ライフサイエンスコーパス: fertilization

1 nuclei from mouse embryos at 8.25 days post-fertilization.

2 a spermatozoon might influence the chance of fertilization.

3 e between crops and under different rates of fertilization.

4 ulation to deliver sperm cells to ovules for fertilization.

5 del, we document that zinc reversibly blocks fertilization.

6 elopment and zygotic genome activation after fertilization.

7 uring epididymal sperm maturation and during fertilization.

8 anges in structure and physiology induced by fertilization.

9 ergo hyperactivation, which is essential for fertilization.

10 roles in cell-cell recognition during double fertilization.

11 e seed coat, embryo, and endosperm following fertilization.

12 ciliates were present on days 8 and 10 post-fertilization.

13 genetic reprogramming that takes place after fertilization.

14 gher HRV and lower heart rate at 5 days post-fertilization.

15 allometric changes associated with nitrogen fertilization.

16 heat grain over time compared to MP and no N fertilization.

17 t control did not decline under experimental fertilization.

18 s to confront both fields to stimulate cross-fertilization.

19 he molecular mechanisms regulating mammalian fertilization.

20 hat sperm donate non-genomic components upon fertilization.

21 th an egg and central cell to achieve double fertilization.

22 s element concentrations in lettuces vs. NPK fertilization.

23 sperm reservoir improves the possibility of fertilization.

24 infertility and negatively impacts in vitro fertilization.

25 unknown mechanisms and moves to the site of fertilization.

26 ck to sperm binding that ensures monospermic fertilization.

27 ng pathway acting on the soma rather than by fertilization.

28 o deliver them to the female gametophyte for fertilization.

29 water, lysin and sp18 are dispersed to drive fertilization.

30 n the fitness of the male gametophyte during fertilization.

31 tive blocks to polyspermy ensure monospermic fertilization.

32 ependent than affected by the applied I + Se fertilization.

33 us and fertilize the egg once at the site of fertilization.

34 in most other species, eggs are activated by fertilization.

35 , which assist in binding female gametes for fertilization.

36 FF and serum from women undergoing in vitro fertilization.

37 pmental time points-80, 87 and 117 days post-fertilization.

38 lve rapidly even if not directly involved in fertilization.

39 d-specific target genes at 96 and 120 h post fertilization.

40 g to offset the acceleration driven by CO(2) fertilization.

41 ation, pollination, seed dispersal, and soil fertilization.

42 trate that TMEM95 is essential for mammalian fertilization.

43 ter inputs, warming, CO(2) enrichment, and N fertilization.

44 ng is essential for natural reprogramming at fertilization.

45 e sperm with defects in capacitation and egg fertilization.

46 llular matrix around the oocyte required for fertilization.

47 e exclusion on soil C and N pools depends on fertilization.

48 ed in the absence of females ever undergoing fertilization.

49 with no mutants surviving past 13 days post fertilization.

50 g primordial germ cell development and after fertilization.

51 arization and germline differentiation after fertilization.

52 y only 13.9%, probably because of historical fertilizations.

53 rnal epigenomes undergo marked changes after fertilization(1).

54 ccessibility, both in gametes(5-8) and after fertilization(5,8-10).

55 ids that are less capable in competition for fertilization; a phenotype that was dependent on RNA pol

56 However, fertilization alone and in combination with herbivore re

57 While N fertilization also plays a role in building or maintaini

58 Fertilization also resulted in a faster increase in GPP(

59 ogenous CaMKII activity in real-time by both fertilization and artificial reagents, such as Sr(2+), w

60 showed significant interactive effects of N fertilization and crop type on BX such that LN and HN si

61 Fertilization and early embryo development are regulated

62 of making NPE resembles some aspects of egg fertilization and early embryo development that lead to

63 g repeat classes during differentiation upon fertilization and embryonic genome activation was eviden

64 n oocytes occurs between their ovulation and fertilization and has been shown to decrease their devel

65 lobally replicated experiment, to assess how fertilization and herbivore removal affected potential (

66 soil net N(min) declined most strongly with fertilization and herbivore removal at sites with lower

67 Yet, to date, little is known about how fertilization and herbivore removal individually, or joi

68 These loci are expressed in ovules before fertilization and in the seed coat, embryo, and endosper

69 Ovulation, fertilization and in vitro development to blastocyst wer

70 is used by many angiosperms to prevent self-fertilization and inbreeding.

71 effects of organic amendments coupled with P fertilization and irrigation on soil physical-chemical p

72 nationwide survey-based reconstruction of N-fertilization and irrigation, and an updated nonlinear m

73 ntrosomes are provided to the oocyte through fertilization and must be positioned properly to establi

74 the 20(th) Century particularly due to CO(2) fertilization and N deposition and compares favorably to

75 Second, CO(2) fertilization and nitro gen deposition are the most impo

76 g embryos with venlafaxine immediately after fertilization and performing spatial distribution of ser

77 We investigated the influences of fertilization and residue incorporation on LOC fractions

78 to oocyte-like cells that were competent for fertilization and subsequent cleavage.

79 ity of vegetation activity was altered after fertilization and the importance of nutrient-water inter

80 rted to the vegetal pole a few minutes after fertilization and then to the future posterior side of t

81 enes in developing seed peaked at 48 h after fertilization and was suppressed by 96 h after fertiliza

82 ing in female gametocytes in preparation for fertilization and zygote development, coinciding with pa

83 machinery required for meiotic progression, fertilization, and embryo development.

84 PPP activity in peroxisomes is essential for fertilization, and immunoblot analyses hinted at the pre

85 ryos and plays vital roles during oogenesis, fertilization, and preimplantation development.

86 es spatial colonization, nutrient predation, fertilization, and symbiosis with growth speeds of up to

87 wering is essential for proper organ growth, fertilization, and yield.

88 se the two sperms that participate in double fertilization are genetically identical.

89 opmental events, starting from the moment of fertilization, are crucial for the acquisition of animal

90 g plants, and prevent its occurrence without fertilization, are not well understood(1).

91 ion strategies that rely on ubiquitous CO(2) fertilization as a driver of increased carbon sinks in g

92 These results show that Potassium fertilization as KCl is an important source of groundwat

93 re is a separation into temporal stages with fertilization as the trigger for transitioning to cell e

94 r climate change, climate variability, CO(2) fertilization as well as both the gradual and rapid ecos

95 ductive tract has revealed new details about fertilization at the molecular level.

96 g on recent findings and potential for cross-fertilization between oncology and infection biology, we

97 face is critical for exocytosis and the post-fertilization block to sperm binding that ensures monosp

98 s are significantly affected by nitrogen (N) fertilization but fertilization effects on spatial distr

99 yte binding and are incompetent for in vitro fertilization, but they can still produce viable offspri

100 damental strategy protecting human eggs from fertilization by multiple sperm may have evolved more th

101 ed live imaging, mutant backgrounds in which fertilization can be controlled, and computational model

102 Tillage and nitrogen (N) fertilization can be expected to alter micronutrient dyn

103 al proteomes were analyzed on days 4-10 post-fertilization; ciliates were present on days 8 and 10 po

104 rove implantation success rates for in vitro fertilization clinics.

105 that higher-order chromatin structure after fertilization coincides with an allele-specific enrichme

106 Importantly, fertilization consistently weakens the contribution of p

107 ent was composed of three treatments: (1) no fertilization (control), (2) chemical fertilizer applica

108 Sanguiin H-10, especially in leaves without fertilization (control).

109 Nitrogen fertilization controlled the response to variations in [

110 upon herbivore exclusion in combination with fertilization correlated with a decrease in aboveground

111 rtilization and was suppressed by 96 h after fertilization, corresponding to syncytial and cellulariz

112 Following fertilization, cortical granules exocytose ovastacin, a

113 Foliar P fertilization could increase P use efficiency; however,

114 source of natural bioactive compounds, while fertilization could increase phenolic compounds content.

115 membrane or penetrate into the ooplasm, and fertilization could only be achieved by mechanical injec

116 eveal that in the glacial Southern Ocean, Fe fertilization critically relies on the dynamic interacti

117 ellular matrices involved in everything from fertilization, development, inflammations, to cancer.

118 Herbivore removal in the absence of fertilization did not alter potential and realized soil

119 Fertilization directly results in Ca(2+) oscillations, b

120 how pronounced sexualization, but productive fertilization does not occur and infection falters.

121 ygous mutant embryos starting at 3 days post fertilization (dpf) that result in lethality by 7 dpf, r

122 ethyl sulfoxide (DMSO) daily from 0-5 d post fertilization (dpf).

123 nic E2 concentrations from 1 to 10 days post-fertilization (dpf).

124 uctures and are not viable past 10 days post fertilization (dpf).

125 her in SG than GG but little differed with N fertilization due to large plot-plot variation.

126 affect red abalone growth as well as reduce fertilization during extreme conditions when compared to

127 boiling, coating, germination, foliar spray, fertilization, dusting are some of the non-destructive t

128 sing atmospheric [CO(2) ], that is the CO(2) fertilization effect (CFE), remains a key area of uncert

129 s of carbon dioxide (CO(2)) [i.e., the CO(2) fertilization effect (CFE)] sustains an important negati

130 res in SOC and TN in both croplands, and the fertilization effect appeared more pronounced in SG.

131 me in certain bioenergy cropland soil when N fertilization effect is evaluated.

132 experimental study of 3 years demonstrated a fertilization effect of increased diffuse radiation frac

133 rests has generally indicated a strong CO(2) fertilization effect on biomass growth(3-5), it is uncle

134 g modelling paradigms, which assume that the fertilization effect on crop yields is mainly attributed

135 eased under dimming, thereby discounting the fertilization effect on crop yields.

136 Yet, whether the c(a)-fertilization effect on forests is modulated by changes

137 The fertilization effect was not attributed to any improved

138 nic climate change, which includes the CO(2) fertilization effect, and land use in driving desertific

139 CO(2) fertilization effects have further profound implications

140 Fertilization effects on potential soil net N(min) were

141 y affected by nitrogen (N) fertilization but fertilization effects on spatial distributions of soil g

142 To prevent these supernumerary fertilizations, eggs have evolved multiple mechanisms.

143 This study suggested that N fertilization elevated central tendency and spatial hete

144 tion of segmental aneuploidies from in vitro fertilization embryo biopsies, the origin and characteri

145 ogramming windows: maternal reprogramming at fertilization, embryonic stem cell (ESC) differentiation

146 ally labeled ammonium and urea to simulate a fertilization event showed nitrification (up to 4.1 +/-

147 Based on a 3-year fertilization experiment in Middle Tennessee, USA, a tot

148 Based on a three-year long fertilization experiment in Middle Tennessee, USA, the t

149 We took advantage of a 10-year field fertilization experiment to investigate the effects of n

150 among icefish species, we performed in vitro fertilization experiments using eggs from a female black

151 subplots had also been subjected to nitrogen fertilization from 2005 to 2010.

152 y guard or cuckoldry during which they steal fertilizations from a nest-holding male using a sneak or

153 In the absence of fertilization, fungal and total eukaryotic community com

154 ity, off-setting and possibly negating CO(2) fertilization gains in future, suggesting projected incr

155 This study demonstrated that N fertilizations generally reduced the plot-level variance

156 though the process is a continuum, mammalian fertilization has been studied as a sequence of steps: s

157 ntact zebrafish embryos at 2 and 5 days post-fertilization highlighted genes that influence HRV (hcn4

158 e) of the total internal amount in 26 h post fertilization (hpf) embryos and between 80 and 49% in 74

159 00 mug/L of fluoxetine from 48 to 120 h post-fertilization (hpf), and the accumulation of fluoxetine

160 rafish embryos causes death within 24 h post-fertilization (hpf).

161 Successful fertilization in angiosperms depends on the proper traje

162 tive tissues to promote proper ovulation and fertilization in C. elegans.

163 se findings suggest that the requirement for fertilization in embryogenesis is mediated by male-genom

164 rigger the initiation of embryogenesis after fertilization in flowering plants, and prevent its occur

165 rtically to offspring obtained from in vitro fertilization in laboratory settings.

166 Following fertilization in mammals, the gametes are reprogrammed t

167 hat oviductal EVs mediate sperm function and fertilization in the cat and provides new insights to im

168 improve sperm cryopreservation and in vitro fertilization in the domestic and wild felids and human.

169 insight into sperm selection for successful fertilization in the female reproductive tract.

170 ntage of the independent transitions to self-fertilization in the genus Capsella to compare the simil

171 zer, but cannot completely replace mineral N fertilization in these systems.

172 the condition of an embryo development after fertilization in vitro (IVF), but the available embryo c

173 proteasome system (UPS) in the regulation of fertilization, including sperm-zona pellucida (ZP) inter

174 We found that fertilization increased p:c ratio in a concentration-dep

175 Assisted fertilization increases the risk of pre-eclampsia, but s

176 The expression analysis of Fie1, a rice FERTILIZATION-INDEPENDENT SEED-POLYCOMB REPRESSOR COMPLE

177 ith elevated autophagy levels at 6 days post fertilization, indicating a more severe genotype-phenoty

178 ming-drying trend, the positive effects of N fertilization induced by N deposition on GPP(max) may be

179 etal hemisphere approximately 20 s after the fertilization-induced [Ca(2+)] increase.

180 ivestock, herbivores consumed the additional fertilization-induced biomass, supporting the consumer-c

181 Fertilization-induced Ca(2+) oscillations are essential

182 The awakening of the genome after fertilization is a cornerstone of animal development.

183 Fertilization is a key biological process in which the e

184 e biological process of gamete fusion during fertilization is a proven target for this approach.

185 lenium (Se) concentration of staple crops by fertilization is a valuable pathway to increase Se in th

186 The fusion of gamete membranes during fertilization is an essential process for sexual reprodu

187 n (H3K9me3) in the paternal pronucleus after fertilization is catalysed by SUV39H2 and that pericentr

188 or transgenic Bt crops (Bt crops), but the N fertilization is considered to be an effective method to

189 Deep learning in in vitro fertilization is currently being evaluated in the develo

190 Fertilization is essential for species survival.

191 h the carpel toward the ovules, where double fertilization is executed.

192 This challenges the view that CO(2) fertilization is the dominant cause of emergent SCA tren

193 hereafter used as oocyte donors for in vitro fertilization (IVF) and as recipients for embryo transfe

194 ncy loss, congenital anomalies, and in vitro fertilization (IVF) failure in humans.

195 In vitro fertilization (IVF) is the most common assisted reproduc

196 We refined ovarian stimulation and in vitro fertilization (IVF) methods established for Chinese cyno

197 ee text]), and black carbon (BC) on in vitro fertilization (IVF) outcomes.

198 This study investigates changes in in vitro fertilization (IVF) rates among health plan enrollees be

199 avage-stage embryogenesis following in vitro fertilization (IVF)(1-3), its rate in naturally conceive

200 RT procedures: hormone stimulation, in vitro fertilization (IVF), embryo culture and embryo transfer.

201 and intended infertility treatment (in vitro fertilization (IVF), non-IVF/study site, and non-IVF/out

202 nd thus is not allowed during human in vitro fertilization (IVF).

203 nceptions and those conceived using in vitro fertilization (IVF).

204 ty of pregnancy in women undergoing in vitro fertilization (IVF).

205 ecific selection of sperm cells for in vitro fertilization (IVF).

206 layers of the egg in order to complete their fertilization journey.

207 ulation, boosting rice yield at low nitrogen fertilization levels.

208 osed that zinc released by mammalian eggs at fertilization may block additional sperm from entering.

209 story factors other than transitions to self-fertilization may influence the rate of parental-conflic

210 ernal age and increased reliance on in vitro fertilization, means that an increasing subset of female

211 the positive role of hurricanes as a natural fertilization mechanism influencing forest productivity.

212 lth on corn yield was 18% the magnitude of N fertilization, Moreover, we found this effect was consis

213 vitamin D null diet between 2-12 months post fertilization (mpf) exhibited diminished somatic growth

214 numerous physiological processes, including fertilization, muscle contraction, apoptosis, secretion,

215 erine insemination (n = 24,962) and in-vitro fertilization (n = 22,666), in which 2,458 (5.3%) mother

216 d assisted reproductive technology (in vitro fertilization [n = 19 448], intracytoplasmic sperm injec

217 Effects of atmospheric CO(2) fertilization, nitrogen deposition, climate, wildland fi

218 change may affect the survival, growth, and fertilization of a representative marine benthic inverte

219 xual reproduction actively guard against the fertilization of an egg by multiple sperm (polyspermy).

220 to successful reproduction is polyspermy, or fertilization of an egg by multiple sperm.

221 Fertilization of an egg cell by more than one sperm cell

222 ibitor of GSK3alpha, BRD0705, also inhibited fertilization of eggs in vitro.

223 Upon fertilization of eggs, modification of ZP2 and ZP3 resul

224 Fertilization of flowering plants requires the organizat

225 The high fecundity and external fertilization of most aquaculture species can facilitate

226 We focused on the ants' active fertilization of their crops and their protection agains

227 While controlled-spawns (single-male fertilizations of pooled eggs) reduced male variance, ov

228 vances our understanding of the effects of N fertilization on ECM fungi and the factors governing nut

229 f water table management (WTM) with nitrogen fertilization on GHG fluxes from corn (Zea mays) agro-ec

230 sediment deposition and associated nutrient fertilization on mangrove productivity and resilience.

231 udies have examined the long-term effects of fertilization on P fractions in a soil profile in Mollis

232 onally, we tested the effect of nitrogen (N) fertilization on protein and AAs trends.

233 the globe and quantify the effect of chronic fertilization on these relationships.

234 and planned infertility treatment (in vitro fertilization, other treatment at a study site, and othe

235 After fertilization, parental genomes are enclosed in two sepa

236 After fertilization, Pol II is preferentially loaded to CG-ric

237 Zebrafish (Danio rerio) swim within days of fertilization, powered by muscles of the axial myotomes.

238 Effects of fertilization practices, mineral (M) and organo-mineral

239 tative status did not differ between the two fertilization practices, whereas some grape juice chemic

240 oid induction (HI), which occurs when double fertilization precedes maternal (egg cell) genome loss.

241 er statistically controlling for irrigation, fertilization, precipitation, temperature and other vari

242 mmals requires distinct cycles of ovulation, fertilization, pregnancy, and lactation often interspers

243 0) allele (Y163X) survive until day 10 after fertilization, presenting with impaired T cell developme

244 Neither fertilization procedure generates incorporation cones.

245 d that carries sperm to eggs to initiate the fertilization process.

246 le selfing produces XX hermaphrodites, cross-fertilization produces 50% XO male progeny.

247 selection can explain the rapid evolution of fertilization proteins, yet sperm proteins evolve rapidl

248 smission, survive until ~10 d dpf (days post fertilization), providing a unique opportunity to explor

249 inflammation and AMH in PCOS, and with BMI, fertilization rate (3 miRNA), insulin resistance, FAI an

250 ioenergy croplands, which little varied with fertilization rate but was more responsive in switchgras

251 The N fertilization rate of 90 kg ha(-1) reduced the accumulat

252 xamined the seasonal effects of nitrogen (N) fertilization rate, application method, formulation and

253 against all tested cell lines regardless of fertilization rate, whereas leaves were effective only a

254 rties of S. minor cultivated under different fertilization rates (control, half rate and full rate) w

255 driven by climate, ecosystem properties, and fertilization regimes.

256 enance of this epigenetic memory during post-fertilization reprogramming, yet incomplete penetrance o

257 and 90% of cloned genes at 2 and 4 days post-fertilization, respectively.

258 We found that disabling of the PKS gene at fertilization resulted in albinism throughout all life s

259 utants exhibited a variety of defects during fertilization/seed set, indicating that GPT1 is essentia

260 Fusion of an egg and sperm, or fertilization, sets off a cascade of developmental event

261 However, the advantages of OW fertilization should be weighed against the potentially

262 al competence of floral organs to respond to fertilization signals may explain the different abilitie

263 illions of ejaculated sperm, a few reach the fertilization site in mammals.

264 AOA and AOB provide the potential for better fertilization strategies that could both increase fertil

265 sperm numbers in turn predicted the relative fertilization success of rival males.

266 by revealing how rodent mating plugs promote fertilization success under competitive conditions.

267 animals and are hypothesized to promote male fertilization success under promiscuous mating.

268 By contrast, in some taxa with external fertilization such as fish, exposure to semen promotes s

269 Alterations in long RNA are maintained after fertilization, suggesting a direct link between sperm an

270 These data indicate that N fertilization supply will increase the Bt toxin content

271 enomenon established in the gametes prior to fertilization that causes differential expression of par

272 Following fertilization, the two specified gametes must unite to c

273 Upon fertilization, this process is potently reversed, which

274 tracer to assemble mouse cell-fate maps from fertilization through gastrulation.

275 ed centrioles are removed around the time of fertilization through incompletely understood mechanisms

276 Third, changes in climate have functioned as fertilization to enhance GPP (1.4 Pg C per annum in the

277 ucial roles in higher organisms, from aiding fertilization to protecting the female reproductive trac

278 Crops may require Si fertilization to sustain yields.

279 e-specific, surface-expressed, essential for fertilization/transmission, and exhibits disulphide isom

280 Females that ate plants from the high fertilization treatment laid lighter eggs.

281 aves and leaves that received one of the two fertilization treatment.

282 d delta(15)N were comparable among different fertilization treatments in both croplands.

283 e effects between nanopesticide exposure and fertilization treatments in both ecosystems.

284 design within two 15-m(2) plots under three fertilization treatments in SG and GG croplands.

285 collected from two 15 m(2) plots under three fertilization treatments in switchgrass (SG: Panicum vir

286 fitness in single- and co-inoculations under fertilization treatments of zero added nitrogen (N) and

287 The fertilization treatments were no N input (NN), low N inp

288 The three fertilization treatments were no N input (NN), low N inp

289 Whether the effects of N fertilization vary with bioenergy crop species also rema

290 To rigorously test for fertilization, we devised a two-component genetic-crossi

291 mbryonic zebrafish (Danio rerio) at 4 h post fertilization were exposed to weathered crude oil and as

292 is is an asexual reproduction system without fertilization, which is an important proliferation strat

293 These results indicated that combining fertilization with crop residues stimulates production o

294 tracycline pollution from feed additives and fertilization with livestock manure.

295 Numerous studies have demonstrated that fertilization with nutrients such as nitrogen, phosphoru

296 f ocean turbulence and a potential for cross-fertilization with other areas of geophysics.

297 out how sperm are processed and prepared for fertilization within female mosquitoes.

298 determine which traits and behaviors predict fertilizations within and between populations.

299 iochemical pathways underlying angiogenesis, fertilization, wound healing and regeneration.

300 otor response (LMR) test in 4 to 5 days post fertilization zebrafish with respect to different modes