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1 motifs shared among them, which may underlie coregulation.
2 A and B forms were overexpressed, suggesting coregulation.
3 cer enrichment dynamics and gene networks of coregulation.
4 ers, which appear subject to transcriptional coregulation.
5 edict the molecular basis of transcriptional coregulation.
6 ve splicing patterns cluster into modules of coregulation.
7 s) of Saccharomyces provide a model for gene coregulation.
8 ation and embryogenesis; and (c) mitonuclear coregulation adapted to accommodate both housekeeping an
9 tosynaptic" genes displayed a lack of global coregulation although small modules of coexpressed genes
11 th the molecular mechanism of transcriptomic coregulation and can scale to matrix with over 100 milli
12 ncrease in entropy at both the level of gene coregulation and chromosomal organization, which we sugg
13 entifying gene pairs with high potential for coregulation and colocalization in a manner consistent w
15 on RBP-RNA interactions and higher-order RBP coregulation and describe approaches that integrate mult
16 on of sequence and chromosomal position, the coregulation and pattern of expression of SNZ1 and SNO1
17 in large-scale gene-expression data implies coregulation and potential gene-gene interactions, but p
18 ith predictions from diverse transcriptional coregulation and proteome interaction data sets to assig
20 provide novel insights into B1/VRK signaling coregulation and support a model in which these enzymes
23 ing of microbial community and immune system coregulation and to develop new diagnostic and therapeut
24 LacD.1-specific and independent regulation, coregulation, and regulation of genes by these pathways
25 stem, mitochondrial metabolites, mitonuclear coregulation, and their critical roles in the emergence
26 g sites, several different mechanisms of EBP coregulation are possible, including the formation of co
27 ts into the conservation of coexpression and coregulation as well as a starting point for comparative
29 or both conductances, suggesting a metabolic coregulation between gs and gm The resulting statistical
34 tightly regulated, possibly involving their coregulation by an evolutionary conserved enhancer clust
36 rough a transcriptional mechanism, and their coregulation by ceftriaxone is not mediated by physical
37 ional regulation by FMRP and transcriptional coregulation by common transcription factors connect the
38 roteolytic degradation and also allows their coregulation by FANCA and FANCM during nuclear localizat
40 ulation of one such miRNA, miR-137, involves coregulation by Sox2, a core transcription factor in ste
42 ndependent growth promotion by CXCR7 and its coregulation by the proinflammatory factor IL-8 in prost
44 proliferation, and underline transcriptional coregulation defects as a novel pathophysiological mecha
45 iminating genes exhibited divergent modes of coregulation, differentiating neurons into discrete clus
50 hanisms: (i) receptor heterodimerization and coregulation, (ii) mutual metabolic modulation, and (iii
51 romatin occupancy facilitators, which confer coregulation in certain contexts via enhancing trans-act
54 detected between raised baseline excitatory coregulation in this network and impulsivity measures, s
57 assessment of gene expression profiles whose coregulation is statistically different from that expect
58 An important example of post-transcriptional coregulation is the selective translational regulation i
62 lanking gene suggesting that transcriptional coregulation may have been important in the neofunctiona
63 ted normal fibroblasts, suggesting that this coregulation may play a role in how uninfected cells res
65 Moreover, our analyses revealed a possible coregulation mechanism connecting hyperlipidemia and axo
66 erms of the number of tissues, the number of coregulation modules, and the number of species in which
67 for correlation with tocopherol profiles by coregulation network and neural clustering approaches.
68 These findings provide new insight into the coregulation of a critical innate immune response by fun
69 ing to positive and negative transcriptional coregulation of a miRNA and its targets-are prevalent in
70 iated protein translation regulation through coregulation of a subset of genes relevant to synaptic f
72 unit A alongside hyperpigmentation suggested coregulation of activity and pigment production (P < 0.0
76 main protein (FADD) represents a paradigm of coregulation of apoptosis and cellular proliferation.
77 lar kinetics and VEGF dependence, suggesting coregulation of blood and lymphatic vascular growth, but
78 we find an uncoupling of the H2Bub1-mediated coregulation of both H3K4 and -K79 methylation, as these
84 Proper cilium function requires the tight coregulation of ciliome gene transcription, which is onl
85 egetative/green tissues, often involving the coregulation of clusters of neighboring genes and global
87 highlights the possibility for crosstalk and coregulation of diverse cellular processes regulated by
88 between activity and stability relies on the coregulation of excitatory and inhibitory inputs onto pr
89 trongly suggest the presence of a functional coregulation of excitatory and inhibitory phenotypes at
93 ter constitutes an operon based partially on coregulation of GabT and GabD activities and the polarit
95 changes in their environment often requires coregulation of gene networks, but little is known about
96 anism for cell type-specific transcriptional coregulation of genes required for the synthesis and pac
98 al network analyses revealed new insights on coregulation of HMs of transcriptional activities in dif
99 athway that directs Mhem macrophages through coregulation of HO-1 (heme oxygenase-1; HMOX1) and lipid
100 st, we demonstrate ancestral transcriptional coregulation of HP6/Umbrea's future insertion site, illu
101 ns in different systems, suggesting that the coregulation of ionic channel expression, by thus linkin
103 edictions from the nominal model showed that coregulation of ionic currents may preserve the key char
105 e lesions reveals a tight, context-dependent coregulation of Krt16 and Krt6 with genes involved in sk
106 metabolism-related genes exhibit evidence of coregulation of lipid metabolism and nervous system deve
107 s is a complex polygenic trait involving the coregulation of many genes and has proved especially cha
109 MPs), has remained unproven despite frequent coregulation of MMPs and TIMPs in other disease states.
112 the presence of nitrite, indicating partial coregulation of NasDEF with the respiratory nitrate redu
115 e first evidence of a molecular link for the coregulation of nitrogenase and hydrogenase biosynthesis
117 sential transcription factor critical in the coregulation of NR1, NR2b, and COX, and coupling exists
119 nscriptional complex via TEAD1, resulting in coregulation of numerous critical pro-proliferation targ
122 stems in marine algae, and the potential for coregulation of Porphyra transporter genes that are asso
123 n vivo framework for dissecting the temporal coregulation of RBP networks as well as providing a reso
127 ay and proteomic data reveal the coordinated coregulation of several interconnected biochemical pathw
128 d network motifs, such as autoregulation and coregulation of sigma and anti-sigma factor pairs, provi
129 ion of regulatory interactions: for example, coregulation of signals and their intracellular effector
130 this dual-tail recognition could facilitate coregulation of spatially proximal genes by promoting co
131 cis-regulatory modules (CRMs) to account for coregulation of specific biological pathways is only par
132 Our analysis suggests global, antagonistic coregulation of splicing by the CELF and RBFOX proteins
134 uromodulatory pathways establishes a dynamic coregulation of synaptic and intrinsic conductances with
135 ences of the syr-syp genes contribute to the coregulation of syringomycin and syringopeptin productio
136 approach to modulate the diverse patterns of coregulation of T-cell exhaustion in this heterogeneous
139 Thus, both phosphorylation cross-talk and coregulation of target genes play a role in the genetic
142 cytokine receptor specific, as evidenced by coregulation of the IL3-Ralpha receptor but not c-Kit.
143 blished transcriptomic data reveals apparent coregulation of the SPI1 and flagellar genes in various
144 fs and modules could be responsible for gene coregulation of the stress response in the lacrimal glan
145 d of telomerase research with a focus on the coregulation of the telomerase gene by both genetic and
146 ogen peroxide and suggest that potentiation (coregulation of the transcript level and translation) is
147 'alpha E(hs1,2) and 3'alpha-hs4, and suggest coregulation of the two enhancers by a common set of fac
148 are expressed at different levels, although coregulation of the two genes remains an interesting pos
149 hree treatments, suggesting coordination and coregulation of the uptake of these three essential mine
151 directions, our results suggest a selective coregulation of these channels as a mechanism for constr
159 ously unknown mechanisms of MAP3K4 and HDAC6 coregulation of TRAF4 in TS cells and highlight these MA
160 of DNA bending for stabilizing chromatin and coregulation of transcription but not for targeted bindi
161 could create an environment that fosters the coregulation of transcription by pol III with transcript
163 cotranscribed multifunctional operon allows coregulation of two enzymes required for the biosynthesi
164 The present study elucidates the potential coregulation of vasculogenesis by the heparan sulfate gl
165 nding illustrates an unprecedented degree of coregulation of voltage-dependent properties in two mole
167 been widely used as a tool for unveiling the coregulations of genes in response to genetic and enviro
168 variation (and probably a tightly controlled coregulation) of ionic conductances can help neurons mai
169 ion cannot be attributed to the pressure for coregulation or formation of selfish gene clusters, thus
171 rough partial correlation (pcor), GGM infers coregulation patterns between gene pairs conditional on
172 priate binarization, BEM was able to extract coregulation patterns consistent with disease subtypes,
173 factorization is an important way to analyze coregulation patterns in transcriptomic data, which can
174 atistical models provide the first hints for coregulation patterns involving primary metabolism plus
181 Research into moderating effects on cortisol coregulation suggests stronger covariation among distres
182 Examples of this are methods that rely on coregulation to infer function of not-yet-annotated gene
184 M pathways exhibit environmentally dependent coregulation, we hypothesized that genes within a SM pat
186 ch to identifying in vivo condition-specific coregulation with cis-regulatory motifs and modules in t
187 A-DR molecules were abnormally enriched, and coregulation with CLEC16A was abolished in blood B cells
188 , C1qb, and C9, which all displayed distinct coregulation with different cis-regulated C-type lectins
189 r, anaerobic growth on arsenate will require coregulation with global regulators such as cAMP-CRP.
190 iR-648), which is subject to transcriptional coregulation with its host gene, MICAL3 (microtubule-ass
191 racterizing Etnppl across development and in coregulation with PEtN-relevant genes, as well as determ
192 e granulosa cell tumor growth via epigenetic coregulation with the disease driver FOXL2C134W, providi