ライフサイエンスコーパス: positive-feedback loop

1 uppresses AR activity and initiation of this positive feedback loop.

2 depends on its position with respect to the positive feedback loop.

3 CDC25A; thus, Cdc25A upregulates itself in a positive feedback loop.

4 expression and odontoblast homeostasis via a positive feedback loop.

5 ase-3 activation, and thus creating a second positive feedback loop.

6 thelin-converting enzyme 1/endothelin 1-SphK positive feedback loop.

7 criptional activation and ATX secretion in a positive feedback loop.

8 c and caspase-3 activity, thereby creating a positive feedback loop.

9 y generated RelA:p52/NF-kappaB activity in a positive feedback loop.

10 expression of CystLT receptors, suggesting a positive feedback loop.

11 targeting Smad7 and HOXD10, hence forming a positive feedback loop.

12 nd consumption of nutritive sugars through a positive feedback loop.

13 like dofetilide sensitize the heart to this positive feedback loop.

14 ronment by enhancing TGF-beta signaling in a positive feedback loop.

15 ACYGY, which enhance DUO1 transcription in a positive feedback loop.

16 cretion, which formed an NF-kappaB/TNF-alpha positive feedback loop.

17 lated each other's expression resulting in a positive feedback loop.

18 d cytohesins may combine in a mixed negative-positive feedback loop.

19 reased in HD cells as a result of overactive positive feedback loop.

20 revents saturation-based distortions in this positive feedback loop.

21 tivate Rac1 at the cell edge, which closes a positive feedback loop.

22 reased killing of cancer cells, setting up a positive feedback loop.

23 affected by a nicotine- and NeuroD1-induced positive feedback loop.

24 ly amplified downstream of Notch, creating a positive feedback loop.

25 amplification of their GEF activity by their positive feedback loop.

26 romotes TNBC cell metastasis, thus forming a positive feedback loop.

27 in the hypothalamus, is a part of estrogen's positive feedback loop.

28 nt tumor suppressor effect generated by this positive feedback loop.

29 EAFY (LFY) directly activates FD, creating a positive feedback loop.

30 lation status maintained by operation of the positive feedback loop.

31 Cbeta, transcriptionally forming a proximate positive feedback loop.

32 r promoted CXCL13 production, establishing a positive feedback loop.

33 rs to be a sialidase - TGF-beta1 - sialidase positive feedback loop.

34 RNP, promotes reperfusion, and eliminates a positive feedback loop.

35 n to further stimulate Eomes expression in a positive feedback loop.

36 al generation by the sperm mitochondria in a positive feedback loop.

37 teoblast differentiation, thereby creating a positive feedback loop.

38 he mitogen-activated protein kinase ERK in a positive feedback loop.

39 tion during pDC differentiation, revealing a positive feedback loop.

40 nduced pro-IL-1beta production, suggesting a positive feedback loop.

41 tent NOTCH2 surface expression, suggesting a positive feedback loop.

42 es, creating a PlGF/leukotriene/Th2-response positive feedback loop.

43 ed TG2/NF-kappaB/IL6 signaling, suggesting a positive feedback loop.

44 ecules might be concomitantly activated in a positive-feedback loop.

45 oblast phenotype and secretome in a salutary positive-feedback loop.

46 e, which bolstered T cell proliferation in a positive-feedback loop.

47 filter undesired model behaviors induced by positive feedback loops.

48 the well-described circadian rhythm negative/positive feedback loops.

49 HPA axis participate in multiple reinforcing positive feedback loops.

50 y involve genetic nonlinear interactions and positive feedback loops.

51 emergent phenomenon propelled by unexplored positive feedback loops.

52 plored tissue-specific gene activation using positive feedback loops.

53 inhibit several stages of disease-associated positive feedback loops.

54 resis, or irreversibility are used to detect positive feedback loops.

55 ave multiple positive direct regulations and positive feedback loops.

56 potent negative regulator of p53, creating a positive feedback loop acting on p53.

57 rect checkpoint pathways from the effects of positive-feedback loops active at the G2/M transition.

58 ate chromatin association of pTEFb through a positive feedback loop and facilitate Pol II transition

59 LMP1, PI3K/AKT, miR-21 and PTEN constitute a positive feedback loop and have a key role in LMP1-induc

60 ll adhesion, which reinforce each other in a positive feedback loop and react from cues from their re

61 polarization is driven by the Bem1-mediated positive feedback loop and reveal novel features of its

62 ocampus, thereby establishing an associative positive-feedback loop and connecting functionally diver

63 ists of a negative feedback loop without any positive feedback loops, and consensus motifs with low d

64 ehavior of important pluripotency-sustaining positive feedback loops, and induce a bifurcation in the

65 ss is dependent on p110beta via p110beta-Rac-positive-feedback loop, and that disruption of this loop

66 Dynamical modeling revealed interlocking positive feedback loop architecture, which exhibits bist

67 In addition, systems with autocatalytic positive feedback loop are shown to be more robust than

68 While positive feedback loops are good at promoting switch-lik

69 pression and drug inhibition are linked in a positive feedback loop arising from an innate, global ef

70 nd DA serve as competing signals, and that a positive feedback loop based on regulation of DA biosynt

71 ulators of AEG-1 transcription, generating a positive feedback loop between AEG-1 and Akt in regulati

72 Our study reveals a positive feedback loop between antigen-specific CTLs and

73 Their initiation is induced by a positive feedback loop between auxin and its transporter

74 In the present study, we discovered a positive feedback loop between BCR-ABL and protein argin

75 ted perturbation of spindle position and the positive feedback loop between chromosome signal-induced

76 pathologically remodel the ECM in IPF via a positive feedback loop between fibroblasts and aberrant

77 ene emission and ozone formation, there is a positive feedback loop between forest communities and oz

78 ematical model incorporating a MMF-inhibited positive feedback loop between H1N1-specific IL-4(+)CD4(

79 Furthermore, we identify a positive feedback loop between HIF-1alpha and aerobic gl

80 at impaired TGFbeta signaling can initiate a positive feedback loop between increasing ECM stiffness

81 ell, Okamoto and Nishimura (2015) identify a positive feedback loop between neuronal cells that maint

82 A positive feedback loop between RTN1A and CHOP was found

83 Overall, our novel data suggest that a positive feedback loop between Snail-nuclear Cat L-CUX1

84 ion of PI3K-AKT-mTOR signaling, suggesting a positive feedback loop between SOX4 and PI3K-AKT-mTOR ac

85 tion and nuclear translocation, indicating a positive feedback loop between STAT3 and GH in somatotro

86 CMEC/D3 cells, suggesting the existence of a positive feedback loop between STAT5 and PRL that promot

87 rve activity, which becomes persistent via a positive feedback loop between sympathetic nerve activit

88 We demonstrate that a positive feedback loop between the aberrant ECM and inte

89 ns, this effect becomes a key component of a positive feedback loop between the GPe and striatum that

90 y touch off a cycle of adaptive potential, a positive feedback loop between the self-system and the s

91 2 is itself an AR-regulated gene, creating a positive feedback loop between the two factors.

92 7 binding site were identified, suggesting a positive feedback loop between the two mesendoderm trans

93 sion in renal epithelial cells, suggesting a positive feedback loop between TNF-alpha and MIF during

94 in G1/S transition and S phase, suggesting a positive feedback loop between UCH37 and E2F1.

95 n suppressed HCC formation by inhibiting the positive feedback loop between YAP/TAZ and Notch signali

96 Here, we demonstrate that a positive-feedback loop between BASL and the MAPK pathway

97 The positive-feedback loop between CIP2A and MYC augments th

98 Our data uncover a positive-feedback loop between circulating plasmablasts

99 Furthermore, we uncovered a positive-feedback loop between MONOPTEROS (ARF5)-depende

100 ion of PKC-alpha and -delta mediates a novel positive feedback loop by promoting ErbB2 entry into the

101 Positive feedback loops can produce multistability, resu

102 In contrast, "positive feedback loops" can develop within these microb

103 dy implies the existence of oncogene-induced positive feedback loops capable of bypassing the continu

104 ggest that an NF-kappaB-HOTAIR axis drives a positive-feedback loop cascade during DDR and contribute

105 Thus, a positive feedback loop connected by the WNT signaling pa

106 These results reveal a positive feedback loop connecting Pten and Ras pathways

107 Together, the network components in this positive feedback loop constitute an emergent property t

108 Regulatory gene circuits with positive-feedback loops control stem cell differentiatio

109 y for full HAE expression, thus completing a positive feedback loop controlling HAE expression.

110 e model predicted that the stimulus-specific positive feedback loop could be responsible for the diff

111 Our results show that although the positive feedback loop determines the range of bistabili

112 m for this competitive advantage is the DDAM positive feedback loop (dissolved organic carbon (DOC),

113 2 from CD44, increasing CD44 expression in a positive feedback loop driven by the Wnt/beta-catenin si

114 es or pseudo-oncogenes and can contribute to positive feedback loops driving cancer progression.

115 This positive feedback loop enables a very rapid and strong h

116 -dependent B-Raf and ERK1/2 activation; this positive feedback loop enhances the invasion of colon ca

117 led-related protein 2 possibly establishes a positive feedback loop enhancing transforming growth fac

118 We opened synthetic positive feedback loops experimentally to obtain open-lo

119 nal target of the Hh pathway, thus forming a positive feedback loop for Gli activation.

120 voring IL-2Ralpha(hi) Treg cells, creating a positive feedback loop for IL-2Ralpha(hi) cell activatio

121 We propose that Panx1 signaling provides a positive feedback loop for inflammatory responses involv

122 modulated by lactate itself, resulting in a positive feedback loop for lactate release.

123 Our results indicate the existence of a positive feedback loop for obtaining sufficient BDNF lev

124 Our results identify a positive feedback loop for the amplification of DNA brea

125 ide the first evidence for the presence of a positive feedback loop for the sustained activation of A

126 Collectively, our findings identified a positive feedback loop formed by FOXM1 and HGF/Met and r

127 Furthermore, we identify a positive feedback loop formed by the exosome and TUT7/4

128 A positive feedback loop from IL-1beta and back to PGE2, w

129 rogresses in large part as a result of three positive feedback loops: i) genetic and epigenetic chang

130 Our results describe a Lat1-EZH2 positive feedback loop illustrated by AA depletion or La

131 main, which is autoinhibitory and supports a positive feedback loop in cytohesins but not in BRAGs, a

132 We conclude that Scl and Kit establish a positive feedback loop in multipotent and MEPs.

133 dly through a ROS-p38 MAPK-NADPH oxidase-ROS positive feedback loop in response to a myocardial hyper

134 Here we identify a positive feedback loop in which C/EBPdelta activates Tlr

135 ting plaque inflammation and uncover a novel positive feedback loop in which cholesterol-laden spleni

136 AMP-signalling, indicating the presence of a positive feedback loop in which Cyr1 and cAMP influence

137 ctively with phosphatidic acid, we propose a positive feedback loop in which DGKalpha generates phosp

138 investigations suggested the existence of a positive feedback loop in which exDNA promotes expressio

139 y restoring EZH2 expression, thus defining a positive feedback loop in which EZH2 controls GC B cell

140 ockout mice or knockdown cells, suggesting a positive feedback loop in which once accumulated, glycog

141 We demonstrate the existence of a tight positive feedback loop in which SA-miRNAs activate and r

142 data indicate that there is an uncontrolled positive feedback loop in which the damaged cells releas

143 ew evidence on the role of microRNA-mediated positive feedback loops in conferring robustness to the

144 tions are often rapid and switch-like due to positive feedback loops in the regulatory network.

145 mselves induce EC activation, we postulate a positive-feedback loop in leukemia that exists to suppor

146 We also identified a positive-feedback loop in which ERK/EGR1 signaling promo

147 emonstrate the physiological importance of a positive-feedback loop in which Swe1p activity inhibits

148 These waves result from a positive feedback loop, in which a metabolic trigger ind

149 sults demonstrate that Itk helps orchestrate positive feedback loops integrating multiple T cell sign

150 Importantly, a positive feedback loop involving autocrine LIF, LIFR, an

151 These findings demonstrate a deleterious positive feedback loop involving elevated intracellular

152 ynamin-1 (Dyn1) and its activation through a positive feedback loop involving enhanced epidermal grow

153 2 transcript levels are maintained through a positive feedback loop involving GL2 activation of MYB23

154 HrpV and HrpG, and may be enhanced through a positive feedback loop involving HrpA, the main componen

155 ocytogenesis in Plasmodium consistent with a positive feedback loop involving PbAP2-G that could be e

156 A positive feedback loop involving RAS and SOS, which lead

157 This distinct cell cycle is driven by a positive feedback loop involving Rb inactivation and red

158 Previously, we described a positive feedback loop involving regulation of Neu5Gc ex

159 Together, these results suggest that a positive feedback loop involving sialidases potentiates

160 These data establish a positive feedback loop involving TAZ and LM511 that cont

161 This pulse growth required a key positive feedback loop involving the sporulation kinases

162 module coupled with three microRNA-mediated positive feedback loops involving miR-192, miR-34a, and

163 ative analysis, we find that inhibiting self-positive feedback loop is a more robust and effective tr

164 This positive feedback loop is critically dependent on the sm

165 ntrast, the invocation of an Abr-independent positive feedback loop is required to account for Cdc42

166 The conducive environment then triggers a positive feedback loop leading to adaptation and persist

167 induction of profibrotic genes, supporting a positive feedback loop leading to myofibroblast activati

168 ed "oncogene-addicted" cancer cells engage a positive feedback loop leading to Stat3 activation, cons

169 at the core of the dynamical behavior of the positive feedback loop linking inflammation to cell tran

170 olon, pancreas, and lung, disruption of this positive feedback loop may be an important strategy for

171 uman mammary epithelial cells in an apparent positive feedback loop mechanism and regulate breast CSC

172 ective antiviral interferons is amplified by positive-feedback loops mediated by inducible interferon

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

174 In this mutant lacking the Snf1-mediated positive feedback loop, Msn2 responds similarly to gluco

175 se inhibitor (CKI)-cyclin-dependent kinase 2 positive-feedback loop, normally generated by APC-Cdh1-m

176 her, these observations suggest a functional positive feedback loop of an intronic miRNA on transcrip

177 act in the extraembryonic YSL to initiate a positive feedback loop of Bmp signaling within the embry

178 Taken together, our findings reveal a positive feedback loop of cGAS signaling generated by TR

179 ivate CaMKII and thereby form a pathological positive feedback loop of ever-increasing CaMKII activit

180 ced expression of GhMAPK3K15, constituting a positive feedback loop of GhWRKY59-regulated MAP kinase

181 ogical control of hemodynamics, permitting a positive feedback loop of increasing blood flow and vess

182 ex intracellular reaction cascades forming a positive feedback loop of the autocrine signaling.

183 e Smad inhibitor Smad7 and participates in a positive feedback loop on NOX1 up-regulation.

184 tic stress observed in vivo and found that a positive feedback loop on protein kinase A mediated by t

185 g pulling force through stress fibers with a positive feedback loop on very stiff substrates.

186 yeast suggested the presence of two parallel positive-feedback loops, one operating as a diffusion-ba

187 ous system (CNS) may interrupt a destructive positive feedback loop present in CNS inflammation.

188 een light initiates multiple radical-forming positive-feedback loops, rapidly producing visible level

189 ppressors) or activators (oncogenes) of this positive feedback loop regulate the occurrence of the ep

190 sible for oscillations, and two antagonistic positive feedback loops (regulated by phosphatases Wip1

191 This positive feedback loop regulating BMI1 expression may be

192 that OCT4, SFRS2, and MBD2 participate in a positive feedback loop, regulating proteome diversity in

193 on ( approximately 60%) of Id1, suggesting a positive feedback-loop regulatory mechanism between Id1

194 This positive-feedback loop reinforces STAT3 activation and d

195 iating component of the CXCL13:LTalpha1beta2 positive feedback loop required for WP ontogeny, and CXC

196 activity and disrupt the nuclear AURKA/FOXM1-positive feedback loop, respectively, resulting in a mor

197 ibitor PF-04691502 does not induce an mTORC2 positive feedback loop similar to other PI3K inhibitors

198 s bimodal, which indicates the presence of a positive feedback loop somewhere in the regulatory envir

199 riven primarily by activation of I(NaP) in a positive feedback loop starting near -70 mV and providin

200 and that HIF-1alpha and iNOS are linked by a positive feedback loop that amplifies macrophage activat

201 Here, we have uncovered a distinct positive feedback loop that arises from the reciprocal s

202 We propose the existence of a positive feedback loop that connects Cdk1 and Plk1 activ

203 de release from soils represent an important positive feedback loop that could influence twenty-first

204 critical "trigger" of active MPF promotes a positive feedback loop that employs Polo kinase to boost

205 ggesting that GIV is required to establish a positive feedback loop that enhances integrin-FAK signal

206 , indicating that SOX9 is at the center of a positive feedback loop that enhances Wnt/beta-catenin si

207 s with the Shh signaling pathway to create a positive feedback loop that fuels hair follicle growth.

208 ate that the PI3-K-->Akt pathway serves as a positive feedback loop that further enhances noncanonica

209 This results in a positive feedback loop that has implications for the ret

210 ulated Mo miR-34a expression, resulting in a positive feedback loop that increased subsequent capacit

211 ad an increased RANKL/OPG ratio, providing a positive feedback loop that increased the number of oste

212 to p53 phosphorylation, which constitutes a positive feedback loop that increases p53 protein levels

213 dynactin to the oocyte posterior, creating a positive feedback loop that increases the length and per

214 ate these TGFbeta-specific effects through a positive feedback loop that integrates TGFbeta/Smad and

215 the discovery of a splice isoform-dependent positive feedback loop that is essential to sustain PI3K

216 ion factor c-Jun in Ctx(R) cells, creating a positive feedback loop that maintained EGFR activation b

217 e 2 (IRS2) at serine 388, thereby creating a positive feedback loop that maintains adipocyte insulin

218 which indicates that USP28 and c-MYC form a positive feedback loop that maintains high c-MYC protein

219 ant macroH2A1 is a critical component of the positive feedback loop that maintains SASP gene expressi

220 of CD147-CD44-EGFR complexes, thus forming a positive feedback loop that may amplify invasiveness.

221 the aggregation of Abeta42 is promoted by a positive feedback loop that originates from the interact

222 pulated by traumatic cues, contributing to a positive feedback loop that perpetuates the effects of t

223 turn, is regulated by this interaction in a positive feedback loop that promotes leukemia survival a

224 TSC-mTOR pathway is a central component of a positive feedback loop that promotes network activity by

225 s maintain DSpd-2 within the PCM, creating a positive feedback loop that promotes robust PCM expansio

226 CynA and regions of responsiveness creates a positive feedback loop that restricts CynA to the rear a

227 ukin (IL)-1beta is part of a proinflammatory positive feedback loop that sustains a persistent proinf

228 ds to the translocated enhancers, creating a positive feedback loop that sustains its expression.

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

230 Thus, EPS production is subject to a positive feedback loop that ties its synthesis to its ow

231 hosphoinositide 3-kinase-dependent manner, a positive feedback loop that we find is completely lost i

232 This mechanical catalysis makes possible a positive feedback loop that would help localize the form

233 ix minimal classes based on the structure of positive feedback loops that activate and localize Cdc42

234 distribution is regulated by auxin-dependent positive feedback loops that are not well-understood at

235 These principles include positive feedback loops that are required to destabilize

236 We further identified two positive feedback loops that integrate epigenetic regula

237 nscription of regulatory elements produces a positive-feedback loop that contributes to the stability

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

239 BTK-mediated signaling in B cells involves a positive-feedback loop that establishes T cell-propagate

240 These results demonstrate a novel positive-feedback loop that links the myofibroblast phen

241 locus for rapid activation and establishes a positive-feedback loop that maintains elevated GATA3 exp

242 n turn increased Wnt signaling, generating a positive-feedback loop that may function during the prol

243 us, Tril is a novel component of a Bmp-Gata2 positive-feedback loop that plays an essential role in h

244 he exocyst tethering complex, thus forming a positive-feedback loop that prepares the secretory vesic

245 etween PP2A(Cdc55) and APC/C(Cdc20) (i.e., a positive feedback loop) that controls APC/C(Cdc20) activ

246 Thus, MKK7 alternative splicing represents a positive feedback loop through which JNK promotes its ow

247 of Mos mRNA translation, thus establishing a positive feedback loop to amplify Musashi function.

248 aling pathways formed an autocrine/paracrine-positive feedback loop to drive the progression of the F

249 e possibility that TSLP may be involved in a positive feedback loop to enhance allergic inflammatory

250 A and FOXM1 participate in a tightly coupled positive feedback loop to enhance BCSC phenotype.

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

252 d VIC deposition of GAGs, thereby creating a positive feedback loop to further enrich GAG content and

253 rates to increase ABA synthesis as part of a positive feedback loop to modulate seedling establishmen

254 ial dysfunction during obesity could evoke a positive feedback loop to perpetuate poor ingestive beha

255 tch from GATA-2 to GATA-1, thus completing a positive feedback loop to promote erythroid maturation.

256 TSP-1 functioned in a positive feedback loop to stabilize p53 by interacting d

257 intestinal epithelial cells, establishing a positive feedback loop to support tumor development.

258 ydrogen peroxide-stimulated Mst1 activates a positive feedback loop to sustain an oxidizing cellular

259 them, implying the presence of some form of positive feedback loop to sustain the response.

260 all circuit of transcription factors forming positive feedback loops to stabilise otic progenitor ide

261 hat BACH1 acts in a double-negative (overall positive) feedback loop to inhibit RKIP transcription in

262 emerged: the first is the requirement for a positive-feedback loop to drive self-recruitment of dete

263 onse to tissue damage may therefore act in a positive-feedback loop to drive the pathophysiology of s

264 Crossveinless 2 functions at this time in a positive-feedback loop to locally enhance BMP activity,

265 Our study reveals the use of interlinked positive-feedback loops to control autoregulation dynami

266 ell, Schuijers et al. (2015) report an Ascl2 positive feedback loop, tuned by previous Wnt pathway ac

267 delling suggests that the NICD/HES5/FBW7beta positive feedback loop underlies Fbw7 haploinsufficiency

268 essed but their efficacy is limited due to a positive feedback loop via mTOR complex 2 (mTORC2), resu

269 complex picture involving both negative and positive feedback loops was observed on IFNgamma treatme

270 A positive-feedback loop was discovered between miR-200c a

271 ng an in vitro model of the HIV Tat-mediated positive-feedback loop, we previously demonstrated that

272 ed beta1-integrin mechanosignaling engaged a positive feedback loop whereby STAT3 signaling promotes

273 previous studies in budding yeast suggested positive feedback loops whereby Cdc42 becomes polarized,

274 These data highlight a novel positive-feedback loop whereby Notch1-dependent furin ex

275 e data provide a mechanistic framework for a positive feedback loop, whereby sleep loss and neuronal

276 s to ANG2 antagonism of Tie2 and initiates a positive feedback loop wherein FOXO1-driven ANG2 express

277 t posits that symmetry breaking occurs via a positive feedback loop, wherein the adaptor protein Bem1

278 ounteract Hippo pathway activity, creating a positive feedback loop, which depends on stabilization o

279 ontributes to carcinogenesis by amplifying a positive feedback loop, which increases both extracellul

280 s interlocked network motifs consisting of a positive feedback loop, which is used to restore the int

281 propose that MET signaling via BRAF fuels a positive feedback loop, which maintains high levels of P

282 scherichia coli lac operon is regulated by a positive feedback loop whose potential to generate an al

283 e polarization of BASL is made possible by a positive feedback loop with a canonical mitogen-activate

284 SA acts in a positive feedback loop with ACCELERATED CELL DEATH6 (ACD

285 of the IRE1alpha signalosome, which forms a positive feedback loop with ASK1 through Txnip.

286 T3-ITD AML stem cells, potentially through a positive feedback loop with c-MYC, highlighting SIRT1 as

287 Prkci is a HH target gene that forms a positive feedback loop with GLI and exists at increased

288 r substrate, the nurse cells, functions in a positive feedback loop with Rac and actin assembly to st

289 cuit models differing in the location of the positive feedback loop with respect to the gene can all

290 lorectal cancer (CRC) metastasis and forms a positive feedback loop with TGF-beta signalling.

291 rotein with an ankyrin domain that acts in a positive feedback loop with the defense signal salicylic

292 iments revealed that Notch signaling forms a positive feedback loop with the Hippo signaling effector

293 ch activity is asymmetrically amplified by a positive feedback loop with the super elongation complex

294 attract CLL-specific Th cells and initiate a positive feedback loop with upregulation of T-bet, CD38,

295 Mechanistically, Ret is engaged in a positive feedback loop with Wnt/Wingless signalling, mod

296 dicating that innate lymphocytes engage in a positive-feedback loop with monocytes that promotes clea

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

298 The activity of TRAP150 defines a positive feedback loop within the clock and provides a p

299 IF promotion of GA accumulation represents a positive feedback loop within the molecular framework dr

300 a2) is required for the LTalpha1beta2:CXCL13 positive feedback loop without which SLO cannot properly