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1 bridized to all but two of the probes in the cDNA array.
2 op designed microarray experiment using a 4k-cDNA array.
3 bridization intensities of the probes on the cDNA arrays.
4 ive study of gene expression utilizing human cDNA arrays.
5 f false positives with radioactively-labeled cDNA arrays.
6 of differential display and high-sensitivity cDNA arrays.
7  weeks using high-density nylon filter-based cDNA arrays.
8 ese, seven were positive by hybridization to cDNA arrays.
9 hese astrocytes were examined with Atlas rat cDNA arrays.
10 lot analysis on 120 selected mRNAs on custom cDNA arrays.
11 pression of over 120 genes, as identified by cDNA arrays.
12 rom these fractions were used to interrogate cDNA arrays.
13 enerate probes for differential screening of cDNA arrays.
14 sing chromatin immunoprecipitation linked to cDNA arrays.
15  risk, LCM-LA RNA from ACF was hybridized to cDNA arrays.
16 n gene expression levels were analyzed using cDNA arrays.
17 nt transcripts, which can now be detected on cDNA arrays.
18 ion of distinct subsets of mRNAs detected by cDNA arrays.
19 eveloping wheat caryopses was analyzed using cDNA arrays.
20 with those obtained using complementary DNA (cDNA) arrays.
21 an cells and genomic profiling by array-CGH (cDNA arrays, 100 kb resolution) and by real-time PCR (si
22 f each sample were then hybridized with 5760 cDNA arrays (5289 unique cDNA sequences) printed on indi
23 r of technical replicates for Affymetrix and cDNA arrays, achieving variance stabilization can be dif
24 ts obtained by quantitative real-time PCR or cDNA array analyses by using a total of 43 lung tumor an
25                                      Lastly, cDNA array analyses indicate that several hematopoietic
26                                              cDNA array analyses revealed that alterations in gene ex
27 ne expression were determined by comparative cDNA array analyses, and the approach was validated by i
28                                              cDNA array analyses, together with real time PCR, reveal
29 y extracellular matrix and adhesion molecule cDNA array analysis and confirmed by real-time quantitat
30 n examined patterns of gene expression using cDNA array analysis and Restriction Landmark Genomic Sca
31 ne in lung, FIZZ1/RELMalpha, first through a cDNA array analysis and then confirmed by RT-PCR.
32                                   Subsequent cDNA array analysis confirmed multiple PI3K-AKT pathway
33                                        Using cDNA array analysis for differential gene expression, we
34                                              cDNA array analysis further revealed that genes ontologi
35 at evaluation of mRNA expression profiles by cDNA array analysis is a powerful approach to characteri
36 utions to gene expression are assessed using cDNA array analysis of an en masse nuclear run-on assay
37                            We previously did cDNA array analysis of LGD1069-treated breast cells usin
38                                              cDNA array analysis of Mac-1-clustered compared with -no
39  downstream targets, we performed Affymetrix cDNA array analysis of Monc-1 cells and identified a gen
40                                              cDNA array analysis of RNA from cells overproducing the
41                                              cDNA array analysis of the polyribosome fraction demonst
42 ination of laser capture microdissection and cDNA array analysis provides a powerful new tool to unra
43                                              cDNA array analysis showed that eugenol caused deregulat
44 ting a set of genes previously determined by cDNA array analysis to be rapidly up-regulated by LAQ824
45 ntisense RNA amplification was combined with cDNA array analysis to examine effects of aging on D1-D5
46                    We then used differential cDNA array analysis to investigate the molecular changes
47 racted sufficient total RNA (3-6 microg) for cDNA array analysis using HgU95-Av2 GeneChip.
48  total RNA (3 to 6 microg) was extracted for cDNA array analysis using the Affymetrix HgU95-Av2 GeneC
49                                              cDNA array analysis was used to identify large-scale cha
50                                           By cDNA array analysis, 334 of 4132 genes studied were expr
51                                           By cDNA array analysis, ADAMTS8, ECM1, MMP8, PLAU, SELP, an
52 To test these ideas, we have made use of the cDNA array analysis, which can provide a more global vie
53 xpression of the subset of genes examined by cDNA array analysis.
54 (d) gene expression changes as determined by cDNA array analysis.
55 ion methodology coupled with custom-designed cDNA array analysis.
56 hemistry, RT-PCR, and membrane-based focused cDNA array analysis.
57  levels of HNF6 targets in the liver using a cDNA array and found that their expression was similar i
58                                We screened a cDNA array and identified the bCL2 family member A1/BFL1
59                                              cDNA array and immunoblot analysis of gene expression re
60                                   We show by cDNA array and immunohistochemical analysis that EGF, EG
61  expression was examined 2 hours later using cDNA array and reverse transcriptase-polymerase chain re
62  and high-throughput screening methods using cDNA array and tissue microarray (TMA) technology, there
63                                              cDNA array and tumor microarray analysis shows that mRNA
64 red with the PC-3 low invasive cells through cDNA array and Western blot analyses.
65 ith FKN mRNA being subsequently evaluated by cDNA array and/or RT-PCR and FKN protein by enzyme-linke
66 is of PREX1 mRNA expression in breast cancer cDNA arrays and a METABRIC cohort revealed that higher P
67 resultant upregulated genes were screened by cDNA arrays and confirmed by quantitative real-time poly
68 istical methods that have been developed for cDNA arrays and describe how the methods can be directly
69 onchoalveolar lavage cells with high density cDNA arrays and found that CXCR4 mRNA is increased in pa
70                                        Using cDNA arrays and quantitative PCR, we discovered nine gen
71                                  Using human cDNA arrays and ribonuclease (RNase) protection assays,
72                Differential hybridization of cDNA arrays and RNase protection studies determined that
73 essed in ovarian cancer through studies with cDNA arrays and serial analysis of gene expression.
74 lysis of human RCC tumor tissue microarrays, cDNA arrays and tumor biopsy samples demonstrated V2R ex
75 is accompanied by up-regulation of A1 on the cDNA array, and this up-regulation was confirmed by semi
76 ed RNA from isolated microglia with relevant cDNA arrays, and identified approximately 30 transcripts
77                               By using human cDNA arrays, approximately 2,000 putatively differential
78                                        Since cDNA arrays are being increasingly used to rapidly disti
79                   Here, expression data from cDNA arrays are ranked and curve-fitted.
80                                          The cDNA array-based approach described here can be applied
81                                              cDNA array-based approaches to assess the stability and
82  traits, we have extended the application of cDNA array-based comparative genomic hybridization (aCGH
83 llular genes influenced by LANA, we employed cDNA array-based expression profiling.
84 hip, Affymetrix) with a laboratory-developed cDNA array by assaying test RNA samples from an experime
85              We have expanded the utility of cDNA arrays by using them to assist in elucidating combi
86 ndicate that studies of gene expression with cDNA arrays can aid the discovery of leukemia markers.
87                 Our results demonstrate that cDNA arrays can be effectively used to identify new diag
88 mparative genomic hybridization performed on cDNA arrays (cDNA aCGH) is a common method to investigat
89  the progression of breast carcinoma, we did cDNA array comparative genomic hybridization (CGH) on a
90 n profiles were also generated using a mouse cDNA array composed of 4000 elements representing known
91                     These were hybridized to cDNA arrays comprising 268 genes and exposed to x-ray fi
92 ression analysis was performed using a novel cDNA array consisting of 277 genes functionally associat
93 anges associated with AMPH toxicity, we used cDNA arrays consisting of 1176 genes to detect different
94 of macaque aorta and vena cava media using a cDNA array containing 4048 known human genes, approximat
95 mplified, [33]P-labeled, and hybridized to a cDNA array containing 4325 known genes.
96  of ARE-mediated mRNA turnover with a custom cDNA array containing probes for 950 ARE mRNAs.
97 AML vs normal probes were then hybridized to cDNA arrays containing genes related to cancer and apopt
98 n reading frames (ORFs) and also constructed cDNA arrays containing probes designed to detect all kno
99 ation function that improves the accuracy of cDNA array data.
100                      Our previously reported cDNA array datasets from neonatal wild-type and Cx43-/-
101                                              cDNA array detected 76.9% of the differentially expresse
102 isplay (DD) to detect global differences and cDNA arrays enriched for cancer-associated genes using m
103  to normal pancreatic tissue in our previous cDNA array experiments prompted us to look in more detai
104                                              cDNA array expression analysis of known genes identified
105 all, these data support the effectiveness of cDNA array expression profiling to investigate the pleio
106 be revealed through analysis of differential cDNA array expression.
107 xpression, we have constructed a specialized cDNA array for the study of ovarian cancer.
108          Clonal populations were analyzed by cDNA array gene expression analysis, which showed differ
109                 We apply the method to Atlas cDNA arrays, GeneFilters, and Affymetrix GeneChip.
110  chain reaction (RAP-PCR) fingerprinting and cDNA arrays (here termed "RAP-array") to identify genes
111 pression was detected in many tumor types by cDNA array hybridization analysis, and TWEAK protein exp
112 GSE-induced drug resistance were analyzed by cDNA array hybridization and reverse transcription-PCR.
113                                              cDNA array hybridization showed that p21 expression sele
114 s of different origin and p53 status using a cDNA array hybridization technique.
115                  In this study, we have used cDNA array hybridization to identify genes regulated by
116                                        Using cDNA array hybridization, the expression profiles of the
117 human dermal endothelial cells (HDMEC) using cDNA array hybridization.
118 levels of gene expression as observed in the cDNA array hybridization.
119  lines were simultaneously monitored using a cDNA array hybridization.
120 n of their expression could be made from the cDNA array hybridization.
121 nd HuR-bound target mRNAs were identified by cDNA array hybridization.
122 of several differentially expressed genes in cDNA array (I-kappaB, VCAM-1 and MIP-3) were further con
123 of 1200 selected mouse genes using the Atlas cDNA array in highly purified hematopoietic stem cells (
124                        In this study we used cDNA arrays in an attempt to identify genes that exhibit
125                 Comparative hybridization of cDNA arrays is a powerful tool for the measurement of di
126 onal difference analysis (RDA) combined with cDNA arrays is an effective approach to identify differe
127 ial cells (HBMECs) by using a human cytokine cDNA array kit.
128 rrayed collections of genome-scale siRNA and cDNA arrayed libraries enable the comprehensive global a
129 alysis of mRNA expression data obtained from cDNA array methods.
130 ser capture microdissection and high density cDNA arrays now provides a unique opportunity to generat
131 c cell lines and in primary AML blasts using cDNA arrays, oligonucleotide arrays and real-time revers
132 ession were assessed by using 4,146 cellular cDNAs arrayed on nitrocellulose filters and real-time re
133 han one method (U133 oligonucleotide arrays, cDNA arrays or serial analysis of gene expression), and
134 problem through development of a three-color cDNA array platform whereby printed probes are tagged wi
135 ntical reference RNA source to a custom-made cDNA array platform.
136  125) genes evaluated on the custom-designed cDNA array platform.
137 icroarray platforms, oligonucleotide arrays, cDNA arrays printed on glass slides and cDNA arrays prin
138 ays, cDNA arrays printed on glass slides and cDNA arrays printed on nylon membranes.
139                                   Multimeric cDNA arrays probably arise during chromosomal break repa
140 f both Affymetrix and printed 75mer oligomer cDNA arrays produced from the same samples provides an o
141                                Assessment of cDNA array profiles should further help us to design a w
142                                              cDNA array profiling demonstrated clustering with sporad
143  2 hours posthepatectomy was examined with a cDNA array representing 588 highly regulated mouse genes
144                                      We used cDNA arrays representing 588 genes to investigate the ro
145                                          The cDNA array results were confirmed by Northern and Wester
146 on of a large number of genes displayed on a cDNA array revealed that significant changes in gene exp
147     In addition, regular mRNA profiling with cDNA arrays revealed correlations between mRNA and H3K9m
148 d comparative genomic hybridization (CGH) to cDNA arrays revealed specific somatic genetic alteration
149                             Interrogation of cDNA arrays revealed that platelet-derived mRNAs are pri
150                                 High density cDNA array screening of colon, lung, and breast cancer c
151  DISH genes were also evaluated by microchip cDNA array screening.
152 m our serial analysis of gene expression and cDNA array studies for their relevance to ovarian cancer
153 cible, robust, and cost-effective customized cDNA array system based on established nylon membrane te
154 oding the cell cycle protein p55Cdc by using cDNA array technique.
155 00 human genes were analyzed and compared by cDNA array techniques.
156 g PCR-selected subtractive hybridization and cDNA array techniques.
157 g PCR-selected subtractive hybridization and cDNA array techniques.
158                                              cDNA array technology has proven to be a powerful way to
159 ssion in three glioblastoma cell lines using cDNA array technology in which the expression of 588 cel
160                                 We have used cDNA array technology to characterize the differences in
161  out a gene expression profiling study using cDNA array technology with 24 primary glioma tissues of
162 hen gene expression was analyzed on a custom cDNA array that contained 2304 known genes, infection wi
163 sly identified a small number of genes using cDNA arrays that accurately diagnosed patients with Seza
164                                  We prepared cDNA arrays that are specifically enriched for genes exp
165                                  Using human cDNA arrays that contained 41,126 cDNAs, corresponding t
166 ith an average insert size of 34 kbp against cDNA arrays, the density of previously characterized exp
167                              The use of this cDNA array to analyze RAP-PCR fingerprints allowed for a
168  of human tumor using Atlas human cancer 1.2 cDNA array to analyze the expression profile of 1187 tum
169 urvival molecule, midkine, was identified by cDNA array to be expressed only in drug-resistant cells.
170 re first analyzed using an erythroid-focused cDNA array to define steady-state transcription levels.
171 the parent cell line SKOV-3, was analyzed by cDNA array to evaluate transcript expression profiles.
172 rly events in lung carcinogenesis, we used a cDNA array to screen for genes that are expressed differ
173 approach that extends the current utility of cDNA arrays to allow the evaluation of the relative role
174 ort, we have tested the feasibility of using cDNA arrays to compare the global changes in expression
175 nscribed, labeled, and used to hybridize 10K cDNA arrays to determine biomarkers for confluence state
176                                     By using cDNA arrays to examine global p53-dependent gene express
177                                Here, we used cDNA arrays to examine transcript profiles in Medicago t
178                Here, we used pathway-focused cDNA arrays to identify additional T. gondii-regulated t
179        In this paper, we describe the use of cDNA arrays to identify subsets of mRNAs contained in en
180 nt of research has been devoted to two-color cDNA arrays to improve experimental design, normalizatio
181                                      We used cDNA arrays to investigate differentially expressed gene
182                                 We have used cDNA arrays to investigate gene expression patterns in p
183              This study has used large-scale cDNA arrays to monitor changes in gene expression patter
184             Using the Atlas Human Cancer 1.2 cDNA arrays to quantitate gene expression in the 31 tumo
185                                We used Atlas cDNA arrays to study gene expression profiles after ER a
186  Mouse Genome 430 2.0 GeneChip and a spotted cDNA array using a mouse model of angiotensin II-induced
187 l problem, we constructed a new multiprimate cDNA array using probes from human, chimpanzee, oranguta
188                             Hybridization of cDNA arrays using RNA from each fraction revealed a subs
189            Some types of microarray, such as cDNA arrays, usually contain a considerable portion of m
190                       The bias observed with cDNA arrays was predictable for fold-changes <250-fold b
191 e bacteria, hybrid selection on high density cDNA arrays was used to characterize the mRNA expression
192  RNA expression changes profiled on the same cDNA array, we detected very little consistent contribut
193       With the use of the Clontech Atlas Rat cDNA Array, we further discovered that the gene expressi
194                 Using a matched normal/tumor cDNA array, we identified a reduced expression of BCCIP
195 ranscription and mRNA amplification to probe cDNA arrays, we found that neurotrophin-3 (NT3) and trkB
196                        In this report, using cDNA arrays, we have examined the changes in gene expres
197 AMH expression profiles obtained by SAGE and cDNA arrays, we observed numerous quantitative discrepan
198                           Using high-density cDNA arrays, we profiled gene expression of small cell l
199                                          The cDNA arrays were hybridized with fluorescent labeled pro
200 fold-change measurements generated by custom cDNA arrays were more accurate than those obtained by co
201                                              cDNA arrays were used to examine gene induction in CALU-
202                                              cDNA arrays were used to identify p53-responsive genes f
203                              Here, we used a cDNA array with 9240 clones relevant to cancer biology a
204                           Using Atlas cancer cDNA arrays with 588 cancer-related genes, we describe g
205 he virtues of probing commercially available cDNA arrays with either radiolabeled cDNA pools or radio
206 erns by interrogating commercially available cDNA arrays with labeled target cDNA prepared from poole
207  were used for comparative hybridizations to cDNA arrays with pooled mRNA from normal cells.

 
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