ライフサイエンスコーパス: cell nuclei

1 hology is NSs filament formation in infected cell nuclei.

2 RNA secondary structure in hair and nonhair cell nuclei.

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

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

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

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

7 spatial gene repositioning in breast cancer cell nuclei.

8 tretching and imaging the lamina of isolated cell nuclei.

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

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

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

12 chromosomes to segregate episomes to progeny cell nuclei.

13 imity of cytoplasmic hybridization signal to cell nuclei.

14 visualization of positions and identities of cell nuclei.

15 from concatemers that accumulate in infected cell nuclei.

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

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

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

19 ominant active isoform in corneal epithelial cell nuclei.

20 ient translocation into the proximal tubular cell nuclei.

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

22 ns of achieving the reprogramming of somatic cell nuclei.

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

24 f a monoallelically expressed gene in single cell nuclei.

25 referred spatial positions within interphase cell nuclei.

26 mmunofluorescence measurements at individual cell nuclei.

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

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

29 ced green fluorescent protein exclusively to cell nuclei.

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

31 and delivered the fluorescent label into the cell nuclei.

32 to detect nanoparticles inside fractionated cell nuclei.

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

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

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

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

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

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

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

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

41 of the nuclear envelope and causes misshapen cell nuclei.

42 ng mismatch-selective metal complexes inside cell nuclei.

43 0-green fluorescent fusion protein entered B-cell nuclei.

44 requent localization of the enzyme to cancer cell nuclei.

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

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

47 the subcellular fractions of brain including cell nuclei.

48 rthermore, Sun2 is enriched in purified HeLa cell nuclei.

49 the asymmetric sorting of Ash1p to daughter cell nuclei.

50 t cDNA localized to dividing and nondividing cell nuclei.

51 quiescent, pericentromeric regions in mouse cell nuclei.

52 between ACBP and HNF-4 alpha in rat hepatoma cell nuclei.

53 he GA-induced disappearance of RGA from root cell nuclei.

54 r under cell cycle control in isolated human cell nuclei.

55 nfluency cell cultures with many overlapping cell nuclei.

56 ed RPL4 expression and redistributed RPL4 to cell nuclei.

57 oplasmic vesicles and is present in infected cell nuclei.

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

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

60 s and viral particles in swollen endothelial cell nuclei.

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

62 t phosphorylation siteswere retained in hair cell nuclei.

63 protocols for the isolation and analysis of cell nuclei.

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

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

66 were still localized to the somatic support cell nuclei.

67 s capable of inducing totipotency in somatic cell nuclei.

68 leic acid band intensities across individual cell nuclei.

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

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

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

72 Deformations of cell nuclei accompany a number of essential intracellula

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

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

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

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

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

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

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

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

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

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

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

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

85 developmental programming of differentiated cell nuclei and impose pluripotency.

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

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

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

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

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

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

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

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

94 protein is expressed and localized in plant cell nuclei and that expression of L1 in plants is enhan

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

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

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

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

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

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

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

102 shown that UNC-98 resides at M-lines, muscle cell nuclei, and possibly at dense bodies.

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

104 ally by counting the neovascular endothelial cell nuclei anterior to the inner limiting membrane.

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

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

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

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

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

110 Changes in the size and texture of cell nuclei as a result of neoplastic transformation and

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

112 ince both proteins are localized within cyst cell nuclei as spermatocytes differentiate from amplifyi

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

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

115 e stress also redistributed activated PKD to cell nuclei, as revealed by PKD indirect immunofluoresce

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

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

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

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

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

121 (BrdU) incorporation throughout the follicle cell nuclei at stages undergoing gene amplification.

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

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

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

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

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

127 contrast, full-length WTIP was excluded from cell nuclei, but after the addition of leptomycin B, an

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

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

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

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

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

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

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

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

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

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

138 Binuclear cell nuclei combine their genomes on a single metaphase

139 demonstrated a 41% reduction in neovascular cell nuclei compared with control mice (P <0.01).

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

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

142 Stratified squamous cell and goblet cell nuclei contained TrkC.

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

144 s, TCC patients with >20% proHB-EGF-positive cell nuclei demonstrated markedly reduced survival compa

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

146 als derived by nuclear transfer from somatic cell nuclei develop to the blastocyst stage but die afte

147 related changes in the ONL and photoreceptor cell nuclei did not represent a toxic effect, because th

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

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

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

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

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

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

154 t cloned embryos derived from differentiated cell nuclei fail to establish a population of truly plur

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

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

157 Cell nuclei from old individuals acquire defects similar

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

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

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

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

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

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

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

165 st the cytoplasmic tail domain, localized to cell nuclei in a manner that correlated positively with

166 ression have been localized within mammalian cell nuclei in a speckled distribution that predominantl

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

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

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

170 colocalized in the paranuclear cytoplasm and cell nuclei in basal, as well as suprabasal, cells of ad

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

172 Each lentiviral integrase localized to cell nuclei in close association with chromatin while th

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

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

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

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

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

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

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

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

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

182 ntally regulated migrations of photoreceptor cell nuclei in the eye.

183 centage of phosphoCREB (PCREB) immunolabeled cell nuclei in the hypothalamic paraventricular nucleus

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

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

186 ion in both Xenopus sperm chromatin and HeLa cell nuclei in vitro.

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

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

189 ystem successfully delivered ASOs and DOX to cell nuclei, inhibited MRP1 and BCL2 protein synthesis,

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

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

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

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

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

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

196 tion of chromosomal DNA replication in human cell nuclei is not well understood because of its comple

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

198 s by which only a very small fraction of the cell nuclei is traversed by a particle track.

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

200 molecular beacons are rapidly sequestered in cell nuclei, leaving little time for them to find and bi

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

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

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

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

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

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

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

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

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

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

211 d androgen receptor proteins can be found in cell nuclei of prostate cancer tissue samples.

212 3alpha, which is normally expressed in basal cell nuclei of stratified squamous epithelia.

213 lting c-fos immunoreactivity within neuronal cell nuclei of the dorsal motor nucleus (DMN), nucleus t

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

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

216 A 92% inhibition of neovascular cell nuclei on light microscopy was observed in mice tre

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

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

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

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

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

222 dynamic behavior of speckles in Arabidopsis cell nuclei provides significant insight into understand

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

248 rogramming by the transplantation of somatic cell nuclei to eggs (in second meiotic metaphase) is alw

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

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

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

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

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

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

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

256 Marker-free P-DNAs are transferred to plant cell nuclei together with conventional T-DNAs carrying a

257 Cell nuclei translocate into these dilations in saltator

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

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

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

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

262 t that 4.1 and actin colocalize in mammalian cell nuclei using fluorescence microscopy and, by higher

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

264 al repeat circle accumulation in nondividing cell nuclei was also equivalent to that of LEDGF/p75 wil

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

266 Strong punctate staining of tumor cell nuclei was observed in 47 of 153 (31%) breast cance

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

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

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

270 Cell nuclei were closely associated with the TM structur

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

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

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

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

275 Some nonneuronal cell nuclei were very strongly immunoreactive, including

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

291 e and T157A-p27 shuttled from NIH3T3 to HeLa cell nuclei with similar frequencies.

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

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

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

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

296 due to the presence of persistent apoptotic-cell nuclei within phagocytic cells in nuc-1 mutants.

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

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

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

300 expressed ataxin-1[82Q]-A776 within Purkinje cell nuclei, yet the ability of ataxin-1[82Q]-A776 to in