ライフサイエンスコーパス: feedback inhibition

1 (+) inhibits Na(+) transport via ENaC (Na(+) feedback inhibition).

2 ([Na(+)]i) through a process known as Na(+) feedback inhibition.

3 k circuits, neither receiving nor generating feedback inhibition.

4 he enzyme level by allosteric regulation and feedback inhibition.

5 ependent recruitment of OLM interneurons for feedback inhibition.

6 ortical inputs, implying a prevalent role in feedback inhibition.

7 inhibiting channel opening to provide vital feedback inhibition.

8 at these early ages despite the presence of feedback inhibition.

9 imulus, and that does not rely on long-range feedback inhibition.

10 drenal glands by restoring adrenal alpha2-AR feedback inhibition.

11 rd input is sufficient to implement divisive feedback inhibition.

12 rrelation have been proposed, among which is feedback inhibition.

13 mbination within the time required to signal feedback inhibition.

14 1-positive tuft cells, suggesting a model of feedback inhibition.

15 synapses, arguing for the importance of the feedback inhibition.

16 nhibition, which differs from feedforward or feedback inhibition.

17 feedback loop with a built-in time delay in feedback inhibition.

18 with respect to their sensitivity to serine feedback inhibition.

19 e (KD of 22-43 muM), which indicates product feedback inhibition.

20 iated inflammation by enhancing the negative feedback inhibition.

21 s (FSNs), which then synchronize the PCs via feedback inhibition.

22 tion is required for starvation-induced PI3K feedback inhibition.

23 lation and eNOS/Cav-1 binding, that is, eNOS feedback inhibition.

24 d, IKK-mediated p85 phosphorylation and PI3K feedback inhibition.

25 boxylase (ACCase) as the enzymatic target of feedback inhibition.

26 s are hyperactivated to trigger the negative feedback inhibition.

27 proposal that beta-endorphin acts to provide feedback inhibition.

28 rk mechanisms of gamma oscillations based on feedback inhibition.

29 on gene regulation, enzymatic activity, and feedback inhibition.

30 endently from receptors mediating reciprocal feedback inhibition.

31 is not caused by the secondary engagement of feedback inhibition.

32 he transcriptional and biochemical levels by feedback inhibition.

33 ium and glutamate, is regulated by glutamine feedback inhibition.

34 nin secretion by interrupting angiotensin II feedback inhibition.

35 e mTORC1, effectively bypassing S6K-mediated feedback inhibition.

36 reduced Xbp1 splicing, suggesting a positive feedback inhibition.

37 ion from pyramidal cells, produce late-onset feedback inhibition.

38 I and L174F enzymes were highly resistant to feedback inhibition.

39 p in which PERIOD (PER) is rate-limiting for feedback inhibition.

40 system combining feed-forward excitation and feedback inhibition.

41 , which in turn suppressed photosynthesis by feedback inhibition.

42 astogenesis via endogenous IFN-beta-mediated feedback inhibition.

43 neurons monitor local excitation, providing feedback inhibition.

44 ng the levels of folding factors removed the feedback inhibition.

45 nt sensitizes nociceptor presynapses to this feedback inhibition.

46 hich is consistent with a loss of retrograde feedback inhibition.

47 compromised CCK-INT-mediated feedforward and feedback inhibition.

48 vel KAT that may be susceptible to metabolic feedback inhibition.

49 primarily to differences in the strength of feedback inhibition.

50 n, passing repeatedly through zones of local feedback inhibition.

51 of a two-tiered microbial 'food chain' with feedback inhibition, after applying an appropriate dimen

52 aeruginosa infections, our data suggest that feedback inhibition allows P. aeruginosa to direct its e

53 nism: endogenously driven gain modulation of feedback inhibition among competing channels.

54 We demonstrate that feedback inhibition among SPNs is strong enough to contr

55 ensitivity of the MtDHDPS2 protein to lysine feedback inhibition and a severely reduced activity of t

56 Furthermore, the sites responsible for feedback inhibition and allosteric activation control fi

57 BAergic interneurons mediate feedforward and feedback inhibition and have a key role in gamma oscilla

58 group also defined roles for leptin receptor feedback inhibition and hypothalamic mTor signaling in m

59 Relaxed feedback inhibition and increased expression of the muta

60 The mechanism of feedback inhibition and its role in pathogenesis are unc

61 positions previously shown to be involved in feedback inhibition and of residues important for cataly

62 e is in-frame, Trbv5 evades TCRbeta-signaled feedback inhibition and recombines by inversion to the D

63 -2 tg mice, both the glucocorticoid negative feedback inhibition and spatial learning and memory were

64 scribe general rules for feed-forward versus feedback inhibition and suggest GGN is potentially capab

65 rtical circuits by providing feedforward and feedback inhibition and synchronizing neuronal activity.

66 a permissible environment for MAPK negative feedback inhibition and thus regulated mammary branching

67 )H for lysine biosynthesis, releasing lysine feedback inhibition, and boosting oxaloacetate supply.

68 g data about the regulation of excitability, feedback inhibition, and network oscillations in area CA

69 ufficiently strong recurrent excitation; (3) feedback inhibition; and (4) simple spatial properties o

70 L-IPSCs, confirming that these two types of feedback inhibition are mediated by distinct and converg

71 e underlying mechanisms of which, especially feedback inhibition, are underexplored.

72 Feedback inhibition arises from a hydrogen bond network

73 he l-lysine epsilon-ammonium group, abrogate feedback inhibition, as do substitutions of residues wit

74 o exogenous CRH stimulation, inferring rapid feedback inhibition at the anterior pituitary.

75 from the synaptic cleft nor by metabotropic feedback inhibition, because it is resistant to blockade

76 rolling a brain size set-point that involves feedback inhibition between wnt11-6/wntA/wnt4a and notum

77 s revealed that, as a consequence of altered feedback inhibition, burst activity arising in CA3 is mo

78 ese findings, an R62A mutation abrogates Gln feedback inhibition but does not affect catalysis.

79 Exogenous expression of BRAF V600E disrupts feedback inhibition but does not sensitize cells to AZD6

80 ior and the impaired glucocorticoid negative feedback inhibition, but not the memory deficit, implyin

81 al aqueous cavity and exhibiting synergistic feedback inhibition by AMP and Fru-6-P.

82 Mathematical modeling indicates that feedback inhibition by BMP ligands acts on the ventral s

83 rns of activity within layer 4 to potentiate feedback inhibition by boosting the strength of FS <-->

84 to provide a pathway for activation and for feedback inhibition by branched-chain amino acids.

85 d releases SAT from substrate inhibition and feedback inhibition by cysteine, the final product of th

86 e important for both enzyme activity and the feedback inhibition by DHNA.

87 Apparent negative-feedback inhibition by ferrous ions is documented at nan

88 A feature of SAT is its feedback inhibition by L-cysteine.

89 shown that MtIPMS is subject to slow-onset, feedback inhibition by l-leucine, the first instance of

90 the dark period, reducing its sensitivity to feedback inhibition by malate and thus enhancing nocturn

91 hat this complex relieves NadE(Gln) negative feedback inhibition by NAD(+) This mechanism is conserve

92 of the pyrophosphate by-product, and blunts feedback inhibition by NAD(+).

93 Such mutations render PSS1 insensitive to feedback inhibition by PS levels.

94 Feedback inhibition by Sox2 on Wnt signaling and by the

95 -23R might not be a major target of negative feedback inhibition by suppressor of cytokine signaling

96 Targeting this feedback inhibition can improve insulin sensitivity.

97 At the network level, modulation of feedback inhibition can result in reduction of variabili

98 Wnt signaling, suggesting that regulation of feedback inhibition controls the binary head-tail regene

99 ound that the balance between excitation and feedback inhibition depended on stimulus frequency; at s

100 Feedback inhibition does not involve translocator insert

101 levates Vbeta rearrangement frequency before feedback inhibition, dramatically increasing the frequen

102 red, resulting in a profound loss of initial feedback inhibition during synchronous CA1 pyramidal act

103 Thus, despite general roles in feedback inhibition, DUSP1 plays a transient, often part

104 s dual regulatory strategies, with classical feedback inhibition enhancing metabolic efficiency and d

105 of IMPDH2 makes the enzyme less sensitive to feedback inhibition, explaining why assembly occurs unde

106 and inhibits BMP-9 thereby providing strong feedback inhibition for BMP-9/ALK1 signaling rather than

107 ons require different strength and timing of feedback inhibition for optimal processing.

108 ogens (typically Geobacter species) relieves feedback inhibition for the fermentative consortia, allo

109 ose principal neurons, Kenyon cells, receive feedback inhibition from a non-spiking interneuron calle

110 GABAergic feedback inhibition from amacrine cells shapes visual si

111 activity in single granule cells can recruit feedback inhibition from Golgi cells.

112 rom pyramidal cells could drive synchronized feedback inhibition from interneurons.

113 expression suppresses S6K1 but, by relieving feedback inhibition from mTORC1 to PI3K signaling, activ

114 ween -65 and -50 mV is sufficient to produce feedback inhibition from periglomerular neurons.

115 This suggests that feedback inhibition from surviving neurons may skew neur

116 tation from olfactory projection neurons and feedback inhibition from the anterior paired lateral neu

117 instead, it appears that another mechanism, feedback inhibition from the giant GABAergic neuron, ser

118 This negative feedback inhibition functions to restrain PI3K activity

119 Feedforward and feedback inhibition generated by these circuits is likel

120 This feedback inhibition has prevented scientists from engine

121 or the nature of competition (feedforward or feedback inhibition) has been revealed by experiments.

122 g striatal projection neurons (SPNs) called "feedback inhibition," have been proposed to endow the st

123 nent quantitative changes in the dynamics of feedback inhibition in a rat model of chronic epilepsy (

124 adaptive neural network that receives global feedback inhibition in addition to local recurrent proje

125 sible manner, demonstrating the existence of feedback inhibition in an oil-accumulating tissue.

126 beta) accessibility but was still subject to feedback inhibition in DP thymocytes.

127 eta) and DJ(beta) gene segments both enforce feedback inhibition in DP thymocytes.

128 ent of end product accumulation and possible feedback inhibition in isoprene-emitting hybrid aspen (P

129 common and underlies the origins of negative feedback inhibition in many metabolic and signaling path

130 ntry of the proteins into NTCs and abrogated feedback inhibition in Notch signaling assays in culture

131 Our results clarify the source of feedback inhibition in the E. coli PhoQ-PhoP system and

132 that provide either feedforward or recurrent/feedback inhibition in the lobe.

133 al role in providing dynamic feedforward and feedback inhibition in the retina.

134 However, the impact of feedback inhibition in the striatal network has remained

135 The lack of feedback inhibition in these cells requires phagocytic u

136 analysis shows that regulation of the local feedback inhibition increases both the entropy and the F

137 Surprisingly, feedback inhibition is abrogated in phagocytic cells.

138 The Wnt5a-induced feedback inhibition is active both during in vitro LPS s

139 Instead, feedback inhibition is due, in part, to a loss of the ac

140 ated Na+ channels, and the spatial extent of feedback inhibition is expanded by gap junction connecti

141 A mechanism for feedback inhibition is proposed in which reduced demand

142 the role of the Glu304 residue in glutamine feedback inhibition is proposed.

143 Feedback inhibition is recruited steeply with a low dyna

144 CCAP) continually present, the impact of the feedback inhibition is reduced, prolonging protraction a

145 Allosteric feedback inhibition is the mechanism by which metabolic

146 iments reveal that GABAergic feedforward and feedback inhibition is unaffected by carbamazepine and a

147 cation limits NHX-7 proton transport through feedback inhibition, likely to prevent metabolic acidosi

148 Moreover, pApA is involved in a feedback inhibition loop that limits GdpP-dependent c-di

149 g enough to destabilize visual responses but feedback inhibition maintains stability.

150 endosymbiotic systems suggest that substrate feedback inhibition may be mechanistically important in

151 lls may act as an inbuilt activation-induced feedback inhibition mechanism against excessive or chron

152 disulfide-isomerase can be inactivated by a feedback inhibition mechanism involving unfolded protein

153 These findings suggest that a SUMO-driven feedback inhibition mechanism is an intrinsic feature of

154 regulated by a TPP-binding riboswitch via a feedback inhibition mechanism.

155 ed astrocyte proliferation via a phospho-ERK feedback inhibition mechanism.

156 tory fiber activity promotes feedforward and feedback inhibition mediated by PV(+) interneuron activi

157 by the time course of I(MI-MCN1) buildup and feedback inhibition-mediated decay, respectively, in LG.

158 ata and localization, we propose a substrate feedback inhibition model in which the accumulation of t

159 Feedback inhibition of 1-deoxy-D-xylulose-5-phosphate sy

160 acteria that possess a stringent biochemical feedback inhibition of ACC and malonyl-CoA formation tri

161 on evoked dopamine release, suggesting that feedback inhibition of acetylcholine release was not inv

162 r guanine nucleotide pools by regulating the feedback inhibition of adenosine derivatives on de novo

163 Feedback inhibition of adenylyl cyclase III (ACIII) via

164 ggesting one mechanism through which loss of feedback inhibition of Akt may occur in mTORC1 hyperacti

165 ts that mTORC1 activation is associated with feedback inhibition of Akt, a substrate of mTORC2.

166 sosomal biogenesis by mTORC1 was mediated by feedback inhibition of AKT, and a resulting suppression

167 essing of 6-TG probably through its negative feedback inhibition of Akt.

168 SHP, within a single physiological pathway, feedback inhibition of bile acid biosynthesis, by differ

169 Genetic variation in negative feedback inhibition of bile acid synthesis may affect CD

170 ted transnitrosylation cascade that provides feedback inhibition of bile salt synthesis.

171 Our data reveal feedback inhibition of cellulose synthase by UDP but not

172 ed intestinal factors that mediate bile acid feedback inhibition of cholesterol 7alpha-hydroxylase ge

173 closely related proteins, are essential for feedback inhibition of cholesterol biosynthesis.

174 separation of the loops and facilitating the feedback inhibition of cholesterol synthesis.

175 Numerous studies suggest that feedback inhibition of CLOCK-BMAL1 is mediated by time-d

176 he proinflammatory response through negative-feedback inhibition of cytokine receptors.

177 , prolongs DA transients and facilitates the feedback inhibition of DA and glutamate release from the

178 lective loss of D2 autoreceptors impairs the feedback inhibition of DA release and amplifies the effe

179 erapy-resistance mechanism involving reduced feedback inhibition of de novo purine biosynthesis and c

180 ese data suggest that DUSP5 functions in the feedback inhibition of ERK1/2 signaling in response to T

181 nhibitor (TFPI) produces factor Xa-dependent feedback inhibition of factor VIIa/tissue factor-induced

182 anism presents an opportunity for mitigating feedback inhibition of fatty acid synthesis in crop plan

183 s is in agreement with the stronger in vitro feedback inhibition of free SAT by cysteine compared wit

184 rk on multiple pulse depression, reveal that feedback inhibition of GABAergic afferents to hilar moss

185 respiration in naked mole-rat tissues avoids feedback inhibition of glycolysis via phosphofructokinas

186 The resultant loss of feedback inhibition of GNE-epimerase activity by CMP-sia

187 Activating BRAF mutants cause feedback inhibition of GTP-bound RAS, are RAS-independen

188 ed in plasma and liver, leading to secondary feedback inhibition of hepatic SREBP2 activity.

189 function of cellular membranes and requires feedback inhibition of HMGR, a rate-limiting enzyme of t

190 Irgm1(-/-) animals, suggesting that negative feedback inhibition of IFN signaling by Irgm1 is necessa

191 ibits Akt/mTOR signaling because it relieves feedback inhibition of IGF1R and other receptors and thu

192 Taken together, our findings suggest a feedback inhibition of IL-15-mediated NK cell activity b

193 ose that mitotic regulators and SHP2 promote feedback inhibition of IR, thereby limiting the duration

194 s consistent with a role for Tyr(317) in the feedback inhibition of Jak2 kinase activity after recept

195 Loss of EPHA2 releases feedback inhibition of KRAS, resulting in activation of

196 )-induced Ca(2+) release and activates STIM1 feedback inhibition of L-type Ca(2+) channels.

197 We identified a powerful type of feedback inhibition of layer II neurons, mostly generate

198 a, may generate regulatory lipids that cause feedback inhibition of LXRalpha in macrophages.

199 d RNA silencing revealed a transient role in feedback inhibition of MAPKs and inflammatory gene expre

200 h waxes and wanes periodically due to phasic feedback inhibition of MCN1 transmitter release.

201 t the loss of electron transport is inducing feedback inhibition of metabolic capabilities that suppr

202 or example, by amyloid beta peptides, causes feedback inhibition of MPP, leading ultimately to accumu

203 altered by Arath;WEE1 expression, suggesting feedback inhibition of native WEE1 transcription.

204 ing their clearance in the bone marrow, with feedback inhibition of neutrophil production via the IL-

205 data in this study also indicated a negative feedback inhibition of nicotine biosynthesis.

206 trations of H2S in a reaction that may allow feedback inhibition of NO production under conditions of

207 ng chemosensitivity due to microRNA-mediated feedback inhibition of p73.

208 hanisms regulating sorting of PDGFRalpha and feedback inhibition of PDGFRalpha signaling at the ciliu

209 nsulin/IGF-1 signaling pathway may result in feedback inhibition of PI3K through IRS1 and reduce APP

210 that myr-Akt overexpression may be inducing feedback inhibition of PI3K, resulting in impaired APP t

211 We also define A2bR/A2aR-mediated autacoid feedback inhibition of proinflammatory/profibrotic cytok

212 The feedback inhibition of PtDXS by IDP and DMADP constitute

213 ng (VIP) interneurons in the cortex regulate feedback inhibition of pyramidal neurons through suppres

214 Physiologic feedback inhibition of RAF/MEK signaling down-regulates

215 Activated BRAF mutants evade feedback inhibition of RAS by either of two mechanisms.

216 bited ERK phosphorylation, but also relieved feedback inhibition of RAS, resulting in induction of pM

217 nation and internalization of PDGFRalpha for feedback inhibition of receptor signaling.

218 hrough monoallelic initiation and subsequent feedback inhibition of recombinational accessibility.

219 within the dorsal raphe nucleus (DR) induces feedback inhibition of serotonin neuron activity and con

220 promoting Ngn1 expression, and that negative feedback inhibition of Sox2 by Ngn1 is an essential step

221 y related proteins that are required for the feedback inhibition of SREBP and HMG-CoA reductase (HMGR

222 chanism in which enterocyte apoptosis breaks feedback inhibition of stem cell division.

223 TRN that promotes the TRN-mediated cortical feedback inhibition of thalamic neurons.

224 Furthermore, the feedback inhibition of the BCR signalosome and most of i

225 Recently, a feedback inhibition of the chloroplastic 1-deoxy-D-xylul

226 m the cytoplasm of donor cells, which delays feedback inhibition of the corresponding amino acid bios

227 ian ORMDL proteins (ORMDL1, 2 and 3) mediate feedback inhibition of the de novo synthesis pathway of

228 osynthesis in plants is tightly regulated by feedback inhibition of the end product on the first enzy

229 Feedback inhibition of the first committed step of a pat

230 levels in failing hearts, with corresponding feedback inhibition of the heme synthetic enzymes and no

231 -Idol pathway is an important contributor to feedback inhibition of the LDLR by sterols and a biologi

232 phosphorylation stabilized Grb10, leading to feedback inhibition of the phosphatidylinositol 3-kinase

233 ) excitation of the pFRG and postinspiratory feedback inhibition of the preBotC, can provide a phase-

234 imulated with IGF-1 and TNFalpha via reduced feedback inhibition of the STAT3 and mTOR pathways.

235 that this increase was due to the relief of feedback inhibition of translation as a consequence of m

236 This relieves feedback inhibition of upstream EGFR family kinases, res

237 of a functional TCR beta-chain gene triggers feedback inhibition of V(beta)-to-DJ(beta) recombination

238 Feedback inhibition of V(D)J recombination enforces Ag r

239 onal AgR gene on one allele, with subsequent feedback inhibition of V(D)J recombination on the other

240 r chains expressed from one allele to signal feedback inhibition of V-to-(D)J recombination on the ot

241 Our findings suggest that TCRbeta-mediated feedback inhibition of Vbeta14 rearrangements depends on

242 eveal an essential role for ligand-dependent feedback inhibition of vertebrate HH signaling governed

243 on of SBF and MBF transcription factors, and feedback inhibition of Whi5 by G1-S cyclins.

244 not due to differential mTORC1 activation or feedback inhibition on Akt.

245 y due to its ability to block IL-10-mediated feedback inhibition on cytokine transcription in macroph

246 rowing sink organs and reducing Suc-mediated feedback inhibition on photosynthesis.

247 R-3085-3p, but in this instance, it exerts a feedback inhibition on signaling with SMAD3 and SMAD4 sh

248 nucleic acid-induced signaling that provides feedback inhibition on specific TLR9-dependent responses

249 tigated the effect of locally regulating the feedback inhibition on the global dynamics of a large-sc

250 in the outer membrane and the corresponding feedback inhibition on the T3SS.

251 Because of the competition mediated by feedback inhibition, only the most excited DG cells fire

252 ing mice suggested that both feedforward and feedback inhibition onto granules cells were diminished

253 C-triggered gastric mill rhythm is shaped by feedback inhibition onto projection neurons from a CPG n

254 y postnatal days as was both feedforward and feedback inhibition onto pyramidal neurons underscoring

255 -1 signaling pathway is tightly regulated by feedback inhibition pathways, we hypothesized that myr-A

256 default-mode network, whereas regulation of feedback inhibition prevents this.

257 This suggests that altered dynamics of feedback inhibition promote the transmission of epilepti

258 on activation is crucial to synchronize, via feedback inhibition, pyramidal cells in the gamma freque

259 Feedback inhibition regulates the strength and speed of

260 c inhibition, whereas PLC-mediated GABAergic feedback inhibition remains responsive to leptin.

261 This feedback inhibition renders the concentration of dNTPs a

262 n is dynamically balanced by feedforward and feedback inhibition, resulting in suppression of dendrit

263 eCBs are retrograde messengers that provide feedback inhibition, resulting in the suppression of neu

264 y, complete loss of PTCH2-, HHIP1- and PTCH1-feedback inhibition results in ectopic specification of

265 Dynamic clamp simulation of feedback inhibition revealed differential effects of thi

266 important for transcriptional initiation and feedback inhibition serving as signaling platform for ch

267 However, to be effective, feedback inhibition should arise from synchronized pools

268 Additionally, net feedback inhibition shows frequency-dependent facilitati

269 tion of two functional rearrangements before feedback inhibition silences one allele.

270 ." Strong balanced amplification arises when feedback inhibition stabilizes strong recurrent excitati

271 In network models deduced from our data, feedback inhibition supports coexistence of theta-nested

272 These results suggest that feedback inhibition suppresses Kenyon cell activity to m

273 tions in odor concentration by adjusting the feedback inhibition that KCs receive from an inhibitory

274 osynthesis and is a key control point in the feedback inhibition that regulates this pathway.

275 tory interneurons that mediate strong, local feedback inhibition that scales with excitation.

276 wnt11-6/wntA/wnt4a undergoes feedback inhibition through canonical Wnt signaling but

277 of the cerebellum, providing feedforward and feedback inhibition through mossy fiber and parallel fib

278 erior outgrowth, whereas DSH-1 also provides feedback inhibition to attenuate the signaling to allow

279 ethods to show that locally constraining the feedback inhibition to compensate for the excess of long

280 xpressing ectopic PEPC forms with diminished feedback inhibition to examine the role of PEPC in carbo

281 s (MFs) and grcs and provide feedforward and feedback inhibition to grcs.

282 that both feedforward and to a lesser extent feedback inhibition to MSNs in HD can potentially be sou

283 interneurons (PIIs), which provide powerful feedback inhibition to neuronal networks.

284 single A17 amacrine cells provide reciprocal feedback inhibition to presynaptic bipolar cells via hun

285 2+) influx upon repolarization and increases feedback inhibition to produce subthreshold modulation o

286 transcriptional repression of PDE4D9 acts as feedback inhibition to regulate dopaminergic signaling.

287 ar cells and A17 amacrines provide GABAergic feedback inhibition to rod bipolar cells.

288 receives input from relay cells and supplies feedback inhibition to them in return.

289 Collectively, our data suggest that feedback inhibition to VTA DA neurons, mediated by GIRK

290 atin accessibility and locus conformation to feedback inhibition using two novel TCR alleles.

291 recombinational accessibility is subject to feedback inhibition, we analyzed TCRbeta rearrangements

292 s predicted by the accepted model of TCRbeta feedback inhibition, we found that expression of these p

293 nthesis is regulated by end product negative feedback inhibition where the levels of sterols and oxys

294 r, Nodal expression declines by day 4 due to feedback inhibition, whereas TGFbeta persists.

295 e that use of this capacity is restricted by feedback inhibition, which is relaxed at lower night tem

296 We show that this data-based form of feedback inhibition, which is softer than that of winner

297 ating disynaptic recurrent, feedforward, and feedback inhibition within and across the two projection

298 y regulated by UzcR, provides a mechanism of feedback inhibition within the UzcRS circuit.

299 spatial exploration, are generated by local feedback inhibition without recurrent excitation, and ha

300 inhibition but reduced total GLP-1 and GIP (feedback inhibition) without affecting the numerical con