ライフサイエンスコーパス: coregulation

1 A and B forms were overexpressed, suggesting coregulation.

2 ers, which appear subject to transcriptional coregulation.

3 edict the molecular basis of transcriptional coregulation.

4 s) of Saccharomyces provide a model for gene coregulation.

5 motifs shared among them, which may underlie coregulation.

6 tosynaptic" genes displayed a lack of global coregulation although small modules of coexpressed genes

7 This is consistent with the known coregulation and association of SM and free cholesterol

8 ncrease in entropy at both the level of gene coregulation and chromosomal organization, which we sugg

9 entifying gene pairs with high potential for coregulation and colocalization in a manner consistent w

10 Coregulation and coordinated horizontal gene transfer ar

11 on of sequence and chromosomal position, the coregulation and pattern of expression of SNZ1 and SNO1

12 in large-scale gene-expression data implies coregulation and potential gene-gene interactions, but p

13 ith predictions from diverse transcriptional coregulation and proteome interaction data sets to assig

14 Coregulation and RNA editing of PRUNE2 and PCA3 were con

15 The loss of coregulation and the changes in current levels were prev

16 ing of microbial community and immune system coregulation and to develop new diagnostic and therapeut

17 LacD.1-specific and independent regulation, coregulation, and regulation of genes by these pathways

18 g sites, several different mechanisms of EBP coregulation are possible, including the formation of co

19 ts into the conservation of coexpression and coregulation as well as a starting point for comparative

20 Coregulation, as measured by correlation of gene express

21 or both conductances, suggesting a metabolic coregulation between gs and gm The resulting statistical

22 joint probability model, characterizing gene coregulation between multiple experiments.

23 Since there exists a coregulation between these neuropeptides and the protein

24 S promoter proximal gene, SSO3017, exhibited coregulation but not cotranscription with lacS.

25 ses ECs and SMCs to enable complex paracrine coregulation but shields SMCs from flow.

26 We examined two loci as case studies of coregulation by AphA and LuxR.

27 rough a transcriptional mechanism, and their coregulation by ceftriaxone is not mediated by physical

28 ional regulation by FMRP and transcriptional coregulation by common transcription factors connect the

29 roteolytic degradation and also allows their coregulation by FANCA and FANCM during nuclear localizat

30 ulation of one such miRNA, miR-137, involves coregulation by Sox2, a core transcription factor in ste

31 ndependent growth promotion by CXCR7 and its coregulation by the proinflammatory factor IL-8 in prost

32 iption complex assembly >300 bp away and how coregulation coevolved with coding sequences.

33 Endogenous coregulation during development and homeostatic scaling

34 these binding sites, suggestive of a common coregulation for many target genes.

35 would be desirable to find the mechanism of coregulation for these gene groups.

36 These coregulations have been used, in a few instances, to inf

37 romatin occupancy facilitators, which confer coregulation in certain contexts via enhancing trans-act

38 ranscription, even in the absence of obvious coregulation in gene expression data sets.

39 delta, thus strongly suggesting their likely coregulation in human tumors.

40 ing a shared evolutionary origin of cortisol coregulation in vertebrates.

41 This binding-dependent coregulation is specific for CLOCK/BMAL1 interaction, as

42 assessment of gene expression profiles whose coregulation is statistically different from that expect

43 An important example of post-transcriptional coregulation is the selective translational regulation i

44 Whether cortisol coregulation is unique to humans or can also be found in

45 However, the mechanism of PIAS1 coregulation is unknown.

46 The loss of conductance coregulation may be a mechanism to facilitate the recove

47 lanking gene suggesting that transcriptional coregulation may have been important in the neofunctiona

48 ted normal fibroblasts, suggesting that this coregulation may play a role in how uninfected cells res

49 From an adaptive perspective, cortisol coregulation may serve to reduce risk in challenging, po

50 Moreover, our analyses revealed a possible coregulation mechanism connecting hyperlipidemia and axo

51 erms of the number of tissues, the number of coregulation modules, and the number of species in which

52 for correlation with tocopherol profiles by coregulation network and neural clustering approaches.

53 These findings provide new insight into the coregulation of a critical innate immune response by fun

54 ing to positive and negative transcriptional coregulation of a miRNA and its targets-are prevalent in

55 iated protein translation regulation through coregulation of a subset of genes relevant to synaptic f

56 e apoptotic pathway reveal a cell autonomous coregulation of activation.

57 unit A alongside hyperpigmentation suggested coregulation of activity and pigment production (P < 0.0

58 other PIAS family members counteracted PIAS1 coregulation of androgen receptor transactivation.

59 This coregulation of apoE, interleukin-6, and IGFBPs was repl

60 main protein (FADD) represents a paradigm of coregulation of apoptosis and cellular proliferation.

61 lar kinetics and VEGF dependence, suggesting coregulation of blood and lymphatic vascular growth, but

62 we find an uncoupling of the H2Bub1-mediated coregulation of both H3K4 and -K79 methylation, as these

63 Coregulation of cancer metabolism by Myc and MondoA prov

64 In this study, we document coregulation of CD8 T cell exhaustion by Tim-3 and PD-1

65 ntial role of cpRNPs in the signal-dependent coregulation of chloroplast genes.

66 egetative/green tissues, often involving the coregulation of clusters of neighboring genes and global

67 highlights the possibility for crosstalk and coregulation of diverse cellular processes regulated by

68 between activity and stability relies on the coregulation of excitatory and inhibitory inputs onto pr

69 trongly suggest the presence of a functional coregulation of excitatory and inhibitory phenotypes at

70 act, might have reflected some mechanism for coregulation of expression.

71 endent, and may promote fibrogenesis through coregulation of fibrogenic gene targets.

72 ere these shared, indicating minimal genetic coregulation of final number.

73 ter constitutes an operon based partially on coregulation of GabT and GabD activities and the polarit

74 This procedure identified conserved coregulation of gene expression between environments rel

75 changes in their environment often requires coregulation of gene networks, but little is known about

76 anism for cell type-specific transcriptional coregulation of genes required for the synthesis and pac

77 regulatory mutation of GJB2 and of potential coregulation of GJB2 and GJB6.

78 al network analyses revealed new insights on coregulation of HMs of transcriptional activities in dif

79 ns in different systems, suggesting that the coregulation of ionic channel expression, by thus linkin

80 Such a coregulation of ionic channels is uniquely observable in

81 edictions from the nominal model showed that coregulation of ionic currents may preserve the key char

82 rease the evolutionary possibilities for the coregulation of juxtaposed sequences.

83 e lesions reveals a tight, context-dependent coregulation of Krt16 and Krt6 with genes involved in sk

84 metabolism-related genes exhibit evidence of coregulation of lipid metabolism and nervous system deve

85 s is a complex polygenic trait involving the coregulation of many genes and has proved especially cha

86 the formation of these structures is key to coregulation of MHC-II genes and the locus.

87 MPs), has remained unproven despite frequent coregulation of MMPs and TIMPs in other disease states.

88 omplex techniques for analyzing coexpression/coregulation of multiple variables are applied.

89 We propose that coregulation of NAD(P)H in dopamine neuron mitochondria

90 the presence of nitrite, indicating partial coregulation of NasDEF with the respiratory nitrate redu

91 ucleoside diphosphate kinase (Ndk), implying coregulation of Ndk and Scs in alginate synthesis.

92 Coregulation of NF90 and NF45 is a posttranscriptional p

93 e first evidence of a molecular link for the coregulation of nitrogenase and hydrogenase biosynthesis

94 Transcriptional coregulation of novel DNA methyltransferase (SmDnmt2) an

95 sential transcription factor critical in the coregulation of NR1, NR2b, and COX, and coupling exists

96 We tested the precision of coregulation of numbers of neurons, glial cells, and end

97 nscriptional complex via TEAD1, resulting in coregulation of numerous critical pro-proliferation targ

98 Intra- and interregional coregulation of opioid genes: broken symmetry in spinal

99 stems in marine algae, and the potential for coregulation of Porphyra transporter genes that are asso

100 We find that coregulation of ribosome- and tRNA-affiliated proteins i

101 gulation effected by the RcsC/RcsB system to coregulation of RpoS with capsule and FtsZ.

102 Coregulation of select target genes by PR-B and STAT5 is

103 ay and proteomic data reveal the coordinated coregulation of several interconnected biochemical pathw

104 d network motifs, such as autoregulation and coregulation of sigma and anti-sigma factor pairs, provi

105 ion of regulatory interactions: for example, coregulation of signals and their intracellular effector

106 this dual-tail recognition could facilitate coregulation of spatially proximal genes by promoting co

107 cis-regulatory modules (CRMs) to account for coregulation of specific biological pathways is only par

108 Our analysis suggests global, antagonistic coregulation of splicing by the CELF and RBFOX proteins

109 Consistent with the coregulation of stripes 4 and 6 by a single cis-element,

110 uromodulatory pathways establishes a dynamic coregulation of synaptic and intrinsic conductances with

111 ences of the syr-syp genes contribute to the coregulation of syringomycin and syringopeptin productio

112 approach to modulate the diverse patterns of coregulation of T-cell exhaustion in this heterogeneous

113 We propose that coregulation of target gene expression by oncogenic/tumo

114 Coregulation of target genes by Foxa1/a2 and either the

115 Thus, both phosphorylation cross-talk and coregulation of target genes play a role in the genetic

116 Coregulation of the expression of IFN-driven chemokines

117 The lack of uniform coregulation of the genes within this multifunctional cl

118 cytokine receptor specific, as evidenced by coregulation of the IL3-Ralpha receptor but not c-Kit.

119 blished transcriptomic data reveals apparent coregulation of the SPI1 and flagellar genes in various

120 fs and modules could be responsible for gene coregulation of the stress response in the lacrimal glan

121 d of telomerase research with a focus on the coregulation of the telomerase gene by both genetic and

122 ogen peroxide and suggest that potentiation (coregulation of the transcript level and translation) is

123 'alpha E(hs1,2) and 3'alpha-hs4, and suggest coregulation of the two enhancers by a common set of fac

124 are expressed at different levels, although coregulation of the two genes remains an interesting pos

125 hree treatments, suggesting coordination and coregulation of the uptake of these three essential mine

126 We propose that the precise coregulation of the voltage-dependent kinetics of multip

127 directions, our results suggest a selective coregulation of these channels as a mechanism for constr

128 However, the coregulation of these loading steps is unclear.

129 to a body of literature finding evidence for coregulation of these transporters.

130 Coregulation of these two pathways was essential and suf

131 of long-term memory are coordinated through coregulation of these two processes.

132 We observed coregulation of TLR2 and TLR6 expression correlating wit

133 of DNA bending for stabilizing chromatin and coregulation of transcription but not for targeted bindi

134 could create an environment that fosters the coregulation of transcription by pol III with transcript

135 Mechanisms for coregulation of transcription of tandem genes in yeast r

136 cotranscribed multifunctional operon allows coregulation of two enzymes required for the biosynthesi

137 The present study elucidates the potential coregulation of vasculogenesis by the heparan sulfate gl

138 nding illustrates an unprecedented degree of coregulation of voltage-dependent properties in two mole

139 These results provide a model for studying coregulation of yeast tandem genes.

140 been widely used as a tool for unveiling the coregulations of genes in response to genetic and enviro

141 variation (and probably a tightly controlled coregulation) of ionic conductances can help neurons mai

142 ion cannot be attributed to the pressure for coregulation or formation of selfish gene clusters, thus

143 GGM displayed known coregulation pathways as subnetworks and added novel com

144 rough partial correlation (pcor), GGM infers coregulation patterns between gene pairs conditional on

145 atistical models provide the first hints for coregulation patterns involving primary metabolism plus

146 ion, by enabling researchers to identify the coregulation patterns of thousands of genes.

147 Our results suggest that current coregulation places constraints on neuronal intrinsic pl

148 interactions, a potential mechanism of their coregulation, remained unclear.

149 We propose that M. xanthus uses an EBP coregulation strategy to make expression of EBP genes th

150 Research into moderating effects on cortisol coregulation suggests stronger covariation among distres

151 We have analyzed the level of gene coregulation, using gene expression patterns measured ac

152 M pathways exhibit environmentally dependent coregulation, we hypothesized that genes within a SM pat

153 Cortisol coregulation, which is the up- or down-regulation of par

154 ch to identifying in vivo condition-specific coregulation with cis-regulatory motifs and modules in t

155 , C1qb, and C9, which all displayed distinct coregulation with different cis-regulated C-type lectins

156 r, anaerobic growth on arsenate will require coregulation with global regulators such as cAMP-CRP.

157 iR-648), which is subject to transcriptional coregulation with its host gene, MICAL3 (microtubule-ass