ライフサイエンスコーパス: regulatory factor

1 horylation dependent binding of a proteasome regulatory factor.

2 tes maturation through secondary postmitotic regulatory factors.

3 y which Dbp5 and mRNA export is modulated by regulatory factors.

4 culating hormones, neural signals, and local regulatory factors.

5 is was an indirect effect through additional regulatory factors.

6 highly dose-sensitive in its use of crucial regulatory factors.

7 itates binding and recruitment of additional regulatory factors.

8 ources of data to improve predictions for AS regulatory factors.

9 enzymes, architectural proteins, and immune regulatory factors.

10 k data, to characterize the cooperativity of regulatory factors.

11 iled understanding of relevant developmental regulatory factors.

12 I interferon (IFN) signaling and interferon regulatory factor 1 (IRF-1) expression is required to en

13 The transcription factor interferon regulatory factor 1 (IRF-1) has a demonstrated role in s

14 nt-associated swelling.IMPORTANCE Interferon regulatory factor 1 (IRF-1) is a transcription factor th

15 Interferon regulatory factor 1 (IRF-1) is a tumor suppressor that i

16 or beta (TGF-beta) signaling, and interferon regulatory factor 1 (IRF-1) transactivation.

17 ransient nature in the absence of interferon-regulatory factor 1 (IRF-1), a transcription factor with

18 uble-stranded RNA, depends on the interferon regulatory factor 1 (IRF1) and IRF2 transcription factor

19 cells are defective in inducible interferon regulatory factor 1 (IRF1) expression by occluding RelA

20 and blocking the activating function of IFN regulatory factor 1 (IRF1).

21 with the PDZ protein, Na(+) /H(+) exchanger regulatory factor 1 (NHERF-1/EBP50).

22 caffolding protein sodium-hydrogen exchanger regulatory factor 1 (NHERF1) interacts with the calcium

23 ctors of 53BP1, including replication timing regulatory factor 1 (RIF1) and Pax transactivation domai

24 irus 8 (HHV-8) gene product viral interferon regulatory factor 1 (vIRF-1) is targeted to mDRM during

25 Viral interferon regulatory factor 1 (vIRF1), a Kaposi sarcoma herpesviru

26 One such protein, viral interferon regulatory factor 1 (vIRF1), targets STING by preventing

27 dietary antigen was dependent on interferon regulatory factor 1 and dissociated from suppression of

28 -->induction of cAMP-->downregulation of IFN regulatory factor 1 expression and binding to the p28 IF

29 and macrophage recruitment (e.g., interferon regulatory factor 1, CD97), adaptive immune response (in

30 IFN regulatory factor-1 (IRF-1) is a nuclear transcription f

31 on was STAT3-dependent and we identified IFN regulatory factor-1 (IRF1) as the STAT3-inducible mediat

32 induced nuclear translocation of interferon-regulatory factor-1 (IRF1) in hepatocytes in vivo, and C

33 Interferon regulatory factor-1 (IRF1) is a tumor suppressor that re

34 Additionally, infected IFN regulatory factor-1 and IFNAR KO macrophages had reduced

35 However, activation of NF-kappaB, IFN regulatory factor-1, and MAPKs, all of which regulate CC

36 In this study, we demonstrate that IFN regulatory factor 2 (IRF2), an ISG and a negative regula

37 on factor C3 (RFC3), FAM111A, and interferon regulatory factor 2 (IRF2)-were confirmed by custom assa

38 ion of the transcription cofactor interferon regulatory factor 2-binding protein 2 (IRF2BP2), and gen

39 erferon genes-TANK-binding kinase-interferon regulatory factor 3 (cGAS-STING-TBK1-IRF3) signaling pat

40 ear factor kappaB (NF-kappaB) and interferon regulatory factor 3 (IRF-3) at a step subsequent to thei

41 ear factor kappaB (NF-kappaB) and interferon regulatory factor 3 (IRF-3), classically inducing IFNbet

42 We show that influenza B virus induces IFN regulatory factor 3 (IRF3) activation and IFN-lambda1 ge

43 )-dependent signaling pathway leading to IFN regulatory factor 3 (IRF3) activation and induction of I

44 Early activation of IFN regulatory factor 3 (IRF3) and NF-kappaB was observed in

45 to sequential phosphorylation of interferon regulatory factor 3 (IRF3) and p65/RelA.

46 Interferon regulatory factor 3 (IRF3) and type I interferons (IFNs)

47 l infection by degradation of the interferon regulatory factor 3 (IRF3) has been subject of conflicti

48 viral signaling protein (MAVS) or interferon regulatory factor 3 (IRF3) in the IFN induction pathways

49 Interferon regulatory factor 3 (IRF3) is a transcription factor inv

50 rmed that these miRNAs potentiate interferon regulatory factor 3 (IRF3) phosphorylation and transloca

51 Interferon regulatory factor 3 (IRF3) regulates hepatocyte apoptosi

52 P-AMP synthase (cGAS), STING, and interferon regulatory factor 3 (IRF3) signaling.

53 orylates the transcription factor interferon regulatory factor 3 (IRF3) to promote interferon express

54 capable of blocking activation of interferon regulatory factor 3 (IRF3) via the retinoic acid inducib

55 expression and phosphorylation of interferon-regulatory factor 3 (IRF3) was decreased in EML-TA cells

56 Interferon regulatory factor 3 (IRF3), a key signal mediator/transc

57 in this study show that cFLIPL inhibits IFN regulatory factor 3 (IRF3), a transcription factor centr

58 nding kinase 1 (TBK1) to activate interferon regulatory factor 3 (IRF3), resulting in production of t

59 e of inoculation independently of interferon regulatory factor 3 (IRF3)-, IRF7-, and IFNAR1-mediated

60 terferons (IFNs), despite maintenance of IFN regulatory factor 3 (IRF3)-dependent IFN-stimulated gene

61 TANK-binding kinase 1 (TBK1) and interferon regulatory factor 3 (IRF3).

62 /or suppressing the activation of interferon regulatory factor 3 (IRF3).

63 y facilitating the degradation of interferon regulatory factor 3 (IRF3).

64 activate the transcription factor interferon regulatory factor 3 (IRF3).

65 the transcription factors NF-kappaB and IFN regulatory factor 3 (IRF3).

66 romoter when it was stimulated by interferon regulatory factor 3 (IRF3)/5D or its upstream molecules

67 and increases LPS-induced NF-kappaB and IFN regulatory factor 3 activation and IL-10 secretion, indi

68 factors was increased, including interferon regulatory factor 3 and 7 (IRF-3 and IRF-7) and STAT-1,

69 increased baseline expression of interferon regulatory factor 3 and 7 mRNAs and production of distin

70 phosphorylation of TANK-binding kinase 1/IFN regulatory factor 3 and production of IFN-beta.

71 e activation of the transcription factor IFN regulatory factor 3 and the molecule UNC93B1, indicating

72 , and mice with disruption of the interferon regulatory factor 3 gene (Irf3(-/-)), with or without di

73 ction, type I IFN signaling by STING and IFN regulatory factor 3 is detrimental to the host during F.

74 to a self-Ag, DC-intrinsic expression of IFN regulatory factor 3 is required to induce optimal prolif

75 ain-containing adapter inducing IFN-beta-IFN regulatory factor 3 pathway is required for Ezrin-defici

76 gregation, and TANK-binding kinase 1 and IFN regulatory factor 3 phosphorylation in inflammasome-defi

77 binding kinase-1, resulting in decreased IFN regulatory factor 3 phosphorylation.

78 serine/threonine kinase 1)-IRF3 (interferon regulatory factor 3) signaling cascade leading to IFN-be

79 ation of the transcription factor IRF-3 (IFN regulatory factor 3).

80 hol-induced hepatic steatosis and interferon regulatory factor 3-mediated apoptosis.

81 dited knockout human cells, we show that IFN regulatory factor 3-mediated IFN induction and downstrea

82 MOV10 enhanced IFN regulatory factor 3-mediated transcription of IFN.

83 1, TAK1, and phosphorylation of TBK1 and IFN regulatory factor 3.

84 pressed IFN-I signaling via an AKT/FOXO3/IFN regulatory factor 3/7 pathway.

85 (HSV)-infected cells and initiate interferon regulatory factor-3 signaling, but it has been unclear h

86 works of transcription factors involving IFN regulatory factor 4 (IRF4) and IRF8, and are specialized

87 In this study, we report that IFN regulatory factor 4 (Irf4) is highly expressed in murine

88 The interferon regulatory factor 4 (IRF4) is known to be highly express

89 production, lung histopathology, interferon regulatory factor 4 (IRF4) mRNA expression, and nuclear

90 roducts, the transcription factor interferon regulatory factor 4 (IRF4) promotes regulatory T cell (T

91 Here, we demonstrated that interferon regulatory factor 4 (IRF4) was a key transcriptional det

92 ssion of the transcription factor interferon regulatory factor 4 (IRF4).

93 IL-2Ralpha, T-bet, IFNgammaR, and interferon regulatory factor 4 (IRF4).

94 and reduced protein expression of interferon regulatory factor 4 and B-cell lymphoma 6 (BCL6) in huma

95 molecule inhibition downregulate interferon regulatory factor 4 and MYC, and provides an explanation

96 hermore, expansion of both Th2-promoting IFN regulatory factor 4(+) programmed death ligand 2(+) dend

97 omide are associated with reduced interferon regulatory factor 4, a downstream target of cereblon.

98 g transcription factors including E4BP4, IFN regulatory factor 4, and GATA3.

99 rentiation is associated with defects in IFN regulatory factor 4, B cell-activating transcription fac

100 reg cells used the transcription factor, IFN regulatory factor 4, to dampen harmful Th2 cell response

101 es CCL17 production by acting through an IFN regulatory factor 4-dependent (IRF4-dependent) pathway i

102 und to be driven by 2 variants of interferon regulatory factor 4-dependent dermal type 2 conventional

103 Taken together, induction and IFN regulatory factor 4-dependent localization of Treg cells

104 IFN regulatory factor 4-positive (IRF4+) DCs constitutively

105 ng Jun family members, GATA3, E4BP4, and IFN regulatory factor 4.

106 Interferon (IFN)-regulatory factor 5 (IRF-5) is a transcription factor th

107 Gain-of-function polymorphisms in IFN regulatory factor 5 (IRF5) are associated with an increa

108 Transcription factor interferon regulatory factor 5 (IRF5) has been implicated in polari

109 Interferon regulatory factor 5 (IRF5) is a key transcription factor

110 Interferon regulatory factor 5 (IRF5) is a member of the IRF family

111 Interferon regulatory factor 5 (IRF5) is a molecule of interest in

112 have shown that the transcription factor IFN regulatory factor 5 (IRF5) polarizes macrophages toward

113 ted LMP1 expression, we find that interferon regulatory factor 5 (IRF5), a direct target of p53, is a

114 tivity controls the activation of interferon regulatory factor 5 (IRF5), a transcription factor impli

115 inhibited both TLR7/8- and TLR9-induced IFN regulatory factor 5 and NF-kB p65 nuclear translocation.

116 e to decreased P-STAT1 (Y701) and interferon regulatory factor 5 compared with NOD mice.

117 a 5 bp CGGGG length polymorphism in the IFN regulatory factor 5 gene (IRF5) was genotyped by PCR.

118 To discover the regulatory factors, 5 candidate 12-HETER1 promoter cis e

119 or-alpha, the chemokine CCL2, and interferon regulatory factor-5 (IRF5), a marker of inflammatory mac

120 Interferon regulatory factor 6 ( IRF6) acts as a tumor suppressor a

121 tions and common polymorphisms in interferon regulatory factor 6 ( IRF6) are associated with both syn

122 Interferon Regulatory Factor 6 (IRF6) and TWIST1 are transcription

123 ' risk allele increased transcription of the regulatory factor 6 (RFX6) gene, increased homeobox B13

124 Mutations in IRF6 (Interferon Regulatory Factor 6) and GRHL3 (Grainyhead-like 3) cause

125 pression by hMPV was dependent on interferon regulatory factor 7 (IRF-7) expression but not on IRF-3

126 ignaling leading to NF-kappaB and interferon regulatory factor 7 (IRF7) activation has not been inves

127 mains of TRIF and RIP1 to disrupt interferon regulatory factor 7 (IRF7) activity, a critical type I I

128 ers showed increased basal expression of IFN regulatory factor 7 (IRF7) and IFN-beta, as well as incr

129 rve that RelA inducibly binds the native IFN regulatory factor 7 (IRF7) promoter in an ATM-dependent

130 ral immunity by downregulation of interferon regulatory factor 7 (IRF7), an immune factor with a pivo

131 e downstream transcription factor interferon regulatory factor 7 (IRF7), and type I interferons (IFN-

132 , IL-33 downregulated viperin and interferon regulatory factor 7 gene expression and rapidly degraded

133 roduction of distinct isoforms of interferon regulatory factor 7 protein.

134 Lastly translocation of interferon regulatory factor 7(IRF7) from the cytosol to the nuclei

135 The transcription factor IRF7 (interferon regulatory factor 7) is a key regulator of type I interf

136 ession of antiviral host factors (interferon regulatory factor 7, CXCL10 [gamma interferon-inducible

137 encodes the transcription factor interferon regulatory factor 7, in an otherwise healthy child who s

138 masome by reducing the mRNA stability of IFN regulatory factor 7, which regulated AIM2 transcription.

139 IL-6 in autoantibody production, but not IFN regulatory factor 7.

140 The transcription factor (TF) interferon regulatory factor 8 (IRF8) controls both developmental a

141 IFN regulatory factor 8 (IRF8) is constitutively expressed i

142 The homozygous K108E mutation of interferon regulatory factor 8 (IRF8) is reported to cause dendriti

143 Here we show that interferon regulatory factor 8 (IRF8) is required for the expressio

144 ffect of the transcription factor interferon regulatory factor 8 (IRF8), which is highly expressed in

145 the IFN-gamma response and repressed the IFN regulatory factor 8-regulated network that controls cent

146 no-1 and the transcription factor interferon regulatory factor 8.

147 In vitro, increased expression of interferon regulatory factor-9 and IRG1 and itaconic acid treatment

148 miR93 inhibits interferon regulatory factor-9 to decrease IRG1-itaconic acid produ

149 1 is not an miR93 target but that interferon regulatory factor-9, which can regulate IRG1 expression,

150 cted to examine the role of miR93-interferon regulatory factor-9-immunoresponsive gene-1 (IRG1)-itaco

151 togenes is mainly controlled by the positive regulatory factor A (PrfA), a member of the Crp/Fnr fami

152 se brain, including reduced levels of myelin regulatory factor and myelin basic protein, and decrease

153 O), an essential adaptor bridging interferon-regulatory factor and NF-kappaB activation.

154 clusters are enriched in binding of specific regulatory factors and are therefore defined as 'Regulat

155 A complex system comprised of regulatory factors and energy metabolic machinery, encod

156 , there is relatively little known about the regulatory factors and mechanisms that govern the spread

157 elective recruitment of cis-proline-specific regulatory factors and region-specific modulation of the

158 sured along with markers of RNA polymerase I regulatory factors and regulators of protein synthesis.

159 in our understanding of the transcriptional regulatory factors and signaling networks that serve to

160 emonstrated that TRIM29 inhibited interferon-regulatory factors and signaling via the transcription f

161 vironmental stimuli and a complex network of regulatory factors are known to modulate expression of V

162 If spike rate is modulated by common regulatory factors as seizures then spikes may be useful

163 tations in IRF8, which encodes an interferon regulatory factor, as a cause of familial NK cell defici

164 PDI5 and NAI2 are negative regulatory factors, as pdi5, nai2, and pdi5-2nai2-3 muta

165 he ParB centromere-binding protein and other regulatory factors at the poles.

166 d populations of these states changed as the regulatory factors complexin and Munc13 were added.

167 propose that the Mcl-1L/S balance is a novel regulatory factor controlling the mitochondrial fusion a

168 n cord versus peripheral blood and to define regulatory factors controlling this proliferation, we co

169 cture and DNA modifications [i.e., chromatin regulatory factors (CRF)] and genes encoding histone pro

170 tein 1 (ZBP1)/DNA-dependent activator of IFN-regulatory factors (DAI) that contain receptor-interacti

171 rect molecular interactions between multiple regulatory factors during neuronal differentiation in mi

172 as measurable ATPase activity alone, several regulatory factors (e.g., RNA, nucleoporin proteins, and

173 erentiation and altered expression of muscle regulatory factors, embryonic myogenesis and formation o

174 Abl suppresses the actin-regulatory factor Enabled, and we find that Abl also act

175 expression may be controlled by its internal regulatory factors, exclusively, or by external subsyste

176 Here, we demonstrate that EGFL6, a stem cell regulatory factor expressed in ovarian tumor cells and v

177 s from Nuclear Factor (NF)-kB and Interferon Regulatory Factor families.

178 Members of the IFN regulatory factor family play critical roles in DC devel

179 13B/Blys) and APRIL (TNFSF13) are important regulatory factors for lymphocyte activation and surviva

180 RC2, and TrxG complexes, which are essential regulatory factors for the maintenance of transcriptiona

181 s controlled by the combinatorial effects of regulatory factors from different biological subsystems

182 Mutations of Chromatin regulatory factor genes were identified at a lower frequ

183 DNA-binding proteins, including the general regulatory factors (GRFs) Reb1p, Rap1p, and Abf1p, and P

184 ontain binding sites for one or more General Regulatory Factors (GRFs), most frequently Abf1 and Reb1

185 receptor (MOR) gene two decades ago, various regulatory factors have been shown to interact with the

186 still lack an integrated view of how all the regulatory factors identified interact or crosstalk to o

187 ne-4 of histone H3 (H3K4men) is an important regulatory factor in eukaryotic transcription.

188 ur findings indicate that CK is an important regulatory factor in plant adaptation to arsenic stress.

189 icted by CENTIPEDE analysis to be bound by a regulatory factor in sperm were correlated with genomic

190 ion to a cytosolic AKAP-PKA interaction as a regulatory factor in the control of canonical Wnt signal

191 The offspring thermogenesis and related regulatory factors in adipose tissue were evaluated.

192 permidine revealed the interplay of multiple regulatory factors in B. burgdorferi gene expression.

193 ession and association of T-bet, GATA-3, and regulatory factors in CD8(+) T cells isolated from the b

194 me the roles of NuA4 KAT and other chromatin regulatory factors in controlling antisense transcriptio

195 ansformations occur upon removal of specific regulatory factors in many different cellular contexts,

196 ation for understanding the role of multiple regulatory factors in modulating Fshb gene activity.

197 the past few years upon removal of specific regulatory factors in organisms from Caenorhabditis eleg

198 However, SlmA is distinct from other regulatory factors in that it must be DNA-bound to inter

199 tly improved the gene expression of myogenic regulatory factors in vitro, suggesting myogenic activat

200 Variation in regulatory factors, including microRNAs (miRNAs), contri

201 m cells (ESCs) and are controlled by diverse regulatory factors, including pluripotent factors, epige

202 It is governed by multiple regulatory factors, including RNA-binding proteins (RBPs

203 These genes encode key regulatory factors, including the SOX trio proteins, and

204 A small number of regulatory factors influence transcription elongation on

205 Kinetic studies of regulatory factor interactions at the PPARgamma2 promote

206 opmentally important genes, especially those regulatory factors involved in amphioxus development, an

207 To further define regulatory factors involved in gH/gL trafficking, a CMV

208 network of chaperones, proteasomes and other regulatory factors involved in their clearance.

209 tion of transcription factors NF-kappaB, IFN regulatory factor (IRF) 1, and IRF5 driving the expressi

210 TRIF, resulting in activation of interferon regulatory factor (IRF) 3.

211 week-old mice triply deficient in interferon regulatory factor (IRF) as a model, we show that blood-b

212 cyte inflammation, members of the interferon regulatory factor (IRF) family may also play a role in t

213 IRF4 is a unique member of the interferon regulatory factor (IRF) family playing critical regulato

214 tes excess c-di-AMP activates the interferon regulatory factor (IRF) pathway with enhanced levels of

215 The transcription factor interferon regulatory factor (IRF)-5 is an important modulator of m

216 ce (nonallergic) and identified CCL7 and IFN regulatory factor (IRF)-7 among the most upregulated mRN

217 One integral player is IFN regulatory factor (IRF)-8, which promotes monocyte/dendr

218 anscription synergy of Il6 and Il12b via IFN regulatory factor (IRF)1 (TLR3-TIR domain-containing ada

219 ma cell-generating transcription factors IFN regulatory factor (IRF)4 and Blimp1, and paradoxically a

220 IFN regulatory factor (IRF)7 is a critical regulator of type

221 nthase (cGas), as well as the downstream IFN regulatory factors (IRF) 3 and 7 in type I IFN induction

222 e fusion protein of porcine interferon (IFN) regulatory factors (IRF) 7 and 3 [IRF7/3(5D)] strongly i

223 a fusion protein of porcine interferon (IFN) regulatory factors (IRF) 7 and 3 delivered by an adenovi

224 Interferon regulatory factors (IRF) have critical functions in lymp

225 These include the interferon regulatory factor, IRF1, and the chemokine, CXCL10.

226 1 transcriptional repressors, the interferon regulatory factors IRF2 and IRF2BP2, which likely leads

227 ation of the transcription factor interferon regulatory factor (IRF4), which, along with the environm

228 ough host sensory pathways that activate IFN regulatory factors (IRFs) and nuclear factor kappaB.

229 dback loops mediated by inducible interferon regulatory factors (IRFs) and retinoic acid inducible ge

230 The key role of Interferon regulatory factors (IRFs) as controllers of the human La

231 te that BAFF is a bona fide ISG and that IFN regulatory factors (IRFs) control the expression of BAFF

232 Interferon (IFN) regulatory factors (IRFs) have crucial roles in immune r

233 IFN regulatory factors (IRFs) help to shape the immune respo

234 t three KSHV homologs of cellular interferon regulatory factors (IRFs), known as viral IRFs (vIRFs),

235 code viral homologues to cellular interferon regulatory factors (IRFs), known as vIRFs.

236 ress viral homologues to cellular interferon regulatory factors (IRFs), termed viral IRFs (vIRFs).

237 The differential expression of MMP-9 and its regulatory factors is also examined.

238 that the plasticity accommodated by certain regulatory factors is conserved, despite substantial cha

239 miR-198 by suppressing the expression of the regulatory factor, KSRP (KHSRP).

240 As the regulatory factors, lncRNAs play critical roles in embry

241 We identified mitochondrial assembly regulatory factor (Marf), a mitochondrial fusion factor

242 Interactions with specific regulatory factors may provide a general mechanism to di

243 epetitive phosphorylation among central gene regulatory factors, may represent an important general p

244 compounds that inhibit the transcription co-regulatory factor MED1.

245 ression thus indicating a role for different regulatory factors modulating expression of the gene.

246 Myogenic regulatory factor (MRF) genes, MYOD1, MYOG, MYF6 and MYF

247 The myogenic regulatory factor (MRF) MYF5 is the earliest to be expre

248 ared regulatory programs that require muscle regulatory factor (MRF)-family genes.

249 The myogenic regulatory factor MRF4 is highly expressed in adult skel

250 Myogenic regulatory factors (MRFs), including Myf5, MyoD (Myod1)

251 Market requirements and regulatory factors must be considered in parallel with s

252 The myogenic regulatory factor MyoD has been implicated as a key regu

253 f myelin genes that are downstream of myelin regulatory factor (MYRF or MRF), a transcriptional regul

254 Myelin-gene Regulatory Factor (MyRF) is one of the master transcript

255 HFE), fatty acid desaturase 2 (FADS2)/myelin regulatory factor (MYRF), transmembrane protease, serine

256 he scaffolding proteins Na(+)/H(+) exchanger regulatory factor (NHERF) 1 and 2.

257 NHE3 directly binds Na(+)/H(+) exchanger regulatory factor (NHERF) family scaffolding proteins th

258 In this study, Na(+)/H(+) exchanger regulatory factor (NHERF)-1 loss-of-function and gain-of

259 nd several scaffold proteins, including NHE3 regulatory factors (NHERFs), inositol trisphosphate (IP(

260 lt2, indicating that CmSlt2 was a downstream regulatory factor of CmNox1 and was involved in conidiat

261 datasets: mRNA expression and the associated regulatory factors of miRNA and lncRNA, and ALV gene exp

262 2 and DNA-dependent activator of interferon regulatory factor) opened a new paradigm: Nucleic acid s

263 phoinositide 3-kinase (PI3K), and interferon regulatory factor pathways.

264 1, MAGI-2, and MAGI-3], Na(+)/H(+) exchanger regulatory factor proteins (NHERFs) (NHERF1, NHERF2, PDZ

265 Dynactin, another ubiquitous dynein-regulatory factor, releases dynein from an autoinhibited

266 Pharmacological inhibition of chromatin co-regulatory factors represents a clinically validated str

267 To test this, we inhibited the cytoskeletal regulatory factor Rho kinase.

268 The store-operated Ca(2+)entry-associated regulatory factor (SARAF) has recently been identified a

269 ed in silencing lines, suggesting that other regulatory factors should participate in pollen formatio

270 lving CREB1, NF-kappaB, STAT, and interferon regulatory factor signaling.

271 y step in NMD and occurs when SMG-1, its two regulatory factors SMG-8 and SMG-9, and UPF1 form a comp

272 ipt accumulation of important soybean embryo regulatory factors such as ABSCISIC ACID INSENSITIVE3 an

273 erts mucoprotective effects and that counter-regulatory factors such as dietary iron and luminal lipo

274 LIS1 concentration and the presence of other regulatory factors such as dynactin and may provide new

275 h vessel patterning might involve modulatory regulatory factors such as R-spondin 1 (Rspo1), an extra

276 se results indicate that posttranscriptional regulatory factors, such as microRNAs, influence the ass

277 n response to small changes in the levels of regulatory factors, such as the maternal Bicoid gradient

278 Of the various regulatory factors tested, only transforming growth fact

279 ephaly-1 (LIS1) is a highly conserved dynein-regulatory factor that binds directly to the dynein moto

280 tified hepatocyte nuclear factor 4alpha as a regulatory factor that bound endogenous CLDN7 promoter i

281 regulatory protein 2 (ESRP2) as a conserved regulatory factor that controls the neonatal-to-adult sw

282 We conclude that Slr1796 is a novel regulatory factor that modulates PSI titer.

283 ochondrial fission, Mff and Drp1 also act as regulatory factors that control mitochondrial fission an

284 Identifying the genomic regions and regulatory factors that control the transcription of gen

285 To identify regulatory factors that control the transcription of P5C

286 However, the origin and regulatory factors that maintain MHC II(+) macrophages r

287 versity and long-term balancing selection of regulatory factors that modulate HLA-C expression.

288 s suggested that miR858a targets a number of regulatory factors that modulate the expression of downs

289 Therefore, TbTim62 acts as a novel regulatory factor to maintain the levels of TIM in T. br

290 that allows for efficient activation of IFN regulatory factors to drive the antiviral transcriptome.

291 l's epigenome arises from interactions among regulatory factors-transcription factors and histone mod

292 Among these regulatory factors, we identify AHR, the aryl hydrocarbo

293 To uncover Gram-positive PBP regulatory factors, we used transposon-sequencing (Tn-Se

294 cited by SBI-756, DNA damage, and cell-cycle regulatory factors were prominent, with mutations in mel

295 xpress in a coordinated fashion the myogenic regulatory factors, while down-regulating the satellite

296 The regulatory factor X (RFX) family of transcription factor

297 trikingly and specifically enriched in islet Regulatory Factor X (RFX) footprints.

298 y indicated posttranscriptional increases in regulatory factor X 5 mRNA and protein expression in OAD

299 and miR-195 to the 3'-untranslated region of regulatory factor X 5.

300 egulated by the class II trans-activator and regulatory factor X, two transcription factors dedicated