ライフサイエンスコーパス: be negatively regulated by

1 We further show that Id-1 expression is negatively regulated by 2ME(2), which may be an addit

2 lin T1, a key enzyme in HIV-1 transcription, is negatively regulated by 7SK RNA and the HEXIM1 protei

3 , and glycoprotein E, and these interactions are negatively regulated by a C-terminal domain (CTD).

4 The MAPKs are negatively regulated by a family of dual-specificity

5 These sensor proteins are negatively regulated by a key immune regulator, SNI1

6 apoptosis the caspase inhibition by IAPs can be negatively regulated by a mitochondrial protein secon

7 c and helminth immunity and this process can be negatively regulated by a vertebrate chitinase.

8 Here, we demonstrate that yabE is negatively regulated by a cis-acting antisense RNA wh

9 , we provide evidence that Ras/PKA signaling is negatively regulated by a deubiquitinating enzyme, Ub

10 MTD-mediated mitochondrial targeting of Vms1 is negatively regulated by a direct interaction with the

11 The expression of this locus is negatively regulated by a GntR family regulator encod

12 MED13, in turn, is negatively regulated by a heart-specific microRNA, mi

13 signaling molecules and adaptor proteins and is negatively regulated by a number of cell surface and

14 These inflammatory responses were negatively regulated by a unique CD1d(hi)CD5(+) B c

15 d (Ena), an actin polymerization factor that is negatively regulated by Abl tyrosine kinase, identifi

16 Here, we show that G6PD is negatively regulated by acetylation on lysine 403 (K4

17 B-Raf autoinhibition was negatively regulated by acidic substitutions at phos

18 The suppressor effects of the cytokine can be negatively regulated by activation of survival signal

19 ied through larval brain ChIP-Seq for Adf-1, is negatively regulated by Adf-1, and manipulations of t

20 ) and that both this IRES and the c-myc IRES are negatively regulated by AKT activity.

21 es in cell survival and oxidative stress and are negatively regulated by Akt-mediated phosphorylation

22 box O1 (FoxO1), a transcription factor that is negatively regulated by Akt, was activated, transloca

23 Gal-1 ligand activity conferred by O-glycans was negatively regulated by alpha2,6 sialyltransferase S

24 izes to lysosomes and that such localization is negatively regulated by amino acid availability.

25 e first time that the mechanoreceptor ICAM-1 is negatively regulated by an actin-binding adaptor prot

26 of the P22 cro gene (O/P(cro)) (P(R)), which is negatively regulated by an arabinose-inducible P22 c2

27 The mast cell activation is negatively regulated by an inhibitory IgG-receptor.

28 We found that C/EBPbeta expression is negatively regulated by androgen receptor (AR) activi

29 Murine autoreactive anti-Smith (Sm) B cells are negatively regulated by anergy and developmental arr

30 te-inducible, carbon-metabolism-involved) as being negatively regulated by AP3 and PI.

31 report a novel tumor promoter, ZBTB46, which is negatively regulated by AR signaling via microRNA (mi

32 P-TEFb activity has been shown to be negatively regulated by association with the small nu

33 Here, we report that Sirt1 is negatively regulated by ATP, which binds to the C-ter

34 Notably, DNA binding by MksB is negatively regulated by ATP, which sets it apart from

35 ochorismate synthase (ICS1); SA biosynthesis is negatively regulated by autoinhibitory feedback at IC

36 Wnt signaling is negatively regulated by Axin, a scaffolding protein t

37 GPCR signalling is negatively regulated by beta-arrestins, adaptor molec

38 sis, T(H)1 differentiation, and autoimmunity are negatively regulated by beta1,6GlcNAc-branched N-gly

39 Endogenous DEPTOR levels are negatively regulated by betaTrCP.

40 (bcs), suggesting that cellulose production is negatively regulated by BinA.

41 Mks1p is negatively regulated by binding to Rtg2p and positive

42 the expression of the proapoptotic gene Bim is negatively regulated by Bmi-1 and that Bim knockdown

43 esting that formation of endoderm precursors is negatively regulated by BMPs on the ventral side.

44 The growth of muscle fibers can be negatively regulated by bovine myostatin.

45 e mediated by BLNK-independent pathways that are negatively regulated by c-Cbl, and further suggest t

46 e transition from c-Kit(lo) to c-Kit(hi) HSC is negatively regulated by c-Cbl.

47 The aspartate pool in L. lactis is negatively regulated by c-di-AMP, and high aspartate

48 on by LTA-stimulated pulp fibroblasts, which is negatively regulated by C5aR activation, has a role i

49 Bundling is negatively regulated by Ca(2+), but the mechanism of

50 Ca2+ influx is negatively regulated by Ca2+ -activated K+ channels (

51 Accordingly, GSK3 activity, which is negatively regulated by canonical Wnt signaling, incr

52 zed by endothelial NO synthase (eNOS), which is negatively regulated by caveolin-1 (Cav-1), the prima

53 d AMPK phosphorylation, suggesting that AMPK is negatively regulated by caveolin-1.

54 ion through ERK activation, and this process is negatively regulated by Cdc42 activity.

55 IN-9 is a cell cycle regulatory protein that is negatively regulated by CDK4/cyclin D.

56 ENaC is negatively regulated by CFTR and, in patients with CF

57 ctional CFTR, we report that MUC4 expression is negatively regulated by CFTR.

58 een Cdc45 and Mcm7 at origins of replication is negatively regulated by Chk1 in a Cdk2-independent ma

59 fine a novel response pathway whereby NFATc3 is negatively regulated by class II histone deacetylases

60 s of siRNAs targeting eight kinases known to be negatively regulated by Csk were then examined; knock

61 nal mediated by the RAR-SRC interaction that is negatively regulated by CSK and is required for RA-in

62 RapGAP1 localization is negatively regulated by Ctx, an F-actin bundling prot

63 sis and Northern blotting that several genes are negatively regulated by CyaR, including ompX, encodi

64 mediates INCENP's microtubule binding, which is negatively regulated by Cyclin-dependent kinase-media

65 of which expression was previously shown to be negatively regulated by D(5)R.

66 The neuroprotective activity of ATM may be negatively regulated by deacetylation since mutations

67 kinase inhibitor 1c (cdkn1c), a p57 homolog, is negatively regulated by Delta-Notch signaling and tha

68 ase in vivo and that this enzymatic activity is negatively regulated by dMyc, which binds to Lid's Jm

69 ontaining repeats in their promoter regions, are negatively regulated by DNA methylation.

70 L1 splicing can also be negatively regulated by EBV SM protein known to alter

71 nslation initiation factor 4E (eIF4E), which is negatively regulated by eIF4E-binding protein 1 (4E-B

72 We found that Slit2, which is negatively regulated by endothelial EphA2 receptor, i

73 This suggested that microglial activation is negatively regulated by EP2 signaling through suppres

74 R71, cardiac and Wnt signaling pathway genes were negatively regulated by ER71.

75 The osteoblast insulin signaling cascade is negatively regulated by ESP, a tyrosine phosphatase d

76 demonstrate that the Drosophila Dpp pathway is negatively regulated by eukaryotic translation initia

77 The expression level of this operon is negatively regulated by exogenous TPP and is mediated

78 pression is positively regulated by ExsA and is negatively regulated by ExsD.

79 sion is positively regulated by ExsA, and it is negatively regulated by ExsD.

80 FAK-cortactin binding is negatively-regulated by FAK activity and associated w

81 It is negatively regulated by FLIP, cIAP1, cIAP2, and XIAP.

82 Here, we identify a p53/TACE pathway that is negatively regulated by FOS and show that the FOS/p53

83 FOXM1 is negatively regulated by FOXO3A, supports cell surviva

84 tested the possibility that VEGF expression is negatively regulated by FOXO3a.

85 of cardiac Fox transcription factors, which is negatively regulated by FoxOs and positively regulate

86 e expressed at the valve-replum boundary and are negatively regulated by FUL and RPL in the valves an

87 n and occupancy at the center of the synapse are negatively regulated by GAKIN to tune the output of

88 uroD and the expression of Bhlhb5 and NeuroD is negatively regulated by ganglion cell-competence fact

89 late amino acid export, a process that could be negatively regulated by GDU1 ubiquitination and LOG2

90 tion within the transcribed regions of genes is negatively regulated by gene transcription and may be

91 This process is negatively regulated by GPIbalpha, as seen in mice wi

92 Autophagy is a catabolic process that is negatively regulated by growth and has been implicate

93 One of the transcription factors that is negatively regulated by GSK-3beta is CREB, which itse

94 VDR target genes CYP24A1, IGFBP-3, and TRPV6 were negatively regulated by GW0742.

95 sigma(Fah) is negatively regulated by host SpoIIAB, an anti-sigma f

96 smic side of the ER membrane, whose activity is negatively regulated by Hsp90 through the TPR domain.

97 The expression of LAT-encoded miRNAs is negatively regulated by ICP4, the major viral transac

98 e that pathogenic NLRP3 activity in CF could be negatively regulated by IL-1Ra and provide a proof-of

99 lance against established metastatic disease is negatively regulated by IL-13 and requires the induct

100 Exhausted CD8(+) T cells function poorly and are negatively regulated by inhibitory receptors.

101 This event is negatively regulated by inhibitory killer Ig-like rec

102 the FoxO forkhead transcription factors that are negatively regulated by insulin/IGF-1 signaling, the

103 etch force, and the expression level of Tcap is negatively regulated by integrin-link kinase (ILK), a

104 sion and these functional properties of Ars2 are negatively regulated by interaction with 7SK RNA.

105 IRT1 activity in vitro was recently found to be negatively regulated by interaction with the deleted

106 a site-specific DNA-binding activity, which is negatively regulated by interaction with certain HSPs

107 Our results indicate that the Tec kinase Itk is negatively regulated by intermolecular clustering and

108 The enzyme is negatively regulated by intramolecular interactions o

109 We suggest that basal autophagic flux may be negatively regulated by IP(3)R-dependent Ca(2+) signa

110 ransport systems, Feo and Fbp, were found to be negatively regulated by iron and Fur.

111 Like E. coli ryhB, V. cholerae ryhB is negatively regulated by iron and Fur and is required

112 r region and find that H2-T6SS transcription is negatively regulated by iron.

113 treptococcal iron acquisition) operon, which was negatively regulated by iron in the parent strain.

114 , we show that the blr7895 and bll6680 genes are negatively regulated by Irr as determined by derepre

115 We found that Nedd4 is negatively regulated by ISG15.

116 Expression of PpCSP1 is negatively regulated by its 3'-untranslated region (3

117 erfamily members, dynamin's function in vivo is negatively regulated by its GAP activity.

118 Rheb is a direct target of TSC2 and is negatively regulated by its GTPase-activating protein

119 The activity of GSK3beta is negatively regulated by its phosphorylation at Ser9.

120 on during the differentiation of neurons and is negatively regulated by JNK3 via phosphorylation of A

121 nsporter containing SLC3A2, whose expression is negatively regulated by K-RAS.

122 We show that cellular FtsA concentration is negatively regulated by KhpA/B at the post-transcript

123 issues during development, and this activity is negatively regulated by kinases in the Hippo signalin

124 ncer cell lines confirm that Sox9 expression is negatively regulated by KLF5.

125 res IL-23 receptor (IL-23R) signaling, which is negatively regulated by let-7f microRNA.

126 In aged fly brain, dAgo1 protein level was negatively regulated by LRRK2.

127 This autophagic response is negatively regulated by mammalian target of rapamycin

128 The steady-state level of mntH mRNA was negatively regulated by manganese, but was unaffecte

129 ZEBs are negatively regulated by members of the miR-200 micro

130 E2Fs are negatively regulated by members of the retinoblastom

131 MAPK activity is negatively regulated by members of the dual specifici

132 smooth muscle cells and stromal fibroblasts is negatively regulated by members of the Pur family of

133 The levels of this complex may be negatively regulated by merlin.

134 As Axl is negatively regulated by merlin and positively regulat

135 th linker DNA between nucleosomes, which may be negatively regulated by methylation of H3K36.

136 norB and tet38 transcription was negatively regulated by MgrA.

137 Some of the genes that are negatively regulated by miR-101 expression include h

138 In turn, we show that PHA-4 and SKN-1 are negatively regulated by miR-228, whereas miR-71 repr

139 Endothelial CXCR4 is negatively regulated by miR-139-5p, whose transcripti

140 o provide evidence that fatty acid oxidation is negatively regulated by miR-29 overexpression, potent

141 c effects of bile acid signaling, whereas it is negatively regulated by miR-34a, a pathogenic microRN

142 P-1), one of the Ets-1 downstream mediators, was negatively regulated by miR-199a-5p.

143 scular endothelial growth factor receptor 2, were negatively regulated by miR-200b.

144 sm, Jin et al. (2014) show that this process is negatively regulated by mitochondrial electron transp

145 here that macrophage expression of IFN-beta is negatively regulated by mitogen- and stress-activated

146 Erk activation is negatively regulated by mitogen-activated protein kin

147 ng the turnover of cytoplasmic constituents, is negatively regulated by mTOR.

148 an mTOR-interacting protein whose expression is negatively regulated by mTORC1 and mTORC2.

149 cused on ULK1, a key autophagy protein which is negatively regulated by mTORC1, to assess its potenti

150 Muscle growth is negatively regulated by myostatin (MSTN) and activins

151 The transcriptional activity of PITX2 is negatively regulated by N-terminal phosphorylation an

152 nscription factor of CSNK1A1 (CK1alpha) that is negatively regulated by NIFK.

153 negatively regulated by miR-1, which itself was negatively regulated by Nkx2-5 in the mouse heart an

154 of HDAC4 and its association with chromatin is negatively regulated by NMDA receptors.

155 iated by a ubiquitin-proteasome pathway that is negatively regulated by NO.

156 nd closure requires actin polymerization and is negatively regulated by nonmuscle myosin.

157 Finally, we show that insm1a is negatively regulated by Notch-Delta signaling.

158 On the other hand, Atp1a1 is negatively regulated by NRF-1.

159 ptive responses to hypoxia, and its activity is negatively regulated by O2-dependent binding of the v

160 HOTAIR expression is negatively regulated by oestrogen, positively regulat

161 BAergic neuron progenitors from PCPs to PIPs is negatively regulated by Olig2 and positively by Gsx1,

162 on U6 promoter, suggesting that U6 promoter is negatively regulated by p38 kinase.

163 lished, studies suggest that VEGF expression is negatively regulated by p53, a master regulator and t

164 CM5 and its transcriptional regulator, E2F1, is negatively regulated by p53.

165 However, rTh markers are negatively regulated by Pax6, which itself is down-r

166 p1 at the LHR promoter, and this interaction is negatively regulated by PC4 phosphorylation.

167 de requires pre-existing CD8(+) T cells that are negatively regulated by PD-1/PD-L1-mediated adaptive

168 Here we report that Tax was negatively regulated by PDLIM2, which promoted Tax K

169 HIF, which is negatively regulated by PHD, activates numerous genes

170 sitide-dependent protein kinase-1 (PDK1) and is negatively regulated by phosphatase and tensin homolo

171 ing support for a model in which CP activity is negatively regulated by phosphatidic acid in vivo.

172 the Abl interactor protein Abi2 is shown to be negatively regulated by phosphorylation of serines 63

173 binding motif (PBM), an interaction that can be negatively regulated by phosphorylation of the E6 PBM

174 eractions are not constitutive, and they can be negatively regulated by phosphorylation within the E6

175 Pdc is negatively regulated by phosphorylation followed by b

176 f SNX18 in membrane tubulation and autophagy is negatively regulated by phosphorylation of S233.

177 Cofilin-1-severing/depolymerization activity is negatively regulated by phosphorylation of serine 3.

178 n particular, the general belief is that Lck is negatively regulated by phosphorylation of tyrosine 1

179 and lipid binding and that lipin 1 activity is negatively regulated by phosphorylation.

180 FKHRL1 activity was negatively regulated by phosphorylation catalyzed by

181 Further, expression of FHY3 and FAR1 is negatively regulated by phyA signaling.

182 Consistently, BRC1 is negatively regulated by phytochrome B.

183 duced preferential translation of Hsp70 mRNA is negatively regulated by PI3K-mTORC1 signaling.

184 of the prototypic AHR responsive gene Cyp1a1 was negatively regulated by PMA and IL-1beta treatment.

185 ere identified among direct targets of PPD2, being negatively regulated by PPDs and KIX8/9.

186 However, glutamate release probability is negatively regulated by presynaptic mGluR2/3, and suc

187 Pan1p activity is negatively regulated by Prk1 kinase phosphorylation a

188 ansmitter release by catecholaminergic cells is negatively regulated by prohormone cleavage products

189 lternative mechanism in which group I mGluRs are negatively regulated by proline-directed kinases tha

190 e mitochondrial apoptotic signaling that can be negatively regulated by prosurvival Bcl-2 proteins.

191 d that the production of IL-23 but not IL-12 was negatively regulated by protein phosphatase 2A (PP2A

192 itively regulated, whereas approximately 32% were negatively regulated by PrrA, which is in excellent

193 link, we determined that IGFBP-2 expression is negatively regulated by PTEN and positively regulated

194 ht to determine whether Mst2, in addition to being negatively regulated by Raf-1, might itself recipr

195 These activities are negatively regulated by REPLUMLESS (RPL), which divi

196 alpha-ketoacid dehydrogenase complex (BCKDC) is negatively regulated by reversible phosphorylation.BC

197 nd Arp2/3-dependent actin polymerization and is negatively regulated by Rho and nonmuscle myosin.

198 with tumor suppressor activity that we found is negatively regulated by Rhox5 in the testis in vivo.

199 igh-affinity receptors for IgE (FcepsilonRI) is negatively regulated by rictor independently of mTOR.

200 y showed that the transcription factor BACH1 is negatively regulated by RKIP and promotes breast canc

201 model whereby CD1d-mediated Ag presentation is negatively regulated by ROCK via its effects on the a

202 SigH is negatively regulated by RshA, its cognate anti-sigma

203 rt that MAPK and CREB-mediated transcription are negatively regulated by SCOP (suprachiasmatic nucleu

204 Recent studies indicate that Wnt signalling is negatively regulated by secreted Wnt antagonists such

205 Although cofilin is negatively regulated by Ser3 phosphorylation, the ups

206 r isoforms, alpha and beta, whose activities are negatively regulated by serine phosphorylation but p

207 Although p53 is well known to be negatively regulated by several ubiquitin ligases inc

208 tic enzyme phosphoglycerate mutase-1 (PGAM1) is negatively regulated by Sirt1, a member of the NAD(+)

209 ed by anti-8-hydroxydeoxyguanosine staining, was negatively regulated by Sirt1.

210 eported that the antiviral activity of RIG-I is negatively regulated by specific E3 ubiquitin ligases

211 m(6)A modification, while the protein itself is negatively regulated by SPI1.

212 negative regulator of flowering that itself is negatively regulated by SPL11, possibly via ubiquitin

213 or of genes used to combat oxidative stress, is negatively regulated by sRNA MgrR.

214 The gene, which is negatively regulated by Sum1, Hst1, and Rfm1, fully r

215 stimulation of C5a receptor 1 (C5aR1), which is negatively regulated by surface-expressed C5aR2.

216 mine and serotonin, with release of dopamine being negatively regulated by synapsins, specifically sy

217 Socs3, and Tcf7 (TCF-1) as gene targets that are negatively regulated by T-bet.

218 ted upon tyrosine phosphorylation, and hence is negatively regulated by TbPTP1.

219 The nucleolytic activity of SLX1-SLX4 is negatively regulated by telomeric DNA-binding protein

220 r, although its expression has been shown to be negatively regulated by TetC and not inducible by tet

221 Here, we show that Sca-1 expression is negatively regulated by TGF-beta1 and that this inhib

222 We found that, besides being negatively regulated by TH at the transcriptional

223 document that HSC development and functions are negatively regulated by the E3 ubiquitin ligase c-Cb

224 , we show that the levels of apical CAR(Ex8) are negatively regulated by the PDZ domain-containing pr

225 TG16L all promote cell-cycle progression and are negatively regulated by the phosphatase and tensin h

226 in destruction and tumor suppressor function are negatively regulated by the prolyl isomerase Pin1.

227 E2Fs are negatively regulated by the retinoblastoma (RB) fami

228 ize how the Jak-Stat pathways in these cells are negatively regulated by the Suppressor of cytokine s

229 S6K1, two key effectors of cell growth that are negatively regulated by the TSC1-TSC2 complex.

230 Ft signaling was recently shown to be negatively regulated by the atypical myosin Dachs [10

231 Plant CNGCs are hypothesized to be negatively regulated by the Ca(2+) sensor calmodulin

232 helial/mesenchymal cell motility is known to be negatively regulated by the catenin protein plakoglob

233 nduction of antizyme expression was found to be negatively regulated by the peptide transporter PEPT-

234 Antizyme itself is negatively regulated by the antizyme inhibitor.

235 bio) biosynthetic operon of Escherichia coli is negatively regulated by the BirA protein, an atypical

236 osphate interconversion in Bacillus subtilis is negatively regulated by the Central glycolytic genes

237 ted NF-kappaB activation requires CARMA1 and is negatively regulated by the deubiquitinase CYLD.

238 athway that controls the cell wall integrity is negatively regulated by the deubiquitinating enzyme U

239 4 gene products of the icaADBC operon, which is negatively regulated by the divergently transcribed i

240 Futsch is negatively regulated by the Drosophila Fragile X ment

241 previously observed that expression of farAB is negatively regulated by the FarR repressor.

242 Genetic studies have indicated that TRA-1 is negatively regulated by the fem-1, fem-2, and fem-3 g

243 NIK expression is negatively regulated by the full-length isoform of TN

244 The gal operon of Escherichia coli is negatively regulated by the Gal repressosome, a highe

245 This GTPase is negatively regulated by the GTPase-activating protein

246 Sphingolipid (SL) biosynthesis is negatively regulated by the highly conserved endoplas

247 vator yes-associated protein 1 (YAP1), which is negatively regulated by the Hippo pathway, in human m

248 otein), a key transcriptional co-factor that is negatively regulated by the Hippo pathway, is crucial

249 flammasome activity during Candida infection is negatively regulated by the IL-22/NLRC4/IL-1Ra axis.

250 ead box O transcription factor (FOXO), which is negatively regulated by the insulin-signaling pathway

251 w also that DeltaNp63alpha protein stability is negatively regulated by the interaction with the prol

252 e PDZ domains of EBP50, and this interaction is negatively regulated by the intramolecular associatio

253 CML42 up-regulation is negatively regulated by the jasmonate receptor Corona

254 her mutated or absent in >50% of cancers and is negatively regulated by the mouse double minute (MDM2

255 rate that MprAB-mediated signal transduction is negatively regulated by the MprB extracytoplasmic dom

256 ns, PLD2 expression and concomitant activity is negatively regulated by the mTOR/S6K signaling pathwa

257 that formation of the p50/p50/Bcl-3 complex is negatively regulated by the p105 precursor.

258 The PI3K-Akt pathway is negatively regulated by the phosphatase and tensin ho

259 een shown to mediate IPC, and Akt activation is negatively regulated by the phosphatase PTEN, but whe

260 Rim15p is negatively regulated by the phosphate-sensing kinase

261 The E2F1 transcription factor, which is negatively regulated by the pRB/p16(INK4a) tumor supp

262 CXCL13 is negatively regulated by the presence of B cells, as i

263 activation of canonical Wnt signaling, which is negatively regulated by the primary cilium and severa

264 Here, we show that Eco1 is negatively regulated by the protein kinase Cdk1.

265 Mst2 is negatively regulated by the proto-oncoprotein Raf-1 i

266 This process is negatively regulated by the Pten phosphatase, which i

267 transcriptional regulators VpsR and VpsT and is negatively regulated by the quorum-sensing transcript

268 Cell cycle progression is negatively regulated by the retinoblastoma family of

269 f this operon, and therefore PQS production, is negatively regulated by the rhl quorum-sensing system

270 ptional activator of methionine biosynthesis is negatively regulated by the SCFMet30 ubiquitin ligase

271 SpyCEP expression is negatively regulated by the signal transduction syste

272 hrough a variant clathrin-binding motif that is negatively regulated by the Sla1p SHD2 domain.

273 etoacid dehydrogenase complex (BCKDC), which is negatively regulated by the specific BCKD kinase (BDK

274 TGFbeta signaling, we demonstrate that BST2 is negatively regulated by the TGFbeta axis in epithelia

275 toxic products during hypoxic metabolism and is negatively regulated by the transcriptional repressor

276 This movement is negatively regulated by the translating ribosome and,

277 inate overproduction, also known as mucoidy, is negatively regulated by the transmembrane protein Muc

278 ral controller of growth and metabolism that is negatively regulated by the tumor suppressor tuberous

279 the control of a single promoter, P1, which is negatively regulated by the two-component regulatory

280 We show that LpxL1 is negatively regulated by the two-component system PhoP

281 FlhD(4) C(2) activity is negatively regulated by the type 3 secretion chaperon

282 tor of the Fat and Hippo signaling pathways, is negatively regulated by the Warts kinase.

283 , and CsfV, induce their own expressions and are negatively regulated by their cognate anti-sigma fac

284 The activities of both mTORC1 and mTORC2 are negatively regulated by their endogenous inhibitor,

285 ch period (Per) and cryptochrome (Cry) genes are negatively regulated by their protein products.

286 ch Period (Per) and Cryptochrome (Cry) genes are negatively regulated by their protein products.

287 artner of Bassoon and Piccolo whose activity is negatively regulated by their conserved zinc finger d

288 ression of the Period and Cryptochrome genes is negatively regulated by their protein products.

289 entary to that of TSH4, consistent with tsh4 being negatively regulated by this microRNA.

290 We report here that CD44 is negatively regulated by thyroid hormone (T(3)) throug

291 a and tissue factor (TF), remains intact but is negatively regulated by tissue factor pathway inhibit

292 er TLR7-driven spontaneous models of SLE and is negatively regulated by TLR9.

293 phagy, which can protect against cell death, is negatively regulated by TOR, and disruption of autoph

294 nd miR-125b and miR-504, the human TP53 gene is negatively regulated by two more miRNAs: miR-25 and m

295 RING domain dimerization efficiency is negatively regulated by upstream sequence.

296 Importantly, BMP4 expression was negatively regulated by vascular endothelial growth

297 Here, we showed that ECT2 is negatively regulated by wild-type p53 but not tumor-d

298 onse to RA treatment or Notch activation and are negatively regulated by Wnt/beta-catenin signalling.

299 such substrate is protein kinase Fpk1, which is negatively regulated by Ypk1.

300 These results indicate that PRR5 is negatively regulated by ZTL, which likely mediates it