ライフサイエンスコーパス: STM

1 STM activates cytokinin (CK) biosynthesis in the SAM, bu

2 STM and 2D-WAXS experiments reveal that both in solution

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

4 STM and organ boundary genes CUP SHAPED COTYLEDON1 (CUC1

5 STM detection is a fast test of suprathreshold auditory

6 STM images show 1-D and 2-D periodic super-lattices orig

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

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

9 STM is also required for proper meristem organisation an

10 STM measurements in combination with density functional

11 STM reveals a clear energetic preference for methane bin

12 STM sensitivity was most critical in predicting SRTs for

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

14 Participants then completed a STM retrieval task using either random or patterned digi

15 We demonstrate interspecific silencing of a STM gene in dodder driven by a vascular-specific promote

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

17 ontrolling the competing interactions with a STM probe tip and the electric field from a back-gate el

18 tability to undergo repeated scanning with a STM tip as well as other electrochemical investigations.

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

23 id interface in a combined approach using an STM break junction (STM-BJ) and a mechanically controlle

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

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

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

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

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

29 tion we provide the first UHV-STM images and STM-based current-voltage (I-V) and orbital mediated tun

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

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

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

33 ecules results in mixed-valence species, and STM images of mixed-valence meta-Fe2 show pronounced asy

34 atus, serial serum tumor markers (STMs), and STM changes over time.

35 lso report here the synthesis, structure and STM current-imaging studies of DNA oligonucleotides cont

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

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

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

39 owed strong topographic and current peaks by STM imaging, suggesting a potential strategy to directly

40 Combined STM imaging and gap-mode Raman experiments provide struc

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

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

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

44 hological investigations (X-ray diffraction, STM, AFM).

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

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

47 750 patients during SWS and 461 (61%) during STM (p<0.0001).

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

49 equency and cause of patient symptoms during STM.

50 Inhibition of TrkB during STM training blocked such consolidation.

51 density functional theory molecular dynamics STM image simulations.

52 rochemical scanning tunneling microscopy (EC-STM) techniques and macroscopic electrochemical measurem

53 rochemical scanning tunneling microscopy (EC-STM).

54 High-resolution EC-STM images show individual peptide molecules forming cha

55 The EC-STM imaging revealed uniform surface coverage with suffi

56 e spectroelectochemistry and electrochemical STM, we suggest that the single-molecule redox reaction

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

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

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

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

61 monotonically increasing neural encoding for STM.

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

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

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

65 lity improves retrieval speed of digits from STM, regardless of set configuration.

66 ding geometry, which cannot be inferred from STM alone, was determined from atomic force microscopy i

67 lted in faster retrieval of information from STM for both stimulus types.

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

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

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

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

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

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

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

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

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

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

78 etaining dynamic sounds and static images in STM.

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

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

81 the apparent heights of excited molecules in STM images, a direct manifestation of probing electronic

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

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

84 veral coexisting auditory representations in STM.

85 n among different representational states in STM.

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

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

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

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

90 mbined approach using an STM break junction (STM-BJ) and a mechanically controlled break junction (MC

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

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

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

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

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

96 ine Trim32 corresponding to the human LGMD2H/STM pathogenic mutation c.1459G > A (p.D487N).

97 factors, including SHOOT MERISTEMLESS-like (STM).

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

99 emperature scanning tunneling microscopy (LT-STM) to reveal the graphene growth intermediates at diff

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

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

102 core based primarily on serum tumor markers (STMs) that could predict short cancer-specific survival

103 ological status, serial serum tumor markers (STMs), and STM changes over time.

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

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

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

107 cervical swab and specimen transport medium (STM) cervical swab samples were collected from 135 patie

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

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

110 k training, which induces short-term memory (STM) but not LTM, can be consolidated into LTM by exposi

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

112 vo to synapses to support short-term memory (STM) formation.

113 ular task to study visual short-term memory (STM) in humans [1-4].

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

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

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

117 al priming on recall in a short-term memory (STM) task.

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

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

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

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

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

123 the shoot meristem genes SHOOT MERISTEMLESS (STM) and CUP-SHAPED COTYLEDON2 (CUC2), in addition to de

124 dopsis class-1 KNOX gene SHOOT MERISTEMLESS (STM) encodes a homeodomain transcription factor essentia

125 US), CLAVATA3 (CLV3) and SHOOT MERISTEMLESS (STM).

126 the homeodomain protein SHOOT MERISTEMLESS (STM).

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

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

129 g a cryogenic scanning tunneling microscope (STM).

130 itations in a scanning tunneling microscope (STM).

131 lation in the scanning tunneling microscope (STM).

132 shed with the scanning tunneling microscope (STM).

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

134 ere we use a scanning tunnelling microscope (STM) to induce a sequence of targeted bond dissociation

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

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

137 estigated via Scanning Tunneling Microscopy (STM) and first-principle theoretical simulations.

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

139 Through scanning tunneling microscopy (STM) and point I-V measurements, the current study revea

140 hene layer by scanning tunneling microscopy (STM) and scanning tunneling spectroscopy (STS) measureme

141 easured using scanning tunneling microscopy (STM) and scanning tunneling spectroscopy (STS).

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

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

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

145 ic resolution scanning tunneling microscopy (STM) experiments conducted at 165 degrees C showing inta

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

147 esolution UHV scanning tunneling microscopy (STM) images confirm the one-dimensional ordering of the

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

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

150 , and in situ scanning tunneling microscopy (STM) in aqueous biological buffer under electrochemical

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

152 Scanning tunneling microscopy (STM) is used to image these species at 77 K under ultrah

153 Scanning tunneling microscopy (STM) is used to study two dinuclear organometallic molec

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

155 2 ne(2)/h in scanning tunneling microscopy (STM) measurements which would show strong (weak) signals

156 n the in situ scanning tunneling microscopy (STM) molecular break junction configuration.

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

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

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

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

161 ere imaged by scanning tunneling microscopy (STM) using a low tunneling current of 10 pA.

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

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

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

165 is studied by scanning tunneling microscopy (STM), and thermodynamic data are derived.

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

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

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

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

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

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

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

173 w-temperature scanning tunneling microscopy (STM).

174 w-temperature scanning tunneling microscopy (STM).

175 signature in scanning tunneling microscopy (STM).

176 strates using scanning tunneling microscopy (STM).

177 r level using scanning tunneling microscopy (STM).

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

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

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

181 in bulk, but scanning tunnelling microscopy (STM) could provide such data for surfaces.

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

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

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

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

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

187 Scanning tunnelling microscopy (STM) measurements show the formation of self-assembled m

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

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

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

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

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

193 Although the monkeys' STM was well fit by a one-item fixed-capacity memory mod

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

195 phy type 2H (LGMD2H), sarcotubular myopathy (STM) and Bardet Biedl syndrome.

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

197 Novel STM-based conductance measurements combined with quantum

198 ve for any high-risk HPV types, and 24.6% of STM samples were positive for any high-risk HPV types.

199 Acquisition of STM for FC can occur even in the presence of protein syn

200 ogy to better understand the neural basis of STM.

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

202 The field dependence of STM images and point I-V curves indicates a spin polariz

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

204 Expression of STM was activated in these ectopic meristems but not oth

205 thaliana STM locus, indicating that loss of STM expression in A. thaliana leaves may have been fixed

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

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

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

209 information among representational states of STM.

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

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

212 The reduced efficacy of dodder infection on STM RNA interference transgenics results from defects in

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

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

215 ot act specifically in either the WUS/CLV or STM pathway regulating meristem function.

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

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

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

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

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

221 uding ambient pressure XPS, ambient pressure STM, X-ray absorption spectroscopy and others.

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

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

224 ting transcription factor SHOOTMERISTEMLESS (STM), similar to the expansion of WUS expression in the

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

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

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

228 c imaging scanning tunnelling microscopy (SI-STM) to image the evolution of URu(2)Si(2) electronic st

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

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

231 bsorption scanning tunneling microscopy (SMA-STM).

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

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

234 nning tunneling microscopy and spectroscopy (STM and STS) of NG revealed the presence of localized st

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

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

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

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

239 High-temperature STM imaging shows virtually no fluctuation of Na-TPA isl

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

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

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

243 inally, Carf KO mice show normal short-term (STM) and long-term memory (LTM) in a novel object recogn

244 nce for a selective sweep at the A. thaliana STM locus, indicating that loss of STM expression in A.

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

246 We propose that STM has dual cellular and meristem-organisational functi

247 Here we show that STM inhibits cellular differentiation and endoreduplicat

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

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

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

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

252 Much of this work suggests that STM has a fixed capacity of 4 +/- 1 items [1-6].

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

254 The STM images display an unexpected honeycomb feature, whic

255 The STM images show extended and homogeneous domains, offeri

256 The STM images suggest that each Alm is shared between the t

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

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

259 The STM topographies reveal a symmetry-breaking distortion o

260 selective molecular sites controlled by the STM tip.

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

262 insulin sensitivity were estimated from the STM and by frequently sampling intravenous glucose toler

263 ity of the surface species proposed from the STM images, finding that the most stable state of a wate

264 Electron injection from the STM tip into the adsorbed CO(2) induces the dissociation

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

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

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

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

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

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

271 In particular, the STM is used to study the reversible binding of O(2) with

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 rve (AUC0-120) of glucose in response to the STM as compared with G2, and G3 (P < 0.01).

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

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

278 -risk HPV DNA was detected in three of their STM samples and in five of their dry samples.

279 c neural correlates of auditory attention to STM.

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

281 one-dimensional ordering as verified by UHV STM and ambient atomic force microscopy (AFM).

282 In particular, UHV STM, sum frequency generation (SFG), and density functio

283 this communication we provide the first UHV-STM images and STM-based current-voltage (I-V) and orbit

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

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

286 ng molecules to synaptic junctions underlies STM.

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

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

289 by fast scanning tunneling microscopy (video STM) and dispersion corrected density functional theory

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

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

292 ynthesis in the SAM, but the extent to which STM function is mediated through CK is unclear.

293 ork resolves the long-standing puzzle of why STM is more challenging for layered manganites than for

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

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

296 symmetric electron density when imaged with STM under ultrahigh-vacuum conditions at 77 K.

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

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

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

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