ライフサイエンスコーパス: regulate

1 about how the activity of these proteins is regulated.

2 dered inaccurate and they need to be tightly regulated.

3 differentiation into the NKT cell subsets is regulated.

4 to the nucleoli, suggesting that p-T153/Y155 regulates a previously unappreciated function of TDP-43

5 H2S regulates a wide range of physiological processes, namel

6 umber of genes (n = 263) were differentially regulated according to the source of infection, enriched

7 lation as an important feedback mechanism to regulate acetyltransferases.

8 and CLEC3B were significantly differentially regulated across all three -omics levels, confirming the

9 such as the LIM domain kinase (LIMK), which regulates actin activity through phosphorylation of cofi

10 The autophagy protein Beclin1 regulates activation of Rab5 and endosomal-mediated degr

11 e for the PLCbeta-PKCalpha pathway, possibly regulating activation of SFKs, which are crucial for ini

12 main of Brassica napus DGAT1 (BnaDGAT11-113) regulates activity based on acyl-CoA/CoA levels.

13 which increased cytosolic Ca(2+) negatively regulates adipokine secretion and have uncovered an evol

14 wing treatment with different drugs known to regulate alpha-SYN expression; while exogenous promoter-

15 trolled in part by RNA-binding proteins that regulate alternative splicing decisions through interact

16 how the assembly of IL-12 family members is regulated and controlled in the cell.

17 vel long intergenic non-coding RNA with MyoD-regulated and skeletal muscle-restricted expression that

18 d to explore in detail how HIV-1 splicing is regulated and, with moderate throughput, could be used t

19 Cellular proteins regulating and targeting lentiviral and gammaretroviral

20 9% of them during early maturation were down-regulated, and preferentially associated with DNA replic

21 fearful fear stimuli, making it difficult to regulate anxiety.

22 revealed that TrkC-miR2 is significantly up-regulated ( approximately 70 times) in colorectal tumor

23 dentified to be highly sensitive to androgen-regulated AR action, such as NOV and ST6GalNAc1, were ma

24 the CHH context were transcriptionally down-regulated as seeds mature: 99% of them during early matu

25 Gene expression is extensively regulated at the levels of mRNA stability, localization

26 al SRP receptor, FtsY, interacts with and is regulated at the target membrane remain unclear.

27 The innate immune response is regulated at various stages, from hematopoiesis to monoc

28 erellin, GA1, by UV-B in this zone, which is regulated, at least in part, by the expression of GRF1 a

29 hile phosphorylation of tyrosine 447 (PY447) regulates auto-inhibition.

30 ulatory components LKB1 and AMPKalpha, which regulate autophagy induction through their kinase activi

31 Our data demonstrate that mTORC1-regulated autophagy is necessary and sufficient for star

32 dynein-Snapin-mediated retrograde transport regulates BACE1 trafficking in axons and APP processing

33 However, the mechanisms regulating BACE1 distribution in axons and beta cleavage

34 gra pars compacta and ventral tegmental area regulate behaviours such as reward-related learning, and

35 nt component of the destruction complex that regulates beta-catenin levels.

36 as neutrophils, we show that FlnA negatively regulates beta2 integrin adhesion to complement componen

37 y estrogen response that were differentially regulated between WT, Cyp1a1-/- and Cyp1a2-/- mice.

38 additional role of environmental factors in regulating birth and mortality rates can lead to erroneo

39 -binding proteins, which may thus recruit or regulate Blm at telomeres.

40 on-like peptide 1), a critical incretin that regulates blood glucose homeostasis.

41 nalogous to the role of blood vessel tone in regulating blood flow.

42 Elevated miR-15a and miR-16 levels down-regulated BMI1 and other polycomb group proteins like RI

43 e-scale studies have revealed how editing is regulated both in cis and in trans.

44 Runx2 was up-regulated by 6.4-fold during IL-13-induced goblet cell d

45 Taken together, we show that the NGB gene is regulated by a cell type-specific loop formed between it

46 pression during erythroid differentiation is regulated by alternative pre-mRNA splicing.

47 During health, animal sleep is regulated by an internal clock and by the duration of pr

48 These functions are spatially regulated by association of dynein and its accessory com

49 hat insulin secretion in pancreatic cells is regulated by Ca(2+) and ROS signaling through Ca(2+)-ind

50 The protein stability of FOXO3A is regulated by Casein Kinase 1 alpha (CK1alpha) in an onco

51 BRI1 abundance is regulated by endosomal recycling and vacuolar targeting,

52 The number of items in working memory can be regulated by external excitation, enabling the system to

53 , the PiT1-PiT2 heterodimerization was still regulated by extracellular Pi levels.

54 These functions are differentially regulated by individual isoforms, necessitating a deeper

55 In cells, actin dynamics are regulated by kinases, such as the LIM domain kinase (LIM

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

57 We found that GCH1 was regulated by NF-E2-related factor 2, a key mediator of t

58 els, that is that inflorescence branching is regulated by novel localized signaling centers.

59 t to identify novel actin signaling pathways regulated by NPM-ALK, a comprehensive phosphoproteome an

60 performed and 263 genes were differentially regulated by RpoE, and surprisingly, the rseA mutant str

61 Holocene alternates between being primarily regulated by sea ice or glacial discharge from the surro

62 and triglyceride synthesis that are normally regulated by SREBP-1c.

63 e matricellular protein CCN1/CYR61 is highly regulated by stiffness in endothelial cells.

64 cate that SOCE and KATP channel activity are regulated by STIM1.

65 Two MAF1 species, MAF1L and MAF1S, are regulated by the C-box YSY motif, which, when mutated, a

66 tional acetylation modification of CREBH are regulated by the circadian clock.

67 d endoplasmic reticulum, with its expression regulated by the external inorganic carbon concentration

68 GF-1, respectively, and IGF-1 expression was regulated by the Sonic Hedgehog (Shh) pathway.

69 at lysosomal functions are transcriptionally regulated by transcription factor EB (TFEB) through the

70 Its binding to mRNA is regulated by tyrosine 396 phosphorylation, and this part

71 ted that voltage-gated Ca(2+) channels, CaV, regulate Ca(2+) homeostasis in excitable cells following

72 (up to +153%) release, suggesting that down-regulating CAD1 is a promising strategy for improving li

73 y to renal physiology, but how renal tubules regulate capillary development remains unclear.

74 inding (Id) proteins play important roles in regulating cardiac development via paracrine signaling.

75 fraction of the human genome was believed to regulate cell function and development.

76 sine kinases acts in signaling pathways that regulate cell migration, cell adhesion, and proliferatio

77 ughout development and across the metazoa to regulate cell polarity.

78 back interactions within the ERK pathway can regulate cell proliferation and transformation, and sugg

79 xicity of Inh2-B1, and its abilities to down-regulate cell wall hydrolase genes and disrupt the biofi

80 In plants, regulated cell death (RCD) plays critical roles during d

81 or responds to various cellular stresses and regulates cell fate.

82 at can be transferred to recipient cells and regulate cellular processes in an autocrine or paracrine

83 strating that these enzymes are important in regulating cellular NEIL1 steady state protein levels.

84 These cytokines regulate central nervous system neurons to induce sleep.

85 vely, our results indicate that ZO-1 binding regulates channel accrual, while disengagement from ZO-1

86 , which interact in a coordinated fashion to regulate chemorepulsion exerted by the muscle.

87 ight environment by a single sigma factor to regulate chloroplast transcription.

88 centrations, suggesting that bacteria likely regulate choanoflagellate mating in nature.

89 etal dysplasia, identifying a mechanism that regulates chondrogenesis via modulation of SOX9 ubiquiti

90 an chondrocytes demonstrates that the region regulates CHSY1 expression.

91 te a common behavioral output, and that Lef1 regulates circuit development that is fundamentally impo

92 e-binding site and a distinct, independently regulated, co-agonist-binding site.

93 We hypothesized that bile acids regulate colonic HbetaD expression and aimed to test thi

94 131Arg) variants have an impaired ability to regulate complement activation and may benefit more from

95 We revealed that Skp2 regulates CRPC through Twist-mediated oncogenic function

96 roRNA regulation of DCC and suggest that, by regulating DCC, miR-218 may be a switch of susceptibilit

97 geneous, and distinct subsets are thought to regulate different behaviors.

98 the identification of several other reflexes regulating discrete immune functions.

99 ARR activation, and basis by which cytokinin regulates diverse aspects of growth and development as w

100 cleoprotein complexes, and that Lon may help regulate DNA replication in response to growth condition

101 on dopaminergic afferents and can negatively regulate dopamine release.

102 he expression of many miRNAs is dramatically regulated during functional maturation of the mouse visu

103 ed that the biomarker was significantly down-regulated during inflammation induced by acute contact h

104 Gene expression is precisely regulated during the inflammatory response to control in

105 ng cell-cycle progression itself and must be regulated dynamically during cyclic re-entry to ensure e

106 However, genetic alterations in the RB-regulated E2F family of transcription factors are infreq

107 nsequences for both provisioning and climate regulating ecosystem services.

108 eviously unrecognized function of the CSN in regulating EGFR neddylation has broad-reaching implicati

109 ate the roles of tumor-associated signals in regulating endothelial cell contractility and adherens j

110 endothelial cell maintenance and function by regulating eNOS activity.

111 t retinoschisin, the protein encoded by RS1, regulates ERK signaling and apoptosis in retinal cells.

112 et1A catalytic methyltransferase activity in regulating ESC differentiation but not self-renewal and

113 e molecular mechanisms that enable HD-PTP to regulate ESCRT function are unknown.

114 omatin, and how chromatin domains in general regulate essential nuclear functions.

115 eins that bind to specific DNA sequences and regulate expression of genes.

116 A)-induced AML cell differentiation, through regulating expression of targets such as ASB2 and RARA b

117 ple species, we hypothesized that PAI-1 also regulates fibrosis during cardiac injury.

118 tic peptides (NPs), atrial NP and B-type NP, regulate fluid homeostasis and arterial BP through renal

119 rofolate reductase (DHFR) is a key enzyme to regulate folate metabolism, however folate/DHFR activity

120 However, the niche that regulates follicular melanocytes is not well characteriz

121 that members of the Notch signalling pathway regulate further differentiation of the progenitors into

122 sociated with altered expression of proteins regulating GABAergic and glutamatergic signaling in the

123 RF2 demonstrates its role in developmentally regulated gamma-globin gene expression and the ability t

124 Noncoding RNAs (ncRNAs) regulate gene expression in all organisms.

125 Riboswitches are widespread RNA motifs that regulate gene expression in response to fluctuating meta

126 MicroRNAs (miRNAs) regulate gene expression through interactions with targe

127 ationale for the powerful ability of BAP1 to regulate gene-environment interaction in human carcinoge

128 tudy, we showed that knockdown of taurine up-regulated gene 1 (TUG1) induces marked inhibition of cel

129 Estrogen receptor alpha (ERalpha) regulates gene transcription through two activation func

130 to mediate their effects on lipid traits by regulating gene expression.

131 ed with AR at specific sites on chromatin to regulate genes relevant to disease progression.

132 1 as a fluid mechanosensor that functions to regulate genes that promote metastasis.

133 erved significant enrichments of haloperidol-regulated genes in schizophrenia GWAS loci and in schizo

134 In the atria, MEF2A regulated genes involved in fibrosis and adhesion, where

135 s of some markers for AML subtypes and c-MYC regulated genes were considered potential predictors of

136 r, the role of brown adipose tissue (BAT) in regulating gestational metabolism is unknown.

137 Here the authors show that MRAP2 also regulates ghrelin receptor signalling in the hypothalamu

138 that this mechanism is essential for insulin-regulated glucose homeostasis.

139 that MYBS1 and MYBS2 play opposite roles in regulating glucose and ABA signaling in Arabidopsis duri

140 Soluble klotho down-regulates growth factor-driven PI3K signaling, contribut

141 Bacteria may play a role in regulating harmful algal blooms, but little is known abo

142 Here we demonstrate that eIF4E regulates HAV IRES-mediated translation by two distinct

143 ant interest has emerged in how inflammation regulates HSC fate and how it affects the long-term func

144 g Zfp521-deficient mice revealed that ZFP521 regulates HSC self-renewal and differentiation.

145 ergence on common transcriptional targets to regulate human RMS growth.

146 en, suggesting that HOXA4 may play a role in regulating human growth by epigenetic mechanisms.

147 genesis in an Egr-2-dependent manner that up-regulates Id2, the repressor of the receptor activator o

148 MEFs lacking AMPK activity also failed to up-regulate IFN-beta and TNF-alpha after treatment with DMX

149 ions in genes encoding protein products that regulate immune function or cell adhesion and tumor cell

150 Many of the miRNAs were regulated in a tissue/organ-specific manner.

151 senescence marker CD57 was significantly up-regulated in CD8(+) T cells from patients with hepatitis

152 little is known about how LMP1 expression is regulated in epithelial cells, and there are conflicting

153 tely expressed genes that are differentially regulated in latent vs. replicative states of infection.

154 ence, expression of RTN1 and RTN3 is tightly regulated in mouse brains.

155 of these properties in nanomedicine to down-regulate inflammatory pathways or to be employed as diag

156 that neuronal circuits operating reflexively regulate innate and adaptive immunity.

157 activation stimulates neuronal circuits that regulate innate and adaptive immunity.

158 gnaling intermediates in murine macrophages, regulating innate immune responses through the initiatio

159 ntify mechanisms through which FGF signaling regulates inner cell mass lineage restriction and cell c

160 ATPase activity, rather than being regulated, instead gradually becomes uncoupled as nucleo

161 a model for identifying molecular mechanisms regulating intercellular bridges.

162 docytic recycling following constitutive and regulated internalization.

163 t signaling and has previously been shown to regulate ISV patterning.

164 nslational modification of HBx by HDM2 which regulates its stability, subcellular localization, and f

165 s a flower-specific jasmonate repressor that regulates JAs, (E)-alpha-bergamotene, TPIs, and a defens

166 Only a few hundreds of protein kinases regulate key processes in human cells, and protein kinas

167 PKC) in the cytosol and extracellular signal regulated kinase (ERK) in the cytosol and nucleus.

168 The stimulatory effect on extracellular regulated kinase (ERK1/2) was blocked by the Src family

169 gnaling events, such as extracellular signal-regulated kinase 1/2 and label free, in a parallel manne

170 ncluding phosphorylated extracellular signal-regulated kinase, phosphorylated protein kinase B, phosp

171 Activation of apoptosis signal-regulating kinase 1 (ASK1) in hepatocytes is a key proce

172 butes to atherogenesis in Apoe (-/-) mice by regulating lesion and systemic inflammation.

173 e DUBs USP7 and USP10, which are involved in regulating levels of p53 and MDM2.

174 and regenerative signaling, is here shown to regulate ligand-specific Notch signaling.

175 ry, as well as tegument proteins involved in regulating lytic replication, but lacked capsid proteins

176 Our studies identified a highly up-regulated mammalian lncRNA, FOXD3-AS1, known as linc1623

177 LHX1 regulates many genes other than Vip, yet activity rhythm

178 Lipin-2 regulates MAPK activation, which mediates synthesis of p

179 roteins and the related SCs of other species regulate meiotic DSB formation to form crossovers crucia

180 ogated not only the alterations in PPARgamma-regulated metabolic pathways, but also the increases in

181 led miR-132 as one of the most severely down-regulated miRNAs at the intermediate and late Braak stag

182 monstrate that the Mdm30-Ubp2-Rsp5 crosstalk regulates mitochondrial fusion by coordinating an intric

183 Hnt's role in regulating Mmp2 and Oamb can be replaced by its human ho

184 enous MSK1 levels concomitantly increased to regulate MOR gene expression during neuronal differentia

185 cal models of how the brain selects actions, regulates movement initiation and execution, and switche

186 let-7 activity and hence expression of let-7-regulated mRNAs.

187 Expression of miss-regulated mutant variants of RabA2 resulted in an increa

188 ctor receptor-associated factor 2 (Traf2) in regulating myocardial necroptosis and remodeling using g

189 ne-protein kinase 2 (Abl2) has a key role in regulating myofiber length, as a loss of Abl2 leads to e

190 osed that SlCBL10 mediates salt tolerance by regulating Na(+) and Ca(2+) fluxes in the vacuole, coope

191 s an important role in antiviral immunity by regulating natural killer and CD8(+) T cells, epigenetic

192 eloping vertebrate nervous system evolved to regulate neurogenesis.SIGNIFICANCE STATEMENT The Src fam

193 Neuraminidases 3 and 4 regulate neuronal function by catabolizing brain ganglio

194 ifying an important role for CaV1.3 L-CDF in regulating neuronal excitability.

195 protein modulates osteoclastogenesis by down regulating NF-kappaB activation.

196 AT3 tyrosine705 phosphorylation cooperate in regulating NKG2D expression in NK cells.

197 editing occurred, generating B cells with up-regulated Nod1, including follicular and marginal zone B

198 proteins are histone demethylases that both regulate normal cell fates during development and contri

199 SF30-L mediates nitrate signaling in part by regulating NRT1.1 expression, thus adding an important c

200 s with beta-N-acetylglucosamine (GlcNAc) and regulates numerous biological processes.

201 ubiquitin-like modifier (SUMO) modification regulates numerous cellular processes.

202 lular and the extracellular microenvironment regulating oligodendrocyte properties and discuss stem c

203 teracts with DAXX and, in turn PTEN directly regulates oncogene expression by modulating DAXX-H3.3 as

204 electronics owing to their discrete voltage regulated operational levels.

205 plementarity and governs the HNH nuclease to regulate overall catalytic competence.

206 (+) T cells, suggesting that miR-155 and ICB regulate overlapping pathways to promote antitumor immun

207 , encodes a ubiquitin ligase that negatively regulates p53 levels by ubiquitination.

208 However, the role of PD-L1 and PD-1 in regulating pain and neuronal function is unclear.

209 Several transcription factors regulating pancreas lineage specification have been iden

210 ation, chromosome condensation and precisely regulated partitioning of chromosomes into daughter cell

211 udy uncovers a novel molecular mechanism for regulating PD-L1 protein stability by a cell cycle kinas

212 Nuclear hormone receptors (NRs) regulate physiology by sensing lipophilic ligands and ad

213 s carotenoid levels by posttranscriptionally regulating phytoene synthase (PSY).

214 el in which dorsoventral genes coordinate to regulate plant development by localizing auxin response

215 has been shown to interact with nephrin and regulate podocyte cytoskeleton and slit diaphragm dynami

216 e goal should be to prohibit or more closely regulate potentially injurious ingredients and thus prom

217 that piRNAs and piRNA biogenesis components regulate precursor mRNA splicing of P-transposable eleme

218 ow vascular endothelial growth factor (VEGF) regulates PRKCB promoter function in CLL cells, stimulat

219 biofilm formation, and also influences cAMP-regulated processes.

220 is a host defense response that directly up-regulates production of keratin-derived AMPs (KAMPs) by

221 These results together suggest that NRTIs up-regulate proinflammatory cytokines via a Wnt5a signaling

222 hyll switch; pufQ is found within the oxygen-regulated pufQBALMX operon encoding the reaction centre-

223 mportant role of litter-leached DOC input in regulating rain-induced soil CO2 pulses and microbial co

224 understanding of the mechanism by which IreB regulates resistance, we initiated a structure-function

225 thway in a pattern consistent with a role in regulating RGC axon outgrowth.

226 We show that FER acts as a RALF-regulated scaffold that modulates receptor kinase comple

227 expression levels and cytosolic conformation regulate sensitivity to BTSA1.

228 This work regulates several key variables of PbS NC assembly (e.g.

229 Btk has been demonstrated to regulate signaling downstream of the B-cell receptor (BC

230 Additionally, miR-124 regulates Smed-slit-1, which encodes an axon guidance pr

231 tant organs with different time kinetics and regulate spatiotemporal tumour plasticity.

232 results demonstrate how sensory information regulates state-dependent reflexes in the lower urinary

233 m has been emerged as signaling molecules to regulate stem cell behaviors such as migration.

234 ndings of the compounds' unique abilities to regulate stem cell fate provides opportunities for devel

235 However, the mechanisms that regulate stem cell fates under such widely varying condi

236 The cell surface receptor CD6 regulates T cell activation in both activating and inhib

237 However, the interplay of factors regulating target selectivity is not well understood and

238 eterodimer that protects chromosome ends and regulates telomerase-mediated telomere extension.

239 the structure as a thermostat that uniformly regulates thalamic activity through negative feedback.

240 in olfactory bulb (MOB), inhibitory circuits regulate the activity of principal cells precisely to dr

241 sulting in downstream activation of STAT3 to regulate the balance between IL-12/IL-23 subunits causin

242 wever, it remained unclear how cryptochromes regulate the BIC gene activity.

243 ls and the mechanisms by which these signals regulate the disruption of avascular privilege in photor

244 In addition, we verified miR-449b could regulate the expression levels of CDK6, c-MYC, HDAC1 and

245 These miRNAs were found to regulate the expression of the proapoptotic Bcl-2 protei

246 lational modifications have been reported to regulate the function of epidermal growth factor recepto

247 odification and ubiquitin-proteasome systems regulate the major events of meiotic prophase in mouse.

248 Multiple protein complexes regulate the Rag GTPases in response to amino acids, inc

249 How GABAergic interneurons regulate the segregation and communication among intermi

250 on: Is there an optimal feedback strategy to regulate the synthesis of a protein to ensure that an ev

251 gi of hair cells, suggesting that Tomt might regulate the trafficking of other MET components to the

252 proposed to function downstream of mTORC1 to regulate the translation of 5'TOP mRNAs such as those en

253 NS is well recognized, how these progenitors regulate the vasculature outside the CNS remains largely

254 While microRNAs (miRNAs) regulate the vast majority of protein-encoding transcrip

255 Our findings suggest that AMPK regulates the activity of the chromatin modifying COMPAS

256 tors at specific region of the cell; it also regulates the activity of these receptors.

257 hosphorylation provide a phospho-switch that regulates the cellular activity of ATG4B to control LC3

258 Our findings reveal how UTX regulates the development of iNKT cells through multiple

259 ether the microtubule-associated protein tau regulates the differentiation and survival of mDANs duri

260 s, RRM1 and RRM2, and post-transcriptionally regulates the fate of target RNAs.

261 difying enzyme histone deacetylase 3 (Hdac3) regulates the formation of both lymphovenous valves, whi

262 ecifically, we found that GnT-III expression regulates the levels and activation of the heavily glyco

263 l migration.Adenomatous polyposis coli (APC) regulates the localization of some mRNAs at cellular pro

264 that PTH1R signaling directly and indirectly regulates the paracellular Ca(2+) transport pathway by m

265 horylation by calcineurin, PKCbeta1, and p38 regulates the transition to differentiation.

266 the physiological role of the type-B ARRs in regulating the cytokinin response, mechanism of type-B A

267 t endogenous GDNF plays an important role in regulating the function of dopamine transporters in the

268 Kv1.3, regulating the membrane potential, facilitates downstrea

269 otic spindle into a polar body by negatively regulating the rho pathway rather than through direct in

270 hedral capsids of specific size and shape by regulating the spatial arrangement of the hexameric and

271 of Nt17 post-translational modifications in regulating the structure and aggregation of Httex1 and s

272 By regulating the thermal-pyrolysis temperature and ratio o

273 Molecular mechanisms that shape and regulate their expression profiles are largely unknown.

274 s interact with other cell types to actively regulate their extracellular environments for tissue mai

275 ic regulatory T cells directly or indirectly regulate their influx by altering the chemotactic milieu

276 tes to produce proinflammatory cytokines, up-regulated their C5aR and FcRIII expression, and released

277 a-related protein 1 (LARP1) binds TOP mRNAs, regulating their stability and translation.

278 ative pathway proteins or the molecules that regulate this pathway were detected in 71% of the women,

279 f integrin tension was shown to be spatially regulated through two myosin-signaling pathways, myosin

280 However, the role of this gradient in regulating tissue size is a topic of intense debate as p

281 n of the promoter and 5'-UTR of the androgen-regulated TMPRSS2 (transmembrane protease, serine 2) gen

282 o ask questions about how these cells can be regulated to mitigate the collateral destruction associa

283 d that ECONEXIN is a potential oncogene that regulates TOP2A by sponging miR-411-5p in glioma.

284 sition of mRNAs can alter gene expression by regulating transcript localization, stability and/or tra

285 The epigenetic mechanisms that (dys)regulate transcription of Dlg4/PSD95, or other plasticit

286 RXRA regulates transcription as part of a heterodimer with 14

287 H2AZ regulates transcriptional activation as well as the main

288 ce of context-specific H3K4 methylation that regulates transcriptional outputs during ESC pluripotenc

289 Codon optimality has been shown to regulate translation elongation speed in fungal systems,

290 cts the morphology of the fusion product and regulates transporter protein degradation.

291 Thus, GCK-dependent glycolysis regulates Treg cell migration.

292 e SLCF-mediated apnea and bradycardia via up-regulating TRPV1 expression and excitation of laryngeal

293 LL-associated factor 2 (EAF2) is an androgen-regulated tumor suppressor and its intracellular localiz

294 croarray analysis C-82 treatment strongly up-regulated two clusters of genes that correlate negativel

295 ontrol of West Nile virus (WNV) infection by regulating type I IFN (IFN-I) response.

296 Hydrogen sulfide (H2S) regulates various physiological processes, including neu

297 f the transmembrane receptor NOTCH1 directly regulates vascular barrier function through a non-canoni

298 s in the extracellular matrix can direct and regulate vaspin interaction with target proteases or oth

299 g reports about whether it plays any role in regulating viral lytic reactivation.

300 ins with the small modifier, ubiquitin (Ub), regulates virtually every known cellular process in euka