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1 n of citrate AuNPs decorated with a specific nucleic acid probe.
2 as they must be detected with a single short nucleic acid probe.
3 flow-FISH with a fluorescein-labeled peptide nucleic acid probe.
4 denaturing dsDNA and hybridizing fluorescent nucleic acid probes.
5 chieved by in situ hybridization with locked nucleic acid probes.
6  by hybridization with labeled complementary nucleic acid probes.
7 ative to traditional fluorophore labeling in nucleic acid probes.
8 rane by molecular hybridization with labeled nucleic acid probes.
9 , mycolic acid analysis, and narrow-spectrum nucleic acid probes.
10 tly from positive ESP-Myco bottles by use of nucleic acid probes.
11 iously identified by biochemical test and/or nucleic acid probes.
12 dies with fluorogenic protease substrates or nucleic acids probes.
13 n-embedded tissues were hybridized to locked nucleic acid probes against 752 human miRNAs (representi
14  paper with BioPen using "ink" consisting of nucleic acid probes and nucleic acid-modified gold nanop
15                           In silico-designed nucleic acid probes and primers often do not achieve fav
16 cal isolates that test negative with the MAC nucleic acid probes and suggest that standard methods us
17 SELEX) to identify glioblastoma TIC-specific nucleic acid probes-aptamers-that specifically bind TICs
18                                              Nucleic acid probes are used for diverse applications in
19 1% to 6.0%) when the clinics switched from a nucleic acid probe assay to a ligase chain reaction test
20 ternative method uses a signal-amplification nucleic acid probe assay, which measures RNA directly by
21                                   Meanwhile, nucleic acid probes based on Watson-Crick base-pairing r
22 ent T790M resistance mutation with a peptide nucleic acid probe-based real-time PCR.
23 l in a number of assay procedures, including nucleic acid probe-based systems.
24      A commercially available, nonamplified, nucleic acid probe-based test system (BD Affirm VPIII) w
25 detected in live cells employing appropriate nucleic acid probes bearing a tetrazine-reactive NIR flu
26 ve a significant advantage over conventional nucleic acid probes because they exhibit a higher degree
27                        Fluorescently labeled nucleic acid probe binding and subsequent denaturation f
28  detection of M. tuberculosis in culture and nucleic acid probes, but biochemicals are preferred for
29 imal hybridization parameters for 130 locked nucleic acid probes by recording nucleic acid melting te
30                          With this approach, nucleic acid probes complementary to RNA targets trigger
31  The isolates were initially hybridized with nucleic acid probes complementary to the rRNA of the res
32 r-beacons are single-stranded hairpin shaped nucleic acid probes composed of a stem, with fluorophore
33  electrophoretically mobilized bead-(peptide nucleic acid probe) conjugates upon hybridization with t
34                            A new concept for nucleic acid probe design is reported.
35 i protein farnesyltransferase (TB-PFT) using nucleic acid probes designed from partial amino acid seq
36              Carbohydrate antigen detection, nucleic acid probe detection, and bacterial culture are
37 ic acid sensors based on fluorogenic peptide nucleic acid probes embedded in permeable, physically cr
38 cleotide-templated reactions between peptide nucleic acid probes embedded within permeable agarose an
39 hat l-DNA is useful for designing functional nucleic acid probes especially for biological applicatio
40                               We used locked nucleic acid probes for in situ hybridization analysis o
41  to obtain the complete primary structure or nucleic acid probes for the alpha3(V) chain or its biosy
42                                      Hairpin nucleic acid probes have been highly useful in many area
43 re (29%); rapid (radiometric methods, use of nucleic acid probes, high-performance liquid chromatogra
44 s, several did intratypic differentiation by nucleic acid probe hybridization, and 2 sequenced wild p
45  making these modified PNAs ideal for use as nucleic acid probes in genomic analysis.
46                               We used locked nucleic acid probes in in situ hybridisation reactions t
47  situ hybridization (flow-FISH) using locked-nucleic acid probes is combined with rolling circle ampl
48 e derivatives have been covalently linked to nucleic acid probe molecules and have been further chara
49                       The design of modified nucleic acid probes, primers, and therapeutics is improv
50 miologic markers nor molecular analysis with nucleic acid probes reliably distinguishes between virus
51 ated with Raman probes and carrying specific nucleic acid probe sequences can be uptaken by the proto
52 ch case, fluorescence intensity of a peptide nucleic acid probe specific for telomeric sequence was e
53                       Commercially available nucleic-acid probes specific for the Mycobacterium avium
54  are both necessary and sufficient to design nucleic acid probe systems with consistently high specif
55 aluated in three clinical settings against a nucleic acid probe test method according to the personne
56                   The structural features of nucleic acid probes tethered to a solid support and the
57 n (QUAL) probes are a class of self-reacting nucleic acid probes that give strong fluorescence signal
58 identify interactions and characteristics of nucleic acid probes that maximize BSI signal upon bindin
59                      We have developed novel nucleic acid probes that recognize and report the presen
60                                          The nucleic acid probe tiles have been used to study positio
61 by short staple segments, was used to create nucleic acid probe tiles that are molecular analogs of m
62                         PICh uses a specific nucleic acid probe to isolate genomic DNA with its assoc
63               These then were used as unique nucleic-acid probes to isolate a 12-kb RPS24 gene fragme
64              Using hybridization with locked nucleic acid probes, we directly detected abortive trans
65 rs are conjugated to high-affinity antisense nucleic acid probes, which show highly selective fluorog
66 se-long RNA target to an immobilized peptide nucleic acid probe, while fragmented mRNA targets from t
67        Molecular beacons are self-reporting, nucleic acid probes whose structure includes complementa
68 from this polypeptide was used to generate a nucleic acid probe with which the corresponding cDNA was
69 , hybridization of cellular DNA with peptide nucleic acid probes with cells intact, and analysis by f
70  the unique recognition properties of locked nucleic acid probes with enzyme-labeled fluorescence.

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