ライフサイエンスコーパス: cell division

1 s involved in transcription, DNA repair, and cell division.

2 d reliably to the two daughter cells through cell division.

3 er the role of Nek8445 in regulating Giardia cell division.

4 ates that are asymmetrically retained during cell division.

5 orchestrating chromosome segregation during cell division.

6 ll septal PG synthesis and regulation during cell division.

7 rsors by favouring symmetric over asymmetric cell division.

8 in is targeted to growing cell plates during cell division.

9 glycan synthase relocation to midcell during cell division.

10 viral genome to the daughter cells following cell division.

11 assembled at the future division site during cell division.

12 late more biomass than larger cells prior to cell division.

13 as focal adhesion formation and turnover and cell division.

14 me and space and could play similar roles in cell division.

15 and in activating some of the key players in cell division.

16 h as endocytosis, vesicular trafficking, and cell division.

17 hanges in DNA condensation, segregation, and cell division.

18 llocation theory and the structural model of cell division.

19 actions between cytoskeletal networks during cell division.

20 family of serine/threonine kinases vital for cell division.

21 ss, rather than the activities preparing for cell division.

22 del for cell cycle regulation and asymmetric cell division.

23 cell expansion is properly coordinated with cell division.

24 regulating key cellular processes, including cell division.

25 me, they were detected at the midbody during cell division.

26 ism for maintaining cell identity throughout cell division.

27 the transcriptional program and TADs during cell division.

28 in re-establishing the epigenetic code upon cell division.

29 zation and segregation leading to a block in cell division.

30 ignaling pathway that leads to an asymmetric cell division.

31 y the spindle, which then guides the axis of cell division.

32 uired for cell function or processes such as cell division.

33 optimal pairing of sister ter regions until cell division.

34 n which DNA is replicated without subsequent cell division.

35 ubiquitous processes of polarised growth and cell division.

36 resulting in SOS induction and inhibition of cell division.

37 egumes is sufficient to induce root cortical cell division.

38 k1 substrates that are essential to complete cell division.

39 The cyclin-dependent kinase 1 (Cdk1) drives cell division.

40 ent on the rate of aneuploidy generation per cell division.

41 ene sets, despite fundamental differences in cell division.

42 ny cell processes, including lens epithelial cell division.

43 postmitotic cells that undergo very limited cell division.

44 e body macrophages and were sites of ongoing cell division.

45 A-containing chromatin and are essential for cell division.

46 d to meet phase-specific demands of eukaryal cell division.

47 mouse oocytes to undergo asymmetric meiotic cell division.

48 shed from the tissue surface and replaced by cell division.

49 anizing, and activating proteins involved in cell division.

50 g that the proteome is heavily geared toward cell division.

51 n protein key to kinetochore assembly during cell division.

52 known to control the metabolism, growth, and cell division.

53 cally separates daughter cells and completes cell division.

54 or generating two distinct cells through one cell division.

55 ed PG synthesis in ovococcal bacteria during cell division.

56 concentrations of key metabolites needed for cell division.

57 hese factors are operating in the context of cell division.

58 ir accurate alignment and segregation during cell division.

59 g cell that undergoes predominant asymmetric cell division.

60 lomere segregation, and it ultimately delays cell division.

61 ntral to the spatial and temporal control of cell division.

62 cytoplasmic reorganization, before the first cell division.

63 regulatory step in the process of bacterial cell division.

64 uncated transmembrane proteins essential for cell division.

65 's genome in S phase and segregate it during cell division.

66 tified previously unknown modes of bacterial cell division.

67 could be attributed to apoptosis and reduced cell division.

68 ntaining bacterial cell shape and permitting cell division.

69 the assumption that germline mutations track cell divisions.

70 ome duplication during synchronous embryonic cell divisions.

71 wth, molting, and the proper pattern of seam-cell divisions.

72 cesses including cell migration and oriented cell divisions.

73 ty to change and dedifferentiate without any cell divisions.

74 somes that may contribute to asymmetric stem cell divisions.

75 aneuploidy, a possible outcome of polyploid cell divisions.

76 e asymmetries featured in self-renewing stem cell divisions.

77 al (2D) plane through a series of asymmetric cell divisions.

78 rs during mitotic rather than during meiotic cell divisions.

79 propose that SlGBP1 acts as an inhibitor of cell division, a function conserved with the human hGBP-

80 ar organelles into two daughter cells during cell division, a process known as cytokinesis.

81 is primarily driven by iterative asymmetric cell divisions (ACDs) in stomatal progenitors, which gen

82 which may underlie the drastic reduction in cell division activity in both shoot and root apical mer

83 ponents of the MRN-ATM pathway, which limits cell division after DNA damage and telomere attrition(11

84 cardiomyocyte karyokinesis, also facilitates cell division and cardiac regeneration.

85 7 did not negatively impact the synchrony of cell division and cell cycle progression during diel gro

86 IL-8 and TNFalpha, associated with abnormal cell division and cell death, respectively.

87 Here we show that defects in both cell division and cell expansion underlie the dwarfism o

88 rowth is widely accepted to be determined by cell division and cell expansion, but, unlike that in an

89 elates with the two periods of organ growth, cell division and cell expansion.

90 Because archaea share similar cell division and chemotaxis machinery with other domain

91 rimarily known for its essential activity in cell division and cortical granule exocytosis, in develo

92 r to enforce homeostatic equilibrium between cell division and death [1, 2].

93 icellular organisms requires coordination of cell division and differentiation across tissues.

94 rk, depends on the intricate balance between cell division and differentiation in specialized regions

95 roposed systemic mechanism for uncoupled SCN cell division and differentiation.

96 Root growth depends on spatially distinct cell division and elongation activities in the root meri

97 Controlled spatiotemporal cell division and expansion are responsible for floral b

98 ity to migrate, plant cells rely on targeted cell division and expansion to regenerate wounds.

99 to class II TCP genes as major regulators of cell division and floral patterning in model core eudico

100 from endogenous murein hydrolases governing cell division and from bacteriocins produced by microbia

101 Microscopic analyses of cell division and gene expression in expanding leaves, a

102 mental for myriad cellular processes such as cell division and growth.

103 ity to IP(3) could play a role in regulating cell division and homeostasis in the lens.

104 mosome segregation is essential for faithful cell division and if not maintained results in defective

105 human cholangiocarcinoma cells by inhibiting cell division and inducing apoptosis.

106 superfamily, which serves important roles in cell division and intraorganellar transport.

107 growth requires not only tight regulation of cell division and metabolism, but also concerted control

108 in utero electroporation to label and track cell division and movement within embryos and observed t

109 n-2 is essential for processes as diverse as cell division and muscle contraction.

110 growth are driven by a branching process of cell division and mutation accumulation that leads to in

111 sion on microtubules is important for proper cell division and neuronal development.

112 or a range of cellular activities, including cell division and organelle transport.

113 Cell division and organismal development are exquisitely

114 is linked to pathogenicity and regulation of cell division and PG synthesis.

115 ger signal, and consequently limits aberrant cell division and potential cellular transformation thro

116 e initiated and maintained during continuous cell division and proliferation.

117 tioning in mitotic cells, affecting oriented cell division and promoting kidney cysts in conditions o

118 ed in the synthesis of the procuticle during cell division and provide a template for further cutin d

119 ICs) are defective in maintaining asymmetric cell division and responsible for tumor recurrence.

120 microtubule network integrity and dynamics, cell division and survival, with biological response on

121 Cell divisions and cell-fate decisions require stringent

122 Considering the high number of cell divisions and delaminations taking place during emb

123 g aspects of motility, membrane trafficking, cell division, and death), but others are more unique fe

124 to vehicle control, enhanced new epithelial cell division, and increased the quality and quantity of

125 esults in decreased cell curvature, impaired cell division, and predominant formation of shorter, dou

126 erties, the protein number partitioning upon cell division, and the modeling of cell communication (j

127 They can also inhibit bacterial cell division, and trigger production of reactive oxygen

128 ity of the spindle is crucial for the proper cell division, and two centrosomes in animal cells natur

129 enable morphogenesis and motility, organize cell division, and withstand diverse environmental force

130 binary cell-fate decisions during asymmetric cell divisions, and what are the cellular mechanisms inv

131 Cell divisions are essential for tissue growth.

132 als, is important for understanding how stem cell divisions are maintained.

133 ecently discovered at many structures during cell division as a possible mechanism for properly local

134 In this role, FtsZ functions in cell division as the counterpart of the cell shape-deter

135 of Corynebacterium glutamicum SepF, the only cell division-associated protein from Actinobacteria kno

136 ssion of a growth inhibitor and promotion of cell division at primordial leaf margins.

137 nearly in time - and suggested crowding from cell division at the apical surface drives basalward mot

138 symmetrization events of normally asymmetric cell divisions at the fourth larval stage, leading to th

139 MinD is a cell division ATPase in Escherichia coli that oscillates

140 positions can be specified via orienting the cell division axis during cytokinesis.

141 en implied in specifying and reorienting the cell division axis, but how general such reorientation e

142 down-regulation of genes involved in mitotic cell division but an up-regulation of genes involved in

143 er membrane constriction is coordinated with cell division by active mobilisation-and-capture of Pal

144 nsically disordered protein (IDP), regulates cell division by causing cell cycle arrest when bound in

145 pe cyclin induced pavement cells to re-enter cell division by establishing mitotic microtubule arrays

146 ng ploidy levels and cell expansion but that cell division can substitute for endoreplication without

147 ith the integrity of the cell wall, disrupts cell division, cell separation, and impairs the fitness

148 ation of programs and processes that control cell division, cell-type specification, cell migration,

149 During embryonic cell divisions, cell size changes rapidly in both C. ele

150 It is critical in cell division, centriole biogenesis, and neuronal morpho

151 t does not require established centromere or cell division components.

152 between the intracellular calcium level and cell division, consistent with the existence of calcium

153 o APC adaptors, CDC20-homologue 1 (CDH1) and cell division cycle 20 (CDC20).

154 Here we report that cell division cycle 23 (Cdc23, also known as APC8) plays

155 nal REM (rat sarcoma exchange motif), CDC25 (cell division cycle 25), and PR (proline-rich) tail doma

156 The small GTPase cell division cycle 42 (CDC42) plays essential roles in

157 inhibition of Rac family small GTPase 1 and cell division cycle 42 activation, as well as downstream

158 1, resulting in the activation of downstream cell division cycle 42/Rac family small GTPase 1 signali

159 breast cancer cell cycle, is associated with Cell Division Cycle 6 (CDC6), Cyclin-dependent kinase 2

160 hat cell growth during the G(1) phase of the cell division cycle dilutes the cell cycle inhibitor Ret

161 Anaphase-promoting complex (APC/C) bound to Cell division cycle protein 20 (CDC20), and ends upon mi

162 ined impacts of the cht7 mutation during the cell division cycle under nutrient deficiency in light-d

163 ablish the basic mechanism of the eukaryotic cell division cycle.

164 ng transitions into and exit from a phase of cell-division cycle oscillations.

165 state stably propagates through at least 14 cell division cycles.

166 in is stably transmitted through consecutive cell division cycles.

167 sing parasites have a life cycle with unique cell-division cycles, and a repertoire of divergent CDKs

168 During eukaryotic cell division, cyclin-specific docking motifs help cycli

169 and transcriptional changes, and tracing of cell divisions demonstrates that the increased clonogeni

170 interphase cell axis, setting up the axis of cell division, despite rounding up as they enter mitosis

171 ve modular structure and are associated with cell division, development, and stress responses.

172 for fundamental cellular processes including cell division, differentiation, and motility.

173 Past studies of embryonic cell division discovered that calcium concentration incr

174 The screen uncovered novel connections to cell division, DNA replication/repair, signal transducti

175 ion and chromosome segregation errors due to cell division during development, growth, renewal, and r

176 that Dw2 modulates endomembrane function and cell division during sorghum internode growth, providing

177 Hence, this cell division-enabled leaf system predicts hypothesized

178 in a variety of cellular processes including cell division, endosomal vesicle trafficking, and viral

179 arction, resulted in increased cardiomyocyte cell division, enhanced cardiac function, and improved l

180 tional cascade that is triggered by a single cell division error-chromosome bridge formation-that rap

181 des an excellent model for understanding how cell division, expansion and differentiation are coordin

182 erly arrest growth, nuclear replication, and cell division following N deprivation.

183 nals, and initiates legume-specific cortical cell division for de novo nodule organogenesis and accom

184 During cell division, FtsK translocates double-stranded DNA unt

185 ction during cell elongation (RodA-PBP2) and cell division (FtsW-FtsI), and we are still uncovering t

186 Hippo signaling pathway is known to regulate cell division furrow position, and Hippo molecules local

187 roliferation pathways, indicating a role for cell division genes in somatic evolution in healthy skin

188 th loss of G cells, increased symmetric stem cell division, glandular fission, and more rapid stem ce

189 tress, can enter a protective state in which cell division, growth, and metabolism are down-regulated

190 of abundance of molecules of interest during cell division has been a long-standing goal of cell cycl

191 Cell division has been implicated in fate decisions in m

192 pindle MTOC inheritance patterns during stem cell division have been associated with accelerated cell

193 mechanisms through which cell growth drives cell division have remained elusive.

194 c chromosome assembly and segregation during cell divisions, however, little is known about their fun

195 nhibit differentiation but also promote stem cell division in adjacent cells.

196 Cell division in bacteria is mediated by a multiprotein

197 cs in mitosis and is required for successful cell division in confinement.

198 However, Cep55 is dispensable for cell division in embryonic or adult tissues.

199 minates, is the last to be segregated before cell division in Escherichia coli.

200 Cell division in eukaryotes requires the regulated assem

201 ect3/ect4 mutants exhibit decreased rates of cell division in leaf and vascular primordia.

202 use an additional transgenic assay to follow cell division in mouse esophagus and the epidermis at mu

203 ct of deleting OCRL on endocytic traffic and cell division in newly created human PT CRISPR/Cas9 OCRL

204 e differentially inherited during asymmetric cell division in organisms ranging from yeast to humans.

205 Here, in exploring the mechanism of cell division in S. acidocaldarius, we identify a role f

206 ate flower developmental stages by promoting cell division in the distal and ventral portion of the l

207 y that class II TCP genes also contribute to cell division in the leaf, the gynoecium and the ovules

208 nism through which a SUMO protease regulates cell division in the mat3-4 mutant of Chlamydomonas and

209 c changes during B cell differentiation with cell division in vivo.

210 migration is critical for planar-orientated cell divisions in densely packed epithelia.

211 ferred to as rhizobia, and the initiation of cell divisions in the root cortex.

212 t, WOX3/NS1 does not traffic, and stimulates cell divisions in the same cells in which it is transcri

213 aximal ASC induction requires at least eight cell divisions in vivo, with BLIMP-1 being required for

214 riggers an innate immune response and drives cell division independently of known density-dependent p

215 Tubulins play crucial roles in cell division, intracellular traffic, and cell shape.

216 The inheritance of regulators through cell division is a key deterministic force, but identify

217 ext, the use of molecular signals triggering cell division is a puzzle, because any molecule inducing

218 ed, which causes cells to grow so large that cell division is defective.

219 Chromosome segregation during cell division is driven by mitotic spindle attachment to

220 into mitotic bioenergetics and suggest that cell division is not a highly energy demanding process.

221 Cell division is often regulated by extracellular signal

222 Bacterial cell division is tightly coupled to the dynamic behavior

223 The outcome of a given cell division is unpredictable but, on average, the like

224 fection of plant cells, the control of plant cell division leading to nodule development, autoregulat

225 eins, we reconstituted part of the bacterial cell division machinery using its purified components Ft

226 chanism that does not require the FtsZ-based cell division machinery.

227 le and regulates the spatial position of the cell division machinery.

228 ing the view that co-option of components in cell division may have led to the innovation of programm

229 (and specifically terminus) segregation and cell division may result in asymmetric division in damag

230 aluation of an alternative ESCRT-independent cell division mechanism.

231 Partitioning of this local pool at each cell division modulates nuclear growth kinetics and dict

232 ng size for excessively large cells; and (2) cell division occurs as per the Adder model (division is

233 correlates with a dramatic loss of oriented cell division (OCD).

234 r LIS1 in controlling the length of terminal cell divisions of outer radial glial (oRG) progenitors,

235 o the tumors had segregated within the first cell divisions of the zygote, without being preceded by

236 urring throughout the cell cycle, coupled to cell division or birth yet independent of cell cycle pro

237 erience strenuous cellular processes such as cell division or ciliary beating while performing their

238 ked growth the fastest, whereas inactivating cell division or outer membrane protein synthesis blocke

239 -CLE and SHR converge to regulate additional cell divisions outside of the ground tissues.

240 o longer arrest but prioritize completion of cell division over repair of DNA damage.

241 cell divisions that coincide with different cell division planes and growth directions enable the de

242 When PLK4 is chemically inhibited, cell division proceeds without centrosome duplication, g

243 rther, we applied this device to control the cell division process by microgravity.

244 Cell divisions produce a steady cellular stream which ad

245 It revealed that quiescent centre cell divisions produce two identical cells, that may acq

246 apid cycles of DNA replication, mitosis, and cell division, producing up to 16 daughter cells.

247 ect upon the polymerization of the bacterial cell division protein FtsZ (a homolog of tubulin); 5) is

248 rent activating subunits, known in plants as CELL DIVISION PROTEIN20 (CDC20) and CELL CYCLE SWITCH52

249 e heterochromatin can be transmitted through cell division provided the counteracting demethylase Epe

250 tal age of the organism, irrespective of the cell division rate of different cell lineages.

251 These differences are related to the cell division rate of the studied cells and thus suggest

252 and FBF-2 activities serve to modulate stem cell division rate simultaneously with the rate of meiot

253 Furthermore, faster cell division rates should be a key factor in genetic ad

254 sidering cell number regulation that acts on cell division rates such that the number of cells in the

255 tion of other factors such as alterations in cell division rates that affect the strength of purifyin

256 Here we targeted the cell division regulator FtsZ, which resulted an elongate

257 During cell division, remodelling of the nuclear envelope enabl

258 Cell division requires the assembly and organization of

259 their specialized functions in apoptosis and cell division respectively, they appear to have retained

260 teins belonging to the resistance-nodulation-cell division (RND) superfamily play significant roles i

261 elopment, coordinated cell shape changes and cell divisions sculpt tissues.

262 cells, in which filaments circle around the cell division site(2,3).

263 dicating that SepF has multiple roles at the cell division site, involving FtsZ bundling, Z-ring teth

264 he distribution of single-cell growth rates, cell division sizes and replication initiation volumes.

265 fy numerous lncRNAs involved in key steps of cell division such as chromosome segregation, mitotic du

266 overlapping functions with co-regulators of cell division such as the cohesin subunits SMC1, SMC3, N

267 38 combination induces cell death within 1-2 cell divisions, suggesting that combined treatment could

268 n late G1 phase that underlies commitment to cell division, termed Start.

269 Meiosis is the specialized cell division that generates haploid gametes and is ther

270 is propagated during "tandem duplication," a cell division that remodels the parental cell into two d

271 Asymmetric cell divisions that coincide with different cell divisio

272 decisions that take place during asymmetric cell divisions that give rise to the sensory organs of D

273 ensively studied, how cell shape changes and cell divisions that occur concurrently in epithelia infl

274 During the initial stages of cell division, the cytoskeleton is extensively reorganiz

275 During cell division, the machinery responsible for PG synthesi

276 At cell division, the mammalian kinetochore binds many spin

277 e multiple alternative alleles in successive cell divisions, thereby generating both multiallelic and

278 which inhibits DNA replication, mitosis, and cell division; this suggests some aspect of cell prolife

279 emonstrate a method to probe and control the cell-division timing in Caenorhabditis elegans embryos u

280 Understanding the coordination of cell-division timing is one of the outstanding questions

281 ility of our genomes is essential for normal cell division, tissue homeostasis, and cellular and orga

282 bscission as a key cellular process coupling cell division to fate transitions.

283 essential for many cellular functions, from cell division to lysosome degradation and autophagy.

284 chanism that integrates gene expression with cell division to preserve cell identity.

285 mal cells the capacity to undergo periclinal cell division to repopulate the vascular stem cell pool.

286 ides can aid in diverse processes, including cell division, transcription regulation, and cell signal

287 Because it can be retained through cell divisions, transcriptional memory allows cells to c

288 ell rounding and cortical stiffening promote cell division under confined conditions that are similar

289 budding yeast mutants that were defective in cell division was reported.

290 role in conveying epigenetic memory through cell division, we report on the isolation of unfixed, na

291 A disproportionate number of germ cell divisions were observed at the DTC-Sh1 interface.

292 sis stomatal development requires asymmetric cell division, where the nucleus moves to the division s

293 lly inherited by outer daughter cells during cell division, where they stabilize the cortex to promot

294 ng of proteins in cells underlies asymmetric cell division, which is an important driver of developme

295 tRNAs' are induced upon normal and cancerous cell division, while the 'differentiation-tRNAs' are act

296 east once to become OSNs, demonstrating that cell division with amplified centrioles, known to be tol

297 s essential to couple genome duplication and cell division with the establishment and maintenance of

298 ion but also by limited numbers of symmetric cell divisions with some characteristics reminiscent of

299 hypothesis was that the cells preparing for cell division would consume more energy and metabolites

300 Investigations of plant cell division would greatly benefit from a fast, inducib