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1 y use of the same platform (Affymetrix U133A GeneChip).
2 in Todd-Hewitt broth and a custom Affymetrix GeneChip.
3 d using the Affymetrix Mouse Genome 430 v2.0 GeneChip.
4 analysis was performed using Affymetrix U95 GeneChip.
5 profiles were analysed on Affymetrix Hu133A GeneChip.
6 -wide expression profiling is the Affymetrix GeneChip.
7 trix Arabidopsis (Arabidopsis thaliana) ATH1 GeneChip.
8 ysis utilizing the match/mismatch feature of GeneChip.
9 xpression profiling on Affymetrix 430A mouse GeneChips.
10 , a model of X-linked EDMD, using Affymetrix GeneChips.
11 r population were genotyped using Affymetrix GeneChips.
12 es by using Affymetrix HG-U133A and HG-U133B GeneChips.
13 nd labeling strategy for use with Affymetrix GeneChips.
14 trains was not tiled as a reference in these GeneChips.
15 gnal response to concentration of Affymetrix GeneChips.
16 time points using custom B. thetaiotaomicron GeneChips.
17 rhd2-1, were compared using Affymetrix ATH1 GeneChips.
18 cortex and hybridized to Affymetrix HG-U133A GeneChips.
19 iptional units not represented on Affymetrix GeneChips.
20 hage activation measured by using Affymetrix GeneChips.
21 th monosomy 7 and trisomy 8 using Affymetrix GeneChips.
22 which then was used to hybridize Affymetrix GeneChips.
23 ided insights for the analysis of Affymetrix GeneChips.
24 as assessed with Affymetrix HG-U133 Plus 2.0 GeneChips.
25 nome-wide association study using Affymetrix GeneChip 100K arrays was performed in a discovery cohort
26 rspective of ancestry, we analyze Affymetrix GeneChip 500K genotype data from African Americans (n =
32 Expressional profiling was done using U133A GeneChip (Affymetrix), which represent approximately two
35 re generated with a gene microarray (rat U34 GeneChips; Affymetrix, Santa Clara, CA) and compared to
39 with both single mutants in combination with GeneChip analyses identified a posttranscriptional defec
47 rica serovar Typhimurium, Affymetrix porcine GeneChip analysis of pig mesenteric lymph nodes was used
58 gonucleotide Affymetrix Mouse Genome 430 2.0 GeneChip and a spotted cDNA array using a mouse model of
60 ene expression profiles were evaluated using GeneChip and confirmed by real-time PCR, and chemokine c
64 ncer (CaP) patients (n=114; 228 specimen) by GeneChip and quantitative real-time RT-PCR, identifies E
66 data set using the Human HG_U133A Affymetrix GeneChip and RMA normalization there is significant bias
69 es were determined using Affymetrix MGU74Av2 GeneChips and confirmed by real-time polymerase chain re
71 (CTLs) was analyzed using Affymetrix 430 2.0 GeneChips and quantitative polymerase chain reaction (PC
72 Yale, (ii) commercially available Affymetrix GeneChips and spotted arrays and (iii) custom arrays mad
73 ow UPEC adapts to life in IBCs, we have used GeneChips and/or quantitative reverse transcriptase PCR
78 ld-type TIP30 or mutant TIP30, by Affymetrix GeneChip array, real-time quantitative PCR, and Western
79 Using the Affymetrix murine genome U74Av2 GeneChip array, we observed >100 candidate genes having
85 ained from SAGE and EST data with those from GeneChip arrays showed that the consistency of the two p
86 reactive astrocyte state, we used Affymetrix GeneChip arrays to profile gene expression in population
88 ssion profiles using whole genome Affymetrix GeneChip arrays, we found that 83 genes were induced mor
89 between different generations of Affymetrix GeneChip arrays, we propose a method of filtering probes
94 terature, thus validating the R. sphaeroides genechip as a powerful and reliable tool for studying un
99 em; one method, adapted from similar work on GeneChip brand microarrays, is based on modeling array s
100 probe level data from the popular Affymetrix GeneChips, but it is difficult to identify the best meth
101 determined from this array and an Affymetrix GeneChip, by quantitative RT-PCR, and by spiking known a
106 sources to a high-density custom Affymetrix GeneChip containing all open reading frames (ORFs) of th
108 in cold acclimation, we used the Affymetrix GeneChip containing probe sets for approximately 24,000
109 ble and that the smallpox virus resequencing GeneChips could differentiate the 14 smallpox virus stra
110 g cDNA cloning, Affymetrix (Santa Clara, CA) genechips covering all the mouse olfactory receptor gene
112 ach GEM and SFP marker were ascertained with GeneChip data from parental accessions as well as RILs;
113 icroarray hybridization theory to Affymetrix GeneChip data has been a recent focus for data analysts.
114 These findings may be generally applicable: GeneChip data sets from 471 human neoplasms revealed tha
116 ments, we sought to characterize features of GeneChip data to better compare and evaluate analyses fo
122 ic NE tumors and cell lines, and analysis of GeneChip datasets of human NE tumors with good or poor p
124 usion experiments and seed mRNA localization GeneChip datasets showed that the seed-specific TF genes
126 oarray analyses using the Affymetrix soybean GeneChip directly compared Peking syncytia undergoing a
129 the mistargeted probes was confirmed in two GeneChip experiments, in which these probes showed a 20-
132 amental quantitative differences, Affymetrix GeneChip expression arrays were used to compare murine l
135 two types of genetic markers from Affymetrix GeneChip expression data to generate detailed haplotypes
140 cently developed a set of seven resequencing GeneChips for the rapid sequencing of Variola virus stra
141 g rhesus monkey gene microarrays (Affymetrix GeneChip), further corroborated the histological finding
142 ssion in two muscle types was analyzed using GeneChip Gene 1.0 ST arrays: biceps, which typically sho
143 trix has recently developed whole-transcript GeneChips-'Gene' and 'Exon' arrays-which interrogate exo
144 nd the subsequent availability of Affymetrix GeneChip genome arrays, several laboratories have survey
146 also suggests that high-density resequencing GeneChips have potential biodefense applications and may
148 ed gene expression changes, using Affymetrix GeneChips (HG-U133A), of infected primary human cells an
151 termined by Gene Logic Inc. using Affymetrix GeneChip HU_95 arrays containing approximately 12,000 kn
152 evaluation of performance between Affymetrix GeneChip Human 133A cartridge and plate arrays with an e
153 orthwest Spain) samples using the Affymetrix GeneChip Human 20k cSNP Kit, followed by a replication s
164 in, and gene expression using the Affymetrix GeneChip Human Mapping 500K (n = 30 cases) and Human U13
165 th studies was performed with the use of the GeneChip Human Mapping 500K Array Set (Affymetrix).
166 mal human brain samples using the Affymetrix GeneChip Human Mapping 500K Array Set and Illumina Human
168 dentified by genotyping, with the Affymetrix GeneChip Human Mapping 500K array, a population sample w
169 compared between groups using the Affymetrix GeneChip hybridization protocol and hierarchical cluster
170 e we report the use of a custom B. anthracis GeneChip in defining the gene expression patterns that o
171 We evaluated the diagnostic performance of GeneChip in detecting resistance to rifampin (RMP) and i
175 f involvement of an entire pathway using the GeneChip included genes involved in the ubiquitin protea
176 rganized probes on more than a dozen popular GeneChips into gene-, transcript- and exon-specific prob
177 p in the analysis of experiments using these GeneChips is to summarize each of these probe sets into
178 ated RNA can be used directly for Affymetrix GeneChip labeling or real-time RT-PCR without further pu
179 tending the SNP-MaP method to the Affymetrix GeneChip Mapping 100K Array set provides a useful screen
181 hole-genome linkage analysis with Affymetrix GeneChip Mapping 10K Array defined a 7-Mb critical regio
184 enome-wide linkage analysis using Affymetrix GeneChip Mapping 10K data from 12 affected members of th
185 Genome-wide linkage analysis with Affymetrix GeneChip Mapping 10K mapping data from 13 members of thi
186 we can also now accept data from Affymetrix GeneChips (MAS5/GCOS or dChip), Agilent Catalog or Custo
189 g these pathologies, we performed Affymetrix GeneChip microarray analysis of 1-, 3-, and 6-month-old
190 vestigated the pathways regulated by MyoD by GeneChip microarray analysis of gene expression in wild-
192 te-related genes was investigated using both genechip microarray and real-time PCR (qPCR) molecular t
199 del species Arabidopsis by using Arabidopsis GeneChip microarrays for whole-genome transcript profili
208 9 matched controls using both the Affymetrix GeneChip miRNA 2.0 and Human Exon 1.0 ST Arrays to furth
209 sion profiling was performed with Affymetrix GeneChip miRNA 3.0 arrays; and results were validated wi
212 samples were hybridized to microarray chips (GeneChip Mouse Genome 430 2.0; Affymetrix, Santa Clara,
214 eward) was determined using Affymetrix wheat GeneChip oligonucleotide arrays which have probes for 55
216 fferentially expressed genes generated using Genechip Operating System (GCOS) or modified PM-only met
217 that is either specific at the level of the GeneChip or up-regulated with respect to genes active at
220 gene expression by a high-density Affymetrix GeneChip platform, encompassing more than 1 million geno
221 EL files relating to 10 different Affymetrix GeneChip platforms and involving nearly 1000 experiments
224 xamined the effect of the SNPs on Affymetrix GeneChip probe set summaries and the expression quantita
225 orresponded with results from representative GeneChip probesets, and showed similar effects of sex st
226 d the procedure to 507 Affymetrix microarray GeneChips processed with RNA from human peripheral blood
228 ction of Arabidopsis thaliana stamen AZs and GeneChip profiling to reveal the AZ transcriptome respon
232 for gene expression microarrays, Affymetrix GeneChip(R) arrays, have as many as ten or more probe se
235 rodent pineal transcriptome using Affymetrix GeneChip(R) technology to obtain a more complete descrip
236 pose a new filtering strategy for Affymetrix GeneChips(R), based on principal component analysis of p
240 and ERBB2 mRNA as measured by the Affymetrix GeneChip reliably and reproducibly establish oestrogen-r
242 gh-density oligonucleotide DNA microarray, a genechip, representing the 4.6-Mb genome of the facultat
244 Analysis of the data indicated that the GeneChip resequencing by hybridization was fast and repr
251 pression profiles in hearts using Affymetrix GeneChips showed statistically significant differences i
253 he design of the smallpox virus resequencing GeneChips; similar information for the remaining strains
256 ts application on two independent Affymetrix GeneChip studies that compared the gene expression of bi
266 sion profiles generated using the Affymetrix GeneChips technology were originally developed for a rat
268 l Genomics Resource Center and an Affymetrix GeneChip that collectively represent the genomes of all
270 We analysed, with Affymetrix Human U133a GeneChips, the expression of 22000 transcripts from tota
271 etwork of Bacillus subtilis using Affymetrix GeneChip time-series data and show how the inferred netw
272 ne-mediated defense, we used the 22K Barley1 GeneChip to compare and contrast time-course expression
274 utrient sensing, we used B. thetaiotaomicron GeneChips to characterize their expression in gnotobioti
275 trolled by FNR, we used Affymetrix Antisense GeneChips to compare global gene expression profiles fro
276 s from this bioassay using Affymetrix U74Av2 GeneChips to determine gene expression changes associate
277 ng those unique to seeds, we used Affymetrix GeneChips to profile Arabidopsis genes active in seeds f
278 A was processed and hybridized to Affymetrix GeneChips, to determine expression of over 47,000 transc
281 transcriptome analysis using the Affymetrix GeneChip U133A in gastric cardia adenocarcinomas (n = 62
283 iles of 21 JPAs, determined using Affymetrix GeneChip U133A, were compared with subjects with normal
285 ys (HDONAs), such as the Affymetrix HG-U133A GeneChip, use sets of probes chosen to match specified g
288 normalized data sets generated on Affymetrix GeneChips were analyzed using Significance Analysis of M
290 In the current study, Affymetrix S. aureus GeneChips were used to define transcriptome changes in r
291 ize the AlgR regulon, Pseudomonas Affymetrix GeneChips were used to generate the transcriptional prof
293 to characterizing these processes, S. aureus GeneChips were used to simultaneously determine the mRNA
295 s after CPT treatment using Affymetrix U133A GeneChips, which include all annotated human genes (22,2
297 development, we designed a custom Affymetrix GeneChip with the complete S. meliloti genome and approx
298 this study, we attempted to hybridize these GeneChips with some known non-Variola orthopoxvirus isol
299 present on the Affymetrix Rat Toxicology U34 GeneChip, with a focus on how the gene products relate t
300 ile data are derived using heterologous rice GeneChips, with about half of the total rice gene set, t
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