ライフサイエンスコーパス: autoregulatory

1 ether and that the domain interaction can be autoregulatory.

2 eyond ribosomal RNA, and that they are often autoregulatory.

3 ulatory network we study is that of a single autoregulatory activator gene, and the two copies of the

4 Differentiation-associated and autoregulatory activities of BRN3A are respectively impa

5 wn renders some PyVs more susceptible to the autoregulatory activities of the miRNA, restoring miRNA

6 that simultaneous loss of both Sox15 and the autoregulatory activity of Su(H) reveals an important ro

7 The autoregulatory activity of this element was demonstrated

8 repertoires (targetomes) while their direct autoregulatory activity on virus-encoded early gene prod

9 alternative, as this creates a surface with autoregulatory activity upon exposure to blood.

10 h other's transcripts to create a network of autoregulatory and cross-regulatory feedback controls.

11 Both autoregulatory and dual feedback motifs were enriched in

12 s are composed of many positive and negative autoregulatory and feedback loops.

13 master switch itself is under both positive (autoregulatory) and negative control.

14 as the set of promoters for each TF itself (autoregulatory) and the immediately upstream and downstr

15 dback loop illustrates an unexpected mode of autoregulatory behavior of a transcription factor, is co

16 at residue 2, specifically R2G, disrupt the autoregulatory capability of the wild-type beta-tubulin

17 hat might play an important part in cerebral autoregulatory capacity after TBI.

18 uctural and functional changes that decrease autoregulatory capacity and increase susceptibility to a

19 inactive, but JAK2 JH2 was found to have low autoregulatory catalytic activity.

20 In vivo trafficking analysis revealed that autoregulatory CD8 T cells are dependent on neuroinflamm

21 These autoregulatory CD8 T cells required in vivo MHC class Ia

22 nces, pMHC-nanoparticle-induced expansion of autoregulatory CD8(+) T cells can effectively suppress t

23 Here we examine the dynamics of memory autoregulatory CD8(+) T cells specific for islet-specifi

24 n of autoantigen-loaded APCs by the expanded autoregulatory CD8(+) T cells.

25 Our results reveal how an autoregulatory cell cycle timer integrates growth and sp

26 nt, potentially missing important changes in autoregulatory characteristics.

27 ndings identify a novel Notch-dependent HRT2 autoregulatory circuit coordinating transcriptional regu

28 target of MYC transactivation, generating an autoregulatory circuit in myeloma cells.

29 thway during cardiogenesis and identifies an autoregulatory circuit in which tin limits its own expre

30 Thus, there is a recurrent autoregulatory circuit involving expression of p53, E2F1

31 An autoregulatory circuit is identified involving the contr

32 brafish larvae, wound repair is driven by an autoregulatory circuit that generates pro-migratory tiss

33 This shift establishes an autoregulatory circuit that maintains durable expression

34 functions as an integral part of a positive autoregulatory circuit to control cell fate.

35 frameshift is the sensor and effector in an autoregulatory circuit.

36 rocally upregulates KLF2, forming a positive autoregulatory circuit.

37 The Csr system of E. coli contains extensive autoregulatory circuitry, which governs the expression a

38 The uORF-mediated polyamine responsive autoregulatory circuits found in polyamine pathway mRNAs

39 nome engineering to delete a transcriptional autoregulatory, cis-acting motif in the che-1 zinc-finge

40 arinic m2 receptors (M2Rs) are implicated in autoregulatory control of cholinergic output neurons loc

41 tably maintained in an on or an off state by autoregulatory control of Sxl premRNA processing.

42 on communication was decreased indicating an autoregulatory control of the connexins.

43 rm to assess the integrity of cardiovascular autoregulatory control systems for risk assessment in he

44 a stable and coherent oscillatory dynamic of autoregulatory control via respiratory entrainment of th

45 We also report autoregulatory crosstalk between K7ac and S5p via RPRD p

46 reductase-thioredoxin system, generating an autoregulatory cycle that persists until the thiol-deple

47 Inhibition of the proteasome induces autoregulatory de novo formation of 20S and 26S proteaso

48 Recently, the C-terminal diaphanous-autoregulatory domain (DAD) and the C terminus (CT) of f

49 binds actin monomers through its diaphanous autoregulatory domain (DAD) that resembles a Wiskott-Ald

50 domain (mDiaN) and the C-terminal Diaphanous-autoregulatory domain (DAD).

51 itory domain (DID) and C-terminal diaphanous autoregulatory domain (DAD).

52 y domain (DID) and its C-terminal diaphanous autoregulatory domain (DAD).

53 endent localization and cleavage, C-terminal autoregulatory domain and regulation by an upstream open

54 iaphanous inhibitory domain and a Diaphanous autoregulatory domain.

55 partial truncation of the DIAPH1 diaphanous autoregulatory domain.

56 cycle is regulated by interaction partners, autoregulatory domains, and off-cycle states.

57 The Golgi Arf-GEFs contain multiple autoregulatory domains, but the precise mechanisms under

58 ting the interaction between the DID and DAD autoregulatory domains, which releases the FH2 domain to

59 Cerebral autoregulatory dysfunction after traumatic brain injury

60 Furthermore, intronic miR-421 may exert an autoregulatory effect on miR-374b and miR-545.

61 or their abilities to bind predicted AT-rich autoregulatory element (ARE) boxes within the sabRAS reg

62 The 5' 2.3 kb sequence functions as an autoregulatory element and directs reporter gene express

63 des the native Dll promoter, functions as an autoregulatory element by directly binding Dll.

64 egl-5 in the P12.pa cell is influenced by an autoregulatory element that is essential in wild type, b

65 r data show that sRNAs from 3' UTRs serve as autoregulatory elements allowing negative feedback contr

66 It has been shown recently that the main autoregulatory elements of PDZRhoGEF, the autoinhibitory

67 like their eukaryotic counterparts, possess autoregulatory elements that influence how hexameric mot

68 Sfpi1 gene by displacing PU.1 from positive autoregulatory elements.

69 Circadian rhythms are autoregulatory, endogenous rhythms with a period of appr

70 cket cell of external sensory organs, via an autoregulatory enhancer called the ASE.

71 nscription in a site-dependent manner via an autoregulatory enhancer containing a combination of mono

72 gesting a mechanism for priming the 3' Atoh1 autoregulatory enhancer needed for hair cell expression.

73 Mutations in an autoregulatory enhancer resulted in reduced levels of PT

74 domain is complemented by an adjacent 2.3-kb autoregulatory enhancer that is able to activate a heter

75 oncentrations and the mammary-specific Stat5 autoregulatory enhancer.

76 tion by Crispr/Cas9-mediated deletion of the autoregulatory exon induces expression of all SR protein

77 ranscriptional regulator, deformed epidermal autoregulatory factor 1 (Deaf1), that can regulate PTA e

78 the transcription factor Deformed Epidermal Autoregulatory Factor 1 (DEAF1).

79 widely deployed in cell lineages, where the autoregulatory factor controls the activity of a battery

80 cade is inhibited by farnesol, a C. albicans autoregulatory factor, and small molecules such as dodec

81 tional regulatory factor, deformed epidermal autoregulatory factor-1 (DEAF-1), also contributes to th

82 ated to atrophy, inflammation, or changes in autoregulatory factors or growth factors remains to be d

83 delayed ischemic deficits due to vasospasm, autoregulatory failure, and intravascular volume contrac

84 sites for transcription factors involved in autoregulatory feedback circuits.

85 e metabolism of FICZ, thereby disrupting the autoregulatory feedback control of cytochrome P4501 syst

86 These results demonstrate that autoregulatory feedback is necessary for the early-actin

87 These findings not only reveal an autoregulatory feedback loop between ATBF1 and estrogen-

88 We have previously identified an autoregulatory feedback loop between iASPP and p63, whic

89 ere, we show the existence of a proapoptotic autoregulatory feedback loop between p73, YAP, and the p

90 These results suggest that there is an autoregulatory feedback loop between the AhR and cytochr

91 We demonstrate that this autoregulatory feedback loop controls cell migration in

92 nism for genetic disease by disruption of an autoregulatory feedback loop critical for maintenance of

93 A positive autoregulatory feedback loop for Sxl was known to mainta

94 ings suggest the presence of a c-Myb-miR-15a autoregulatory feedback loop of potential importance in

95 provides a full-loop mechanism for a classic autoregulatory feedback loop proposed ~25 years ago.

96 hormone target and is involved in a positive autoregulatory feedback loop that modulates thyroid horm

97 ere we show that a hippocampal BDNF-positive autoregulatory feedback loop via CCAAT-enhancer binding

98 We demonstrate a novel autoregulatory feedback loop which controls crucial phys

99 ic marks, along with its participation in an autoregulatory feedback loop with genes known to transfo

100 to its own promoter, defining a new negative autoregulatory feedback loop within the core clock.

101 Thus, SCM participates in an autoregulatory feedback loop, enabling cells engaged in

102 intain its own expression through a positive autoregulatory feedback loop.

103 a9 and Meis1, indicating the existence of an autoregulatory feedback loop.

104 miRNAs identified act as part of a negative autoregulatory feedback loop.

105 vel, providing a substrate for an ultrashort autoregulatory feedback loop.

106 omposed of a transcription-translation-based autoregulatory feedback loop.

107 ostatic hypotheses by explicitly emphasizing autoregulatory feedback loops and known synaptic biology

108 splicing events that could be implicated in autoregulatory feedback loops in RBM39, HNRNPM, and U2AF

109 The clockworks are driven by autoregulatory feedback loops that lead to oscillating l

110 Autoregulatory feedback loops, where the protein express

111 followed by RNA-seq, to identify novel such autoregulatory feedback loops.

112 transcription in SLE T cells, we propose an autoregulatory feedback mechanism between CREM and AP-1.

113 irst miRNA that monitors c-Myc levels via an autoregulatory feedback mechanism in response to serum s

114 criptional reprogramming includes a positive autoregulatory feedback mechanism in which ectopic PHF7

115 current noncoding mutations in disrupting an autoregulatory feedback mechanism, thereby deregulating

116 gth viral genome, this mechanism promotes an autoregulatory feedback that decreases expression of tat

117 e a requirement for positive transcriptional autoregulatory feedback to attain the level of the neuro

118 RecADeltaC17 mutants, lacking a C-terminal autoregulatory flap, also promote strand exchange in a 5

119 in-specific CD8 T cells to optimally perform autoregulatory function in vivo.

120 ation of HdrR prevents the positive feedback autoregulatory function of HdrR, thereby maintaining a l

121 Myogenic vasoconstriction is an autoregulatory function of small arteries.

122 portant in patients with already compromised autoregulatory function.

123 he substrate binding site that might play an autoregulatory function.

124 f the link between genetic polymorphisms and autoregulatory function.

125 Autoregulatory gene circuits can be physically encoded w

126 and Sox9 induce MaSCs by activating distinct autoregulatory gene expression programs.

127 very of viral master circuits: virus-encoded autoregulatory gene networks that autonomously control v

128 ve more interactions with microRNAs than non-autoregulatory genes and 89% of autoregulatory TFs were

129 These transcription factors form an autoregulatory hormonal network that influences estrogen

130 Our findings establish the DnaB collar as an autoregulatory hub that controls the ability of the heli

131 rives monocyte proinflammatory processes and autoregulatory IL-10 in a serum IgE-dependent manner.

132 nd induced secretion of TNF-alpha, IL-6, and autoregulatory IL-10.

133 nsfer function analysis (gain and phase) and autoregulatory index (ARI) fit from spontaneous oscillat

134 blood flow, cerebral perfusion pressure, and autoregulatory index decreased markedly during hypotensi

135 NP did not prevent reductions in CBF, CPP or autoregulatory index during combined hypotension and FPI

136 blood flow, cerebral perfusion pressure, and autoregulatory index during hypotension in females but i

137 artery diameter, intracranial pressure, and autoregulatory index were determined before and after fl

138 We calculated autoregulatory indices for adjacent short segments of in

139 ndividuals in all (steady-state and dynamic) autoregulatory indices, ranging from low (almost absent)

140 s, thereby demonstrating the conservation of autoregulatory infrastructure across the IpaH enzyme fam

141 es provided evidence for crossregulatory and autoregulatory interactions among components of this com

142 ong with controlling membrane binding, these autoregulatory interactions inhibit the ability of Nwk-S

143 rritories by both cross-inhibitory and cross-autoregulatory interactions.

144 by eIF2alpha phosphorylation destabilizes an autoregulatory intramolecular interaction within eIF2alp

145 HAT assays suggest that the RING domain, the autoregulatory loop (AL) within the HAT domain, and the

146 thesis, our observations reveal a GATA1-heme autoregulatory loop and implicate GATA1 and heme as the

147 d middle meiotic promoter through a positive autoregulatory loop and is repressed in vegetative cells

148 monstrating the presence of another feedback autoregulatory loop between Cul3-Rbx1 and Nrf2.

149 An autoregulatory loop between INrf2 and Nrf2 regulates the

150 port a previously unrecognized bidirectional autoregulatory loop between MTA1 and tumor suppressor al

151 Previously we have shown a feedback autoregulatory loop between Nrf2 and INrf2 indicating th

152 We propose that a positive autoregulatory loop between Ntl/Bra and canonical Wnt si

153 these mechanisms Blimp-1 participates in an autoregulatory loop by which IL-2 induces Prdm1 expressi

154 It can function in an autoregulatory loop consisting of RAP80, HDM2, and the p

155 dent manner demonstrating the presence of an autoregulatory loop during growth.

156 d that Ntl functions normally to protect the autoregulatory loop from endogenous RA by directly activ

157 ence of a nuclear KIT-driven NFKBIB-RELA-KIT autoregulatory loop in GIST tumorigenesis, which are pot

158 A novel autoregulatory loop interdependent on HMGA2 and EZH2 exp

159 tes the activity of Spo0A through a positive autoregulatory loop involving KinC, a histidine kinase t

160 ory circuitry of ES cells, which includes an autoregulatory loop involving the pluripotency regulator

161 newly identified control should result in an autoregulatory loop limiting the amount of OmrA/B sRNAs.

162 A Dpp > dpp autoregulatory loop maintains BMP signaling, which limit

163 e NDRs, established by OCT4, in ensuring the autoregulatory loop of pluripotency and, furthermore, th

164 occupancy of the Etv1 gene itself, and this autoregulatory loop preceded ETV1 binding and activation

165 that SHH and Atoh1 contribute to a positive autoregulatory loop promoting neuronal precursor expansi

166 The autoregulatory loop terminates by 48 h after training wi

167 CL6 gene alterations is to bypass a negative autoregulatory loop that controls its transcription.

168 and revealed a novel STARS-SRF feed-forward autoregulatory loop that could play an essential role in

169 factors OCT4, NANOG and SOX2 form a positive autoregulatory loop that is pivotal for maintaining the

170 A2 and 1B1, thereby also participating in an autoregulatory loop that keeps its own steady-state conc

171 ating that these proteins may function in an autoregulatory loop that maintains appropriate levels of

172 ase, in part through the up-regulation of an autoregulatory loop that promotes podosome formation.

173 r cells, the enhancer and PTF1a establish an autoregulatory loop that reinforces and maintains Ptf1a

174 ion, whereas ER71 and SOX9 participate in an autoregulatory loop to sustain each other's expression a

175 y interfering with IL-13's negative feedback autoregulatory loop under MEK/ERK-dependent conditions.

176 tudy, we characterize a Neurogenin3 positive autoregulatory loop whereby this factor may rapidly indu

177 dence that CEH-17 participates in a positive autoregulatory loop with CEH-14 in ALA, and that CEH-10,

178 ow that TAL1 forms a positive interconnected autoregulatory loop with GATA3 and RUNX1 and that the TA

179 vertebrate embryo depends on a Brachyury/Wnt autoregulatory loop within the posterior mesodermal prog

180 Together, we identified a novel p53-RNPC1 autoregulatory loop, and our findings suggest that RNPC1

181 t the BDNF gene is a subject to an extensive autoregulatory loop, where TrkB signaling upregulates th

182 which are normally controlled by a negative autoregulatory loop.

183 phenotype is stabilized by a GATA3-dependent autoregulatory loop.

184 AM transcripts, thus establishing a feedback autoregulatory loop.

185 ressing IL-22R1 generate IL-22 in a positive autoregulatory loop.

186 etic corepressor ETO-2 and an ETO-2-negative autoregulatory loop.

187 plying that Greatwall participates in an MPF autoregulatory loop.

188 n, suggesting the presence of a GL3 negative autoregulatory loop.

189 a as well as Igf2bp3 mRNA itself, forming an autoregulatory loop.

190 a repressor complex that is reinforced by an autoregulatory loop.

191 r BMP-2-induced NFATc1 expression through an autoregulatory loop.

192 The autoregulatory loops of the circadian clock consist of f

193 Indeed, the trimeric PTF1 complex forms dual autoregulatory loops with the Ptf1a and Rbpjl genes that

194 tworks should often be dominated by positive autoregulatory loops.

195 Many varieties of autoregulatory malfunction occur within the cardiovascul

196 resynaptic receptors on POMC terminals in an autoregulatory manner to limit continued transmission.

197 otubule motor-cargo interface and associated autoregulatory mechanism can be manipulated using a smal

198 first to implicate ligand dimerization as an autoregulatory mechanism for growth factor bioactivity a

199 fine enzyme activity-dependent sorting as an autoregulatory mechanism for protein trafficking.

200 ependent inactivation (CDI) is a fundamental autoregulatory mechanism in Ca(V)1 and Ca(V)2 voltage-ga

201 The system employs an autoregulatory mechanism in perceiving a sucrose-control

202 These data suggest an autoregulatory mechanism in which Gcn5 performs both the

203 SII repair, and psbA translation, suggest an autoregulatory mechanism in which the light-induced degr

204 A1 represent a p53-independent bidirectional autoregulatory mechanism in which these two opposites ac

205 This novel autoregulatory mechanism is capable of tuning uptake cap

206 omes of opioid drugs, which suggests that an autoregulatory mechanism may function in opioid systems.

207 is critically dependent on a self-sustaining autoregulatory mechanism mediated by the Pit-1 protein.

208 Furthermore, we found an autoregulatory mechanism of progranulin whereby a feed-f

209 This autoregulatory mechanism of repression implies that the

210 a saiR mutant required SpxA2, indicating an autoregulatory mechanism of spxA2 control.

211 n FUS expression achieved by saturating this autoregulatory mechanism produces a rapidly progressive

212 The authors further define an autoregulatory mechanism that likely controls AKAP350A's

213 eptide products and reveal clues for a novel autoregulatory mechanism that might have significant imp

214 Here we demonstrate an autoregulatory mechanism used by Mediator to repress tra

215 report that Nanog is subjected to a negative autoregulatory mechanism, i.e., autorepression, in ESCs,

216 , a pathway triggered by a negative-feedback autoregulatory mechanism.

217 rate region, indicating a common type II PAK autoregulatory mechanism.

218 V segregation by fueling this non-autonomous autoregulatory mechanism.

219 um following D-V segregation by fueling this autoregulatory mechanism.

220 the life of the respective cell type via an autoregulatory mechanism.

221 on of individual proteins correlate to known autoregulatory mechanisms and extend the network of ribo

222 of aqueous humor dynamics suggests possible autoregulatory mechanisms in the eye.

223 osomal protein genes are often controlled by autoregulatory mechanisms in which a protein encoded in

224 cterizations have provided new insights into autoregulatory mechanisms of LYP function.

225 Here, we report unique autoregulatory mechanisms that control protein phosphory

226 Both autoregulatory mechanisms usually suppress the average (

227 neurons in mice relies on a transcriptional autoregulatory module initiated via transient activity o

228 aB in a novel feed-forward, self-amplifying, autoregulatory module regulated by the ERBB family of gr

229 roved that the oligopeptide functioned as an autoregulatory molecule responsible for the density-depe

230 Here we report the discovery of a new autoregulatory motif within the clathrin adaptor Gga2 th

231 Moreover, how specific autoregulatory motifs are selected during evolution and

232 Identified autoregulatory motifs involve 56% of transcription facto

233 tion is highly conserved in the beta-tubulin autoregulatory MREI (methionine-arginine-glutamic acid-i

234 ptimization and truncation of the putatively autoregulatory N terminus of TMEM165.

235 sigmas and their promoters by leveraging the autoregulatory nature of ECF sigmas as a means of promot

236 e that Chtop expression is controlled via an autoregulatory negative feedback loop whereby Chtop bind

237 d supply induces Pten expression creating an autoregulatory negative feedback loop, whereas complete

238 s establishing a mechanism for a miRNA/Dicer autoregulatory negative feedback loop.

239 Eukaryotic circadian clocks employ autoregulatory negative feedback loops to control daily

240 eukaryotic circadian oscillators consist of autoregulatory negative feedback loops.

241 ormed parameter searches to demonstrate that autoregulatory negative-feedback loops of the redundant

242 Here, we study a common autoregulatory network motif, the negative single-input

243 We estimate the parameters of an autoregulatory network providing results both for simula

244 We further show that for autoregulatory networks with negative feedback, the prot

245 This objective is achieved through autoregulatory neural and hormonal systems in close asso

246 se to an ASE-driven phase, ASE being another autoregulatory Nodal enhancer.

247 This work both reveals a new autoregulatory pathway governing SMN expression, and ide

248 The mutation disrupts an autoregulatory PAX6 binding site, causing loss of enhanc

249 Thus, C. neoformans produces an autoregulatory peptide that matures extracellularly but

250 osophila circadian oscillator is composed of autoregulatory period/timeless (per/tim) and Clock (Clk)

251 teins reflects the operation of an adaptive, autoregulatory process of functionally significant aggre

252 then by creating an environment in which an autoregulatory process restricts the immune response to

253 Several of the PDZ-kinases show autoregulatory properties similar to natural SFKs.

254 ogene and that Erk molecules possess unusual autoregulatory properties, some of them independent of T

255 CaMKII isozymes have complex structural and autoregulatory properties.

256 Levels of PU.1 were sustained through autoregulatory PU.1 binding to an upstream enhancer that

257 exhibit high activity of the BRN3A proximal autoregulatory region.

258 ains the stalk but not the cargo-binding and autoregulatory regions.

259 transcriptional regulator, QapR, which is an autoregulatory repressor.

260 indicates low perfusion pressure and limited autoregulatory reserve.

261 light (functional hyperemia) is a well-known autoregulatory response driven by increased neural activ

262 -resolved OCT angiography to investigate the autoregulatory response in the 3 parafoveal retinal plex

263 ngiography was able to show that the retinal autoregulatory response to hyperoxia affects only the de

264 lloon catheter in the aorta to determine the autoregulatory response to hypertension.

265 values in the NoDR group likely represent an autoregulatory response to increased metabolic demand, w

266 Autoregulatory restoration of renal blood flow to baseli

267 ectively, these findings indicate a positive autoregulatory role for INSL3 signaling in maintaining t

268 Discovery of this autoregulatory role for the mammalian CRY1 tail and cons

269 We defined the autoregulatory role of LANA and identified a cellular RN

270 This study sheds light on the autoregulatory role of LANA to modulate its expression a

271 ion of POMC neurons such that attributing an autoregulatory role to opioids must include consideratio

272 h the idea that the 2B subdomain may have an autoregulatory role.

273 tors and demonstrates an unexpected level of autoregulatory scaffolding in mammalian stress-activated

274 re dedicated protein kinases regulated by an autoregulatory segment C terminus of the catalytic core

275 Potential contributions of autoregulatory segment to cMLCK activity were analyzed w

276 talytic activity, substrate recognition, and autoregulatory self-association.

277 S. acidiscabies, a gene cluster encoding GBL autoregulatory signaling homologs was identified and cha

278 ce DUSP1 mRNA expression, suggesting that an autoregulatory signaling loop may be activated by Stxs.

279 Qsp1 mediates autoregulatory signaling that modulates secreted proteas

280 lector gene engrailed is silenced through an autoregulatory silencing mechanism that requires the PRC

281 omal rearrangements, mutations of a negative autoregulatory site in the BCL6 promoter region and aber

282 0 vs. 3.7 +/- 0.8 mmHg) while increasing the autoregulatory slope (0.10 +/- 0.05 vs. 0.24 +/- 0.08 cm

283 ation, establishment, and maintenance of the autoregulatory state.

284 , trauma severity, intracranial pressure, or autoregulatory status, and thus represent a discrete phe

285 tivity as a result of altered activating and autoregulatory switch-off mechanisms.

286 reventing cachexia, we developed a molecular autoregulatory system involving a single recombinant ade

287 influenced by the maturing neurovascular and autoregulatory systems of the neonatal brain.

288 eation of splicing-based protein sensors and autoregulatory systems.

289 der the control of gamma-butyrolactone (GBL) autoregulatory systems.

290 tive CD4(+) clonotypes into antidiabetogenic autoregulatory T cells.

291 l clonotypes, promoting their deviation into autoregulatory T cells.

292 4) forms several H-bonds with the N-terminal autoregulatory tail but is far from the catalytic Fe(II)

293 NAs than non-autoregulatory genes and 89% of autoregulatory TFs were found in dual feedback motifs wi

294 d organismal physiology are controlled by an autoregulatory transcription-translation feedback loop t

295 ablished by transcription of clock genes and autoregulatory transcriptional feedback loops.

296 e circadian clock in mammals is driven by an autoregulatory transcriptional feedback mechanism that t

297 ically integrated circuits that use bistable autoregulatory transcriptional feedback to retain memory

298 ulator with control of its expression via an autoregulatory transcriptional loop.

299 as selective removal of I-E on DCs abrogated autoregulatory Treg formation and T1D protection, select

300 cy is established when the expression of the autoregulatory viral trans-activating factor Tat is redu