei in various gastric tumors and lymph node met

189 ntral-posterior marker genes and localize to cell nuclei in Xenopus animal caps, highlighting its rol

190 ure correct splitting of apparently touching cell nuclei independent of their shape, size or intensit

191 -Sight (LoS) to separate apparently touching cell nuclei into approximately convex parts.

192 The transfer of somatic cell nuclei into oocytes can give rise to pluripotent st

193 The transfer of mammalian somatic cell nuclei into Xenopus oocytes induces transcriptional

194 fer of cloned embryos, reconstructed with ES cell nuclei, into recipients resulted in live offspring.

195 Maintenance of nucleosomal structure in the cell nuclei is essential for cell viability, regulation

196 transfer of DNA from Agrobacterium to plant cell nuclei is initiated by a cleavage reaction within t

197 The identification of fluorescently stained cell nuclei is the basis of cell detection, segmentation

198 However, reports of beta-cell nuclei labeling with both BrdU and gamma-phosphoryl

199 We propose that somatic cell nuclei lack factors needed to direct normal SCC for

200 Mislocalization of viral capsids in infected cell nuclei likely contributes to the observed decrease

201 G(1) and G(2) of the cell cycle, progenitor cell nuclei migrate back-and-forth across the proliferat

202 d size and ultrastructural defects affecting cell nuclei, mitochondria, and autophagosomes.

203 n for the first 12 cell cycles, some somatic cell nuclei must remember a developmentally activated ge

204 In ooc-5-mutant germ cell nuclei, nucleoporins (Nups) were mislocalized in la

205 a lesions with increased expression in tumor cell nuclei of advanced cancers.

206 AR was not expressed in renal epithelial cell nuclei of androgen-deficient rats but was displayed

207 was displayed in most tubule and mural cyst cell nuclei of androgen-replete rats.

208 HIF-1alpha was detected in tumor cell nuclei of both hemangioblastomas and CC-RCCs.

209 gen that lives exclusively inside epithelial cell nuclei of its crab host.

210 3alpha, which is normally expressed in basal cell nuclei of stratified squamous epithelia.

211 th LXRalpha and LXRbeta are expressed in the cell nuclei of the epithelium of the choroid plexus and

212 apoptosis was detected in the photoreceptor cell nuclei of the retina.

213 cromolecules in complex media (e.g., tumors, cell nuclei, or the extracellular matrix).

214 al analysis revealed retention of lens fiber cell nuclei owing to impeded terminal differentiation.

215 a high percentage of egg chambers with nurse cell nuclei persisting past stage 13, indicating a block

216 munocytochemistry to Iba1 in samples of free cell nuclei prepared with the isotropic fractionator fro

217 the Cell attests, the nonchemical aspects of cell nuclei present a new frontier to biologists and bio

218 physiologic salt and when microinjected into cell nuclei, producing dense and dynamic droplets.

219 isms that maintain nuclear integrity as germ cell nuclei progress through meiotic development and mig

220 istochemistry showed tightly compact bipolar cell nuclei (protein kinase C alpha/calbindin positive)

221 (TEL-FISH) coupled with 3D imaging of buccal cell nuclei], providing high-resolution data amenable to

222 FI16 recognized the HSV-1 genome in infected cell nuclei, relocalized, and colocalized with ASC in th

223 Structure of interphase cell nuclei remains dynamic and can undergo various chan

224 exogenous plasmid DNA (pDNA) into mammalian cell nuclei represents a key intracellular obstacle to e

225 Proper localization of pU(L)25 in infected cell nuclei required pU(L)17, pU(L)32, and the major cap

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

227 amp electrophysiology of isolated insect Sf9 cell nuclei revealed a consistent and high probability o

228 et al., 2019), another study, and new single-cell/nuclei RNA-sequencing data, we investigated the exp

229 Cell nuclei rupture following exposure to mechanical for

230 We present an advanced three-dimensional cell nuclei segmentation algorithm that is accurate and

231 ore, a major difficulty of three-dimensional cell nuclei segmentation is the decomposition of cell nu

232 novel and fully automated three-dimensional cell nuclei segmentation method incorporating LoS decomp

233 Most applications require reliable cell nuclei segmentation.

234 family of transcription factors localized in cell nuclei, sensing specific ligands and fine-tuning a

235 nstrate that ultrasound can deliver DNA into cell nuclei shortly after sonication and that the rest o

236 demonstrated that DNA from DNASE1L3-digested cell nuclei showed a median length of 153 bp with CC mot

237 the perinuclear space of intestinal and germ cell nuclei, similar to defects reported in torsin-mutan

238 h its detection in two-thirds of CHI-D delta-cell nuclei, similar to the fetal pancreas, and implied

239 e stained with acridine orange, which stains cell nuclei, skeletal muscle, and collagenous stroma.

240 tly reprogram transplanted mammalian somatic-cell nuclei such that they have an embryo-like pattern o

241 nuclei segmentation is the decomposition of cell nuclei that apparently touch each other.

242 Second, transposition is limited to germ-cell nuclei that contain donor elements, but the transpo

243 HRDE-1 directs gene-silencing events in germ-cell nuclei that drive multigenerational RNAi inheritanc

244 required for bulk mRNA export from the nurse cell nuclei that supply most of the material to the grow

245 In ovarian amplification-stage follicle cell nuclei, the largest subunit, Mip130, is a negative

246 troduce leukaemia-targeting CAR genes into T-cell nuclei, thereby bringing about long-term disease re

247 stranded DNA genomes that replicate in plant cell nuclei through double-stranded DNA intermediates th

248 e mammalian preribosomal complexes by lysing cell nuclei through mild sonication.

249 ociated with an increase in the size of beta-cell nuclei throughout the whole of the pancreas and mos

250 in the mammalian oocyte to reprogram somatic cell nuclei to an undifferentiated state.

251 The transplantation of somatic cell nuclei to enucleated eggs has shown that genes can

252 a result of translocation of HMGB1 from the cell nuclei to the cytoplasm and subsequent release into

253 ature oocyte cytoplasm can reprogram somatic cell nuclei to the pluripotent state through a series of

254 eveals the organization of ON-center bipolar cell nuclei to the upper portion of the inner nuclear la

255 Reprogramming of somatic cell nuclei to yield induced pluripotent stem (iPS) cell

256 e DNA constructs are microinjected into HeLa cell nuclei, to follow the fates of the transcripts.

257 ssay, based on the analysis of unfixed brain cell nuclei, to study whether p75(NTR)-dependent neurona

258 Cell nuclei translocate into these dilations in saltator

259 Notably, HeLa cell nuclei treated with L, or those from EMCV-infected

260 criptional regulator Ikaros into mouse pre-B cell nuclei triggered immediate binding to target gene p

261 and TIF2 coexist in mouse testicular Sertoli cell nuclei under normal conditions.

262 ytochrome c is shown to be translocated into cell nuclei upon induction of DNA damage, but not upon s

263 o deliver the created gene construction into cell nuclei, usually through the deployment of virus-der

264 calization of nucleolin and UL44 in infected cell nuclei was observed by immunofluorescence assays.

265 of 5-methylcytosine in Purkinje and granule cell nuclei, we detected the presence of an unusual DNA

266 king and mass spectrometry on embryonic stem cell nuclei, we identified and mapped, at peptide resolu

267 staining was defined as negative (<1% tumour cell nuclei), weak (1 to <50%), or strong (>/=50%).

268 Cell nuclei were closely associated with the TM structur

269 The frequencies of misshapen cell nuclei were lower in Lmna(csmHG/+) and Lmna(csmHG/c

270 dition, an abnormal number and morphology of cell nuclei were noticed in a subset of Cre-expressing R

271 The cell nuclei were segmented using a high-pass filter algo

272 Cell nuclei were stained with 4',6'-diamino-2-phenylindo

273 Some nonneuronal cell nuclei were very strongly immunoreactive, including

274 t of the DNA damage-induced kinase ABL1 into cell nuclei where it bound the CSF1 gene promoter and en

275 spectrin (alphaIISp) is present in mammalian cell nuclei where it is important in repair of DNA inter

276 evious evidence that PDC localizes to cancer cell nuclei where it plays a role in histone acetylation

277 rage protein, but it also localizes to tumor cell nuclei where it seems to protect DNA from oxidative

278 S100PBPR was found to localize to cell nuclei where S100P is also present, and the two pro

279 NANOS3 expression was highest in human germ cell nuclei where the protein co-localized with chromoso

280 r microsomes and achieves rapid ingress into cell nuclei where the putative molecular target is locat

281 r virus (VZV) is delivered to newly infected cell nuclei, where it initiates VZV replication by trans

282 ated enzyme present in all higher eukaryotic cell nuclei, where it plays key roles in the maintenance

283 n, ORF29p is localized primarily to infected-cell nuclei, whereas during latency it appears in the cy

284 ATF-3 expression was evident in many Schwann cell nuclei, whereas no neuronal nuclei were ATF-3 immun

285 of fluorescently labelled DNA delivery into cell nuclei, which is necessary for gene transfection.

286 entially targeted EGFR to mouse corticotroph cell nuclei, which resulted in higher Pomc expression an

287 ing degenerating neurons with Fluoro-Jade C, cell nuclei with DAPI and activated astrocytes with GFAP

288 amework for the segmentation and tracking of cell nuclei with high accuracy and speed.

289 Incubation of purified human endometrial cell nuclei with rMG_186 resulted in DNA degradation and

290 fluorescence complementation interaction in cell nuclei with, the DELLA proteins RGA-LIKE2 and RGA-L

291 ell-cycle state identification of individual cell-nuclei with widely varying morphologies embedded in

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

293 adult rat brain was present predominantly in cell nuclei, with only light to moderate cytoplasmic sta

294 resence of NF-kappaB p50 and p65 in melanoma cell nuclei, with p50 being more prevalent.

295 Segmenting cell nuclei within microscopy images is a ubiquitous tas

296 NA molecules are preferentially delivered to cell nuclei within minutes.

297 measured the dry mass content of individual cell nuclei within spheroids.

298 y demonstrates that Yy1 is expressed in hair cell nuclei within the cochlea.

299 tributions of pCREB/CREB values obtained for cell nuclei within the external nucleus of the inferior

300 ferences of microenvironmental myoepithelial cell nuclei without any direct information about neoplas