ライフサイエンスコーパス: be regulated by

1 Lipid droplet (LD) functions are regulated by a complement of integral and peripheral

2 Mitochondrial dynamics are regulated by a complex system of proteins representi

3 riptomic analysis identified other RNAs that are regulated by a similar mechanism.

4 t al. (2017) demonstrate that Id2 expression is regulated by a cell type-specific cis-regulatory elem

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

6 Finally, we show that ligand exchange is regulated by a checkpoint mechanism, an apparent prer

7 Transcript co-expression is regulated by a combination of shared genetic and envi

8 The gene is regulated by a combination of TFs in close proximity.

9 an transcriptional response to high salinity is regulated by a core set of pCREs and provide a genome

10 namic, oriented cell intercalation during CE is regulated by a group of core proteins identified orig

11 gated beta-barrel channels in which opening is regulated by a helical plug connected to an extended

12 ling and genome editing revealed that AMIGO2 is regulated by a melanoma-specific BRD2/4-bound promote

13 The Escherichia coli lac operon is regulated by a positive feedback loop whose potential

14 ematode Caenorhabditis elegans, this process is regulated by a thermosensitive membrane TRP channel a

15 the fission yeast Schizosaccharomyces pombe is regulated by a third strategy: the size-dependent exp

16 man toxoplasmosis), and other protists, Skp1 is regulated by a unique pentasaccharide attached to hyd

17 Plasmodesmal flux is regulated by a variety of environmental cues but the

18 This process hinders VZV and is regulated by a viral glycoprotein, gB.

19 pothesized that the levels of ESX substrates were regulated by a feedback-control mechanism, linking

20 istent with a model in which IQGAP1 cleavage is regulated by acetylation of the cleavage sites.

21 er, we hypothesized that Brg1 activity might be regulated by additional kinases.

22 integration of miRNAs into the Ago complexes is regulated by additional mechanisms.

23 immune cells to the aorta in atherosclerosis is regulated by adhesion molecules, chemokines and cytok

24 urce specific aspects of their morphology to be regulated by adjacent body parts or organs.

25 feration of pre-existing cardiomyocytes, and is regulated by aerobic-respiration-mediated oxidative D

26 We hypothesize that slincR is regulated by AHR2 and transcriptionally represses sox

27 the chemotactic response towards As(III) and is regulated by AioR.

28 idence that the initiation of TH 2 responses is regulated by airway epithelial cell-derived factors,

29 Furthermore, the PP2Cs HAI1 to HAI3 were regulated by all RCARs, and the ABA receptor RCAR4/

30 expression during erythroid differentiation is regulated by alternative pre-mRNA splicing.

31 PTK7 as an AMIGO2 interactor whose function is regulated by AMIGO2.

32 Thus, multiple cellular events that are regulated by an array of signaling molecules and pat

33 in other differentiated tissues, and that it is regulated by an alternative promoter whose activity i

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

35 -bond dynamics of the D-channel residue N139 is regulated by an interplay of protonation in the D-cha

36 Integrin binding is regulated by an intramolecular interaction between th

37 DSCs, suggesting that the expression of iNOS is regulated by an IRF8-independent mechanism under path

38 ed that mycobacterial cell-cycle progression is regulated by an unprecedented mechanism involving par

39 ce, we found that IL-10 induction in B cells was regulated by an ERK1/2- and p90 ribosomal S6 kinase-

40 indings suggest that the expression of AURKA is regulated by androgen in prostate cancer cells that h

41 lyses suggested that Aurora kinase A (AURKA) is regulated by androgens in prostate cancer cells that

42 tor cells than in memory precursor cells and was regulated by antigenic stimulation and signals from

43 cretion in type A intercalated cells (A-ICs) is regulated by apical vesicle recycling and stimulated

44 nhances kinetochore-microtubule coupling and is regulated by Aurora B kinase.

45 partite interaction, each component of which is regulated by Aurora B kinase.

46 that the stability of kinetochore attachment is regulated by Aurora B/Ipl1 kinase and this regulation

47 The Ska complex regulates, and is regulated by, Aurora B [13].

48 Furthermore, FOF2 mRNA expression is regulated by autonomous pathway gene FCA, and the rep

49 ed lipid content in these cells, which could be regulated by autophagy.

50 stricted promoter activity in galls/GCs that was regulated by auxins through auxin-responsive factors

51 Starvation-induced autophagy, which is regulated by beclin 1, was particularly inhibited in

52 rientation within the tumor microenvironment is regulated by beta2-adrenergic receptor (beta-AR) sign

53 s protein clients and its chaperone function are regulated by binding of ATP/ADP to mtHsp70's nucleot

54 WNK4 levels are regulated by binding to Kelch-like 3, targeting WNK4

55 in large-for-gestational age infants and may be regulated by BMAL1.

56 hese damaged telomeres is interdependent and is regulated by both ATR and Chk1.

57 origin and expansion of biological diversity is regulated by both developmental trajectories and limi

58 strongly dependent on glucose abundance and is regulated by both glucose-sensing pathways, ATP is la

59 t that insulin secretion in pancreatic cells is regulated by Ca(2+) and ROS signaling through Ca(2+)-

60 eEF-2K is regulated by Ca(2+) ions and multiple upstream signal

61 ility assays to demonstrate that the carrier is regulated by calcium via a locking pin mechanism invo

62 ubiquitin ligase and reveal that the enzyme is regulated by calmodulin.

63 studies to search for potential factors that are regulated by caloric restriction and act as caloric

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

65 severe, enhanced Th2-mediated AAD, which can be regulated by CD8(+) T cells.

66 To identify genes likely to be regulated by CDX2 directly, we performed CDX2 ChIP-Se

67 port that the piRNA biogenesis in BmN4 cells is regulated by cell density.

68 Multifunctionality resistance was regulated by changes in microbial composition (relat

69 The activity of the colon is regulated by chemical signaling, of which serotonin (

70 reveals a mechanism that the Warburg effect is regulated by CHIP through its function as an E3 ligas

71 complex substrate and that their interaction is regulated by CK2 phosphorylation.

72 ng vesicle fusion or fission, processes that are regulated by coat proteins.

73 predicts that many of the dysregulated genes are regulated by common transcription factors, one of wh

74 sized that GSs from the same cancer type may be regulated by common regulatory motifs.

75 whose activities and substrate specificities are regulated by complex co-factors.

76 the communication between EpAT and the heart is regulated by complex bidirectional pathways, since no

77 lism-driven extracellular volume control and is regulated by concerted liver, muscle, and renal actio

78 Animal lifespan is regulated by conserved metabolic signalling pathways

79 s a discrete global brain activity mode that is regulated by context-dependent neuromodulators and ac

80 We found that SNF1 activity in the nucleus is regulated by controlled relocalization of the SNF1 ac

81 idney, tissue-specific beta-catenin activity is regulated by cooperation with cell type-specific tran

82 fic for several genes previously reported to be regulated by CR: Fmo3, Mup4, Serpina12 and Cyp4a12, w

83 Igf-1 expression is regulated by CR and by the circadian clock, we found

84 , we propose that the proliferation of CySCs are regulated by crowdedness, or confluency, of cells in

85 Here we show that PD-L1 protein abundance is regulated by cyclin D-CDK4 and the cullin 3-SPOP E3 l

86 Altogether, we show that LAMP2A trafficking is regulated by cystinosin, Rab11, and RILP and that CMA

87 Thus, flux through the CIA pathway can be regulated by degradation of the substrate-specifying

88 esis and cell expansion can be uncoupled and are regulated by different mechanisms.

89 ch biological outcomes of caspase activation are regulated by differential amplification of IAP antag

90 ll as RNA selectivity in granule composition are regulated by distinct concentration regimes of A2.

91 phosphorylation-dependent force development is regulated by distinct signalling modules involving pr

92 main potassium (K2P) channel ion conductance is regulated by diverse stimuli that directly or indirec

93 Here we report that APE2 resection activity is regulated by DNA interactions in its Zf-GRF domain, a

94 V) latency and its associated carcinogenesis are regulated by dynamic changes in DNA methylation of b

95 rt that traction forces generated by T cells are regulated by dynamic microtubules (MTs) at the inter

96 of how food intake behavior and body weight are regulated by endogenous central GLP-1.

97 Moreover, this pathway is regulated by endogenous cGMP/PKG2 signaling, and can

98 BRI1 abundance is regulated by endosomal recycling and vacuolar targeti

99 c metabolism, as well as how ILC biology can be regulated by environmental changes in host metabolism

100 wth factor 8 (Fgf8) in the HAA anlage, which was regulated by enzymes that degrade retinoic acid (RA)

101 infected primary human cultures from trachea were regulated by epithelial-specific ets homologous fac

102 This sex difference may be regulated by estrogens, such as estradiol, that are s

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

104 Endogenous CaCCs are regulated by extracellular protons; however, the mol

105 nels that mediate electrogenic ion transport are regulated by extracellular purinergic signals that s

106 surface delivery of newly synthesized GPCRs is regulated by extracellular signals is less understood

107 Developmental responses to auxin are regulated by facilitated uptake and efflux, but deta

108 We found that plasma uridine levels are regulated by fasting and refeeding in mice, rats, an

109 ical properties imparted to plasma membranes are regulated by fatty acid chain profiles.

110 , indicating that human molecular clocks may be regulated by feeding time and could underpin plasma g

111 dicate that unlike lung IL2Cs, uterine ILC2s are regulated by female sex hormones, which may speciali

112 tyrosine phosphorylation, which is known to be regulated by focal adhesion kinase (FAK).

113 Although this process is known to be regulated by follicular helper T (TfH) cells, the mec

114 n of a considerable number of these circRNAs is regulated by FUS.

115 ynaptic transmission at cone ribbon synapses is regulated by Gbetagamma/SNAP-25 interactions indicate

116 ntain physiological NADPH homeostasis, which is regulated by glucose-6-phosphate dehydrogenase and AM

117 gether, our data suggest that FGFs/FGFRs can be regulated by glutamate transmission to modulate/stabi

118 nd CD8(+) T cells in type 1 conditions (Th1) were regulated by glutamine and alpha-ketoglutarate (alp

119 Pituitary gonadotropin hormones are regulated by gonadotropin-releasing hormone (GnRH) v

120 ciferins, major seed storage proteins, which were regulated by Group VII Ethylene Response Factor (ER

121 howed that fear expression, but not anxiety, is regulated by GRs in glutamatergic neurons of the BLA.

122 endothelial cells, as a critical factor that is regulated by gut microbiota and determines thrombus g

123 l differentiation, such as JAK2 and IL12RB2, are regulated by H3K27me3.

124 anism for Smo activation by sumoylation that is regulated by Hh and Smo interacting proteins.

125 Pathway analyses revealed that the signature was regulated by HIF1alpha and TP53 and included nine HI

126 n of Adipoq during adipocyte differentiation is regulated by histone acetylation and the binding prot

127 However, how VP35 function is regulated by host cellular factors is poorly understo

128 he rate constant for the polymerization step is regulated by hydrogen-bonding interactions made betwe

129 Many angiogenic growth factors are regulated by hypoxia-inducible factor, and hypoxia-i

130 Also, fewer proteins were regulated by hypoxia in neutrophils from AMPKalpha2

131 The activity of IL-22 is regulated by IL-22 binding protein (IL-22BP); however

132 role in these cells and how these cells can be regulated by individual physiologic stimuli.

133 e results we suggest that ZIKV transcription is regulated by inflammasomes.

134 To date every identified ArsR is regulated by inorganic As(III).

135 The growth phase dependent transcription was regulated by Integration Host Factor (IHF), which bo

136 adhesion, motility, and rigidity adaptation are regulated by integrin-mediated adhesion to the extra

137 In mice, we found TICE to be regulated by intestinal FXR via induction of its targ

138 ely, nuclear volume and its gross morphology are regulated by intracellular outward pulling forces ex

139 subtle changes in the structure of CFTR that are regulated by intracellular pH, in part, at ATP-bindi

140 Insulin exocytosis is regulated by ion channels that control excitability a

141 ing movement, and we show that this activity is regulated by Ipl1/Aurora B phosphorylation during cel

142 und that the nuclear localization of Gene 33 is regulated by its 14-3-3-binding domain and that the c

143 rmal growth factor receptor (EGFR) signaling is regulated by its accumulation within CCPs.

144 ease of Ca via the ryanodine receptor, which is regulated by its interacting proteins junctin and tri

145 BiP's activity is regulated by its intrinsic ATPase activity that can b

146 This enzyme is regulated by its movement from a soluble form (largel

147 y JAK2 knockdown, we questioned whether TFEB is regulated by JAK2.

148 ression of IL-10 and TIMP-3 in CD146(+) TSCs are regulated by JNK/signal transducer and activator of

149 ylation levels at histone H3 lysine 4 (H3K4) is regulated by KDM1A (LSD1).

150 Reuptake is regulated by kinase pathways and drug exposure, allow

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

152 extent to which a chloroplast target of SIG5 is regulated by light-induced changes in SIG5 expression

153 Interestingly, FOF2 expression is regulated by light.

154 he nucleus and cytoplasm by a mechanism that is regulated by lipotoxic and oxidative stress.

155 es whose biogenesis, structure, and function are regulated by many signaling pathways.

156 ncreasingly clear that start codon selection is regulated by many trans-acting initiation factors as

157 This transcriptional program is regulated by many transcription factors (TFs).

158 the activity of the TNFR2/TRAF1 pathway that is regulated by MAVS signaling.

159 dation to dissect further how Piezo channels are regulated by mechanical force.

160 h markedly increases its affinity for IGF-I, is regulated by mechanistic target of rapamycin (mTOR) a

161 that specific limbs of the immune system can be regulated by microbiota in a time-restricted period d

162 Moreover, metastasis is regulated by microenvironmental and systemic processe

163 e demonstrate that ILC2s and IL-33 signaling are regulated by miR-155 in allergic airway inflammation

164 , we were interested in other genes that may be regulated by miR-15/16, which may target other driver

165 and Idh2p were assessed because their levels are regulated by mitochondria.

166 and then cytoplasmic sites in a manner that is regulated by molecular chaperones and requires TORC1

167 with each other and with MAD2 conformers and are regulated by MPS1 kinase, providing critical insight

168 synthase kinase 3 (GSK3) MoGSK1 in M. oryzae is regulated by Mps1 MAP kinase, particularly under the

169 ic behavior and organization of the MT array is regulated by MT-associated proteins (MAPs), which inc

170 Tfh-Teff cell fate commitment is regulated by mutual antagonism between the transcript

171 This process is regulated by mutually antagonistic signals: Notch sig

172 size, connectivity, spacing, and orientation are regulated by myosin activity.

173 f CSB-mediated chromatin remodeling that can be regulated by NAP1L1.

174 RNA polymerase activity is regulated by nascent RNA sequences, DNA template sequ

175 However, the molecular mechanisms that are regulated by NECL4 and affect peripheral myelination

176 l cell population and in mammary tumors, and is regulated by NF-kappaB signaling.

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

178 Ascl2 expression is regulated by Notch signaling, a key governor of satel

179 models, that is that inflorescence branching is regulated by novel localized signaling centers.

180 ding Wiskott-Aldrich syndrome protein (WASp) were regulated by NPM-ALK.

181 lity as an origin of genome instability that is regulated by nuclear architecture and mirrors mutagen

182 eabsorption in the distal kidney nephron and is regulated by numerous hormones, including the mineral

183 as a transcriptional factor and its activity is regulated by numerous post-translational modification

184 promotes ILC2 responses, how ILC2 responses are regulated by other stimuli remains poorly understood

185 diator complex and the activity of Cdk8-CycC is regulated by other Mediator components.

186 However, it is not clear whether Smo is regulated by other post-translational modifications,

187 Other RTKs have been reported to bind, and be regulated by, over-expressed SOCS proteins.

188 ting that the protein stability of HIPK2 can be regulated by p300-mediated acetylation.

189 Trafficking of myomaker is regulated by palmitoylation of C-terminal cysteine re

190 hat CAIII is highly expressed in osteocytes, is regulated by parathyroid hormone both in vitro and in

191 Deficiency in pGP3 alone, which is regulated by pGP4, largely reproduced the in vivo but

192 CSR and SHM are regulated by phosphorylation on AID serine38 (pS38),

193 hened (Smo) acts as a signal transducer that is regulated by phosphorylation and ubiquitination, whic

194 At-NPF6.3 imports and senses nitrate and is regulated by phosphorylation at Thr-101 (T101).

195 exocytosis and endocytosis, which can often be regulated by physiological stimuli.

196 PDR1 expression is regulated by phytohormones and by the soil phosphate

197 tress conditions, wild-type Sec3 degradation is regulated by Pib1 and the 26S proteasome.

198 Rs are laid down during their biogenesis and are regulated by post-transcriptional RNA editing, splic

199 nt on the AMPA receptor subunit GluA4, which is regulated by presynaptic expression of the synaptogen

200 This process is regulated by proapoptotic and prosurvival members of

201 We found that 15 microRNAs (miRNAs) are regulated by progesterone via PR-A, but not the long

202 C and showed that SCARF-1 expression by HSEC is regulated by proinflammatory cytokines and bacterial

203 in part by PID1, involves NFkappaB, and may be regulated by proteasomal degradation.

204 In contrast, Cdr2-T166 phosphorylation is regulated by protein phosphatase 2A but not by the Sd

205 or protein homologous to mammalian RIP1 that is regulated by proteolytic cleavage and Lys-63-polyubiq

206 t approximately 15 kDa (PEA15), and its mRNA are regulated by PS1/gamma-secretase.

207 CB, and UL16-binding protein 2 were shown to be regulated by RBPs and microRNAs, usually resulting in

208 ptosis is a form of programmed necrosis that is regulated by receptor-interacting protein kinases (RI

209 s, cornea anteriorly and sclera posteriorly, are regulated by region-specific molecular mechanism rem

210 idocaldarius, biosynthesis of the archaellum is regulated by regulatory network proteins that control

211 iating the idea that global species richness is regulated by resource availability.

212 Intracellular polyamine metabolism is regulated by reversible acetylation and dysregulated

213 Of importance, both pathways are regulated by Rho/myocardin-related transcription fac

214 lation but not SM myosin RLC phosphorylation is regulated by RhoA GTPase during ACh stimulation, and

215 Gene expression in metazoans is regulated by RNA polymerase II (Pol II) promoter-prox

216 nduced proinflammatory endothelial responses are regulated by rosuvastatin in a mechanism that appear

217 erythroleukemia cells, indicating that PCTP is regulated by RUNX1.

218 al and cellular N-myristoylated proteins can be regulated by selectively sequestering myristate.

219 While TbetaRII targeting was shown to be regulated by sequences between amino acids 529 and 53

220 ar distribution and dynamics of mitochondria are regulated by several motor proteins and a microtubul

221 Dim-light vision is regulated by several adaptive mechanisms.

222 ed to sex chromosomes themselves or found to be regulated by sex chromosome genes.

223 ed a subset of Forkhead box (Fox) genes that are regulated by Shh signaling during lip morphogenesis.

224 elative proportions of red and far red light was regulated by SIG5 through phytochrome and photosynth

225 The stability of mRNAs is regulated by signals within their sequences, but a sy

226 ved melanoblasts in turtle Trachemys scripta is regulated by similar mechanisms as in other amniotes,

227 to form the new Golgi and that this process is regulated by small GTPases.

228 ctivated transcription factor whose activity is regulated by small molecules provided by diet, commen

229 s and mice to show that IFN-lambda signaling is regulated by SOCS1 but not by SOCS3 or USP18.

230 Here the authors show that this process is regulated by SOCS3 via a mechanism dependent on IL-6

231 expression of Dct, Tyrp1 and Tyr, genes that are regulated by SOX10 and MITF and for chromatin remode

232 f the functional pools of cAMP/PKA/EPAC that are regulated by specific cAMP-PDEs (the PDE-regulated p

233 We have also shown that NKG2D transcription is regulated by STAT3 phosphorylation.

234 the central output controlling fertility and are regulated by steroid feedback.

235 indicate that SOCE and KATP channel activity are regulated by STIM1.

236 The paradigm protein synthesis rate is regulated by structural complexity of the 5'untransla

237 hese data indicate the position of lysosomes is regulated by synaptic activity and thus plays an inst

238 documented; however, whether the transporter is regulated by synaptic inhibition is unknown.

239 e further provided evidence that these genes are regulated by T3 and likely involved in the T3-induce

240 t may facilitate understanding diseases that are regulated by TFs.

241 l timing that take place in the striatum and are regulated by the amygdala.

242 e anaerobic respiratory genes, many of which are regulated by the anaerobic transcriptional regulator

243 Two MAF1 species, MAF1L and MAF1S, are regulated by the C-box YSY motif, which, when mutate

244 nslational acetylation modification of CREBH are regulated by the circadian clock.

245 iron export from the tissues into the plasma are regulated by the liver-derived peptide hepcidin.

246 l guanosine triphosphatases (GTPases), which are regulated by the opposing actions of guanine nucleot

247 ell proliferation and migration are known to be regulated by the Notch receptor, which plays an essen

248 GTA production can be regulated by the producing organism and coordinated t

249 ess1 mutant, suggesting that these genes may be regulated by the tasiRNA pathway.

250 Rev's shuttling into and out of the nucleus is regulated by the antagonistic activities of both a pe

251 es polarized NC morphology and motility, and is regulated by the asymmetrically localized RhoGAP Dele

252 Iron entry into the brain is regulated by the blood-brain barrier (BBB).

253 it from the galaxy, and the gas infall rate is regulated by the brightness of the active galactic nu

254 The role of TopBP1 in host DNA replication is regulated by the class III deacetylase SIRT1; activat

255 In animal cells, spindle orientation is regulated by the conserved Galphai-LGN-NuMA complex,

256 It is regulated by the counter-activities of protein tyrosi

257 marker, whose mRNA stability and translation is regulated by the CUG-binding protein 2 interacting wi

258 Here we report that Ets-1 destruction is regulated by the deubiquitinating enzyme, Usp9x, and

259 Here we report that the stability of ARTs is regulated by the deubiquitinating enzymes (DUBs) Ubp2

260 echanism in developing mammalian hearts that is regulated by the dynamic interaction of DNMT3B-mediat

261 is expressed in embryonic mammary glands and is regulated by the Eda pathway.

262 that odorant responsiveness and OR transport is regulated by the Hedgehog pathway.

263 ER stress-induced apoptosis is regulated by the highly labile and ER-associated BCL-

264 This immune response process is regulated by the major histocompatibility complex (MH

265 , we reveal that the breast epithelial clock is regulated by the mechano-chemical stiffness of the ce

266 VWF is regulated by the metalloprotease ADAMTS13, which in t

267 gan-boundary intestinal stem cells (OB-ISCs) is regulated by the neighboring hindgut, a developmental

268 inding to dynein and that this stoichiometry is regulated by the nucleotide state of dynein's AAA3 do

269 The activity of CPR-4 is regulated by the p53 homologue CEP-1 in response to r

270 hanism of DENND3 intramolecular binding that is regulated by the phosphorylation of a single tyrosine

271 The signal-mediated pathway is regulated by the phosphorylation of the DXXLL-motif s

272 nt of symbiotic nitrogen-fixation in legumes is regulated by the plant hormone ethylene, but it has r

273 rker FoxA1 by promoter-methylation, and that is regulated by the Plk1 phosphorylation sites in FoxM1b

274 of Ubiquitin-conjugating enzyme E2S (UBE2S) is regulated by the PTEN/Akt pathway and that its degrad

275 her show MT depolymerization within biofilms is regulated by the SrbA hypoxic transcription factor an

276 ned unclear whether and how its biosynthesis is regulated by the symbiotic pathway.

277 Brown adipose tissue (BAT) is regulated by the sympathetic nervous system via beta3

278 Here we show that FDH abundance is regulated by the ubiquitin proteasome system (UPS).

279 opeptide antibiotics in clinical enterococci is regulated by the VanSARA two-component signal transdu

280 entre called the zone of polarizing activity is regulated by the ZRS enhancer.

281 endent delayed induction of GluA1 (24 hours) was regulated by the activation of CaMKII.

282 TKS5 overexpression was regulated by the intracellular metabolic environment

283 TBC1D23 localized at the trans-Golgi and was regulated by the small GTPases Arl1 and Arl8, sugges

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

285 iological age and sex-hormone regulation and was regulated by the transcription factor VGLL3, which a

286 The functions of glycoproteins are regulated by their dynamics to adapt the ever-changi

287 brane localization of SK2 (KCa 2.2) channels is regulated by their interacting proteins.

288 pproaches identified potential pathways that are regulated by these miRNAs.

289 e-specific strain-biased gene expression may be regulated by tissue-specific enhancers or by post-tra

290 How NLRP3 activation is regulated by transcriptional and posttranslational me

291 Glutamatergic receptor expression is regulated by tropomyosin-related kinase receptor subt

292 metabolic pathways previously established to be regulated by Trxs.

293 melanogaster, where gap genes were found to be regulated by two nonredundant "shadow" enhancers.

294 Ammonium assimilation in Escherichia coli is regulated by two paralogous proteins (GlnB and GlnK),

295 Its binding to mRNA is regulated by tyrosine 396 phosphorylation, and this p

296 6 is an E2 ubiquitin-conjugating enzyme that is regulated by USP7.

297 Floral initiation is regulated by various genetic pathways in response to

298 Thus, sprout anastomosis parameters are regulated by VEGFA signaling, and stable connections

299 the cellular response, which in gnathostomes is regulated by von Willebrand factor (VWF), a glycoprot

300 knowledge on how the collaborative features are regulated by workers' activities because we lack met