ライフサイエンスコーパス: be regulated by

1 Biofilm formation is regulated by 3',5'-cyclic diguanylate (c-di-GMP) and

2 sity and central specificity of pSNs and MNs are regulated by a common set of determinants, thus link

3 aling in endothelial cells (ECs), where they are regulated by a novel TNF-alpha-responsive microRNA,

4 sly showed that two such genes, wg and Wnt6, are regulated by a single damage-responsive enhancer tha

5 gesting that multiple justice intuitions may be regulated by a common social-evaluative psychology.

6 transport activity of ABCB1 was suggested to be regulated by a physical interaction with FKBP42/Twist

7 Moreover, we show that CDC48 at the INM may be regulated by a subgroup of PUX proteins, which determ

8 that basal stem/progenitor cell maintenance is regulated by a balance between BMP5 self-renewal sign

9 The connectivity of mitochondria is regulated by a balance between fusion and division.

10 We find that shape change is regulated by a beta-catenin-mediated decrease in RhoA

11 This is regulated by a brainstem reflex pathway.

12 arasite Plasmodium falciparum Its life cycle is regulated by a cGMP-dependent protein kinase (PfPKG),

13 Here, we report that insulin secretion is regulated by a circular RNA containing the lariat seq

14 t in the brain of suicide completers, MAALIN is regulated by a combination of epigenetic mechanisms i

15 the specificity for longer chain fatty acids is regulated by a conformational change in the C-termina

16 Nuclear gene expression is regulated by a diversity of retrograde signals that t

17 The switch between these roles is regulated by a DNA sequence called Chi.

18 he SMP domain, while the size of formed MLOs is regulated by a domain predicted to engage in protein

19 Activity of mtHsp70 is regulated by a heterodimeric complex of two J-domain

20 Eukaryotic gene transcription is regulated by a large cohort of chromatin-associated p

21 However, whether this protein interaction is regulated by a mechanism other than the abundance of

22 We show here that the SMPD1 gene is regulated by a microRNA (miR), miR-15a, in endothelia

23 Vascular stem cell maintenance is regulated by a peptide signaling involving Tracheary

24 ansduction channel and that channel function is regulated by a phospholipid-sensing domain in TMIE wi

25 pends primarily on microtubule number, which is regulated by a reaction-diffusion system when cells a

26 IL-17R, we established that IL-17 signaling is regulated by a robust negative feedback loop mediated

27 organelles and their progenitor prokaryotes is regulated by a series of proteases including the case

28 eudomonas aeruginosa, expression of the T3SS is regulated by a signaling cascade involving the protei

29 Hsp70 is regulated by a suite of co-chaperone molecules that b

30 The ABC galactose transport system is regulated by a three-component sensing system.

31 bservations, we propose that shade avoidance is regulated by a three-layered gas-and-brake mechanism

32 The expression of emhABC was regulated by a TetR-family transcription factor EmhR

33 d that the expression of GATA6-AS1 and GATA6 were regulated by a bidirectional promoter within the in

34 Filaments are regulated by actin-binding proteins, but the nucleot

35 ts/regulators to inhibit YAP, a process that is regulated by actin cytoskeleton tension.

36 Gene transcription by RNA polymerase II is regulated by activator proteins that recruit the coac

37 hereas others are ubiquitously expressed but are regulated by AD risk variants within myeloid enhance

38 y, astrocyte-induced DMS neuronal activities are regulated by adenosine metabolism, receptor signalin

39 RNA editing, a fundamental RNA modification, is regulated by adenosine deaminase (AD) domain containi

40 A myriad of cellular events are regulated by allostery; therefore, evolution of this

41 tivity required for mitotic error correction is regulated by alpha-tubulin detyrosination remains unk

42 dimer reveals how the activity of plant CRYs is regulated by alternative protein-protein interactions

43 that Rho/ROCK and actinomyosin contractility are regulated by AMP/ATP levels independently of AMPK, a

44 orylation occurs in the absence of PINK1 and is regulated by AMPK-dependent signaling.

45 Their endogenous levels are regulated by an extracellular mammalian N-acyl amino

46 We show that AWC(ON) sensory activity is regulated by an absolute signal threshold that contin

47 al transition to a sparse conformation which is regulated by an alpha-helical capping "switch" at the

48 PDCD4 mRNA translation is regulated by an interplay between the oncogenic micro

49 Purine nucleotide levels are regulated by anabolic processes and by nucleotidases

50 Further, as the title suggests, the KP is regulated by, and in turn regulates multiple other ph

51 miRNA that controls neuronal gene expression is regulated by antipsychotics.

52 within the late transcript of the phage and are regulated by antitermination of the P(R') late promo

53 ect sequencing (ChIP-seq), we show that CA12 is regulated by AP-2gamma through binding with its promo

54 the magnitude of the DR-cell population may be regulated by apoptosis.

55 The activity of many enzymes is regulated by associative processes.

56 "Closing" of dimers around clients is regulated by ATP binding, co-chaperones, and post-tra

57 ression and chromatin loading of PRIMPOL and is regulated by ATR activity.

58 These cells are regulated by autocrine signaling by parathyroid horm

59 Human dynein is regulated by autoinhibition, whereby intermolecular c

60 To identify genes that might be regulated by AW112010, we used chromatin isolation by

61 The surface receptor abundance is regulated by background signal-dependent receptor end

62 Apoptosis is regulated by BCL-2 family proteins.

63 However, whether BCR signaling is regulated by BCR mobility, and what factors mediate t

64 The interaction of dynein with dynactin is regulated by binding between the intermediate chain (

65 RGS14 membrane localization is regulated by binding Galphai-GDP, whereas RGS14 nucle

66 Activity of these neurons is regulated by bodily sodium content, and their activat

67 n immune activation and disease presentation are regulated by both host genetic diversity and pathoge

68 RNA regulatory mechanism, 2) MyD88 splicing is regulated by both the MyD88- and TRIF-dependent arms

69 reas in B cells, NF-kappaB and MAPK pathways were regulated by both BTK and IRAK4.

70 ts plant height and biomass accumulation and is regulated by brassinosteroid signaling, auxin transpo

71 nal stem cell (ISC) plasticity is thought to be regulated by broadly permissive chromatin shared betw

72 tification of 90 new actinobacteria that may be regulated by butenolides, two of which are experiment

73 Here we show that RBOHD is regulated by C-terminal phosphorylation and ubiquitin

74 Importantly, these processes are regulated by Ca(2+) signals that occur at rest.

75 nature, these spontaneous fusion events can be regulated by Ca(2+) signaling pathways.

76 Striated muscle contraction is regulated by Ca(2+) -dependent modulation of myosin c

77 Glucose-stimulated insulin secretion (GSIS) is regulated by calcium (Ca(2+) ) entry into pancreatic

78 Mitochondrial bioenergetics is regulated by calcium uptake through the mitochondrial

79 opolysaccharide binding and S-layer assembly is regulated by calcium.

80 amate receptor subtype 5 (mGluR5) in the VMH is regulated by caloric status in normal mice and reduce

81 nduced signaling in the extracellular matrix is regulated by catalytic activity of matrix metalloprot

82 LPA-mediated mitochondrial homeostasis is regulated by CDK1-mediated SIRT3 phosphorylation, whi

83 Cell shape is regulated by cell adhesion and cytoskeletal and membr

84 abundance of a gap junction molecule, which is regulated by cell-autonomous function of the worm hom

85 with task engagement, which, in turn, could be regulated by chemogenetic excitation and inhibition.

86 t of leukocytes, a hallmark of inflammation, is regulated by chemokines, which activate chemokine rec

87 that expression of m(6)A demethylase ALKBH5 is regulated by chromatin state alteration during leukem

88 Glucagon secretion is regulated by circulating glucose, but it has turned o

89 onger checkpoint in germline precursor cells is regulated by CMT-1, the ortholog of p31(comet), which

90 of the voltage-gated KCNQ1 potassium channel is regulated by co-assembly with KCNE auxiliary subunits

91 Favored interactions within TADs are regulated by cohesin and CTCF through distinct mecha

92 re used to compete for limited resources and are regulated by complex sensory cues and the organism's

93 f coral holobionts, and how this functioning is regulated by complex doses and interactions among env

94 Heart valve development is regulated by complex interactions between different c

95 PKM2 is expressed in many human cancers and is regulated by complex mechanisms that promote tumor gr

96 le for synthesis of NO in endothelial cells, is regulated by complex posttranslational mechanisms.

97 In most streptococci, competence is regulated by ComRS signaling, a system based on the m

98 -associated herpesvirus (KSHV) transcription is regulated by CTCF and cohesin, with both proteins pre

99 This overwhelming immune response is regulated by damage-associated molecular patterns (DA

100 demonstrated that cotranslational mRNA decay is regulated by developmental cues.

101 enes in the model plant Arabidopsis thaliana are regulated by diel cycles via pathways independent of

102 Emerging evidence shows that Ca(v)1.2 is regulated by different mechanisms in cardiomyocytes c

103 This process is regulated by DNM2 binding to LC3 and is increased by

104 Here, we show that this process is regulated by E3 ubiquitin ligase RNF41 and define a n

105 xperiments, we concluded that hypoxia in IHs is regulated by EPAS1 (HIF-2alpha) instead of HIF-1alpha

106 the promoters and enhancer repertoires that are regulated by epigenetic mechanisms and transcription

107 A(250) groups, with 115 of them predicted to be regulated by estradiol and 57 associated with female

108 genes in loop ends associated with these SEs are regulated by estrogen.

109 loci in ~377 Mb super-enhancer regions that are regulated by evolutionarily conserved, well-position

110 ng Galphai-GDP, whereas RGS14 nuclear export is regulated by Exportin 1 (XPO1).

111 ell wall biosynthesis and how these pathways are regulated by external and internal cues.

112 these results suggest that NIPAL1 expression is regulated by extracellular magnesium and that down-re

113 activating cell-intrinsic mechanisms, which are regulated by extrinsic signal interactions.

114 erparts and that TERRA transcription in mice is regulated by factors others than Dnmt3b.

115 We found that expression of these genes was regulated by FOXM1 and/or p38 MAPK.

116 d inward rectifier potassium (GIRK) channels are regulated by G proteins and PIP(2).

117 Besides being regulated by G-protein-coupled receptors, the acti

118 was originally discovered in neutrophils and is regulated by G protein betagamma subunits and the lip

119 Many developmental processes in plants are regulated by GA hormones.

120 Proteasome function is regulated by gates derived from the termini of alpha-

121 Flowering is regulated by genes that respond to changing daylength

122 wever, it is not known whether cell motility is regulated by global or local inhibition of Rho activi

123 nsmission, and many other neuronal processes are regulated by glycans.

124 differentiation through Nrp-1 and Grn which are regulated by Gsalpha signaling.

125 sed in llgl1 morphants, whereas Notch, which is regulated by hemodynamic forces and participates in v

126 To investigate whether gastric BA changes were regulated by hepatic BA synthesis, C57BL/6J mice we

127 The transcriptional kinase activity of CDK7 is regulated by HER2, and by the receptor tyrosine kinas

128 Cell differentiation is regulated by HetR which activates the synthesis of it

129 ory domain and has recently been reported to be regulated by highly curved membranes.

130 a quarter of the IAV-induced splicing events are regulated by hnRNP K, a host protein required for ef

131 cellular copper (Cu) in eukaryotic organisms is regulated by homeostatic systems, which rely on the a

132 h, the exocrine scent glands express vvl and are regulated by Hox genes.

133 anscript (NICI) on chromosome 12p13.31 which is regulated by hypoxia via HIF-1 promoter-binding in mu

134 vealed 19 new cases of genes whose integrity is regulated by IGEs (including dut, eccCa1, gntT, hrpB,

135 We investigated microRNAs that are regulated by IL1B and their effects on expression of

136 Transcription of F3 was regulated by IL1beta, whose secretion decreased upon

137 Identification of specific miRs that are regulated by increasing load magnitude, as well as t

138 Biomineralization is regulated by inorganic pyrophosphate (PP(i)), a poten

139 on and scaling growth, and their mRNA levels are regulated by insulin receptor signaling.

140 INF2 is regulated by interaction between its N-terminal diaph

141 death can transpire via diverse pathways and is regulated by interactions with commensal and pathogen

142 Body weight is regulated by interoceptive neural circuits that track

143 , and uptake of immune cell-derived exosomes are regulated by intracellular proteins and extracellula

144 ISC function is regulated by intrinsic, local, and systemic stimuli t

145 ontributes to macrophage polarization, which is regulated by itchy E3 ubiquitin ligase (ITCH), a nega

146 d that the subcellular distribution of Hsp82 is regulated by its co-chaperone Ppt1.

147 cipation of DNA2 in these different pathways is regulated by its interactions with distinct groups of

148 the transcriptional coactivator beta-catenin is regulated by its phosphorylation in a complex that in

149 echanism, 2) indicate that transcription may be regulated by KAP1 abundance aside from canonical regu

150 nal movements of hexatopic ligand L(4) could be regulated by L(1) to promote the subsequent coordinat

151 n different organs revealed that SlBBX genes are regulated by light and their transcripts accumulatio

152 he mechanism by which plastid protein import is regulated by light during photomorphogenesis in Arabi

153 eases but also provide evidence that PTP may be regulated by LLPS that can be therapeutically targete

154 The relative weight of both pathways is regulated by local inhibitory interneurons.

155 yl hydrolase activity and that this activity is regulated by Lpg2505.

156 phosphorylation of Frizzled3 at T598 and can be regulated by LRRK2 in a kinase activity-dependent way

157 e expression levels of small GTPase proteins are regulated by m(6)A modulators.

158 al anodes and high voltage cathodes, and can be regulated by manipulating the solvation structure.

159 Microglial proliferation is regulated by many factors, but colony stimulating fac

160 nvestigated potential cellular pathways that are regulated by MDV U(S)3 and identified chicken CREB (

161 propose a revised model of how CDK8 activity is regulated by MED12, but also offer a path forward in

162 ry loci, monitored by promoter capture Hi-C, was regulated by metabolic status in distinct fashion de

163 ptic ion and metabolite channel, pannexin-1, is regulated by metabotropic NMDAR signaling through Src

164 nal villus structural and functional decline is regulated by mTORC1, a sensor of nutrients and growth

165 Muscle wasting and atrophy are regulated by multiple molecular processes, including

166 HSF1 is known to be regulated by multiple post-translational modification

167 ty of Cullin3 substrate adaptor protein BPM1 is regulated by multiple environmental cues pointing on

168 The catalytic activity of RNase J is regulated by multiple mechanisms which include oligom

169 Here, we show that IME1 transcription is regulated by multiple sequence-specific transcription

170 in tight association with increasing N/C and is regulated by N/C.

171 at ANKS6-NEK8 density within the compartment is regulated by NEK8.

172 of brain endothelial genes whose expression is regulated by neuronal activity.

173 body temperature as low as 20 degrees C(6), is regulated by neurons in the medial and lateral preopt

174 ry conditions undergo a metabolic shift that is regulated by NF-kappaB activation, leading to reprogr

175 fically inhibited synaptic plasticity, which is regulated by NFIA in astrocytes through calcium-depen

176 on (C) pools and plant community composition are regulated by nitrogen (N) and phosphorus (P) availab

177 transcription was observed in genes known to be regulated by NMD.

178 Microenvironments are regulated by noncovalent interactions, such as hydro

179 and neuronal differentiation of enteric glia are regulated by Notch signalling.

180 Moreover, APELIN expression is regulated by Notch signaling in human ECs, and its fu

181 Vascular smooth muscle cell (VSMC) function is regulated by Nox-derived reactive oxygen species (ROS

182 This process was regulated by nucleocytoskeletal connections, Par3 cl

183 ermore, the studies showed that the reaction is regulated by off-cycle acid-base and ligand exchange

184 ward system, in which GABA neurotransmission is regulated by opioid neuropeptides, including dynorphi

185 ltiple reports suggest that sirtuin activity is regulated by oxidative post-translational modificatio

186 Responses to hypoxia are regulated by oxygen-dependent degradation of kingdom

187 agine hydroxylation, suggesting that Cezanne is regulated by oxygen levels.

188 dsRNA in the human infant airway epithelium are regulated by p38-MAPK and NF-kB signalling.

189 gh its expression was previously reported to be regulated by p53, our data show that the increase in

190 However, the mechanism by which virulence is regulated by PE synthesis is only partially understoo

191 enes with increased expression were known to be regulated by peroxisome proliferator-activated recept

192 Given that expression of pstSCAB is regulated by PhoPR, these findings suggest that overa

193 cation and suggest that this interaction can be regulated by phosphorylation of E2 Y138.IMPORTANCE Pa

194 We show here that this interaction is regulated by phosphorylation of Frizzled3 at T598 and

195 Here, we provide evidence that Mis4 activity is regulated by phosphorylation of its cohesin substrate

196 us findings were obtained when consciousness was regulated by physiological sleep.

197 Shade avoidance is regulated by PHYTOCHROME INTERACTING FACTORs, a group

198 ticular, the timing of this dynamic response is regulated by PIN2,(5)(,)(6) but the underlying molecu

199 Terrestrial photosynthesis is regulated by plant phenology and environmental condit

200 involving a direct relocalization mechanism, is regulated by Polo-mediated phosphorylation, whereas P

201 ulation, over 60% of activated transcriptome is regulated by polymerase pause-release and a transient

202 (GPCR) biogenesis, trafficking, and function are regulated by post-translational modifications, inclu

203 Intriguingly, PKR can also be regulated by PRKRA (protein interferon-inducible doub

204 directed activities of both PIKfyve and Fig4 are regulated by protein-directed activities within the

205 Here, we show that the oxidation of Y(356) is regulated by proton release involving a specific resi

206 Lactate flux into and out of cells is regulated by proton-coupled monocarboxylate transport

207 Genes were regulated by proximal chromatin states; repressive

208 a top overexpressed miR, and its expression was regulated by RAS/MAPK signaling.

209 Since the prolactin receptor (Prlr) is regulated by reproductive hormones and is female-sele

210 fibrosis post-myocardial infarction (MI) can be regulated by resident cardiac cells with a fibrogenic

211 15), whose expression in the visual thalamus is regulated by retinal input.

212 romatin adopts different configurations that are regulated by reversible covalent modifications, refe

213 Thus, irreversible junction deformations are regulated by RhoA-mediated contractility, membrane t

214 The former is regulated by RNA polymerase II (pol II) de novo recru

215 ciated protein 4 (MAP4), the latter of which was regulated by ROS production.

216 e-5'-phosphate (PAP) and it's in vivo levels are regulated by SAL1/FRY1, a phosphatase enzyme located

217 ng and explaining the necessity for MTHFR to be regulated by SAM.

218 Autophagy can be regulated by several energy sensing pathways, includi

219 Genetically, most phenotypes seem to be regulated by several hormones, but transcriptional pr

220 ice sites by the core spliceosomal machinery is regulated by several protein factors that predominant

221 Hematopoietic stem cells (HSCs) are regulated by signals from the bone marrow (BM) niche

222 an important bacterial lipid transporter may be regulated by small proteins, and raises the possibili

223 The activity of SERCA is regulated by small membrane protein subunits, the mos

224 Social behaviours in termites are regulated by sophisticated chemical communication sy

225 Levels of RA in tissues are regulated by spatiotemporal expression patterns of g

226 The Orai1 channel is regulated by stromal interaction molecules STIM1 and

227 trusion formation during cell migration that is regulated by subcellular mitochondrial trafficking.

228 g were conducted to evaluate how osteoclasts were regulated by T cells during the bone remodeling pro

229 ndividuals, and its expression and signaling are regulated by T1D genetic risk variants and viral inf

230 Conversion was regulated by TAK1.

231 nd of targets of the AUXIN RESPONSE FACTOR 6 are regulated by TCP15 and often contain putative TCP re

232 logical processes and 27 molecular functions were regulated by TGF-beta1.

233 identified specific signaling networks that are regulated by TGFbetaR.

234 primate-specific MER41 family, some of which are regulated by the cardiogenic transcription factor TB

235 s than promoters, suggesting that most genes are regulated by the combined action of multiple enhance

236 Cell cycle entry and quiescence are regulated by the E2F transcription factors in associ

237 tream genes and physiological processes that are regulated by the endo siRNAs to affect longevity.

238 ptinemia and leptin resistance, effects that are regulated by the endocannabinoid (eCB)/CB(1)R system

239 The endogenous levels of this peptide are regulated by the feeding state, with reduced levels

240 ulated by FXR in mouse and human liver cells are regulated by the FXRalpha2 isoform via specific bind

241 metric VO(2) and that electronic transitions are regulated by the interplay between charge fluctuatio

242 -regulated potassium (K(ATP) ) channels that are regulated by the intracellular ATP/ADP ratio.

243 Identifying the genes that are regulated by the miRNA-183 cluster provides research

244 Intriguingly, we found that MmpL11 levels are regulated by the phosphorylation of threonine in the

245 NET1 guanine nucleotide exchange factor, and are regulated by the tumor-suppressor protein APC.

246 oregularity, and their molecular weights can be regulated by the loading of Grubbs initiators or by t

247 en by molecular motor forces and should thus be regulated by the mechanical load acting on the MT arr

248 s building evidence that suggests Piezo1 can be regulated by the membrane environment, with the activ

249 ds in heteromultivalent binding with GM1 may be regulated by the positions of the internal Gal-linked

250 es adaptor function and how this process can be regulated by the Rsp5-associated deubiquitinase, Ubp2

251 and additional experiments revealed that it is regulated by the activities of cAMP-dependent protein

252 to account for this effect, where imitation is regulated by the agreement between the learner and th

253 The activity of AMPK is regulated by the availability of nutrients, such as c

254 e demonstrate that cell shape in V. cholerae is regulated by the bacterial second messenger cyclic di

255 Muscle atrophy is regulated by the balance between protein degradation

256 s involve repression of the G6pc gene, which is regulated by the carbohydrate-response element-bindin

257 Thus, the competence state in cyanobacteria is regulated by the circadian clock and can adapt to sea

258 the Drosophila larval neuromuscular junction is regulated by the conserved RNA binding protein Syncri

259 timing of the G1-S cell cycle transition and is regulated by the corresponding increase in the level

260 cells that Fes1 oxidation is reversible and is regulated by the cytoplasmic methionine sulfoxide red

261 Stomatal patterning is regulated by the EPIDERMAL PATTERING FACTOR (EPF) fam

262 This is regulated by the ExuR transcription factor.

263 While BP is regulated by the function of kidney, vasculature, and

264 This process is regulated by the HAP complex in yeast.

265 h the adjacent CDKN1A locus, DINO expression is regulated by the histone demethylase KDM6A.

266 Expression of SOX4 is regulated by the integrin alphavbeta6 receptor on the

267 ere, we report that endoderm differentiation is regulated by the interaction between the long non-cod

268 translational stabilization of UNC5B by PyST is regulated by the interaction of PyST with PP2A.

269 ans and cnidarians, epithelial cell-polarity is regulated by the interactions between Par proteins, W

270 Emerging evidence suggests that this process is regulated by the mesoscale compartmentalization of th

271 Muscle contraction is regulated by the movement of end-to-end-linked tropon

272 the TLR signaling pathway, 3) MyD88 splicing is regulated by the NF-kappaB transcription factor, and

273 This mechanism is regulated by the organization and dynamics of the cor

274 tinal-tract-specific lncRNA (LINC00675) that is regulated by the pioneer transcription factor FOXA1 a

275 for how mitochondrial inner-membrane fusion is regulated by the ratio of two forms of Opa1.

276 internalization of the dopamine D2 receptor is regulated by the receptor tyrosine kinase ALK.

277 ntact more frequently than expected and that is regulated by the same group of transcription factors.

278 Here we show that RepoMan abundance is regulated by the same mechanisms that control Aurora

279 g outcome), and for all records, the outcome is regulated by the same set of known fixed effects and

280 Pore opening is regulated by the signaling lipid PIP2.

281 Furthermore, the differential adhesion code is regulated by the sonic hedgehog morphogen gradient.

282 0E-triggered oviposition in these mosquitoes is regulated by the stress- and immune-responsive c-Jun

283 In vertebrates, epithelial permeability is regulated by the tight junction (TJ) formed by specia

284 The folding capacity of the ER is regulated by the unfolded protein response (UPR) and

285 Furthermore, NICI expression is regulated by the von Hippel-Lindau (VHL) tumor suppre

286 mouse mammary tumor cells, PD-L1 expression was regulated by the nuclear receptor NR4A1/Sp1 complex

287 Here, we report that Th17 cells were regulated by their own signature cytokine, IL-17A.

288 ignals that activate them and the genes that are regulated by them.

289 n of the thylakoid proton motive force (pmf) is regulated by thylakoid ion transport.

290 lectin (MBL) and surfactant protein D (SP-D) are regulated by tissue fibroblasts at extravascular sit

291 to chronic hypothalamic inflammation, which is regulated by Tlr4 and Ikbke signaling.

292 How these roles are regulated by transcription factors is unknown.

293 Expression of all 18 genes is regulated by transcription factor AP2-G, which is req

294 Their function and activity are regulated by transcriptional changes, yet how such c

295 ent-20% higher in the CPE-supplemented group-was regulated by treatment and not by total fat content;

296 nd that T cell expression of PD-L1 in cancer was regulated by tumor antigen and sterile inflammatory

297 in import into a subcellular compartment can be regulated by ubiquitination and deubiquitination by E

298 ts modulates the plant's response to ABA and is regulated by ubiquitination.

299 Human periodontal ligament cells (hPDLCs) are regulated by vitamin D(3) and play a fundamental rol

300 ng and closing of voltage-gated ion channels are regulated by voltage sensors coupled to a gate that