ライフサイエンスコーパス: high mobility

1 sity of states near the band edges, and 4) a high mobility.

2 ort-range ordered aggregates, which leads to high mobility.

3 High mobility (132 cm(2)/Vs), electrical stability, and

4 istance (~ 160 Omega square(-1) at 10 K) and high mobility (~2,000 cm(2) V(-1) s(-1) at 10 K) are obs

5 used as a target feature to design/discover high-mobility 2D semiconductors.

6 fabricated from the full-coverage films show high mobility (33 and 49 cm(2) V(-1) s(-1) for the mono

7 Here we report the preparation of high-mobility 4-inch wafer-scale films of monolayer moly

8 as a suitable quasi-2D Dirac semimetal with high mobility (~85000 cm(2)V(-1)s(-1)) and large nontriv

9 haracterized by notable properties such as a high mobility, a tunable density and, in topological ins

10 charge carriers that is responsible for the high mobility also makes it difficult to control their m

11 on with the membranes due to its small size, high mobility and concentration.

12 e processed at near ambient temperature with high mobility and device performance.

13 solved chromatin domains ranging from low to high mobility and displaying different subnuclear locali

14 xceptional physical properties such as ultra-high mobility and extremely large magnetoresistances.

15 overy after photobleaching, we demonstrate a high mobility and fast exchange of RNase H2 at sites of

16 s niche applications that involve graphene's high mobility and high sensitivity nature.

17 istributed receptor populations, one showing high mobility and low lateral restriction and the other

18 spital-acquired blood stream infections with high mobility and mortality.

19 Its high mobility and the moderate band gap make it very pro

20 istance give nearly zero effective mass with high mobility and the nontrivial Berry phase.

21 nding to and engulfing insoluble substrates, high mobility, and stability of the catalytic centers.

22 For high-mobility applications, both rigid and flexible radi

23 st attractive graphene analogue owing to its high mobility approaching that of graphene, and its thic

24 These record high mobilities are achieved by controlled orientation o

25 emiconductors with appropriate band gaps and high mobilities are highly desired.

26 ion of ambipolar organic semiconductors with high mobilities, as indicated by charge transport measur

27 tically competent, with both too low and too high mobility being detrimental for its activity.

28 - through milliseconds reveals its unusually high mobility, both free and assembled on polymeric micr

29 , quantum-mechanical transport phenomena and high mobility can be observed.

30 o others oxides, and to realize devices with high-mobility carriers and interesting magnetoelectronic

31 ls of SrTiO3 introduces oxygen vacancies and high-mobility carriers in the bulk SrTiO3, and the three

32 hese requirements and has been proposed as a high-mobility channel material, a light emitting medium

33 rd to their respective mobility with low- or high-mobility chromatin.

34 The emergence of high-mobility, colloidal semiconductor quantum dot (QD)

35 eal 75% of VGLUT1-containing vesicles have a high mobility, comparable to that at ribbon synapses.

36 rate, all-polymer solar cells composed of a high-mobility, crystalline, naphthalene diimide-selenoph

37 Further, a third high mobility domain is observed.

38 thiophen-2-yl)thieno[3,2-b]thiophene], and a high mobility donor-acceptor polymer, poly(isoindigo-bit

39 se is captured by a narrow Drude peak from a high-mobility electron pocket of double Weyl quasipartic

40 e chain length and QD size distributions for high-mobility electron transport in 1D QDCs.

41 ansistor arrays, demonstrating that DPA is a high mobility emissive organic semiconductor with potent

42 magneto-transmission and Faraday rotation in high-mobility encapsulated monolayer graphene using a cu

43 As a result, the polymer films maintain high mobility even at very low concentrations.

44 nteracting with the DNA phosphates exhibited high mobility, forming dynamic interfaces.

45 ected microwave power from the photo-excited high mobility GaAs/AlGaAs 2D device has been measured ov

46 o vary the observed magnetoresistance in the high mobility GaAs/AlGaAs 2D electron system.

47 t that appears around zero magnetic field in high mobility GaAs/AlGaAs 2DES (~10(7) cm(2)/Vs) is expe

48 m = 0.067, the standard value, even in these high mobility GaAs/AlGaAs devices, at very large filling

49 nduced magnetoresistance oscillations in the high mobility GaAs/AlGaAs heterostructure two dimensiona

50 High mobility graphene field-effect devices, fabricated

51 arly ideal electron fluid in charge-neutral, high-mobility graphene at room temperature(4).

52 ic Poiseuille profile for electron flow in a high-mobility graphene channel near the charge-neutralit

53 Our high-mobility graphene device enabled observation of suc

54 In a series of experiments using high-mobility graphene devices, we demonstrate the abili

55 Recently, high-mobility graphene has emerged as an ideal two-dimen

56 We report measurements of high-mobility graphene superlattices where the complete

57 ltage of electronic flow through channels of high-mobility graphene.

58 Such mutations cluster in the SRY high mobility group (HMG) box, a conserved motif of spec

59 High mobility group (HMG) proteins concentrate in the nu

60 urons to transactivate the expression of the high mobility group (HMG)-box transcription factor SOX-2

61 histones and architectural proteins such as high mobility group (HMGB) proteins.

62 es on the gene encoding WDHD1 (WD repeat and high mobility group [HMG]-box DNA-binding protein), one

63 NAMPT expression is regulated by high mobility group A (HMGA) proteins during senescence.

64 High Mobility Group A2 (HMGA2), an architectural transcr

65 We identified HMGA2 (high mobility group A2) as an important regulator of PAR

66 ession of the chromatin architectural factor High Mobility Group AT-hook 1 (HMGA1) in pulmonary arter

67 High mobility group AT-hook 2 (HMGA2) protein is compose

68 rboring different genetic drivers, including high mobility group AT-hook 2 (HMGA2) rearrangements, me

69 itectural transcription factor and oncogene, high mobility group AT-hook 2 (HMGA2), as a target of in

70 id 2-like 2 activity; high lin-28 homolog B, high mobility group AT-hook 2, spalt-like transcription

71 We illustrate these measures on High Mobility Group B (HMGB) box proteins and a dataset

72 tical tweezers (OT) experiments to show that high mobility group B (HMGB) proteins strongly disrupt n

73 The high mobility group box (HMGB) architectural protein fam

74 requires the thymocyte selection-associated high mobility group box (TOX) protein(13-15).

75 High mobility group box 1 (HMGB1) (an endogenous ligand

76 We show that high mobility group box 1 (HMGB1) acts as a cofactor in

77 The alarmin high mobility group box 1 (HMGB1) can be released under

78 High mobility group box 1 (HMGB1) is a chromatin-binding

79 High Mobility Group Box 1 (HMGB1) is a nuclear protein t

80 Here, we investigated whether the alarmin high mobility group box 1 (HMGB1) mediates age-associate

81 Previously, we found that the high mobility group box 1 (HMGB1) protein bound to tripl

82 evious studies showed the involvement of the high mobility group box 1 (HMGB1) protein in the patholo

83 beta-Lapachone-induced high mobility group box 1 (HMGB1) release activates the

84 High mobility group box 1 (HMGB1) serves as an inflammat

85 High Mobility Group Box 1 (HMGB1) was a dominant mediato

86 In our study, expression of high mobility group box 1 (HMGB1) was demonstrated to be

87 novo brain and blood generation of disulfide high mobility group box 1 (HMGB1), a neuroinflammatory m

88 d with de novo brain and blood generation of high mobility group box 1 (HMGB1), a neuroinflammatory m

89 s work, we investigated the participation of high mobility group box 1 (HMGB1), an important modulato

90 The inflammatory mediator, high mobility group box 1 (HMGB1), is a key regulator of

91 combination of lipopolysaccharide (LPS) and high mobility group box 1 (HMGB1).

92 epithelial cells resulted in the release of high mobility group box 1 and leukotriene B4 from the ep

93 rs of the innate immune system-specifically, high mobility group box 1 protein (HMGB1) and mitochondr

94 molecular pattern (DAMP) molecules, such as high mobility group box 1 protein (HMGB1), but the recep

95 ssues tonically release DAMPs, including the high mobility group box 1 protein (HMGB1).

96 Patients with a high high mobility group box 1 protein concentration between

97 Our aim was therefore to determine high mobility group box 1 protein concentration kinetics

98 The causal role of the prototype alarmin high mobility group box 1 protein in systemic inflammati

99 Total plasma high mobility group box 1 protein levels were analyzed w

100 Two distinct high mobility group box 1 protein release phases were id

101 High mobility group box 1 protein was released in two co

102 In contrast, a second high mobility group box 1 protein wave peaking 3-6 hours

103 Only the second high mobility group box 1 protein wave was a significant

104 g of these effector molecules, including the high mobility group box 1 protein, was involved in the i

105 ter trauma might hypothetically benefit from high mobility group box 1 protein-specific antagonist th

106 Detectable levels of the RAGE ligand high mobility group box 1 were present in serum from at-

107 mediates upregulation of the alarmin HMGB1 (High Mobility Group Box 1) in wound-induced papillomas.

108 to RSV bronchiolitis pathogenesis via HMGB1 (high mobility group box 1) release.Methods: Nasopharynge

109 High mobility group box 1-induced prolactin expression i

110 cally induced pressure, oxidative stress, or high mobility group box 1.

111 hepatocellular cytoplasmic translocation of high mobility group box 1.

112 In this study, we report that high mobility group box 2 (HMGB2) orchestrates the chrom

113 The chromatin protein high mobility group box 2 (HMGB2) was identified as an S

114 epressed expression of 1392 genes, including High Mobility Group Box 2 (HMGB2), a chromatin-associate

115 High mobility group box protein 1 (HMGB1) is an architec

116 Thymocyte selection-associated high mobility group box protein family member 2 (TOX2) i

117 Moreover, thymocyte selection-associated high mobility group box protein TOX (TOX) promoted the p

118 ution at a conserved back surface of the SRY high mobility group box) markedly destabilizes the domai

119 lix bundle with structural similarity to the high mobility group box, a domain that is well known as

120 Here, high mobility group box-1 (HMGB-1) protein was explored

121 omarkers, kidney injury molecule (KIM-1) and high mobility group box-1 (HMGB-1) simultaneously in buf

122 identified 2 novel miR-193a-3p targets, the high mobility group box-1 (HMGB1) and the hypoxia upregu

123 High mobility group box-1 (HMGB1) is highly induced duri

124 iral load was associated with the release of high mobility group box-1 (HMGB1) which triggered airway

125 vide mechanistic insights (keratin-18 [K18], high mobility group box-1 [HMGB1], and glutamate dehydro

126 GAM5), dynamin-related protein 1 (Drp1), and high mobility group box-1 protein (HMGB1).

127 t glycoprotein VI, integrin-linked kinase-1, high mobility group box-1 protein, chemokine CXCL4, and

128 Baseline sputum uric acid, high mobility group box-1, CXCL8 mRNA, sputum neutrophil

129 idative stress, and prevented the release of high mobility group box1 during OGD/R.

130 We investigated the effects of histone H1, high mobility group D1 (HMGD1), and methyl CpG binding p

131 he TOX family that shares a highly conserved high mobility group DNA-binding domain with the other TO

132 The chromatin-modifying protein high mobility group nucleosomal binding domain 2 (HMGN2)

133 patients also had a significant increase in high mobility group protein 1 (HMGB1), a sterile danger

134 th the chromatin structures of the host gene high mobility group protein A1 (HMGA1) and viral long te

135 The mammalian high mobility group protein AT-hook 2 (HMGA2) is a multi

136 High mobility group protein B1 (HMGB1) binds to the inte

137 vs. 3.6 [0.6-17.1] pg/mL, p < 0.01), whereas high mobility group protein B1 remained unchanged.

138 eins, Ctcf (CCCTC-binding factor) and Hmgb2 (high mobility group protein B2), in regulating pathologi

139 The mammalian high mobility group protein HMGA2 contains three DNA bin

140 3) with stroke, and the LHFPL2 gene (lipoma high mobility group protein I-C fusion partner-like 2) w

141 The high mobility group-domain containing transcription fact

142 determining factor SRY comprises a conserved high-mobility group (HMG) box DNA-binding domain and poo

143 ription factor A mitochondria (TFAM), a dual high-mobility group (HMG) protein involved in maintenanc

144 to O(2)-nBudT-containing DNA, whereas three high-mobility group (HMG) proteins (i.e., HMGB1, HMGB2,

145 Here we show that the high-mobility group (HMG) transcription factors Tcf1 and

146 High-mobility group A1 (Hmga1) chromatin remodelling pro

147 Elevated expression of high-mobility group AT hook 2 (HMGA2) has also been freq

148 importance for human placental development [high-mobility group AT-hook 1 (HMGA1), transcriptional r

149 e present study, a beta-catenin coactivator, high-mobility group AT-hook 1 protein (HMGA1), was detec

150 es revealed that a beta-catenin coactivator, high-mobility group AT-hook 1 protein (HMGA1), was readi

151 ors coordinate with the epigenetic regulator high-mobility group AT-hook 2 (Hmga2) to regulate self-r

152 p-regulates that of the transcription factor high-mobility group AT-hook 2 (HMGA2), which activates t

153 Adipose tissue-derived high-mobility group B1 (HMGB1) protein activates Toll-li

154 lture, plasmin directly, and in synergy with high-mobility group B1, stimulated Kupffer cells and bon

155 Extracellular high-mobility group box (HMGB)1 mediates inflammation du

156 g cell-surface Tim-3 binding to the alarmin, high-mobility group box 1 (HMGB-1).

157 associated molecular pattern (DAMP) molecule high-mobility group box 1 (HMGB1) and its receptor for a

158 We previously showed that high-mobility group box 1 (HMGB1) can engage receptor fo

159 Despite high-mobility group box 1 (HMGB1) clearly being involved

160 High-mobility group box 1 (HMGB1) is a multifunctional p

161 High-mobility group box 1 (HMGB1) is a nuclear protein t

162 High-mobility group box 1 (HMGB1) is an abundant chromat

163 damage-associated molecular pattern molecule high-mobility group box 1 (HMGB1) is upregulated by acti

164 Here, we have identified the high-mobility group box 1 (HMGB1) protein as an interact

165 e chemokines CXCL4 and CXCL7 and cytoplasmic high-mobility group box 1 (HMGB1) protein, but not membr

166 associated with increased airway epithelial high-mobility group box 1 (HMGB1) translocation and rele

167 High-mobility group box 1 (HMGB1), a prototypic alarmin,

168 acellular translocation of the injury-sensor high-mobility group box 1 (HMGB1), a trigger of inflamma

169 ducts (RAGE) and one of its primary ligands, high-mobility group box 1 (HMGB1), are required for opti

170 incRNA-Tnfaip3 physically interacts with the high-mobility group box 1 (Hmgb1), assembling a NF-kappa

171 ve contribution of specific DAMPs, including high-mobility group box 1 (HMGB1), is ill defined.

172 by neutralizing the proinflammatory cytokine high-mobility group box 1 (HMGB1).

173 damage-associated molecular patterns such as high-mobility group box 1 (HMGB1).

174 The high-mobility group box 1 (HMGB1)/TLR4 axis is a key ini

175 h necroptosis and release of danger molecule high-mobility group box 1 are eliminated by the absence

176 High-mobility group box 1 exerts powerful proinflammator

177 Included among these networks is the high-mobility group box 1 gene (HMGB1), a nonhistone chr

178 larmins such as IL-1alpha, IL-33, IL-16, and high-mobility group box 1 in cellular and physiological

179 ATX also significantly decreased high-mobility group box 1 nuclear translocation and secr

180 High-mobility group box 1 potently activated WT PAEC, in

181 a cava inferior, we identified blood-derived high-mobility group box 1 protein (HMGB1), a prototypica

182 changes of the intracellular distribution of high-mobility group box 1 protein.

183 ntestinal epithelial TLR4 activation induced high-mobility group box 1 release from the intestine, wh

184 nificantly higher expression of IL-10, TLR4, high-mobility group box 1, IFN-gamma, TRIF-related adapt

185 ystem for genes Toll-like receptor-4 (TLR4), high-mobility group box 1, nuclear factor kappa beta, my

186 eceptor for advanced glycation end-products, high-mobility group box 1, uric acid, IL-33, or inflamma

187 terns such as heat shock proteins (HSPs) and high-mobility group box 1.

188 atic release of secretory cytokines, such as high-mobility group box 1.

189 cells by targeting the chromatin-associated high-mobility group box 3 (HMGB3) protein.

190 Recombinant high-mobility group box protein 1 (HMGB1) increased blad

191 d levels of a key initiator of inflammation, high-mobility group box protein 1 (HMGB1), have been ass

192 Here, we show that high-mobility group box protein 4 (HMGB4), a protein pre

193 In this study, we overexpressed a high-mobility group box protein, TDP1, which was suffici

194 The high-mobility group box transcription factor SOX4 is the

195 d by the coexpression of CD4 and TOX (thymus high-mobility group box), in the skin and blood of CTCL

196 Extracellular high-mobility group box-1 (HMGB1) was identified as the

197 nalysis of the PPMS NPC secretome identified high-mobility group box-1 (HMGB1), which was found to be

198 nd mediators of islet destruction, including high-mobility group box-1, tissue factor, and IL-1beta.

199 POU factor OCT4, acting in concert with the high-mobility group genes Sox-2 and Sox-17.

200 We report that the mRNA encoding the high-mobility group N5 (HMGN5) chromatin binding protein

201 Present study defined the role of high-mobility group protein (HMGB1) in EDR related to di

202 High-mobility group protein B-1 (HMGB1) is a highly cons

203 NETs contain the high-mobility group protein B1 (HMGB1), a DNA-binding pr

204 , TLR4), which sense double-stranded RNA and high-mobility group protein B1 (HMGB1), respectively, as

205 portional to tumor necrosis factor-alpha and high-mobility group protein B1 cytokine expression.

206 ustaining, pathologic inflammation involving high-mobility group protein B1, interleukin-23, and the

207 neutrophil gelatinase-associated lipocalin, high-mobility group protein B1, intracellular cell adhes

208 Enrollment levels of high-mobility group protein B1, neutrophil gelatinase-as

209 ammation (suppressors of cytokine signaling, high-mobility group protein B1, oxidative stress, and ne

210 epigenetic factors of the histone family and high-mobility group protein B2 (HMGB2), suggesting their

211 The Saccharomyces cerevisiae high-mobility group protein Hmo1p has been implicated in

212 Loss of the nonhistone high-mobility group protein Nhp6 reduces histone occupan

213 Y) encode proteins containing a single HMG (high-mobility group) domain.

214 ination region of Y chromosome (SRY)-related high-mobility group-Box gene 9 (Sox9), one of the earlie

215 ine RSS binding by RAG1/2 and their cofactor high-mobility group-box protein 1 (HMGB1) as they procee

216 ted the PDI-ELISA method using the mammalian high-mobility-group protein AT-hook 2 (HMGA2) as the pro

217 e inflammatory protein-2, interleukin 6, and high-mobility groups protein 1.

218 ver, in recent reports of devices with ultra-high mobility (>40 cm(2) V(-1) s(-1)), the device charac

219 this assumption has been challenged, because high mobility has been reported for semiconducting polym

220 Such high mobility has significant influence on several magma

221 Although both the electron/hole high mobilities have been calculated for BAs, there is a

222 portant for DC function, as DCs expressing a high-mobility ICAM-1 mutant lacking the cytoplasmic doma

223 y expressed genes and those distinguished by high mobilities in the present study, in support of the

224 Our work emphasizes the need to achieve high mobility in combination with strongly suppressed ch

225 eir high physicochemical stability (and thus high mobility in soils).

226 Thanks to the inherent wide band gap and high mobility in the 2D plane, covalent organic framewor

227 t, which have both a low Urbach energy and a high mobility in thin-film-transistor (TFT) devices.

228 tilized and suggest design principles toward high-mobility indacenodithiophene-based polymers.

229 aterials in the same group, we find that the high mobility is closely related with its electronic str

230 The high mobility is supposed to promote reactivity, while t

231 Surface high mobility is unexpected since bismuth is not a topol

232 phosphorene represents the much sought after high-mobility, large direct band gap two-dimensional lay

233 obility to 560 cm(2) V(-1) s(-1), yielding a high mobility-lifetime product of 1.8 x 10(-2) cm(2) V(-

234 These results suggest that high mobility materials will be indispensable for variou

235 vior in two-dimensional (2D) systems such as high mobility metal-oxide field effect transistors, insu

236 of low-dimensional metallic systems such as high-mobility metal oxide field-effect transistors, the

237 oint, in addition to orbital MR expected for high mobility metals.

238 mportant molecular design guidelines for new high-mobility molecular semiconductors is suggested.

239 map of the transient localization lengths of high-mobility molecular semiconductors to identify what

240 directly to the SOC strength in a series of high-mobility molecular semiconductors with strong poten

241 disorder in some of the most widely studied high-mobility molecular semiconductors, state-of-the-art

242 compatible dielectrics, batch fabrication of high-mobility monolayer 2H-MoTe(2) field-effect transist

243 o observed Shubnikov-de Haas oscillations in high-mobility monolayer and few-layer MoS2.

244 A broad range of band gaps and high mobilities of a 2D semiconductor family, composed o

245 variable amounts of negative charges provide high mobilities of glycoconjugates on polyacrylamide gel

246 t (RH) showed hole-dominated carriers with a high mobility of 3.05 x 10(4) cm(2) V(-1) s(-1) at 3 K.

247 horus (a-RP) films are semiconductive with a high mobility of 387 cm(2) V(-1) s(-1) and a current swi

248 t only do hydrogen storage materials require high mobility of hydrogen in the solid state, but the ef

249 The anomalously high mobility of hydroxide and hydronium ions in aqueous

250 logue switching capability(6,7) owing to the high mobility of metal ions in the Si switching medium(8

251 After controlling for the relatively high mobility of persons from farm origins, we find that

252 ming the core of the filament as well as the high mobility of the CARD relative to this core.

253 roperties allow both high concentrations and high mobility of the charge carriers to be realized simu

254 The bandgap gradient and high mobility of the ternary telluride core/shell struct

255 of rapid cis-autophosphorylation suggesting high mobility of this region.

256 ation of perovskite single-crystal FETs with high mobility of up to ~15 cm(2) V(-1) s(-1) at 80 K.

257 OH(-) + HA --> A(-) + H2O; the conversion of high-mobility OH(-) to lower mobility A(-) results in a

258 overcoming this effect, allowing low-voltage high-mobility operation.

259 rategy for the design of new classes of very high mobility organic semiconductors with a low degree o

260 also opens up new avenues in the search for high-mobility organic semiconductors.

261 harge transfer, is a logical strategy toward high-mobility p-type polymers.

262 operational and environmental degradation of high-mobility, p-type polymer FETs and demonstrate an ef

263 ansfer integrals in the two-dimensional (2D) high-mobility plane protect the semiconductor from the e

264 Controlled device parameters of high-mobility polymer field-effect transistors (FETs) ar

265 Fluorescence enhancement of a high-mobility polymer semiconductor is achieved via ener

266 esign and OPV implementation of high-purity, high-mobility polymers, and other soft materials that ha

267 pe organic thermoelectric materials based on high-mobility polymers.

268 gand treatments and doping that have enabled high-mobility QD solids, as well as the experiments and

269 holes (N center) as charge carriers of very high mobility, reaching values of up to ~8 x 10(3) cm(2)

270 S) provides a promising new tool that offers high mobility resolution and compatibility with high-per

271 The high mobility resolution and preservation of labile sulf

272 s highlight the need to use IMS devices with high mobility resolving power for better separation of i

273 an be measured using OSA-TIMS-FT-ICR MS with high mobility resolving powers (RIMS up to 250), high ma

274 hich demonstrate excellent air stability and high-mobility semiconducting behaviour.

275 sistive-type trace oxygen sensor based on 2D high-mobility semiconducting Bi(2) O(2) Se nanoplates.

276 High-mobility semiconducting polymers offer the opportun

277 High-mobility semiconducting ultrathin films form the ba

278 suggests a simple and general principle for high-mobility semiconductor design/discovery.

279 resonance excitations of electron liquids in high-mobility semiconductor quantum wells or graphene sh

280 High mobility Si(0.15) Ge(0.85) film on sapphire was gro

281 degrees C, the lowest substrate temperature, high mobility Si(0.15)Ge(0.85) film with continues morph

282 High-mobility (Smx Bi1-x )2 Se3 topological insulators (

283 ower, possibly due to an increased number of high-mobility spiral surface modes based on spin-split b

284 external magnetic field, we observe that our high mobility TaAs samples become more conductive as a m

285 with massless carriers and, thus, extremely high-mobility that is due to the character of the band s

286 are deposited to form high-conductivity and high-mobility thin-film electrodes and channel layers of

287 but also possess suitable energy levels and high mobility to afford high VOC and FF.

288 ne serves as both the tunnel barrier and the high-mobility transport channel.

289 d by a photoconductive semiconductor, into a high mobility two-dimensional electron system.

290 portance for the physics of devices based on high-mobility two-dimensional electron gas (2DEG) since

291 lex (and less studied) hole-like states in a high-mobility two-dimensional electron gas in GaAs-AlGaA

292 Here we report induced superconductivity in high-mobility two-dimensional electron gas in gallium ar

293 local electric field and spatially isolated, high mobility, two-dimensional electron and hole conduct

294 ure, low crystallinity upon passivation, and high mobility under bias.

295 Multilayer MoSe2 transistors exhibit high mobility up to 121 cm(2) V(-1) s(-1) and excellent

296 s since high-performance devices necessitate high mobility values.

297 ecently been utilized (TIF-BT and TBIDT-BT), high mobilities were still attained in these polymers ow

298 These composites are observed to maintain high mobilities when strained and after repeated applied

299 ecular pools in living cells; one pool shows high mobility with transient incorporation into nanodoma

300 arc deposition technique is used to produce high-mobility ZnO thin films for low voltage thin-film t