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1 y(phenylene) based model cationic conjugated oligo- (2QA-CCOE, 4QA-CCOE) and polyelectrolytes (CCPE),
2 and flexibility of the individual n-mers in oligo-(9,9-dioctylfluorene) from controlled Suzuki-Miyau
3 tally dependent on dsRNA activation of 2'-5' oligo (A) synthetase (OAS), it is likely that the primar
6 feature of all genomes was the abundance of oligo- and di-peptide permeases (oppABCDF and dppABCDF)
7 ause cleavages within linker regions produce oligo- and mono-nucleosomes, whereas cleavages within nu
10 ndent B<-->A conformational transition in 24 oligo- and polymeric duplexes yield optimal dimeric and
11 nd synthesis, the efficient use of synthetic oligo- and polymeric helical chiral catalysts is still v
13 n of structurally defined, sulfo-phenylated, oligo- and polyphenylenes that incorporate a novel tetra
15 otential applications of rationally designed oligo- and polyphosphodiesters reside in the areas of dr
16 ucan side chain (de)branching, regulation of oligo- and polysaccharide chain length, and formation of
17 simulation of (13)C and (1)H NMR spectra of oligo- and polysaccharides and their derivatives, includ
18 pathways for the utilization of mono-, di-, oligo- and polysaccharides by analysing the distribution
21 Comparison of the activities of CSA and CSB oligo- and polysaccharides with a similar sulfation patt
26 OS) is a heterogeneous condition, defined by oligo-/anovulation, hyper-androgenism and/or polycystic
27 ysis duration (P = .01), and the duration of oligo-/anuria (P = .005) were associated with the develo
28 half adaptor" (HA), generated by annealing P oligo (carrying a phosphate group at the 5' end) and T o
29 rying a phosphate group at the 5' end) and T oligo (carrying a T-tail at the 3' end), for efficient l
30 ath(D)K(10), containing the FKFL linker with oligo-(D)-lysine, and (iii) pH(D)Cath(D)K(10), containin
31 ncubated with sucrose as glucosyl donor and (oligo-)dextran as acceptor, transferring glucosyl residu
33 y modifications, such as the low-fermentable oligo-, di-, and monosaccharides and polyols (FODMAP) di
38 en associated with diets rich in fermentable oligo-, di-, monosaccharides, and polyols (FODMAPs), and
39 table short-chain carbohydrates (fermentable oligo-, di-, monosaccharides, and polyols [FODMAPs]) has
40 bed, short-chain carbohydrates (fermentable, oligo-, di-, monosaccharides, and polyols [FODMAPs]) in
42 ferentiated spermatogonia were captured with oligo (dT)-conjugated beads after UV-crosslinking and pr
44 ssion levels of 18S-RNA and the precision of oligo-(dT) primed first-strand synthesis, we have develo
45 is, we have developed a method that combines oligo-(dT) with an 18S-RNA-specific primer in the initia
46 hese MNPs were attached with 5'-NH(2)-tagged oligo-(dT)(25) primer and were used to isolate mRNA from
47 ssic and important biocompatible polymers of oligo (ethylene glycol) (OEG) and cyclic poly(epsilon-ca
49 genes antibody (mAb-Lis) to amino terminated oligo (ethylene glycol)-capped gold nanoparticles (NH(2)
51 lot plant extraction of cocoa bean shell CBS oligo- (hCHO) and polysaccharide (CHO) extracts using al
53 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/
54 omal endopeptidase cathepsin B, connected to oligo-(L)-lysine for nucleic acid binding, (ii) pHCath(D
58 encompassed five factors: gestational age at oligo- or anhydramnios, gestational age at birth, functi
60 had provirus integration patterns that were oligo- or monoclonal and limited to the tumor cells, sug
61 ulomas from single immunized mice had unique oligo- or monoclonal populations of presumptive NP-speci
69 Here, we systematically designed a set of (oligo-)para-phenylene bridged 2,2'-linked pentacene dime
71 tailed internal bond structure of individual oligo-(phenylene-1,2-ethynylenes) on a (100) oriented si
72 only retained for anthocyanins and flavanol oligo + polymers [anthocyanins Q3 vs. Q1 HR (95% CI): 0.
74 of total flavonoids, flavonols, and flavanol oligo + polymers-had a 12% [HR (95% CI): 0.88 (0.81, 0.9
76 ies, and repurposed it to detect any DNA/RNA oligo (target) in a complex mixture by conducting voltag
77 hing rGrGrG 3'-end of the template-switching oligo (TSO), allowing the reverse transcriptase (RT) to
78 and activated p53 protein was increased in T-oligo- vs. diluent-pretreated skin at the time of irradi