ライフサイエンスコーパス: circular

1 ts cross-section significantly deviates from circular.

2 roidal vessels in a 6-mm-diameter submacular circular.

3 conventional or surround flow irrigation and circular ablation catheters with open irrigation (nMARQ)

4 In this study, two circular ACP mitogenome sequences from California (mt-CA

5 ng close to cool stars are expected to be on circular, aligned orbits because of strong tidal interac

6 oom-temperature lasing in protein rings, and circular and elliptical pillars with customized beam sha

7 Using x-ray magnetic circular and linear dichroism techniques, we demonstrate

8 and estimates the expression values of both circular and linear transcripts using an existing model-

9 43 RNP granules in the proximal axon is less circular and shows spiculated edges, whereas more distal

10 oups of microrobots were moved along linear, circular, and arbitrary 2D trajectories.

11 ical area and transition from a polygonal to circular apical shape to achieve robust mitotic rounding

12 The CB was defined as a circular area of approximately 100 mum composed of dense

13 rs were asked to judge the average tilt in a circular array of high-contrast gratings, relative to an

14 a strong potential in a future sustainable, circular bioeconomy.

15 Results from the circular blister test, however, display seemingly anomal

16 creating reproducible, central, and precise circular capsulotomy.

17 Circular carrier plasmid DNA is included during subseque

18 Hepatitis B virus (HBV) covalently closed circular (CCC) DNA functions as the only viral template

19 he hepatitis B virus (HBV) covalently closed circular (CCC) DNA, by serving as the viral transcriptio

20 b-on-a-chip capable of mechanically inducing circular cell-free areas within confluent cell layers.

21 jured cells were found along the edge of the circular cell-free areas, thus allowing reliable and rep

22 identify target genes of these DREs, we used circular chromosome conformation capture (4C) sequencing

23 Circular chromosome conformation capture (4C-seq) identi

24 s for human atherosclerotic disease based on circular chromosome conformation capture followed by seq

25 By circular chromosome conformation capture followed by seq

26 tierella elongata and assembled the complete circular chromosome of its endosymbiont, Mycoavidus cyst

27 sponsible for duplicating the entire 4.6 Mbp circular chromosome.

28 lted in four contiguous sequences: two large circular chromosomes and two smaller putative plasmids.

29 cently uncovered tens of thousands of unique circular (circ)RNAs, but their complete sequences, genes

30 The SNAREpins self-organized into a circular cluster at the fusion site, driven by entropic

31 a proportion of iPS cells spontaneously form circular colonies, each of which is composed of four con

32 multiple state of canting spin stripes is a circular configuration with zero skyrmion charge number.

33 sumption system to naturally evolve toward a circular configuration.

34 consensus reads derived from at least 7 full circular consensus sequencing rounds significantly reduc

35 By using 7 passes of circular consensus sequencing, the error rate was reduce

36 er, the first tool that can extract complete circular contigs from sequence data of isolate microbial

37 e structural units: the N-terminal unit, the Circular Cradle, and the Head.

38 ng a variety of nontrivial phenomena such as circular dichiroism for chiral molecules, magnetic Skyrm

39 By careful circular dichroism (CD) analyses of daptomycin with Ca(2

40 up to four NOTAs was still functional; (iii) circular dichroism (CD) analysis confirmed the complexat

41 Circular dichroism (CD) and mass spectrometry studies wi

42 ally selective damage of biomolecules due to circular dichroism (CD) can generate EE of correct hande

43 g the "sergeant-and-soldiers" approach using circular dichroism (CD) experiments, we are able to obta

44 calculate electronic absorption (UV-vis) and circular dichroism (CD) spectra of typical biomolecules

45 Circular dichroism (CD) spectroscopy experiments indicat

46 pproach produced quantitative agreement with circular dichroism (CD) spectroscopy in detecting the do

47 Circular dichroism (CD) spectroscopy is a well-establish

48 Circular dichroism (CD) spectroscopy is extensively util

49 relates with the strength of the acceptor QD circular dichroism (CD) spectrum.

50 Using circular dichroism (CD) we find that in solution the cor

51 -modified DNA films was characterized by UV, circular dichroism (CD), and X-ray photoelectron spectro

52 structure were confirmed by Western Blot and Circular Dichroism (CD), respectively.

53 in structure and activity was analyzed using circular dichroism (CD), Site-Directed Spin Labeling (SD

54 and by comparison of experimental electronic circular dichroism (ECD) data with TDDFT-ECD calculation

55 pproaches including solution NMR, electronic circular dichroism (ECD), and single-crystal X-ray diffr

56 nt for high-throughput synchrotron radiation circular dichroism (HT-SRCD) has been developed to satis

57 Induced circular dichroism (ICD) of DNA-binding ligands is well

58 We show that magnetic circular dichroism (MCD) of sun's ultraviolet C light by

59 ic resonance (EPR), absorption, and magnetic circular dichroism (MCD) spectroscopies show that CuZ de

60 ibed with an emphasis on the use of magnetic circular dichroism (MCD) spectroscopy to validate the re

61 spectroscopic methods ((119)Sn-NMR, magnetic circular dichroism (MCD), electron paramagnetic resonanc

62 wine, was analyzed by Synchrotron Radiation Circular Dichroism (SRCD) spectroscopy.

63 pendent density functional theory-electronic circular dichroism (TDDFT-ECD) calculations of the solut

64 ) using a focused X-ray beam, X-ray Magnetic Circular Dichroism - Photo Emission Electron Microscopy

65 xibility and structural shifting hypothesis, circular dichroism analysis of rSp0032 suggests that it

66 Circular dichroism analysis shows the alt-PASs adopt a r

67 etics for racemization of 28 compounds using circular dichroism and (1) H NMR spectroscopy.

68 material, the AOS is attributed to magnetic circular dichroism and angular momentum transfer between

69 ine probe to capture the target compound for circular dichroism and fluorescence sensing analysis.

70 condary structure of kafirin as evaluated by circular dichroism and Fourier-transform infrared red sp

71 Protein solubility, zeta potential, circular dichroism and gel strength of the collagen extr

72 chick embryo skeletal development, and using circular dichroism and matrix least-squares Henderson-Ha

73 was assessed using ultraviolet spectroscopy, circular dichroism and native gel electrophoresis.

74 Circular dichroism and NMR experiments confirmed the dis

75 ich was further established with the help of circular dichroism and Raman spectroscopy.

76 We used circular dichroism and site-directed spin labeling coupl

77 n mPPCs and Abeta monomer/oligomers based on circular dichroism and Thioflavin T fluorescence assays.

78 est LC-MS/MS for sequence determination, and circular dichroism and tryptophan fluorescence spectrosc

79 d on measurements of UV-vis spectrum, far-UV circular dichroism and tryptophan fluorescence, and the

80 mentary DNA molecules were examined by using circular dichroism and UV-vis spectroscopy in comparison

81 Using electron microscopy, circular dichroism and X-ray fiber diffraction, we have

82 ctra of porphycenes: Absorption and magnetic circular dichroism are discussed, together with their an

83 Circular dichroism as high as 0.6 is experimentally obse

84 sense chiral molecules with inherently weak circular dichroism at visible and near-infrared frequenc

85 1-108-alphaS fibrils have a unique negative circular dichroism band at approximately 230 nm, a featu

86 The Protein Circular Dichroism Data Bank (PCDDB) has been in operati

87 gold standard' set obtained from the Protein Circular Dichroism Data Bank (PCDDB).

88 tron paramagnetic resonance spectroscopy and circular dichroism data indicate MDPs do not act by bind

89 It started from the observation of strong circular dichroism during the synthesis of individual na

90 e interactions were verified here by NMR and circular dichroism experiments as well as investigated u

91 A combination of solid-state NMR and circular dichroism experiments found the latter orientat

92 Kinetic and circular dichroism experiments with C69G-GES-5 demonstra

93 We provide evidence from magnetic circular dichroism measurements supporting the hypothesi

94 ctrical recording, molecular simulations and circular dichroism measurements to provide high-resoluti

95 Circular dichroism measurements yielded a melting point

96 eraction, an observation consistent with our circular dichroism measurements.

97 Circular dichroism peaks in the visible range change fro

98 Oriented Circular Dichroism results showed that the peptide was o

99 Molecular dynamics and circular dichroism revealed an amphipathic helix within

100 Circular dichroism spectra also supported these evidence

101 was proved by the comparison of the NMR and circular dichroism spectra and of the specific optical r

102 Circular dichroism spectra in far UV and thermal denatur

103 nantiomers have pronounced features in their circular dichroism spectra resulting solely from topolog

104 in the 1D-IR (FTIR), 2D-IR, and vibrational circular dichroism spectra.

105 5 years as a public repository for archiving circular dichroism spectroscopic data and associated bio

106 xylate-oxygen is an M(+) ligand, and EPR and circular dichroism spectroscopies reveal that both the s

107 tween the NDI units probed by absorption and circular dichroism spectroscopies, electrochemistry and

108 (DSC), fluorescence-quenching, infrared and circular dichroism spectroscopies.

109 ere also investigated through application of Circular Dichroism spectroscopy (CD).

110 Circular dichroism spectroscopy and dynamic light scatte

111 EHMT1 p.P809L was also studied using far UV circular dichroism spectroscopy and intrinsic protein fl

112 Synchrotron radiation circular dichroism spectroscopy confirmed that purified

113 es compared to Abeta (1-42), as indicated by circular dichroism spectroscopy data.

114 Circular dichroism spectroscopy in combination with dyna

115 ht scattering, stopped-flow fluorescence and circular dichroism spectroscopy in combination with ther

116 Small angle neutron scattering and circular dichroism spectroscopy showed no substantial ch

117 Circular dichroism spectroscopy shows strong Cotton effe

118 atography, small-angle x ray scattering, and circular dichroism spectroscopy suggest partial unfoldin

119 Far-UV circular dichroism spectroscopy was used to confirm the

120 Circular Dichroism spectroscopy was used to investigate

121 spectrometry, size-exclusion chromatography, circular dichroism spectroscopy, and electron microscopy

122 icroscopy, small angle x-ray scattering, and circular dichroism spectroscopy, showing that it assumes

123 Results from circular dichroism spectroscopy, size exclusion chromato

124 ase with BA was measured by fluorescence and circular dichroism spectroscopy.

125 at is typically detectable with conventional circular dichroism spectroscopy.

126 data as well as investigation of the UV and circular dichroism spectrum in trifluoroethanol for comp

127 compute from first principles the electronic circular dichroism spectrum of a (modeled or experimenta

128 me, which exhibits a pronounced shift in its circular dichroism spectrum under a modest level of exci

129 re most important in determining the near-UV circular dichroism spectrum.

130 Circular dichroism studies indicated that self-assembly

131 Solution circular dichroism studies show that compound 1 also for

132 peptides using variable-temperature NMR and circular dichroism suggests that preorganization of line

133 A combination of UV-vis and circular dichroism were used to determine thermal stabil

134 achiral structure, yet they can give rise to circular dichroism when the experiment itself becomes ch

135 ubstitutions, electronic absorption, near-UV circular dichroism, and electron paramagnetic resonance

136 biochemical and biophysical tools involving circular dichroism, fluorescence, Raman spectroscopy, an

137 ation of mutated sw ApoMb were studied using circular dichroism, Fourier transform infrared spectrosc

138 ed region (UTR) of NRF2 mRNA, as measured by circular dichroism, nuclear magnetic resonance, and dime

139 ion Fourier transform infrared spectroscopy, circular dichroism, scanning electron microscopy and tra

140 xcitonic transport properties with prominent circular dichroism, superradiance, and fast delocalized

141 Using circular dichroism, we find that the tC(O)-modified RNA

142 he absolute configuration was established by circular dichroism.

143 e x-ray scattering and both near- and far-UV circular dichroism.

144 teins, as demonstrated by gel filtration and circular dichroism.

145 electronic states by means of X-ray magnetic circular dichroism.

146 associated a strong chiroptical signature in circular dichroism.

147 ve intermediates including covalently closed circular DNA (cccDNA) are present.

148 bly, capsid uncoating, and covalently closed circular DNA (cccDNA) formation.

149 ies in the accumulation of covalently closed circular DNA (cccDNA) in nuclei of infected cells.

150 HBV covalently closed circular DNA (cccDNA) plays an essential role in HBV per

151 te or inactivate the viral covalently closed circular DNA (cccDNA), which is a stable episomal form o

152 e detected eccDNAs were also associated with circular DNA enrichment efficiency.

153 , taurocholate uptake, HBV covalently closed circular DNA formation, and expression of all HBV marker

154 During infection, the circular DNA genome of HPV persists within the nucleus,

155 nd, which would nevertheless preserve closed circular DNA in either single-stranded (SS) or double-st

156 formation of H-NS nucleoprotein complexes on circular DNA molecules having different arrangements of

157 Using one- and two-site circular DNA substrates we show that CglI does not requi

158 e cure (ie, eradication of covalently closed circular DNA) of CHB, several challenges in basic resear

159 used with different DNA sequences, linear or circular DNA, bulk genomic DNA, recombinant or native Dr

160 urface (HBs) antigens, and covalently closed circular DNA, was observed in HUHEP and HIS-HUHEP mice.

161 y removing all DNA species other than closed circular DNA.

162 nally includes loss of HBV covalently closed circular DNA.

163 Extrachromosomal circular DNAs (eccDNAs) have been reported in most eukar

164 Circular dorsal ruffles (CDRs) are actin-rich structures

165 tually all plastid (chloroplast) genomes are circular double-stranded DNA molecules, typically betwee

166 Our images show a nearly circular, dust-free atmosphere, which is very compact an

167 s finding has important implications for the circular economy concept, indicating that quite a long p

168 eliorate this situation by introducing a new circular element assembly algorithm, leveraging assembly

169 nces likely to be plasmids, phages and other circular elements.

170 Circular elliptical microstructures produce smooth flow

171 genes can be amplified in chromosomes or in circular extrachromosomal DNA (ecDNA), although the freq

172 Loss of circular fibres led to a bifurcated anterior-posterior a

173 ne, nkx1-1, is required for the formation of circular fibres, oriented along the medial-lateral axis.

174 densities, decreased flight speeds, followed circular flight paths, and vocalized frequently.

175 crofluidic channels by embedding sacrificial circular gelatin vascular templates in collagen, which w

176 ted and in humans contain a 16,569-base-pair circular genome (mtDNA) encoding 37 genes required for o

177 scripts can be visualized on both linear and circular genome browsers.

178 DNA replication of circular genomes generates physically interlinked or cat

179 Mitochondria organelles have small circular genomes with substantial structural and genetic

180 re more globally collapsed, hairpin-like, or circular, giving rise to the observed heterogeneous broa

181 However, very little is known about circular granular ratchets, startling devices able to co

182 ations of the operational characteristics of circular granular ratchets.

183 in the energy of angular-momentum states in circular graphene p-n junction resonators when a relativ

184 for all population sizes, and in the case of circular graphs, randomness delays mutant fixation for N

185 of treatment to eradicate covalently closed circular HBV DNA, and development of immunotherapy for C

186 raction or entrapment of the non-protonated, circular helical (blue) structure of phycocyanin and the

187 escent state, the viral genome persists as a circular, histone-associated episome, and transcription

188 lizing with chitin, in patterns ranging from circular (Histoplasma capsulatum) to punctate (Cryptococ

189 riments showed that the AuNPs and AgNPs were circular in shape with an average diameter of 5 and 8nm,

190 fibroblasts into rectangular anisotropic or circular isotropic geometries and stimulated them with T

191 tion within the MFGM with growth, leading to circular lipid domains.

192 monolayer morphology changes from dispersed circular liquid-condensed (LC) domains in a continuous l

193 , we used excision of chromosomal regions as circular "loop outs" to convert sister chromatid intertw

194 ayer form they host electrons with quantized circular motion and associated valley polarization and v

195 The four circular mt genomes have an estimated size of 12.6, 12.5

196 tify the boundaries of longitudinal (LM) and circular muscle (CM) layers.

197 graft-derived neurons formed a plexus in the circular muscle layer.

198 , long rectilinear arrays of neurites within circular muscle/secondary plexus or longitudinal muscle/

199 re located between the muscularis mucosa and circular muscular layer of the human gut.

200 nificantly dependent on the chirality of the circular nanomagnet and is asymmetric with respect to th

201 d the dynamic response of a vortex core in a circular nanomagnet by manipulating its dipole-dipole in

202 le handpiece with a soft collapsible tip and circular nitinol cutting element.

203 nm) with a loop structure at one end with a circular opening approximately 6 nm in diameter.

204 R that degrades linear RNAs but not RNAs in circular or lariat-like conformations.

205 y light to induce local conduction blocks of circular or linear shapes.

206 se complexes depended on whether the DNA was circular or not.

207 The circular orbit is unlikely to be the result of tides and

208 toward chaotic behavior as the radius of the circular orbit of the point mass increases (other parame

209 cal shell and caused to move in a prescribed circular orbit relative to the shell.

210 to manipulate the charge carriers by using a circular p-n junction whose size can be continuously tun

211 The division plane typically has a circular periphery and the growth starts from the periph

212 rmation and deamination, we have developed a circular permutation synthesis strategy for positioning

213 tions allow us to unambiguously identify the circular photo-galvanic effect as the dominant mechanism

214 The circular photogalvanic effect (CPGE) is the part of a ph

215 ting, visualized by the sudden appearance of circular pits with uniform diameters of 6-7 mum and dept

216 process long double-stranded DNAs, including circular plasmid DNAs and genomic DNAs.

217 fficiency by twofold to fivefold relative to circular plasmid donors at one genomic locus in 293 T ce

218 sion phase during which the extremity of the circular plate seeks contact with the mother wall and br

219 s were trained to run many trials on a large circular platform, either to LED-cued goal locations or

220 Here we demonstrate the conversion of the circular polarization of incident femtosecond laser puls

221 l elimination was drastically increased when circular polarization of incident photons matched to the

222 rent that switches depending on the sense of circular polarization of the incident light.

223 Indeed, both the circular polarization of the light that excites the elec

224 In this paper, we aim to control the circular polarization states, e.g., left-hand, or right-

225 horescence with unusually long lifetimes and circular polarization that depends on both the helical N

226 or radial directions to effectively convert circular polarization to linear polarization and induce

227 rm phase front, both in orthogonal states of circular polarization.

228 e conversion between linear polarization and circular polarization.

229 nly permit the conversion of left- and right-circular polarizations (spin states) into states with op

230 a metasurface that converts left- and right-circular polarizations into states with independent valu

231 provide distinctive responses from opposite circular polarizations.

232 pers, beam splitters, terahertz wave plates, circular polarizers and other polarization devices.

233 flat films and show uniform textures between circular polarizers when suspended in sub-millimeter siz

234 ermal conductivity for the case with aligned circular pores, confirming a significant thermal transpo

235 ase in thermal transport with respect to the circular pores.

236 We show formation of a reinforced circular port-hole in the prey wall, L,D-transpeptidaseB

237 p and ill-understood process, from a relaxed circular (RC) DNA, in which neither of the two DNA stran

238 tep and ill-understood process, from relaxed circular (RC) DNA.

239 ze constraints, efficiency was optimal via a circular receiver coil wrapped into a half-cylinder with

240 dard deviation of attenuation measured in 14 circular regions of interest.

241 ing to 6 viral families, as well as numerous circular Rep-encoding single-stranded DNA (CRESS DNA) vi

242 aper, we report the analysis of a concentric circular ring plasmonic optical antenna (POA) array usin

243 r-field and their mutual interactions in the circular ring POA array.

244 The currents in the circular rings of the POA array and their mutual couplin

245 Circular RNA (circR)-284 is a potential inhibitor of miR

246 Circular RNA (circRNA) is a class of noncoding RNA whose

247 controls back-splicing reactions leading to circular RNA (circRNA) production.

248 Moreover, inhibition of Ttn-derived circular RNA increased the susceptibility of cardiomyocy

249 s largely unknown how the ratio of linear to circular RNA is controlled or modulated.

250 n of the cleavage/polyadenylation machinery, circular RNA levels were similarly increased.

251 ected into alternative pathways that lead to circular RNA production.

252 larization of an exon of the PVT1 gene, as a circular RNA showing markedly reduced levels in senescen

253 g and long noncoding transcripts, as well as circular RNA species that were also experimentally valid

254 Circular RNAs (circRNAs) are a class of non-coding RNAs

255 Recent studies have shown that circular RNAs (circRNAs) are abundant, widely expressed

256 Circular RNAs (circRNAs) are covalently closed RNA molec

257 Circular RNAs (circRNAs) are single-stranded RNAs that a

258 Circular RNAs (circRNAs) have recently emerged as a larg

259 Circular RNAs (circRNAs) represent a class of endogenous

260 uences, and (ii) thousands of novel intronic circular RNAs (IcircRNAs) are expressed in cells.

261 ogy, such as the functions of enhancer RNAs, circular RNAs and chemical modifications to RNA in cellu

262 identified regulated expression of specific circular RNAs derived from Ttn (Titin), Fhod3 (Formin ho

263 Seq), we compared the expression patterns of circular RNAs in proliferating (early-passage) and senes

264 harmacologically, the steady-state levels of circular RNAs increased while expression of their associ

265 ti et al. (2017) demonstrate that endogenous circular RNAs may generate proteins, thereby expanding t

266 , including short microRNAs, long ncRNAs and circular RNAs, across various heart diseases indicates t

267 y eukaryotic genes generate linear mRNAs and circular RNAs, but it is largely unknown how the ratio o

268 t the first cell type-specific expression of circular RNAs-a neuron-specific and nuclear-enriched RNA

269 drug doxorubicin and their interaction with circular RNAs.

270 ets are a major source of miRNAs, YRNAs, and circular RNAs.

271 -state output of protein-coding genes toward circular RNAs.

272 ffect of doxorubicin via regulating a set of circular RNAs.

273 ere measured by two radiologists using three circular ROIs (three-ROIs), single-section (SS), and who

274 Circular sequencing (CirSeq) is a method by which the er

275 s, including fusion with rapid relaxation to circular shape, shear stress-induced deformation, and ra

276 circles" active contour model, which favors circular shapes but allows slight variations around them

277 Under particular load patterns, the circular shells display novel mechanical behaviour such

278 ontributions (EC)) and the other forcing it (circular sib mating (CM)).

279 In the case of the ubiquitous human circular single-stranded DNA virus family Anelloviridae,

280 Circular single-stranded DNA viruses infect archaea, bac

281 Potato spindle tuber viroid (PSTVd) is a circular, single-stranded, noncoding RNA plant pathogen

282 DNA polymerases depend on circular sliding clamps for processive replication.

283 Circular "SPHINX" DNAs <5 kb were previously isolated fr

284 m-infecting, lipid-containing phage), with a circular ssDNA genome and an internal lipid membrane enc

285 agen fiber alignment as a vector field using Circular Statistics.

286 highlighted by the observation of some large circular structures with 2.5-5 degrees curvature angles

287 s collectively composed of three distinctive circular structures: a 60-stranded vertical beta-barrel

288 Hetero-oligomers of TatB and TatC form circular substrate-receptor complexes with a central bin

289 s formed a spheroid with a smoother and more circular surface when co-cultured with osteoblasts.

290 nal swimming but is at risk of giving futile circular swimming paths in the presence of biological no

291 rees C from both double- and single-stranded circular template DNA using specific primer pairs.

292 ength, amount of expression and the ratio of circular to linear transcripts, had impacts on quantific

293 neurons were recorded while rats traversed a circular track bidirectionally in which the track was ei

294 y and move steadily along either straight or circular trajectories, and the motile behavior is sensit

295 ate transcript expression of both linear and circular transcripts from RNA-seq data.

296 On the other hand, the consideration of circular transcripts in expression quantification from r

297 we proposed a novel strategy that transforms circular transcripts to pseudo-linear transcripts and es

298 had impacts on quantification performance of circular transcripts.

299 he three strands at each crossing point in a circular triple helicate, while structural constraints o

300 ise become stronger, and centers become more circular while maintaining differences between RGC types