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1 e stably expressed NtPDR1 in N. tabacum BY-2 suspension cells.
2 NA library derived from sucrose-starved rice suspension cells.
3 to produce monoclonal antibodies in HEK293E suspension cells.
4 present at a 1:3 M ratio with total actin in suspension cells.
5 starch purified from Arabidopsis plants and suspension cells.
6 bidopsis and stably transformed tobacco BY-2 suspension cells.
7 llets derived from roots, inflorescence, and suspension cells.
8 clin D1 cooperate to rescue proliferation in suspension cells.
9 into the cytoplasm of numerous adherent and suspension cells.
10 an Rb cDNA can induce pigmentation in maize suspension cells.
11 ame mechanism is used by Tax in adherent and suspension cells.
12 rapidly activated a 48-kD kinase in tobacco suspension cells.
13 cid-induced protein kinase (SIPK) in tobacco suspension cells.
14 nt phosphorylation of both cPLA2 and ERK2 in suspension cells.
15 ll as GPCR drug responses in LCLs, which are suspension cells.
16 aigremontiana and unable to attach to carrot suspension cells.
17 capable of alkalinizing the media of soybean suspension cells, a response that is generally associate
18 Within 2 days after injection of single-cell suspensions, cells aggregated to form cysts lined with a
19 e generated tobacco (Nicotiana tabacum; NT1) suspension cells and Arabidopsis plants with altered lev
20 eptidase Y and other proteins in Arabidopsis suspension cells and cause these proteins to be secreted
23 promoters in both maize Black Mexican Sweet suspension cells and in stably transformed maize plants.
24 genase (MTD) in celery (Apium graveolens L.) suspension cells and plants showed that MTD is a cytopla
26 l for plant mitochondria in vivo, transgenic suspension cells and tobacco plants expressing GFP with
29 oplasm and nucleus of interphase Arabidopsis suspension cells but much stronger staining of the mitot
32 s originally identified in Nicotiana tabacum suspension cells (BY2), in which its expression was indu
33 ctron microscope analysis confirmed that the suspension cells carry plastids that are significantly s
35 e and increase in DNA content in hematologic suspension cells, correlates with the capability of thes
36 fy highly active L1 RNP complexes from human suspension cell culture and characterize the copurified
37 ptides that rapidly increase the pH of plant suspension cell culture medium and inhibit root growth.
40 ere we use a newly characterized Arabidopsis suspension cell culture to establish that the rhythmic c
41 ntification of highly expressing cell lines, suspension cell cultures are scaled up in a facile manne
42 acts from Arabidopsis (Arabidopsis thaliana) suspension cell cultures can accurately cleave different
44 eferential expression in BMS and embryogenic suspension cell cultures vs. endosperm-derived suspensio
48 ynamics simulation and complete retention of suspension cells experimentally demonstrated within the
53 ranscript and protein changes in Arabidopsis suspension cells in response to ABA using microarrays an
54 on constructs in tobacco (Nicotiana tabacum) suspension cells, indicated mitochondrial, plastidial, a
55 Bright Yellow 2 tobacco (Nicotiana tabacum) suspension cells labeled with an environment sensitive f
58 copy expression levels by 24-fold in tobacco suspension cell lines stably transformed by microproject
64 e report development of a dark-grown tobacco suspension cell model system to investigate the transfor
65 nology can be applied to LCLs, despite their suspension cell nature, in order to serve as an in vitro
66 in cells with low autofluorescence, such as suspension cells or trichomes, but masked in green tissu
70 haride preparation from strain C58 to carrot suspension cells prior to inoculation with the bacteria
71 is finding suggests that the T. caerulescens suspension cells represent cells of the Zn/Cd transport
72 tation experiments with Arabidopsis thaliana suspension cells revealed homooligomerization of all fiv
74 escence microscopic analyses of tobacco BY-2 suspension cells serving as an in vivo import system.
75 ine-phalloidin in permeabilized tobacco BY-2 suspension cells, showing that the fusion protein can sp
76 bles studies of a wide range of adherent and suspension cell subpopulations, which we anticipate will
77 2-yl)carbamoyl]acet ate (YH439)]-treated and suspension cells, suggesting a common mechanism of targe
79 can efficiently deliver oligonucleotides to suspension cells that are known to be very difficult to
81 RKII W109L, and PTP1B C215S activated ERK in suspension cells, the latter two constructs also disrupt
83 us, AOX functions in leaves and roots, as in suspension cells, to ameliorate ROS production when the
85 In a previous study on Arabidopsis thaliana suspension cells transiently infected with the microtubu
86 lear extracts isolated from embryogenic rice suspension cells treated with the phytohormone abscisic
87 t mammalian NOS to tobacco plants or tobacco suspension cells triggered expression of the defense-rel
88 ing of fluorescently labeled SNV to Tanoue B suspension cells using a high-throughput flow cytometer.
89 sue of wheat embryos but their expression in suspension cells was compromised, compared with transien
91 gy was absolutely clear when semiadherent or suspension cells were used in this multistep experimenta
92 ed full-length cDNA was conducted in tobacco suspension cells where its expression resulted in the ac
93 tosol to peroxisomes in Arabidopsis and BY-2 suspension cells, whereas AtMDAR2 and AtMDAR3 accumulate
94 possible to stably transform T. caerulescens suspension cells, which will allow us to alter the expre
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