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1 tally dependent on dsRNA activation of 2'-5' oligo (A) synthetase (OAS), it is likely that the primar
5 ndent B<-->A conformational transition in 24 oligo- and polymeric duplexes yield optimal dimeric and
6 nd synthesis, the efficient use of synthetic oligo- and polymeric helical chiral catalysts is still v
8 n of structurally defined, sulfo-phenylated, oligo- and polyphenylenes that incorporate a novel tetra
10 ucan side chain (de)branching, regulation of oligo- and polysaccharide chain length, and formation of
11 simulation of (13)C and (1)H NMR spectra of oligo- and polysaccharides and their derivatives, includ
14 Comparison of the activities of CSA and CSB oligo- and polysaccharides with a similar sulfation patt
18 ysis duration (P = .01), and the duration of oligo-/anuria (P = .005) were associated with the develo
19 half adaptor" (HA), generated by annealing P oligo (carrying a phosphate group at the 5' end) and T o
20 rying a phosphate group at the 5' end) and T oligo (carrying a T-tail at the 3' end), for efficient l
21 ath(D)K(10), containing the FKFL linker with oligo-(D)-lysine, and (iii) pH(D)Cath(D)K(10), containin
22 ncubated with sucrose as glucosyl donor and (oligo-)dextran as acceptor, transferring glucosyl residu
26 table short-chain carbohydrates (fermentable oligo-, di-, monosaccharides, and polyols [FODMAPs]) has
27 bed, short-chain carbohydrates (fermentable, oligo-, di-, monosaccharides, and polyols [FODMAPs]) in
30 ssion levels of 18S-RNA and the precision of oligo-(dT) primed first-strand synthesis, we have develo
31 is, we have developed a method that combines oligo-(dT) with an 18S-RNA-specific primer in the initia
32 hese MNPs were attached with 5'-NH(2)-tagged oligo-(dT)(25) primer and were used to isolate mRNA from
35 micro g (P>0.05); (4) 60 micro g/5 microl AS oligo (i.c.v. treatment on days 1, 3 and 5) against OFQ/
36 omal endopeptidase cathepsin B, connected to oligo-(L)-lysine for nucleic acid binding, (ii) pHCath(D
40 had provirus integration patterns that were oligo- or monoclonal and limited to the tumor cells, sug
41 ulomas from single immunized mice had unique oligo- or monoclonal populations of presumptive NP-speci
48 tailed internal bond structure of individual oligo-(phenylene-1,2-ethynylenes) on a (100) oriented si
49 and activated p53 protein was increased in T-oligo- vs. diluent-pretreated skin at the time of irradi
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