ライフサイエンスコーパス: DNA chip

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 The MAS is adaptable to the fabrication of DNA chips containing probes for thousands of genes, as w

31 Developments in the field of DNA chip design have now made it possible to measure the

32 onstraints, we present a novel gene-specific DNA chip design.

33 uclease-treated chromatin-immunoprecipitated DNA (ChIP-exo).

34 or the first time, the generation of a viral DNA chip for simultaneous expression measurements of nea

35 lity of high-density oligonucleotide arrays (DNA chips) for obtaining sequence information from homol

36 Nevertheless, recent studies using DNA chips have made inroads into the molecular character

37 High density oligonucleotide arrays (DNA chips) have been used in two color mutational analys

38 Coupled with DNA chip hybridization using a high-density 60-nucleotid

39 RFC and PCNA together were flowed across the DNA chip in the presence of ATP, a signal was observed s

40 y, and is compatible with current generation DNA chips in which DNA spots are deposited in micro- and

41 n) procedure, where multiple probes are on a DNA chip, in our applications we perform a series of exp

42 We previously identified by DNA chip interleukin (IL)-27 p28 and transforming growth

43 ase (CAT)-transgenic (Tg) mice were used for DNA chip microarray analysis.

44 ression profiles using oligonucleotide-based DNA chip microarrays representative of approximately 12,

45 (iii) Unlike DNA chips or DNA microarrays, no additional instrumentat

46 riety of biomedical applications, such as in DNA chips, protein and cellular microarrays.

47 DNA microarrays, or DNA chips, provide the means to measure simultaneously w

48 tandard microscope rather than sophisticated DNA chip scanners.

49 eq) and immunoprecipitation-enriched genomic DNA (ChIP-Seq) coupled with histone H3 lysine 4 trimethy

50 Most DNA chip syntheses have been assayed using in situ coupl

51 The complete DNA chip synthesis process is accomplished on a regular

52 racteristics of the commonly utilized planar DNA chip technologies.

53 methoxysilane and the application of this to DNA chip technology are described.

54 DNA chip technology enables simultaneous examination of

55 Microarray or DNA chip technology is revolutionizing biology by empowe

56 In this study, we used DNA chip technology to systematically identify new progn

57 uggest applications in oligonucleotide array/DNA chip technology when higher hybridisation temperatur

58 ocess, and it is enabling the development of DNA chip technology, which will permit the analysis of g

59 e also been achieved through improvements in DNA chip technology.

60 Host gene expression profiles (using DNA-chip technology) may also provide clues as to the po

61 Our goal was to create a DNA chip that is as easy, convenient, and inexpensive as

62 it is desirable to have synthesis methods of DNA chips that are highly flexible in sequence design an

63 is of great importance in the development of DNA chips that use the simple concept of the covalent at

64 30 bp in length) that need to be placed on a DNA chip to capture the variation implied by the trainin

65 rmed otic vesicle RNA hybridizations against DNA chips to not only confirm the efficacy of the librar

66 This DNA chip was used to study 17 paired tissues of breast t

67 The thermal gradient DNA chips were then tested for genotyping, and the resul

68 These 1.0-cm2 DNA "chips" were used to quantitatively monitor differen