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1 moter-promoter interactions are enriched for co-expression.
2 eric in the absence of stimulation and ErbB2 co-expression, a small fraction was present as constitut
4 pport observations that PGE exhibits ordered co-expression, although mechanisms underlying this instr
7 ate essential lincRNAs was then subjected to co-expression analyses using independent data from ENCOD
10 combining adipose transcriptome datasets in co-expression analysis and in differential expression an
15 tistical EcoToxModules were identified using co-expression analysis of publicly available microarray
20 eneNetwork database is a unique resource for co-expression analysis using data from a variety of tiss
21 further analyzed using correlation analysis, co-expression analysis, clustering, differential gene ex
27 filtrate as well as increased GFAP and S100B co-expression and decreased HuC/D protein expression in
31 irs and the relationship between development co-expression and phenotypes resulting from the knockout
33 QTL enrichment, functional fine-mapping, RNA co-expression, and patterns of physiological association
34 ata on protein cellular concentrations, gene co-expression, and protein-protein interactions in the w
38 oaches for in silico doublet identification: Co-expression based doublet scoring (cxds) and binary cl
40 d phenotypes, and relationships such as gene co-expression, biochemical regulation, and biomolecular
42 tein-protein interaction (PPI) network, gene co-expression (CE) network and pathway information to id
43 assess the cell-type specificity of AD gene co-expression changes and estimate cell-type proportion
45 48 analyzed tissues in GTEx, 26 have variant co-expression clusters of four highly expressed and panc
46 Here we test macroevolutionary hypotheses on co-expression, co-regulation, and diversification of the
47 ted by EMMPRIN (CD147) as determined through co-expression/co-immunoprecipitation studies, and siRNA-
51 schizophrenia genetic signals and modules of co-expression converged on one module showing not only a
53 ted by predicting gene function from RNA-seq co-expression data processed uniformly from the gene exp
56 genomes display extensive redistribution of co-expression domains with expanded and newly-appearing
58 f cell-type composition on correlation-based co-expression estimation for any cell types of interest.
59 nition of bacterial effectors by plant NLRs, co-expression experiments with matching Mla-AVR(a) pairs
60 ated from multiple sources including TF-gene co-expression from RNA-seq studies, TF-target associatio
61 f features including protein sequences, gene co-expression, functional association, and phylogenetic
63 inheritance of parental expression patterns, co-expression gene network properties, and genomic loci
65 ith Igf2bp3, another RBP, and their enforced co-expression in adult HSPCs reactivated fetal-like B-ce
68 e expression under the normal state and gene co-expression in the human brain has not been fully defi
69 dence for adrenergic receptor expression and co-expression in the subregions of the mouse auditory mi
71 of miRNA target predictions with target gene co-expression information to model genome-wide gene regu
72 n across multiple networks highlights robust co-expression interactions and improves the functional c
74 ify lncRNA signatures in clinically-relevant co-expression lncRNA-mRNA networks residing in pertinent
76 he desired methods (2) calculating gene-gene co-expression measurements for adjusted datasets (3) eva
77 show significant clustering within a single co-expression module of genes highly expressed during ea
78 d frameworks consider the common latent gene co-expression modules and gene-sample biclusters underly
79 transcriptomic data can provide insights via co-expression modules and hubs, alternative forms of com
80 heritability of psychiatric disorders in the co-expression modules enriched for dystonia-associated g
81 um score regression was used to test whether co-expression modules enriched for dystonia-associated g
82 ariants that regulate the expression of gene co-expression modules in the aging human brain; we disco
83 response networks involved multiple discrete co-expression modules including those related to Th2-, t
86 from 32 normal controls showed that distinct co-expression modules were mostly enriched in neurogenes
87 at can identify biologically meaningful gene co-expression modules with genes that are not all highly
88 roportion changes in human AD by integrating co-expression modules with single-cell transcriptome dat
96 intent in this study was to construct a gene co-expression network (GCN) for the normal brain using R
103 essed genes (DEGs) and also by Weighted Gene Co-expression Network Analysis (WGCNA) to identify modul
104 pression data were analyzed by weighted gene co-expression network analysis (WGCNA) to identify trait
107 highly associated for COPD in Weighted Gene Co-Expression Network Analysis (WGCNA) was enriched for
111 regating-based Markov random field, weighted co-expression network analysis and supervised regulatory
113 form the localized (cell subpopulation) gene co-expression network analysis from large-scale scRNA-se
114 tive gene modules generated by Weighted Gene Co-expression Network Analysis from purified leukocyte p
123 one cancer and CTCs to perform weighted gene co-expression network analysis to systematically detect
125 ly used to perform different aspects of gene co-expression network analysis, and Modularity Maximizat
126 s, pathway enrichment analysis, differential co-expression network analysis, prediction, clustering a
128 l gene expression analysis and weighted gene co-expression network analysis, we identified both cruci
133 a statistical framework built on considering co-expression network changes across time from time seri
134 reds and on average have significantly fewer co-expression network connections suggesting that a subs
135 f change point detection to characterize the co-expression network dynamics, and the use of kernel fu
136 We demonstrate early alterations in a gene co-expression network enriched for myelin and oligodendr
139 networks, forming a single highly integrated co-expression network module, maximizing potential for s
141 genes (OLIGs), whereas a multicellular gene co-expression network of plaque-induced genes (PIGs) inv
142 it were multiple times more likely to form a co-expression network than other genes expressed in an o
143 transcription factor (TF) and lncRNA-TF-mRNA co-expression network were constructed with high specifi
149 ophrenia cases; all Caucasians) to construct co-expression networks and detect "modules" of co-expres
151 CNA algorithms use correlation to build gene co-expression networks and identify modules with highly
152 se low-rank representation to construct gene co-expression networks and local maximal quasi-clique me
153 n immunoinflammatory pathways and associated co-expression networks and their relationships to sympto
155 ld potentially disrupt genetic networks, the co-expression networks are highly conserved across envir
160 determined the enrichment of these genes in co-expression networks constructed from 10 human brain r
163 Here we explore the role of genetics and co-expression networks in regulating these genes in the
164 ighlights complex relationships between gene co-expression networks in the brain and clinical state a
165 s and identify risk clusters using BrainSpan co-expression networks of early- and mid-fetal periods.
167 ntially expressed genes and constructed gene co-expression networks on mRNAs of pigs under different
168 tage of subspace clustering to generate gene co-expression networks rather than using correlation as
169 ed a combined analysis of metabolic and gene co-expression networks to explore how the soil microbiom
170 e-collecting Steiner forest-based problem on co-expression networks, adapted to model neurodevelopmen
172 f the TCGA transcriptome data, identified 12 co-expression networks, and demonstrated that CXCL13, CX
173 ologies and are also hub proteins of protein co-expression networks, as promising targets for future
174 d by additional lines of evidence, including co-expression networks, metabolite analyses, and direct
175 approaches that combine gene regulatory and co-expression networks, proteomics, metabolomics, lipido
176 hough those applications focus on miRNA-mRNA co-expression networks, SmCCNet is applicable to a varie
182 a highly multiplexed screen to quantify the co-expression of 351 surface molecules on millions of hu
185 of single-cell RNA sequencing data show that co-expression of ACE2 and TMPRSS2 is elevated in absorpt
186 ormation in Arabidopsis, we demonstrate that co-expression of AcMYB123 and AcbHLH42 is a prerequisite
190 or subtypes in a single IC cell, we measured co-expression of alpha(1) , alpha(2A) , and beta(2) rece
193 ene expression analysis revealed significant co-expression of beta-adrenergic pathway genes PKA regul
194 activation (+47 mV at 12 um matrix Ca(2+) ) Co-expression of BK(Ca) with the BK-beta1 subunit in HeL
198 nal feature of non-CG methylation (mCH), but co-expression of Brn2 and Mytl1 was required to establis
200 ngth and sample age on PCR amplification and co-expression of candidate genes on apparent expression
203 dent for epigenetic regulators with enhanced co-expression of chromatin- and dendrite-related genes i
205 , its role in reactions and pathways and the co-expression of complex components in the tissues of mu
207 rotein modules for breast tumor groups, with co-expression of EGFR and MET marking ductal carcinoma i
210 ecific regulatory B cells were identified by co-expression of fluorescence-conjugated ovalbumin and I
213 ions of reprogramming factors, we found that co-expression of GMT in individual fibroblasts is suffic
214 sis in dorsal telencephalic progenitors, the co-expression of Gsx2 with Ascl1 inhibits neurogenesis.
216 T171-120Q forms inclusions but is benign and co-expression of HTT171-120Q with non-aggregating pathog
217 cancer have limited effector function, high co-expression of inhibitory receptors and extensive tran
218 ssion of INMT transcript in rats and humans, co-expression of INMT and AADC mRNA in rat brain and per
220 n transport pathway, codon optimization, and co-expression of molecular chaperones to promote express
221 or SRSF2 imparted distinct splicing changes, co-expression of mutant IDH2 altered the splicing effect
223 e a rosette pluripotent state defined by the co-expression of naive factors with the transcription fa
224 ic reticulum (ER)-like neighborhood, whereas co-expression of OsPIP2;2 recruited OsPIP1;3 to the plas
225 data and, employing a binomial model for the co-expression of pairs of genes, yields interpretable do
226 Using patch clamp recordings, we found that co-expression of Phactr1 with wild-type Slack channels r
227 Further, employing the GBM BioDP, we found co-expression of PIK3CA with the neuronal stem/progenito
229 depleted the cells of LDs, but unexpectedly, co-expression of PNPLA3(wild type [WT] or 148M) with ATG
233 ls expressing SLC26A9 alone or with WT-CFTR, co-expression of SLC26A9 with F508del-CFTR reduced total
236 f the tuberigen activation complex, and that co-expression of StCEN blocks activation of the StSP6A g
237 d dysregulated transcriptional programs with co-expression of stemness and myeloid priming genes and
238 s and dendritic cells, were characterized by co-expression of surface proteins corresponding to HLA-D
242 in, Rv2514c, induces bacteriostasis and that co-expression of the cognate antitoxin Rv2515c restores
244 his is associated with different patterns of co-expression of the glutamatergic phenotype along the r
245 om those that are preserved, suggesting that co-expression of the glutamatergic phenotype in DA cells
247 ated inhibition of mTORC1 activity; however, co-expression of the phospho-deficient mutant of PRAS40
249 was to evaluate the regional expression and co-expression of the transporter proteins for serotonin
250 ociated with mainly increased expression and co-expression of the transporters for serotonin and dopa
251 hastic bursts of transcription result in the co-expression of these antagonistic transcription factor
253 A-Seq dataset of aortic tissue to assess the co-expression of TLR4, MD2, and subunits of the vascular
255 onally unspecialized state, characterized by co-expression of transcription factors that become restr
256 vivo and that polymodal nociception requires co-expression of TrpA1 isoforms, providing novel insight
259 overexpression of PTEN, there was increased co-expression of type I interferon-associated genes with
265 experiments, we examined the effects of CLN3 co-expression on the KChIP3-mediated modulation of Kv4.2
266 ll mice, we investigated the impact of GPR88 co-expression on the signaling of opioid receptors in vi
267 ork analysis (WGCNA) was applied to identify co-expression patterns among CXCL13-CXCR5, associated ge
268 ene subnetworks that represent specific gene co-expression patterns are inferred from the components
269 e drug sensitvity biomarkers with concordant co-expression patterns between the PDXs and pretreatment
270 Single-cell RNA sequencing studies on gene co-expression patterns could yield important regulatory
271 e based on the consistency level between the co-expression patterns in the given sample and samples i
273 association to vascular diseases and cancer co-expression patterns reported in the relevant database
274 e common functionalities as reflected by the co-expression patterns, which are distinct from samples
277 primary prostate tumors by investigating the co-expression profiles of patient samples and their corr
282 sion inhibits eVP40 VLP egress and that Amot co-expression rescues budding of eVP40 VLPs in a dose-de
283 rom biopsies of cancer patients can identify co-expression signatures representing particular biomole
286 and posterior ventral thalamus, while lower co-expression was noted in the dorsomedial thalamus.
287 ependent on K19 expression, and K19-cyclin D co-expression was observed in human breast cancer tissue
289 ntial expression, variance partitioning, and co-expression, we identify the following trade-offs for
290 order to incorporate phenotypic context into co-expression, we recently developed an epistasis-expres
291 a database of mouse brain anatomy and gene (co-)expression with sophisticated visualization and sess
297 urther, NEDD8 correlation analysis indicated co-expression with RBX1, a key component in cullin-RING
298 eural progenitor cells based on differential co-expression with Tc-six3/optix, Tc-six4, Tc-chx/vsx, T
300 re robustly defined each showing patterns of co-expression within individual cells, which were mainly