ライフサイエンスコーパス: positive-feedback loop

1 ed hypoxia inside the tumor mass, creating a positive feedback loop.

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

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

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

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

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

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

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

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

10 , further accelerating mass recruitment in a positive feedback loop.

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

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

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

14 expression and odontoblast homeostasis via a positive feedback loop.

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

16 ells upregulates IL-12 secretion by DCs in a positive feedback loop.

17 hore distance-dependent manner, indicating a positive feedback loop.

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

19 itochondrial dysfunction and IL-6 exist in a positive feedback loop.

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

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

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

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

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

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

26 levels in neurons, forming a transcriptional positive feedback loop.

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

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

29 cytokine expression in macrophages through a positive feedback loop.

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

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

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

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

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

35 induced IL-10 production in ILC2s through a positive feedback loop.

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

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

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

39 y promote the recruitment of each other in a positive feedback loop.

40 da induces its own gene expression through a positive feedback loop.

41 e activity and promoting ATM activation in a positive feedback loop.

42 rotein amplifies amphiregulin signaling in a positive feedback loop.

43 ation post-transcriptionally, establishing a positive feedback loop.

44 undreds of genes in oncogenic pathways via a positive feedback loop.

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

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

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

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

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

50 urther recruit T cells to the skin through a positive-feedback loop.

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

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

53 posure contributes to induction of IRF5 in a positive-feedback loop.

54 ases in astrocytic Ca(2+) and resulting in a positive-feedback loop.

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

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

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

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

59 ave multiple positive direct regulations and positive feedback loops.

60 filter undesired model behaviors induced by positive feedback loops.

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

62 HPA axis participate in multiple reinforcing positive feedback loops.

63 y involve genetic nonlinear interactions and positive feedback loops.

64 emergent phenomenon propelled by unexplored positive feedback loops.

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

66 te of tissue damage and thereby results in a positive feedback loop, amplifying GBM necrosis developm

67 regulatory network composed of a fast-acting positive feedback loop and a delayed negative feedback l

68 dynamically enhancing plaque targeting via a positive feedback loop and dual action of cholesterol de

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

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

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

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

73 hanced FKBP5 response to NF-kappaB through a positive feedback loop and was present in individuals wi

74 predictions for the switching properties of positive feedback loops and that these differences decre

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

76 gh SigM activity results from a dysregulated positive feedback loop, and can be suppressed by overexp

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

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

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

80 A physiological consequence of this positive feedback loop appears to be decreased GBM cell

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

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

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

84 There is also an important positive feedback loop as T(b) influences BMR(1-3).

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

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

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

88 A positive feedback loop between cytoskeletal signaling an

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

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

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

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

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

94 Overall these results suggest a positive feedback loop between lamellar disruption and c

95 macological inhibition of Bcl6, suggesting a positive feedback loop between MLL and BCL6.

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

97 suggests that early-life stress initiates a positive feedback loop between peripheral inflammatory c

98 A positive feedback loop between RTN1A and CHOP was found

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

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

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

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

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

104 2 is itself an AR-regulated gene, creating a positive feedback loop between the two factors.

105 ion is induced by beta-catenin, triggering a positive feedback loop between the two proteins.

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

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

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

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

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

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

112 We identified a positive-feedback loop between PPARD and interferon gamm

113 ters appear to facilitate this crosstalk and positive-feedback loops between multiple types of immune

114 hese direct effects and by the disruption of positive-feedback loops between tumour cells and the bon

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

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

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

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

119 cal-chemical integration occurring through a positive feedback loop centred on FGF20, which induces c

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

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

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

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

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

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

126 ISPR-based methods, suggesting an amplifying positive feedback loop due to increasing gRNA dosage.

127 icroglia activation in a microglia-astrocyte positive feedback loop during brain inflammation.

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

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

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

131 which then becomes self-sustained through a positive feedback loop established among the tumor-secre

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

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

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

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

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

137 wer channel activity, thereby establishing a positive feedback loop for PI(4,5)P(2) microdomain compa

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

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

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

141 Here, we present a novel mechanism of a positive feedback loop, formed by a reciprocally activat

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

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

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

145 Depletion of Zeb1 disrupts this positive feedback loop in the tumor perivascular niche,

146 teins, and our results are consistent with a positive feedback loop in which amino acids bound to sel

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

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

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

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

151 We also identified a positive feedback loop in which TGF-beta signaling promo

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

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

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

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

156 reveal C/EBPdelta as a link that engages two positive feedback loops, in part by directly targeting t

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

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

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

160 2 transcript levels are maintained through a positive feedback loop involving GL2 activation of MYB23

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

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

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

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

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

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

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

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

169 This positive feedback loop is thought to be important for th

170 lecules and suggest that the function of the positive feedback loop is to stabilize the oscillations

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

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

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

174 Here, we uncovered an NFIB-calpain 1-positive feedback loop mediated through CAST and calcine

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

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

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

178 MAD1-dependent pool of CDK1-CCNB1 creates a positive feedback loop necessary for timely recruitment

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

180 lux from the deep ocean to the atmosphere, a positive feedback loop not included in most future proje

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

182 adjacent cells, which is likely to create a positive feedback loop of cellular senescence within the

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

184 ropose a testable hypothesis that, a vicious positive feedback loop of des-Arg(9)-bradykinin- and bra

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

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

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

188 A TaVrt2-mediated positive feedback loop of TaVrn1 during vernalization wa

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

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

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

192 The resulting positive feedback loops rapidly lock larvae into evolvin

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

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

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

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

197 This positive-feedback loop reinforces STAT3 activation and d

198 Akt signaling and activate Dyn1 to create a positive feedback loop required for rapid recycling of E

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

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

201 3beta (GSK3beta) signaling pathway through a positive-feedback loop, resulting in N-Myc stabilization

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

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

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

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

206 HOCl, constitutes a potentially detrimental positive feedback loop that can only be attenuated throu

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

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

209 eractions between Spd-2, Polo and Cnn form a positive feedback loop that drives the dramatic expansio

210 id (ATRA) induces VCP expression, creating a positive feedback loop that enhances degradation.

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

212 Their combination constitutes a positive feedback loop that exponentially amplifies thei

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

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

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

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

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

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

219 elop therapeutic strategies that disrupt the positive feedback loop that leads to persistent airway c

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

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

222 ept of stable motif, i.e., a self-sustaining positive feedback loop that maintains an associated stat

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

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

225 ental HIF-1alpha expression, which creates a positive feedback loop that promotes FLT-1 expression le

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

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

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

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

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

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

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

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

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

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

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

237 ting that SARS-CoV-2 infections could create positive feedback loops that increase ACE2 levels and fa

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

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

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

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

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

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

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

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

246 urface-dependent lasR induction initiating a positive feedback loop through the small RNA, Lrs1.

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

248 ctional tight junctions, which establishes a positive feedback loop to accommodate lumen growth.

249 hydrocholesterol (7-DHC) accumulation form a positive feedback loop to amplify innate immune response

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

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

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

253 he lytic switch protein, thereby providing a positive feedback loop to ensure successful completion o

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

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

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

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

258 d hyperactivity, demonstrating an unexpected positive feedback loop to persistently promote pain.

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

260 actin assembly to PI3K activation to form a positive feedback loop to support lateral membrane exten

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

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

263 ream targets including MYC and JUN, drives a positive feedback loop to up-regulate multiple other RTK

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

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

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

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

268 Chemotherapeutic drugs triggered a positive feedback loop via ATM/E2F1/STAT signaling, ampl

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

270 6 targeting in the plaques by establishing a positive feedback loop via the reciprocal regulation of

271 suggest that AN may arise from pathological positive feedback loops: voluntary food restriction acti

272 In 4T1BR5 cells, there was a positive feedback loop whereby astrocytic BDNF induced c

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

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 or complement initiation occurring through a positive-feedback loop wherein surface-deposited C3b par

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 Aurora B and Bub1 form a distance-dependent positive feedback loop, which spatiotemporally may act a

283 t that beta-catenin and Tspan8 are part of a positive feedback loop, which sustains a high Tspan8 exp

284 These interactions form an engine-like positive feedback loop, which sustains a shared elongati

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

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

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

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

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

292 e IL-6 in the aorta, which participates in a positive feedback loop with the impaired vascular mitoch

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

294 ive of specific movements is maintained by a positive feedback loop with the thalamus.

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

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

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

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

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