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1 human blood basophils in whole-transcriptome microarray analyses.
2 inhibitory genes, as revealed by genome-wide microarray analyses.
3 r PARG in MCF-7 cells followed by expression microarray analyses.
4 h early OA and normal controls in 2 separate microarray analyses.
5 e bone microarchitecture and extract RNA for microarray analyses.
6 nisms, C/EBPalpha targets were identified by microarray analyses.
7 ease-associated mutations were identified by microarray analyses.
8 er, real-time reverse transcription-PCR, and microarray analyses.
9 d on expression of neuronal markers and cRNA microarray analyses.
10 ia to profile gene expression patterns using microarray analyses.
11 rum sensing are prominently displayed in our microarray analyses.
12 gene transcription profiles were studied by microarray analyses.
13 ve expression in reciprocal hybrids based on microarray analyses.
14 for 1, 4, 24, 48, and 72 h using large scale microarray analyses.
15 RNAs containing AREs were assessed by custom microarray analyses.
16 gene expression changes were compared using microarray analyses.
17 and capture many changes not observed by DNA microarray analyses.
18 ed by helminth-specific immune responses and microarray analyses.
19 analyzed and also used in complementary DNA microarray analyses.
20 , compared with non-tumor tissues, in tissue microarray analyses.
21 s were assessed by using whole transcriptome microarray analyses.
22 nd then subjected to miRNA and messenger RNA microarray analyses.
23 ed from the 3 groups of Ts cells and used in microarray analyses.
24 amplification of cDNA ends (RACE), and tiled microarray analyses.
26 odel of heterotopic heart transplantation by microarray analyses and a unique profile was detected in
28 CD8+ T cells in vitro were determined by DNA microarray analyses and confirmed by RT-PCR analyses and
31 antibody co-immunoprecipitation, followed by microarray analyses and downstream bioinformatics, 'RIP-
32 -regulated transcriptome via gene expression microarray analyses and ER ChIP-Seq, and to examine resp
33 with type 2 diabetes and control subjects by microarray analyses and found significant differences in
36 ng whole-exome sequencing and/or chromosomal microarray analyses and/or direct Sanger sequencing.
37 tail these Hoxa1(-/-) ES cells by performing microarray analyses, and by this technique we have ident
38 ent of larger sample collections, chromosome microarray analyses, and high-throughput sequencing.
39 prostate cancer relevant gene signatures in microarray analyses, and inhibited growth of ERG-positiv
40 he power of distributed computing to perform microarray analyses, and provides seamless access to res
41 global transcription patterns determined by microarray analyses, and the implications of the D39 gen
42 l subjects was interpreted to be "normal" by microarray analyses, and their rearrangements would not
43 lax treatment with death pathway inhibition, microarray analyses, and/or electron microscopy indicate
44 obulin reactivity data obtained from protein microarray analyses; and (ii) known protective antigens
47 s of BAHD genes by "in silico" northern- and microarray-analyses based on public databases, and by RT
49 ated genes are not identified in traditional microarray analyses, but may theoretically be closely fu
50 le describes methods to improve the power of microarray analyses by defining internal standards to ch
52 Protease- and protease inhibitor-specific microarray analyses (CLIP-CHIP) of laser-dissected leuko
66 and following temperature-shift, comparative microarray analyses demonstrated unequivocally that RpoS
67 tions of miR-301a to GALNT13 corroborated by microarray analyses demonstrating an inverse correlation
69 isomeric oligosaccharides and demonstrate by microarray analyses distinct binding activities of antib
73 d after 7 to 14 days of therapy was used for microarray analyses exploring EGFR pathway activity and
74 ranscriptomics was performed by whole genome microarray analyses followed by functional pathway analy
76 elayed-early genes (DEGs, at 120 minutes) by microarray analyses, followed by quantitative real-time
77 as isolated from snap-frozen IEN lesions for microarray analyses, followed by quantitative reverse tr
85 l analysis of primary library expression and microarray analyses, here we have shown that nuclear fac
96 istology was used to validate the results of microarray analyses in a larger cohort of long-term surv
97 ssion level changes in previous ChIP-seq and microarray analyses in Isl1-deficient cell lines, we fou
98 ute to excessive drinking, here we performed microarray analyses in laser microdissected rat ACC afte
99 consequences of loss of sacsin, we performed microarray analyses in sacsin knockdown cells and ARSACS
100 using AGO2 immunoprecipitation (AGO2-IP) and microarray analyses in two breast cancer cell lines, MCF
104 expression studies combined with genome-wide microarray analyses indicate that LecRK-VI.2 positively
110 on treatment of NK cells with HIV gp120, DNA microarray analyses indicated up-regulation of several c
112 te RNA coimmunoprecipitation with downstream microarray analyses indicates that GRN mRNA is directly
116 re we present single-nucleotide polymorphism microarray analyses of a single CLL patient over 29 year
124 the behavioral phenotype was examined using microarray analyses of dentate gyrus and nucleus accumbe
128 s of virulence gene expression is limited to microarray analyses of expression at selected time point
132 nal gene expression profiles is essential if microarray analyses of genetic profiles are to produce r
134 list of potential target genes from previous microarray analyses of human peripheral blood-derived (p
136 A3 and NR4A1, was altered by insulin in cDNA microarray analyses of human skeletal muscle, we studied
138 protein sequence phylogeny with whole-genome microarray analyses of induced cell cultures and develop
139 proteases involved, we performed genome-wide microarray analyses of invasive human melanomas and beni
151 pression in p53 knockout cells, we conducted microarray analyses of p53(+/+) and p53(-/-) immortalize
154 schizophrenia and comparison subjects and by microarray analyses of pooled samples of individually di
155 of this disease in the kidney, we performed microarray analyses of renal biopsy samples from patient
157 ified previously as an altered transcript in microarray analyses of samples from human AD cases.
158 We compared the results of karyotype and microarray analyses of samples obtained after delivery.
159 ts unique to the Atoh1-derived lineage using microarray analyses of specific bHLH-sorted populations
168 EMs based on in vitro drug sensitivities and microarray analyses of the NCI-60 cancer cell line panel
175 favorable prognosis, we performed expression microarray analyses on FOXA1-positive and ER-positive (M
176 performed quantitative mass spectrometry and microarray analyses on protein and RNA isolated from the
181 ong HemEPCs, HemECs, and cbEPCs, revealed by microarray analyses, provided further indication of an E
185 scription-PCR, real-time PCR, and Affymetrix microarray analyses) resulted in the identification of f
189 ure isolation of RNA from larval neurons and microarray analyses reveal that balboa is also highly en
197 ic effect in female Wwox(hep-/-) mice, where microarray analyses revealed an increase in plasma trigl
210 Fluorescence-activated cell sorting and cDNA-microarray analyses revealed that each subclone was comp
224 In this study, we report lymphatic tissue microarray analyses, revealing for the first time stage-
225 vitro-cultured pollen tubes were assayed by microarray analyses, revealing over 500 transcripts spec
227 function of Rv2302 is still unknown, recent microarray analyses show that Rv2302 is upregulated in r
229 IAM accelerated chromosomal instability, and microarray analyses showed reduced NIAM mRNA expression
243 d immunohistochemical and whole human genome microarray analyses to characterize human skin in situ t
244 t cell functions, we carried out comparative microarray analyses to characterize the global transcrip
249 d the meaning of these changes, we conducted microarray analyses to examine the following: (i) the on
252 laria (ECM) and high-density oligonucleotide microarray analyses to identify host molecules that are
255 the Idd9 genotype and its phenotype, we used microarray analyses to investigate the gene expression p
256 In this study, we performed time series microarray analyses to investigate transcriptome dynamic
257 unoprecipitation (CLIP) with subsequent ChIP microarray analyses to profile miR responses and their d
258 e quantitative polymerase chain reaction and microarray analyses to show that it represses the transc
259 ombinatorial approach, including mRNAseq and microarray analyses, to identify targets co-regulated by
265 okines in HSCs and progenitors, we performed microarray analyses using Lineage(-) Sca-1(+) c-Kit(+) (
266 erformed oligonucleotide-based transcriptome microarray analyses using RNA isolated from mutant fly s
268 Using cell-based knockdown approaches and microarray analyses we found that (1) MYT1L is required
271 Using both protein immunohistochemistry and microarray analyses, we demonstrate that MERTK expressio
275 ng the down-regulated genes revealed by cDNA microarray analyses, we identified Aurora-A, a centrosom
277 Combination of in silico prediction and microarray analyses, we identified that miR-4487 and miR
278 uencing, in vivo functional studies and gene microarray analyses, we investigated the role of WWOX in
281 unds in athymic mice, and biopsy samples for microarray analyses were collected at multiple in vitro
292 ed with copper under multiple conditions and microarray analyses were previously performed to better
294 ed and an integrated series of bioinformatic microarray analyses were used to identify altered genes
298 Here, we combined extensive statistical microarray analyses with behavioral testing to comprehen
299 as aeruginosa was characterized by phenotype microarray analyses with single and double mutants and t
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