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1 evealed greater expression after metamorphic climax.
2 hey became free-swimming through metamorphic climax.
3 s showed minima during the period of biomass climax.
4  11) in the exocrine pancreas at metamorphic climax.
5 (NF62) and reexpressed again near the end of climax.
6 a-cells does not change during the 8 days of climax.
7 escendo (amplitude increase) with a terminal climax.
8 t also prevents aggregation of beta-cells at climax.
9 ne projections degenerate during metamorphic climax.
10  of the epithelial cells into many layers at climax.
11   The scale is 0-100 with 100 as the nominal climax.
12 ally appears in the tail only at metamorphic climax.
13  vaginal lubrication (39%), and inability to climax (34%).
14  altered, enabling the identification of the climax and attack communities that were proposed in an e
15 he role of disturbance in the coexistence of climax and colonist species.
16 lly distinct phases: introduction, build-up, climax and let-down.
17 ratching, swallowing, micturition and sexual climax, are episodic: even in the absence of sensory inp
18 appearing from day 13 and rapidly reaching a climax around weaning time on day 28, compared to the si
19                           During metamorphic climax, best frequencies significantly increase, and sen
20                               At metamorphic climax, both TH-induced cell division and D2 expression
21 tration of T4 that is reached at metamorphic climax cannot induce the final morphological changes.
22             During prolonged hiatal periods, climax communities develop, which include endolithic coc
23 ieved, and creating relationships resembling climax communities.
24 from soil profiles (0-80 cm) from a regional climax community and a degraded land.
25 collapse within a year, suggesting that this climax composition actually causes the collapse of the c
26           Experimentally imposing this fatal climax composition on colonies caused 80% of communities
27  into functional categories (i.e., colonist, climax, disturbance-generalist, and rare).
28 ng linear transects in colonising, mixed and climax forest habitats, representing different levels of
29 cognised in the fossil data (i.e. Stage III: climax; II: transitional; I: pioneer; 0: highly disturbe
30 fferentiation of the tadpole acinar cells at climax is a necessary step in the formation of a mature
31 lated in the tail at the peak of metamorphic climax just before it is resorbed are suppressed in the
32                               By metamorphic climax, limb movement is impaired, ranging from uncoordi
33                       Before the metamorphic climax, most of the cells have already transformed from
34 wn regulated at the beginning of metamorphic climax (NF62) and reexpressed again near the end of clim
35 Their acinar cells do not dedifferentiate at climax, nor do they down-regulate exocrine-specific gene
36 lies that the end-Permian extinction was the climax of a protracted environmental crisis.
37                                   During the climax of amphibian metamorphosis many tadpole organs re
38 modeling of the tadpole intestine during the climax of amphibian metamorphosis.
39 observed no PRMT1 recruitment to TREs at the climax of intestinal remodeling when both PRMT1 and T3 w
40 DS/EVI are expressed in the intestine at the climax of metamorphosis and are induced by T3.
41 rphosis, these transgenic animals die at the climax of metamorphosis before tail resorption has begun
42                                       At the climax of metamorphosis in Xenopus laevis (when the TH l
43                                       At the climax of metamorphosis thyroid hormone (TH) induces ded
44                                       At the climax of metamorphosis thyroid hormone (TH) induces the
45                                       At the climax of metamorphosis, D2 expression is activated spec
46                                       At the climax of metamorphosis, tail muscle down-regulates more
47 phosis and leads to tadpole lethality at the climax of metamorphosis.
48 e onset of the negative feedback loop at the climax of metamorphosis.
49 e took place within weeks of each other in a climax of scientific excitement during the summer of 196
50                                          The climax of this strategy of catalysis boosting by means o
51 (i.e. social status) with the high-amplitude climax phase, and context (reflecting activity of the ca
52 ow-amplitude introduction and high-amplitude climax phases.
53 n found repeatedly in significant numbers in climax saltern crystallizer communities.
54                                    After the climax, SFB quickly declined to very low levels in the s
55  in or capable of pathogen transmission than climax species.
56 n) but was present just prior to metamorphic climax (stage 58, during TH secretion).
57 ail cells remain as larval cells even at the climax stages of metamorphosis.
58                                       During climax the increase in insulin cluster size is not cause
59      Shortly before the onset of metamorphic climax, there is a brief "deaf" period during which no a
60     D. odorata (Leguminosae), a slow growing climax tree, occurs at very low densities, whereas J. co
61                           During metamorphic climax when the exocrine pancreas dedifferentiates to pr
62 Ptf1a) undergo almost complete extinction at climax, whereas PDX-1, Notch-1, and Hes-1, genes implica
63  Intestinal colonization begins at birth and climaxes with the acquisition of two dominant groups of

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