ライフサイエンスコーパス: negative feedback loop

1 tive feedback loops and coupled positive and negative feedback loops).

2 tive inhibition by L-methionine, much like a negative feedback loop.

3 nd regulates cell proliferation by forming a negative feedback loop.

4 ing it constitutes a key component of an IFN negative feedback loop.

5 stent viral infection via an IL-10-dependent negative feedback loop.

6 ed mobilization of IRF3, thus constituting a negative feedback loop.

7 ed the generation of Th1 effector cells in a negative feedback loop.

8 ole in controlling Th2 development through a negative feedback loop.

9 bitor thrombospondin-1, thereby triggering a negative feedback loop.

10 ced TSH suppresses osteoclast formation in a negative feedback loop.

11 er targeted DNMT-1 expression resulting in a negative feedback loop.

12 N, AURKB, and LIN28, the latter via a double-negative feedback loop.

13 by NPY, but stress overrides this autocrine negative feedback loop.

14 xpression, thus disturbing the CRY1-mediated negative feedback loop.

15 gnaling 1, a key regulator that enhances the negative feedback loop.

16 expression of amino acid-related genes in a negative feedback loop.

17 s, signaling via NLRC3 and TLR constitutes a negative feedback loop.

18 p70 S6 kinase or S6K1 can activate Akt via a negative feedback loop.

19 C-2 are the core components of the circadian negative feedback loop.

20 ghly repressed by CodY, creating a potential negative feedback loop.

21 maB network to function as an ultrasensitive negative feedback loop.

22 scade reactions "OFF", thus establishing the negative feedback loop.

23 (IFNs) and limits their production through a negative feedback loop.

24 with the growth regulator melted in a double-negative feedback loop.

25 R-200, independent of Zeb1, to form a double-negative feedback loop.

26 rwhelming immune reaction by engagement of a negative feedback loop.

27 it bone resorption by osteoclasts, forming a negative feedback loop.

28 egrin receptors at the RPE cell surface as a negative feedback loop.

29 on in mammary adipose tissue through a novel negative-feedback loop.

30 single Cdk/cyclin complex and APC wired in a negative-feedback loop.

31 effect driven by the partial preservation of negative feedback loops.

32 -bacterial interactions in both positive and negative feedback loops.

33 found that AKT was involved in all detected negative feedback loops.

34 inuria with hypertriglyceridemia through two negative feedback loops.

35 d by a delicate balance between positive and negative feedback loops.

36 teoclast signaling intermediaries or through negative feedback loops.

37 ith oscillatory features mediated by delayed negative feedback loops.

38 ealing a network of interlocked positive and negative feedback loops.

39 and limiting activation of Ca(2+)-dependent negative feedback loops.

40 torage, and export and are connected through negative feedback loops.

41 e highly recursive positive feed-forward and negative feedback loops.

42 ling regulates corolla limb opening and a JA-negative feedback loop; (2) production of floral volatil

43 scriptionally coupled IkappaBalpha/NF-kappaB negative feedback loop, a pivotal regulatory node of inn

44 of macroH2A1 from SASP genes results from a negative feedback loop activated by SASP-mediated endopl

45 n cells decreases exon 7 inclusion through a negative feedback loop affecting the splicing of its own

46 mediated NMD inhibition, breaking the normal negative feedback loop and allowing the aberrant increas

47 uency is a hard-wired feature of the primary negative feedback loop and not a function of the stimulu

48 d miR-155 relieves chronic inflammation by a negative feedback loop and plays a protective role durin

49 imal chemical oscillator containing a single negative feedback loop and study numerically the effects

50 lar modules, including genetic components, a negative feedback loop and the size of the crowding mole

51 sufficient to maintain both the T4-dependent negative feedback loop and thyroid economy.

52 ork, which places downstream enzymes under a negative feedback loop and upstream ones under a positiv

53 rs indicate that PTSD subjects have a strong negative feedback loop and, as a result, the predicted o

54 lations out of two simple types of circuits (negative feedback loops and coupled positive and negativ

55 iod depends on the sum of delays inherent to negative-feedback loops and inhibitor half-lives.

56 ion by Cdc42-GTP inhibit Cdc42 activity in a negative feedback loop, and this inhibition depends on C

57 dic dynamics, the elements with two positive/negative feedback loops are the minimalist elements to h

58 nscriptional repressors within the molecular negative feedback loops at the heart of the SCN clockwor

59 PKC activation amplifies negative feedback loops at the level of G protein-couple

60 Here we show that a CDK1-mediated negative-feedback loop attenuates cyclin production befo

61 plants, is more complex than expected, with negative feedback loops based on the repression of gene

62 In essence, these results suggest a double-negative feedback loop between a tumor suppressor (miR-1

63 Additionally, we uncover a negative feedback loop between actin remodeling and flg2

64 Here, we identify a novel double-negative feedback loop between APC and a translation inh

65 Here the authors show a negative feedback loop between C/EBPalpha and miR-182 an

66 These findings reveal a negative feedback loop between CCN2 and HIF-1alpha in NP

67 s a novel AR-repressed gene, suggestive of a negative feedback loop between CHK2 and AR.

68 a mechanism that is likely due to the double negative feedback loop between Clp1/Cdc14 and Cdc25 that

69 regulation of ERK and define a novel double-negative feedback loop between EpCAM and ERK that contri

70 We describe the negative feedback loop between graft mesenchymal and Tef

71 the mature, processed microRNA, suggesting a negative feedback loop between miR-1247 and its target S

72 lated by the insulin signaling pathway via a negative feedback loop between miR-34 and DAF-16/FOXO.

73 We also demonstrate the existence of a negative feedback loop between miR-378, IGF1R, and IGF1

74 Our results describe a double-negative feedback loop between MIR100HG and the transcri

75 A negative feedback loop between odd-skipped-related genes

76 sults reveal a previously undescribed double-negative feedback loop between sponge lncRNA and target

77 pools of stem cells that are maintained by a negative feedback loop between the CLAVATA pathway and t

78 of miR-31 transcription, suggesting a cross-negative feedback loop between the expression of miR-31

79 us transcription factors, including a double-negative feedback loop between the microRNA-200 (miR-200

80 The double-negative feedback loop between the microRNA-200 family a

81 We report a negative feedback loop between the signaling protein pho

82 Here we identified a double-negative feedback loop between the transcription factors

83 A double negative feedback loop between the Warts kinase of the H

84 Our data point to the existence of negative feedback loops between these two regulatory pro

85 Here, we define a negative-feedback loop between the Caenorhabditis elegan

86 Negative-feedback loops between transcription factors an

87 l assays confirmed that the L1 interrupted a negative feedback loop by blocking ST18 repression of it

88 Interrupting this negative feedback loop by PMEPA1 knockdown increased pro

89 BXL3) ubiquitin ligase complex controls this negative feedback loop by promoting CRY ubiquitination a

90 loop and that MMP-9-SDC1 activity creates a negative feedback loop by regulating the expression of m

91 rectly represses the MDFIC gene, revealing a negative feedback loop by which glucocorticoids limit MD

92 By contrast, Ripply1 induces a negative-feedback loop by promoting Tbx6 protein degrada

93 B pathway can exhibit oscillatory dynamics-a negative feedback loop causes oscillatory nuclear-cytopl

94 Circadian negative feedback loop (CNFL) genes play important roles

95 gether, these results describe a tri-element negative feedback loop composed of p53, Apela, and hnRNP

96 ally induces phyB degradation, in a mutually-negative, feedback-loop configuration.

97 mness-regulatory mechanism in which a double-negative feedback loop consisting of PRMT7 and miR-24-3p

98 tructure unbiasedly reveals four interlocked negative feedback loops contributing to circadian rhythm

99 These models suggested that a negative-feedback loop controlled by Wnt is crucial for

100 This creates a potential negative feedback loop controlling PRC1 activity.

101 ell surface expression of c-Mpl, whereas the negative feedback loop controlling THPO serum levels req

102 ilon therefore create a spatially restricted negative feedback loop counteracting Aurora B in anaphas

103 The negative feedback loop created by MSCs through TSG-6 att

104 ich enables their rapid removal; and (iii) a negative-feedback loop created by CsrA repression of Csr

105 d Dok2 proteins are involved in an intrinsic negative feedback loop downstream of NK-cell-activating

106 atially and temporally coordinated through a negative-feedback loop driving pathological angiogenesis

107 The model also includes a negative feedback loop due to inhibition of calcium infl

108 replication forks, revealing an ATR-mediated negative feedback loop during replication.

109 h CAL-101 [idelalisib]), interrupts a double-negative feedback loop, enhancing GC-regulated transcrip

110 e speed of Sic1 destruction through a double-negative feedback loop, ensuring a robust all-or-none tr

111 ent cullin and proteasome activity provide a negative feedback loop, ensuring that adhesion assembly

112 ts GIV's GEF function and generates a unique negative feedback loop for downregulating the GIV-Gi axi

113 Our findings have identified a negative feedback loop for the signaling between ATM and

114 n-generating/consuming enzymes with pairs of negative-feedback loops for pH homeostasis.

115 odels simulations suggest that, although the negative feedback loop formed by cAMP, cAMP-dependent pr

116 A double-negative feedback loop formed by the morning genes CIRCA

117 Two auxiliary negative feedback loops, from ERK to MEK and RAF, placed

118 lations demonstrate that the CSP-1-dependent negative feedback loop functions in glucose compensation

119 This potentially constitutes a negative feedback loop governing this critical checkpoin

120 to a highly self-cooperative transcriptional negative-feedback loop (Hill coefficient approximately 7

121 A potentially important negative feedback loop in blood pressure homeostasis is

122 e Polycomb group protein EZH2 disrupted this negative feedback loop in both CRPC and enzalutamide-res

123 ishes the molecular basis of a Mg(2+)-driven negative feedback loop in CorA as the key physiological

124 nse signaling molecule salicylic acid form a negative feedback loop in defense and cell death control

125 rotein stabilizes DUX4 mRNA through a double-negative feedback loop in FSHD muscle cells.

126 We uncovered a negative feedback loop in M2 myeloid cells, wherein inte

127 by a conserved transcriptional/translational negative feedback loop in mammals.

128 nthesis of IkappaBalpha, thus accelerating a negative feedback loop in NFkappaB signaling, and direct

129 and inflammatory cytokines form a functional negative feedback loop in NP cells that may be important

130 he result of activation of the S6K-dependent negative feedback loop in PHLPP knockdown cells.

131 ed AR/miR-190a/YB-1 forms an auto-regulatory negative feedback loop in prostate cancer: miR-190a expr

132 ygenase type 2 (COX-2), which functions in a negative feedback loop in TGFbeta and ERbeta signaling p

133 lly repressed by p53, defining an additional negative feedback loop in the p53 network.

134 irst time demonstrate a calpain/PTP1B/VEGFR2 negative feedback loop in the regulation of VEGF-induced

135 derstood from mathematical modeling of a key negative feedback loop in the underlying regulatory circ

136 Thus, our results uncover a negative feedback loop in which CREBH regulates NEFA flu

137 on to all circadian systems, consisting of a negative feedback loop in which KaiC regulates its own p

138 us, Treg cell development is controlled by a negative feedback loop in which mature progeny cells ret

139 mmalian circadian rhythms are generated by a negative feedback loop in which PERIOD (PER) proteins ac

140 Our results identified a negative feedback loop in which SET9 controls DNA methyl

141 Circadian clocks in mammals are built on a negative feedback loop in which the heterodimeric transc

142 Circadian clocks in mammals are based on a negative feedback loop in which transcriptional repressi

143 and this was assumed to occur due to strong negative feedback loops in the HPA axis.

144 se lower jaw, in part through establishing a negative-feedback loop in which Hand2 represses Dlx5 and

145 Here we describe evidence of a negative feedback loop, in which PGE2 augments the expre

146 We propose a negative feedback loop, in which sphingosine inhibits GB

147 This is consistent with a negative-feedback loop, in which newly generated neurons

148 Ca(2+)-dependent negative feedback loops, including activation of phospho

149 tion is predicted to depend on delays in the negative-feedback loop, including, most importantly, the

150 Here, we report the definition of a double-negative feedback loop involving AP4 and miR-15a/16-1 th

151 We further demonstrate that a negative feedback loop involving miR-135a can restore AR

152 In summary, our results define a double-negative feedback loop involving miR-15a/16-1 and AP4 th

153 antly induce miR-132 expression via a double-negative feedback loop involving Rest inhibition.

154 Thus, a negative feedback loop involving Tal regulates the forma

155 Furthermore, our results suggested that a negative feedback loop involving TGF-beta signaling and

156 SAC silencing is thus promoted by a negative feedback loop involving the Mps1-dependent recr

157 how that partial adaptation arises through a negative feedback loop involving the small protein MgrB.

158 A negative-feedback loop involving the CLAVATA (CLV) signa

159 The SNAIL1/miR-34 double-negative feedback loop is responsible for the reversible

160 e to IFNs and its modulation by positive and negative feedback loops is incompletely understood.

161 CTH2 transcript, we demonstrate that a Cth2 negative-feedback loop is required for the efficient dec

162 et gene expression abrogates their intrinsic negative feedback loops, leading to accumulation of phos

163 induced FBXL5 protein level, demonstrating a negative feedback loop limiting excessive accumulation o

164 data suggest that TAZ and Nek1 constitute a negative feedback loop linked through phosphorylation an

165 thesis that high stress intensity and strong negative feedback loop may cause hypersensitive neuro-en

166 This negative-feedback loop may provide a safety mechanism to

167 paBalpha protein and impaired NF-kappaB self-negative feedback loop mediated less newly synthesis of

168 A different negative feedback loop, mediated by phosphodiesterase-2

169 This regulation establishes a negative feedback loop necessary to maintain cAMP/CaMKII

170 n still be grouped into two general classes: negative feedback loop (NFBL) and incoherent feed-forwar

171 Only two circuit motifs generate adaptation: negative feedback loops (NFLs) and incoherent feed-forwa

172 rrectly projecting contralateral fibers, the negative feedback loop normally regulating OKR can turn

173 robe, which upon irradiation strengthens the negative feedback loop of a CRN that produces oscillatio

174 ulation results suggest that, while a single negative feedback loop of either one- or two-gene elemen

175 he nuclear response of NF-kappaB through the negative feedback loop of NF-kappaB pathway.

176 induced RNA (TMEPAI), which is involved in a negative feedback loop of TGF-beta signaling.

177 mor suppressor 1/2) kinases, to constitute a negative feedback loop of the Hippo pathway in both cult

178 ly, depletion of Sox2 revealed the potential negative feedback loop of TLX expression that is antagon

179 searches to demonstrate that autoregulatory negative-feedback loops of the redundant repressor Her d

180 DA currents, providing an activity-dependent negative feedback loop on NMDA receptor activity.

181 nstitutively active PI3K or (ii) relief of a negative feedback loop on PI3K by prolonged inhibition o

182 This revealed that Ca(2+) entry exerted a negative feedback loop on rituximab-induced apoptosis, s

183 To study the effects of the positive and negative feedback loops on the dynamical stability of BC

184 Our data indicate that a negative feedback loop operates to repress transcription

185 iron transport and utilization enzymes with negative-feedback loop pairs for iron homeostasis.

186 at a combination of interlinked positive and negative feedback loops plays an important role in setti

187 Thus, mGluRs establish a local negative feedback loop positioned to regulate IHC activi

188 n summary, pneumococci recognition induces a negative feedback loop, preventing excessive inflammatio

189 to investigate how interlinked positive and negative feedback loops process EGF signals into ERK pul

190 to ICAM-1, suggesting that a tension-induced negative feedback loop promotes ICAM-1-mediated neutroph

191 and it is widely accepted that intracellular negative-feedback loops regulate oscillatory gene expres

192 200 family and ZEB1, which exist in a double-negative feedback loop regulated by TGF-beta, serve impo

193 The regulatory core is controlled by two negative feedback loops (regulated by Mdm2 and Wip1) res

194 A negative feedback loop regulates the RQC, and Hsf1 sense

195 represses its own expression as part of the negative feedback loop regulating the TGF-beta pathway.

196 and E2F3, thereby establishing a unilateral negative feedback loop required for the cell-cycle exit

197 hat AtMYB93 is part of a novel auxin-induced negative feedback loop stimulated in a select few endode

198 sitive feedback introduces a hierarchy among negative feedback loops, such that the effect of a negat

199 plication stress and is thereby engaged in a negative feedback loop that attenuates oncogene-dependen

200 SUMOylation and degradation, establishing a negative feedback loop that attenuates SnRK1 signaling a

201 fear-induced miRNAs, act as components of a negative feedback loop that blocks neuronal hyperactivit

202 cadian transcription factor, WC-1, forming a negative feedback loop that can influence the core oscil

203 on of SK channels by mGluR1, which removes a negative feedback loop that constitutively regulates NMD

204 y miR-146a as an important new member of the negative feedback loop that controls TCR signaling to NF

205 it is also part of a previously unidentified negative feedback loop that degrades glucagon and regula

206 is oscillatory, revealing the presence of a negative feedback loop that disperses the factors.

207 nment at the nuclear periphery establishes a negative feedback loop that enables the GAL locus to res

208 like responses to inputs, is nested within a negative feedback loop that encompasses RAS and RAF, MEK

209 L4P activity (L4-22K/33K), which establish a negative feedback loop that ensures the transient activi

210 RSPO2-induced, LGR5-dependent Wnt signaling-negative feedback loop that exerts a net growth-suppress

211 These elements typically have one negative feedback loop that generates oscillations, and

212 0 produced extrinsically, but also through a negative feedback loop that induces "intrinsic" IL-10 ex

213 This allows plasma T4 to signal a negative feedback loop that inhibits production of thyro

214 porulation sigma factor sigma(F) to create a negative feedback loop that inhibits sigma(F) -directed

215 rq and qrf transcription thus forms a double negative feedback loop that is interlocked with the core

216 pic glutamate signalling establishes a local negative feedback loop that is positioned to regulate in

217 We show that it is part of a negative feedback loop that limits proinflammatory and p

218 ne that functions as an afferent signal in a negative feedback loop that maintains homeostatic contro

219 ator of TGFbeta signalling, thus mediating a negative feedback loop that may potentially restrain TGF

220 on, epigenetic barrier crossing coupled to a negative feedback loop that mechanistically differs from

221 d CaMKI and PME-1 networks thus constitute a negative feedback loop that modulates the phosphatase ac

222 ng with its promoter, completing a CCA1-ELF3 negative feedback loop that places ELF3 within the oscil

223 d CaN in a complex on the InsP3R, creating a negative feedback loop that prevents exaggerated Ca(2+)

224 hat the paracrine actions of Ucn3 activate a negative feedback loop that promotes somatostatin releas

225 gene 6 protein (TSG-6) and thereby create a negative feedback loop that reduces inflammation in zymo

226 08, and Blimp1 and Otx2 were shown to form a negative feedback loop that regulates the level of Otx2,

227 A negative feedback loop that relies on the coordination-c

228 These results suggest a negative feedback loop that responds to signaling events

229 egf and Dll4/Notch signalling cooperate in a negative feedback loop that specifies endothelial tip an

230 suppresses AR expression, this results in a negative feedback loop that suppresses AR protein expres

231 anism that is responsible for generating the negative feedback loop that sustains the clock.

232 onent of the interlinked positive and double-negative feedback loops that constitute the bistable mit

233 or degradation, suggesting both positive and negative feedback loops that control Nod factor levels d

234 Eukaryotic circadian oscillators consist of negative feedback loops that generate endogenous rhythmi

235 ated computational models to interrogate the negative feedback loops that regulate the dynamic activi

236 The intensity of ERK signaling, negative feedback loops that regulate the pathway, and c

237 is complex, involving multiple positive and negative feedback loops that result in the establishment

238 evels of cGMP and Ca(2+) stimulate competing negative feedback loops that shape cGMP dynamics.

239 dsDNA viruses induces a regulatory temporary negative-feedback loop that blocks TLR9 transcription an

240 l secretory cells, establishing a reciprocal negative-feedback loop that ensures the full differentia

241 article, we report that STAT3 also drives a negative-feedback loop that limits the formation of IL-1

242 critical involvement of Dok-1 and Dok-2 in a negative-feedback loop that prevents overactivation of C

243 f the chemicals is regulated by a biomimetic negative feedback loop, the "repressilator" network.

244 To close the transcription-based negative feedback loop, the FRQ-FRH complex inhibits the

245 The resulting bioelectronic and microfluidic negative-feedback loop then serves to regulate the conce

246 e analyzed dynamics-determining positive and negative feedback loops, thereby elucidating the attract

247 s and dopamine release of SN DA neurons in a negative feedback loop through activation of G-protein c

248 n modeled, and we provide evidence for a new negative feedback loop through PPM1A upregulation.

249 regulated by VEGF and therefore disrupts the negative-feedback loop, thus generating constant, but lo

250 uentially produce IFN-gamma, which acts in a negative feedback loop to ameliorate iNKT hepatitis by i

251 Our studies thus delineate a negative feedback loop to attenuate Ang II signaling in

252 n decreased miR863-3p levels, thus forming a negative feedback loop to attenuate immune responses aft

253 nd RagA(GTP) hydrolysis, thereby providing a negative feedback loop to attenuate mTORC1 lysosomal rec

254 CCN3/NOV inhibits AR signaling and acts in a negative feedback loop to block AR function.

255 ZEB1 acts in a negative feedback loop to block expression of miR-200, w

256 d translational repression combine to form a negative feedback loop to control Cpeb4 protein levels w

257 , a mechanism that might serve normally as a negative feedback loop to control immune responses that

258 Our data suggest that miR-323-3p acts in a negative feedback loop to control the production of IL-2

259 duced p105 proteolysis, therefore, induced a negative feedback loop to downregulate NF-kappaB-depende

260 onmental stimulation amplifies an endo-siRNA negative feedback loop to dynamically repress cognate ge

261 data suggest that PIFs and HECs constitute a negative feedback loop to fine-tune photomorphogenesis i

262 ivated protein kinase Snf1 is coupled with a negative feedback loop to generate the characteristic pu

263 SNAI2 and miR-203 formed a double negative feedback loop to inhibit each other's expressio

264 gers assembly of the GADD34/PP1 complex in a negative feedback loop to inhibit Yap and promote apopto

265 200 expression via a self-reinforcing double negative feedback loop to promote the mesenchymal state.

266 e, which is used as a signal in an autocrine negative feedback loop to regulate cell proliferation.

267 It has been shown to provide a negative feedback loop to regulate glucose uptake into c

268 ent up-regulation of miR-125b, which forms a negative feedback loop to repress p38alpha activation an

269 Finally, Ebf1 participates in a negative feedback loop to repress Zfp521 as differentiat

270 S6K in turn acted through a negative feedback loop to restrain Akt3 expression.

271 y the E3 ligase beta-TrCP1, thus providing a negative feedback loop to tightly control cellular Akt o

272 manner, thereby unveiling a novel inducible negative feedback loop to tightly control NF-kappaB-depe

273 uodenum to sense nutrient influx and trigger negative feedback loops to inhibit glucose production an

274 of ancestral RNAi by, for example, employing negative feedback loops to reset the transmission of epi

275 he CUL7/Fbxw8 ubiquitin ligase constitutes a negative-feedback loop to restrain the activity of HPK1

276 hese data suggest that Ub binding provides a negative feedback loop upon NOD-dependent activation of

277 wo decades ago the WUSCHEL/CLAVATA (WUS/CLV) negative feedback loop was established as being essentia

278 to be decent substrates of OGT, exhibiting a negative feedback loop when phosphorylated at the P-3 si

279 s Pten expression creating an autoregulatory negative feedback loop, whereas complete loss of PTEN ma

280 pression is controlled via an autoregulatory negative feedback loop whereby Chtop binds its own mRNA

281 Finally, we show for the first time a negative feedback loop whereby miR-137 downregulates CAR

282 In addition, we discovered a negative feedback loop whereby the tumour suppressor FBX

283 to be a transcription-and-translation-based negative feedback loop, wherein progressive and controll

284 downmodulation of a phosphatase-mediated MET-negative feedback loop, which accompanies receptor inter

285 cytohesins and BRAGs, EFA6 is regulated by a negative feedback loop, which is mediated by an alloster

286 e the integrity of adherens junctions, and a negative feedback loop, which is used to limit beta-cate

287 and impaired dPER function in the circadian negative feedback loop, which manifests into changes in

288 a component of the Neurospora core circadian negative feedback loop, which was thought to generate su

289 ing the presence of interlinked positive and negative feedback loops, which are common in polarity pa

290 depends on a self-sustaining transcriptional negative feedback loop with a built-in time delay in fee

291 ntial for generating a slow, self-sustaining negative feedback loop with a period close to 24 hr, the

292 Importantly, Irf8 forms a negative feedback loop with Cebpb, a monocyte-derived DC

293 b gene of the M4 module (NaLRRK1) mediates a negative feedback loop with JA signaling.

294 positive feedforward loop with Stat1/2 and a negative feedback loop with Stat3.

295 A negative feedback loop with time delays due to slow bind

296 We then proposed a negative feedback loop with upregulation of the phosphat

297 nterplay between fast (min) and slow (min-h) negative feedback loops with maximal information transfe

298 Two negative feedback loops with Notch and Pros allow Kon to

299 ogy of highly druggable motifs consists of a negative feedback loop without any positive feedback loo

300 This negative feedback loop would cause a substantial drop in