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1 he ejaculates of different males compete for fertilisation.
2 ity to mount appropriate Ca(2+) responses at fertilisation.
3 differences between conventional and organic fertilisation.
4 rectification mechanism to support mammalian fertilisation.
5 re-acquire pluripotency, by cycling through fertilisation.
6 is required for normal egg activation during fertilisation.
7 ar process happens to the sperm NE following fertilisation.
8 ant larvae fail to thrive beyond 6 days post-fertilisation.
9 ignificant in gamete interactions leading to fertilisation.
10 NOS) is implicated in gamete interaction and fertilisation.
11 + transients which trigger egg activation at fertilisation.
12 plasmic changes which prepare the oocyte for fertilisation.
13 imulates destruction of CSF during mammalian fertilisation.
14 e and the resulting battle of the sexes over fertilisation.
15 both species reproducing by predominant self-fertilisation.
16 n mouse eggs indistinguishable from those at fertilisation.
17 ty resistance to climate change and nitrogen fertilisation.
18 ie by apoptosis between 35 and 45 hours post fertilisation.
19 play sperm-triggered calcium oscillations at fertilisation.
20 y falls to reach low levels 25 minutes after fertilisation.
21 mozygous for this deletion arrest soon after fertilisation.
22 d most active between 8.5 and 10.5 days post-fertilisation.
23 l role of sperm is to activate the oocyte at fertilisation, a process initiated by phospholipase C ze
24 umber of opportunities for productive 'cross-fertilisation' among the (largely independent) bodies of
25 The generation of calcium oscillations at fertilisation and during mitosis appears to be controlle
28 r 500 species before and following identical fertilisation and fencing treatments at 39 grassland sit
29 activity is elevated again 15 minutes after fertilisation and finally becomes inactivated 25 minutes
30 The effects of the application of foliar fertilisation and pesticide on nutritional quality of ma
31 k labelled poly(A) is 'masked' shortly after fertilisation and remains so until the larval stage.
32 l to reach maximal activity 10 minutes after fertilisation and subsequently falls to reach low levels
34 al mRNAs that are deadenylated shortly after fertilisation, and are likely to be degraded thereafter.
35 suggesting that children born after in-vitro fertilisation by intracytoplasmic sperm injection (ICSI)
37 rrest at metaphase I is achieved and how the fertilisation Ca(2+) transient overcomes the arrest in t
40 results indicate that in normal development fertilisation contributes to setting up embryonic patter
42 zebrafish embryos (Danio rerio) 4 days after fertilisation following egg injection with the construct
43 hence, after in vitro maturation and in situ fertilisation, for the generation of transgenic plants.
45 n reaches stigmas links pollination to ovule fertilisation, governing subsequent siring success and s
48 d in 114 fields across Europe, we found that fertilisation had the strongest positive effect on yield
49 tion in the female reproductive tract before fertilisation has been circumstantially associated with
51 ere measured in embryos from 6 to 120 h post fertilisation (hpf) by enzyme linked immunosorbent assay
53 analyses strongly implicate autonomous self-fertilisation in causing this relationship, as it is not
54 istance, a floral trait associated with self-fertilisation in this species, exhibits a nonlinear rela
55 IC FLOWER2 (EMF2), VERNALISATION2 (VRN2) and FERTILISATION INDEPENDENT ENDOSPERM2 (FIS2) genes encode
56 d respond to an appropriate Ca(2+) signal at fertilisation is largely unchanged by advancing maternal
57 erstand what affects the success of in-vitro fertilisation (IVF) and the rate of resulting twin birth
61 reproductive technologies, such as in-vitro fertilisation (IVF) with intracytoplasmic sperm injectio
63 e invasive option than conventional in-vitro fertilisation (IVF), which can be successful even when s
65 species are more likely to survive when (1) fertilisation occurs inside or close to an adult, (2) ma
71 Of the eight oocytes suitable for in-vitro fertilisation, one fertilised normally and developed int
73 during but erroneous belief is that the post-fertilisation period is irrelevant for axis development
74 effect of crop cover on juice delta(18)O and fertilisation practices on pulp delta(15)N was demonstra
78 l cues experienced by either parent prior to fertilisation results in a modification of offspring rea
79 ntimicrobial defences, sperm maturation, and fertilisation, revealing a functionally complex SF prote
80 ss 18 time points from 1 cell to 5 days post-fertilisation sampling individual and pools of embryos.
83 potential for inbreeding by facultative self-fertilisation, substantial levels of polymorphism were f
85 intain the potential for rare heterospecific fertilisation that typically cause rapid diversification
91 genous histone H1) and falls 5 minutes after fertilisation to remain at low levels for 5 minutes.
93 to persistence at low density is successful fertilisation (union between egg and sperm), and chronic
95 dentify three waves of gene activity: a post-fertilisation wave involving polyadenylation of maternal
97 ng at secondary regions is established after fertilisation, whereas imprinting is established during
98 eased water-use efficiency (WUE) due to CO2 -fertilisation, which we simulated as increased effective
99 sful, and the alternative-immediate in vitro fertilisation with cryopreservation of embryos-is not al
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