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1 levels of unamplified and amplified RNA on a cDNA microarray.
2 me database and a large-scale songbird brain cDNA microarray.
3 al neoplasia using a sequence-verified human cDNA microarray.
4 pression data derived from the public tomato cDNA microarray.
5 nal degeneration on a 12,325-feature retinal cDNA microarray.
6 (ES) cells and amplified them to construct a cDNA microarray.
7 er activation of LFY using a flower-specific cDNA microarray.
8 ata sets: two Affymetrix microarrays and one cDNA microarray.
9 cessing streams, we designed a custom ferret cDNA microarray.
10 es that had previously been characterized by cDNA microarray.
11 purge were investigated using a 23 K element cDNA microarray.
12 rential hybridization using mouse tooth germ cDNA microarrays.
13 icle regions were obtained and analyzed with cDNA microarrays.
14 E), 18 BEs, and nine EACs were hybridized to cDNA microarrays.
15 to elevated [CO(2)] were investigated using cDNA microarrays.
16 paired MK and EB cultures and compared using cDNA microarrays.
17 , reverse transcribed, and hybridized to rat cDNA microarrays.
18 racterized genetically by using whole-genome cDNA microarrays.
19 lobal expression patterns was assessed using cDNA microarrays.
20 gy considerably increases the sensitivity of cDNA microarrays.
21 ene expression profiling on mouse Lymphochip cDNA microarrays.
22 sentations (LCRs) of mRNA as the targets for cDNA microarrays.
23 insulin were assessed by endocrine pancreas cDNA microarrays.
24 and hybridized to approximately 42,000 clone cDNA microarrays.
25 liferation genes identified previously using cDNA microarrays.
26 beled DA cells to screen the RIKEN 19k mouse cDNA microarrays.
27 harvested and profiled using 20,000 element cDNA microarrays.
28 occus radiodurans following DNA damage using cDNA microarrays.
29 interrogated by transcriptome profiling with cDNA microarrays.
30 were compared by using canine retinal custom cDNA microarrays.
31 ored at 1, 2, 4, and 6 hours after PHx using cDNA microarrays.
32 4, with an adult sample type (leaf 9) using cDNA microarrays.
33 at in the fellow ONH (n = 6/group), by using cDNA microarrays.
34 ysis typically applied to complementary DNA (cDNA) microarrays.
38 , NR4A3 and NR4A1, was altered by insulin in cDNA microarray analyses of human skeletal muscle, we st
44 Among the down-regulated genes revealed by cDNA microarray analyses, we identified Aurora-A, a cent
52 ferentially expressed genes were detected by cDNA microarray analysis and confirmed by Northern blot
55 t the tumor-bone interface using comparative cDNA microarray analysis and quantitative reverse transc
64 ure of EpCAM-positive HCCs was identified by cDNA microarray analysis of 40 HCC cases and validated b
65 tively down-regulated in MSI-H cancers using cDNA microarray analysis of 41 primary colon cancers.
66 tive lupus glomerulonephritis was studied by cDNA microarray analysis of gene expression in glomeruli
76 n parental cells and sublines by genome-wide cDNA microarray analysis revealed several potential medi
82 expressing a mutant mTOR, we have performed cDNA microarray analysis to compare global gene expressi
85 collected using an in vivo invasion assay to cDNA microarray analysis to identify the gene expression
91 of apoptosis-related genes as determined by cDNA microarray analysis, and increased cellular sensiti
105 clinical biomarker for lung cancer, we used cDNA microarray and 2D protein analyses to demonstrate t
106 . mansoni, was hybridized to the custom made cDNA microarray and 98 differentially expressed genes or
107 of wild-type plants using a flower-specific cDNA microarray and a whole genome oligonucleotide array
108 cancer samples between data sets produced by cDNA microarray and Affymetrix gene-chip platforms.
110 f lncRNAs in human CML cells using an lncRNA cDNA microarray and identified an lncRNA termed lncRNA-B
112 in highly tumorigenic breast cancer cells by cDNA microarray and RNA interference (RNAi) analysis, an
113 ay studies were carried out using 20 K human cDNA microarray and select genes were validated using qu
114 ted to be downregulated in ovarian cancer by cDNA microarray and suppression subtraction cDNA (SSH) a
117 trol cultures by using a custom human retina cDNA microarray and were validated by quantitative real-
120 cytes for gene expression using high-density cDNA microarrays and analyzed T cell subsets, CD4 and CD
121 ression profiling in plants with emphasis on cDNA microarrays and discussion of both experimental des
122 profiles were compared by using genome-wide cDNA microarrays and label-free quantitative proteomics,
125 with the rate of muscle weight loss, we used cDNA microarrays and RT-polymerase chain reaction to ana
126 rat models of glaucoma by using whole genome cDNA microarrays and were further validated by quantitat
127 ession data obtained from complementary DNA (cDNA) microarrays and corresponding DNA copy number vari
129 ated melanoma phenotypes was hybridized to a cDNA microarray, and their signature genes were studied.
130 ferentially expressed genes were analyzed by cDNA microarray, and they were validated by immunohistoc
131 s for Microarray Data (LIMMA) for processing cDNA microarrays, and differential gene expression analy
132 astrointestinal stromal tumors (GISTs) using cDNA microarrays, and found that the gene FLJ10261 (DOG1
134 arried out with oligonucleotide microarrays, cDNA microarrays, and reverse transcription (RT)-PCR ass
138 port here the adaptation and evaluation of a cDNA microarray-based CGH method for the routine charact
148 ith this autopolyploid series using a potato cDNA microarray containing approximately 9000 genes.
150 ve performed gene expression profiling using cDNA microarrays containing 42,578 clones and used artif
152 cimens and nine lymph node metastases, using cDNA microarrays containing approximately 26,000 genes.
153 is indicates that existing data generated by cDNA microarrays containing IMAGE clone ESTs should be f
157 y integrating a database of TRN information, cDNA microarray data analyzers, bioinformatics modules,
158 tant for cancer stem-like cells, we analyzed cDNA microarray data and identified nine pathways that w
164 Evaluation of transcriptional profiles using cDNA microarrays demonstrated that there were similariti
166 lysis of expression data from two single-dye cDNA microarray experiments showed that ESTs whose seque
172 ds and techniques emphasizing fabrication of cDNA microarrays, fluorescent labeling, cDNA hybridizati
176 lor, spotted microarrays was developed using cDNA microarrays from in vivo and in vitro dose-response
177 and measured expression of 40000 genes using cDNA microarrays from the fifty-nine publicly available
178 hydrates, lipids, hormones, various RNAs and cDNAs, microarrays) have been discovered and correlated
179 nscript abundance levels were quantitated by cDNA microarray hybridization and confirmed by quantitat
182 examined by gene expression profiling using cDNA microarray hybridizations, generated from a porcine
184 our methods for gridding and segmentation to cDNA microarray images from an HIV infection experiment.
185 th a Salmonella enterica serovar Typhimurium cDNA microarray in order to identify genes important for
187 ses in the stress-induced ORFs identified by cDNA microarray indicates that helicases might be playin
188 human gliomas of various histogenesis, using cDNA microarrays, inferential and descriptive statistics
190 gs demonstrated that the zebra mussel byssus cDNA microarray is an efficient tool for the studies of
191 e evidence that cross-species application of cDNA microarrays is a useful strategy for investigating
194 comparative genomic hybridization (n = 109), cDNA microarray (n = 76), and tissue array (n = 504).
200 eal clock, and herein we employ high density cDNA microarrays of pineal gland transcripts to determin
202 Based on analyses of two-dimensional gel and cDNA microarrays, our laboratory and others have demonst
205 aluated in trabecular meshwork (TM) cells by cDNA microarray, q-PCR, fluorescence microscopy, and imm
209 zation of CNAs in murine tumors, using mouse cDNA microarrays representing approximately 14,000 diffe
210 in a set of 18 colon cancer cell lines using cDNA microarrays representing approximately 21,000 diffe
211 zation on a set of 24 SCLC cell lines, using cDNA microarrays representing approximately 22,000 human
214 s from these aggregates using a whole genome cDNA microarray revealed the induction of a putative exo
219 nts based on expression technologies such as cDNA microarrays, RNA-Seq, and cell imaging-based assays
220 with various expression technologies such as cDNA microarrays, RNA-Seq, and cell imaging-based assays
222 ty and transparency of the mouse lens, using cDNA microarray, RT-PCR, immunoblot, pharmacological inh
224 d Dickkopf-3, the top candidate genes from a cDNA microarray screen, are differentially expressed in
225 Hrpt2(+/+) and Hrpt2(-/-) MEFs were used in cDNA microarray, semiquantitative reverse transcription-
226 and resident ATMs using real-time RT-PCR and cDNA microarrays showed that recruited ATMs overexpress
230 fying conditions, we conducted whole-genome, cDNA microarray studies to explore this topic systematic
233 ults of an initial cell cycle analysis and a cDNA microarray study showed effects consistent with inh
234 d cultured preadipocytes using an Affymetrix cDNA microarray technique and validated with quantitativ
235 utility of cross-species application of the cDNA microarray technique for investigating differential
240 ling are not completely understood; however, cDNA microarray technology may enable rapid and accurate
241 ression during the PPD response we have used cDNA microarray technology to carry out a large-scale an
242 these clinical manifestations, we first used cDNA microarray technology to measure METH-induced trans
245 m single oocytes and embryos for analysis by cDNA microarray technology, thus lending credence to add
250 dized the RNA from each animal to individual cDNA microarrays that contained more than 100 target gen
251 ous source of error intrinsic to all spotted cDNA microarrays that use IMAGE clones of expressed sequ
253 SS effectors in disease formation, we used a cDNA microarray to analyze the expression of approximate
254 ysis of gene expression in AS using a custom cDNA microarray to compare expression patterns from lymp
256 m patients with melanoma was hybridized to a cDNA microarray to identify lesions with the transcript
259 e used a new "three-genome" maize biogenesis cDNA microarray to track abundance changes in nuclear, c
260 sion signatures of disease progression using cDNA microarrays to analyze RNA from laser-captured micr
262 regulating mutational processes, we used 8K cDNA microarrays to compare the patterns of gene express
263 ns in alphabeta T cells provoked us to apply cDNA microarrays to explore the potential pleiotropy of
264 array comparative genomic hybridization, and cDNA microarrays to gain insights into the structural an
265 ssion in the gastrointestinal tract, we used cDNA microarrays to identify 114 genes with altered leve
272 acute lymphoblastic leukemia (ALL), we used cDNA microarrays to obtain a genome-wide view of gene ex
273 As a second step, we constructed a custom cDNA microarray using a subset of the differentially reg
278 tudy, genome-wide expression profiling using cDNA microarrays was conducted for resistant Hofer and s
285 for E-cadherin and high density (27k) mouse cDNA microarrays, we identified 474 genes that are more
288 o waveforms were applied to cultured EC, and cDNA microarrays were used to analyze the differential p
293 ated primary human skeletal myocytes using a cDNA microarray, which contains 501 mitochondria-related
296 about possible gene function, we hybridized cDNA microarray with probes derived from wild-type Arabi
298 rine gene expression were investigated using cDNA microarrays with complementary physiological and hi
300 rstand the zebra mussel's byssus activity, a cDNA microarray (ZMB) including 716 genes, generated fro
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