ライフサイエンスコーパス: microcrystal

1 tude via varying the thickness of the MoS(2) microcrystal.

2 roelastic domains in a defected Al-doped VO2 microcrystal.

3 to nitrogen--vacancy centers in the diamond microcrystal.

4 c ferroelectric diisopropylammonium chloride microcrystal.

5 ng exactly at saturation without introducing microcrystals.

6 ers from hundreds of thousands of individual microcrystals.

7 lease in human neutrophils activated by CPPD microcrystals.

8 determination by serial X-ray diffraction of microcrystals.

9 y for determining structures from showers of microcrystals.

10 DPPH standard in the form of water-insoluble microcrystals.

11 ectron diffraction experiments on individual microcrystals.

12 chronic articular responses to inflammatory microcrystals.

13 nts of c.d. and of electron diffraction from microcrystals.

14 o record x-ray diffraction data from protein microcrystals.

15 on that can generate bending and twisting in microcrystals.

16 tion and confinement in pseudo-spherical ZnO microcrystals.

17 mination of material crystal structures from microcrystals.

18 ied by delamination to elastic quasicircular microcrystals.

19 ng substrate or ligand solutions with enzyme microcrystals.

20 and less so in the detergent environment of microcrystals.

21 the measurement of hundreds to thousands of microcrystals.

22 rocess to promote the growth of inclined ZnO microcrystals.

23 uch larger, cryocooled granulovirus granulin microcrystals.

24 nolayer-thick cap at the external surface of microcrystals.

25 e leaky field beyond the boundary of the ZnO microcrystals.

26 ffect photomechanical deformations of single microcrystals.

27 ity of the framework is maintained in porous microcrystals.

28 When excited by using laser light, such bent microcrystals act as active optical microwaveguides that

29 Structures of 13 of these microcrystals all reveal steric zippers, but with variat

30 thanolic suspensions leads to exfoliation of microcrystals along the 2 0 0 planes, giving rise to 1.5

31 responsive properties of 2D cyclo-octasulfur microcrystals (alpha-S8 MCs), produced using a quick, si

32 nerozoic limestones characterized by rhombic microcrystals also exhibit petrographic and/or geochemic

33 well on proton-rich systems, such as organic microcrystals and biomolecular assemblies.

34 lso showed distinct conformations for single microcrystals and confirms that crystallization properly

35 ed here for two proteins, alpha-spectrin SH3 microcrystals and hydrophobin functional amyloids.

36 triisopropylsilylethynyl)pentacene (TIPS-Pn) microcrystals and Mn-phthalocyanine islands, confirming

37 lection of electron diffraction data from 3D microcrystals and nanocrystals of radiation-sensitive bi

38 are much less deformable than the desolvated microcrystals and shatter completely at very low applied

39 The aggregation of COM microcrystals and their attachment to epithelial cells a

40 c guests, including drugs, in both water and microcrystals, and drugs absorbed in microcrystals can b

41 ange of 0-4 GPa for individual 1.2 mum ZIF-8 microcrystals, and the deformed microcrystals partially

42 H(2)O from unit cells at the surface of the microcrystals, and the rate of diffusion of H(2)O across

43 1 cocrystals; the size distribution of these microcrystals, and the resulting polymer chains, can be

44 Microcrystals are continuously rotated during data colle

45 decahedron, supports the proposal that these microcrystals are cubic crystals twinned about an icosah

46 pproach, liquid solutions containing protein microcrystals are deposited on carbon-coated electron mi

47 These microcrystals are ideal for investigation by microcrysta

48 When these microcrystals are illuminated with light of lambda=405 n

49 e phonon polaritons in mono- and bilayer hBN microcrystals are imaged.

50 Individual microcrystals are located by raster-scanning a several-m

51 Methanol-solvated ZIF-8 microcrystals are much less deformable than the desolvat

52 For loading, the suspended microcrystals are pipetted onto the chip and excess moth

53 e also show variations in the density of GaN microcrystal arrays that depend on the ionicity of subst

54 Here, using tetrakaidecahedral Zn2SnO4 microcrystals as an example, we employed alternating cur

55 sing the atomic resolution structures of the microcrystals as the starting points, we show that the R

56 erial femtosecond X-ray crystallography from microcrystals at an X-ray free electron laser.

57 electrosolution, revealing aggregates of 20 microcrystals at the corners of a pentagonal dodecahedro

58 photoelectrochemical experiments on a single microcrystal attached to a nanoelectrode tip revealed a

59 lude surface plasmon resonance (SPR), quartz microcrystal balance (QMB) and surface acoustic wave (SA

60 1 mug cm(-2) using an electrochemical quartz microcrystal balance.

61 ection more practical and also extendable to microcrystals, both enabling and requiring the study of

62 his protocol gives advice on how to identify microcrystals by light microscopy or by negative-stain e

63 The growth of microcrystals can be controlled by a variety of agents,

64 The silica-infused microcrystals can be directly observed in the dry state,

65 We also show that the solubility of the microcrystals can be further tuned by varying the thickn

66 ter and microcrystals, and drugs absorbed in microcrystals can be released to water with selectivity.

67 is still often limiting data collection, as microcrystals can clog both field- and flow-focusing noz

68 ine to the mother liquor in contact with the microcrystals, consistent with a conformational rearrang

69 ming created erroneous results because of UA microcrystal contaminants triggering IL-1beta release.

70 al investigation of slowly compressed nickel microcrystals, covering three orders of magnitude in nom

71 ous laboratory experiments show that calcite microcrystals crystallizing under conditions similar to

72 the rhombic form/morphology, whereas calcite microcrystals crystallizing under conditions similar to

73 manno-octulosonate-8-phosphate synthase from microcrystals delivered in droplets revealing distinct s

74 elf-organize into turbid hydrogels or bigger microcrystals depending on the component substituents.

75 ed to high resolution (~2.5 A) using protein microcrystals deposited on an ultra-thin silicon nitride

76 f a thioimidate covalent intermediate in ICH microcrystals during catalysis.

77 f an advanced intermediate was elucidated by microcrystal electron diffraction (MicroED) analysis.

78 ideally suited to structure determination by microcrystal electron diffraction (MicroED) and serial f

79 ast, low-dose, event-based electron counting microcrystal electron diffraction (MicroED) data collect

80 Single-crystal X-ray diffraction (SCXRD) and microcrystal electron diffraction (MicroED) data show a

81 lar proteins were determined ab initio using microcrystal electron diffraction (MicroED) data that we

82 The emergence of microcrystal electron diffraction (MicroED) expands the

83 Additionally, we demonstrate the use of microcrystal electron diffraction (MicroED) for direct s

84 ate the coupling of divergent synthesis with microcrystal electron diffraction (MicroED) for rapid as

85 Microcrystal electron diffraction (MicroED) has advanced

86 Microcrystal electron diffraction (MicroED) is an electr

87 Microcrystal electron diffraction (MicroED) is an emergi

88 Here we report the use of microcrystal electron diffraction (MicroED), an emerging

89 s of two of the products were determined via microcrystal electron diffraction (MicroED), and we repo

90 microcrystals are ideal for investigation by microcrystal electron diffraction (MicroED), but the gel

91 tructure of an ApePgb variant, determined by microcrystal electron diffraction (MicroED), reveals tha

92 Microcrystal electron diffraction (microED), with it's i

93 ryogenic electron microscopy (cryoEM) method microcrystal electron diffraction (MicroED).

94 quality of data obtained is investigated by microcrystal electron diffraction (MicroED).

95 ectron microscopy (cryo-EM) technique called microcrystal electron diffraction (MicroED).

96 ndent anion channel (VDAC) was determined by microcrystal electron diffraction (MicroED).

97 In the hands of experts, microcrystal electron diffraction (microED, a 3D ED meth

98 yogenic electron microscopy (cryoEM) method, microcrystal electron diffraction (microED, a 3D ED tech

99 mental and theoretical approaches, including microcrystal electron diffraction and DFT analysis, we r

100 n the presence of fullerenes, is revealed by microcrystal electron diffraction and single-crystal X-r

101 Microcrystal electron diffraction demonstrates that the

102 s were determined de novo using the emerging microcrystal electron diffraction method.

103 work (MOF) material Cu(3) (C(6) O(6) )(2) by microcrystal electron diffraction with sub-angstrom prec

104 nm;) characterized by X-Ray crystallography, microcrystal electron diffraction, UV/Vis, fluorescence,

105 via the cryoelectron microscopy technique of microcrystal electron diffraction.

106 structure of the crystal is confirmed using microcrystal electron diffraction.

107 rphology proved intractable for conventional microcrystal electron diffraction.

108 hly selective detection of individual chiral microcrystals, enabling insights into the fundamental me

109 It was also found that GaN microcrystal ensembles are dominated by slight tensile s

110 The x-ray powder pattern of the microcrystals, extending to 0.9-A resolution, yields the

111 d with rapid energy transfer through the MOF microcrystal facilitates amplified quenching with a 7000

112 A diamond microcrystal fixed on the fiber tip is heated by laser r

113 erformance multiphoton excited hybrid single microcrystal for future optoelectronic and micro-nano ph

114 for growth and delivery of membrane protein microcrystals for crystallographic data collection.

115 for the preparation and characterization of microcrystals for LCP-SFX applications.

116 Screening microcrystals for quality diffraction takes roughly an h

117 okinetic injector for efficiently delivering microcrystals for serial femtosecond X-ray crystallograp

118 ng this pipeline, we successfully identified microcrystals for ~ 16% of the tested protein set, which

119 hermore, the hypothesis that rhombic calcite microcrystals form exclusively in meteoric environments

120 ns, it is proposed here that rhombic calcite microcrystals form exclusively in meteoric environments.

121 the SONICC and TEM techniques to screen for microcrystal formation within living insect cells.

122 t a metastable state toward beta-sheet-based microcrystals formation.

123 mestones are comprised of diagenetic calcite microcrystals formed during mineralogical stabilization

124 UA with NaOH avoided this artifact, and this microcrystal-free preparation suppressed LPS- or MSU cry

125 age size of silver phenylselenolate (AgSePh) microcrystals from <5 um to >1 mm, while simultaneously

126 We extracted microcrystals from arm tip photophores and identified th

127 cribe time resolved experiments on PSII nano/microcrystals from Thermosynechococcus elongatus perform

128 ll exists over large areas of the surface of microcrystals from Valonia, one of the most highly cryst

129 rms amyloid-like fibrils and closely related microcrystals, from which we have determined the atomic

130 on to study the structural properties of GaN microcrystals grown by ES-SAG.

131 n serotonin receptor using sub-10-micrometer microcrystals grown in a membrane mimetic matrix known a

132 he effectiveness of milling membrane protein microcrystals grown in viscous media using a focused ion

133 d to the prototypical case of Ge/Si vertical microcrystals grown on deeply patterned Si substrates.

134 Microcrystal growth and characterization methods are dis

135 To this goal, Si vertical microcrystals have been grown, while for Ge the fitting

136 These microcrystals have been obtained by thermolysis of (AuCl

137 changes during the dissolution of a calcite microcrystal in aqueous solution.

138 we developed acoustic 2D focusing of protein microcrystals in capillaries that enables real-time onli

139 await Land, who oriented fragile herapathite microcrystals in extruded polymers, a process that produ

140 we have unraveled structural dynamics of GaN microcrystals in growth structures of different dimensio

141 o 100 kPa through the rational design of BAs microcrystals in polymer composite.

142 chrotron single-crystal X-ray diffraction on microcrystals in situ, demonstrates the capabilities of

143 Compared with SFX methods for microcrystals in solution using liquid injectors, LCP-SF

144 sensors (charcoal particulates and LiNc-BuO microcrystals) in 22 patients was performed to evaluate

145 Cholesterol microcrystal injection into the kidney artery of wild-ty

146 to the crystal flow, which focused lysozyme microcrystals into a single line inside a silica capilla

147 ly show that grain refinement of the initial microcrystals into nanocrystals (approximately 5 nm) occ

148 Although every microcrystal is exposed to a dose of 33 MGy, no signs of

149 idues at the intermolecular interface of the microcrystal lattice, which we attribute to intermediate

150 high-resolution structural information from microcrystals (less than 1 micrometer by 1 micrometer by

151 Kidney stones, aggregates of microcrystals, most commonly contain calcium oxalate mon

152 abits), as opposed to the typical polyhedral microcrystals obtained under bulk crystallization condit

153 temperature X-ray diffraction data of PS II microcrystals obtained using ultrashort (< 50 fs) 9 keV

154 structures and the solution phase synthesis, microcrystals of 2D RP perovskites can be quite heteroge

155 Single microcrystals of a 1:1 solid solution of n-C32H66/n-C36H

156 ecular orientation of CO2 adsorbed in single microcrystals of a functionalized metal-organic framewor

157 ial variations of excitons and biexcitons in microcrystals of a series of 2D RP perovskites BA(2)MA(n

158 Microcrystals of an essential mutant of VDAC grew in a v

159 the precipitation of antimonite [Sb(III)] as microcrystals of antimony trioxide.

160 We report on the electrochemical growth of microcrystals of bismuth selenide, Bi(2)Se(3), in the me

161 ut quartz, NOSE microscopy was performed for microcrystals of both naproxen and glucose isomerase.

162 Microcrystals of calcium pyrophosphate dihydrate (CPPD)

163 nes are aggregates, most commonly containing microcrystals of COM as the primary inorganic constituen

164 oute for the production of antimony trioxide microcrystals of commercial significance to the nanotech

165 la elaborated with synthetic antioxidant and microcrystals of curcumin in relation to its physicochem

166 Microcrystals of desired sizes are important in a range

167 We used the injector to analyze microcrystals of Geobacillus stearothermophilus thermoly

168 oscopy, we video the intercalation of single microcrystals of graphite in concentrated sulfuric acid.

169 nts that control the growth and stability of microcrystals of monovalent or multivalent inorganic sal

170 We used microcrystals of photoactive yellow protein (a bacterial

171 RD) and x-ray emission spectroscopy (XES) of microcrystals of photosystem II (PS II) at room temperat

172 high-resolution structural information from microcrystals of proteins.

173 We confirmed that microcrystals of rctt-tetrakis(4-pyridyl)cyclobutane wit

174 icroscopy (EM) grids containing proteinase K microcrystals of similar sizes from the same crystalliza

175 3)C spectra have been acquired from hydrated microcrystals of site-directed (13)C-enriched ubiquitin.

176 Microcrystals of TD grown by drop casting piperidine sol

177 Microcrystals of tetra-/hexamethoxypyrene as donors with

178 precipitation has been used to grow branched microcrystals of the anthracene derivative 4-fluoroanthr

179 present X-ray diffraction data recorded from microcrystals of the Blastochloris viridis photosyntheti

180 microporous polymer membranes incorporating microcrystals of the complex show identical vapochromic

181 elength anomalous scattering measurements on microcrystals of the well-established model system lysoz

182 Microcrystals of this peptide also share the principal p

183 tilever tip, mechanically compliant acicular microcrystals of three N-benzylideneanilines were bent t

184 e fragmentation and morphological changes in microcrystals of ZIF-8 at lower shock pressures ( approx

185 ssembly of emissive carbon quantum dot (CQD) microcrystals on organized cellulose nanocrystals templa

186 arbon black, charcoal particulates, LiNc-BuO microcrystals) on FDG-PET/CT imaging after implantation

187 gmentation of large, imperfect crystals into microcrystals or nanocrystals can provide a simple path

188 hoton-pumped solid-state laser in single MOF microcrystal (or nanocrystal) for future optoelectronic

189 ing proteins that form amyloid-like fibrils, microcrystals, or usually both.

190 rystallography on photoactive yellow protein microcrystals over a time range from 100 femtoseconds to

191 .2 mum ZIF-8 microcrystals, and the deformed microcrystals partially recovered after pressure release

192 ar cavity, containing a birefringent organic microcrystal (perylene) and exhibiting emergent optical

193 Identifying microcrystals, preparing samples and setting up the micr

194 gel-like LCP with embedded membrane protein microcrystals, providing a continuously renewed source o

195 PHE was present as microcrystals, providing non-limiting conditions for gro

196 /or do not produce the copious quantities of microcrystals required for flowing jet methods.

197 These protein microcrystals, roughly a micron across, accrue within in

198 ein expression and purification, and in vivo microcrystal screening for structural studies.

199 d about an icosahedral seed, with each cubic microcrystal sharing a threefold axis and three symmetry

200 The mortadella with curcumin microcrystals showed significantly lower TBARS values at

201 sible in electron micrographs or needle-like microcrystals showing a cross-beta diffraction pattern.

202 rectly onto TEM grids for later soaking with microcrystal slurries, and complexes with noncovalent li

203 transfer 2.5 nL droplets from the surface of microcrystal slurries, through the air, onto mounting mi

204 s the study of enzyme-catalyzed reactions in microcrystal slurries.

205 ion with the cocrystallized enzyme-substrate microcrystal slurry, a ferric-hydroperoxo intermediate i

206 sm in atomic detail, we determined eight new microcrystal structures of fiber-forming segments of Abe

207 (g)) was delivered to or swept away from the microcrystal surfaces.

208 ty to the conditions under which the various microcrystal textures form.

209 By linking calcite microcrystal textures to specific diagenetic environment

210 photophores are densely packed with protein microcrystals that catalyse the bioluminescent reaction

211 h a solubility of ~1 mM and can readily form microcrystals that lead to cystine stone formation, espe

212 photoactivation experiment by employing PSII microcrystals that retained all protein subunits after c

213 HG) imaging, enabled detection of homochiral microcrystals that survived only a few seconds before be

214 sections led to detection of the presence of microcrystals that were demonstrated as precipitates of

215 Crystallization efforts consistently yielded microcrystals that were unsuitable for single-crystal X-

216 ed membrane proteins by MicroED using single microcrystals that would be impossible with other crysta

217 bdenum disulfide and hexagonal boron nitride microcrystals, the most-promising van der Waals semicond

218 These attached microcrystals then grow larger over time during immersio

219 have permitted transport through individual microcrystals to be evaluated semiquantitatively.

220 For work with very small microcrystals to be realized in practice, however, it is

221 t microfluidic system for delivering protein microcrystals to X-ray beams for diffraction data collec

222 1 degrees C (for larger solution-synthesized microcrystals) to 455 degrees C, thereby mitigating ther

223 X-ray-probe experiment employing haemoglobin microcrystals transported via a liquid jet into the XFEL

224 Finally, data for microcrystals up to 12 layers thick reveal how the respo

225 The resulting large microcrystals up to 200 mum across show unusually high e

226 urcumin content by incorporation of curcumin microcrystals upon electrospraying.

227 The crystal structure was determined from microcrystals using precession-assisted electron diffrac

228 homogeneous behaviour of even individual VO2 microcrystals using pump-probe microscopy and nanoimagin

229 Here, we spatially image TIPS-pentacene microcrystals using ultrafast two-dimensional white-ligh

230 were observed in XFEL-irradiated ferredoxin microcrystals using unusually long pulses of 80 fs.

231 broad range of materials, i.e. subwavelength microcrystals, van-der-Waals materials, or topological i

232 ltraprecise nanoscale measurements on nickel microcrystals, we directly determined the size of discre

233 n the mechanical behavior of ZIF-8 nano- and microcrystals were also investigated.

234 Lysozyme microcrystals were frozen on an electron microscopy grid

235 Microcrystals were identified using a scanning electron

236 BCP microcrystals were internalized into vacuoles of human m

237 imidazolate framework (ZIF-8) micro- and sub-microcrystals were observed under compression.

238 uman lactate dehydrogenase isozyme 1 (LDH-1) microcrystals were separately dissolved and subsequently

239 erminations from the measurement of multiple microcrystals which were previously considered too small

240 tensities from a heterogeneous population of microcrystals, while at the same time modeling the X-ray

241 tracompact fiber-optic probe where a diamond microcrystal with a well-defined orientation of spin qua

242 o 150 mW results in increase of the yield of microcrystals with high curvatures (10-20 mm(-1)) from 2

243 ight at 365 nm, 405 nm, and 445 nm generates microcrystals with high curvatures (11-12 mm(-1)), while

244 ttleneck: many hybrid materials are obligate microcrystals with low symmetry and severe radiation sen

245 d sensitive and selective imaging of protein microcrystals with negligible contributions from solvate

246 orthorhombic (bco) phases in bipyramidal Au microcrystals with penta-twinned tips.

247 mically thin transition metal dichalcogenide microcrystals with previously unattainable 20 nm resolut

248 igh resolution diffraction data from protein microcrystals with sizes of 4 micrometers and smaller.

249 y waveguide modes can be supported in MoS(2) microcrystals with suitable thicknesses.

250 et state sparsely distributed throughout the microcrystals, with higher concentrations at edges and m