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1 proliferating and endocycling domains of the root apex.
2  and the sinus membrane is elevated over the root apex.
3  of the phytohormone auxin from the shoot to root apex.
4 egulation of oxIAA levels in the Arabidopsis root apex.
5 abolically active cells found in the growing root apex.
6 d in epidermal and hypodermal tissues at the root apex.
7 edons and a reduction in auxin levels in the root apex.
8 n distribution and stem cell function at the root apex.
9 rtex cells within the elongation zone of the root apex.
10 ion (CEJ), CEJ to root apex, and cusp tip to root apex.
11 opetal, post-phloem movement of auxin to the root apex.
12 spect of the root, occasionally reaching the root apex.
13 inly involves decreased cell division at the root apex.
14 distribution of auxin within the Arabidopsis root apex.
15 rominent in the proliferating regions of the root apex.
16 MS medium, except in regions proximal to the root apex.
17 on, specifically from epidermal cells of the root apex.
18 specific cell populations within the primary root apex.
19 rinsically lower H(+)-ATPase activity in the root apex, (2) greater salt-induced membrane depolarizat
20       In cells only from the rapidly growing root apex, a hyperpolarization-activated calcium current
21 us, both lateral corrective bending near the root apex and root tip impedance could be due to differe
22 postproliferation phase of elongation at the root apex and this was associated with extensive radial
23 to the cemento-enamel junction (CEJ), CEJ to root apex, and cusp tip to root apex.
24 l infection and death of border cells at the root apex appears to selectively suppress fungal growth
25     We show that salinity application to the root apex arrests root growth in a highly tissue- and tr
26 he central stele and then, upon reaching the root apex, auxin is transported basipetally through the
27 f 10 (out of 25 detected) amino acids in the root apex but not in the mature zone and changed the org
28 creased auxin-induced gene expression in the root apex, but decreased expression in regions where lat
29  sometime between tooth crown completion and root apex closure.
30  Na(+) uptake was about 4-fold higher in the root apex compared with the mature zone, mature root cel
31 f the auxin permease AUX1 in the Arabidopsis root apex has revealed a novel phloem-based IAA transpor
32  and stem cell maintenance must occur at the root apex in order to ensure the continuous growth of pl
33 hibit reduced shootward IAA transport at the root apex in radiotracer experiments and reduced gravitr
34 involved in organizing the distal end of the root apex, including the extent and pattern of cell divi
35 ts in epidermal cells of the rapidly growing root apex, mature epidermal cells, cortical and epiderma
36 ncentrations were observed internally at the root apex (meristem), with As also accumulating in the r
37                                     Near the root apex, Na declined across the cortex in roots from t
38  (mu-SXRF) showed that Hg accumulated at the root apex of alfalfa and was distributed through the vas
39  rhizosphere induces citrate efflux from the root apex of the Al-tolerant maize (Zea mays) hybrid Sou
40 ne and the apical region (much poorer in the root apex) of the root.
41 tance from the cementoenamel junction to the root apex, on radiographs).
42                              A Carboniferous root apex reiterates the importance of the fossil record
43  lateral root cap tissues of the Arabidopsis root apex reveals that the auxin permease regulates a se
44 dapted plants, such as rice, it is typically root apexes, sites of rapid entry for water/nutrients, w
45                               In the growing root apex, the hyperpolarization-activated calcium curre
46          The Fe flux to the DGT resin at the root apexes was 3-fold higher than the anaerobic bulk so
47 Carazinho extends TaMATE1B expression to the root apex, where it confers citrate efflux and enhanced

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