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 Devices show high mobility (0.2 cm(2) V(-1) s(-1)) and close to zero

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

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

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

8 High mobility ambipolor organic thin-film transistors ba

9 Moreover, specific high-mobility analytes were extracted and enriched from

10 istence of a small number of holes with very high mobility and a large number of electrons with low m

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

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

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

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

15 nitude smaller in BLG devices that have both high mobility and low extrinsic doping.

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

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

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

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

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

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

22 These record high mobilities are achieved by controlled orientation o

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

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

25 ale transport of charges in these materials (high mobility at short length scales, low mobility at lo

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

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

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

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

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

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

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

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

34 ort a comparative transport study of several high-mobility conjugated polymers by field-effect-modula

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

36 nzothia diazole)] with a bandgap of 1.38 eV, high mobility, deep highest occupied molecular orbital.

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

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

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

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

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

44 High mobility graphene field-effect devices, fabricated

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

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

47 ermining region on the Y chromosome)-related high mobility group (HMG) box) proteins require the calc

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

49 Specific DNA binding is mediated by a high mobility group (HMG) box.

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

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

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

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

54 ch induce expression of the embryonic factor high mobility group A2 (HMGA2), which causes mesenchymal

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

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

57 ation of the minor groove DNA-binding factor high mobility group AT-hook 2 (HMGA2) as a driver of ERM

58 eting the architectural transcription factor high mobility group AT-hook 2 (HMGA2) induces TET1.

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

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

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

62 c proepithelial mesenchymal transition (EMT) high mobility group AT-hook 2 gene (HMGA2) mediates the

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

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

65 olves abundant architectural factors such as high mobility group B (HMGB) proteins.

66 epatocyte necrosis, necrotic tissue releases high mobility group B1 (HMGB1) and exogenous HMGB1 is ab

67 hitectural chromatin protein is an essential high mobility group box (HMGB) protein facilitating Pol

68 matically determined the role of Sry-related high mobility group box (Sox) 4 and the underlying molec

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

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

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

72 of neutrophils, initiated by the release of high mobility group box 1 (HMGB1) from UV-damaged epider

73 High mobility group box 1 (HMGB1) is a 25-kDa chromatin-

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

75 High mobility group box 1 (HMGB1) is a nuclear and cytos

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

77 Extracellular high mobility group box 1 (HMGB1) is an important mediat

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

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

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

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

82 The alarmin high mobility group box 1 (HMGB1) was released by platel

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

84 gene expression is regulated in part through high mobility group box 1 (HMGB1), an endogenous proinfl

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

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

87 llular nuclear proteins, histone H4 (H4) and high mobility group box 1 (HMGB1), released by injured c

88 iapoptotic functions, and down-regulation of high mobility group box 1 (HMGB1)-mediated, toll-like re

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

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

91 This study focused on the effect of high mobility group box 1 protein (HMGB1) on these criti

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

93 Hb also led to secretion of high mobility group box 1 protein (HMGB1), which synergi

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

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

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

97 HMGB1 (high mobility group box 1) modulates gene expression in

98 HMGB1 (high mobility group box 1), a nuclear protein released b

99 nologic synapse-related proteins myosin IIA, high mobility group box 1, and the TCR Vbeta-chain.

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

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

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

103 ry-conditioned medium, dead cell debris, and high mobility group box chromosomal protein 1 (HMGB-1).

104 h factor receptor 2 gene (FGFR2) and the TOC high mobility group box family member 3 gene (TOX3) were

105 rate TCFs contain two DNA binding domains, a High Mobility Group box for recognition of the Wnt Respo

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

107 biomarkers such as glutamate dehydrogenase, high mobility group box protein 1, and microRNA-122 coul

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

109 determining region Y (SRY)-box 9 protein], a high mobility group box transcription factor, plays crit

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

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

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

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

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

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

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

117 roRNA-122 (miR-122; high liver specificity), high mobility group box-1 (HMGB1; marker of necrosis), f

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

119 rferon gene expression by directly targeting high mobility group box-1 and interferon regulatory fact

120 After multivariate modeling, only high mobility group box-1 protein (HMGB-1, mean=5.84 [lo

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

122 interleukin-10, tumor necrosis factor-alpha, high mobility group box-1, and NO(2)/NO(3) were signific

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

124 -2 as well as serum levels of interleukin-6, high mobility group box-1, interleukin-10, and brain his

125 ells into the lung leading to the release of high mobility group box-1, which in turn stimulates the

126 crosis factor-alpha, BAX, interleukin-6, and high mobility group box-1; and increased those of Bcl-2

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

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

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

130 was regulated by FOXM1, PLK1, chromobox, and high mobility group families of transcription factors.

131 most vertebrate cells contain members of the high mobility group N (HMGN) protein family, which bind

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

133 High mobility group protein 1 (HMGB1) interacts with DNA

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

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

136 ctivity (toll-like receptor 4 expression and high mobility group protein B1 [HMGB-1] release) and nor

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 rRNA processing by regulating binding of the high mobility group protein Hmo1 and the small ribosomal

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

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

143 LEF/TCFs have a DNA sequence-specific high-mobility group (HMG) box that binds Wnt response el

144 egulatory network consisting of a quartet of high-mobility group (HMG) box transcription factors, SOX

145 chondrial transcription factor A (TFAM) is a high-mobility group (HMG) protein at the nexus of mitoch

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

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

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

149 low-frequency c.136-14_136-13insC variant in high-mobility group A1 (HMGA1) may strongly contribute t

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

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

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

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

154 the 3' UTR and suppresses the expression of high-mobility group AT-hook 2 (HMGA2), leading to inhibi

155 We use Hmga2 (High-mobility group AT-hook 2) an epigenetic regulator,

156 Eukaryotic High-Mobility Group B (HMGB) proteins alter DNA elastici

157 High-mobility group B (HMGB) proteins bind duplex DNA wi

158 analyze chromatin-related proteins, of which high-mobility group B (HMGB) proteins consistently cofra

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

160 ure, diminished cytoplasmic translocation of high-mobility group box (HMGB) 1 and suppressed NF-kappa

161 We detected high levels of high-mobility group box (HMGB)-1 in blood and skin lesio

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

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

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

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

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

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

168 anslocation and extracellular release of the high-mobility group box 1 (Hmgb1) nuclear protein, activ

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

170 ely aerobic glycolysis, in the regulation of high-mobility group box 1 (HMGB1) release.

171 duction and sequestration of proinflammatory high-mobility group box 1 (HMGB1) to prevent it from eng

172 Circulating levels of high-mobility group box 1 (HMGB1) were significantly red

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

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

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

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

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

178 molecules (DAMPs) such as S100 proteins and high-mobility group box 1 (HMGB1).

179 including interleukin (IL)-1beta, IL-18 and high-mobility group box 1 (HMGB1).

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

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

182 DNA curvature-inducing proteins including high-mobility group box 1 and histones H2A and H2B signi

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

184 High-mobility group box 1 exerts powerful proinflammator

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

186 also upregulated the endogenous TLR4 ligand high-mobility group box 1 in diabetic nephropathy.

187 populations were mediated by increased free high-mobility group box 1 in tm24KO mice.

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

189 ch could trigger T-cell immunity mediated by high-mobility group box 1 protein (HMGB1) and calreticul

190 We show that high-mobility group box 1 protein (HMGB1) orchestrates b

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

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

193 One such protein is HMGB1 (high-mobility group box 1).

194 -CSF, and endogenous danger signals, such as high-mobility group box 1, uric acid, and ATP, that acti

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

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

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

198 dents wherein impaired nuclear export of the high-mobility group box and import-dependent phosphoryla

199 the ubiquitous DNA-binding/-bending proteins high-mobility group box protein (HMGB)1 or HMGB2.

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

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

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

203 Two subtle variants (V60L and I90M in the high-mobility group box) define inherited alleles shared

204 HMGB (high-mobility group box) proteins are members of a class

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

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

207 erleukin-18, monocyte chemotactic protein-1, high-mobility group box-1 and tumor necrosis factor-alph

208 increase after rewarming was demonstrated on high-mobility group box-1 concentrations in the jugular

209 ut not monomers and fibrils, and the alarmin high-mobility group box-1 protein (HMGB-1) could promote

210 Gene expression profiling revealed high-mobility group box-1 protein (HMGB1) as a key regul

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

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

213 tudy, we report the identification of HMGN1 (high-mobility group nucleosome-binding protein 1) as a n

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

215 s-inducing factor (AIF), and proinflammatory high-mobility group protein B1 (HMGB-1) was effectively

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

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

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

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

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

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

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

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

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

225 SOX family proteins belong to the high-mobility-group (HMG) domain-containing transcriptio

226 ll lines, in the present study, we show that high-mobility-group box-1 (HMGB-1), a proinflammatory cy

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

228 factor A (mtTFA/TFAM) is a nucleus-encoded, high-mobility-group-box (HMG-box) protein that regulates

229 associated molecular-pattern molecule called high-mobility-group-box-1 (HMGB1) that promotes endothel

230 ntiation of myelinating glia, among them the high-mobility-group-domain-containing protein Sox10.

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

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

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

234 Such high mobility has significant influence on several magma

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

236 ysics that allows reaching such unexpectedly high mobilities in these weakly van der Waals bonded and

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

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

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

240 The high mobility is insensitive to the polymer molecular we

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

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

243 eling uptake in PSMs in which chemicals have high mobility, its validity is questionable for PSMs suc

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

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

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

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

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

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

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

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

252 , structurally planar, solution-processable, high-mobility, molecular, and macromolecular semiconduct

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

254 However, high-mobility n-type conjugated polymers are still rare.

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

256 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.

257 Consequently, slow sedimentation and high mobility of agglomerated AgNP could be expected und

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

259 Given the high mobility of Swi6 protein and that increased levels

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

261 after photobleaching experiments revealed a high mobility of the ZYX-1 protein within muscle cells,

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

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

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

265 nt long-range order but outperform the best, high-mobility, ordered semiconducting polymers to date.

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

267 conjugated copolymer and its application in high-mobility organic field-effect transistors.

268 High-mobility p-type and ambipolar conjugated polymers h

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

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

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

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

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

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

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

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

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

278 ured polydimethylsiloxane dielectric and the high-mobility semiconducting polyisoindigobithiophene-si

279 ientation and microstructure of films of the high-mobility semiconducting polymer poly(N,N-bis-2-octy

280 We argue that charge transport in high-mobility semiconducting polymers is quasi one-dimen

281 High-mobility semiconducting polymers offer the opportun

282 High-mobility semiconducting ultrathin films form the ba

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

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

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

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

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

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

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

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

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

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

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

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

295 uantum well created in GaAs and supporting a high-mobility two-dimensional electron gas.

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

297 ain and in the lateral direction, leading to high-mobility unipolar n-channel transport in field-effe

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

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