ライフサイエンスコーパス: daughter

1 ased incidence of adult breast cancer in the daughter.

2 premenopausal breast cancer incidence in the daughter.

3 ry, a mother gets inspiration from her young daughter.

4 TC and Sh1, and Sh1 grew over the Sh1-facing daughter.

5 nance or loss of basal contact by the apical daughter.

6 ng a standardized portrayal of the patient's daughter.

7 rrant Wnt target activation in anterior cell daughters.

8 actomyosin ring that cleaves a cell into two daughters.

9 tomatic cerebral arteriopathy resembling her daughters.

10 egnancy and pubertal development in sons and daughters.

11 symmetric division to produce two hair cell daughters.

12 alpha-emission dosages from (225)Ac and its daughters.

13 r cell proliferation, (3) more proliferative daughters.

14 by heating, to yield a litter of autonomous daughters.

15 the strategic interests of both parents and daughters.

16 ed cytokinesis, produces individual invasive daughters.

17 nd semen with the methylation profile of his daughters.

18 t most are cATS in differentiating stem cell daughters.

19 posed mothers produced more anxious sons and daughters.

20 s inhibited by high concentration of Ash1 in daughters.

21 ting their phenotypic effects in sons versus daughters.

22 is differential scaling causes Start in both daughter and mother cells across growth conditions.

23 boosts Ash1 accumulation in both mothers and daughters and show that Ash1 inhibits promoter recruitme

24 king site, to investigate public mentions of daughters and sons on social media.

25 te expansion leads to extrusion of veil cell daughters and squamous cells, suggesting veil cell fate

26 thers avoid reproductive conflict with their daughters, and offer increased benefits to their grandof

27 vely associated with HIV prevalence in their daughters (aOR 0.36, 0.15-0.82, per increase in level at

28 We tested the adaptive hypothesis that daughters are more responsive to cues from their mother,

29 mework for both mitosis detection and mother-daughters association in fluorescence microscopy data.

30 their terminally differentiated Paneth cell daughters at crypt bottoms.

31 X-ray absorptiometry (DXA) were measured in daughters at Tanner B4.

32 with mother compartments giving rise to two daughters at the end of each mitotic cycle.

33 nature signal-such as the observation of the daughter atom in the decay-that cannot be generated by r

34 136)Xe could be established by detecting the daughter atom, (136)Ba(2+), in its doubly ionized state(

35 ncies switch in a graded manner as stem cell daughters begin differentiation.

36 uantify age-specific reproductive success of daughters born to mothers differing in age.

37 n the favorable lower elevation environment, daughters born to older mothers also had greater age-spe

38 Contrary to prediction, daughters born to older mothers had greater annual repro

39 her elevation environment on the other hand, daughters born to older mothers tended to die before rea

40 annual reproductive success on average than daughters born to younger mothers, and this translated i

41 Simulations show that when a daughter branch is appended, the buckling resistance of

42 n actin outcrop with 8 generations of mother-daughter branching produced the linear, nonlinear, and c

43 d to assess the association between EGWG and daughters' breast composition (% of fibroglandular volum

44 in the offspring; however, its effect on the daughters' breast density is unclear.

45 RSCs generate daughters by asymmetric Notch signaling, yet RSCs remain

46 ling from the SPB that is delivered into the daughter cell (dSPB) during anaphase and the SPB that re

47 and, surprisingly, loss of viability of one daughter cell at division, suggesting specific impairmen

48 n, acting as a contractile ring to establish daughter cell boundaries.

49 that all intestinal regeneration arises from daughter cell dedifferentiation, marking the coming-of-a

50 d to chemotherapy-induced damage by altering daughter cell fates.

51 f dividing Chlamydia trachomatis cells where daughter cell formation occurs, and peptidoglycan regula

52 but the process arrests at an early stage of daughter cell growth.

53 n of CDK1-driven mitotic translation reduces daughter cell growth.

54 divisions, which are highly asymmetric: one daughter cell inherits the vacuole, the other the growin

55 Every daughter cell inherits two things from its mother: genet

56 n clearance, and the physical sealing of the daughter cell membranes.

57 mes and TR DNA to segregate virus genomes to daughter cell nuclei.

58 mitotic chromosomes to segregate genomes to daughter cell nuclei.

59 echanism, the asymmetric distribution to the daughter cell of the mRNA for a specific glucose transpo

60 observe defects in cell-cell communication, daughter cell orientation and the juxtanuclear accumulat

61 Erythroid progenitor daughter cell pairs have similar transcriptomes with or

62 Daughter cell positions can be specified via orienting t

63 o important for subsequent progenitor and/or daughter cell proliferation in the brain.

64 ransmitted through cell division such that a daughter cell recapitulates the spatial genome organizat

65 that the OPC-enriched gene, PCDH15, mediates daughter cell repulsion and facilitates proliferation.

66 t amidase activity alone is insufficient for daughter cell separation and that lytic transglycosylase

67 1 in regulating neural progenitor cell (NPC) daughter cell separation.

68 lity is tightly controlled to execute proper daughter cell separation.

69 ds of division are dynamically determined by daughter cell shape.

70 ral and spatial control to produce different daughter cell types in proper numbers and sequence.

71 n factories toward the tip of the developing daughter cell, where protein synthesis is most heavily r

72 nes are enriched towards the differentiating daughter cell.

73 leading to their inheritance by the germline daughter cell.

74 elf-renewing stem cell and a differentiating daughter cell.

75 one set of sister chromatids to each nascent daughter cell.

76 self-renewed stem cell and a differentiating daughter cell.

77 Successful separation of two daughter cells (i.e., cytokinesis) is essential for life

78 tep of mitosis that physically separates two daughter cells [1, 2].

79 herichia coli, FtsEX is required to separate daughter cells after cell division and for viability in

80 n in rDNA is highly correlated in mother and daughter cells after cell division, indicating that the

81 ants are observed at the apical membranes of daughter cells and are much more abundant in early-stage

82 ssion, the process that physically separates daughter cells and completes cell division.

83 It controls the final separation of the daughter cells and has been involved in cell fate, polar

84 ols the proliferation-quiescence decision in daughter cells and thereby couples protein production wi

85 thousands of individual pairs of mother and daughter cells and track their fates.

86 ony-a process wherein components for several daughter cells are produced within a common cytoplasm an

87 ts, which can segregate cleanly to different daughter cells at anaphase.

88 at the intercellular bridge between the two daughter cells at the end of mitosis.

89 of amoebas, fungi, and animal cells into two daughter cells at the end of the cell cycle depends on a

90 4), is selectively induced in alae-secreting daughter cells but is repressed in hypodermal daughter c

91 centrosome loss prevent the growth of unfit daughter cells by activating a pathway involving 53BP1,

92 After mitosis, fate-committed daughter cells delaminate from this germinative zone.

93 The developmental asymmetry of fission yeast daughter cells derives from inheriting 'older Watson' ve

94 he genome has partitioned between mother and daughter cells during anaphase.

95 chinery for the transmission of propagons to daughter cells during cell division and cytoplasmic tran

96 the duplicated cellular organelles into two daughter cells during cell division, a process known as

97 ins become asymmetrically inherited by outer daughter cells during cell division, where they stabiliz

98 idases that participate in the separation of daughter cells during cell division.

99 Force plays a central role in separating daughter cells during cytokinesis, the last stage of cel

100 n of the chromosomal content between the two daughter cells during division.

101 accurate segregation of genetic material to daughter cells during mitosis depends on the precise coo

102 omolecules (such as RNAs and proteins) among daughter cells during the division of a cancer cell.

103 ount for the cell shape and demonstrate that daughter cells emerging from wave-mediated cytofission e

104 After mitosis, the majority of daughter cells extend a long, basally oriented filopodia

105 cient segregation of the viral genome to the daughter cells following cell division.

106 ead, DNA lesions segregate, unrepaired, into daughter cells for multiple cell generations, resulting

107 ir integrity and are inherited by developing daughter cells in a She2p/She3p-dependent manner.

108 i of cells; partitioning the viral genome to daughter cells in dividing cells; avoiding recognition b

109 oning duplicated chromosomes equally between daughter cells is a microtubule-mediated process essenti

110 HO expression in daughter cells is inhibited by high concentration of Ash

111 Because of this movement, daughter cells may be born displaced from the tissue lay

112 To examine in detail differences between the daughter cells of a proliferative division of procyclic

113 of cells that divide asymmetrically to give daughter cells of different size and fate.

114 body remnants are more often retained on the daughter cells of early proliferative divisions.

115 During brain development, the daughter cells of neural stem cells have to make a choic

116 romatin-bridge formation, and micronuclei in daughter cells of proband skin fibroblasts.

117 is, which enables the physical separation of daughter cells once mitosis has been completed, is execu

118 Spindles polarized, pairs of daughter cells oriented between the DTC and Sh1, and Sh1

119 Daughter cells received equal shares of preinitiation fa

120 anscriptional memory and reactivation in the daughter cells remain unclear.

121 es phenotypic differences between mother and daughter cells similar to other pathogenic yeasts.

122 hydrolyse crosslinked peptidoglycan between daughter cells so that they can separate(7).

123 ing that there may be glycan bridges between daughter cells that cannot be resolved by amidases.

124 s in a short pulse of ERK inactivity in both daughter cells that correlates with elevated endpoint NA

125 ments divide asymmetrically, producing short daughter cells that tend to be devoid of damage and have

126 ofound loss of division symmetry, generating daughter cells that vary widely in size and eventually g

127 nformation is segregated reliably to the two daughter cells through cell division.

128 ic information is transmitted from mother to daughter cells through mitosis.

129 y, the PPARgamma-homologue Eip75B drives ISC daughter cells towards absorptive enterocyte lineage ens

130 se, when sister chromatids must transit into daughter cells uninterrupted.

131 complete separation and isolation of the two daughter cells via abscission.

132 Stem cells produced daughter cells with an extraordinarily high rate of turn

133 site where they build the partition between daughter cells(2-4).

134 h of the septum to form the new poles of the daughter cells(4).

135 region compromised segregation of TR DNA to daughter cells, as assessed by retention of green fluore

136 the region reduced segregation of TR DNA to daughter cells, but not episome maintenance.

137 heir accurate segregation and propagation to daughter cells, but the mechanisms ensuring coordination

138 cell in two identical halves can be used in daughter cells, irrespective of its orientation in relat

139 he cell cycle before symmetric division into daughter cells, leading to polyploidy and multinucleatio

140 l as 'hyper-proliferation' of progenitor and daughter cells, promoted by PRC2-mediated repression of

141 to the production of properly sized, viable daughter cells, the mechanisms underlying division site

142 remodeling, especially during separation of daughter cells, which depends heavily upon the activity

143 cell divisions and generate a core of small daughter cells, which is a prerequisite for lateral root

144 ly, proliferative cell divisions produce two daughter cells, which look similar but are not identical

145 compact, as required for clean separation to daughter cells, while maintaining close parallel alignme

146 Cytokinesis-the division of a cell into two daughter cells-is a key step in cell growth and prolifer

147 tosis, and cell division, producing up to 16 daughter cells.

148 s manner, LytN facilitates the separation of daughter cells.

149 d the accurate segregation of chromosomes to daughter cells.

150 te and eventually pinch off to form separate daughter cells.

151 arental chromosomes into a single nucleus in daughter cells.

152 rrow ingression and led to frequent lysis of daughter cells.

153 ansient protein structure connecting the two daughter cells.

154 mmetry and differential cell fate of the two daughter cells.

155 some unlinking and faithful segregation into daughter cells.

156 r released or rapidly degraded by one of the daughter cells.

157 differentiated, effector-molecule-expressing daughter cells.

158 ought to be formed de novo in the developing daughter cells.

159 itioning of cellular components into the two daughter cells.

160 ithful segregation of the genome between two daughter cells.

161 sis, with GSCs failing to abscise from their daughter cells.

162 chromosome distribution into the two forming daughter cells.

163 and accurate segregation of chromosomes into daughter cells.

164 ansmission of altered genetic information to daughter cells.

165 Geminin family members modulate the fate of daughter cells.

166 cess, producing two morphologically distinct daughter cells.

167 g to the retention of seam cell fate in both daughter cells.

168 tin at the intercellular bridges between GSC-daughter cells.

169 mulation and asymmetric partitioning between daughter cells.

170 viral genomes to hitchhike or piggyback into daughter cells.

171 enome and divide the duplicated DNA into two daughter cells.

172 process of equal chromosome segregation into daughter cells.

173 ependent segregation of mitochondria between daughter cells.

174 e elongation and position chromosomes within daughter cells.

175 gate the origin of replication region to new daughter cells.

176 aughter cells but is repressed in hypodermal daughter cells.

177 hfully passed on through many generations of daughter cells.

178 actile ring drives the separation of the two daughter cells.

179 s, localize to puncta and associate with the daughter cells.

180 ce that contributes to PM ingression between daughter cells.

181 ced state in the mother cell is inherited in daughter cells.

182 rpC redistributes to the growing edge of the daughter cells.

183 ion that remodels the parental cell into two daughter cells.

184 torial furrowing and separation into the two daughter cells.

185 inant control mechanism for S phase entry of daughter cells.

186 ation is passed on to the next generation of daughter cells.

187 nt must also be properly distributed between daughter cells.

188 re and faithfully segregate chromosomes into daughter cells.

189 is leading to the physical separation of the daughter cells.

190 to ensure the correct separation of the two daughter cells.

191 of sister chromatids to each of the nascent daughter cells.

192 ectives, or they develop clonally via mother-daughter cellular adhesion.

193 apid loss of centrosomes due to a failure in daughter centriole duplication, suggesting that Alms1a h

194 substrate Centrobin (Cnb) accumulate on the daughter centriole during mitosis, thereby generating mo

195 olo-mediated phosphorylation, whereas Polo's daughter centriole enrichment requires both Wdr62 and Cn

196 lation of Ana2 at the procentriole to induce daughter centriole formation.

197 ase 4 (Plk4) and initiates in S-phase when a daughter centriole grows from the side of a pre-existing

198 The daughter centriole invariably migrated ahead of the MC f

199 ls, contain an older "mother" and a younger "daughter" centriole.

200 Stem cells either inherit the mother or daughter-centriole-containing centrosome, providing a po

201 y generating molecularly distinct mother and daughter centrioles before interphase.

202 stem cell selectively inherits the mother or daughter centrosome.

203 how asymmetric behavior of the mother versus daughter centrosomes, whereby the self-renewing stem cel

204 on, indicating distinct states of mother and daughter centrosomes.

205 4 tetramers are randomly distributed between daughter chromatids during DNA replication, rare occurre

206 A supercoiling, which may intertwine (braid) daughter chromatin fibers to form precatenanes, posing t

207 l demonstrated that (134)Ce (and its (134)La daughter) could be used as a PET imaging candidate for (

208 usions, (3) three-phase inclusions with NaCl daughter crystals, and (4) CO(2)-aqueous inclusions.

209 In multivariable analysis, daughter-daughter angle was directly, and parent artery

210 During 403,786 years of follow-up, 865 daughters developed incident cases of invasive breast ca

211 As GSC daughters differentiate into nurse cells and oocytes, nu

212 The daughter DNA duplexes are packaged with an equal amount

213 om entry of parental DNA into CMG to exit of daughter DNA from PCNA.

214 ed aneurysm wall irregularity, presence of a daughter dome, presence of hypoplastic or aplastic A1 ar

215 osity and low surface tension induce a small daughter droplet encapsulated by a larger air shell bubb

216 eparating the cleaved fragments in different daughter droplets on the basis of their net charge.

217 sed by dipole-dipole coalescence between the daughter droplets.

218 ng in the generation of biomolecule-enriched daughter droplets.

219 inlet of the Hele-Shaw channel from unfused daughter droplets.

220 d and used as templates for the synthesis of daughter duplexes with identical sequences.

221 Among 30,921 mother-daughter dyads from the Nurses' Mothers' Cohort (2001) a

222 We used data from 35,133 mother-daughter dyads of the Nurses' Health Study (NHS) II and

223 y increase the reproductive success of their daughters even after they are nutritionally independent

224 osity of Z chromosome blocks was produced by daughter-father backcrosses, and inferred from marker lo

225 g barbed end growth, CP favors nucleation of daughter filaments at the functionalized surface where t

226 amage to manifest as 53BP1 nuclear bodies in daughter G(1) cells leading to G(1) arrest, whereas WEE1

227 S phase entry is mitogen-independent in the daughter G1 phase, but remains sensitive to DNA damage,

228 e the parent gene (RNASE1) is conserved, the daughter gene (RNASE1B) has multiple amino acid substitu

229 or cell in the zebrafish's lateral line, the daughter hair cells differentiate with opposite mechanic

230 s assembly and stability, especially for the daughter half, by regulating filament pairing and the fu

231 ndle establishment or positions of HCs since daughter HCs are known to switch positions with each oth

232 of zebrafish neuromasts divides to form two daughter HCs of opposite hair bundle orientations.

233 on factor Emx2, expressed in only one of the daughter HCs, generates this bidirectional HC pattern (J

234 hannels continued to grow unperturbed, but a daughter hypha gradually branched into the opening and f

235 le system, followed by the formation of two "daughter" hyphae growing in opposite directions along th

236 en the two daughters, with the new-flagellum daughter in particular re-modelling rapidly and extensiv

237 h men and women mention sons more often than daughters in their posts.

238 ulations may be violated (e.g. more than two daughter lineages may coalesce to a parent at low popula

239 In daughters, maternal smoking was associated with earlier

240 r H(2) through precipitation of Fe(III)-rich daughter minerals results in conditions that are conduci

241 The impact of fullerene C(60) water soluble daughter molecules - fullerols C(60)(OH)(24) nanoparticl

242 15 s, followed by nucleation 16 s later of a daughter MT at a 36 degrees branch angle.

243 enitor cells from the normal delamination of daughter neuroblasts in the developing mouse neocortex.

244 downregulation is necessary for delaminated daughter neuroblasts to escape from anoikis.

245 ng acentric chromosome fragments that rejoin daughter nuclei are associated with nuclear membrane but

246 to a contractile ring positioned between the daughter nuclei by different mechanisms in fungi and ani

247 arks and localize to the cytoplasm following daughter nuclei formation and cytokinesis where they for

248 owing late-segregating chromosomes to rejoin daughter nuclei remain underexplored.

249 hin the narrow bridge that links segregating daughter nuclei.

250 ir nuclear envelope to produce two identical daughter nuclei.

251 zone to prevent the leakage of material from daughter nuclei.

252 e re-established at the nuclear periphery in daughter nuclei.

253 altered metaphase progression and ploidy of daughter nuclei.

254 deform it, which results in fission into two daughter nuclei.

255 or Ace2, which localizes specifically to the daughter nucleus, where it drives a daughter-specific tr

256 nderthal fossils-as well as Denisova 11, the daughter of a Neanderthal and a Denisovan(4)-date to bet

257 This work demonstrates that the two daughters of a proliferative division of T. brucei are n

258 Daughters of women who had EGWG had higher levels of AFG

259 their large size did not propagate to their daughter packs.

260 are recycled from the mother to the forming daughter parasites using a highly dynamic F-actin networ

261 ferring membrane to the megakaryocyte and to daughter platelets.

262 e peptidoglycan (PG) cell wall that caps the daughter poles and prevents osmotic lysis of the newborn

263 After separating the daughter products into nine fractions (MA1-MA9) accordin

264 , it provides the first understanding on the daughter products of bioelectrochemical hydrocarbon degr

265 e early Solar System are known because their daughter products were preserved in high-temperature con

266 he immobilization of uranium and some of its daughter products, significantly improves in response to

267 sport of aqueous uranium and radioactive its daughter products, were observed on activated carbons im

268 Between 2012 and 2017, sons and daughters provided information on a wide range of pubert

269 ) strain isolated prior to treatment and the daughter (resistant) strain obtained from the same patie

270 eir pregnancy with the nurse and their nurse daughter's early life experience.

271 1), the following information was collected: daughter's television viewing time and physical activity

272 ent of "hippo" signaling that induces mother-daughter separation.

273 c cell divisions, a key concept is utilizing daughters' similarity.

274 on pressures maintain the morphs in multiple daughter species?

275 y to the daughter nucleus, where it drives a daughter-specific transcriptional network.

276 odifications must be faithfully passed on to daughter strands.

277 al profiles in their offspring, and sons and daughters strongly differed in the ways in which their b

278 f methylomes within patrilines (i.e., father-daughter subfamilies) than between patrilines in each co

279 p = 1.0) but were more likely to inform the daughter that her father was sick enough to die (68% vs

280 ficient parasites develop inviable conjoined daughters that contain components for multiple cells.

281 balance self-renewal with the production of daughters that leave the niche to differentiate.

282 re we were, celebrating with her now-married daughters, their husbands, and three beautiful grandchil

283 can transfer epigenetic information to their daughters through DNA methylation.

284 wing the new-flagellum and the old-flagellum daughters to be distinguished.

285 father (i.e. predator-exposed F0 males to F1 daughters to F2s), a predator-exposed paternal grandfath

286 parents and daughters, with parents coercing daughters to marry early for the parents' economic benef

287 lemental compositions in O(2) species, where daughter transformation products doubled relative to par

288 Daughters typically remained attached throughout their ~

289 The old-flagellum daughter undergoes a different G1 re-modelling, however,

290 ast cells confer a growth advantage to their daughters using a novel mechanism, the asymmetric distri

291 should initially reduce genetic variation in daughter versus parental species, a common pattern is th

292 ameters and angles of surrounding parent and daughter vessels.

293 ameters and angles of surrounding parent and daughter vessels.

294 The daughters were heterozygous and the mother was a somatic

295 ffspring, females that weaned more sons than daughters when aged between 2 and 7 y experienced faster

296 trains with P-elements cause severe GD in F1 daughters when Har fathers mate with mothers lacking P-e

297 a conflict of interests between parents and daughters, with parents coercing daughters to marry earl

298 ct morphological differences between the two daughters, with the new-flagellum daughter in particular

299 -specific patterns (e.g. by pooling sons and daughters) would have underestimated the magnitude of pa

300 cellularization, to create and release many daughter 'zoospores'.