ライフサイエンスコーパス: regulator

1 with chronicity, with FOXK1 acting as immune regulator.

2 ntified agonists of this important metabolic regulator.

3 was demonstrated to be an indole-responsive regulator.

4 ession of miRNA-485, as a PGC1alpha upstream regulator.

5 their post-translational and transcriptional regulators.

6 ns, assess network topology and identify key regulators.

7 incomplete cytokinesis or muscle fusion pore regulators.

8 ated by transcription factors and epigenetic regulators.

9 ased on the input from expert scientists and regulators.

10 an by altered acetylation of other autophagy regulators.

11 rive expression of key viral transcriptional regulators.

12 RNAs also function as global transcriptional regulators.

13 he recruitment and the ejection of chromatin regulators.

14 dentify severe asthma genes and their master regulators.

15 functionally, due to IFN-I-induced negative regulators.

16 within the leucine zipper-like transcription regulator 1 (LZTR1).

17 of LZTR1 (leucine zipper-like transcription regulator 1), an adaptor for CUL3 (CULLIN3) ubiquitin li

18 AmrZ, another alginate regulator(6), is triggered to repress CRISPR-Cas immunit

19 a reduction in expression of the autoimmune regulator (Aire), a critical mediator of central immune

20 mutation implicated a membrane and ESCRT-III regulator, Alx1, in this alternate pathway.

21 Gene network inference and master regulator analysis (MRA) have been widely adopted to def

22 ion control Ras' competence to bind multiple regulator and effector proteins.

23 lts convey the potent role of DR3 as an ILC2 regulator and introduce DR3 agonistic treatment as a nov

24 der-recognized multifactorial role as both a regulator and target of stress hormone signaling within

25 These data were analyzed to predict upstream regulators and affected signaling pathways following ars

26 by combining new targeted agents with immune regulators and chimeric antigen receptor-expressing natu

27 Thus, DiNeR successfully extracted hub regulators and discovered well-known risk genes.

28 six antimicrobial peptides, two plant immune regulators and eight chemicals which inhibit Candidatus

29 mensions can control local concentrations of regulators and influence the emergent behavior of mitoti

30 Six1 targets a wide range of hair-bundle regulators and late Six1 deletion disrupts hair-bundle p

31 ering ab initio the binding motifs for known regulators and some unknown ones.

32 xtraordinary opportunity to pinpoint crucial regulators and target genes responsible for complex dise

33 It is a known mitotic regulator, and it is well-described that KIF11 is necess

34 PTB domains as a scaffold for a range of Rab regulators, and also the VPS13 family of proteins which

35 nsporters, surface proteins, transcriptional regulators, and metabolic pathways.

36 own to also activate the nonrelated response regulators ArcA, CpxR, RcsB, and PhoQ.

37 Regulators are evaluating the use of noninterventional r

38 CFH), a major alternative complement pathway regulator, are associated with the development of age-re

39 Activating mutations of EZH2, an epigenetic regulator, are present in approximately 20% of patients

40 unsaturated PA in foods is a concern to food regulators around the world because these compounds have

41 Pi promoted beclin 1 binding to its negative regulator BCL2, which impairs autophagy flux.

42 NA (siRNA)-based down-regulation of an actin regulator, by pharmacological inhibition of actin polyme

43 insufficient oxygen through transcriptional regulators called hypoxia-inducible factors (HIFs).

44 Because shared upstream regulators can ensure correlated gene expression, the se

45 eased Tnf expression, decreased a cell cycle regulator (Ccnb1), and increased apoptotic factors (Aifm

46 on and downregulation of the transcriptional regulators CEBPD and IkappaBalpha.

47 oexpressed with CF transmembrane conductance regulator (CFTR) along with transcription factors that h

48 s, cystic fibrosis transmembrane conductance regulator (CFTR)-rich ionocytes, and immune cells(1,2).

49 The response regulator CheY increased motor switching from counterclo

50 Genetic studies of seed maturation regulators, combining transcriptomics and network analys

51 ERalpha) is a ligand-dependent transcription regulator, containing two transactivation functional dom

52 ffected the gene encoding the carbon storage regulator CsrA.

53 e mitochondrial permeability transition pore regulator cyclophilin D (CypD) promotes NGSIS, but not g

54 egulates expression of the key seed dormancy regulator, DELAY OF GERMINATION1, is a typical represent

55 e canonical FtsZ-membrane anchors and Z-ring regulators described for E. coli.

56 Putative regulators described here add information to this hypoth

57 map, and a knockout of a predicted upstream regulator disrupts normal regeneration, validating our p

58 e development in vivo The competence shutoff regulator DprA was highly expressed during pneumonia-der

59 els to temporally delete essential autophagy regulators during carcinoma progression.

60 nding to VEGFRs is an important angiogenesis regulator, especially the earliest-known isoform, VEGF-A

61 of proteins belonging to the type-B Response Regulator family of cytokinin response activators.

62 -induced hepatic expression of the metabolic regulator fibroblast growth factor 21 (FGF21) was blunte

63 hroughput CRISPR screening using a ubiquitin regulator-focused single-guide RNA library in HL lines c

64 r work reveals TiPARP as a negative-feedback regulator for multiple oncogenic transcription factors,

65 nd myosin-7B (MYO7B) as critical endocytosis regulators for alpha-Syn preformed fibrils (PFFs).

66 gnalling but also requires inhibition by the regulator fructose 1,6-bisphosphate, which senses the up

67 lling their clonal expansion through the Wnt-regulator FZD8.

68 homeotic mutation in the co-transcriptional regulator gene NODULE ROOT1 (MtNOOT1) converts legume-ty

69 Comparative analysis of the master regulator genes followed by validation testing in indepe

70 comitant changes in the expression of floral regulator genes suggest that these processes are a prere

71 ation in the sorbitol operon transcriptional regulator gutR was associated with increased bacterial g

72 ding the mode of action of these non-protein regulators has been an intense area of research in recen

73 ylation, and thereby activation, of response regulators has been demonstrated to occur by their cogna

74 in adulthood, including the transcriptional regulator Hmga1.

75 light-regulated genes, including the master regulator HY5.

76 matrix modifiers (MMP12 and SPARCL1), immune regulators (IDO1, SOCS3, and IL10), and a proinflammator

77 n B1, and increased expression of the immune regulators IL6 and IL8 followed by cell death.

78 findings strongly implicate TSPAN-7 as a key regulator in determining the set-point of glucose-stimul

79 tor alpha (ERalpha) is a key transcriptional regulator in the majority of breast cancers.

80 The downregulation of this cytokinin regulator in the Yh haplotype may be sufficient to trigg

81 a genome-wide annotation of transcriptional regulators in A. fumigatus and construction of a library

82 are the most common type of transcriptional regulators in prokaryotes and function by altering gene

83 Adult-specific manipulation of homeostatic regulators in the fly's auditory neurons accelerated - o

84 matrix, but little is known about integrin's regulators in the glia.

85 of transcriptional and post-transcriptional regulators, including microRNAs (miRNAs), coordinate the

86 ting of selected stress-response and cambium regulators indicated ERF-1 as a potential key checkpoint

87 on the immune receptors and transcriptional regulators involved in T cell quiescence and activation,

88 this context, the expression of the "master regulator" is necessary and sufficient to activate linea

89 e to nutrient stress, including the upstream regulator KLF15, aminoacid catabolizing enzymes, notably

90 ergenic non-coding RNA-Nucleotide Metabolism Regulator (lincNMR) is a long non-coding RNA (lncRNA) wh

91 LysR-type transcriptional regulators (LTTRs) are the most common type of transcrip

92 d to identify enriched pathways and upstream regulators.Measurements and Main Results: Responses to R

93 Ubiquitously expressed chromatin regulators modulate these networks, yet the mechanisms g

94 In this study, we report that immune regulator Monocyte chemotactic protein-1-induced protein

95 utive loss or acute inhibition of the Arp2/3 regulator, N-WASP, which is associated with enhanced sig

96 In bioinformatics analysis of upstream regulator networks, the Cxcl8 pathway exhibited dominanc

97 ctile ring formation, we show that the ECT-2 regulator NOP-1, but not centralspindlin, is essential f

98 deposition, and targeting the plant defense regulator NPR1 and analyses receptor FLS2.

99 and thus we identify a role of Ppargamma as regulator of a functionally related class of AF-miRNAs.

100 Therefore, TrkB signaling is a key regulator of a previously uncharacterized neuronal popul

101 he activity of heparan sulfate, an important regulator of a wide range of biological cell functions.

102 nding protein annexin A3 (AnxA3), a negative regulator of adipocyte differentiation, is down-regulate

103 GABA is a key regulator of adult-born dentate granule cell (abDGC) mat

104 ted in the presence or absence of the master regulator of antioxidant defense nuclear factor erythroi

105 ntly examined the role of a newly identified regulator of atherosclerotic burden in miR-144 knockout

106 i CDK-related kinase 5 (CRK5), is a critical regulator of atypical mitosis in the gametogony and is r

107 domain containing 66 (CCDC66) and TOG array regulator of axonemal microtubules 1 (TOGARAM1) as ARMC9

108 ivity toward its substrate Notch, a critical regulator of B cell and T cell development.

109 X-A and OX-B, is firmly established as a key regulator of behavioral arousal, sleep, and wakefulness

110 SynGAP is a potent regulator of biochemical signaling in neurons and plays

111 Proteolysis is a major posttranslational regulator of biology inside and outside of cells.

112 These results suggest that LINGO1 is a regulator of BK channels, which causes a "functional kno

113 TRADD(4-6), an adaptor protein, as a direct regulator of both cellular homeostasis and apoptosis.

114 lcium-dependent protein kinase CPK3 is a key regulator of both pattern-triggered immunity and effecto

115 ntify alphaV-integrin (CD51) as an essential regulator of cardiac PW1(+) cells fibrogenic behavior.

116 demonstrate that the CTK complex is negative regulator of cat-3 expression by affecting its chromatin

117 ivation of mTOR Complex 1 (mTORC1), a master regulator of cell growth and metabolism.

118 of rapamycin complex 1 (TORC1) is a central regulator of cell growth.

119 e blebbing is now recognized as an important regulator of cell migration, cancer cell invasion, and v

120 nt protein kinase kinase-2 (CaMKK2) is a key regulator of cellular and whole-body energy metabolism.

121 es initiating chondrogenesis, SOX9 acts as a regulator of cellular metabolism by suppressing oxidatio

122 Levels of glutathione, a key regulator of cellular redox status, are reduced in the m

123 -related, matrix-associated, actin-dependent regulator of chromatin, subfamily D, member 2) has recen

124 r implicates the JNK pathway as an important regulator of cortical development.

125 although NTA has gained recognition as a key regulator of crucial processes such as protein turnover,

126 ling pathway has been considered as a master regulator of cytoprotective genes, and exists in many ce

127 he ortholog of the ASD risk gene Taok2, as a regulator of dendritic arborization in sensory neurons.

128 R subdomains defined by seipin (Fld1), and a regulator of diacylglycerol (DAG) production, Nem1.

129 Hyperglycemia is a potent regulator of endogenous glucose production (EGP).

130 MP-activated protein kinase (AMPK), a master regulator of energy metabolism, in response to ZIKV chal

131 ytokine interleukin-22 (IL-22) is a critical regulator of epithelial homeostasis.

132 motes the expression of twist1b-a well-known regulator of epithelial-to-mesenchymal transition.

133 , a gene encoding a putative transcriptional regulator of ETT2 associated genes.

134 ltogether, these data show that bHLH121 is a regulator of Fe homeostasis that acts upstream of FIT in

135 ing transcription factor 4 (ATF4) as a novel regulator of fetal gamma-globin gene expression in human

136 sor, RbsR, was also defined as a pleiotropic regulator of flotation and virulence factor elaboration

137 cular studies within this region highlighted regulator of G-protein signaling 4 (Rgs4) within laser-c

138 multifaceted and therapeutically targetable regulator of GC responses.

139 t is transcriptionally silent, is a critical regulator of gene expression.

140 e or nonsense variants in a known epigenetic regulator of gene expression: ten-eleven translocation m

141 Our results establish H1 as a critical regulator of gene silencing through localized control of

142 rect transcriptional repressor of the master regulator of growth, Myc.

143 actor like growth factor (HB-EGF), a crucial regulator of heart valve development in mice.

144 rginine methyltransferase 1 (PRMT1) is a key regulator of hepatic immune responses.

145 VuPOB1 is shown to be a positive regulator of HR since silencing of VuPOB1 expression in

146 we can block EHT, identifying an additional regulator of HSPC development.

147 -regulated anion channels (VRAC), as a vital regulator of hypotonicity-induced, but not DAMP-induced,

148 Here, we identified c-Maf as an essential regulator of ILC3 homeostasis and plasticity that limits

149 a novel role for this cytokine as a central regulator of immunity in lymphatic organs.

150 noxide, bilirubin, and iron, is an important regulator of inflammation and epithelial responses in th

151 has recently been implicated as an essential regulator of inflammation in the oral cavity.

152 2 (CITED2) as a critical intrinsic negative regulator of inflammation, which broadly attenuates pro-

153 Thus, [Ca(2+)](ER) is a major regulator of InsP(3)R channel activity and InsP(3)R-medi

154 tly interacts with IR to serve as a feedback regulator of insulin action in control of liver metaboli

155 A key regulator of insulin- and exercise-stimulated glucose up

156 The (pro)renin receptor (PRR), a key regulator of intrarenal renin-angiotensin system (RAS),

157 In this review, we focus on PIP(2) as a regulator of ion channels in smooth muscle cells and end

158 in (HTT) protein has emerged as an important regulator of its localization, structure, aggregation, c

159 A central regulator of leukocyte recruitment is Rac1.

160 antly expressed in hepatocytes as a critical regulator of lipid metabolism, and clinical trials targe

161 hat transcription factor EB (TFEB), a master regulator of lysosomal biogenesis and autophagy(4,5), is

162 of transcription factor EB (TFEB), a master regulator of lysosomal biogenesis and autophagy.

163 signal regulatory protein alpha, a negative regulator of macrophage phagocytosis allowing repression

164 methylcytosine (5mC), the central epigenetic regulator of mammalian DNA.

165 how that transcription factor AP2 (Tfap2), a regulator of mammalian germ lines, acts to commit adult

166 Here we identified CD177 as a novel regulator of mammary epithelial proliferation and breast

167 They include the entire Nodal pathway, a key regulator of mesoderm development and left-right axis sp

168 BACKGROUNDInsulin is a key regulator of metabolic function.

169 AMPK is a central regulator of metabolism and autophagy.

170 211 has previously been shown to be a direct regulator of metabolism in BRAF(V600E)-mutant melanoma c

171 e Tricornered (Trc) as a Pavarotti-dependent regulator of microtubule sliding in neurons.

172 MNRR1 (CHCHD2) is a bi-organellar regulator of mitochondrial function that directly activa

173 abenula complex is appreciated as a critical regulator of motivated and pathological behavioral state

174 ase enzyme Katanin is emerging as a critical regulator of MT dynamics.

175 f DNA damage responses 1 (REDD1), a negative regulator of mTOR/protein kinase B, is poorly understood

176 Signaling by G-CSF, a regulator of neutrophil development, trafficking, and fu

177 xpectedly, one top hit was Traf3, a negative regulator of NF-kappaB signaling that has never previous

178 ous studies suggested that NRARP, a negative regulator of Notch signaling, could have a suppressive r

179 ur identification of EGLN3, a known negative regulator of nuclear factor kappaB (NF-kappaB), as a dir

180 responsive behavior, functioning as a global regulator of organismal responses to stress.

181 rator-activated receptor (PPAR) delta as key regulator of osteoblast metabolism.

182 ace adhesion receptor CD44 as a key positive regulator of PD-L1 expression in these cancers.

183 ligase by Egr2, the central transcriptional regulator of peripheral myelination, to its target genes

184 While PKA is a well-known regulator of physiological and oncogenic events, the rol

185 findings suggest that TRIM32 functions as a regulator of PKCzeta that controls the differentiation o

186 Our results establish BIN2 as a central regulator of platelet activation in thrombosis and throm

187 Together our data identify LYN as a key regulator of pMo development and a potential therapeutic

188 patterning, identifying Nkx2.1 as a negative regulator of prethalamic identity.

189 PI3Kdelta is a key regulator of regulatory T (Treg) cell function.

190 l role in cell growth control as the central regulator of RNA polymerase (Pol) III activity.

191 n conclusion, we identified FOSL1 as a novel regulator of sepsis-induced deviant angiogenic signaling

192 SCYL-1/SCYL1 is an evolutionarily conserved regulator of Slo2 channels.

193 e alpha (RPTPalpha) is an important positive regulator of SRC kinase activation and a known promoter

194 ults identify mTOR signaling as an important regulator of striatal functions through an intricate mec

195 he E3 ubiquitin ligase Peli1 as an important regulator of T cell metabolism and antitumor immunity.

196 the tumor microenvironment and as a negative regulator of T-cell tumor infiltration and patient survi

197 ific role of PFN2 as a stable interactor and regulator of the actin N-terminal acetyltransferase NAA8

198 reprogramming and upregulates NRF2, a master regulator of the antioxidant network.

199 o, MCs hindered activation of cMET, a master regulator of the basal program, and simultaneously promo

200 TM kinase is a tumor suppressor and a master regulator of the DNA damage response.

201 ulum (ER), is a recently identified negative regulator of the ER-associated retinal pigment epitheliu

202 gy and that UBQLN2 functions as an important regulator of the expression and stability of ATP6v1g1.

203 irectional promoter with MAP3K4, an upstream regulator of the MAPK signaling pathway, and regulates i

204 ction of NIN-LIKE PROTEIN 7 (NLP7), a master regulator of the nitrogen signaling pathway in plants.

205 hsa-miR-223-3p was a key regulator of the TLR and Th17 pathways in the sputum of

206 Carboxylesterase Notum is a negative regulator of the Wnt signaling pathway.

207 dings highlight cell metabolism as a crucial regulator of these processes.

208 if-containing protein 1 (SARM1) is a central regulator of this neurodegenerative process(5-8), and it

209 indings demonstrate that EphA4 is a negative regulator of Tie2 receptor signaling, which limits pial

210 subunits GluN1 and GluN2A as well as KEAP1 (regulator of transcription factor NRF2).

211 ediator complex, which is a deeply conserved regulator of transcription in eukaryotes.

212 (PGC)-1alpha, has been proposed as a master regulator of tumor oxidative phosphorylation.

213 plemented a comprehensive screen to discover regulators of (i)Mg(2+) dynamics.

214 Fs) Kalirin and Trio have emerged as central regulators of actin dynamics at the synapse.

215 monomeric GTPases Rac and Rho are important regulators of actin.

216 s in gene expression levels of key enzymatic regulators of biochemical reactions linked to transmethy

217 cytidine residues, are now recognized as key regulators of both cellular and viral mRNA function.

218 l-surface proteomic profiling in discovering regulators of brain wiring.

219 ic entry due to overaccumulation of negative regulators of cell cycle such as Wee1-like protein kinas

220 Phosphoinositides (PI) are key regulators of cellular organization in eukaryotes and ge

221 iology analyses reveal new insights and gene regulators of cellular senescence.

222 gram was driven by the receptor CXCR2 and by regulators of circadian cycles.

223 d highlights the genomic context of putative regulators of cyanobacterial sigma factors.

224 ole of actin elongation factors as potential regulators of developmental axon regrowth.

225 he expression profiles of central epigenetic regulators of DNA methylation, histone modifications and

226 feasibility of this approach for identifying regulators of dosage-sensitive genes.

227 adhesion, whereas the expression of negative regulators of E-cadherin was decreased.

228 e show that MADS78 and MADS 79 are essential regulators of early seed developmental transition and im

229 Histone deacetylases (HDACs) are important regulators of gene expression that are aberrantly regula

230 s (miRNAs) are critical post-transcriptional regulators of gene expression.

231 iew, we posit that SPs are central chromatin regulators of gene silencing that establish immune cell

232 ple GRNs within a species to detect putative regulators of important plant pathways and provides pote

233 anscriptomic signatures enriched in negative regulators of inflammation.

234 nd tribbles pseudokinase 3 (TRIB3), negative regulators of innate immune signaling, in HT-29 intestin

235 sulinemia through targeting several critical regulators of insulin secretion and beta cell proliferat

236 e in the S/G2 phase as potent inhibitors and regulators of L1 activity.

237 ormation by trafficking PA and/or PIP, known regulators of membrane trafficking between organellar su

238 um and reactive oxygen species, are also key regulators of mitochondrial cell death pathways.

239 molecules (dscam and dscaml1) are essential regulators of neural circuit assembly, but their roles i

240 Additionally, they are negative regulators of nuclear RNAi triggered from exogenous sour

241 an important role for two WRKYs as positive regulators of plant immunity against bacterial and poten

242 ptor) alpha and gamma, known transcriptional regulators of postnatal mitochondrial biogenesis and fun

243 tein degradation have emerged as fundamental regulators of proteome complexity that regulate stem cel

244 , we identified PTEN and DNA-PK as essential regulators of replication checkpoint arrest in response

245 Although multiple upstream regulators of RhoA have been identified, the temporal re

246 ytically inactive, similar to known negative regulators of RNA editing.

247 AMTA2, and CAMTA3 (CAMTA123) serve as master regulators of salicylic acid (SA)-mediated immunity, rep

248 Negative regulators of stress signaling, such as ENHANCED DISEASE

249 of DC-mediated priming in identifying novel regulators of T cell differentiation.

250 analyses identify Pbx3 and Meis1 as critical regulators of tail regeneration and axon organization.

251 Jasmonates are key regulators of the balance between defence and growth in

252 junctions and connexin hemichannels are key regulators of the biology of neural progenitors during d

253 as a broad transcriptional repressor of key regulators of the cell cycle, in turn influencing contac

254 MicroRNAs (miRNAs) are key regulators of the immune system, yet their variation and

255 Sproutys are negative regulators of the Ras/Raf/MAPK signaling pathway and inv

256 that were previously identified as negative regulators of the type-II interferon response (for examp

257 rion and its associated proteins are crucial regulators of these responses and related pathways such

258 of circulating miRNAs, which were predicted regulators of transcripts downregulated in the bone marr

259 BC200 and the rodent analog BC1 as negative regulators of translation in both cell-based and in vitr

260 oplastic monocytic cells have emerged as key regulators of tumor maintenance and progression.

261 yeast one-hybrid assay to identify potential regulators of vascular identity.

262 tations in the NLR gene SNC1 or the immunity regulator PAD4.

263 HC class I and down-regulation of checkpoint regulator PD-L1 on the cancer cells.

264 patiotemporal expression of the plasmodesmal regulator PDLP5 in cells overlying LRP, creating a negat

265 unomodulatory and antibiofilm innate defense regulator peptide (IDR)-1018 based on three different sy

266 t activation of the glucose/lipid metabolism regulator peroxisome proliferator-activated receptor gam

267 growth of leukemia cells via the glycolytic regulator PFKFB3.

268 We identify a quartet of transcriptional regulators promoting hPSC self-renewal including ZNF398,

269 (PaFtsZ) and the effects of its two positive regulator proteins, ZipA and ZapA.

270 ntly limited knowledge about transcriptional regulators regulating these repair programs.

271 eveal that, in planta, the majority of these regulators repress the transcription of genes encoding c

272 crease E2F signaling by binding E2F negative regulator Retinoblastoma-1 (RB).

273 through the up-regulation of the EMT master regulator Slug, a process that is dependent on both MEK/

274 NSCs, where it colocalizes broadly with NSC regulator SOX2.

275 ubunit and activation of the transcriptional regulator STAT5.

276 Mutations in epigenetic regulators such as DNMT3A and TET2 confer an advantage b

277 ion and degradation of several transcription regulators, such as LMO2, LMO4, LHX2, LHX3, LDB1, and th

278 use shorter FLS interact with SNX9, an actin regulator that binds phosphoinositides during endocytosi

279 We identified a new Fur-controlled regulator that is upregulated upon iron starvation.

280 identify TEX15 as a new essential epigenetic regulator that may function as a nuclear effector of MIL

281 Tfap2c and Tead4 induce expression of actin regulators that control the recruitment of apical protei

282 significantly expand the list of epigenetic regulators that impact nuclear morphology.

283 tiotemporal localization dynamics of the key regulators that master the two intertwined and transient

284 st that ringer acts as a hub for microtubule regulators that relays cellular status information, such

285 luding calcium transporters and cytoskeletal regulators, that are associated with the RB and may be i

286 The inheritance of regulators through cell division is a key deterministic

287 our data reveal that -31CBS acts as critical regulator to define +19-enhancer and the leukemic prone

288 demic researchers, clinicians, patients, and regulators to discuss methods to advance the development

289 evelopment of allosteric HDAC inhibitors and regulators to improve the therapy for several disease st

290 ress, bacteria utilize iron-dependent global regulators to sense the iron status of the cell and regu

291 s study, we found that another key virulence regulator, ToxR, was important for V. cholerae resistanc

292 ridization to identify novel transcriptional regulators, we show that chromatin remodeler Hmga1 is hi

293 c epithelial cells expressing the autoimmune regulator were detected within 10 days of gene transfer,

294 Protein and transcript levels of cell cycle regulators were examined in breast cancer cells.

295 to enhance translation of key morphogenetic regulators, while also destabilizing sentinel mRNAs that

296 The actin cytoskeletal regulator Wiskott Aldrich syndrome protein (WASp) has be

297 4 (BRD4) is a transcriptional and epigenetic regulator with intrinsic kinase and histone acetyltransf

298 these codes to predict CIGs and their master regulators with high accuracy.

299 size through control of the transcriptional regulators YAP (yes-associated protein) and TAZ.

300 activity of the prosurvival transcriptional regulator Yes-associated protein.