ライフサイエンスコーパス: cell cycle-dependent

1 egative bacterial species and observed to be cell cycle dependent.

2 ions to retroviral infections are themselves cell cycle dependent.

3 the mode of binding of HMGNs to chromatin is cell cycle dependent.

4 BHK-propagated virus to infect CHO cells was cell cycle dependent.

5 ensitize cells to apoptosis may be, in part, cell cycle dependent.

6 Expression of Aurora-A is cell cycle-dependent.

7 ution at GVBD is therefore dynein-driven and cell cycle-dependent.

8 ase, the subcellular localization of Epac is cell cycle-dependent.

9 the thermodynamic stability of PGK-FRET are cell cycle-dependent.

10 flammatory response following DNA damage are cell-cycle dependent.

11 e helicase (BLM) that is phosphorylation and cell-cycle dependent.

12 le-dependent AAV2 rep expression facilitates cell cycle-dependent AAV2 DNA replication and inhibits H

13 We conclude that cell cycle-dependent AAV2 rep expression facilitates cel

14 Cell cycle-dependent accumulation of cyclin D1 negativel

15 gulation of RICTOR, which is associated with cell cycle-dependent activation of mammalian target of r

16 lly antagonistic, particularly with the more cell cycle-dependent agents such as cytarabine.

17 is regulated by interactions with Rb and by cell cycle-dependent alterations in E2F-1 abundance.

18 We observed that AAV2 rep gene expression is cell cycle dependent and gives rise to distinct time-con

19 fferentiation of a number of tissues in both cell cycle-dependent and -independent manners.

20 Both cell cycle-dependent and DNA damage-dependent phosphoryl

21 rther, MEK activation in the early embryo is cell cycle-dependent and Raf independent and increases i

22 he HSC response to genotoxic stress via both cell-cycle-dependent and cell-cycle-independent mechanis

23 itochondrial functionality is cell size, not cell cycle, dependent, and it results in an optimal cell

24 Moreover, using cell-cycle-dependent Ara-C chemotherapy to produce minim

25 This regulation of p53 by E2F1 is cell cycle dependent, as the cellular distribution of Se

26 Primary cilia undergo cell-cycle-dependent assembly and disassembly.

27 Taken together, these results suggest that cell cycle-dependent association and dissociation of LSD

28 Consistent with the cell cycle-dependent association of Gwl and PP1, Gwl and

29 cells with anti-Orc3 antibodies demonstrate cell cycle-dependent association with a nuclear structur

30 Ube2S depends on the cell cycle-dependent association with the APC/C activato

31 We suggest that the cell cycle-dependent binding of dynein/dynactin to the n

32 ted using N5-2OH in combination with two non-cell cycle dependent boron delivery agents, boronophenyl

33 wn that telomere elongation by telomerase is cell cycle dependent, but the mechanism underlying this

34 ution of an intermediate state, in which the cell cycle-dependent Ccq1-Est1 interaction is coupled to

35 on pathway may play an important role in the cell cycle-dependent Cdt1 degradation in mammalian cells

36 Cell cycle-dependent Cdt1 degradation plays an essential

37 The cell-cycle-dependent change in GCL localization provides

38 lei of dividing neural progenitors undergo a cell-cycle-dependent change in position along the apico-

39 ombe using synchronized cells to investigate cell cycle dependent changes in genome organization and

40 ated that this zinc finger protein undergoes cell cycle-dependent changes in association with DNA tha

41 Cell cycle-dependent changes in central carbon metabolis

42 ysis of the data revealed one component with cell cycle-dependent changes in expression at the 99% co

43 FtsZ assembly is governed primarily through cell cycle-dependent changes in FtsZ polymerization kine

44 expressed in COS-1 cells undergoes dramatic cell cycle-dependent changes in its PM localization, hav

45 We suggest that Aurora B and PP1 coordinate cell cycle-dependent changes in kinetochore assembly tho

46 These cell cycle-dependent changes in Kv2.1 localization and t

47 Here we present evidence that dynamic cell cycle-dependent changes in levels of UbcH7 regulate

48 The cell cycle-dependent changes in localization and phospho

49 Their cell cycle-dependent changes in localization may be impo

50 sms for generating Tyr(P) ERK by determining cell cycle-dependent changes in localized phosphatase ac

51 In addition, Zds1 undergoes cell cycle-dependent changes in phosphorylation.

52 hese results provide novel insights into the cell cycle-dependent changes in PM protein localization

53 Previous studies have suggested that cell cycle-dependent changes in the affinity of the orig

54 8 and 13 [Klp10A]) seem to be controlled by cell cycle-dependent changes in their localizations.

55 Mps1 regulation is mediated by cell cycle-dependent changes in transcription and protei

56 iplexed quantitative proteomics, we analyzed cell cycle-dependent changes of the human proteome.

57 dy various combinations of multiple doses of cell-cycle dependent chemotherapies and radiation therap

58 lls), inhibitors of signal transduction with cell cycle-dependent chemotherapy, antiangiogenic agents

59 This cell cycle-dependent choreography suggests that similarl

60 These nucleosomes were subject to cell cycle-dependent chromatin remodeling and histone mo

61 Our data suggest that cell cycle-dependent chromosome occupancy of H1 is gover

62 tide-3-kinase (PI3K) pathway triggers PTEN's cell cycle-dependent chromosome region maintenance 1-med

63 r RcdA recognition and uncovering additional cell-cycle-dependent ClpXP substrates.

64 These results demonstrate a cell cycle-dependent compartmentalization of phospholipa

65 ction of MRN with BRCA1, we propose that the cell cycle-dependent complex formation of BRCA1, CtIP, a

66 This band comigrated with a cell cycle-dependent component identified from single-ce

67 oligomers whose size may be regulated by the cell cycle-dependent concentration of NAP1.

68 ed in cup1Delta and sod1Delta cells, whereas cell cycle-dependent Cu resistance was suppressed in sod

69 Mammalian cells also display a cell cycle-dependent cytoplasmic polyadenylation, sugges

70 states and to analyse the effect of various cell-cycle dependent cytotoxic drugs.

71 Recombination defects were correlated with a cell cycle-dependent defect in the ability of RAG-1 to r

72 iquitin ligase and thus is important for the cell cycle dependent degradation of Cdt1 in mammalian ce

73 re, we investigate the mechanisms underlying cell cycle-dependent degradation of ORC1.

74 These results suggest that cell cycle-dependent degradation of s80(HER4) limits its

75 evel depends on its compartment-specific and cell cycle-dependent degradation.

76 long-term centromere identity, propagation, cell-cycle-dependent deposition, maintenance, function,

77 e via two distinct mechanisms to accommodate cell cycle-dependent differences in NE topology.

78 These patterns are cell cycle-dependent, disappearing during mitosis.

79 tic subunits of PP2A (PP2Ac) is required for cell cycle-dependent distribution of actin.

80 Epstein-Barr virus OriP confers cell cycle-dependent DNA replication and stable maintena

81 We show here that the cell cycle-dependent DNA-binding and transcriptional act

82 c3 led to a delay in cell-cycle progression, cell-cycle-dependent DNA damage, and apoptosis in mouse

83 ilitates Foxp3 induction in part by opposing cell cycle-dependent Dnmt1 recruitment, leading to locus

84 containing several Sp1 canonical, Sp1-like, cell cycle-dependent element/cell cycle gene homology re

85 clin A promoter, we have identified CDE-CHR (Cell cycle-Dependent Elements-Cell cycle genes Homology

86 ry factor-2 (IRF-2) oncoprotein controls the cell cycle-dependent expression of histone H4 genes duri

87 These novel observations of cell cycle-dependent expression of TR suggest that diffe

88 ata demonstrate that Citron-K has a distinct cell cycle-dependent expression pattern and cellular loc

89 on factors to activate or repress genes with cell cycle-dependent expression patterns.

90 Although the three proteins have variable cell cycle-dependent expression profiles, they can only

91 t of the cell cycle regulators in hESCs show cell cycle-dependent expression, thus revealing importan

92 Fkh2p act in a DNA-bound complex to regulate cell-cycle dependent expression of the CLB2 cluster in S

93 This process is temporally controlled by cell-cycle-dependent factors, but its biochemical mechan

94 ptional activity of FoxM1 is controlled in a cell cycle-dependent fashion by temporally regulated pho

95 reover, KEAP1 associates with chromatin in a cell cycle-dependent fashion with kinetics similar to th

96 ion, which is active during the S phase in a cell cycle-dependent fashion.

97 re recruited to bivalent gene promoters in a cell cycle-dependent fashion.

98 e polo-like kinase Plk1 and Numb cycles in a cell-cycle-dependent fashion along with this mitotic reg

99 he p34 subunit of RPA is phosphorylated in a cell-cycle-dependent fashion and is hyperphosphorylated

100 RPA-p34 is phosphorylated in a cell-cycle-dependent fashion primarily at Ser-29 and Ser

101 form" solutions and add to the evidence that cell-cycle dependent feedback robustly leads to cell-cyc

102 ns models of large populations of cells with cell-cycle dependent feedback.

103 Similar cell cycle-dependent findings also were observed for end

104 phase from an asynchronous mixture based on cell cycle-dependent fluctuations in size.

105 Cell cycle-dependent formation and activation of this tr

106 These data suggest a novel cell cycle-dependent function for p38, suppression of th

107 ich cannot be replaced by AUG8, and that the cell-cycle-dependent function of augmin can be different

108 The majority of the identified genes are cell cycle-dependent (GAPDH Associated Cell Cycle, or GA

109 E2F-mediated transcriptional repression of cell cycle-dependent gene expression is critical for the

110 How the marks facilitate cell cycle-dependent gene expression is poorly understoo

111 rent mechanism for determining the timing of cell cycle-dependent gene expression that involves compe

112 nd available data suggest that they regulate cell cycle-dependent gene expression through opposing tr

113 es in common with known master regulators of cell cycle-dependent gene expression.

114 actor that allows it to specifically control cell cycle-dependent gene expression.

115 We used our algorithm to compare cell-cycle-dependent gene expression in wild-type and kn

116 ion for the polo kinase Cdc5p in controlling cell-cycle-dependent gene expression that is crucial for

117 oblastoma], E2F, and MuvB) complex represses cell cycle-dependent genes during quiescence.

118 but not pRB, and mediates the repression of cell cycle-dependent genes in quiescence.

119 ption factors function in condensin loading, cell cycle-dependent genome organization and mitotic chr

120 A polarisome mediates cell cycle dependent growth in yeast and pseudohyphae.

121 al several dynamic features of the SPB core: cell cycle-dependent growth and reduction, growth in res

122 maging provides a unique method for studying cell cycle-dependent growth.

123 cell line, exhibited relatively restrictive, cell cycle-dependent hCNT1 expression and transport.

124 myelocytic leukemia cells, expression of the cell cycle-dependent histone genes is downregulated at t

125 Foamy virus replication is cell cycle dependent; however, the genome is found in th

126 We therefore propose that CYREN is a direct cell-cycle-dependent inhibitor of cNHEJ that promotes er

127 Cell cycle dependent interactions were captured between

128 rest is associated with up-regulation of the cell cycle-dependent kinase inhibitor p27kip1, the induc

129 ary cells and demonstrate that silencing the cell cycle-dependent kinase inhibitors CDKN2C/p18 or CDK

130 sure to LAQ824 induced the expression of the cell cycle-dependent kinase inhibitors p21 and p27 and c

131 We correlated this phenomenon with loss of cell-cycle-dependent kinase 1 (CDK1), which mediates lam

132 expression of p21WAF1/CIP1, an inhibitor of cell cycle-dependent kinases and a downstream mediator o

133 Although this loss activates the cell-cycle-dependent kinases CDK4/6, which have been con

134 This cell cycle-dependent localization requires AIR-2/AuroraB

135 Par-1 shows a cell cycle-dependent localization to the spectrosome, a

136 A carboxy-terminal domain from HDHB confers cell cycle-dependent localization, but not the focal pat

137 le for Polo kinase in directly mediating Nuf cell cycle-dependent localization.

138 our results demonstrate that PRL-1 exhibits cell cycle-dependent localization; in non-mitotic HeLa c

139 isrupt phosphodependent interactions abolish cell-cycle-dependent localization and provide compelling

140 ion on multiple serine residues in vivo in a cell cycle dependent manner and that only unphosphorylat

141 MCM is controlled in a subunit-specific and cell cycle dependent manner.

142 -TuSC oligomerization and MT nucleation in a cell cycle dependent manner.

143 Bni4 is phosphorylated in a cell cycle-dependent manner and Bni4(V831A/F833A) is bot

144 n the nucleus of renal epithelial cells in a cell cycle-dependent manner and in connecting cilia of p

145 eleased, TR expression levels increased in a cell cycle-dependent manner and peaked to 30-40% cells e

146 hat JMJD2A protein levels are regulated in a cell cycle-dependent manner and that JMJD2A overexpressi

147 e, we show that BARD1 is phosphorylated in a cell cycle-dependent manner and that the hyperphosphoryl

148 ated by CDK2, in the absence of damage, in a cell cycle-dependent manner and we identify serine 687 a

149 enhances tau-induced neurodegeneration in a cell cycle-dependent manner and, when ectopically activa

150 p27, for example, is polyubiquitylated in a cell cycle-dependent manner by a ubiquitin ligase comple

151 he budding yeast Dpb2 is phosphorylated in a cell cycle-dependent manner during late G(1) phase.

152 We show that E2f1 protein is destroyed in a cell cycle-dependent manner during S phase of cycles 15

153 ssociated directly at the PHO5 promoter in a cell cycle-dependent manner in chromatin immunoprecipita

154 ciated protein that is highly expressed in a cell cycle-dependent manner in hematopoietic lineage cel

155 ation of GAPDH is regulated by ceramide in a cell cycle-dependent manner parallel with the inhibition

156 A-PKcs autophosphorylation is regulated in a cell cycle-dependent manner with attenuated phosphorylat

157 t phosphorylation of KIBRA is regulated in a cell cycle-dependent manner with the highest level of ph

158 slin is phosphorylated by CDK2/cyclin E in a cell cycle-dependent manner, and its phosphorylation sta

159 ted for ubiquitin-dependent degradation in a cell cycle-dependent manner, but the identity of the ubi

160 Expression of Claspin fluctuates in a cell cycle-dependent manner, but the mechanisms involved

161 binds to chromatin in a DDB1-independent and cell cycle-dependent manner, increasing from early S thr

162 Elm1 is expressed in a cell cycle-dependent manner, primarily at S and G(2)/M.

163 ylation, which is dynamically regulated in a cell cycle-dependent manner, reflects a balance of coord

164 ermore, ERK phosphorylates TRAP220/Med1 in a cell cycle-dependent manner, resulting in peak levels of

165 lizes with the satellite component PCM1 in a cell cycle-dependent manner, similarly to the satellite

166 Expression of BRCA1 fluctuates in a cell cycle-dependent manner, such that low steady-state

167 g machinery components may be regulated in a cell cycle-dependent manner, thereby coordinating [Ca(2+

168 ligase Mdm2 and promotes AR degradation in a cell cycle-dependent manner, while PIM-1L-induced Thr-85

169 rate that FOXC2 expression is regulated in a cell cycle-dependent manner, with FOXC2 protein levels a

170 CDK1) at threonine residues 345 and 487 in a cell cycle-dependent manner.

171 phase and repress CTCF-regulated genes in a cell cycle-dependent manner.

172 F binding sites and bound CTCF proteins in a cell cycle-dependent manner.

173 ores, microtubules, and the cell cortex in a cell cycle-dependent manner.

174 binding to multiple G(1) gene promoters in a cell cycle-dependent manner.

175 s and excluded from sites of DNA repair in a cell cycle-dependent manner.

176 ex with CtIP and MRN (Mre11/Rad50/Nbs1) in a cell cycle-dependent manner.

177 ated that E2F1, Rb, and LSD1 bind to Cp in a cell cycle-dependent manner.

178 t Mnd2 is phosphorylated during mitosis in a cell cycle-dependent manner.

179 S224 indicate that it is phosphorylated in a cell cycle-dependent manner.

180 Ialpha, unlike XRCC1, is phosphorylated in a cell cycle-dependent manner.

181 nic transformation events are regulated in a cell cycle-dependent manner.

182 ed both in a cell cycle-independent and in a cell cycle-dependent manner.

183 90 participates in kinetochore assembly in a cell cycle-dependent manner.

184 Bir1 is phosphorylated in a cell cycle-dependent manner.

185 lize at, subnuclear foci (Cajal bodies) in a cell cycle-dependent manner.

186 actin gene transcription in a cell type- and cell cycle-dependent manner.

187 like that of p27, is regulated by Skp2 in a cell cycle-dependent manner.

188 action with the D-box of its substrates in a cell cycle-dependent manner.

189 mutant blocks the translocation of RPA in a cell cycle-dependent manner.

190 , are transcriptional factors regulated in a cell cycle-dependent manner.

191 core exhibits both exchange and growth in a cell cycle-dependent manner.

192 tion of endogenous RFCp145 is modulated in a cell cycle-dependent manner.

193 igase does not regulate CDK9 expression in a cell cycle-dependent manner.

194 to the promoter in an Spt21-dependent and a cell cycle-dependent manner.

195 Protein distribution is regulated in a cell cycle-dependent manner.

196 in-dependent kinase 1 (CDK1) expression in a cell cycle-dependent manner.

197 in eukaryotic cells is often controlled in a cell cycle-dependent manner.

198 associates with the mitotic spindle/NPC in a cell cycle-dependent manner.

199 ed break sites is resected up to 3.5 kb in a cell cycle-dependent manner.

200 lates the pathway choice of NHEJ and HR in a cell cycle-dependent manner.

201 key structures of the mitotic apparatus in a cell cycle-dependent manner.

202 s and localization only upon DNA damage in a cell cycle-dependent manner.

203 ciates with the replisome protein And-1 in a cell cycle-dependent manner.

204 Its protein level is regulated in a cell cycle-dependent manner.

205 nds of chromosomes in a telomere length- and cell-cycle-dependent manner [1-4].

206 N terminus, that is hyperphosphorylated in a cell-cycle-dependent manner and in response to DNA damag

207 Nuclear PDC levels increased in a cell-cycle-dependent manner and in response to serum, ep

208 hat both PBK/TOPK and P38 are activated in a cell-cycle-dependent manner in neuronal progenitor cells

209 of triacylglycerols (TGs) is regulated in a cell-cycle-dependent manner, by activation of the Tgl4 l

210 obacter crescentus, tmRNA was localized in a cell-cycle-dependent manner.

211 nd both are co-localized in the nucleus in a cell-cycle-dependent manner.

212 to regulate histone gene transcription in a cell-cycle-dependent manner.

213 h the host cellular DNA, and only once, in a cell-cycle-dependent manner.

214 y axoneme and to mitotic spindle fibers in a cell-cycle-dependent manner.

215 antly, they reveal the existence of a novel, cell cycle-dependent mechanism through which PKCdelta st

216 These data show that cell cycle-dependent mechanisms can control ciliary leng

217 This protein is thus an essential, cell cycle-dependent mediator of sister chromatid cohesi

218 rfamily suggested a common mechanism for the cell cycle-dependent modulation of DNA-binding affinity

219 Cell cycle-dependent morphogenesis of unicellular organi

220 and that phosphorylation of Vac17 parallels cell cycle-dependent movement of the vacuole.

221 ous studies have demonstrated a key role for cell cycle-dependent multi-site phosphorylation of Ngn2

222 the negative regulator GSK-3beta, causing a cell cycle-dependent nuclear accumulation of GSK-3beta.

223 Through these analyses, we show that the cell cycle-dependent nuclear import of the Saccharomyces

224 na tabacum) Bright Yellow-2 cells revealed a cell cycle-dependent nuclear localization pattern but no

225 glial progenitor cells exhibit bidirectional cell cycle-dependent nuclear oscillations.

226 at TacA degradation is controlled during the cell cycle dependent on the ClpXP regulator CpdR and tha

227 PodJ(L) substrate cooperatively control the cell cycle-dependent onset of Rip.

228 Knockdown of FOXJ3 and FOXK1 eliminated cell cycle-dependent oscillations and resulted in decrea

229 In summary, these data indicate that the cell cycle-dependent pattern of BRCA1 expression is dete

230 /subdistal regions of mature centrioles in a cell cycle-dependent pattern.

231 ory role, we found that INPP5E expression is cell cycle dependent, peaking at mitotic entry.

232 calized to chromatin fractions and underwent cell cycle-dependent phosphorylation and dephosphorylati

233 g and transformation, and they indicate that cell cycle-dependent phosphorylation of C/EBPbeta on Ser

234 silencing, (ii) quantitatively determine the cell cycle-dependent phosphorylation of Ser-1126 of huma

235 Cell cycle-dependent phosphorylation of Sil is required

236 e to the modulation of Byr4, which undergoes cell cycle-dependent phosphorylation presumed to regulat

237 tivation of Fus2p in mitosis is prevented by cell cycle-dependent phosphorylation that overrides the

238 ty is regulated by both Survivin binding and cell cycle-dependent phosphorylation.

239 Here we demonstrate the cell-cycle-dependent phosphorylation of a key reprogramm

240 In this study, we examined the cell-cycle-dependent phosphorylation of the Nup107-160 s

241 tercellular communication, and regulation of cell cycle-dependent physiological processes.

242 ure of this signaling network is the dynamic cell cycle-dependent polar localization of its component

243 These results demonstrate that cell-cycle-dependent post-translational modification of

244 ize and the persistent memory pool size: the cell cycle dependent probability of apoptosis, and the p

245 monstrate that phosphorylation of Sec4p is a cell cycle-dependent process associated with cytokinesis

246 y that the centrosome may coordinate various cell-cycle-dependent processes by synchronizing mitosis

247 which is involved in DNA replication and has cell cycle dependent properties.

248 Study of cell cycle-dependent protein expression is important in

249 animal cell, is in large part controlled by cell cycle-dependent protein phosphorylation.

250 Citron Kinase (Citron-K) is a cell cycle-dependent protein regulating the G(2)/M trans

251 otein are controlled post-translationally by cell cycle-dependent proteolysis, wherein Ski is degrade

252 luctuations in their protein levels owing to cell cycle-dependent proteolysis.

253 tional factors are inexplicably required for cell-cycle-dependent proteolysis.

254 The observed variation in cell cycle-dependent purinosome formation between the tw

255 eract at two defined sites to coordinate the cell cycle-dependent rearrangement and scaffolding activ

256 y is regulated in fission yeast, we analysed cell cycle-dependent recruitment of telomere-specific pr

257 n is tightly regulated through selective and cell cycle-dependent recruitment, retention, and removal

258 The cell cycle-dependent redistribution of ParC occurs by it

259 Thus, the cell cycle-dependent regulation of pyrimidine biosynthes

260 Interestingly, we also observe a cell cycle-dependent regulation of Smad3 in both cell ty

261 at telomeres and provide a mechanism for the cell cycle-dependent regulation of telomere synthesis in

262 , depletion of endogenous Dyrk2 disrupts the cell cycle-dependent regulation of TERT and elicits the

263 romoter construct failed to recapitulate the cell cycle-dependent regulation of the endogenous hPCNA

264 Our data provide a novel mechanism for the cell cycle-dependent regulation of the FA pathway.

265 itotic, differentiated cells, to examine the cell cycle-dependent regulation of the human PCNA gene (

266 echanism by which this occurs, we reproduced cell cycle-dependent regulation of the V(D)J recombinase

267 Our results reveal a mechanism of cell-cycle-dependent regulation of basal transcription.

268 Knowledge about the cell-cycle-dependent regulation of membrane and storage

269 in and reptin peaks in S phase, evidence for cell-cycle-dependent regulation of TERT.

270 analysis revealed little overlap between the cell cycle-dependent regulons of CtrA and DnaA in S. mel

271 Our findings suggest that cell cycle-dependent repression results from recruitment

272 Distinct cell cycle-dependent response patterns comprised a large

273 Our results provide vital insight into cell cycle-dependent RNR regulation under conditions of

274 ignificantly expand our understanding of the cell-cycle-dependent roles of 53BP1 in DSB repair.

275 In this issue, Ouenzar et al. uncover cell cycle-dependent sequestration of the telomerase RNA

276 ffinity and support a model wherein a single cell cycle-dependent Ser/Thr kinase could simultaneously

277 A cell-cycle-dependent shuffling of multiple centromeric u

278 ubiquitin-conjugating enzyme Cdc34 mediates cell cycle-dependent Ski degradation both in vitro and i

279 process is consistent with a simple model of cell cycle-dependent stochastic priming of progenitors t

280 and their temporal fate changes appear to be cell cycle-dependent, such that the same numbers and typ

281 igration and neurogenesis and suggest that a cell cycle-dependent switch between distinct microtubule

282 In addition, we found that Sba1p displayed a cell cycle-dependent telomere interaction that parallele

283 t the expression of Bdbd strongly suppressed cell cycle-dependent transcription activation of Cyclin

284 MADS box protein Mcm1p are key regulators of cell cycle-dependent transcription at both the G2/M and

285 Cell cycle-dependent transcription factor binding permit

286 e identified a regulatory module controlling cell cycle-dependent transcription of G2-M genes and exp

287 or function of CBF by which it regulates the cell cycle-dependent transcription of the topo II alpha

288 ovide a more detailed and integrated view of cell cycle-dependent transcription.

289 e results suggest that CITED1 functions as a cell cycle-dependent transcriptional cofactor whose acti

290 directly measure the effects of lineage and cell cycle-dependent transcriptional profiles of single

291 ific methyltransferase that is implicated in cell-cycle-dependent transcriptional silencing and mitot

292 of PRC1 in midzone formation, indicate that cell cycle-dependent translocation of PRC1 by Kif4 is es

293 In contrast, cell cycle-dependent up-regulation of a group of mitosis

294 However, the mechanism for this cell cycle-dependent vulnerability is unknown.

295 In some cases 14-3-3 binding was cell cycle-dependent, whereas in other cases the binding

296 We show that iPLA(2) activity is cell cycle-dependent with peak activity during G(2)/M an

297 ime that RASSF10 subcellular localization is cell-cycle dependent with RASSF10 colocalizing to centro

298 for BBS4, FOP localization to satellites is cell cycle dependent, with few satellites labeled in G1,

299 R function and phosphorylation is remarkably cell cycle dependent, with the highest activity in S pha

300 SBDS localization was cell-cycle dependent, with nucleolar localization during