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1 thin a 3D colonic epithelium using Intestine-Chip technology.
2 de range of myocardial diseases using lab-on-chip technology.
3 development and application of organoid-on-a-chip technology.
4  Stokes flow and the accessibility of lab-on-chip technology.
5 ng two-photon hyperentanglement and photonic-chip technology.
6 s with ImmunoCAP Immuno-solid-phase Allergen Chip technology.
7 drial damage, a unique advantage of organ-on-chip technology.
8 on was resequenced using hybridization-based chip technology.
9 alyses with chromatin immunoprecipitation-on-chip technology.
10 ts on the same chip to produce true lab-on-a-chip technology.
11 to develop a mass-spectrometry-based protein chip technology.
12 lular mRNA accumulation was analyzed by gene chip technology.
13 so been achieved through improvements in DNA chip technology.
14 sts (CFs) within an organotypic microfluidic chip technology.
15 rixes compatible with organoids and organ-on-chip technology.
16 capsulated into liposomes using microfluidic chip technology.
17 ing the PamGene PamStation kinome microarray chip technology.
18 DMF have pushed the barriers of this "lab-on-chip" technology.
19  substrate is essential for realizing lab-on-chip technologies.
20 iniaturized medical diagnostics and lab on a chip technologies.
21 ticated fluid manipulation tools in lab-on-a-chip technologies.
22 as sensing, medical diagnostics and lab-on-a-chip technologies.
23 inities, more suitable for phage-display and chip technologies.
24 eristics of the commonly utilized planar DNA chip technologies.
25 lling, stem cell and microfluidic organ-on-a-chip technologies.
26 ted on-chip, using microfluidic and lab-on-a-chip technologies.
27 that make them promising for nanophotonic on-chip technologies.
28 rking an important step forward for heart-on-chip technologies.
29 ved cardiomyocytes, organoid, and organ-on-a-chip technologies.
30 e credited to chromatin immunoprecipitation (ChIP) technologies.
31 ative functional relevance were genotyped by chip technology (24 polymorphisms) or MALDI-TOF-MS (40 p
32 fields: (1) wireless technology, (2) digital chip technology, (3) hearing science, and (4) cognitive
33                      Microfluidic organ-on-a-chip technology aims to replace animal toxicity testing,
34 n used in conjunction with Ciphergen protein chip technology (also referred to as SELDI-Surface Enhan
35  and using Affymetrix (Santa Clara, CA) gene chip technology, altered gene expression of different en
36 supercapacitors are attractive for system on chip technologies and surface mount devices due to their
37 LDI-ToF) mass spectrometry utilizing protein chip technology and artificial neural networks (ANN).
38 -of-care diagnostics by integrating lab-on-a-chip technology and electrochemical analysis.
39                                              CHIP technology and high-throughput sequencing promise t
40     By use of single-nucleotide-polymorphism chip technology and homozygosity mapping, a common regio
41                           By combining Organ-Chip technology and human iPSC-derived tissue, we have c
42       Such brain-on-a-chip and organoid-on-a-chip technologies are promising platforms for studying t
43 oxysilane and the application of this to DNA chip technology are described.
44            The use of organoids and organ-on-chip technologies as nonanimal methodologies in drug dis
45        In this Review, we explore organ-on-a-chip technology as a platform to fulfill this need and e
46  can potentially allow a multiplexed "QCR-on-chip" technology, bringing a paradigm shift in speed, ac
47 n this review, we discuss how the Organ-on-a-Chip technology can have critical roles in different pre
48                                       Lab-on-Chip technology comprises one of the most promising tech
49 is end, we have evaluated the use of Protein Chip technology, coupled with bioinformatics analysis to
50                                   The lab-on-chip technology described by A. M. Cabibbe et al. potent
51                                          DNA chip technology enables simultaneous examination of how
52          Evolutions in instrument and sensor chip technology, experimental methodology, and data anal
53 gn and validation of a microfluidic Lab-on-a-Chip technology for automation of the zebrafish embryo t
54 l handheld analyzer with disposable lab-on-a-chip technology for the electrical detection of the anes
55 ere next generation-sequenced (semiconductor chip technology) for the MYH7, MYBPC3, TNNT2, TNNI3, ACT
56  rapidly increased compared to semiconductor chip technology, for example.
57                The application of microarray chip technology has led to an explosion of data concerni
58                         Sequencing and exome-chip technologies have motivated development of novel st
59                                     Lab-on-a-chip technologies have the potential to deliver signific
60     Recent genetic approaches including gene chip technology have been used to elucidate the gene exp
61  In this context, microfluidics and lab-on-a-chip technology have emerged as the most promising avenu
62 e review recent developments in 'spores-on-a-chip' technologies, highlighting how they could be explo
63 otechnology, microfluidics and laboratory-on-chip technology in advancing the field.
64                            Microarray or DNA chip technology is revolutionizing biology by empowering
65                                         Gene chip technology is still a relatively new technology, an
66 rotein kinases and demonstrates that protein chip technology is useful for high-throughput screening
67                With the advent of microarray chip technology, large data sets are emerging containing
68     Host gene expression profiles (using DNA-chip technology) may also provide clues as to the possib
69 system referred to as nano fraction analysis chip technology (nanoFACT) is reported.
70                    Microfluidics or lab-on-a-chip technology offer clear advantages over conventional
71                                      Protein chip technology permits analysis of the expression and m
72         Using chromatin immunoprecipitation (ChIP) technologies, protein-DNA interactions are routine
73                          Microarray and gene chip technology provide high throughput tools for measur
74 lumes are determined using compact sensor-on-chip technology, retrieved in a digital format, and stor
75 iposomes and lipid-based nanoparticles by on-chip technologies that are applicable in a laboratory an
76            We have developed a novel protein chip technology that allows the high-throughput analysis
77 ethod offers an improved approach to protein chip technology that should prove useful for diagnostics
78   Here we describe, with the use of proteome chip technology, the in vitro substrates recognized by m
79                  The McMOA exploits lab-on-a-chip technologies to fully integrate complex autonomous
80 his scientific issue through the use of gene chip technology to identify clock-regulated genes in an
81                 We have used Affymetrix gene chip technology to look for changes in gene expression c
82                   In this study, we used DNA chip technology to systematically identify new prognosti
83     Here, we unite organoids with organ-on-a-chip technology to unravel disease pathology and develop
84    Here, we combined organoids and Organs-on-Chips technology to create a human Duodenum Intestine-Ch
85              Here we leveraged the Organs-on-Chips technology to develop a human Brain-Chip represent
86                           We applied Protein Chip technology toward discovery of allograft response m
87           We imagine a future where lab-on-a-chip technologies utilize novel predictive markers of RB
88                  Metagene analysis with gene chip technology was performed on 326 CRCs, which were th
89                      Microfluidic organ-on-a-chip technology was used to assess for detachment of pod
90 ometry in conjunction with Ciphergen protein chip technology we have used relative importance values,
91 sive materials and the microfluidic lab-on-a-chip technology, we also present the stimuli-responsive
92                                  Using Organ-Chip technology, we created an entirely human BBB-Chip w
93                        Using Affymetrix gene chip technology, we first identified that PGF2alpha dram
94                        By means of a protein-chip technology, we identified a cluster of proteins tha
95                                   Using gene chip technology, we isolated a murine gene, designated T
96 st applications in oligonucleotide array/DNA chip technology when higher hybridisation temperatures a
97 s, and it is enabling the development of DNA chip technology, which will permit the analysis of gene
98         It is hoped that application of gene chip technologies will address the global profile of van
99 spread interest in combining laboratory-on-a-chip technologies with mass spectrometry (MS)-based anal
100 ectrospun fibers by integrating microfluidic chip technology with a micro-sol oriented electrospinnin
101  we compare a patch-clamp robot using planar-chip technology with human patch-clamp in a functional a

 
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