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1 erence of a conventional microwave frequency synthesizer.
2 ng phosphoramidite chemistry involving a DNA synthesizer.
3 ion of a photonic-based, microwave frequency synthesizer.
4 osition of ligands and fluorophores on a DNA synthesizer.
5 olymerized with excellent control in the DNA synthesizer.
6 ich has already been adapted to a commercial synthesizer.
7 it into the synthesis column of a commercial synthesizer.
8 orated into oligomers using an automated DNA synthesizer.
9 e readily incorporated into DNA by automated synthesizer.
10 amidite approach in an automated solid-phase synthesizer.
11 nucleotides, using a modified maskless array synthesizer.
12 ciently to the 5'-end of DNA on an automatic synthesizer.
13 CAT)(2) on a modified Millipore Expedite DNA synthesizer.
14 e assembled into oligofluor strings on a DNA synthesizer.
15 of several oligosaccharides on a solid-phase synthesizer.
16 low cell reaction chamber connected to a DNA synthesizer.
17  acting as intracellular nanoscale molecular synthesizers.
18 rs in an automated multiplex oligonucleotide synthesizer (AMOS).
19    Our approach requires just a conventional synthesizer and a computer-controllable optical module,
20 between DNA made on a commercially available synthesizer and this unit show that it produces DNA of s
21 chtop without the need of highly specialized synthesizers and at much lower volumes than is currently
22               Recent tools include automated synthesizers and flow reactors.
23 ened up new fields, ripe for attack by young synthesizers and theoreticians.
24  we grew wild-type and a transgenic mannitol synthesizer Arabidopsis thaliana hydroponically with fre
25 ng oil, which were carried out on a parallel synthesizer at 160 degrees C in triplicate in a single d
26 NA oligonucleotides while they remain on the synthesizer column.
27 e is a potent, mismatch-sensitive, automated synthesizer-compatible antisense S-ON modification that
28 igomer was synthesized in a conventional DNA synthesizer, containing neutral nucleotides with a methy
29  was synthesized using a solid-phase peptide synthesizer followed by rhenium cyclization.
30 e inherent flexibility of the maskless array synthesizer for in situ synthesis of thousands of photol
31            Here we describe a maskless array synthesizer (MAS) that replaces the chrome masks with vi
32          This instrument, the Maskless Array Synthesizer (MAS), uses a digital light processor (DLP)
33 lly available Glyconeer 2.1 automated glycan synthesizer, monosaccharide building blocks, and a linke
34                                          The synthesizer performance is comparable to mid-range comme
35 been developed, including molecular muscles, synthesizers, pumps, walkers, transporters and light-dri
36 t to implement into a commercially available synthesizer, restricting access to this radiopharmaceuti
37 esign of the ELIXYS FLEX/CHEM cassette-based synthesizer supports higher temperatures and pressures t
38 sis process is accomplished on a regular DNA synthesizer that is coupled with a UV-VIS projection dis
39 th tetrazole were used with an automated DNA synthesizer to prepare phosphonoacetic acid modified int
40 ctivities (CobP in aerobic adenosylcobalamin synthesizers) to convert adenosylcobinamide (AdoCbi) to
41 he reactions carried out in an automated DNA synthesizer using standard phosphoramidite chemistry.
42 d PMO-DNA chimeras have been prepared on DNA synthesizers using phosphoramidite chemistry.
43                                        A DNA synthesizer was successfully employed for preparation of
44                                        A DNA synthesizer was used to construct several short ODFs car
45 n developed for use in a monomodal microwave synthesizer with direct temperature control using the in

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