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1 and quantify the influence of each factor on co-expression.
2 ced clones demonstrated appropriate MYF5-GFP co-expression.
3 odel training, with canine OS tumor data for co-expression.
4 on, 72 miRNA-target pairs showed significant co-expression.
5 ellular trafficking of HA was affected by NA co-expression.
6 eurons in an experimental design targeted to co-expression.
7 le for multi-factor analysis of differential co-expression.
8 hat CCDDs are associated with increased gene co-expression.
9 that influenced the respective differential co-expression.
10 luence of individual factors on differential co-expression.
11 es we introduce CLIC, CLustering by Inferred Co-expression.
14 analysis (WGCNA), which exploits patterns of co-expression among genes, to brain transcriptome data o
17 nts along with systems-based comparative and co-expression analyses of these transcriptome maps ident
20 een developed for single-factor differential co-expression analysis and applied in a variety of studi
22 f publicly available transcriptomic studies, co-expression analysis combining multiple transcriptomic
28 s of incisor renewal and illustrate how gene co-expression analysis of intact biological systems can
33 d from the following sources: (i) systematic co-expression analysis, (ii) detection of shared selecti
37 r and the capsaicin receptor (TRPV1) exhibit co-expression and complex, but largely unknown, function
40 ylation by protein kinase A during bacterial co-expression and subsequent binding at the amphipathic
41 y, we identify technical factors influencing co-expression and suggest how they can be controlled for
42 a tissue microarray format and analyzed the co-expression and the clinicopathologic data of ERG and
45 tructed cancer or tissue type-specific, gene co-expression based protein interaction networks and dru
47 ulation of each IGF-IR gene, revealing tight co-expression between the IGF-IRa paralogues, but expres
48 As current methods for identification of co-expression cannot cope with this level of complexity,
49 ly, we validated the biological relevance of co-expression cluster memberships with an independent ph
51 d at the level of individual cell types, but co-expression clusters provided clues as to their functi
52 ssue and shown that cytoplasmic PML and CRM1 co-expression correlates with reduced disease-specific s
53 and Cgrpalpha was not mutually exclusive and co-expression could be observed, most abundantly in the
54 mprovement, overcoming the limit of enforced co-expression data retrieval and instead enabling the re
56 Along this line, analysis of differential co-expression (DC) has gained attention in the recent ye
58 likely to overlap with known functions than co-expression derived from bulk data, with functional va
60 onal approach, called ICEGM, to Identify the Co-Expression Gene Modules through a novel mathematical
63 all traits was found in a xylem preferential co-expression group developed in independent experiments
66 risk genes, and showed their interaction and co-expression in a functional network that converged on
73 human breast tumors data sets the MTSS1/p63 co-expression is a negative prognostic factor on patient
77 ssion data sets allowed to observe that high co-expression levels of SCD1, beta-catenin, YAP/TAZ and
79 to the brainstem suggesting that Ctip2/Satb2 co-expression may refine their properties rather than de
80 thods (differential expression, correlation, co-expression, microRNA-mRNA target prediction, co-targe
81 d the power of this approach by showing that co-expression module members Lrig1 and Igfbp5 define pop
84 A subset of these genes belonged to the same co-expression module, mapped to the epidermal differenti
86 ramework that integrates GWAS data with gene co-expression modules from tissues representing three br
87 sulin resistance and height, as well as gene co-expression modules generated by Weighted Gene Co-expr
88 tational analyses, we identified three major co-expression modules of TF genes that may regulate the
92 rom the heterogeneous data, we combined gene co-expression modules with mutation modulators and propo
97 elated Nicotiana species revealed a key gene co-expression network (M4 module) which is co-activated
102 highly associated for COPD in Weighted Gene Co-Expression Network Analysis (WGCNA) was enriched for
120 orming principle component and weighted gene co-expression network analysis, we categorized dorsal ro
123 mutations, gene and protein expression, gene co-expression network and drug pharmacological informati
124 s paper, a method is introduced to construct co-expression network and to extract co-expressed module
125 initial perception of drought, we applied a co-expression network approach to associate rhythmic gen
128 t many tools and methods for construction of co-expression network from gene expression data and for
130 Importantly, these processes are coupled to co-expression network modules associated with cell proli
131 ion of two over-represented PD-specific gene co-expression network modules: the Brown Module (Br) con
133 menon, we generated and integrated a dynamic co-expression network of heart regeneration in the zebra
141 emented with new tools for reconstruction of co-expression networks and feature-and-network-based pri
145 that integration of association mapping and co-expression networks enhances our understanding of com
148 pled method to recover context specific gene co-expression networks from the estimated sparse biclust
152 n Hfe(-/-) x Tfr2(mut) brain with human gene co-expression networks suggests iron loading influences
153 iovascular study cohort, and we recover gene co-expression networks that are differential across ER+
154 single-cell RNA-seq data create confounds in co-expression networks which can be identified and expli
155 ic diversity is supported by analyses of RNA co-expression networks, protein-protein interaction netw
165 the DNA methyltransferase DNMT3A targeted by co-expression of a guide RNA to any 20 bp DNA sequence f
167 pression (DCX) signifies change in degree of co-expression of a set of genes among different biologic
173 vitro and in vivo, which was mitigated upon co-expression of an Eos mutant lacking miR-17 target sit
174 d by dampening neuronal excitability through co-expression of an inwardly rectifying potassium channe
177 g re-assembly of Complex V) following stable co-expression of ATP8 and ATP6 Thus, we report the stabl
185 ammalian N-BAR domains bound calmodulin, and co-expression of calmodulin with endophilin A2 potentiat
189 ls from human primary NSCLC samples based on co-expression of CD73 and CD90 while lacking hematopoiet
190 basal tumor cells (BTCs), as defined by the co-expression of CD90, CD44 and CD49f, directly from pat
191 were implicated in resistance to GLS through co-expression of COI1 and enrichment of genes with the G
194 ional studies of Cx26 in HeLa cells revealed co-expression of Cx26-Asp50Asn and wild-type Cx26 in gap
197 L was a potent inhibitor of Kv4.2 and Kv4.3; co-expression of cytosolic beta subunit KChIP2, which re
203 ectrometry can be utilized to screen for the co-expression of functionally related biomarkers to be r
204 2 cells also increased TAG accumulation, and co-expression of FUS3 and diacylglycerol acyltransferase
206 understanding of how microRNAs influence the co-expression of genes and pathways, and thus ultimately
208 mune/inflammatory response, as determined by co-expression of genes, which is associated with the maj
212 engineered to express Myc and Akt1 in liver, co-expression of Igf2 accelerated formation of liver tum
215 CHO cells expressing integrin alphaIIbbeta3, co-expression of K2 with talin head domain resulted in r
216 rated by wild-type Kar2 can be replicated by co-expression of Kar2 mutants that mimic either the unmo
220 on is conserved in the human orthologue, and co-expression of Minion and the transmembrane protein My
221 alyses include global expression comparison, co-expression of miRNA clusters and the prediction of mi
222 n transport pathway, codon optimization, and co-expression of molecular chaperones to promote express
224 ys with moricin mutant promoters showed that co-expression of MsFkh with Relish-RHD did not have an a
225 basic and translational studies that require co-expression of multiple factors or multi-units of comp
235 However, our results reported here indicate co-expression of PKM1 and PKM2 and their possible physic
236 n consonance, phosphoproteins obtained after co-expression of PknA with mPDE/S20A/T240A/4A displayed
241 genes is supported by the eQTL analyses and co-expression of PTTG1lP with vimentin and E-cadherin1,
244 d that poor survival is associated with high co-expression of SCD1, beta-catenin and the YAP/TAZ down
245 constructs for the temporary, stoichiometric co-expression of six different combinations of the four
250 This morphological phenotype was rescued by co-expression of TCF4 plus calmodulin in a calcium-depen
254 ent virus-like particle trap assay, based on co-expression of the HIV Gag protein, confirmed that thi
256 ide-deletion mutant but could be restored by co-expression of the propeptide in trans SBT3 was inhibi
258 in breast cancer is further supported by the co-expression of these molecules in multiple subtypes of
262 Here we show that post-lesional AAV-assisted co-expression of two soluble proteins, namely insulin-li
264 dult spinal neurons defined by developmental co-expression of VGLUT3 and Lbx1 (VT3(Lbx1) neurons): th
268 k significantly enriched for transcriptional co-expression (P<0.0001) in the frontal cortex during fe
270 516 pairs of lncRNA-mRNAs have differential co-expression pattern, in which the correlation between
271 ast tissue; (2) 291 pairs have dose-response co-expression pattern, in which the correlation is simil
273 Ms help discover tumor subtype specific gene co-expression patterns (modules) that are significantly
276 y-associated) derived from effector function co-expression patterns were used to analyze the results.
279 ents in HEK-293T cells demonstrated that D1R co-expression promotes a switch in GHS-R1a-G protein cou
281 that ID-AGs are substantially enriched with co-expression, protein-protein interactions, and specifi
283 work was constructed, which consisted of 681 co-expression relationships between 164 lncRNAs and 201
284 n, we performed an unbiased analysis of gene co-expression relationships to identify modules of co-ex
286 form the first major analysis of single-cell co-expression, sampling from 31 individual studies.
288 opy number alterations (SCNA), which produce co-expression signatures based on physical proximity rat
289 s expressed in Pichia pastoris and through a co-expression strategy with a molecular chaperone, yield
293 ines, and GDU1 protein levels decreased upon co-expression with active, but not enzymatically inactiv
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