ライフサイエンスコーパス: fertilisation

1 + transients which trigger egg activation at fertilisation.

2 plasmic changes which prepare the oocyte for fertilisation.

3 imulates destruction of CSF during mammalian fertilisation.

4 e and the resulting battle of the sexes over fertilisation.

5 both species reproducing by predominant self-fertilisation.

6 n mouse eggs indistinguishable from those at fertilisation.

7 ie by apoptosis between 35 and 45 hours post fertilisation.

8 play sperm-triggered calcium oscillations at fertilisation.

9 y falls to reach low levels 25 minutes after fertilisation.

10 mozygous for this deletion arrest soon after fertilisation.

11 d most active between 8.5 and 10.5 days post-fertilisation.

12 d physiological mechanisms that prevent self-fertilisation.

13 rval zebrafish tectum from 4 to 15 days post-fertilisation.

14 te the transition back to diploid life after fertilisation.

15 'elimination of paternal mitochondria during fertilisation.

16 fish larvae between four and five days post fertilisation.

17 sitive to ongoing anthropogenic nitrogen (N) fertilisation.

18 bers in regulating pollen tube growth during fertilisation.

19 lity soils in Central Amazonia after 1 yr of fertilisation.

20 ts the initiation of transcription following fertilisation.

21 ion necessary for gametophyte maturation and fertilisation.

22 ed with lizard numerical responses and plant fertilisation.

23 r effect on nutrient availability than CO(2) fertilisation.

24 n males by forcing ejaculates to compete for fertilisation.

25 ty resistance to climate change and nitrogen fertilisation.

26 he ejaculates of different males compete for fertilisation.

27 ity to mount appropriate Ca(2+) responses at fertilisation.

28 differences between conventional and organic fertilisation.

29 ability reacted disproportionately strong to fertilisation.

30 rectification mechanism to support mammalian fertilisation.

31 re-acquire pluripotency, by cycling through fertilisation.

32 is required for normal egg activation during fertilisation.

33 y selected against if present during natural fertilisation.

34 ar process happens to the sperm NE following fertilisation.

35 ant larvae fail to thrive beyond 6 days post-fertilisation.

36 ignificant in gamete interactions leading to fertilisation.

37 NOS) is implicated in gamete interaction and fertilisation.

38 l role of sperm is to activate the oocyte at fertilisation, a process initiated by phospholipase C ze

39 Nitrogen fertilisation affected AM fungal community composition i

40 a separate experiment, we performed in vitro fertilisations after one 2-week period using a split-clu

41 umber of opportunities for productive 'cross-fertilisation' among the (largely independent) bodies of

42 were affected by the interactive effects of fertilisation and AMF application.

43 field-native AMF, particular combinations of fertilisation and AMF inoculation were more effective at

44 The generation of calcium oscillations at fertilisation and during mitosis appears to be controlle

45 tor (PGR) co-ordinately regulates ovulation, fertilisation and embryo implantation through tissue-spe

46 Since 1991, the Human Fertilisation and Embryology Authority (HFEA) has been c

47 In a prospective study of UK Human Fertilisation and Embryology Authority data, we investig

48 r 500 species before and following identical fertilisation and fencing treatments at 39 grassland sit

49 activity is elevated again 15 minutes after fertilisation and finally becomes inactivated 25 minutes

50 and non-sibling ovarian fluid, and assessed fertilisation and hatching success, growth rate and pate

51 Soils and plants were sampled from different fertilisation and lime treatments of the Park Grass long

52 rient limitation and pH-related stress under fertilisation and liming-but has the opposite impact on

53 ing and courtship through to sperm transfer, fertilisation and offspring production.

54 The effects of the application of foliar fertilisation and pesticide on nutritional quality of ma

55 k labelled poly(A) is 'masked' shortly after fertilisation and remains so until the larval stage.

56 of the most important questions in mammalian fertilisation and reproduction.

57 l to reach maximal activity 10 minutes after fertilisation and subsequently falls to reach low levels

58 Yet how krill fishing impacts nutrient fertilisation and the carbon sink in the Southern Ocean

59 We investigated the effect of nitrogen fertilisation and watering reduction on the temporal dyn

60 immobility at 2 days and death by Day 3 post-fertilisation and were rescued by HMGCS1 mRNA.

61 In contrast, external fertilisation and wind- or water-driven passive dispersa

62 al mRNAs that are deadenylated shortly after fertilisation, and are likely to be degraded thereafter.

63 ic CO(2) (ie, carbon nutrient penalty, CO(2) fertilisation, and climate effects on productivity) will

64 y during the processes of oocyte maturation, fertilisation, and pre-implantation development to blast

65 othesis of pangenesis, the role of pollen in fertilisation, and the influence of "conditions of life"

66 niaceae, cytological evidence of meiosis and fertilisation are however yet to be observed in these ta

67 arginine methylation in reprogramming after fertilisation are still poorly understood.

68 y, an embryo's sex is fated at the moment of fertilisation, but in rare instances it is the maternal

69 maphroditism, therefore implicating internal fertilisation by a male stickleback.

70 suggesting that children born after in-vitro fertilisation by intracytoplasmic sperm injection (ICSI)

71 Upon fertilisation by sperm, mammalian eggs are activated by

72 rrest at metaphase I is achieved and how the fertilisation Ca(2+) transient overcomes the arrest in t

73 with the upsweep of the first and subsequent fertilisation Ca2+ spikes.

74 erally, long residue mulches maintain higher fertilisation capacity at advanced stage of decompositio

75 velopment of gametophytes and acquisition of fertilisation competency.

76 n tend to correlate with the position of the fertilisation cone that forms after sperm entry.

77 rical decomposition models and showed that N fertilisation consistently accelerates early-stage but s

78 results indicate that in normal development fertilisation contributes to setting up embryonic patter

79 phase-II arrested eggs to activate following fertilisation declines with advancing maternal age.

80 Nitrogen fertilisation decreased AM fungal spore density (SD), ex

81 The agronomic efficiency of P fertilisation decreased for greater P application rates.

82 e a T. gondii strain that exhibits defective fertilisation, decreased fecundity and generates oocysts

83 sively increases over the first 10 days post-fertilisation (dpf).

84 ost-hatching larvae of 3, 4, and 5 days post fertilisation (dpf).

85 Grassland fertilisation drives non-random plant loss resulting in

86 ver, great uncertainties exist for the CO(2) fertilisation effects, particularly when its interaction

87 Fertilisation experiments have demonstrated that nutrien

88 %) couples in the conventional IVF group had fertilisation failure (absolute difference -0.9%, -4.0 t

89 zebrafish embryos (Danio rerio) 4 days after fertilisation following egg injection with the construct

90 hence, after in vitro maturation and in situ fertilisation, for the generation of transgenic plants.

91 On fertilisation, gametes undergo epigenetic reorganisation

92 ct of increasing CO(2) concentration ('CO(2) fertilisation') gave more realistic estimates of stand-s

93 n reaches stigmas links pollination to ovule fertilisation, governing subsequent siring success and s

94 analysis to modulate fruit shape during post-fertilisation growth of both species.

95 Historical CO(2) fertilisation had a noticeable effect on the Gross Prima

96 ed modest top-down control of algae, whereas fertilisation had no general effect.

97 d in 114 fields across Europe, we found that fertilisation had the strongest positive effect on yield

98 tion in the female reproductive tract before fertilisation has been circumstantially associated with

99 In-vitro fertilisation has been done for nearly 30 years; in deve

100 e of NET2 proteins in pollen development and fertilisation have yet to be elucidated.

101 ere measured in embryos from 6 to 120 h post fertilisation (hpf) by enzyme linked immunosorbent assay

102 main (pMN) sharply declines at 48 hours post-fertilisation (hpf).

103 opposing dorsal retina before (32 hours post fertilisation, hpf), during (48 hpf) and after (56 hpf)

104 analyses strongly implicate autonomous self-fertilisation in causing this relationship, as it is not

105 Predicted increases in fertilisation in emerging economies will accelerate N(2)

106 -analysis to synthesize yield responses to P fertilisation in grasslands, the most common type of agr

107 hough we have a good cellular description of fertilisation in mammals, many of the molecules involved

108 lity alleles (S-alleles), which prevent self-fertilisation in plants, have historically been expected

109 In his book The Effects of Cross & Self-Fertilisation in the Vegetable Kingdom, Charles Darwin h

110 istance, a floral trait associated with self-fertilisation in this species, exhibits a nonlinear rela

111 and experience with predation risk prior to fertilisation in threespined stickleback (Gasterosteus a

112 N fertilisation increases leaf N content but inconsistentl

113 IC FLOWER2 (EMF2), VERNALISATION2 (VRN2) and FERTILISATION INDEPENDENT ENDOSPERM2 (FIS2) genes encode

114 Therefore, efficient fertilisation is crucial.

115 imiting nutrients in agricultural systems, P fertilisation is essential to feed the world.

116 d respond to an appropriate Ca(2+) signal at fertilisation is largely unchanged by advancing maternal

117 l land, to identify under which conditions P fertilisation is most effective.

118 e spermathecae to the ventral receptacle for fertilisation is similar for SR and wildtype male sperm,

119 ibes the origins and development of in vitro fertilisation (IVF) and how it was influenced by, and in

120 selection might improve outcomes of in-vitro fertilisation (IVF) and intracytoplasmic sperm injection

121 erstand what affects the success of in-vitro fertilisation (IVF) and the rate of resulting twin birth

122 of frozen embryo transfer (FET) in in-vitro fertilisation (IVF) has increased.

123 Most aspects of in-vitro fertilisation (IVF) have changed dramatically since intr

124 The success rate of in-vitro fertilisation (IVF) remains low and many women undergo m

125 irths in many western countries and in-vitro fertilisation (IVF) services are growing worldwide.

126 The effectiveness of in-vitro fertilisation (IVF) treatment depends both on the overal

127 reproductive technologies, such as in-vitro fertilisation (IVF) with intracytoplasmic sperm injectio

128 Following in vitro fertilisation (IVF), only about half of normally fertili

129 During in vitro fertilisation (IVF), pharmacological activation of the m

130 e invasive option than conventional in-vitro fertilisation (IVF), which can be successful even when s

131 approach compared with conventional in-vitro fertilisation (IVF).

132 nd adverse pregnancy outcomes after in-vitro fertilisation (IVF).

133 This study demonstrates that high nitrogen fertilisation levels disrupt the temporal dynamics of AM

134 aried with plant development at all nitrogen fertilisation levels, regardless of watering conditions.

135 ) yr(-1) ) but not at high (>= 140) nitrogen fertilisation levels.

136 ding energy production and storage, improved fertilisation methods, and expansion of biodegradable ma

137 would maximise scientific synergy and cross-fertilisation, minimise replication of effort, acquire a

138 a, salamanders henceforth) here we show that fertilisation mode is tied to parental care: male-only c

139 Climate change and spatial redistribution of fertilisation N inputs have driven an increase in global

140 species are more likely to survive when (1) fertilisation occurs inside or close to an adult, (2) ma

141 t the ampullary-isthmic junction (AIJ) where fertilisation occurs, but the mechanisms involved are un

142 Nitrogen fertilisation of agricultural soil contributes significa

143 es (MPF activity and MAP kinase activity) at fertilisation of Ascidiella aspersa oocytes.

144 of T. gondii occurs only in felids, wherein fertilisation of haploid macrogametes by haploid microga

145 Learning which was born as a result of cross-fertilisation of ideas between Quantum Computing and Cla

146 On fertilisation of mouse oocytes, the fusing spermatozoon

147 he biological drawdown of CO(2) is iron (Fe) fertilisation of the high latitudes, but modelling effor

148 Artificial fertilisation of the ocean has been proposed as a possib

149 Fertilisation of these MII oocytes triggers extrusion of

150 tolebias marmoratus, can reproduce with self-fertilisation, offering a unique and useful genetic tool

151 rients as by-products to active and targeted fertilisation on hyperabsorptive sites.

152 mask hypothesised shifts in the effect of N fertilisation on litter decomposition dynamics.

153 revious syntheses evaluating the effect of N fertilisation on litter decomposition relied largely on

154 accurately predicts responses to N and CO(2) fertilisation on tissue allocation, growth and biomass,

155 , market responses, and the effects of CO(2) fertilisation on yield are projected to increase global

156 Of the eight oocytes suitable for in-vitro fertilisation, one fertilised normally and developed int

157 Importantly, internal fertilisation opens the way to terrestrial reproduction,

158 her than for infertility treated by in-vitro fertilisation or gamete intrafallopian transfer.

159 during but erroneous belief is that the post-fertilisation period is irrelevant for axis development

160 effect of crop cover on juice delta(18)O and fertilisation practices on pulp delta(15)N was demonstra

161 We studied how grassland fertilisation propagates change through the plant assemb

162 iR-382-5p and miR-425-3p correlated with the fertilisation rate; miR-127-3p correlated with insulin r

163 Reports of higher fertilisation rates after ICSI suggest that this techniq

164 Secondary outcomes were pregnancy and fertilisation rates associated with each treatment.

165 rs and led to an average of 18% reduction in fertilisation rates in the resulting crosses.

166 In early-larval zebrafish (<10 days post-fertilisation), regenerated hair cells drive action pote

167 , phosphorus-addition effect standardised by fertilisation regime and production measure was consiste

168 e or negative), depending significantly upon fertilisation regime and production measure, but did not

169 rison with the sample of employees (In Vitro Fertilisation Register model: hazard ratio = 1.46 (95% c

170 nish Civil Registration System, the In Vitro Fertilisation Register, and the National Patient Registe

171 At fertilisation, repetitive increases in the intracellular

172 h methylated histone fraction resisting post-fertilisation reprogramming marks developmental genes wh

173 vironmental burdens associated with nitrogen fertilisation, require further consideration.

174 Biomass increase under fertilisation resulted mostly from species that persist

175 l cues experienced by either parent prior to fertilisation results in a modification of offspring rea

176 ntimicrobial defences, sperm maturation, and fertilisation, revealing a functionally complex SF prote

177 ss 18 time points from 1 cell to 5 days post-fertilisation sampling individual and pools of embryos.

178 theory predicts that species undergoing self-fertilisation should have greater population structure t

179 After fertilisation, sperm DNA exchanges protamines for histon

180 ied with biological variables, such as field fertilisation status and intercrop family, and methodolo

181 s and the values were directly linked to the fertilisation strategy.

182 We show that fertilisation strongly increases herbivory in salt marsh

183 potential for inbreeding by facultative self-fertilisation, substantial levels of polymorphism were f

184 es with faster sperm had greater competitive fertilisation success in both seawater conditions.

185 otile sperm per egg is a useful predictor of fertilisation success, using cryopreserved sperm.

186 intain the potential for rare heterospecific fertilisation that typically cause rapid diversification

187 Under fertilisation, the decline in species richness resulted

188 After fertilisation, the punctuate, mitochondrial distribution

189 siderably richer, encompassing the nature of fertilisation, the role of hybridisation in evolution, a

190 ifting maternal investment from pre- to post-fertilisation, thereby reducing a female's reproductive

191 Via gametogenesis and fertilisation this lineage generates a new embryo in the

192 over traits related to courtship, mating and fertilisation through to parental investment.

193 This pathway from ocean fertilisation to aerosol induced cooling of the climate

194 We generated offspring via in-vitro fertilisation to allow us to isolate paternal effects me

195 food system relies on synthetic nitrogen (N) fertilisation to increase crop yields, yet the use of sy

196 We have found that causing fertilisation to occur in the abnormal end of the egg co

197 tant pollen tube growth is stunted, limiting fertilisation to ovules nearest the stigma.

198 genous histone H1) and falls 5 minutes after fertilisation to remain at low levels for 5 minutes.

199 Nucleoli are dynamically reprogrammed post-fertilisation: totipotent early mouse embryos display no

200 In-vitro fertilisation treatment of the recipient and her partner

201 The effects of different fertilisation treatments with arbuscular mycorrhizal fun

202 to persistence at low density is successful fertilisation (union between egg and sperm), and chronic

203 juice from mandarin oranges in which foliar fertilisation was either applied or not.

204 Destabilisation with fertilisation was prevalent but was driven by single nut

205 dentify three waves of gene activity: a post-fertilisation wave involving polyadenylation of maternal

206 psis NET2 proteins in pollen development and fertilisation, we analysed the subcellular localisation

207 Yield responses to P fertilisation were 40-100% higher in (a) tropical vs tem

208 les undergoing their first cycle of in-vitro fertilisation were enrolled from Aug 1, 2016, to June 3,

209 finally becomes inactivated 25 minutes after fertilisation when the pb2 is extruded.

210 tributed into haploid gametes such that upon fertilisation, when two haploid gametes fuse, diploidy i

211 ng at secondary regions is established after fertilisation, whereas imprinting is established during

212 igh sodium plants declined in abundance with fertilisation, whereas low sodium plants increased.

213 eased water-use efficiency (WUE) due to CO2 -fertilisation, which we simulated as increased effective

214 sful, and the alternative-immediate in vitro fertilisation with cryopreservation of embryos-is not al

215 ld with sickle cell disease can use in-vitro fertilisation with preimplantation genetic testing to co