戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ive and attractive probe for the design of a DNA chip.
2 one visit, were analyzed every 12 months via DNA chip.
3 es that are molecular analogs of macroscopic DNA chips.
4 pots to automate the deposition of probes on DNA chips.
5  by using these dual-signaling probes on CMS-DNA chips.
6 uencing and high-density variation-detection DNA chips.
7                                              DNA chip analyses show that only a few transcripts are d
8                                              DNA chip analysis of mRNA from IL-1beta-treated and nont
9                                              DNA chip analysis showed that amphoterin-induced gene an
10 48 of these 50 ORFs responded as they did by DNA chip analysis, with magnitudes displaying a correlat
11 ass of fluorescent nucleotide analogues on a DNA chip and a four-color fluorescent scanner.
12 ntegrated the Si nanonet-based sensor into a DNA chip and we have shown that this selective sensor ca
13 ions for the construction of next-generation DNA chips and functional circuits of DNA-based 1D nanost
14 n advanced biotechnological methods, such as DNA chips and protein-protein interaction screens as wel
15 idization of mRNA to oligonucleotide arrays (DNA chip) and by ELISA.
16 r of classes of tumors using the data from a DNA chip, and class prediction, the problem of accuratel
17                  Oligonucleotide arrays, or 'DNA chips', are miniature, parallel analytical devices,
18    Oligonucleotide microarrays, also called "DNA chips," are currently made by a light-directed chemi
19 y indicates that oligonucleotide probe-based DNA chip assays provide a powerful approach to detect sp
20                                              DNA-chip based assays can be a valuable new technology f
21 ation of high-density oligonucleotide array (DNA chip)-based analysis to determine the distant histor
22                  Oligonucleotide microarray (DNA chip)-based hybridization analysis is a promising ne
23                                              DNA chip-based assays may provide a valuable new technol
24                                              DNA chip-based assays should play a valuable role in hig
25 rothioate moieties have broad application in DNA chip-based gene analysis.
26 ing multiexon PCR amplification protocols in DNA chip-based hybridization analysis was devised and im
27 re, I review current strategies and uses for DNA chip-based resequencing and mutational analysis, the
28                                              DNA chips can be directly prepared by synthesizing oligo
29 airs of high density oligonucleotide arrays (DNA chips) consisting of >96 000 oligonucleotides were d
30                   We utilized the GGP HD150K DNA chip containing 139,376 single nucleotide polymorphi
31   The MAS is adaptable to the fabrication of DNA chips containing probes for thousands of genes, as w
32                 Developments in the field of DNA chip design have now made it possible to measure the
33 onstraints, we present a novel gene-specific DNA chip design.
34 uclease-treated chromatin-immunoprecipitated DNA (ChIP-exo).
35 or the first time, the generation of a viral DNA chip for simultaneous expression measurements of nea
36 lity of high-density oligonucleotide arrays (DNA chips) for obtaining sequence information from homol
37           Nevertheless, recent studies using DNA chips have made inroads into the molecular character
38         High density oligonucleotide arrays (DNA chips) have been used in two color mutational analys
39                                 Coupled with DNA chip hybridization using a high-density 60-nucleotid
40 RFC and PCNA together were flowed across the DNA chip in the presence of ATP, a signal was observed s
41 y, and is compatible with current generation DNA chips in which DNA spots are deposited in micro- and
42 n) procedure, where multiple probes are on a DNA chip, in our applications we perform a series of exp
43                  We previously identified by DNA chip interleukin (IL)-27 p28 and transforming growth
44 ase (CAT)-transgenic (Tg) mice were used for DNA chip microarray analysis.
45 ression profiles using oligonucleotide-based DNA chip microarrays representative of approximately 12,
46                                 (iii) Unlike DNA chips or DNA microarrays, no additional instrumentat
47 riety of biomedical applications, such as in DNA chips, protein and cellular microarrays.
48                          DNA microarrays, or DNA chips, provide the means to measure simultaneously w
49 tandard microscope rather than sophisticated DNA chip scanners.
50                                Using in vivo DNA (ChIP-seq) and RNA (CLIP-seq) data, and validating m
51 eq) and immunoprecipitation-enriched genomic DNA (ChIP-Seq) coupled with histone H3 lysine 4 trimethy
52                                         Most DNA chip syntheses have been assayed using in situ coupl
53                                 The complete DNA chip synthesis process is accomplished on a regular
54 racteristics of the commonly utilized planar DNA chip technologies.
55 methoxysilane and the application of this to DNA chip technology are described.
56                                              DNA chip technology enables simultaneous examination of
57                                Microarray or DNA chip technology is revolutionizing biology by empowe
58                       In this study, we used DNA chip technology to systematically identify new progn
59 uggest applications in oligonucleotide array/DNA chip technology when higher hybridisation temperatur
60 ocess, and it is enabling the development of DNA chip technology, which will permit the analysis of g
61 e also been achieved through improvements in DNA chip technology.
62         Host gene expression profiles (using DNA-chip technology) may also provide clues as to the po
63                     Our goal was to create a DNA chip that is as easy, convenient, and inexpensive as
64 it is desirable to have synthesis methods of DNA chips that are highly flexible in sequence design an
65 is of great importance in the development of DNA chips that use the simple concept of the covalent at
66 30 bp in length) that need to be placed on a DNA chip to capture the variation implied by the trainin
67 rmed otic vesicle RNA hybridizations against DNA chips to not only confirm the efficacy of the librar
68                                         This DNA chip was used to study 17 paired tissues of breast t
69                         The thermal gradient DNA chips were then tested for genotyping, and the resul
70                                These 1.0-cm2 DNA "chips" were used to quantitatively monitor differen
71 E as a robust platform for light-addressable DNA chips with high sensitivity and specificity.
72                             DNA microarrays (DNA chips) with species-specific oligonucleotide probes