ライフサイエンスコーパス: progeny

1 e percentage of haploid progeny versus total progeny).

2 ty to self-renew and produce differentiating progeny.

3 t stem cells (PSCs) and their differentiated progeny.

4 eproduction and creates genetic variation in progeny.

5 rstitial cells, including neuronal cells and progeny.

6 maphrodites and males yield exclusively male progeny.

7 oxins affects physiological responses of the progeny.

8 compared the phenotype of animals of the F2 progeny.

9 ng occurring in their post-mitotic migratory progeny.

10 rbon metabolism during gestation has on mice progeny.

11 for subsequent activation in differentiating progeny.

12 potent but primarily generate megakaryocytic progeny.

13 a detrimental effect in their differentiated progeny.

14 y inhibits the neural differentiation of the progeny.

15 omes compete for transmission from mother to progeny.

16 secondary RNAs, which are then inherited by progeny.

17 are detrimental or fatal to the cell or its progeny.

18 tors that ultimately give rise to all mature progeny.

19 cells also send feedforward signals to their progeny.

20 in contrast to their isogenic differentiated progeny.

21 sible effect that was maintained in cellular progeny.

22 erm capacity to make endocrine fate-directed progeny.

23 umour growth and give rise to differentiated progeny.

24 ghly mannosylated on tick cell-derived viral progeny.

25 ranslate into transposon mobilization in the progeny.

26 h tumor cells and host cells producing virus progeny.

27 dentity of somatic cyst stem cells and their progeny.

28 yield more extra-embryonic than pluripotent progeny.

29 n of stem cells and differentiation of their progeny.

30 ls (HSCs), progenitor cells and their mature progeny.

31 d by lethality of half of the male or female progeny.

32 vitro, followed by isolation of the neuronal progeny.

33 PGCs and displayed developmental defects in progeny.

34 cy, can influence lifelong phenotypes in the progeny.

35 ng sequence and the silencing can persist in progeny.

36 e 5hmC mark in ISCs and their differentiated progeny.

37 iosis II, causing female-biased sex ratio in progeny.

38 d also yielded smaller numbers of infectious progeny.

39 eproduction and creates genetic variation in progeny.

40 iginates from Wnt-responsive cells and their progeny.

41 ppress host defenses and generate infectious progeny.

42 ll mutations were stably inherited to the T2 progeny.

43 ls (LSCs) compared with their differentiated progeny.

44 ved in the production of excess viral (+)RNA progeny.

45 nitor cells, as well as their differentiated progeny.

46 o1) in the hippocampus of cocaine-sired male progeny.

47 eshly isolated club cells and their cultured progeny.

48 ated with glyphosate resistance in pseudo-F2 progeny.

49 to increased incidence of AA and BPD in the progenies.

50 complex, as do the larval type II neuroblast progeny?

51 ception and maternal, gestational, fetal and progeny (Abstract figure).

52 Follicle stem cell (FSC) progeny adopt distinct polar, stalk, and main body cell

53 findings show that ependymal contribution of progeny after SCI is minimal, local and dependent on dir

54 alyzed viral DNA and the production of viral progeny after treatment of primary adult murine neuronal

55 chestrating the generation of both their own progeny and a neighboring lineage to achieve concomitant

56 is sufficient to alter fates of radial glia progeny and define a new paradigm to understand how mito

57 stem results in complete homozygosity in all progeny and has important evolutionary and ecological im

58 appropriate production of lineage-committed progeny and suppressing tumor formation.

59 ich defined a clear cleft between the lesion progeny and the parent bone (n = 9).

60 y human cytokines expressed by both the HSPC progeny and the tumor cells.

61 mal progenitors versus their differentiating progeny and those altered in cancers.

62 lation are closely associated with the viral progeny and thus may potentially be responsible for its

63 L12 is essential for the production of viral progeny and thus provides an attractive, druggable enzym

64 traits in a Populus linkage population (1200 progeny) and a natural population (435 individuals).

65 natural ((40)K, (238)U and (232)Th and their progeny) and artificial radionuclides ((137)Cs) in vario

66 nant baculoviruses produced viral DNA, virus progeny, and some viral proteins earlier during in vitro

67 s it is advantageous for the survival of its progeny, and therefore, P10 presents an enigma.

68 ic stem cell fate together with differential progeny apoptosis contribute to the final sexual dimorph

69 d ganglia to epithelial tissues, where viral progeny are produced in numbers allowing spread to other

70 epopulates itself indefinitely, whereas some progeny are terminated in antigen-presenting cells, ther

71 kocytes ex vivo We conclude that FabT mutant progeny arise during infection, constitute a metabolical

72 ental potential of differentiating stem cell progeny becomes rapidly and stably restricted following

73 and temporarily impedes the release of such progeny by female macrofilariae, but a macrofilaricidal

74 l developmental transition for production of progeny by sexual reproduction in spermatophytes.

75 notypes, and identify 43 genetically diverse progeny by typing with microsatellites and 9230 single-n

76 Progeny (C1) of these plants showed the expected Mendeli

77 on of aging factors from aged cells to their progeny can be a mechanism for modulating longevity.

78 n between a NSC and its descendants, so that progeny can send feedback signals to the 'mother' cell t

79 of matching sequence, and dsRNA that reaches progeny can spread between cells to cause gene silencing

80 upport multilineage engraftment and generate progeny capable of trafficking to secondary tissues incl

81 longation and chain formation, a hallmark of progeny cell separation arrest.

82 IRF8 and PU.1, which was transmitted to most progeny cells and was reinforced by upregulation of IRF8

83 brane-delimited, capsule-embedded cluster of progeny cells and with a frequency that depends on tempe

84 mitogens without producing virus, generating progeny cells that can release infectious virus.

85 required for cell elongation, separation of progeny cells, and cell wall homeostasis in growing cell

86 m is necessary for constructing new poles of progeny cells, and cells cannot elongate without inserti

87 d apoptosis compared to their differentiated progeny cells.

88 isolated a Drosophila mutation, wuho (wh, no progeny), characterized by a severe fertility defect and

89 e detected in 7/171 (4.1%) mothers of MR/DPD progeny, compared with only 1/171 (0.6%) control mother

90 We reveal that clonal progeny contribute exclusively to either luminal or basa

91 tion into an appendage blastema broadens the progeny contributions of a cellular subpopulation that n

92 relative predictive ability of maternal and progeny cues, costs and constraints of plasticity in par

93 o ensure both successful and efficient phage progeny development.

94 ise to transit-amplifying progenitors, whose progeny differentiate into distinct cell types.

95 that harbors a fixed SC pool whose expelled progeny differentiate, asymmetric divisions first specif

96 It promotes GSC progeny differentiation by translationally controlling t

97 ependent manner, which helps explain the GSC progeny differentiation defect.

98 eny, resulting in a rapid GSC loss and a GSC progeny differentiation defect.

99 ds germline stem cell (GSC) self-renewal and progeny differentiation in a Lok kinase-dependent manner

100 t that Aub promotes GSC self-renewal and GSC progeny differentiation.

101 ion to HFD-induced obesity; at 18 months, LP progeny displays a BAT activity comparable to control of

102 at exhibits genetic anticipation of affected progeny due to expansions of a trinucleotide repeat (TNR

103 ogenitor cells, and their neuronal and glial progeny, during development.

104 ns based on the higher predictive ability of progeny environmental cues.

105 r replication in neuronal cells, all PRV180G progeny exclusively contain mRFP-VP26 tagged capsids.

106 capsid protein (CP) in encapsidating the RNA progeny, experimental evidence on positive sense single-

107 y relative to TS1 TN Posttransplant, TS1 TEM progeny expressed higher levels of PD-1 than did TS1 TN

108 ausal relationship between mitotic delay and progeny fate.

109 n target gene expression to direct interzone progeny fates and articular cartilage development and di

110 atin states in animals can be transmitted to progeny for many generations.

111 VR1814 proliferated and released infectious progeny for weeks, producing higher virus titers than la

112 vibrio, accommodating odd- and even-numbered progeny formation by non-binary division.

113 1vtx/vtx mice, we analysed ABR thresholds of progeny from a backcross segregating MRL and B6 alleles.

114 Marker analysis of 13 F2 confirmed mutant progeny from a recombinant mapping population gave a rou

115 n application before conception protected WT progeny from allergy, it aggravated allergic airway infl

116 that first generation and second generation progeny from gestationally SS-exposed mice exhibit exace

117 med this hypothesis by genomic sequencing of progeny from young and old plants.

118 nd constraints of plasticity in parental and progeny generations, and the dynamic nature of the adapt

119 regulate its transcription, replication, and progeny genome packaging.

120 ethodology to label and track blastemal cell progeny has been deficient, restricting our understandin

121 experience can influence development of the progeny has broad potential for improving human health.

122 nsplantations of various stem cells or their progeny have repeatedly improved cardiac performance in

123 reduction in endocrine progenitor cells and progeny hormone-producing cells, indicating that Area II

124 l infection compared to their differentiated progeny; however, the mechanism is mysterious.

125 Linkage analysis in F2 intercross (B6 x MSM) progeny identified several MSM loci controlling resistan

126 Young progenies in a rat model of maternal low-protein (LP) di

127 erism and is able to generate differentiated progenies in post-implantation pig embryos.

128 omous manner in vitro and migration of their progenies in the hippocampus granular layer in vivo.

129 Monitoring specific cell types and their progeny in a non-invasive, longitudinal and quantitative

130 Neonatal B1 B cells and their CLL progeny in aged mice continued to express moderately up-

131 reds of blastemal cells and their respective progeny in living adult zebrafish undergoing fin regener

132 B73 and Mo17 and their reciprocal F1 hybrid progeny in primary roots under control and water deficit

133 SV-2 DNA replication and production of viral progeny in SCG neurons but not in TG neurons.

134 SV-1 DNA replication and production of viral progeny in SCG neurons, but no significant differences w

135 tegy to indelibly mark a single cell and its progeny in situ, combined with tissue clearing and 3D im

136 ction in vivo and passage of HIV DNA to cell progeny in the absence of active viral replication.

137 ction in vivo and passage of HIV DNA to cell progeny in the absence of active viral replication.

138 meiosis and produced extreme male bias among progeny in the absence of any significant reduction in f

139 nti-CD3/CD28 beads and gave rise to CD161(-) progeny in vitro.

140 The percentage of winged female parasitoid progeny increased exponentially with temperature between

141 However, the percentage of male progeny increased significantly with the densities of ma

142 their division, and differentiation of their progeny into mature granule neurons.

143 that stem cells traverse to generate mature progeny is vital for elucidating the mechanisms governin

144 infection and neurodevelopmental defects in progeny is well established, although the biological mec

145 that neither the single Th17 subset, nor its progeny, is solely responsible for immunopathology or au

146 ssed in germline stem cells (GSCs) and early progeny, it remains unclear whether it plays any roles i

147 The affected HSPCs and their progeny lack expression of glycosylphosphatidylinositol

148 ressed higher levels of PD-1 than did TS1 TN progeny, leading us to test the hypothesis that TEM indu

149 Secondarily, progeny lesions became ossified (n = 7) while at the sam

150 te/erythroid progenitors (MEPs) give rise to progeny limited to the megakaryocyte (Mk) and erythroid

151 se cells, together with their differentiated progeny, maintain a stable identity during steady state

152 Furthermore, several ASC progeny markers were downregulated, and regeneration was

153 Their progeny (MET mice) exhibited schizophrenia-like social d

154 that naive B cells and their differentiated progeny move among distinct micro-environments.

155 ine hematopoietic stem cells (HSC) and their progeny MPP1 separated the cells into 3 main clusters wi

156 ssues to be maintained, stem cells and their progeny must migrate and differentiate in the correct po

157 -efficiency entry of BV and the retention of progeny nucleocapsids in the perinuclear space during eg

158 efficient entry of BV and nuclear egress of progeny nucleocapsids of baculoviruses.

159 ons in cells expressing DN NSF revealed that progeny nucleocapsids were retained in a perinuclear spa

160 are required for efficient nuclear egress of progeny nucleocapsids.

161 so necessary for efficient nuclear egress of progeny nucleocapsids.

162 howed reduced sensitivity to darkness and F1 progenies of the cross between opal5 and Atpir-1 display

163 We found that differentially-fated progeny of 4d (germline, segmental mesoderm, growth zone

164 Evaluating progeny of 73 Tc1 births and 112 Ts65Dn births from fema

165 molecular level, with transmission rates to progeny of 91.4 to 99.6%.

166 omonads multiply by binary division, and the progeny of a haptomonad can either remain attached or gr

167 Each clone is the progeny of a single B cell responding to Ag, with divers

168 Each clone consists of the progeny of a single progenitor cell.

169 ity of tracing a single cell and reveal that progeny of a single proliferative MaSC/progenitor are di

170 Truly endothelial, BOEC are progeny of a transplantable cell that originates in bone

171 n, non-Mendelian inheritance was found among progeny of A1cf and Ago2 mutant intercrosses but not in

172 fy plastid DNA transfer, was observed in the progeny of about 50% of lines emerging from the screen.

173 dose clears the skin-dwelling microfilarial progeny of adult worms (macrofilariae) and temporarily i

174 r in vitro and in vivo studies show that the progeny of ALDH1(+)/CD90(-)/Ecad(-) cells residing in th

175 l hypothesis with a urogenital sinus-derived progeny of all prostatic epithelial cells is opposed by

176 High genotype diversity was observed among progeny of both coinfections; however, diversity was mor

177 irculation also contributed to the bulk cell progeny of distal tumors.

178 Lineage tracing also revealed that the progeny of individual VSMCs contributes to both alpha sm

179 When mixed together in the same vial, the progeny of species I replicate preferentially at pH 7.8;

180 entially at pH 7.8; similarly at pH 5.3, the progeny of species II take over the system.

181 old cells being continually replaced by the progeny of stem cell divisions.

182 e found that cartilage renewal occurs as the progeny of superficial cells fully replace fetal chondro

183 uctuating environmental conditions in hybrid progeny of the inbred lines B73 and Mo17.

184 Furthermore, the progeny of these cells reconstitute adult articular cart

185 c CD4CD25FOXP3 regulatory T (Treg) cells are progeny of thymic-derived CD4CD25FOXP3 Treg (tTreg) cell

186 otype was seen in SERT-deficient mice and in progeny of WT dams given the SERT antagonist fluoxetine.

187 Stem cells and their differentiated progeny offer great hope for treating disease by providi

188 enitors produce substantially more apoptotic progeny or neurons.

189 ells (GSCs) relative to differentiated tumor progeny or normal neuronal cells.

190 In contrast, progeny particles appear to be transported unidirectiona

191 and kinesin during entry, whereas egressing progeny particles are exclusively transported by kinesin

192 nsplanted (Y-chromosome(POS)) CPCs (or their progeny) persisted and continued to proliferate, but the

193 Their progeny (PGC1alpha(DeltaIEC) mice) were subjected to 2%

194 If they form in the embryo, do their progeny populate the adult central complex, as do the la

195 , each transposition burst generates a novel progeny population of chromosomally integrated LTR retro

196 However, in the prediction of the subsequent progeny population, this accuracy increase was only obse

197 y born INPs produce morphologically distinct progeny, presumably due to differential inheritance of t

198 w complete because of sterility of F1 hybrid progeny, prezygotic isolation is still incipient.

199 5, thus preventing the inactivation of virus progeny produced upon replication; (ii) the demonstratio

200 Fluctuations in progeny production and failure to reach population equil

201 thesis, while those in the M segment delayed progeny production from infected cells.

202 on to the cells was evidenced by increase in progeny production.

203 09 viruses in pigs, which could give rise to progeny reassortant viruses with enhanced virulence and

204 ion, at will in transplanted cells and their progeny, regardless of which tissue may have incorporate

205 man SI Mf population and suggest a precursor-progeny relationship with PBMos.

206 leading to infected cell death with no phage progeny release.

207 as self-renewing progenitors, some of whose progeny remain at the tips while others populate the gro

208 oss the entire spinal cord, ependyma-derived progeny remained local, did not migrate and contributed

209 f a specific subset of radial glial neuronal progeny residing along the ventricular surface.

210 ors in the BM such that their differentiated progeny respond inefficiently to signals to accumulate a

211 oduce double-strand breaks in GSCs and their progeny, resulting in a rapid GSC loss and a GSC progeny

212 ly into the viral replicase complex to boost progeny RNA synthesis.

213 g cytoplasmic fibrils, likely to be exported progeny RNA.

214 ant during polymerase maturation into active progeny RNPs.

215 namic role in the control of dormancy of her progeny seed in response to environmental signals.

216 ly by using single-family descent mapping in progenies segregating for the traits.

217 acy of progeny than parental cues to predict progeny selective environments.

218 iscernible effect on the entry and egress of progeny Sendai virus.

219 rmoglycemic and insulinopenic 3-month-old LP progeny shows increased body temperature and energy diss

220 to the individual genes due to insufficient progeny sizes for high resolution mapping and the previo

221 ins in the hippocampus of male cocaine-sired progeny, some of which were enhanced near the Dao1 locus

222 ndings and showed significant differences of progeny survival on Bt plants depending on the origin of

223 Together, our results reveal that progeny temporal fate and progenitor decommissioning are

224 Progeny tended to settle close to their parents, with re

225 sis) between Dura, Pisifera and their hybrid progeny Tenera has not yet been well understood.

226 cause of the potentially greater accuracy of progeny than parental cues to predict progeny selective

227 g to these differences, Cvi-0 x Col-0 hybrid progeny that are homozygous for both Cvi-0 HISN6A and Co

228 +) luminal stem cells give rise to Blimp1(-) progeny that are invariably Elf5(+)ERalpha(-)PR(-).

229 dergo quiescence, and produce embryonic-born progeny that contribute to the adult central complex.

230 tph1b-expressing cells contribute fibroblast progeny that remain restricted to joints throughout life

231 vely divide and produce a cohort of neuronal progeny that shows striking spatial configuration and nu

232 Their progeny then homed back to SC niche and supported new cy

233 wo beneficial mutations to generate a fitter progeny; this evidence suggests that the recombination e

234 pe II lineages, which produce highly diverse progeny through intermediate neural progenitors.

235 ors are bona fide multipotent and contribute progeny to all major pancreatic cell lineages, we also i

236 nment, microbes must widely distribute their progeny to colonize new territory.

237 slowly self-renew and produce differentiated progeny to maintain homeostasis throughout the lifespan

238 g the blastema contribute lineage-restricted progeny to regenerating tissue.

239 ssary for the polarized trafficking of viral progeny to the host plasma membrane for assembly.

240 gands Delta1 and Jagged1, expressed by their progeny, together influence NSC recruitment, cell cycle

241 odies fail to divide and make few infectious progeny until the persistence-inducing stressor is remov

242 we generated spontaneous colistin resistant progeny (up to >256 mug/mul) from four colistin suscepti

243 id induction rate (the percentage of haploid progeny versus total progeny).

244 infection and its effect on the transport of progeny viral capsids to the nuclear envelope.

245 R were required for AAV2 DNA replication and progeny virion formation.

246 The support of progeny virion infectivity by RHA is attributable to str

247 short form seems more potent at restricting progeny virion production at later times, indicating tha

248 mature in an acidic environment and release progeny virions in a membrane-mediated cell-to-cell mann

249 ation of the viral DNA and the production of progeny virions in HEK293 cells.

250 AAV2 duplex DNA genome and the production of progeny virions included the HBoV1 NP1 and NS4 proteins

251 virus proteins necessary for the budding of progeny virions needs to accumulate at budozones.

252 initiates viral DNA replication and produces progeny virions that are infectious in HAE.

253 nome replicates in HEK293 cells and produces progeny virions that are infectious in well-differentiat

254 owing multiple iterations of FACS, cells and progeny virions were shown to display higher levels of a

255 hesis and subsequent extensive production of progeny virions.

256 pikes on cells correlated well with those on progeny virions.

257 he host cell for manufacturing components of progeny virions.

258 ed to the plasma membrane for packaging into progeny virions.

259 me of this virus and allow the production of progeny virions.

260 f HBoV1 DNA and the downstream production of progeny virions.

261 -producing cells resulted in less infectious progeny virions.

262 ed to the plasma membrane for packaging into progeny virions.

263 egradation of Vif to regulate infectivity of progeny virions.

264 PG), pose a major problem for the release of progeny virions.

265 al proteins and membrane-mediated release of progeny virions.IMPORTANCE IBDV is the most extensively

266 Yields of progeny virus and cell-to-cell spread of the DeltaM25 mu

267 uction and with an early elevated release of progeny virus comprising largely spherical rather than f

268 he host cell, but budding arrests before the progeny virus escapes.

269 sm, progressive assembly, and packaging into progeny virus particles.

270 BJ/94-like M gene, showed an early surge in progeny virus production and more severe pathology and e

271 F9) significantly inhibited viral spread and progeny virus production of mut-Ad3GFP but not of wt-Ad3

272 al PtDd neutralize HD5 and support spread of progeny virus was an HAdV3 mutant virus in which formati

273 proviral transcription and the production of progeny virus.

274 Infected ECs released infectious progeny virus.

275 me have been shown to decrease production of progeny virus.

276 s-mediated toxicity and reduces the titer of progeny virus.

277 surface of influenza A viruses that releases progeny viruses from the surface of infected cells and p

278 NA is important as it releases progeny viruses from the surface of infected cells and p

279 For the spread of infection, progeny viruses must rapidly exit the infected cells, bu

280 The resultant progeny viruses often suffer fitness defects due to subo

281 ar chromatin and allowing for the passage of progeny viruses to the nuclear envelope, their site of n

282 g signals were incorporated into reassortant progeny viruses.

283 regnant outbred CD1 female mice and the male progeny was crossed for three generations with untreated

284 However, the robust production of viral progeny was not restored by PDGFRalpha overexpression in

285 ith wild-type virus, passage of UnaG through progeny was significantly enhanced by C3P3.

286 gregated, and spinal cords of adult chimeric progeny were examined for motor neurons with cytosolic d

287 Progeny were randomly placed into groups: no drug (UNT),

288 neural stem cells (NSCs) and their immediate progenies, which generate distinct neural lineages.

289 synaptic plasticity impairments only in male progeny, which has significant implications for the male

290 ve isoform of TCF7L2 (dnTCF7L2) in interzone progeny, which may account for the selective regulation

291 reveals a function of Aub in GSCs and their progeny, which promotes translation of self-renewal and

292 ential of stem cells or their differentiated progenies will depend on their capacity to differentiate

293 ntain initial Imp/Syp levels can still yield progeny with a small range of early fates.

294 e crossed into arrays of mutants to identify progeny with increased GCR rates.

295 At 10 months, BAT activity declines in LP progeny with the appearance of reduced protection to HFD

296 f human pluripotent stem cells (PSCs) toward progeny with trophectoderm characteristics, we produced

297 (+/-) females were crossed to generate 6,729 progeny, with 98 F5(L/L)Tfpi(+/-) offspring surviving un

298 o be inherited in both vegetative and sexual progeny, with exhibition related to the age and propagat

299 ap was generated from a set of 1976 full-sib progeny, with the positioning of 8793 expressed genes.

300 mporal information that diversifies neuronal progeny within a single lineage also impacts circuit ass