ライフサイエンスコーパス: STM

1 STM and atomic-resolution non-contact AFM imaging reveal

2 STM and organ boundary genes CUP SHAPED COTYLEDON1 (CUC1

3 STM detection is a fast test of suprathreshold auditory

4 STM imaging of an AAB macrocycle revealed the formation

5 STM imaging of its monolayers revealed large-area, defec

6 STM imaging of two additional sequence-controlled macroc

7 STM is a mobile protein that traffics cell-to-cell, pres

8 STM is also required for proper meristem organisation an

9 STM measurements in combination with density functional

10 STM reveals a clear energetic preference for methane bin

11 STM sensitivity was most critical in predicting SRTs for

12 STMs could enhance their impact by strengthening working

13 STMs send physicians from high-income countries to low a

14 ingle-cell transcriptomics to profile 32,000 STMs and identified phenotypic changes in patients with

15 We defined extreme use as > 12 STM and/or more than four radiographic imaging tests in

16 protein interacts with STM protein to form a STM self-activation loop.

17 mpound of the iron chalcogenides, by using a STM tip with a magnetic cluster at its apex.

18 ta suggest that ATH1 anchors STM to activate STM as well as other axillary meristem regulatory genes.

19 her groups, exposure to IMD and TMX affected STM but not LTM.

20 he chemical identification inferred from AFM/STM.

21 icroscopy/scanning tunneling microscopy (AFM/STM) experiment can both distinguish neutral O2 molecule

22 ly interacts with the metal electrodes of an STM break junction (STM = scanning tunneling microscope)

23 with a major motility disorder by use of an STM than with SWS in the development set (321 [43%] pati

24 d biochemical data suggest that ATH1 anchors STM to activate STM as well as other axillary meristem r

25 kHz) pure-tone average (HFA; R(2 )= .31) and STM sensitivity (R(2 )= .28).

26 oupling of the SOP is detected by nc-AFM and STM.

27 acterized by XPS, electrochemistry, AFM, and STM.

28 s necessary for stable and reliable AFM- and STM-based TERS experiments, together with the specific p

29 SAM and to specify cotyledon boundaries, and STM controls CUC expression post-embryonically at organ

30 ntly from those of peas, as both LFY/FLO and STM are expressed in developing leaves of Bignonieae.

31 ning tunneling microscopy (STM) imaging, and STM break junction (STM-BJ) techniques.

32 The MCBJ and STM-BJ studies on single molecules both showed that DTFs

33 n remarkable agreement with recent X-ray and STM observations.

34 ging by AP scanning tunneling microscopy (AP-STM) shows that the reduction of the oxide films is init

35 ead to substantial variation in the apparent STM layer heights.

36 ochemical potential at the nanostructured Au STM tip.

37 Interestingly, aversive STM requires PDF but not PDFR, suggesting that there are

38 Transcripts of both STM and LFY/FLO were detected in leaf primordia, associa

39 n conclusion, we describe the routes used by STM to spread systemically in the period immediately pos

40 Here we exploit a combined STM/AFM technique to demonstrate the on-surface formatio

41 By combining STM experiments with large-scale density functional theo

42 At 200 K, controlled STM tip-induced unidirectional switching is possible, yi

43 es across the solid surface, allowing direct STM imaging.

44 ete phenotypic clusters within four distinct STM subpopulations with diverse homeostatic, regulatory

45 omprehensive quantum treatment of the dopant-STM system to pinpoint the exact coordinates of the dopa

46 750 patients during SWS and 461 (61%) during STM (p<0.0001).

47 Observations made during STM can establish motility disorders as the cause of oes

48 equency and cause of patient symptoms during STM.

49 density functional theory molecular dynamics STM image simulations.

50 molecule junctions using the electrochemical STM-based break-junction technique in combination with D

51 1) by self-assembly and verify it, employing STM, absorption spectroscopy, and quantum chemical calcu

52 ., fitness-based) progression of co-evolving STM strains.

53 Inclusion criteria were first STM episode, magnetic resonance imaging performed 90 day

54 in cortex (FOF) are considered critical for STM maintenance, and during each trial display a monoton

55 monotonically increasing neural encoding for STM.

56 thresholds were measured over headphones for STM (2cycles/octave density, 4-Hz rate) applied to an 85

57 ion of flowers and uncover the mechanism for STM silencing.

58 Nonappreciation of the potential for STM to occur in NMOSD may lead to increased disability f

59 prevailing insulin sensitivity derived from STM and FSIVGTT, demonstrated larger beta-cell function

60 ed ten SWS, followed by a standardised 200 g STM.

61 The KNOX genes STM and BP were overexpressed in double mutants whereas

62 heir perceptions of the impact of Guatemalan STMs.

63 Herein, STM imaging in combination with electrochemical characte

64 Combined with the HFA, STM sensitivity significantly improved the SRT predictio

65 f catalyst structures; (3) to explore how HP-STM and ETEM can be synergistically used to reveal struc

66 h-pressure scanning tunneling microscopy (HP-STM) and environmental transmission electron microscopy

67 This Review focuses on the development of HP-STM and ETEM, the in situ/operando characterizations of

68 fter TBI demonstrated significantly improved STM at 24h when compared with room air controls (p<0.05)

69 etric mean fold rises (GMFR) after dose 4 in STM, HM, HIV, and autologous-HCT patients were 3.00 (P <

70 ernalization and localization was altered in STM KO mammary epithelial cells, leading to decreased pr

71 ating rows, with two distinct appearances in STM which are assigned to concave and convex intramolecu

72 object, that multiple objects can coexist in STM, and that attention can be deployed to an object in

73 etaining dynamic sounds and static images in STM.

74 h 10ppm INO for 24h showed no improvement in STM.

75 data indicate that information maintained in STM can be represented in qualitatively distinct states.

76 at attention can be deployed to an object in STM.

77 es on the CuPc metal centers are observed in STM images.

78 veral coexisting auditory representations in STM.

79 n among different representational states in STM.

80 onological properties of the items stored in STM from the patterns representing their order.

81 Break junction techniques, including STM break junctions and mechanically controllable break

82 as compared with G2 or G3 (Disposition Index-STM, P = 0.005; DI-FSIVGTT, P = 0.006).

83 o were AQP4-IgG seropositive with an initial STM represented 14% of initial myelitis episodes among p

84 e metal electrodes of an STM break junction (STM = scanning tunneling microscope) and that the zero-v

85 canning tunneling microscopy break junction (STM-BJ) and mechanically controllable break junction (MC

86 g tunneling microscope-based break junction (STM-BJ) device.

87 canning tunneling microscopy break junction (STM-BJ) method is used to bridge tetrafluoroterephthalic

88 canning tunneling microscope-break junction (STM-BJ) technique, thereby enabling direct measurement o

89 scopy (STM) imaging, and STM break junction (STM-BJ) techniques.

90 canning tunneling microscopy break junction (STM-BJ), current sensing atomic force microscopy break j

91 canning tunneling microscopy break-junction (STM-BJ) measurements.

92 g tunneling microscope-based break-junction (STM-BJ) technique.

93 We then used fluorescently labeled STM to identify interactions with immune cells from the

94 emperature scanning tunneling microscopy (LT-STM) and the break junction technique.

95 gle molecule switching realized using the LT-STM tip on surfaces.

96 pothesized that synovial tissue macrophages (STM), which persist in remission, contribute to joint ho

97 o adults with either solid tumor malignancy (STM); hematologic malignancy (HM); human immunodeficienc

98 Preoperative serum tumor markers (STMs) normalized/decreased in 74% of patients.

99 sease-monitoring tests (serum tumor markers [STMs] and radiographic imaging) among women with MBC.

100 inclusion of a standardised solid test meal (STM) to HRM studies increases test sensitivity for major

101 cagon responses to a standardized test meal (STM) were evaluated.

102 effect of two aspects of short term memory (STM) (alpha, tau) and their interplay with conduction ve

103 a significant deficit in short term memory (STM) and strong inflammatory reaction in the ipsilateral

104 or the epsilon4 allele in short-term memory (STM) but the findings have been inconsistent.

105 out (KO) mice show normal short-term memory (STM) for social odor recognition (SOR) and social transm

106 Auditory short-term memory (STM) in the monkey is less robust than visual STM and ma

107 ry Pavlovian fear memory; short-term memory (STM) is intact, whereas long-term memory (LTM) is signif

108 Short-term memory (STM) or long-term memory (LTM) was evaluated in rutabaga

109 s been causally linked to short-term memory (STM), but whether this activity is necessary for forming

110 that spatial and temporal short-term memory (STM), respectively, recruit visual and auditory attentio

111 Short-term memory (STM), the brief maintenance of information in the absenc

112 Appetitive short-term memory (STM), which in wild-type (WT) is time-of-day (TOD) indep

113 ternally but preserved in short-term memory (STM).

114 sented in auditory-verbal short-term memory (STM).

115 aditional view of short-term working memory (STM) is that task-relevant information is maintained 'on

116 the meristem marker gene SHOOT MERISTEMLESS (STM) expression in the leaf axil to enable meristematic

117 the homeodomain protein SHOOT MERISTEMLESS (STM).

118 ed MCs, i.e., septum transversum mesenchyme (STM), in 2D cultures.

119 ming a molecular bridge between the metallic STM tip electrode and the metallic surface electrode.

120 ning tunnelling and atomic force microscope (STM/AFM) was used to dehydrogenate precursor molecules.

121 a commercial scanning tunneling microscope (STM) as a versatile, cost-efficient solution for TERS at

122 ures, using a scanning tunneling microscope (STM) combined with light irradiation at 5 K.

123 based on the scanning tunneling microscope (STM) to selectively couple a series of aniline derivativ

124 Using a scanning tunneling microscope (STM) under suitable bias conditions, binary information

125 g a cryogenic scanning tunneling microscope (STM).

126 c scheme in a scanning tunneling microscope (STM).

127 tions from a scanning tunnelling microscope (STM) tip.

128 the basis of scanning tunneling microscopy (STM) and complementary atomistic simulations, we develop

129 e, time-lapse scanning tunneling microscopy (STM) and density functional theory (DFT)-based calculati

130 on devices by scanning tunneling microscopy (STM) and mechanically controllable break junctions (MCBJ

131 bond-resolved scanning tunneling microscopy (STM) and noncontact atomic force microscopy (nc-AFM).

132 nsistent with scanning tunneling microscopy (STM) and transmission electron microscopy (TEM) images i

133 molecules via scanning tunneling microscopy (STM) at and close to room temperature.

134 ces using the scanning tunneling microscopy (STM) break junction technique.

135 y because UHV-scanning tunneling microscopy (STM) enables control of the quality of narrow step modif

136 een in recent scanning tunneling microscopy (STM) experiments on cuprates.

137 ed by in situ scanning tunneling microscopy (STM) imaging combined with density functional theory mol

138 lar assembly, scanning tunneling microscopy (STM) imaging, and STM break junction (STM-BJ) techniques

139 Scanning Tunneling Microscopy (STM) in combination with X-ray Photoelectron spectroscop

140 Scanning tunneling microscopy (STM) is an ideal tool not only for the characterization,

141 resolution of scanning tunneling microscopy (STM) is intrinsically limited to the extent of molecular

142 according to scanning tunneling microscopy (STM) measurements and density functional theory (DFT) ca

143 2 ne(2)/h in scanning tunneling microscopy (STM) measurements which would show strong (weak) signals

144 opy (AFM) and scanning tunneling microscopy (STM) paved the way for identifying individual reaction p

145 tegrated with scanning tunneling microscopy (STM) studies for supported 2D epitaxial nanoclusters and

146 from NMR and scanning tunneling microscopy (STM) studies, as well as from a new generation of X-ray

147 vacuum (UHV) scanning tunneling microscopy (STM) to elucidate the molecular sensing mechanism in CuP

148 were shown by scanning-tunneling microscopy (STM) to impact the next levels of supramolecular orderin

149 Scanning tunneling microscopy (STM) topography reveals a characteristic modulation of t

150 Herein, scanning tunneling microscopy (STM) was applied to study periodic grain boundaries in m

151 nce (SPR) and scanning tunneling microscopy (STM) were used to characterize the modification of surfa

152 lecular beam, scanning tunneling microscopy (STM), and ab initio molecular dynamics.

153 oscopy (TEM), scanning tunneling microscopy (STM), and transport property measurements.

154 combined with scanning tunneling microscopy (STM), Angstrom-scale topographic resolution.

155 ombination of scanning tunneling microscopy (STM), atomic force microscopy (AFM) with CO-tip, scannin

156 terized using scanning tunneling microscopy (STM), infrared reflection absorption spectroscopy (IRRAS

157 visualized by scanning tunneling microscopy (STM), pairs of molecules adsorb very close to each other

158 Using scanning tunneling microscopy (STM), state-of-the-art density functional theory (DFT),

159 in particular Scanning Tunneling Microscopy (STM), to study the changes in the local geometric and el

160 otor applying scanning tunneling microscopy (STM), which consists of a single acetylene (C(2)H(2)) ro

161 m-temperature scanning tunneling microscopy (STM), X-ray photoelectron spectroscopy, transmission inf

162 R-ARPES), and scanning tunneling microscopy (STM).

163 , observed by scanning tunneling microscopy (STM).

164 opy (TEM) and scanning tunneling microscopy (STM).

165 w-temperature scanning tunneling microscopy (STM).

166 w-temperature scanning tunneling microscopy (STM).

167 onitored with scanning tunneling microscopy (STM).

168 gh-resolution scanning tunneling microscopy (STM).

169 racterized by scanning tunneling microscopy (STM).

170 fraction and scanning tunnelling microscopy (STM) and modelled by ab initio theory.

171 ments by the scanning tunnelling microscopy (STM) break junction technique and electron transport cal

172 ermined from scanning tunnelling microscopy (STM) for CeCoIn5, we conclude that the robust upward-dis

173 e nanoscale, scanning tunnelling microscopy (STM) has proven a very effective technique due to its ex

174 -temperature scanning tunnelling microscopy (STM) imaging and a comprehensive quantum treatment of th

175 his study, a scanning tunnelling microscopy (STM) investigation with atomic resolution revealed previ

176 Scanning tunnelling microscopy (STM) is commonly used to identify on-surface molecular s

177 , we present scanning tunnelling microscopy (STM) measurements of the TCI Pb1-xSnxSe for a wide range

178 We use scanning tunnelling microscopy (STM) to investigate a structural phase transition betwee

179 -temperature scanning tunnelling microscopy (STM) to measure an individual dibutyl sulfide molecule o

180 Within the MLN, STM associates with dendritic cells and B cells but pred

181 long-established standard tunnelling model (STM) of independent TLS.

182 nguistic unaided spectrotemporal modulation (STM) detection test might be a viable option as a surrog

183 uditory function-spectrotemporal modulation (STM) sensitivity-and SRTs in noise was examined for 154

184 c simulations of a Spatio-Temporal Movement (STM) model and 100 stochastic simulations of an Individu

185 Short transverse myelitis (STM; <3 vertebral segments) is considered noncharacteris

186 lation-based patients with AQP4-IgG-negative STM included the following: nonwhite race/ethnicity; ton

187 iently increased at disease-vulnerable NMJs (STM muscle).

188 Novel STM-based conductance measurements combined with quantum

189 are discussed, as well as the capability of STM to manipulate single point defects.

190 monstrate that mTBI produces a disruption of STM which is evident 24h after injury and persists for 2

191 elusive functional and structural drivers of STM bacteria.

192 The different modes of STM imaging and the promising capabilities of non-contac

193 A key prediction of STM is that the noise should vanish at low temperatures.

194 Arabidopsis, and the functional relevance of STM mobility is unknown.

195 lation mediated transcriptional silencing of STM.

196 xploitation pathways in the genetic space of STM, including a strong evolutionary drive through a tra

197 information among representational states of STM.

198 Using a non-mobile version of STM (2xNLS-YFP-STM), we show that STM mobility is requir

199 indings point towards a more nuanced view of STM in which multiple substrates work in concert to supp

200 temalan physicians reported a net benefit of STMs on their careers, they perceived STMs as an imperfe

201 Billing dates of STMs (carcinoembryonic antigen and/or cancer antigen 15-

202 with dysphagia (241 [67%] of 360 patients on STM vs 125 [35%] patients on SWS in the development set,

203 tomography) were recorded; if more than one STM or imaging test were completed on the same day, they

204 Our STM results on such self-organized end-linked molecules

205 ary for forming, maintaining, or reading out STM remains unclear.

206 y, we report that female stathmin knock-out (STM KO) mice are unable to nurse their litters due to fr

207 fit of STMs on their careers, they perceived STMs as an imperfect solution to unmet surgical needs.

208 Therapeutic modulation of MerTK(pos) STM subpopulations could therefore be a potential treatm

209 A low proportion of MerTK(pos) STMs in remission was associated with increased risk of

210 In AQP4-IgG-positive STM cases, subsequent myelitis episodes were longitudina

211 re common in patients with AQP4-IgG-positive STM than in 27 population-based patients with AQP4-IgG-n

212 , postoperative pathology, and postoperative STMs were associated with PFS.

213 .92; P < 0.001) and increasing postoperative STMs (HR, 4.98; P < 0.001) were associated with shorter

214 val (reactivation) and postreactivation (PR)-STM are intact, whereas PR-LTM is significantly impaired

215 probe scanning tunneling microscopy (4-probe STM) under real-time monitoring of scanning electron mic

216 We construct networks where nodes represent STM strains and directed edges represent evolutionary st

217 ETT and ARF4 directly repress STM, while MP acts indirectly, through its target FILAME

218 ect spatial expression of CUC genes requires STM mobility in the meristem.

219 By performing high-resolution STM with a CO-functionalised tip, we clearly identify th

220 y the pluripotency factor SHOOTMERISTEMLESS (STM), is surrounded by transit amplifying cells competen

221 between the pleiotropy of SHOOTMERISTEMLESS (STM) and BREVIPEDICELLUS (BP) homeobox genes and their a

222 onally, the expression of SHOOTMERISTEMLESS (STM), PHANTASTICA (PHAN), and LEAFY/FLORICAULA (LFY/FLO)

223 tions of IMD and TMX and tested their short (STM) and long-term (LTM) olfactory memories.

224 e of environmental conditions, its simulated STM image perfectly matches experimental data, it is mor

225 smission electron microscopy system (in-situ STM-TEM).

226 bsorption scanning tunneling microscopy (SMA-STM).

227 ial biopsy fluorescent activated cell sorted STMs, revealed two STM subpopulations (MerTK(pos)TREM2(h

228 -polarized scanning tunneling microscopy (SP-STM) has been used extensively to study magnetic propert

229 Using SP-STM to visualize magnetic order in strongly correlated m

230 nning tunneling microscopy and spectroscopy (STM/STS), photoemission electron microscopy/spectroscopy

231 scanning tunneling microscopy/spectroscopy (STM/S) and non-contact atomic force microscopy (nc-AFM)

232 Scanning tunneling microscopy/spectroscopy (STM/S) corroborated by ab initio calculations, reveals t

233 scanning tunneling microscopy/spectroscopy (STM/S) to study the engineered quantum impurity in a top

234 scanning tunneling microscopy/spectroscopy (STM/S), which reveals different spectra for each surface

235 scanning tunneling microscopy/spectroscopy (STM/S).

236 ule on Au(111) and demonstrate that standard STM measurements cannot conclusively establish the natur

237 We used SOL and sternomastoid (STM) muscles from SOD1(G37R) mice and performed Ca(2+)-i

238 Specifically, we use low-temperature STM to investigate an ultra thin film (4 atomic layers)

239 ater molecules on Au(111) by low-temperature STM.

240 Room-temperature STM of the Au(111) surface at CO pressures in the range

241 Here, we tested STM performance in a large cohort of individuals (N = 12

242 nique is underpinned by the observation that STM images contain atomic-sized features in ordered patt

243 Here we show that STM inhibits cellular differentiation and endoreduplicat

244 version of STM (2xNLS-YFP-STM), we show that STM mobility is required to suppress axillary meristem f

245 Our results showed that STM detection thresholds were significantly correlated w

246 Our data suggest that STM mobility is critical for its normal function in shoo

247 the context of previous work suggesting that STM sensitivity for low rates and low-frequency carriers

248 The STM episode was defined as the first manifestation of NM

249 The STM images display an unexpected honeycomb feature, whic

250 The STM images show extended and homogeneous domains, offeri

251 The STM parameters are found to play a crucial role for soli

252 The STM tip-enhanced laser light produces a large excited-st

253 The STM topographies reveal a symmetry-breaking distortion o

254 This auto-regulation allows the STM locus to remain epigenetically active.

255 ecules between the Au(111) electrode and the STM tip to measure the single-molecule conductance throu

256 ly confined magnetic interaction between the STM tip and surface atoms, we drive quantum Rabi oscilla

257 combination of quantitative analysis by the STM and density functional theory calculations revealed

258 selective molecular sites controlled by the STM tip.

259 ility disorders reported symptoms during the STM (p=0.0038), compared with 89 (32%) of 277 patients w

260 Transitivity only weakly correlated for the STM model and time-varying IMM model metrics.

261 However, the STM mRNA and protein localization domains are not obviou

262 red with a high-energy molecular beam in the STM can be readily extended to other systems to clarify

263 n physicians was affected by practice in the STM setting.

264 nancial implications of participation in the STM.

265 In maize, the STM homolog KNOTTED1 shows clear differences between mRN

266 Moreover, the STM tip can be used to manipulate the tunneling dynamics

267 rectionality depends on the magnitude of the STM bias voltage.

268 ility disorders is increased with use of the STM compared with SWS, especially in patients with dysph

269 Moreover, approximately half of the STM in lymph are not associated with cells at all and tr

270 Here we show that downregulation of the STM pluripotency gene promotes initiation of flowers and

271 mbled architecture is presented based on the STM tip-induced deprotonation of the inner protons of in

272 Conversely, appropriately positioning the STM tip allows selecting the operating point on the comp

273 Specifically, the STM was used to cleave individual acetyl groups and to f

274 cifically, our results demonstrated that the STM detection test using a low spectral and temporal mod

275 ed patterns that are highly sensitive to the STM tip orbital and the absolute dopant lattice site.

276 res and low microwave power, contrary to the STM.

277 These STMs were potent producers of inflammation-resolving lip

278 c neural correlates of auditory attention to STM.

279 Additionally, transport, STM, neutron-scattering, and optical experiments have pr

280 ent activated cell sorted STMs, revealed two STM subpopulations (MerTK(pos)TREM2(high) and MerTK(pos)

281 volutionary paths-of Salmonella Typhimurium (STM) from nine years of Australian disease surveillance

282 ith Salmonella enterica serovar Typhimurium (STM) to identify changes in intestinal immune cells indu

283 compound 24 were analyzed in preliminary UHV-STM experiments.

284 the CI candidacy evaluation by both unaided STM detection test and the traditional best-aided senten

285 dle-shaped conformation that is stable under STM manipulation.

286 discuss how the neural mechanisms underlying STM are inextricably linked with the cognitive demands o

287 cture of the complex was characterized using STM imaging and spectroscopy.

288 e-molecule electronics is demonstrated using STM-break junction approaches by forming metal-single-mo

289 opment set (321 [43%] patients diagnosed via STM vs 163 [22%] via SWS; p<0.0001) and validation set (

290 We show that viable STM can be carried in the lymph by any subset of migrati

291 TM) in the monkey is less robust than visual STM and may depend on a retained sensory trace, which is

292 A dynamical attractor model in which STM relies equally on cortical and subcortical regions r

293 c through 28 days post-dose 4 in adults with STM, HM, and HIV.

294 sification validated for SWS (CCv3) and with STM (CC-S), respectively.

295 Furthermore, ATH1 protein interacts with STM protein to form a STM self-activation loop.

296 of the different growth modes observed with STM are presented in this review within a general framew

297 in this study may help select patients with STM who are at the highest risk for an NMOSD.

298 Patients with STM who were seronegative for AQP4-IgG among an Olmsted

299 nageable and high personal satisfaction with STM work.

300 As verified with STM, cyclic voltammetry (CV), and temperature-programmed

301 Using a non-mobile version of STM (2xNLS-YFP-STM), we show that STM mobility is required to suppress