ライフサイエンスコーパス: division

1 olved in transcription, DNA repair, and cell division.

2 ce of genes involved in bacterial growth and division.

3 n of enzymes involved in cell elongation and division.

4 curate alignment and segregation during cell division.

5 e segregation, and it ultimately delays cell division.

6 standing the coordination of cell growth and division.

7 to the spatial and temporal control of cell division.

8 lasmic reorganization, before the first cell division.

9 r to progression to metaphase and subsequent division.

10 latory step in the process of bacterial cell division.

11 ed transmembrane proteins essential for cell division.

12 nome in S phase and segregate it during cell division.

13 d previously unknown modes of bacterial cell division.

14 ication and segregation with cell growth and division.

15 be attributed to apoptosis and reduced cell division.

16 ing bacterial cell shape and permitting cell division.

17 is regulated by a balance between fusion and division.

18 iably to the two daughter cells through cell division.

19 e role of Nek8445 in regulating Giardia cell division.

20 for protein import, peroxisomal growth, and division.

21 egulated in order to support cell growth and division.

22 ylation, is stably propagated during mitotic division.

23 that are asymmetrically retained during cell division.

24 rate (Ser) function redundantly in the third division.

25 the bacteria, in particular to assist their division.

26 estrating chromosome segregation during cell division.

27 3 (ARC3), a crucial regulator of chloroplast division.

28 nregulated were critical for cell growth and division.

29 by favouring symmetric over asymmetric cell division.

30 targeted to growing cell plates during cell division.

31 n synthase relocation to midcell during cell division.

32 genome to the daughter cells following cell division.

33 bled at the future division site during cell division.

34 through asymmetric segregation during active division.

35 lobus cells undergo a robust and symmetrical division.

36 simultaneously imaging the cells to measure division.

37 more biomass than larger cells prior to cell division.

38 d space and could play similar roles in cell division.

39 n activating some of the key players in cell division.

40 spindle, which then guides the axis of cell division.

41 ptal PG synthesis and regulation during cell division.

42 chromosome segregation at the first meiotic division.

43 cal adhesion formation and turnover and cell division.

44 tion theory and the structural model of cell division.

45 hey were detected at the midbody during cell division.

46 to control the metabolism, growth, and cell division.

47 tone to bacterial cell wall biosynthesis and division.

48 ocytes progressing through the first meiotic division.

49 fe including cell development, movement, and division.

50 y macrophages and were sites of ongoing cell division.

51 separates daughter cells and completes cell division.

52 nerating two distinct cells through one cell division.

53 synthesis in ovococcal bacteria during cell division.

54 l that undergoes predominant asymmetric cell division.

55 ntrations of key metabolites needed for cell division.

56 factors are operating in the context of cell division.

57 mmetries featured in self-renewing stem cell divisions.

58 neurogenic progenitors arise from asymmetric divisions.

59 D) plane through a series of asymmetric cell divisions.

60 ring mitotic rather than during meiotic cell divisions.

61 -wide whose fluctuations persist for several divisions.

62 ssumption that germline mutations track cell divisions.

63 enishment divisions and consuming neurogenic divisions.

64 with planar-oriented symmetric self-renewal divisions.

65 uplication during synchronous embryonic cell divisions.

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

67 Notch signaling between the second and third divisions.

68 memory in individual cells through multiple divisions.

69 s that are distinct from cell elongation and division?

70 was highest in the East South Central Census Division (14.8 per 1000).

71 in optical-frequency synthesis(4), frequency division(5) and optical clocks(6).

72 ose that SlGBP1 acts as an inhibitor of cell division, a function conserved with the human hGBP-1 pro

73 e layered diagrammatic representation of CNS divisions, according to their arrangement in correspondi

74 h may underlie the drastic reduction in cell division activity in both shoot and root apical meristem

75 transcriptional programs that can drive the division and (trans-)differentiation of non-beta cells t

76 omyocyte karyokinesis, also facilitates cell division and cardiac regeneration.

77 not negatively impact the synchrony of cell division and cell cycle progression during diel growth.

78 Here we show that defects in both cell division and cell expansion underlie the dwarfism of an

79 s with the two periods of organ growth, cell division and cell expansion.

80 ily known for its essential activity in cell division and cortical granule exocytosis, in development

81 ed systemic mechanism for uncoupled SCN cell division and differentiation.

82 of a "transition zone" boundary between the division and elongation zones is critical for efficient

83 o migrate, plant cells rely on targeted cell division and expansion to regenerate wounds.

84 r Cdc42-dependent activity on HSC asymmetric division and fate.

85 utants in the tol-pal locus fail to complete division and form cell chains.

86 Microscopic analyses of cell division and gene expression in expanding leaves, and re

87 l for myriad cellular processes such as cell division and growth.

88 e segregation is essential for faithful cell division and if not maintained results in defective cell

89 family, which serves important roles in cell division and intraorganellar transport.

90 lved in diverse cellular processes including division and membrane remodeling.

91 h requires not only tight regulation of cell division and metabolism, but also concerted control of t

92 Here, we investigated the origin, division and migration patterns of the adult-born neural

93 to perform basic cellular functions such as division and motility.

94 s essential for processes as diverse as cell division and muscle contraction.

95 range of cellular activities, including cell division and organelle transport.

96 Cell division and organismal development are exquisitely orch

97 ignal, and consequently limits aberrant cell division and potential cellular transformation through a

98 the synthesis of the procuticle during cell division and provide a template for further cutin deposi

99 are defective in maintaining asymmetric cell division and responsible for tumor recurrence.

100 r model established the timing of QC and CEI division and suggests that SHR repression of QC division

101 otubule network integrity and dynamics, cell division and survival, with biological response on the t

102 ar decoupling of proliferative replenishment divisions and consuming neurogenic divisions.

103 sary and sufficient to activate SHR-mediated divisions and CYCD6;1 expression.

104 signaling pathway regulating formative root divisions and provides a framework to explore this pathw

105 sses, including PG turnover, cell elongation/division, and antibiotic resistance.

106 ects of motility, membrane trafficking, cell division, and death), but others are more unique feature

107 ociated with compartments - collocalization, division, and merging - which are commonly thought to pl

108 s, the protein number partitioning upon cell division, and the modeling of cell communication (juxtac

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

110 f the spindle is crucial for the proper cell division, and two centrosomes in animal cells naturally

111 sms driving the final steps of mitochondrial division are still unclear.

112 Group divisions are a continual feature of human history, with

113 At caudal levels, the divisions are more laminated in appearance.

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

115 y in time - and suggested crowding from cell division at the apical surface drives basalward motion.

116 trization events of normally asymmetric cell divisions at the fourth larval stage, leading to the ret

117 e. induction of cell death and inhibition of division, at a single-cell level are used as metrics to

118 MinD is a cell division ATPase in Escherichia coli that oscillates from

119 plied in specifying and reorienting the cell division axis, but how general such reorientation events

120 eems to contribute both to PG elongation and division biosynthetic complexes based on its localizatio

121 regulation of genes involved in mitotic cell division but an up-regulation of genes involved in apopt

122 ing protein 3 (PBP3/FtsI) initiate polarized division, but the process arrests at an early stage of d

123 mbrane constriction is coordinated with cell division by active mobilisation-and-capture of Pal at di

124 clin induced pavement cells to re-enter cell division by establishing mitotic microtubule arrays.

125 tubules formed by Drp1 promote mitochondrial division by facilitating ER-mitochondria interactions.

126 The number of divisions carried out depends on the initial size of the

127 ebral bridge (PB), the upper (CBU) and lower division (CBL) of the central body and a pair of globula

128 he integrity of the cell wall, disrupts cell division, cell separation, and impairs the fitness of th

129 Compared with the third division, cell-fate decision in the second division requ

130 During embryonic cell divisions, cell size changes rapidly in both C. elegans

131 ggest that CDKA1 may promote a switch into a division-competent state, and E2F/Dp1 may promote mainte

132 s not require established centromere or cell division components.

133 coextensive model has been proposed in which division-coupled conversion of NSCs into differentiated

134 adaptors, CDC20-homologue 1 (CDH1) and cell division cycle 20 (CDC20).

135 bition of Rac family small GTPase 1 and cell division cycle 42 activation, as well as downstream intr

136 t cancer cell cycle, is associated with Cell Division Cycle 6 (CDC6), Cyclin-dependent kinase 2 (CDK2

137 lization of the cytosol for both the nuclear division cycle and branching.

138 hase-promoting complex (APC/C) bound to Cell division cycle protein 20 (CDC20), and ends upon mitotic

139 impacts of the cht7 mutation during the cell division cycle under nutrient deficiency in light-dark s

140 ersistence is characterized by a halt in the division cycle, aberrant morphology, and, in the case of

141 h the basic mechanism of the eukaryotic cell division cycle.

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

143 During eukaryotic cell division, cyclin-specific docking motifs help cyclin-dep

144 ision and suggests that SHR repression of QC division depends on formation of the SHR homodimer.

145 ability of cells to properly reorient their divisions depends on local tissue tension.

146 dular structure and are associated with cell division, development, and stress responses.

147 Past studies of embryonic cell division discovered that calcium concentration increases

148 Dw2 modulates endomembrane function and cell division during sorghum internode growth, providing insi

149 eprivation and by the occurrence of abortive divisions during N refeeding.

150 ates CYCLIND6;1 (CYCD6;1) to drive formative divisions during root ground tissue development.

151 LIMP-1 being required for differentiation at division eight.

152 variety of cellular processes including cell division, endosomal vesicle trafficking, and viral buddi

153 on, resulted in increased cardiomyocyte cell division, enhanced cardiac function, and improved long-t

154 ptions are thought to originate from meiotic division errors in the female germline, quantitative stu

155 During division, eukaryotic cells undergo a dramatic, complex a

156 n excellent model for understanding how cell division, expansion and differentiation are coordinated

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

158 ive G-protein eliminated the increase in GSC division frequency in mated males.

159 a role for the G-proteins in regulating GSC division frequency, RNA-i against seven out of 35 G-prot

160 During cell division, FtsK translocates double-stranded DNA until bo

161 during cell elongation (RodA-PBP2) and cell division (FtsW-FtsI), and we are still uncovering the im

162 eration pathways, indicating a role for cell division genes in somatic evolution in healthy skin.

163 e MTOC inheritance patterns during stem cell division have been associated with accelerated cellular

164 Rotatory actomyosin flows during division have been implied in specifying and reorienting

165 Thus, distinct modes of NPC division have divergent requirements for Ino80-dependent

166 t differentiation but also promote stem cell division in adjacent cells.

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

168 es, is the last to be segregated before cell division in Escherichia coli.

169 Cell division in eukaryotes requires the regulated assembly o

170 ction with septation is critical to faithful division in Gram-negative bacteria and vital to the barr

171 ect4 mutants exhibit decreased rates of cell division in leaf and vascular primordia.

172 deleting OCRL on endocytic traffic and cell division in newly created human PT CRISPR/Cas9 OCRL knoc

173 ferentially inherited during asymmetric cell division in organisms ranging from yeast to humans.

174 uard, that adjusts the balance of fusion and division in response to increased mitochondrial connecti

175 Here, in exploring the mechanism of cell division in S. acidocaldarius, we identify a role for th

176 lower developmental stages by promoting cell division in the distal and ventral portion of the limb.

177 t class II TCP genes also contribute to cell division in the leaf, the gynoecium and the ovules in A.

178 ation is critical for planar-orientated cell divisions in densely packed epithelia.

179 d to as rhizobia, and the initiation of cell divisions in the root cortex.

180 X3/NS1 does not traffic, and stimulates cell divisions in the same cells in which it is transcribed.

181 l ASC induction requires at least eight cell divisions in vivo, with BLIMP-1 being required for diffe

182 rs an innate immune response and drives cell division independently of known density-dependent prolif

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

184 Mitochondrial division involves Dynamin-related protein-1 (Drp1) oligo

185 The inheritance of regulators through cell division is a key deterministic force, but identifying i

186 hich causes cells to grow so large that cell division is defective.

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

188 Bacterial cell division is tightly coupled to the dynamic behavior of F

189 cell division occurs as per the Adder model (division is triggered upon adding a fixed size from birt

190 homologous chromosomes at the first meiotic division is usually ensured by crossing over.

191 This division is, at least in part, the result of historical

192 on of plant cells, the control of plant cell division leading to nodule development, autoregulation o

193 BC1D15-NuMA1 association impaired asymmetric division machinery by hijacking NuMA from LGN binding, t

194 we reconstituted part of the bacterial cell division machinery using its purified components FtsZ, F

195 d regulates the spatial position of the cell division machinery.

196 sm that does not require the FtsZ-based cell division machinery.

197 Brady Jr." from the "Psychotic Disorders Division, McLean Hospital, Harvard Medical School, Belmo

198 ms to probe the growth, chromosome cycle and division mechanism of Bacillus subtilis L-forms.

199 ere, we report a dual-comb Vernier frequency division method to vastly reduce the required electrical

200 The pre- and post-division migrations are dependent on microtubules and ac

201 Partitioning of this local pool at each cell division modulates nuclear growth kinetics and dictates

202 25 bps) prototype and an 8-channel frequency-division multiplexed (0.5 m x 1,000 bps) prototype are d

203 ze for excessively large cells; and (2) cell division occurs as per the Adder model (division is trig

204 Cytokinesis-the division of a cell into two daughter cells-is a key step

205 ighlight areas of improvement within our own Division of Critical Care Medicine.

206 we sought to systematically characterize the division of labor between YAP and TAZ in non-small cell

207 e implications for both fork restart and the division of labor during leading-strand synthesis genera

208 Together, these results reveal a division of labor in which dissociable neural systems su

209 ms with different DNA binding domains show a division of labor on male aggressive behaviors.

210 w-celled haploid structure that orchestrates division of labor to coordinate successful interaction w

211 ganization, cells in each state exhibit true division of labor, providing growth/survival advantages

212 This has now been corrected to: "Division of Life Sciences, State Key Laboratory of Molec

213 present an updated freshwater biogeographic division of mainland Southeast Asia and describe 12 spec

214 ame available due to closure of the research division of our medical center.

215 distinction is reflected in a medial-lateral division of prefrontal cortex - with lateral frontal pol

216 In vitro, division of primary fibroblasts occurs without Cep55 and

217 D-19 first wave for the 9 departments in the Division of Surgery at The University of Texas MD Anders

218 ivision of the central body (CBU), the lower division of the central body (CBL), and the paired nodul

219 ses the protocerebral bridge (PB), the upper division of the central body (CBU), the lower division o

220 Unexpectedly, division of the large Chlamydomonas chloroplast was dela

221 ange more, and the typical structure shows a division of the society in upper and lower classes.

222 encoding of predator fear in the dorsomedial division of the ventromedial hypothalamus (VMHdm) and th

223 eadfins (Percomorphacea: Polynemidae) is the division of their pectoral fin into an upper, unmodified

224 ) by simultaneously measuring metabolism and division of thousands of individual Saccharomyces cerevi

225 gic therapy and regularly followed up at the divisions of dermatology of several main hospitals in th

226 1 in controlling the length of terminal cell divisions of outer radial glial (oRG) progenitors, sugge

227 tivity is required for supernumerous mitotic divisions of the mat3-4 cells.

228 idence for altered activity within the major divisions of the prefrontal cortex, including orbitofron

229 le-cell measurements of bacterial growth and division often relied on testing preconceived models of

230 edict: chronological age, mortality, mitotic divisions, or telomere length.

231 sterior to anterior, dictates the pattern of divisions over the FSC domain, promotes more posterior F

232 ng changes in anisotropic cell expansion and division patterns [3-5].

233 e tracks and show spatio-temporally flexible division patterns.

234 stent with their distinct roles in polarized division, peptidoglycan organization is different in cel

235 s cellular states permissive for the meiotic division phase.

236 Because the division plane is largely set by the position of the ana

237 m concentration increases transiently at the division plane just before cleavage furrow ingression, s

238 initial cell and the angle of the transition division plane, which sufficiently distinguished a gamet

239 s orientation in relation to the penultimate division plane.

240 divisions that coincide with different cell division planes and growth directions enable the develop

241 When PLK4 is chemically inhibited, cell division proceeds without centrosome duplication, genera

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

243 It revealed that quiescent centre cell divisions produce two identical cells, that may acquire

244 pon the polymerization of the bacterial cell division protein FtsZ (a homolog of tubulin); 5) is comp

245 ts have implicated a conserved subcomplex of division proteins composed of FtsQ, FtsL, and FtsB (FtsQ

246 erochromatin can be transmitted through cell division provided the counteracting demethylase Epe1 is

247 aried by hospital referral region and Census Division (range: 18.6% [East South Central] to 39.1% [We

248 suggests that a 10% change in phytoplankton division rate may be associated with a 50% reduction in

249 These differences are related to the cell division rate of the studied cells and thus suggest an i

250 nmental properties controlling phytoplankton division rates (e.g., nutrients and light), as they omit

251 wound-induced cell expansion and restorative division rates in a dose-dependent manner, leading to tu

252 Furthermore, faster cell division rates should be a key factor in genetic adaptat

253 ing cell number regulation that acts on cell division rates such that the number of cells in the tiss

254 ccurring during periods of declining modeled division rates, an observation that highlights the impor

255 s in the seasonal magnitude of phytoplankton division rates.

256 d division, cell-fate decision in the second division requires a lower level of Suppressor of Hairles

257 Cell division requires the assembly and organization of a mic

258 stems belonging to the resistance-nodulation-division (RND) superfamily are ubiquitous in Gram-negati

259 by efflux pumps of the Resistance-Nodulation-Division (RND) superfamily of proteins creating an effic

260 by active mobilisation-and-capture of Pal at division septa by the Tol system.

261 a highly ordered hourglass structure at the division site [13] is largely unexplored.

262 ell division, where the nucleus moves to the division site based on cellular polarity cues.

263 e structure (Z-ring) assembled at the future division site during cell division.

264 rly spaced "nodes" of TP activity around the division site of predivisional cells.

265 al and have higher levels of Rho1-GTP at the division site than wild-type cells.

266 s, in which filaments circle around the cell division site(2,3).

267 a moving zone of signalling activity at the division site.

268 lapping functions with co-regulators of cell division such as the cohesin subunits SMC1, SMC3, NIPBL

269 PARC6), another key regulator of chloroplast division, suggesting a role of OR(His) in competing with

270 e G1 phase that underlies commitment to cell division, termed Start.

271 opagated during "tandem duplication," a cell division that remodels the parental cell into two daught

272 Asymmetric cell divisions that coincide with different cell division pla

273 ely studied, how cell shape changes and cell divisions that occur concurrently in epithelia influence

274 During cell division, the machinery responsible for PG synthesis loc

275 During mitochondrial division, the mechano-guanosine triphosphatase (GTPase)

276 lls, we found that cell growth is coupled to division through a sizer operating largely in the G1 pha

277 regulation of SHR transcription modulate the division timing of two different specialized cell types

278 sion as a key cellular process coupling cell division to fate transitions.

279 ntial for many cellular functions, from cell division to lysosome degradation and autophagy.

280 ells the capacity to undergo periclinal cell division to repopulate the vascular stem cell pool.

281 hat human OPCs undergo consecutive symmetric divisions to exponentially increase the progenitor pool

282 (NSCs) from proliferative to differentiative divisions to generate neurons.

283 can aid in diverse processes, including cell division, transcription regulation, and cell signaling.

284 ounding and cortical stiffening promote cell division under confined conditions that are similar to t

285 n caudate nucleus and putamen-a striatal sub-division unique to primates-with both dopamine and serot

286 The ventral division (vLGN) connects subcortically, sending inhibito

287 Additional divisions were made based on HER2 status, PR status, cT

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

289 ith MDH, tested and confirmed at our allergy division, were retrospectively evaluated in terms of cli

290 tomatal development requires asymmetric cell division, where the nucleus moves to the division site b

291 nherited by outer daughter cells during cell division, where they stabilize the cortex to promote api

292 proteins in cells underlies asymmetric cell division, which is an important driver of development an

293 in 2 (PBP2) are unable to initiate polarized division, while cells treated with inhibitors that preve

294 ' are induced upon normal and cancerous cell division, while the 'differentiation-tRNAs' are active i

295 me individuals consistently respond to group divisions, while others do not.

296 ential to couple genome duplication and cell division with the establishment and maintenance of cellu

297 ting a fixed fate imbalance of self-renewing divisions with an ever-decreasing proliferation rate.

298 ut also by limited numbers of symmetric cell divisions with some characteristics reminiscent of inter

299 increased the proportion of planar-oriented divisions, without effecting SC viability, fibronectin d

300 thesis was that the cells preparing for cell division would consume more energy and metabolites as bu

301 Investigations of plant cell division would greatly benefit from a fast, inducible sy