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 This autoregulatory activation is further enhanced by cyclin

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

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

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

7 orb regulatory targets is orb mRNA, and this autoregulatory activity is critical for ensuring that Or

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

9 The autoregulatory activity of this element was demonstrated

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

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

12 duced in the mutant, indicating that AoxR is autoregulatory and at least partially controls the expre

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

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

15 e to form regulatory circuitry consisting of autoregulatory and feedforward loops.

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

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

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

19 to sensory cell production involves distinct autoregulatory behaviors of Ngn1 (negative) and Math1 (p

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

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

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

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

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

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

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

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

28 We hypothesized that autoregulatory changes in arteriolar blood volume (aBV)

29 ion cells is physiologically associated with autoregulatory changes of the neural-vascular system.

30 nt, potentially missing important changes in autoregulatory characteristics.

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

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

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

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

35 An autoregulatory circuit is identified involving the contr

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

37 This shift establishes an autoregulatory circuit that maintains durable expression

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

39 functions as a negative regulator in the orb autoregulatory circuit, downregulating orb mRNA translat

40 rocally upregulates KLF2, forming a positive autoregulatory circuit.

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

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

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

44 s generate daily rhythms via cell-autonomous autoregulatory clock gene networks, and, thus, to locali

45 gion structure, suggesting that this mode of autoregulatory control is conserved among higher metazoa

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

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

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

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

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

51 mediated via the induction of a long-lasting autoregulatory cycle by which GDNF positively regulates

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

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

54 One design was an autoregulatory design; one transcription unit used a tet

55 as to printing nested bioarrays and building autoregulatory devices.

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

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

58 n (DID) and the carboxyl-terminal diaphanous autoregulatory domain (DAD).

59 ory domain (DID) and a C-terminal diaphanous autoregulatory domain (DAD).

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

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

62 ctivation is disruption of the juxtamembrane autoregulatory domain by internal tandem duplications (I

63 binding site ("T-site"), thereby keeping the autoregulatory domain displaced and enabling Ca2+/CaM-in

64 iaphanous inhibitory domain and a Diaphanous autoregulatory domain.

65 partial truncation of the DIAPH1 diaphanous autoregulatory domain.

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

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

68 the CK2 phosphorylation of their respective autoregulatory domains.

69 n analysis was used to determine the dynamic autoregulatory efficiency of the renal vasculature.

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

71 e HOXA10 estrogen response element (ERE) and autoregulatory element (ARE) were tested for BPA respons

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

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

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

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

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

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

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

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

80 e in which we have inserted the 107 bp Hoxb1 autoregulatory enhancer into the Hoxa1 promoter.

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

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

83 oncentrations and the mammary-specific Stat5 autoregulatory enhancer.

84 tyrosine phosphorylation is also a critical autoregulatory event.

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

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

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

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

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

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

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

92 sites for transcription factors involved in autoregulatory feedback circuits.

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

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

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

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

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

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

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

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

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

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

103 rmal cells p53 levels are kept low due to an autoregulatory feedback loop where p53 activates the tra

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

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

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

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

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

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

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

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

112 odulates p53 transactivation functions in an autoregulatory feedback loop.

113 e cell and a number of positive and negative autoregulatory feedback loops act upon the p53 response.

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

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

116 Autoregulatory feedback loops, where the protein express

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

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

119 The present studies thus unveil a novel autoregulatory feedback mechanism that negatively contro

120 anscription factor, Ste12, as well as on the autoregulatory feedback of Ste12.

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

122 ranscription start site and the role of this autoregulatory function in EBV latency.

123 and C-terminal domains of SPN, suggesting an autoregulatory function similar to that of importin-alph

124 portant in patients with already compromised autoregulatory function.

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

126 Autoregulatory gene circuits can be physically encoded w

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

128 s that express key elements of the circadian autoregulatory gene network and that the inner nuclear a

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

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

131 Strikingly, the newly generated autoregulatory Hoxa1 gene can deliver the functionality

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

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

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

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

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

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

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

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

140 and cerebral autoregulation, defined by the autoregulatory index, at 6 and 36 hrs; 2) continuous mon

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

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

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

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

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

146 by eIF2alpha phosphorylation destabilizes an autoregulatory intramolecular interaction within eIF2alp

147 The identification of a GDNF-mediated, autoregulatory long-lasting feedback loop could have imp

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

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

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

151 An autoregulatory loop between INrf2 and Nrf2 regulates the

152 demonstrate the presence of a novel feedback autoregulatory loop between INrf2 and Nrf2 that controls

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

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

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

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

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

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

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

160 A conserved transcriptional-translational autoregulatory loop generates molecular oscillations of

161 sequence, the C-terminal extension, and the autoregulatory loop in the reductase domain.

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

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

164 We hypothesize that the Pax6 autoregulatory loop is targeted for repression by the TG

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

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

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

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

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

170 The autoregulatory loop terminates by 48 h after training wi

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

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

173 emonstrate that Greatwall participates in an autoregulatory loop that generates and maintains suffici

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

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

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

177 which interacts functionally with MDM2 in an autoregulatory loop that parallels the p53/MDM2 feedback

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

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

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

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

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

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

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

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

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

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

188 hese data imply that PSMA participates in an autoregulatory loop, wherein active PSMA facilitates int

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

190 AM transcripts, thus establishing a feedback autoregulatory loop.

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

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

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

194 plying that Greatwall participates in an MPF autoregulatory loop.

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

196 which are normally controlled by a negative autoregulatory loop.

197 eam targets, and that a number of unexpected autoregulatory loops exist between Sox17 and Gata4-6, be

198 The autoregulatory loops of the circadian clock consist of f

199 Autoregulatory loops often provide precise control of th

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

201 tworks should often be dominated by positive autoregulatory loops.

202 Many varieties of autoregulatory malfunction occur within the cardiovascul

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

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

205 KE 1 (DCL1), suggesting a second homeostatic autoregulatory mechanism for DCL1 expression; another de

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

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

208 This suggests an autoregulatory mechanism for Rep helicase, which may app

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

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

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

212 This novel autoregulatory mechanism is capable of tuning uptake cap

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

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

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

216 This autoregulatory mechanism of repression implies that the

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

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

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

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

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

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

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

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

225 substrate-binding site, which may reflect an autoregulatory mechanism.

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

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

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

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

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

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

232 Both autoregulatory mechanisms usually suppress the average (

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

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

235 he identification of an 11-mer peptide as an autoregulatory molecule in C. neoformans suggests that a

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

237 These same autoregulatory molecules do not evoke the morphological

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

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

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

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

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

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

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

245 eukaryotic circadian oscillators consist of autoregulatory negative feedback loops.

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

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

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

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

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

251 Specifically targeting this novel autoregulatory pathway may provide new therapeutic appro

252 new role of the TF cytoplasmic domain in an autoregulatory pathway that controls LPS-induced TF expr

253 beta is involved in this novel RANKL/iNOS/NO autoregulatory pathway.

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

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

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

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

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

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

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

261 CaMKII isozymes have complex structural and autoregulatory properties.

262 and vceR, which codes for a transcriptional autoregulatory protein that negatively regulates the exp

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

264 se domains of the constitutive isoforms, the autoregulatory region (AR) and the C-terminal tail regio

265 exhibit high activity of the BRN3A proximal autoregulatory region.

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

267 indicates low perfusion pressure and limited autoregulatory reserve.

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

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

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

271 xl is maintained in the on state by positive autoregulatory RNA splicing [2].

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

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

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

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

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

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

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

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

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

281 Qsp1 mediates autoregulatory signaling that modulates secreted proteas

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

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

284 0 vs. 3.7 +/- 0.8 mmHg) while increasing the autoregulatory slope (0.10 +/- 0.05 vs. 0.24 +/- 0.08 cm

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

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

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

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

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

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

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

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

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

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

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

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

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

298 ign of cellular memory in yeast that employs autoregulatory transcriptional positive feedback.

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