ライフサイエンスコーパス: fertilization

1 ge and blastocyst development after in-vitro fertilization.

2 h that enhances germline proteostasis before fertilization.

3 us to examine whether these fibrils promote fertilization.

4 various families are activated shortly after fertilization.

5 ed immature testes around eleven weeks after fertilization.

6 the female reproductive structures vital for fertilization.

7 staged isogenic and hybrid zygotes following fertilization.

8 other mucoid secretions to reach the site of fertilization.

9 still lacking, especially under nitrogen (N) fertilization.

10 es showed testicular tissue six months after fertilization.

11 of the genome for rapid activation following fertilization.

12 ementations of crop and forestry harvest and fertilization.

13 ransduction to the actin cytoskeleton during fertilization.

14 s, with differences first visible 12 d after fertilization.

15 , two pairs of gametes participate in double fertilization.

16 undantly control gamete fusion during double fertilization.

17 erated directly from gametophytes, bypassing fertilization.

18 that may be of particular importance during fertilization.

19 ency of blastocyst production after in vitro fertilization.

20 e of foliar biomass, season, or nitrogen (N) fertilization.

21 ial exodus of paternal chromosomes following fertilization.

22 It was again inactive after fertilization.

23 sposons, some of which are transcribed after fertilization.

24 and the initiation of seed development after fertilization.

25 rting sperm hyperactivation, thus preventing fertilization.

26 te and produced larger larvae at 5 days post fertilization.

27 n bovine embryos (n = 23) following in vitro fertilization.

28 ential role in male-female communication and fertilization.

29 gous populations of mitochondrial isolate at fertilization.

30 ich like apogamy produce sporophytes without fertilization.

31 tion that may be of particular importance in fertilization.

32 cent state of the egg cell in the absence of fertilization.

33 ered exodus of the paternal genome following fertilization.

34 a to reset centriole number in the zygote at fertilization.

35 dation of the sperm-borne mitochondria after fertilization.

36 s that serve to ensure a diploid genome upon fertilization.

37 roteins repress nucellus degeneration before fertilization.

38 rapid and synchronous cell cycles following fertilization.

39 This process is known as double fertilization.

40 s a quiescent state that is maintained until fertilization.

41 yte is required for sperm release and double fertilization.

42 ayed undifferentiated until six months after fertilization.

43 gametes that produce an entire organism upon fertilization.

44 d C57BL/6N, with the routine use of in vitro fertilization.

45 s of sugarcane pokkah boeng compared to urea fertilization.

46 oice can also occur in species with external fertilization.

47 th in the ovary to support development after fertilization.

48 Sperm capacitation is required for fertilization.

49 blished in the germline and maintained after fertilization.

50 system development from 12 to 48 hours post fertilization.

51 vulation, a timed event that is critical for fertilization.

52 laria parasite and gamete membrane fusion at fertilization.

53 OX isoform expression at 1 and 1.5 days post fertilization.

54 val zebrafish (Danio rerio) at 5.5 days post-fertilization.

55 sperm migration and contribute to successful fertilization.

56 ssed by N fertilization and stimulated by Mo fertilization.

57 lls that houses the sperm and is the site of fertilization.

58 tly the tocopherol and sugar contents than N fertilization.

59 upture, releasing the sperm cells for double fertilization.

60 zation undergoes drastic reprogramming after fertilization.

61 ed post-fertilization when compared with pre-fertilization.

62 ential nuclear cleavages within only 2 hr of fertilization.

63 nce of cytoplasmic determinants displaced by fertilization.

64 ling the restoration of ploidy levels during fertilization.

65 atly diminished higher-order structure after fertilization.

66 proportion of cycles resulting in successful fertilization (10% decrease), implantation (31%), clinic

67 ell reception, gamete interaction, their pre-fertilization activation and fusion, as well as the mech

68 regulates seed development immediately after fertilization, although the controlling mechanisms remai

69 ium transients are a universal phenomenon at fertilization and are required for egg activation, but t

70 Sperm motility, viability, fertilization and blastocyst rates were lower in Prdx6 (

71 reproduction between individuals results in fertilization and can result in barriers to interspecifi

72 Cell fusion is ubiquitous in eukaryotic fertilization and development.

73 porate more manipulative treatments, such as fertilization and drought, and whenever possible, simult

74 preserved, which is critical for successful fertilization and early development.

75 es and eggs, which is fundamental to support fertilization and egg activation.

76 I) is an important mechanism to prevent self-fertilization and inbreeding in higher plants and also i

77 y attributed to the end of Subantarctic iron fertilization and increasing nitrate input from the surf

78 ical early events regulating pollination and fertilization and involve many signaling events.

79 ZGA occurs shortly after fertilization and involves approximately 10% of the geno

80 ogenous levels of deoxyATP (dATP) present at fertilization and is activated as dATP is depleted via D

81 ransportation), and on-farm activities (e.g. fertilization and machinery operation).

82 region, straw returning, optimized nitrogen fertilization and no tillage are all necessary whatever

83 d nutrient enrichment associated with forest fertilization and organic matter influx which may have f

84 rface while providing benefits from enhanced fertilization and outcrossing.

85 ults imply females have greater control over fertilization and potential to exert selection on males

86 RNA and endo-siRNA contents are required for fertilization and preimplantation development.

87 borne sncRNAs truly have any function during fertilization and preimplantation embryonic development.

88 ols pollen tube reception immediately before fertilization and regulates seed development immediately

89 which plays an important role in conspecific fertilization and reproductive isolation of sea urchins.

90 a fail-safe system to prepare the oocyte for fertilization and reproductive success.

91 ses apart these mechanisms by using in vitro fertilization and shows that susceptibility of offspring

92 t, free-living N fixation is suppressed by N fertilization and stimulated by Mo fertilization.

93 ed with improved cultivation practices (i.e. fertilization and straw return) since the early 1980s we

94 gene that functions immediately after double fertilization and supported the model that a passage thr

95 e reception by the female gametophyte before fertilization and the initiation of seed development aft

96 rovides further evidence of the roles of CO2 fertilization and warming-induced respiration, and highl

97 tially increase crop yields while reducing N fertilization and, subsequently, environmental pollution

98 ies selection, grazing and mowing harvest, N fertilization); and (iii) land management practices with

99 quality and maturation of the oocyte before fertilization, and can be predicted through a minimally

100 CO2 18480 microatm) on oyster gametogenesis, fertilization, and early larval development successes.

101 ical process, such as stem cell maintenance, fertilization, and heart development.

102 vailable on how gamete membranes interact at fertilization, and it is unclear how Juno - which was pr

103 es responses to reduced acid deposition, CO2 fertilization, and nitrogen deposition.

104 le during oogenesis, is not translated until fertilization, and produces a protein gradient that func

105 asis of sperm-egg recognition, cross-species fertilization, and the barrier to polyspermy, thereby pr

106 produced by a combination of IR69428 and Zn fertilization applied at panicle initiation (38.5 mug g(

107 ns in mating system from outcrossing to self-fertilization are common; however, the impact of these t

108 ex cellular events that occur in response to fertilization are essential for mediating the oocyte-to-

109 nesis, especially the early events following fertilization are largely unknown in radish.

110 and the details of their functional roles in fertilization are not known.

111 netic instructions delivered by the sperm at fertilization are required for correct regulation of gen

112 he Subantarctic Zone, possibly owing to iron fertilization as a result of higher absolute dust fluxes

113 on cycle dynamics, with biodiversity and CO2 fertilization as secondary factors.

114 to evaluate Se-enriched pasta through foliar fertilization at various rates and timing of application

115 e occurring in approximately 50% of in vitro fertilization attempts.

116 ecosystems and for global projections of CO2 fertilization, because, although direct effects are typi

117 rmones re-establish oocyte proteostasis once fertilization becomes imminent.

118 notype distribution, and potential for cross-fertilization between E. tenella strains.

119 light opportunities and challenges for cross-fertilization between sociology and decision research th

120 ssible to resolve long-standing questions in fertilization biology, and to test the efficacy and safe

121 s showed that soil available-P response to P fertilization but maize yields did not.

122 s diploid egg cells that can develop without fertilization, but haploid pollen.

123 embryonic viability in the first hour after fertilization, but persistently required throughout the

124 orted by the vegetative pollen tube cell for fertilization, but the extent to which they regulate the

125 he change in C storage in forests due to the fertilization by deposited N and P (Cnu dep ), based on

126 ast in part--a combination of dwindling iron fertilization by dust and enhanced deep ocean ventilatio

127 Surprisingly, the fibrils inhibited fertilization by immobilizing sperm.

128 event in several cellular processes, such as fertilization, cell migration, and cell differentiation.

129 lipase A2 (Ca(2+)-iPLA2) activity by MJ33 on fertilization competence of mouse spermatozoa.

130 osis I (MI) are two key stages for producing fertilization-competent eggs.

131 ed in human follicular fluid during in vitro fertilization cycles.

132 Rh, the response ratio (RR) of Rh flux to N fertilization decreased firstly during growing season, i

133 Notably, transgenic THOR knockout produced fertilization defects in zebrafish and also conferred a

134 in oocytes, but increases dramatically after fertilization, directly interacts with, and relieves the

135 eding under European law (from 5.2 days post-fertilization (dpf) at 28.5 degrees C).

136 c, and axenic larvae colonized at 1 day post fertilization (dpf) were evaluated using a standard loco

137 lies greater SOC storage associated with CO2-fertilization-driven increases in C inputs over the comi

138 exhibit abnormal behavior upto 12 days post fertilization due to changes in HTRs.

139 ed to increase C3 crop yield through the CO2 fertilization effect (CFE) by stimulating photosynthesis

140 d to be as much as half of that from the CO2 fertilization effect during 1990-2013.

141 The CO2 fertilization effect is a major source of uncertainty in

142 ings support the hypothesis of a general CO2-fertilization effect on vegetation growth and suggest th

143 However, the magnitude of this CO2 fertilization effect varies from a 20 per cent to a 60 p

144 or litter microbial communities, C, N, and P fertilization effects on microbial stoichiometry were st

145 reduced germination in vitro and with lower fertilization efficiency in vivo.

146 ic stem cells (nt-ESCs), as well as in vitro fertilization embryo-derived ESCs (IVF-ESCs).

147 gy for maximizing spore production from each fertilization event.

148 with a sperm [3], thereby preventing further fertilization events, it is unknown whether plant gamete

149 ses to N deposition, we conducted a two-year fertilization experiment in a semiarid grassland on the

150 Using a fertilization experiment in a tropical rainforest, we ev

151 three types of organic matter over a 30-year fertilization experiment.

152 Although in vitro fertilization experiments suggest that the maize zygote

153 In species with internal fertilization, females can favour certain males over oth

154 may exist in a markedly relaxed state after fertilization, followed by progressive maturation of hig

155 Phosphorus fertilization had no-significant effect on richness of A

156 rogram them for embryonic development during fertilization have historically been considered unique t

157 Following successful pollination and ovule fertilization, heat-stress modified PsACS and PsACO tran

158 in our molecular understanding of mammalian fertilization, highlighting the areas in which genetic a

159 sion of il-2rgammac.a commenced at 16 h post fertilization (hpf) and rose steadily from 4-6 d postfer

160 omal tissue (CHEST) cells from 72-hours post fertilization (hpf) caudal hematopoietic tissue (CHT), t

161 alyze the time-course (24, 48, and 96 h post fertilization (hpf)) of transcriptional and developmenta

162 he equatorial Pacific Ocean to test the dust fertilization hypothesis.

163 sis requires Bmp signaling from 10-18 h post-fertilization, immediately following gastrulation.

164 ly associated with proportions of successful fertilization, implantation, clinical pregnancy, and liv

165 erbaceous legume species to nine levels of N fertilization in a glasshouse.

166 It primarily reproduces by internal self-fertilization in a mixed ovary/testis gonad.

167 suggested higher leaching risk from chemical fertilization in acidic soil of southern China with high

168 egg and sperm is the first necessary step of fertilization in all sexually reproducing organisms.

169 Sperm chemotaxis is essential for fertilization in both animals and early land plants such

170 nce of paternal mitochondria after embryonic fertilization in C. elegans.

171 likely operated synergistically with mode of fertilization in driving the diversification that began

172 Fertilization in flowering plants requires a complex ser

173 hese membrane potential changes critical for fertilization in mouse sperm, and they are only sensitiv

174 C3, associated with sperm mitochondria after fertilization in pig and rhesus monkey zygotes.

175 lack of any clear short-term NEE response to fertilization in such an N-limited system is inconsisten

176 l timescales deep ocean circulation and iron fertilization in the Southern Ocean played a consistent

177 s and for the formation of centrosomes after fertilization in the zygote.

178 y rate, and blastocyst development following fertilization in vitro, compared to the control without

179 A results in striking phenotypes weeks after fertilization; including perinatal lethality and abnorma

180 coli is a Se-hyperaccumulator plant, with Se-fertilization increasing its potential as a functional f

181 uring a whole-genome duplication to generate FERTILIZATION INDEPENDENT SEED2 (FIS2) and MEDEA (MEA),

182 3D microtomographic imagery, we found that N fertilization induced an increase in intra-aggregate por

183 ils, for long-term duration, and with less N fertilization input when compared to PT0.

184 s a late evolutionary adaptation to maximize fertilization inside the mammalian female reproductive t

185 complement of chromosomes in the absence of fertilization involves genome duplication prior to the m

186 t adequately represented in DGVMs, while CO2 fertilization is likely overrepresented.

187 of AM plants differ from those induced by Pi fertilization is poorly understood.

188 Interspecies fertilization is rare, partly due to species separation

189 Fertilization is the culminating event of sexual reprodu

190 r plant species to another in the absence of fertilization is thought to be rare.

191 of genetic variation in cell lineages after fertilization, is increasingly recognized to play a caus

192 Since the discovery of double fertilization, it has been recognized that flowering pla

193 noncoding RNAs (sncRNAs) into oocytes during fertilization, it remains unknown whether these sperm-bo

194 owing parthenogenetic activation or in vitro fertilization (IVF) and tracked their development.

195 urinary phthalate metabolites with in vitro fertilization (IVF) outcomes, accounting for multiple IV

196 ated female uterus partially rescue in vitro fertilization (IVF) that failed with epididymal spermato

197 of PFR metabolites and outcomes of in vitro fertilization (IVF) treatment among couples recruited fr

198 studies of breast cancer risk after in vitro fertilization (IVF) treatment were inconclusive due to l

199 is, suspension feeding, osmotrophy, internal fertilization, jet propulsion, undulatory locomotion, an

200 The success of double fertilization largely depends on compatible communicatio

201 ere examined during 1990-2009 under chemical fertilization, manure incorporation with fertilizer, and

202 ances oocyte proteostasis in anticipation of fertilization may be conserved in other species.

203 n yield increases through only enhanced crop fertilization may have unforeseen, indirect, effects on

204 of plant production is common and therefore fertilization may reduce diversity by reducing the numbe

205 od flow in Zebrafish embryos at 4 days after fertilization, measuring the average speed and the durat

206 ther to child is now a reality with in vitro fertilization mitochondrial replacement techniques.

207 amount of protein into the medium just after fertilization, most likely related to the blocks to poly

208 chness, precipitation, temperature, nitrogen fertilization (N), and grazing intensity.

209 Fertilization occurs during female meiosis in most anima

210 s of bioavailable iron and contribute to the fertilization of coastal waters and the ocean beyond.

211 We propose occasional fertilization of diploid egg cells by haploid pollen, re

212 CO2 seasonal cycle and the magnitude of CO2 fertilization of GPP is almost linear across the entire

213 o consistent emergent constraints on the CO2 fertilization of GPP.

214 cess, creating a lot of discussion and cross-fertilization of ideas from developmental biologists to

215 Cross-fertilization of learning processes across multiple doma

216 Fertilization of nitrogen (N)-limited ecosystems by anth

217 ded as the growth-limiting nutrient in bogs, fertilization of nutrient-poor ecosystems, such as these

218 last glacial period were linked to iron (Fe) fertilization of subantarctic surface waters.

219 Here we show that fertilization of the central cell results in the product

220 In angiosperms, double fertilization of the embryo sac initiates the developmen

221 Cumulus cells sustain the development and fertilization of the mammalian oocyte.

222 d for replication versus transcription after fertilization of the oocyte.

223 ed by carbon cycle feedbacks related to dust fertilization of the Southern Ocean as a consequence of

224 he initiation of substantive dust-borne iron fertilization of the Southern Ocean during peak glacial

225 We studied the impacts of elevated CO2 and N fertilization on EMM production and turnover in a Pinus

226 illustrated, for example, the impacts of CO2 fertilization on litter and SOC dynamics can be easily d

227 tically significant effect of irrigation and fertilization on positive sensorial perception.

228 heterostylous flowers can achieve unimpeded fertilization only on opposite-morph flowers.

229 roach to analyze Cyclin B1-null embryos from fertilization onward.

230 il to achieve pregnancy due to either failed fertilization or embryo arrest during preimplantation de

231 During fertilization, Pollen Receptor-Like Kinases (PRKs) contr

232 mes in the same monkey without deteriorating fertilization potential of eggs until a poor response to

233 nds mammalian eggs, becomes impermeable upon fertilization, preventing the entry of further sperm.

234 red for zygote formation and functions after fertilization; protein-, lipid- and energy-metabolism.

235 In general, N fertilization provides an improvement in the chemical co

236 The adjusted fertilization rate for women in increasing quartiles of

237 )D concentrations were positively related to fertilization rate.

238 At fertilization rates above 100 kg N ha(-1) , NO emissions

239 a increased by up to roughly 2.63 ppbv under fertilization rates of 150 kg N ha(-1) or higher.

240 presumably mediated by the interplay of high fertilization rates, massive spore production and long-d

241 N fertilization reduced the standing EMM biomass C to 57%

242 Quantifying the contribution of various fertilization regimes to soil N storage and loss has bee

243 ts were grown under low, moderate, or high N fertilization regimes.

244 Fertilization releases the meiotic arrest and initiates

245 Oocyte fertilization represents a scenario wherein inappropriat

246 In flowering plants, fertilization requires complex cell-to-cell communicatio

247 report here that translation of nanos1 after fertilization requires Dead-end 1 (Dnd1), a vertebrate-s

248 ic conditions and agronomic operations (e.g. fertilization, residue management and chemical crop prot

249 lute protein and phosphosite dynamics of the fertilization response by mass spectrometry-based proteo

250 sults, we propose that mycorrhization and Pi fertilization share cytokinin-mediated improved shoot gr

251 tence of all these interests and their cross-fertilization should be favored by interdisciplinary, in

252 rainfall years of 2011/2012 and 2012/2013, N fertilization significantly stimulated Rs by 23.9% and 1

253 o1 interaction was shown to be essential for fertilization since mice lacking either gene exhibit sex

254 F community assemblages is correlated with P fertilization, soil depth and crop phenology.

255 plasm is usually a DNA-free zone, but during fertilization, sperm DNA enters oocyte cytoplasm and cou

256 many significant functional terms, including fertilization, sperm motility, calcium channel regulatio

257 Our results would enable design of optimal fertilization strategies to enrich broccoli in Se with m

258 if being eaten sufficiently enhances either fertilization success (mating effort) or offspring numbe

259 on of coral sperm reduced sperm motility and fertilization success in half, thus fresh sperm, capable

260 on of the cryoprotectant treatments affected fertilization success in small- and larger-scale reprodu

261 erm within the bank was not important as the fertilization success of sperm frozen for less than 1 mo

262 It is expected that N fertilization supply may promote the expression of trans

263 ations, as well as for applied research into fertilization technology.

264 selection on males in species with external fertilization than previously thought possible.

265 duced lck:GFP+ thymic T cells by 5 days post-fertilization that persisted into adult stages.

266 hromatin assembly is strongly modified after fertilization, that the egg cell is primed to activate t

267 Fertilization, the culminating event in sexual reproduct

268 Following fertilization, the endosperm expands and the embryo grow

269 Upon fertilization, the genome of animal embryos remains tran

270 After fertilization, the initially distinct parental epigenome

271 oduction in flowering plants involves double fertilization, the union of two sperm from pollen with t

272 Following fertilization, these morphological changes led to format

273 ygosity and produces diploid embryos without fertilization through a truncated meiosis.

274 ies selection, irrigation, wetland drainage, fertilization, tillage, and fire-for (1) their importanc

275 of paternal mitochondria to the matrix after fertilization to degrade mitochondrial DNA.

276 Twelve months elapse from fertilization to fruit abscission.

277 dings confirm the effectiveness of foliar Se fertilization to increase Se concentrations in durum whe

278 Chromatin is reprogrammed after fertilization to produce a totipotent zygote with the po

279 variety of ecosystem benefits, ranging from fertilization to stabilization against erosion.

280 not large enough to provide substantial iron fertilization to the central equatorial Pacific.

281 accessibility is quickly reprogrammed after fertilization to the level similar to maternal chromatin

282 After fertilization, to initiate development, gametes are repr

283 Fertilization triggers assembly of higher-order chromati

284 ere is little if any mtDNA replication after fertilization until the embryo implants.

285 ection of flower organs and mimicry of ovary fertilization unveiled in this study guided the rice pla

286 rate emergent constraints on large-scale CO2 fertilization using observed changes in the amplitude of

287 r sites (AA) is significantly increased post-fertilization when compared with pre-fertilization.

288 ilization, while SOS1 functions mostly after fertilization when seed development begins.

289 ic Erk signaling, except from 1 to 4 hr post-fertilization, when perturbing the spatial extent of Erk

290 entially become a valuable tool for in vitro fertilization, where contrast agents and fluorophores ma

291 ls that transfer sperm between adults during fertilization, whereas animals that broadcast sperm into

292 wed decreased aliphatic GLSs at split dose N fertilization; whereas reduced N increased aliphatic and

293 n on responses of Rs and its components to N fertilization, which should be incorporated into models

294 pting at least three histone marks following fertilization, while PSR avoids self-elimination by evad

295 ons early in reproductive development before fertilization, while SOS1 functions mostly after fertili

296 sting connections and possibilities of cross-fertilization with other domains, including biophysics.

297 ation of de novo meiotic spindles and, after fertilization with sperm, meiosis completion and formati

298 e were subtly, but significantly, altered by fertilization, with higher alpha diversity in fertilized

299 This is the first demonstration that in vivo fertilization without the normal physiological trigger o

300 or ACR neurotoxicity by exposing 5 days post-fertilization zebrafish larvae to 1 mM ACR for 3 days.