ライフサイエンスコーパス: smooth

1 the contrast loss caused by greater temporal smoothing.

2 h time point independently and then performs smoothing.

3 lso generated without any postreconstruction smoothing.

4 Using a smart-sampling Kalman filtering smoothing algorithm improved sensor accuracy.

5 tures or rely on either manual inspection or smoothing algorithms that lose the underlying agent-base

6 by Bayesian Smoothing) capable of producing smooth and accurate nowcasts in multiple disease setting

7 lysis offers unique opportunities to achieve smooth and clean functionalization of drugs by unlocking

8 ese motors coordinate their action to ensure smooth and fast transport along the flagellum without st

9 e and scanning electron microscopy suggest a smooth and homogeneous distribution of grains on the fil

10 om healthy subjects were similar between the smooth and rough morphotypes of M. abscessus However, in

11 nsmission electron microscope testing of the smooth and rough nanoboxes show them to yield at 130 +/-

12 m wall thickness hollow Au-Ag nanoboxes with smooth and rough surfaces.

13 introduction system was designed to ensure a smooth and uninterrupted delivery of desolvated particle

14 our approach to scRNA-seq transformed by kNN smoothing and found that our model successfully classifi

15 ber-band baseline correction, Savitzky-Golay smoothing and standard normal variate transformation.

16 Overall, MAGIC, kNN-smoothing, and SAVER were found to outperform the other

17 The landscape is nearly smooth at low and high concentrations, but the tradeoff

18 00 and 900 cm(-1) followed by Savitzky-Golay smoothing, baseline correction and normalization to Amid

19 Lissencephaly ('smooth brain') is a severe brain disease associated with

20 The membrane surface is smoothed by deposition of the cellulose layer and modifi

21 sian approach, NobBS (Nowcasting by Bayesian Smoothing) capable of producing smooth and accurate nowc

22 ransport can differ from the case of ideally smooth channels.

23 round tissue level implants with a partially smooth collar between patients with thin (<=2 mm) and th

24 This increase is due to the smooth color change presented after the cue rather than

25 and is attributed to an ultra-thin and ultra-smooth copper-doped silver film with low optical loss an

26 We observe a smooth crossover from the disorder-driven superconductor

27 In mice performing rough-smooth discrimination, S1 units exhibit much stronger ph

28 g MNAs fulfill the geometric (sharp tips and smooth edges) and mechanical-strength requirements for f

29 ationary slow motion with hops to a fast and smooth efficient one.

30 als with high anchoring strengths can ensure smooth electrodeposition of lithium metal, thus paving t

31 m channels, and/or internal release from the smooth endoplasmic reticulum) near the postsynaptic dens

32 aller spines contain just a single tubule of smooth ER.

33 target compensate for the reduced vigour of smooth eye movements that occurs with the ingestion of l

34 ffects which are fundamentally impossible in smooth films.

35 Our purpose was to determine the effect of a smoothing filter and partial-volume correction (PVC) on

36 Conclusion: A smoothing filter and PVC had a significant effect on mea

37 inger to rub or tap three textured surfaces (smooth flat, medium rough, and rough) with three levels

38 % lower bending rigidity, thus destabilizing smooth [Formula: see text]um curvature radius structures

39 odel changes in the community structure as a smooth function of time.

40 the logarithm of mean gene counts as sums of smooth functions with the smoothing parameters and coeff

41 th tailored chirality distributions, such as smooth gradients in chirality and micropatterns with tai

42 scalloped hammerhead shark (Sphyrna lewini), smooth hammerhead shark (S. zygaena) and shortfin mako s

43 fter 270 days to be more yellow, rubbery and smooth, have a less sour and lingering aftertaste and ar

44 Smoothed incidence surfaces, environmental and socioecon

45 mogeneous channel formation, indicative of a smooth interface between the TMD and underlying electrol

46 The smooth interfaces and low defect density reduce phonon l

47 latter consisting of multifocal opacity and smooth interlobular septal thickening, possibly with sma

48 illing of a rough clinical isolate and not a smooth isolate, suggesting that unique host-pathogen int

49 assessed using locally-weighted scatterplot smoothing (LOWESS) regression and change-point analyses

50 er detection of lipid A derived from intact (smooth) LPS from host-pathogen MSI studies, proved elusi

51 on vaginal products (KY Jelly, Replens Silky Smooth lubricant, coconut oil, Replens Long-Lasting mois

52 an 10.0 mm with LOS or triangular shapes and smooth margins were benign.

53 and-valley structure and an emerging type of smooth membranes are prepared.

54 EpiSAFARI employs a novel smoothing method for decreasing noise in signal profiles

55 However, it protects the airway smooth muscle (ASM) against a loss of smooth muscle myos

56 n promotes beta-AR desensitization in airway smooth muscle (ASM) and compromises airway relaxation re

57 odorants on the contractile state of airway smooth muscle (ASM) and uncovered a complex mechanism of

58 ns desmin and vimentin in obstructed bladder smooth muscle (BSM).

59 2B subunits are expressed in mouse lymphatic smooth muscle (LSM) and form functional K(ATP) channels

60 yperpolarized both mouse and human lymphatic smooth muscle (LSM).

61 s widely expressed in many tissues including smooth muscle (SM), although its role in the regulation

62 00A4 is expressed in many tissues, including smooth muscle (SM), but its physiologic function is unkn

63 plex crosstalk between endothelial (ECs) and smooth muscle (SMCs) cells.

64 protein] receptor) is expressed in vascular smooth muscle (VSM) and increased VSM PTH1R signaling mi

65 Here we have solved the structure of smooth muscle 10S myosin by cryo-electron microscopy wit

66 Immunostaining with alpha-smooth muscle actin (alpha SMA) revealed a significant r

67 ss fibers, exhibited greater levels of alpha-smooth muscle actin (alpha-SMA) expression, and exerted

68 itative proteomic comparison of mature alpha-smooth muscle actin (alpha-SMA)+ myofibroblasts (verifie

69 ding collagen Ialpha1 (colIalpha1) and alpha-smooth muscle actin (alpha-SMA), and cell migration/woun

70 lls, associated with overexpression of alpha-smooth muscle actin (alpha-SMA), and differential upregu

71 ions in the gene, ACTA2, which encodes alpha-smooth muscle actin (alpha-SMA).

72 nthase 2, HAS2, and PDPN increased and alpha-smooth muscle actin alphaSMA mRNA decreased.

73 s I and VI, and the profibrotic factor alpha-smooth muscle actin compared with placebo in subcutaneou

74 own of GalR1 in cholangiocytes reduced alpha-smooth muscle actin expression in LX-2 cells treated wit

75 uces collagen I, fibronectin, elastin, alpha-smooth muscle actin in human adult dermal (HDFs) and neo

76 Similarly, alpha-smooth muscle actin(alpha-SMA) expression, aortic collag

77 s >60% of fibroblasts formed alphaSMA (alpha-smooth muscle actin) stress fibers and expressed myofibr

78 markers CNN-1 (calponin 1), alpha-SMA (alpha-smooth muscle actin), and SM22-alpha (smooth muscle prot

79 fibrotic markers f-actin, fibronectin, alpha smooth muscle actin, and collagen type 1 were equally di

80 fibrotic markers f-actin, fibronectin, alpha smooth muscle actin, and collagen type 1 were performed.

81 in, alpha(1) -antitrypsin, glypican-3, alpha-smooth muscle actin, and collagen type 1A2 markers were

82 n, hepatic expressions of collagen-1a, alpha-smooth muscle actin, and mononuclear cell infiltration (

83 expression of three fibrotic markers: alpha-smooth muscle actin, collagen 1, and fibronectin.

84 and PECAM1 and increases in collagen, alpha-smooth muscle actin, TGFbeta receptor 1, and the transcr

85 stress to promote fibrosis in the absence of smooth muscle actin-expressing myofibroblasts, a key pro

86 ted hepatic stellate cell; aHSCs) expressing smooth muscle alpha-actin (alphaSMA) and platelet-derive

87 ), a cytoplasmic protein expressed in airway smooth muscle and bronchial epithelium that regulates th

88 he variant were differentiated into vascular smooth muscle and endothelial cells that demonstrated ha

89 tion, a mechanism by which those channels in smooth muscle are thought to be targets of endothelium-d

90 ent of mesenchymal progenitors to the airway smooth muscle bundle.

91 sected advanced atherosclerotic lesions with smooth muscle cell (SMC) and endothelial lineage tracing

92 formation in MFS may be related to distinct smooth muscle cell (SMC) embryologic lineages.

93 sm development and identified a key role for smooth muscle cell (SMC) reprogramming into a mesenchyma

94 Smooth muscle cell (SMC)-specific RyR2 knockout (KO) or

95 a-1 (TGFbeta1) is a major driver of vascular smooth muscle cell (VSMC) phenotypic switching, an impor

96 Vascular smooth muscle cell (VSMC) remodeling is a pathological h

97 between mitochondrial dynamics and vascular smooth muscle cell (VSMC) senescence.

98 ic inflammation and remodeling via decreased smooth muscle cell activation and neutrophil transendoth

99 elastic fiber disruption, and an increase in smooth muscle cell alpha-actin expression compared to un

100 es and evaluates the changes in rat vascular smooth muscle cell biomechanics following statin-mediate

101 holesterol depletion remodels total vascular smooth muscle cell cytoskeletal orientation that may add

102 gene encoding NOTCH3 and results in vascular smooth muscle cell degeneration, stroke, and dementia.

103 imal and medial endothelial, macrophage, and smooth muscle cell function.

104 R-145-5p was strongly associated with airway smooth muscle cell growth in vitro.

105 caspase-1 secretion and attenuated leukocyte-smooth muscle cell interactions under high glucose or li

106 Smooth muscle cell migration is essential for many diver

107 Abi1 knockdown by shRNA reduced human airway smooth muscle cell migration, which was restored by Abi1

108 tics allow the investigation of pericyte and smooth muscle cell physiology and their role in regulati

109 g is associated with an increase in vascular smooth muscle cell proliferation and changes in vessel m

110 nhibition of TRPV4 channels mitigates aortic smooth muscle cell-dependent inflammatory cytokine produ

111 lpha-SMA function within the cerebrovascular smooth muscle cell.

112 f blood outgrowth endothelial cells (BOECs), smooth muscle cells (BO-SMCs), and leukocytes were obtai

113 In cultured coronary arterial smooth muscle cells (CASMCs) from Asah1(fl/fl)/SM(Cre) m

114 on in primary human coronary artery vascular smooth muscle cells (HCASMCs).

115 Human pulmonary artery smooth muscle cells (HPASMCs) demonstrated hypoxic induc

116 involved ongoing proliferation of intestinal smooth muscle cells (ISMC) with expression of platelet-d

117 duced vascular endothelial cells (iVECs) and smooth muscle cells (iSMCs) by direct reprogramming of h

118 Altered metabolism in pulmonary artery smooth muscle cells (PASMCs) and endothelial cells (PAEC

119 Smooth muscle cells (SMC) play a critical role in athero

120 rly stage of atherosclerosis and on vascular smooth muscle cells (SMC) remain to be fully elucidated.

121 Neointima arises from smooth muscle cells (SMCs) and not endothelium.

122 g extra domain A (Fn-EDA) is associated with smooth muscle cells (SMCs) following vascular injury.

123 erations in extracellular matrix and loss of smooth muscle cells (SMCs) in the medial layer of the ao

124 Smooth muscle cells (SMCs) play significant roles in ath

125 phages (in the absence of serum or HDL) onto smooth muscle cells (SMCs) that had been metabolically l

126 se vasodilatory factors that act directly on smooth muscle cells (SMCs) to induce arterial dilation a

127 ediated NO dioxygenation process in vascular smooth muscle cells (SMCs), and the requisite reducing s

128 ontractility and differentiation in vascular smooth muscle cells (SMCs), but the specific function of

129 uman atherosclerotic plaques associated with smooth muscle cells (SMCs), inflammation, extracellular

130 c motor neurons and SIP syncytium, including smooth muscle cells (SMCs), interstitial cells of Cajal

131 tional cells of the SIP syncytium, including smooth muscle cells (SMCs), interstitial cells of Cajal

132 in fully differentiated contractile vascular smooth muscle cells (SMCs).

133 Vascular smooth muscle cells (VSMCs) in the normal arterial media

134 mechanical fluctuations applied to vascular smooth muscle cells (VSMCs) regulates mitochondrial netw

135 a hybrid phenotype of striated and vascular smooth muscle cells (VSMCs), we performed lineage tracin

136 in the vessel wall, is mediated by vascular smooth muscle cells (VSMCs).

137 fication gene, highly expressed in arteries' smooth muscle cells and chondrocytes.

138 tin, MCP-1) in endothelial cells or vascular smooth muscle cells and decreased monocytes adhesion to

139 on PIP(2) as a regulator of ion channels in smooth muscle cells and endothelial cells-the two major

140 controlled proliferation of pulmonary artery smooth muscle cells and fibroblasts.

141 Mural cells (smooth muscle cells and pericytes) are integral componen

142 ese results identify P2Y(2) receptors in RTN smooth muscle cells as requisite determinants of respira

143 We also identify P2Y(2) receptors in RTN smooth muscle cells as the substrate responsible for thi

144 blockade or genetic deletion of P2Y(2) from smooth muscle cells blunted the ventilatory response to

145 gregated within the mitochondria of vascular smooth muscle cells can drive an hour-long disruption.

146 e, mutant transgenic PDE3A overexpression in smooth muscle cells confirmed that mutant PDE3A causes h

147 sed a strategy whereby human endothelial and smooth muscle cells derived from blood progenitors from

148 Compared with renal vascular smooth muscle cells from Add3 transgenic rats, those fro

149 differentiated human macrophages, and aortic smooth muscle cells from humans with diabetes), MCC950 s

150 e-expression of P2Y(2) receptors only in RTN smooth muscle cells fully rescued the CO(2)/H(+) chemore

151 Vascular smooth muscle cells going from a proliferative and motil

152 rimentally by treating human coronary artery smooth muscle cells in an in vitro calcification assay.

153 Endothelial and smooth muscle cells in arterial tissue expressed CARD8 a

154 nd to be expressed predominantly on vascular smooth muscle cells in lesions of athero-prone Apoe(-/-)

155 well as the expression of CD47 from arterial smooth muscle cells in mice.

156 cepted role of the protein Kv2.1 in arterial smooth muscle cells is to form K(+) channels in the sarc

157 l proline-rich repeat 3 (SPRR3), in vascular smooth muscle cells of atheromas.

158 intercellular Ca(2+) waves are generated in smooth muscle cells of colonic longitudinal muscles (LSM

159 gene signatures of mesangial cells, vascular smooth muscle cells of the afferent and efferent arterio

160 Smooth muscle cells of the muscularis mucosa, in close p

161 ed in mice harboring specific endothelial or smooth muscle cells or cardiomyocyte or myeloid cell def

162 ssion of Akt1E17K to endothelial, cardiac or smooth muscle cells resulted in viable offspring and rem

163 crine prostaglandin E(2) signaling in airway smooth muscle cells that eventually triggered cAMP/PKA-d

164 e Kv7.4 and Kv7.5 alpha-subunits in vascular smooth muscle cells to determine which components are es

165 ogy, adhesion, and migration of human airway smooth muscle cells transfected with PKAc variants conta

166 endothelial cells and alpha-SMA(+) vascular smooth muscle cells were detected within all cellular zo

167 neurons(1), cardiomyocytes(2-4) and vascular smooth muscle cells(5), where they are involved in the r

168 nd cell types, including platelets, vascular smooth muscle cells, and neuronal cells.

169 r cells, like endothelial cells and vascular smooth muscle cells, cardiac myocytes and inflammatory c

170 ised intracellular Ca(2+) levels in arterial smooth muscle cells, constricted arterioles ex vivo and

171 ro-inflammatory actions of TWEAK on vascular smooth muscle cells, decreasing NF-kB activation, cytoki

172 Distinct loss of function of IDO in smooth muscle cells, inflammatory cells, or cardiomyocyt

173 ing through activation of nuclear ERalpha in smooth muscle cells, inviting to revisit the mechanisms

174 onmyocyte cardiac lineages, such as vascular smooth muscle cells, pericytes, and fibroblasts.

175 3 and IL-4 in human bronchi and human airway smooth muscle cells.

176 y endothelial cells, pericytes, and vascular smooth muscle cells.

177 diomyocytes compared to neurons and vascular smooth muscle cells.

178 imary human airway epithelial progenitor and smooth muscle cells.

179 ed in lesional macrophages, endothelial, and smooth muscle cells.

180 ood vessels are comprised of endothelial and smooth muscle cells.

181 djacent to the PAA endothelium into vascular smooth muscle cells.

182 quired the presence of the underlying medial smooth muscle cells.

183 sion of CD47 and other oncogenes in arterial smooth muscle cells.

184 to longitudinal proliferation of arteriolar smooth muscle cells.

185 unter to the expectation that the absence of smooth muscle constriction would lead to a more relaxed

186 regression and niche relocation through the smooth muscle contractile machinery that generates centr

187 the first time, that effects of compromised smooth muscle contractility are more important in terms

188 st that directly inhibits calcium influx and smooth muscle contractility, leading to voiding dysfunct

189 l negative feedback mechanism that regulates smooth muscle contractility.

190 a(1A)-adrenoreceptor, a GPCR that stimulates smooth muscle contraction in response to binding noradre

191 expression along with reduced expression of smooth muscle differentiation markers in the carotids.

192 rplasia, diseases linked to loss of vascular smooth muscle differentiation.

193 activating Myocardin, which prevented airway smooth muscle differentiation.

194 ated with the life-threatening multisystemic smooth muscle dysfunction syndrome (MSMDS) due to mutati

195 irway hyperresponsiveness as an indicator of smooth muscle dysfunction, and treating them appropriate

196 agonist Bay k8644 abrogates ketamine-induced smooth muscle dysfunction.

197 In tracheal smooth muscle ex vivo, in organ baths, isometric contrac

198 causing tissue depolarization and increased smooth muscle excitability.

199 myosin heavy chain (smMHC) and several other smooth muscle gene transcripts, indicating these cells a

200 (-/-) mice rendered both bladder and urethra smooth muscle hypercontractile.

201 As rapamycin can attenuate bladder smooth muscle hypertrophy and dysfunction during the gen

202 We show that Poldip2 deficiency in vascular smooth muscle in vitro and in vivo induces the expressio

203 channel localizes to vascular endothelium or smooth muscle is controversial and the distribution and

204 strate that during development, while airway smooth muscle is dispensable for epithelial branching, i

205 ajor constituent alpha-terpinene on tracheal smooth muscle isolated from rats.

206 xcitability and contractility of the uterine smooth muscle layer, the myometrium, increase drasticall

207 senchyme to produce rhythmically contracting smooth muscle layers.

208 t and cardiovascular system, blood, kidneys, smooth muscle lineage and limb skeleton in the developin

209 or DR3 restricted increases in peribronchial smooth muscle mass and accumulation of lung collagen, pr

210 pathogenesis is unclear, although increased smooth muscle mass is present.

211 id cells type 2 (ILCs), and increased airway smooth muscle mass via recruitment of mesenchymal progen

212 However, the role and mechanism of Abi1 in smooth muscle migration are largely unknown.

213 polymerization in vitro of nonphosphorylated smooth muscle myosin filaments by the addition of MgATP

214 PDGFRalpha(+) cells in the PKJ co-expressed smooth muscle myosin heavy chain (smMHC) and several oth

215 airway smooth muscle (ASM) against a loss of smooth muscle myosin heavy chain (SMMHC) expression.

216 nomers assemble into bipolar and side-polar (smooth muscle myosin) filaments.

217 4 h, the myosins form thick bipolar and, for smooth muscle myosin, side-polar filaments.

218 Although it has long been recognized that smooth muscle Na/K ATPase modulates vascular tone and bl

219 ation, revealing extensive expression in the smooth muscle of resistance arterioles supplying skeleta

220 g revealed specific localization of TRPV1 to smooth muscle of terminal arterioles in the heart, adipo

221 ver, in plasma and lung endothelium, but not smooth muscle or adventitia, miR-210 was observed in kno

222 erstanding of the roles of these channels in smooth muscle physiology and disease, particularly in co

223 (alpha-smooth muscle actin), and SM22-alpha (smooth muscle protein 22alpha) and an increase in synthe

224 C processes and indicating the importance of smooth muscle response to vascular stress and phenotypic

225 gain-of-function KATP mutations in vascular smooth muscle resulted in cardiac remodeling.

226 cellular electrode measurements in lymphatic smooth muscle revealed only subtle, but not significant,

227 The periodic cartilage and smooth muscle structures in mammalian trachea are derive

228 s, our study identifies the dermal sheath as smooth muscle that drives follicle regression for reunit

229 Genetic ablation of smooth muscle TRPC3 channels shortened the duration of S

230 Human myenteric ganglia and adjacent smooth muscle were isolated by laser-capture microdissec

231 l mesenchymal specification to cartilage and smooth muscle, coupling epithelial identity with mesench

232 In smooth muscle, cytoglobin (Cygb) functions as a potent n

233 ated support cells that include fibroblasts, smooth muscle, macrophages and other immune cells.

234 -type VGCCs are expressed in mouse lymphatic smooth muscle, they do not play a significant role in mo

235 a-pig urothelium, suburothelium, and bladder smooth muscle, with urothelial predominance.

236 , TPPP3/PRG4+ chondrogenic cells, and ITGA7+ smooth muscle-mesenchymal cells.

237 responses to capsaicin revealing a vascular smooth muscle-restricted signalling mechanism.

238 Smooth muscle-specific expression of a Kir6.1 gain-of-fu

239 Smooth muscle-specific expression of Kir6.1 gain-of-func

240 rlap of these QTLs and their relationship to smooth muscle-specific genes and transcription factors.

241 ation genes (proteins) to the human vascular smooth muscle-specific protein-protein interactome (218

242 and lung inflammation in germline and airway smooth muscle-specific Rgs4(-/-) mice and in mice treate

243 To examine this possibility, we developed a smooth muscle-specific TRPC3 knockout (TRPC3smcKO) mouse

244 n might initiate and spread in this myogenic smooth muscle.

245 tid, which was not myoepithelial or vascular smooth muscle.

246 een in glia, interstitial cells of Cajal, or smooth muscle.

247 g growth factor beta (TGF-beta) signaling in smooth muscle.

248 lar physiology, regulating vascular tone and smooth-muscle cell phenotype.

249 In contrast, smooth-muscle specific deletion of the L-type VGCC, Ca(v

250 lpha5-containing GABA(A) receptors in airway smooth muscles are considered as an emerging target for

251 endothelial cells with 2 abluminal layers of smooth muscles cells and matrix.

252 Smooth muscles of the lower esophageal sphincter (LES) a

253 ion, such that firing probability grows as a smooth nonlinear function of membrane potential; and (2)

254 a smaller task related to factoring: finding smooth numbers, which is an essential step of the Number

255 CaSpER integrates the multiscale smoothing of expression signal and allelic shift signals

256 the changes are attributed to atomic-scale "smoothing" of the surface by preferential sublimation of

257 arious factors such as hydrophobic material, smooth optic surface, and sharp posterior optic edge pla

258 the presence of signs favoring PLC on HRCT (smooth or nodular septal lines, subpleural nodularity, p

259 te that the formation of a relatively thick, smooth oxide sheath can improve the catalytic stability

260 counts as sums of smooth functions with the smoothing parameters and coefficients estimated simultan

261 We estimated smooth percentiles for RR and SpO(2) that varied by age

262 Smooth percentiles for RR and SpO(2) varied by site and

263 th irregular or ulcerated plaque and 27 with smooth plaque; P = .54).

264 Savitsky-Golay (SG) derivative, smoothing points, and polynomial order, and extended mul

265 Thus, Neuralized promotes smooth progression of the differentiation front by coupl

266 We propose smooth q-gram, a variant of q-gram that captures q-gram

267 orithm for detecting overlapping reads using smooth q-gram-based seeds.

268 ysaccharides in IDFs had lower proportion of smooth region and higher proportion of hairy region that

269 the number of elements required to achieve a smooth response.

270 ) as it transcribes a gene is anything but a smooth ride.

271 Ninety-six smooth (S) and 96 minimally rough (R) titanium microimpl

272 raded impact crater in Elysium Planitia on a smooth sandy, granule- and pebble-rich surface with few

273 branes via structural optimization: first, a smooth selective layer should be maintained to ensure un

274 gravity between a millimetric droplet and a smooth solid or a liquid thin film.

275 wo distinct surface characters, wrinkled and smooth spherical.

276 elling, cognitive decline was assessed using smoothing splines and linear mixed effects models.

277 n empirical recurrence rates ratio (ERRR), a smoothing statistic that is gradually gaining currency i

278 (p < 0.01), while the product Replens Silky Smooth stimulated growth (p < 0.01).

279 shear zones and fault planes have spatially smooth stress with predominantly time-dependent stress i

280 m laminar to turbulent flow occurring over a smooth surface is a particularly important route to chao

281 Arrokoth has a lightly cratered, smooth surface with complex geological features, unlike

282 scopy (SEM) images demonstrated a relatively smooth surface with small pore size.

283 tained were oval to round in shape and had a smooth surface.

284 ubSP and the previously identified bumpy and smooth-surfaced spherical particles, may help flavivirus

285 Moreover, the preparation of smooth surfaces is crucial for vertically stacked device

286 m) have been observed to generate remarkably smooth surfaces not predicted by low-pressure deposition

287 Then, the microparticles swelled to form smooth surfaces.

288 at is much faster than that generated during smooth, symmetric vergence eye movements.

289 dingly, protraction-tuned units encode rough-smooth texture better than retraction-tuned units and en

290 of our analyzed phenotypes are sufficiently smooth that some evolutionary paths remain accessible fo

291 g-rate selection assumption proposed by CBGB smooths the transition between limiting rates and always

292 ight propagates inside a thin soap membrane, smooth thickness variations in the film act as a correla

293 benzene-containing materials and showed that smooth topographical cues with proper period and orienta

294 A smooth traceless ligation strategy using an air-stable p

295 d dysmetria in selected trials manifesting a smooth trajectory to the endpoint.

296 This suggests a smooth transition between insulating and metallic layers

297 the host-pathogen interface: OMVs with long (smooth-type) lipopolysaccharide lipids retain their sphe

298 e, combining chipping of outer enameloid and smooth wear of inner enameloid to preserve an efficient

299 the films reveals that these films are very smooth with low roughness, the thin films synthesized at

300 me-of-flight modeling and postreconstruction smoothing with a 5-mm gaussian filter.