ライフサイエンスコーパス: master

1 For measurements with the IOL Master 500 and Pentacam AXL, a mean difference of 0.026

2 700) to a widely used optical biometer (IOL Master 500).

3 ept-source optical coherence tomography (IOL Master 700) to a widely used optical biometer (IOL Maste

4 For measurements with Pentacam AXL and IOL Master 700, a mean difference of -0.019 mm and COR of 0.

5 In contrast, the master adipogenic TF peroxisome proliferator-activated r

6 increase in the Ti content over the range of master alloy additions, causes the grain number density

7 ial purity aluminium with a range of Al3Ti1B master alloy additions.

8 refinement compared to that provided by the master alloy alone.

9 size reduces with increasing addition of the master alloy which adds additional TiB2 particles and Ti

10 nt was found to continuously decrease in the master alloy with increasing cycles of salt-fluxing trea

11 minium contains the smallest amount of added master alloy, ultrasonics caused significant additional

12 factor-erythroid 2-related factor (Nrf-2), a master antioxidant transcription factor, and of heme oxy

13 automatic," performance) can be acquired and mastered at all ages.

14 We assessed 152 masters athletes 54.4+/-8.5 years of age (70% male) and

15 the prevalence of coronary artery disease in masters athletes with a low atherosclerotic risk profile

16 Studies in middle-age and older (masters) athletes with atherosclerotic risk factors for

17 downregulation of cardiac and renal Egr1, a master cardiovascular regulator involved in cardiac hype

18 l-cycle-independent developmental role for a master cell-cycle regulator, the anaphase-promoting comp

19 Elderly adults may master challenging cognitive demands by additionally rec

20 This study showed that IFN-gamma is a master checkpoint regulator for many cytokines.

21 Here, we use the near-explicit Master Chemical Mechanism (MCM v3.2) within a 0D box-mod

22 hese findings into a box model utilizing the Master Chemical Mechanism v3.2, and constraining the mod

23 ticular interest are lncRNAs upstream of the master chondrocyte transcription factor SOX9 locus.

24 tream regulator(s) and relationship with the master chromatin remodeling factor MTA1, continues to be

25 nappreciated role for direct DA input to the master circadian clock and highlight the importance of a

26 vironmental signals.SIGNIFICANCE STATEMENT A master circadian clock in the suprachiasmatic nuclei (SC

27 The master circadian clock is located in the suprachiasmatic

28 The master circadian clock of the suprachiasmatic nucleus sy

29 matic nucleus (SCN)-often referred to as the master circadian clock-is essential in generating physio

30 The master circadian pacemaker in mammals is located in the

31 r and electrophysiological dissection of the master circadian pacemaker, the suprachiasmatic nuclei (

32 y rhythms in astrocytes within the mammalian master circadian pacemaker, the suprachiasmatic nucleus

33 o regulate the function of the s-LNvs as the master circadian pacemaker.

34 w the architectures of these fate-regulating master circuits in HIV-1 and the human herpesvirus cytom

35 Here, we review the discovery of viral master circuits: virus-encoded autoregulatory gene netwo

36 5-hr delay in meals on markers of the human master clock and multiple peripheral circadian rhythms.

37 and metabolic cues, can also phase shift the master clock in the suprachiasmatic nuclei (SCNs) and/or

38 usal in the sleeping period phase shifts the master clock in the suprachiasmatic nuclei and/or slows

39 rhythms of subjective hunger and sleepiness, master clock markers (plasma melatonin and cortisol), pl

40 suprachiasmatic nuclei (SCN), the circadian "master clock," which is DNA methylated in region-specifi

41 n age-independent domain-general strategy to master cognitive challenges.

42 strophy (CBE) found association with ISL1, a master control gene expressed in pericloacal mesenchyme.

43 Paired box 6 (Pax6) is considered to be the master control gene for eye development in all seeing an

44 d the pathways involved in regulation of the master controller of iron metabolism, the hormone hepcid

45 In this study, we identified LGR4 as a master controller of Wnt/beta-catenin signaling-mediated

46 on of mean expression collapse onto a single master curve independent of the strength and number of c

47 imetic and natural branches fall on the same master curve, enlightening the universality of our poroe

48 evolutionary dynamics can be collapsed onto master curves governed by three essential parameters: (1

49 forming growth factor beta1 (TGF-beta1) is a master cytokine in many biological processes, including

50 The master cytokine TGF-beta mediates tissue fibrosis associ

51 lected on 27 major paintings by Old European Masters dating from the 14th to the late 19th centuries

52 harbor recurrent functional mutations of the master DNA damage response kinase ATM, which has been sh

53 internalised into early endosomes, where the master early endosome regulator Rab5b promotes STAT5 pho

54 ransition (EMT) by driving expression of the master EMT regulators and stem cell markers.

55 that S100A4 is an upstream regulator of the master EMT regulators SNAIL2 and ZEB along with other me

56 Collectively, we reveal that Galpha13 is a master endogenous negative switch for osteoclastogenesis

57 elease by stimulating acetylation of ETS1, a master endothelial cell transcriptional regulator.

58 Most lifelong masters endurance athletes with a low atherosclerotic ri

59 results establish MLL3/MLL4 and CBP/p300 as master enhancer epigenomic writers and suggest that enha

60 se-grained molecular dynamics simulation and master equation analysis to elucidate the folding of an

61 Here, with data from ab initio master equation and kinetic-transport simulations, we re

62 We present a Master Equation approach to calculating polymerization d

63 etrized Rice-Ramsperger-Kassel-Marcus (RRKM)-master equation calculations correctly predict the direc

64 Master equation modeling is utilized to compute the ther

65 ology and American Journal of Public Health, Masters et al. reported age-specific hazard ratios for t

66 ecurrence, and lethality in patients, but no master factor coordinating the invasive properties of gl

67 Notably, m(6)A facilitates the master female determinant Sxl, since multiple m(6)A comp

68 ow that CONSTANS (CO/B-BOX PROTEIN1 BBX1), a master flowering regulator, forms a trimer with Arabidop

69 onsider the fabrication of fluidic channels, masters for polymer replication, and tools for the produ

70 function of TFH cells are controlled by the master gene BCL6, but it is largely unclear how this tra

71 ndreds of genes, suggesting the existence of master genetic regulators.

72 mycin complex 1 (mTORC1) protein kinase is a master growth regulator that becomes activated at the ly

73 The mTORC1 kinase is a master growth regulator that senses many environmental c

74 ulatory mechanisms for ordered expression of master hematopoietic regulators during lineage specifica

75 red basophil count-associated locus near the master hematopoietic transcription factor CEBPA The fine

76 rthermore, structural HMIs can help identify master host cell regulator nodes and modules whose tweak

77 on of plants' own defence genes, such as the master immune regulatory gene NPR1 (ref.

78 ial processes that need to be understood and mastered in order to build up potential devices based on

79 In this study, we found that c-Fos, a master inflammatory regulator, was increased in photorec

80 One such mechanism involves Rad3, a master kinase coordinating the DNA damage response.

81 Tumor suppressor and upstream master kinase Liver kinase B1 (LKB1) plays a significant

82 OGT regulates expression of the master lipid regulator the transcription factor sterol r

83 ndings demonstrate that Dmrt1 is a candidate master male sex-determining gene in this TSD species, co

84 ABSTRACT: Sensory input to the master mammalian circadian clock, the suprachiasmatic nu

85 Activation of the master metabolic kinase AMPK enhances autophagy.

86 vation in Caenorhabditis elegans larvae, the master metabolic regulator AMP-activated protein kinase

87 hat AMP-activated protein kinase (AMPK), the master metabolic regulator of the cell, controls muscle

88 a mammalian target of rapamycin) (mTORC1), a master metabolic sensor.

89 that super-enhancers drive the biogenesis of master miRNAs crucial for cell identity by enhancing bot

90 ces in performance: the TaqMan Universal PCR Master Mix failed to correctly quantify DNA with more th

91 We compared the TaqMan Universal PCR Master Mix with two alternative DNA polymerases: ExTaq H

92 positive effect for the TaqMan Universal PCR Master Mix, enabling accurate quantification for 25 pg/n

93 se results support the concept of NFI-A as a master molecular transcriptome switch that controls myel

94 The human capacity to master multiple languages is remarkable and leads to str

95 B11 sits in a pathway directly downstream of master myeloid regulators including PU.1, and TP53 is on

96 ously showed that expression of myostatin, a master negative regulator of skeletal muscle mass, was s

97 rvation, as well as direct inhibition of the master nutrient response regulator target of rapamycin c

98 appeal of the idea that no species can be a master of all trades, there has been a scarcity of linke

99 maximize fitness of all traits leading to a "master of all traits".

100 er MBBS from the University of Queensland, a Master of Science degree in Epidemiology from Harvard Un

101 ools that extend our capabilities, making us masters of our environment.

102 Osteocytes are master orchestrators of bone remodeling; they control os

103 One of the challenges now is to master ordering within the atomic sheets.

104 i (SCN) of the hypothalamus are described as master pacemaker cells for biological rhythms.

105 on in the suprachiasmatic nucleus (SCN), the master pacemaker of circadian physiology.

106 aracteristics distinguishing the s-LNvs, the master pacemaker of the locomotor rhythms, from other cl

107 nding of tumor-promoting p53 mutants and the master proinflammatory regulator NFkappaB that drives al

108 itin (K63-Ub) chains needed to activate the "master" protein kinase TAK1.

109 of 1562 participants in the PHACS Adolescent Master Protocol and IMPAACT P1074 were eligible, and 144

110 ric HIV/AIDS Cohort Study (PHACS) Adolescent Master Protocol and International Maternal Pediatric Ado

111 on between diagnostic companies and the ARLG Master Protocol for Evaluating Multiple Infection Diagno

112 antagonizes activation by acetylation of the master redox regulator NRF2, providing an unusual mode o

113 a well-established network biology approach (master regulator analysis) to combine a transcriptional

114 ation, including a Candida albicans-specific master regulator at the CR1 locus.

115 Conversely, conditional deficiency of the master regulator Bcl6 in CD4(+) T cells resulted in a ma

116 e diverse family solves the problem of how a master regulator can control so many diverse receptors.

117 histocompatibility complex (MHC)-II and its master regulator class II transactivator (CIITA) are dow

118 in this study, we have found that PU.1-a key master regulator for hematopoietic self-renewal and line

119 s can be classified as positive for Runx2, a master regulator for osteoblastogenesis.

120 , which inhibits the expression of ComK, the master regulator for the K-state, and reduces transforma

121 TFEB is a master regulator for transcription of genes involved in

122 t by decreasing acetylation of the Treg cell master regulator Foxp3 mediated by the histone acetyltra

123 This implicates putative master regulator genes in which multiple independent sto

124 the cadherin juxtamembrane domain acts as a master regulator guarding cadherin stability.

125 larmone (p)ppGpp has been determined to be a master regulator in B. burgdorferi.

126 es triggered by VLVs and found that PRDM1, a master regulator in cell differentiation, was significan

127 BES1 functions as a master regulator in the brassinosteroid (BR) pathway tha

128 ETV1 is a master regulator in the intestinal cells of Cajal (ICC),

129 conversion induced by the melanocyte lineage master regulator MITF.

130 in profile of photoreceptors lacking the rod master regulator Nrl is nearly indistinguishable from th

131 m we exhibit that in mESCs, the pluripotency master regulator Oct4, counteracts pro-differentiation i

132 synthetic genetic interaction with Hac1, the master regulator of a second proteotoxic stress response

133 pax6b and mnx1 while downregulating arxa, a master regulator of alpha-cell development and function.

134 n factor EB (TFEB) has recently emerged as a master regulator of autophagosome-lysosome function, con

135 ent by means of hepatic gene transfer of the master regulator of autophagy transcription factor EB or

136 or, Deleted in Colorectal Cancer (DCC), is a master regulator of axonal crossing throughout the neura

137 r (FXR) is a nuclear receptor that acts as a master regulator of bile acid metabolism and signaling.

138 fate of subplate neurons (SPNs), which are a master regulator of brain development that plays critica

139 Overall, our results highlight Wnt5a as a master regulator of brain invasion, specifically TPC, an

140 e affects the immune response by acting as a master regulator of carbohydrate metabolism in the infec

141 Inducer of CBF expression 1 (ICE1) is a master regulator of CBFs, and ICE1 stability is crucial

142 In eukaryotes, protein kinase A (PKA) is a master regulator of cell proliferation and survival.

143 the Notch/Delta-like ligand (Dll) pathway, a master regulator of cell-cell interaction and vascular p

144 mTORC1 is a signal integrator and master regulator of cellular anabolic processes linked t

145 The transcription factor Snail is a master regulator of cellular identity and epithelial-to-

146 The transcription factor RpaA is the master regulator of circadian transcription in cyanobact

147 containing miR-206, which represses Rrbp1, a master regulator of collagen biosynthesis, in fibrogenic

148 CITF1 acts together with a master regulator of copper homeostasis, SPL7 (SQUAMOSA P

149 We propose that PRA is a master regulator of Cx43 expression, GJ formation and my

150 ption factor NRF2, encoded by NFE2L2, is the master regulator of defense against stress in mammalian

151 llectively, this study identifies nRAGE as a master regulator of DSB-repair, the absence of which orc

152 These results demonstrate that SurR is a master regulator of electron flow within P. furiosus, li

153 promotes optimal transcription of Wt1 as the master regulator of embryonic EPDCs.

154 n yeast) is an essential Hsp70 chaperone and master regulator of endoplasmic reticulum (ER) function.

155 osphate-activated protein kinase (AMPK) is a master regulator of energy homeostasis in eukaryotes.

156 or-activated receptor gamma (PPARgamma) is a master regulator of energy metabolism.

157 p63 is a master regulator of epidermal biology, sustaining stemne

158 present in the promoter region of Grp78, the master regulator of ER stress, thereby preventing homeos

159 The conserved small G-protein Cdc42 is a master regulator of eukaryotic cellular polarization.

160 HIF-1alpha is a master regulator of gene expression and might play an im

161 The master regulator of HBC activation is the DeltaN isoform

162 Thus, GATA4 acts as master regulator of hepatic microvascular specification

163 y the hermaphrodite-specific transcriptional master regulator of hermaphroditic cell identity tra-1,

164 ng site for the aryl hydrocarbon receptor, a master regulator of IL-22 production.

165 Hepcidin, the master regulator of iron homeostasis, controls iron flow

166 as well as enhanced expression of MYC2, the master regulator of JA-dependent responses.

167 tivate the transcription factor EB (TFEB), a master regulator of lipid metabolism and lysosomal bioge

168 Our data reveal that Rab29 is a master regulator of LRRK2, controlling its activation, l

169 n leading to the downregulation of Cited2, a master regulator of LSC quiescence.

170 regulator of shear responses, and PROX1, the master regulator of lymphatic development.

171 sed on the transcription factor EB (TFEB), a master regulator of lysosomal biogenesis that detects ly

172 ulation of transcription factor EB (TFEB), a master regulator of lysosomal pathways.

173 pression of the Elf5 transcription factor, a master regulator of mammary alveologenesis and luminal c

174 Upon nutritional starvation, the master regulator of meiosis Mei2 inactivates Mmi1, there

175 sential role as a cellular energy sensor and master regulator of metabolism in eukaryotes.

176 AMPK is a highly conserved master regulator of metabolism, which restores energy ba

177 pharmacological inhibition of miRNA-10b - a master regulator of metastatic cell viability - leads to

178 al models, these findings show that DCC is a master regulator of midline crossing and development of

179 tein mitochondrial Rho GTPase 1 (Miro1) is a master regulator of mitochondrial axonal transport in re

180 controls the transcription of PGC-1alpha, a master regulator of mitochondrial biogenesis.

181 Transcription factor C/EBPalpha is a master regulator of myelopoiesis and its inactivation is

182 OD protein, a transcription factor that is a master regulator of myogenesis, while leaving MYOD mRNA

183 The circadian system is a master regulator of nearly all physiology and its disrup

184 ite growth and define UNC-45A as a novel and master regulator of NMII-mediated cellular processes in

185 newal/differentiation, implicating TET2 as a master regulator of normal and malignant hematopoiesis.

186 abditis elegans was originally heralded as a master regulator of organ differentiation.

187 D1, via H3K4me1 demethylation, represses the master regulator of osteoblast differentiation RUNX2 to

188 suppresses expression of Krox20 (Egr2), the master regulator of PNS myelination.

189 gy 2 domain-containing protein (p66Shc) is a master regulator of reactive oxygen species (ROS).

190 1L is transcriptionally activated by NRF2, a master regulator of redox homeostasis.

191 tion were due to the activation of NRF2, the master regulator of redox stress tolerance.

192 The ATR kinase is a master regulator of replication stress responses.

193 Our data identify CRL2(Lrr1) as a master regulator of replisome disassembly during vertebr

194 ys an essential role in defense, whether the master regulator of SA signaling, NPR1, is targeted by a

195 We identified Srf as a master regulator of SC fusion required in both fusion pa

196 nal activation of ap2-g (PF3D7_1222600), the master regulator of sexual development, from an epigenet

197 MICROSPORES (AMS) transcription factor is a master regulator of sporopollenin biosynthesis, secretio

198 Among these, HSF1, considered the master regulator of stress-induced transcriptional respo

199 Thus, SOX2 is a master regulator of the acinar cell lineage essential to

200 r (erythroid-derived 2)-like 2 (Nrf2) is the master regulator of the antioxidant response, and its fu

201 tor-erythroid 2-related factor-2 (Nrf2) is a master regulator of the antioxidant response.

202 te a role for p53, a previously unrecognized master regulator of the cardiac transcriptome.

203 TOR is a master regulator of the cell's growth and metabolic stat

204 NRF2 is a transcription factor serving as a master regulator of the expression of many genes involve

205 GRP78, also called BiP, is a master regulator of the UPR, reducing ER stress levels a

206 ed into the thermogenic program by PRDM16, a master regulator of thermogenesis.

207 gulation, identify a previously unrecognized master regulator of this critical immune checkpoint and

208 ntify Pib2 (PhosphoInositide-Binding 2) as a master regulator of TORC1.

209 lcium is a known potent second messenger and master regulator of wound-healing programs, it is unknow

210 In addition to identifying the master regulator our method provides an overview of the

211 ated by the pioneer transcription factor and master regulator PHA-4/FoxA, followed by the cytoskeleta

212 propose that this response is driven by the master regulator retinoic acid receptor-related orphan r

213 , it is important to identify and target the master regulator transcription factor for proper underst

214 computational approach for identification of master regulator transcription factor in a genome.

215 t the second step, our method identifies the master regulator transcription factor, if there exists o

216 onably well in validating the existence of a master regulator when the number of subjects in each tre

217 or (erythroid-derived 2)-like 2 (Nrf2), the "master regulator" of genes controlling cellular redox ho

218 Although Aurora B is regarded as the "master regulator" of kinetochore-microtubule attachment,

219 This 'master regulator' transcription factor is at the top of

220 loped a screening method of identifying the 'master regulator' transcription factor just using only t

221 A 'master regulator' transcription factor often appears to

222 curs through the expression of the flagellar master regulator, FlhD4C2.

223 We use three such master regulators (FOXA1, NKX3.1 and androgen receptor,

224 To further identify the Master Regulators (MRs) driving the network function, he

225 of the UPR, and evidence indicates that the master regulators and downstream effectors of the UPR ha

226 atasets, our method ensures the existence of master regulators and identifies biologically meaningful

227 ator LuxO is active and regulates the two QS master regulators AphA, which is induced, and OpaR, whic

228 However, recent studies indicate that the master regulators are often coexpressed.

229 Furthermore, the expression of master regulators can be dynamic and quantitative.

230 tion of MAPK are transcriptionally linked to master regulators essential for neural stem cell identif

231 gest that Oct4 competes with various lineage master regulators for binding promoters and enhancers.

232 ve been shown, in many cases, to function as master regulators for gene expression and thus, they can

233 Ectopic expression of lineage master regulators induces transdifferentiation.

234 Expression of the master regulators of B cell development Ebf1 and Pax5 wa

235 hat poising the fast-activating enhancers of master regulators of differentiation through continual h

236 homeostasis and proper expression of several master regulators of iron metabolism, including iron reg

237 We found that MiT/TFE transcription factors-master regulators of lysosomal and melanosomal biogenesi

238 nd show that these transcription factors are master regulators of neuropsychiatric function.

239 Furthermore, master regulators of Oncopig STS expression were identif

240 Members of the Rab GTPase family are master regulators of vesicle trafficking.

241 nd were regulated by chloroplast maintenance master regulators such as GLK1.

242 III Ca(2+)-sensor protein kinases (CPKs) as master regulators that orchestrate primary nitrate respo

243 can identify cell type specification genes (master regulators) that act synergistically, and demonst

244 nt developmental switches by transcriptional master regulators, chromatin state changes, and hormone

245 further demonstrate that conserved CREs bind master regulators, suggesting that while CREs contribute

246 ators and identifies biologically meaningful master regulators.

247 Development requires the expression of master regulatory genes necessary to specify a cell line

248 Master regulatory genes require stable silencing by the

249 Findings include a master regulatory locus that likely has a role in immune

250 he phosphorylation of sPPases as a potential master regulatory mechanism that could be used to attenu

251 n islets revealed that NKX2.2 is a conserved master regulatory protein that controls the acquisition

252 ecified dynamically by attractor states of a master regulatory TF network.

253 Spatially, master regulatory transcription factors are required to

254 fied by the combinatorial action of homeotic master regulatory transcription factors.

255 3-5 cyclic diguanylic acid (c-di-GMP) to the master repressor, BldD.

256 dUTPases can interact with the SaPIbov1 Stl master repressor, leading to derepression and mobilizati

257 osome, under the control of the SaPI-encoded master repressor, Stl.

258 ed in part by the phosphorylated form of the master response regulator Spo0A (Spo0A approximately P).

259 A) are small, noncoding RNA molecules with a master role in the regulation of important tasks in diff

260 al therapy delivered in pediatric clinics by master's-level clinicians.

261 heck-in calls to support accessing care from master's-level coordinators.

262 The master spindle checkpoint kinase Mps1 senses kinetochore

263 uctures were subsequently utilized to create master stamps for nanoimprint lithography.

264 ein response, GRP78-an endoplasmic reticulum master stress regulator-detaches from three endoplasmic

265 a novel role for the anaphylatoxin C5a as a master switch of the delicate pHi balance in neutrophils

266 esults identify IGF2BP3 as a human ontogenic master switch that restricts megakaryocyte development b

267 gulatory potential of molecular thiol-driven master switches such as Nrf2/Keap1 or NF-kappaB/IkappaB

268 s of MSC reduced expression of the Treg cell master TF Foxp3 and induced TH2 differentiation even und

269 G1 or CHD7 alone showed an enrichment of ESC master TFs binding and active chromatin architecture at

270 ty of the medieval glassmaker allowed him to master the redox kinetics in the glass by rapid shaping

271 ignaling by inducing degradation of STAT3, a master transcription activator involved in multiple cell

272 nized that each lineage expresses a specific master transcription factor and the expression of these

273 o identify candidate TSG implicated GATA4, a master transcription factor driver of hepatocyte epithel

274 enesis by demonstrating that the endothelial master transcription factor ETS1 promotes global RNAPII

275 3-dependent stabilization of ets variant 1-a master transcription factor for ICCs-and consequent up-r

276 nd attenuated activation of ERK/MAPK and the master transcription factor NF-kappaB in response to FGF

277 were targets of both JunB and the iNKT cell master transcription factor PLZF was UTX dependent.

278 alcineurin-dependent activation of NFAT, the master transcription factor regulating IL-2 expression.

279 led to decreased levels of the chondrogenic master transcription factor sox9 and its downstream targ

280 rdinately control the expression of the bone master transcription factor Sp7 (osterix) during mesench

281 Although master transcription factors (TFs) are key to the develo

282 This process is heavily regulated by such master transcription factors as MYOD and members of the

283 -gene Regulatory Factor (MyRF) is one of the master transcription factors controlling myelin formatio

284 , and cell type-specific balance between the master transcription factors in determining heterogeneit

285 type into another by enforced expression of master transcription factors.

286 ming can be achieved by forced expression of master transcription factors.

287 on, including many known targets of NRF2-the master transcriptional factor for the oxidative stress r

288 omated deep-phenotyping of a mutation in the master transcriptional regulator fezf2 not only detects

289 By augmenting macrophage TFEB, the master transcriptional regulator of autophagy-lysosomal

290 that the vitamin D receptor (VDR) acts as a master transcriptional regulator of autophagy.

291 endent kinase inhibitor (CDKI) p18INK4c, the master transcriptional regulator of PC differentiation B

292 nstrating that heat shock factor 1 (HSF1), a master transcriptional regulator of the chaperone respon

293 ike 2 (NFE2L2; hereafter NRF2), which is the master transcriptional regulator of the endogenous antio

294 nse to various stress signals by acting as a master transcriptional regulator.

295 rks can be distilled into a small set of key master transcriptional regulators (MTR), genes that are

296 We further demonstrate that the master transcriptional regulators of phosphate stress re

297 response factors, Msn2 and Msn4, function as master transcriptional regulators of yeast glycolysis vi

298 factor-encoding genes and is considered the "master virulence regulator" in Bordetella pertussis, the

299 XR) is a nuclear receptor considered to be a master xenobiotic receptor that coordinately regulates t

300 ato-refractometry (Topcon), Pentacam HR, IOL Master (Zeiss) axial length measurements and fundus opti