ライフサイエンスコーパス: feedback loop

1 AR activity and initiation of this positive feedback loop.

2 highly variable, unknown input signals via a feedback loop.

3 n-activated protein kinase ERK in a positive feedback loop.

4 gulated autophagy through a miR-221/beclin-1 feedback loop.

5 ng pDC differentiation, revealing a positive feedback loop.

6 ereby creating a compensative RUNX1-p53-CBFB feedback loop.

7 throughput-discovery and materials-by-design feedback loop.

8 e has its origins in the pallido-subthalamic feedback loop.

9 o-IL-1beta production, suggesting a positive feedback loop.

10 H2 surface expression, suggesting a positive feedback loop.

11 pregulation occurs through a Meis1-dependent feedback loop.

12 the activation of Akt through IGFR/PI3k/Akt feedback loop.

13 rk to function as an ultrasensitive negative feedback loop.

14 t premotor noise entering within an internal feedback loop.

15 to blood at a much elevated level due to the feedback loop.

16 feedforward computations are reinforced in a feedback loop.

17 ctions "OFF", thus establishing the negative feedback loop.

18 ar space quantitatively describes this novel feedback loop.

19 to feed decisions and provide an information feedback loop.

20 ing a PlGF/leukotriene/Th2-response positive feedback loop.

21 -kappaB/IL6 signaling, suggesting a positive feedback loop.

22 on its position with respect to the positive feedback loop.

23 ammalian circadian transcription/translation feedback loop.

24 ied OGT as a YAP-regulated gene that forms a feedback loop.

25 anscription-translation-based autoregulatory feedback loop.

26 l activation and ATX secretion in a positive feedback loop.

27 ght be concomitantly activated in a positive-feedback loop.

28 ich enhance DUO1 transcription in a positive feedback loop.

29 lling of cancer cells, setting up a positive feedback loop.

30 NBC cell metastasis, thus forming a positive feedback loop.

31 pothalamus, is a part of estrogen's positive feedback loop.

32 maging mode via a computer-controlled closed-feedback loop.

33 atus maintained by operation of the positive feedback loop.

34 a sialidase - TGF-beta1 - sialidase positive feedback loop.

35 zation of IRF3, thus constituting a negative feedback loop.

36 mary adipose tissue through a novel negative-feedback loop.

37 signaling intermediaries or through negative feedback loops.

38 NFkappaB, ERK, and AKT pathways and multiple feedback loops.

39 behavior via cell-autonomous transcriptional feedback loops.

40 through processes involving ongoing sensory feedback loops.

41 everal stages of disease-associated positive feedback loops.

42 experiments to assess the roles of putative feedback loops.

43 irreversibility are used to detect positive feedback loops.

44 rcadian clock keeps time via transcriptional feedback loops.

45 potential for intricate reaction systems and feedback loops.

46 e way for the powering of integrated medical feedback loops.

47 h, Hedgehog, and JAK/STAT, which all involve feedback loops.

48 iven by the partial preservation of negative feedback loops.

49 ssue-specific gene activation using positive feedback loops.

50 oagulation pathway independently of thrombin feedback loops.

51 re, we find that temporal regulation of this feedback loop, a previously unexplored dimension, is the

52 thereby establishing an associative positive-feedback loop and connecting functionally diverse hippoc

53 K/AKT, miR-21 and PTEN constitute a positive feedback loop and have a key role in LMP1-induced CSCs i

54 relieves chronic inflammation by a negative feedback loop and plays a protective role during atheros

55 olecular assemblies comprising the circadian feedback loop and provide an initial structural view of

56 tion is driven by the Bem1-mediated positive feedback loop and reveal novel features of its regulatio

57 l fates due to the strong effect of noise on feedback loops and missing parameters.

58 systems away from equilibrium, incorporating feedback loops and pushing replication chemistry away fr

59 ons arise in the subthalamic-globus pallidus feedback loop, and occur during movement.

60 g feed-forward loops and their combinations, feedback loops, and circuits made of an sRNA and another

61 f important pluripotency-sustaining positive feedback loops, and induce a bifurcation in the underlyi

62 e or suppress neuronal function for adaptive feedback-loop applications in the future.

63 ical modeling revealed interlocking positive feedback loop architecture, which exhibits bistable or o

64 These feedback loops are initiated by CLOCK-CYCLE (CLK-CYC) he

65 ics, the elements with two positive/negative feedback loops are the minimalist elements to have chaot

66 ncovers the 1q21.3-directed S100A7/8/9-IRAK1 feedback loop as a crucial component of breast cancer re

67 action of transcriptional and translational feedback loops as well as chromatin remodelling events.

68 GLN enzymes and HIF isoforms and discuss how feedback loops based on recently identified noncoding RN

69 Additionally, we uncover a negative feedback loop between actin remodeling and flg22-induced

70 Our study reveals a positive feedback loop between antigen-specific CTLs and APC to a

71 the present study, we discovered a positive feedback loop between BCR-ABL and protein arginine methy

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

73 -based approach to elucidate how the two-way feedback loop between cell contractility (induced by the

74 on of ERK and define a novel double-negative feedback loop between EpCAM and ERK that contributes to

75 ion and ozone formation, there is a positive feedback loop between forest communities and ozone, whic

76 Our results describe a double-negative feedback loop between MIR100HG and the transcription fac

77 A positive feedback loop between RTN1A and CHOP was found leading t

78 rall, our novel data suggest that a positive feedback loop between Snail-nuclear Cat L-CUX1 drives EM

79 cretion subsided, demonstrating a functional feedback loop between the liver and the insulin-secretin

80 ription factors, including a double-negative feedback loop between the microRNA-200 (miR-200) family

81 lf an AR-regulated gene, creating a positive feedback loop between the two factors.

82 sed HCC formation by inhibiting the positive feedback loop between YAP/TAZ and Notch signaling.

83 is A or T), and discuss how self-reinforcing feedback loops between DNA methyltransferases and histon

84 quires tonic sensing of microbes and complex feedback loops between innate and adaptive components of

85 Our data point to the existence of negative feedback loops between these two regulatory proteins tha

86 cillator comprises transcription-translation feedback loops but also requires post-translational proc

87 presses the MDFIC gene, revealing a negative feedback loop by which glucocorticoids limit MDFIC activ

88 novel insights into how and to what extent a feedback loop can enhance or suppress molecular fluctuat

89 In migrating cells, feedback loops can amplify stochastic fluctuations in ac

90 an lead to larger eventual inequalities, (2) feedback loops can embed early-life circumstances, (3) c

91 aints can breed further constraints, and (4) feedback loops can operate over generations.

92 In contrast, "positive feedback loops" can develop within these microbial commu

93 t an NF-kappaB-HOTAIR axis drives a positive-feedback loop cascade during DDR and contributes to cell

94 e mouse bleomycin model, and by breaking the feedback loop, cause a downregulation of sialidase and T

95 Our results reveal a positive mechanical feedback loop: cells pulling on collagen locally align a

96 Circadian negative feedback loop (CNFL) genes play important roles in cance

97 llator consists of transcription-translation feedback loops composed of transcriptional regulators, e

98 olar cell growth is sustained by oscillatory feedback loops comprising three main components that tog

99 ulatory mechanism in which a double-negative feedback loop consisting of PRMT7 and miR-24-3p/miR24-2-

100 transcription factors in the circadian-clock feedback loop, consisting of CCA1 HIKING EXPEDITION (CHE

101 This feedback loop contributes to pathological responses to i

102 ronmental signals and directly implicated in feedback loops controlled by miRNAs, ZEB1 appears to be

103 n integral part of the Wnt and Fgf signaling feedback loop coordinating cell migration and the self-o

104 redicted that the stimulus-specific positive feedback loop could be responsible for the difference be

105 s competitive advantage is the DDAM positive feedback loop (dissolved organic carbon (DOC), disease,

106 They rely on transcriptional/translational feedback loops driven by interacting networks of clock c

107 ated kinase 1 (IRAK1) establish a reciprocal feedback loop driving tumorsphere growth.

108 each a large enough group size, they enter a feedback loop - driving shellfish prey size down with at

109 ession of a negative regulator of the hIL-10 feedback loop, dual-specificity phosphatase 1 (DUSP1), r

110 ced in this region, suggestive of a Shh-Vax1 feedback loop during early development of the forebrain

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

112 This positive feedback loop enables a very rapid and strong host respo

113 model demonstrates that the MazF mRNA-decay feedback loop enables proportional control of MazF in an

114 The feedback loop enables the drift correction of pressure b

115 t B-Raf and ERK1/2 activation; this positive feedback loop enhances the invasion of colon cancer cell

116 gulation amplification by thrombin-dependent feedback loops enhances the risk of thrombosis.

117 ed protein 2 possibly establishes a positive feedback loop enhancing transforming growth factor-beta1

118 [idelalisib]), interrupts a double-negative feedback loop, enhancing GC-regulated transcription to s

119 n and proteasome activity provide a negative feedback loop, ensuring that adhesion assembly predomina

120 Thus a mutually reinforcing feedback loop exists between telomere capping and Wnt si

121 We opened synthetic positive feedback loops experimentally to obtain open-loop functi

122 malian clocks are based on a transcriptional feedback loop featuring the transcriptional activators c

123 t of the Hh pathway, thus forming a positive feedback loop for Gli activation.

124 A double-negative feedback loop formed by the morning genes CIRCADIAN CLOC

125 ors, uncovered a direct and rapid inhibitory feedback loop from ERK to MEK1, and mediated development

126 A positive feedback loop from IL-1beta and back to PGE2, which itse

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

128 This potentially constitutes a negative feedback loop governing this critical checkpoint mechani

129 e-wide analyses of the clock transcriptional feedback loop have revealed a global circadian regulatio

130 b group protein EZH2 disrupted this negative feedback loop in both CRPC and enzalutamide-resistant pr

131 n the TNFAIP3/A20-mediated anti-inflammatory feedback loop in CD4(+) T cells and promotes kinase acti

132 that the primary function of the interlocked feedback loop in Drosophila is to drive rhythmic transcr

133 We uncovered a negative feedback loop in M2 myeloid cells, wherein integrin beta

134 her with PI3K/AKT to regulate a ZEB1-miR-200 feedback loop in PDGFRalpha-driven gliomas.

135 gh a ROS-p38 MAPK-NADPH oxidase-ROS positive feedback loop in response to a myocardial hypertrophic c

136 ype 2 (COX-2), which functions in a negative feedback loop in TGFbeta and ERbeta signaling pathways a

137 ylation in a reciprocal manner, suggesting a feedback loop in the control of the epigenome.

138 ral geniculate nucleus complete the earliest feedback loop in the mammalian visual pathway and regula

139 ssed by p53, defining an additional negative feedback loop in the p53 network.

140 the p53-PCBP4-ZFP871 axis represents a novel feedback loop in the p53 pathway.

141 demonstrate a calpain/PTP1B/VEGFR2 negative feedback loop in the regulation of VEGF-induced angiogen

142 ations, and establishes an AKT1-MARCKS-LAMC2 feedback loop in this regulation.

143 We also identified a positive-feedback loop in which ERK/EGR1 signaling promotes CD44V

144 ng EZH2 expression, thus defining a positive feedback loop in which EZH2 controls GC B cell prolifera

145 We propose the presence of an autocrine feedback loop in which Klotho senses the need for FGF23.

146 The mammalian circadian clock is built on a feedback loop in which PER and CRY proteins repress thei

147 Our results identified a negative feedback loop in which SET9 controls DNA methyltransfera

148 These studies suggest a mechanical-chemical feedback loop in which TCR-triggered T cells generate fo

149 time via a transcriptional/posttranslational feedback loop in which transactivation of Per (period) a

150 sue of Cancer Cell, Wieland et al. uncover a feedback loop in which tumor cells, by augmenting Notch

151 We show here that the number of feedback loops in a network, as well as the eigenvalues

152 d indirect (biochemical via PLD2 and mTORC2) feedback loops in organizing cell polarity and motility-

153 ned movements, highlighting a role for local feedback loops in the brain.

154 the clock is composed of numerous regulatory feedback loops in which REVEILLE8 (RVE8) and its homolog

155 Here we describe evidence of a negative feedback loop, in which PGE2 augments the expression of

156 We propose a negative feedback loop, in which sphingosine inhibits GBA2 activi

157 otor decision making within the sensorimotor feedback loop intrinsic to tracking?

158 Importantly, a positive feedback loop involving autocrine LIF, LIFR, and STAT4 d

159 These findings reveal a feedback loop involving CRL4(CRBN) that adjusts GS prote

160 findings demonstrate a deleterious positive feedback loop involving elevated intracellular calcium a

161 (Dyn1) and its activation through a positive feedback loop involving enhanced epidermal growth factor

162 HrpG, and may be enhanced through a positive feedback loop involving HrpA, the main component of the

163 A positive feedback loop involving RAS and SOS, which leads to bist

164 ether, these results suggest that a positive feedback loop involving sialidases potentiates fibrosis,

165 partial adaptation arises through a negative feedback loop involving the small protein MgrB.

166 ontrol of thyroid hormone homeostasis by the feedback loops involving the hypothalamus-pituitary-thyr

167 lysis, we find that inhibiting self-positive feedback loop is a more robust and effective treatment s

168 ghtness of the active galactic nucleus; this feedback loop is the process by which supermassive black

169 of profibrotic genes, supporting a positive feedback loop leading to myofibroblast activation.

170 BXL5 protein level, demonstrating a negative feedback loop limiting excessive accumulation of iron-re

171 A G-protein signaling-mediated feedback loop maintains cytoplasmic Ca(2+) level, which

172 her contend that the DL to DDi to DDmg to DL feedback loop makes the pattern separation/completion op

173 generation acting effectively in a positive feedback loop, mediating a subsequent surge in procoagul

174 behaviorally triggered stimuli to flies in a feedback-loop mode, and are highly customizable and open

175 is mutant lacking the Snf1-mediated positive feedback loop, Msn2 responds similarly to glucose limita

176 e grouped into two general classes: negative feedback loop (NFBL) and incoherent feed-forward loop (I

177 circuit motifs generate adaptation: negative feedback loops (NFLs) and incoherent feed-forward loops

178 ch upon irradiation strengthens the negative feedback loop of a CRN that produces oscillations of try

179 Here, we report on a positive regulatory feedback loop of alcohol and FGF2 in rodent models.

180 ken together, our findings reveal a positive feedback loop of cGAS signaling generated by TRIM14-USP1

181 onal eNOS and potentially play a role in the feedback loop of damage and repair during homeostasis, b

182 esults suggest that, while a single negative feedback loop of either one- or two-gene element can onl

183 ssion of GhMAPK3K15, constituting a positive feedback loop of GhWRKY59-regulated MAP kinase activatio

184 adrenergic signaling reinforced an autocrine feedback loop of macrophage-derived IL-10 and this syner

185 ular stress-response pathways by mediating a feedback loop of p38-p53 signaling, thereby contributing

186 ggest that Pfn may play a role in a possible feedback loop of the actin/MKL/SRF signaling circuit.

187 es for one another that establish mechanical feedback loops of activation.

188 s observed in vivo and found that a positive feedback loop on protein kinase A mediated by the AMP-ac

189 inputs, both local recurrent and widespread feedback loops, onto DGCs.

190 enhanced quality factor using a regenerative feedback loop operating at 1.4 GHz and an adjustable qua

191 rks in immune cells, such as feedforward and feedback loops or ligand antagonism, sometimes can be un

192 s the protein concentration in the cell with feedback-loop parameters affecting the dynamics of the c

193 Thus, mGluRs establish a local negative feedback loop positioned to regulate IHC activity and ma

194 ar clock relies on transcription/translation feedback loops, posttranscriptional regulation also play

195 tigate how interlinked positive and negative feedback loops process EGF signals into ERK pulses of co

196 , suggesting that a tension-induced negative feedback loop promotes ICAM-1-mediated neutrophil crawli

197 initiates multiple radical-forming positive-feedback loops, rapidly producing visible levels of reso

198 egulatory core is controlled by two negative feedback loops (regulated by Mdm2 and Wip1) responsible

199 oscillations, and two antagonistic positive feedback loops (regulated by phosphatases Wip1 and PTEN)

200 ein CDC6 binds Cyclin E-CDK2 kinase and in a feedback loop removes RB from ORC1, thereby hyper-activa

201 Together, these results describe a novel feedback loop required for lens differentiation and morp

202 and disrupt the nuclear AURKA/FOXM1-positive feedback loop, respectively, resulting in a more effecti

203 Noninvasive PET monitoring of these RTK feedback loops should help to rapidly assess resistance

204 , which indicates the presence of a positive feedback loop somewhere in the regulatory environment of

205 edback introduces a hierarchy among negative feedback loops, such that the effect of a negative feedb

206 HIF-1alpha and iNOS are linked by a positive feedback loop that amplifies macrophage activation.

207 Here, we have uncovered a distinct positive feedback loop that arises from the reciprocal stabilizat

208 uced miRNAs, act as components of a negative feedback loop that blocks neuronal hyperactivity at leas

209 channels by mGluR1, which removes a negative feedback loop that constitutively regulates NMDARs.

210 uated by Fxr1, indicating the existence of a feedback loop that contributes to Fxr1 overexpression an

211 However, the Tat positive-feedback loop that controls HIV's fate decision between

212 latory subunit (PP2A(Rts1)) is embedded in a feedback loop that controls TORC2 signaling and helps se

213 TORC2 signaling cascade represents a vicious feedback loop that elicits unrestrained AKT signaling.

214 onses to inputs, is nested within a negative feedback loop that encompasses RAS and RAF, MEK, and ERK

215 that GIV is required to establish a positive feedback loop that enhances integrin-FAK signaling.

216 l (MIM) capacitors that, via a discrete-time feedback loop that equalizes charging time, digitize tem

217 ted signaling in B cells involves a positive-feedback loop that establishes T cell-propagated autoimm

218 the PI3-K-->Akt pathway serves as a positive feedback loop that further enhances noncanonical Wnt sig

219 miR-34a expression, resulting in a positive feedback loop that increased subsequent capacity to engu

220 to the oocyte posterior, creating a positive feedback loop that increases the length and persistence

221 n sigma factor sigma(F) to create a negative feedback loop that inhibits sigma(F) -directed gene tran

222 InDrosophila, a transcriptional feedback loop that is activated by CLOCK-CYCLE (CLK-CYC)

223 es under constant light illumination, with a feedback loop that is driven by self-shadowing.

224 overy of a splice isoform-dependent positive feedback loop that is essential to sustain PI3K/Akt sign

225 mate signalling establishes a local negative feedback loop that is positioned to regulate inner hair

226 We show that it is part of a negative feedback loop that limits proinflammatory and prothrombo

227 These results demonstrate a novel positive-feedback loop that links the myofibroblast phenotype to

228 unctions as an afferent signal in a negative feedback loop that maintains homeostatic control of adip

229 -scale Langmuir waves; this process closes a feedback loop that maintains the continuous coherent emi

230 netic barrier crossing coupled to a negative feedback loop that mechanistically differs from previous

231 cing of MYB83 is tightly regulated through a feedback loop that might contribute to fine-tuning the e

232 involvement of Dok-1 and Dok-2 in a negative-feedback loop that prevents overactivation of CD8(+) T c

233 ogical and evolutionary processes, closing a feedback loop that promises exciting new avenues of scie

234 Klotho in bone cells is part of an autocrine feedback loop that regulates FGF23 expression during ren

235 A negative feedback loop that relies on the coordination-coupled de

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

237 es AR expression, this results in a negative feedback loop that suppresses AR protein expression in a

238 recruitment of P-TEFb, generating a positive feedback loop that sustains transcription.

239 sitide 3-kinase-dependent manner, a positive feedback loop that we find is completely lost in beta-ce

240 l classes based on the structure of positive feedback loops that activate and localize Cdc42.

241 gene LRCs are intimately linked to identical feedback loops that are involved in potentially chaotic

242 We uncovered gene networks with overlapping feedback loops that are modulated by nuclear hormone rec

243 These principles include positive feedback loops that are required to destabilize a spatia

244 cadian clock is comprised of transcriptional feedback loops that control rhythmic gene expression res

245 other during cell-cell fusion, and the force-feedback loops that ensure robust cytokinesis.

246 resistance to these treatments can arise via feedback loops that increase surface expression of the r

247 We further identified two positive feedback loops that integrate epigenetic regulation and

248 or is a highly complex process with multiple feedback loops that involve both peripheral and central

249 micals is regulated by a biomimetic negative feedback loop, the "repressilator" network.

250 ting bioelectronic and microfluidic negative-feedback loop then serves to regulate the concentration

251 d dynamics-determining positive and negative feedback loops, thereby elucidating the attractor (dynam

252 ed miR863-3p levels, thus forming a negative feedback loop to attenuate immune responses after succes

253 inhibits AR signaling and acts in a negative feedback loop to block AR function.

254 a suggest that miR-323-3p acts in a negative feedback loop to control the production of IL-22 in IL-2

255 The molecule is initiating a feedback loop to enable its own movement.

256 M1 participate in a tightly coupled positive feedback loop to enhance BCSC phenotype.

257 BK and TRPML1 forms a positive feedback loop to facilitate lysosomal Ca(2+) release and

258 est that PIFs and HECs constitute a negative feedback loop to fine-tune photomorphogenesis in Arabido

259 osition of GAGs, thereby creating a positive feedback loop to further enrich GAG content and promote

260 otein kinase Snf1 is coupled with a negative feedback loop to generate the characteristic pulsatile d

261 respond to cellular metabolites, often in a feedback loop to repress synthesis of the enzymes used t

262 is stress induced, is that it functions in a feedback loop to resolve cell stress.

263 al epithelial cells, establishing a positive feedback loop to support tumor development.

264 vides opportunities for the establishment of feedback loops to enhance or suppress surface-derived si

265 ceptor CRYPTOCHROME (CRY) synchronizes these feedback loops to light:dark cycles by binding to and de

266 ral RNAi by, for example, employing negative feedback loops to reset the transmission of epigenetic i

267 it of transcription factors forming positive feedback loops to stabilise otic progenitor identity.

268 initiating double-strand breaks (DSBs) via a feedback loop triggered by crossover designation in C. e

269 time using transcriptional/posttranslational feedback loops (TTFL) in which expression of Cryptochrom

270 Transcriptional-translational feedback loops (TTFLs) are a conserved molecular motif o

271 tion in the behaviour of the Vegf-Dll4/Notch feedback loop underlies the morphogen function of Vegfa

272 eratocyte-to define a set of mechanochemical feedback loops underlying actin network excitability and

273 Altogether, this suggests that a mechanical feedback loop, via microtubules acting both as stress se

274 near waveguides to represent the graph and a feedback loop, we experimentally show that photons trave

275 Using this speckle wavemeter as part of a feedback loop, we stabilize a 780 nm diode laser to achi

276 ent substrates of OGT, exhibiting a negative feedback loop when phosphorylated at the P-3 site.

277 self-consistency via a classically computed feedback loop where quantum gate errors can be partly ac

278 which is a regulator of the positive hIL-10 feedback loop, whereas expression of a negative regulato

279 e have identified an enzymatically amplified feedback loop whereby glucocorticoids boost cAMP to main

280 blockade of autophagy revealed an unexpected feedback loop whereby knocking down the autophagy factor

281 ell-autonomous transcriptional-translational feedback loop, whereby expression of the Period and Cryp

282 We provide direct evidence for a feedback loop, whereby PLD induction upon starvation lea

283 antagonism of Tie2 and initiates a positive feedback loop wherein FOXO1-driven ANG2 expression promo

284 The core feedback loop, which employs CLOCK-CYCLE (CLK-CYC) activ

285 ired dPER function in the circadian negative feedback loop, which manifests into changes in molecular

286 CLK-CYC also activates an interlocked feedback loop, which uses the PAR DOMAIN PROTEIN 1epsilo

287 a coli lac operon is regulated by a positive feedback loop whose potential to generate an all-or-none

288 sive gene constituting a positive regulatory feedback loop with alcohol.

289 Thus, inducible lncRNA can create a feedback loop with its cognate transcription factor to a

290 that innate lymphocytes engage in a positive-feedback loop with monocytes that promotes clearance of

291 ls differing in the location of the positive feedback loop with respect to the gene can all reproduce

292 ion of eve in this spider does not require a feedback loop with run-1, as is found in the pair-rule c

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

294 Further, CD44V6 is part of a positive-feedback loop with TGFbeta1/TGFbetaRI signaling that act

295 vealed that Notch signaling forms a positive feedback loop with the Hippo signaling effector YAP/TAZ

296 IL7 is part of a local feedback loop with the soma because it regulates cumulus

297 ty is asymmetrically amplified by a positive feedback loop with the super elongation complex (SEC) to

298 echanistically, Ret is engaged in a positive feedback loop with Wnt/Wingless signalling, modulated by

299 ion of GA accumulation represents a positive feedback loop within the molecular framework driving rap

300 We identified a feedback loop within the NANCI (Nkx2.1-associated noncod

301 on and motor commands to be intertwined in a feedback loop, yet the neural substrate underlying this