ライフサイエンスコーパス: shell

1 hat are irregularly scattered throughout the shell.

2 r Ag(2) staples further surround this Ag(60) shell.

3 ckness, and the pressure gradient across the shell.

4 edium spiny neurons in the nucleus accumbens shell.

5 the organic matrix extracted from the oyster shell.

6 ost of the RNA genome situated at the capsid shell.

7 elease of the dye molecules from the polymer shell.

8 tion of a rare rhombicosidodecahedral Ag(60) shell.

9 ded by an Ag(25) discontinuous metal-organic shell.

10 ions to the nucleus accumbens (NAc) core and shell.

11 exible necks, initiated by the origin of the shell.

12 erse hexagonal cylindrical morphology in the shell.

13 al shape evolution within the initially flat shell.

14 white, golden, black or partially pigmented shell.

15 aling beta-barrel domain of Teneurin, the YD shell.

16 s that appear to have no contact with capsid shell.

17 me cargo encapsulated within a proteinaceous shell.

18 n prey trapped inside large marine gastropod shells.

19 ed particles with hollow cores and polymeric shells.

20 he sporophyte conchocelis bores into mollusk shells.

21 by a similar mechanism as the foraminiferal shells.

22 g assembly to translocate DNA into procapsid shells.

23 ter comprehend the recycling of waste oyster shells.

24 ites still partially surrounded by solvation shells.

25 vealing that the first dinosaur egg was soft-shelled.

26 to forming chemical bonds that engage the 5f shell(1-3).

27 ed the spread of another foraging strategy, "shelling" [17], whereby some dolphins in this population

28 cross the ventral striatum (medial accumbens shell, accumbens core, lateral accumbens shell) and show

29 the NIR-II optical imaging agent, and a PDA shell, acting as the PA contrast agent.

30 crostructures can range from uniform to core-shell, affected by reagent reactivity and solvent choice

31 We identified six novel SHELL alleles in noncommercial African germplasm populat

32 Four novel SHELL alleles were associated with fruit form phenotype.

33 ir shells serve as mechanical armor, bivalve shells also enable evasive behaviors such as swimming an

34 limbic information, to the nucleus accumbens shell (an area known to be important for reward and moti

35 ramembrane portion of the viral glycoprotein shell and allowed a detailed description of the surface

36 geometries, including porous particles, core-shell and hollow shell structures, and a unique 'fruits-

37 capsulates enzymes into a virus-like protein shell and plays essential roles in photosynthetic carbon

38 intermediate oil layer between the polymeric shell and the gas core prevents rapid outgassing by effe

39 The embedding shell and the occluded Asp act as an integral until whic

40 lysis revealed that SMAPs had a carbon-dense shell and were stored in multicore granules.

41 uire more energy to maintain their calcified shells and acid/base balance with ocean acidification.

42 occupancy of nodes in the inner and outer k-shells and low occupancy in the middle shells of financi

43 Biological materials including shells and wood achieve impressive toughness by using we

44 ens shell, accumbens core, lateral accumbens shell) and showed complex and heterogeneous profiles of

45 prised of three domains: R (RNA binding), S (shell), and P (protruding).

46 citly includes chromatin fibers, the nuclear shell, and coupling with the cytoskeleton.

47 e of Fos expression in the NAc core, but not shell, and Fos was colabeled with both Drd1- and Drd2-MS

48 anized as a T = 19 capsid, confines the core shell, and it is composed of the mature products derived

49 tes the first critical compilation on oyster shell applications, with the aim to provide essential el

50 cle composition and deviations from the core-shell approximation-reconciles absorption enhancement pr

51 n net strength of glutamatergic input to NAc shell arising from midbrain dopamine neurons, it alters

52 r a GRR, to the presence of the native oxide shell around the Ga NPs and their liquid nature, via a m

53 n of lithium ions from their water solvation shell as compared with organic molecules.

54 r, their infectious genome encapsulated by a shell assembled by a multiscale process, starting from a

55 ons of exendin-4 directly into the accumbens shell attenuated oxycodone self-administration and the r

56 for the scalable fabrication of nonperiodic, shell-based ceramic materials with ultralow densities, p

57 recent evidence of birch bark tar, art, and shell beads, the idea that Neanderthals were cognitively

58 Both whole (i.e. in-shell) beans and shelled seeds (cotyledons) were analyse

59 We find IrB(2) O(-) has a closed-shell bent structure (C(s) , (1) A') with BO(-) coordina

60 sional Faddeev integral equation are the off-shell boost two-body t-matrices, which are calculated di

61 oloxidase into polyphenoloxidase accelerated shell browning.

62 aughter droplet encapsulated by a larger air shell bubble, forming an antibubble.

63 tain several examples of enigmatic, putative shell-building metazoan fossils.

64 Chemogenetic activation of thalamo-accumbens shell, but not core, projectors attenuated heroin seekin

65 ace of the inorganic core and organic ligand shell by so-called "exciton-delocalizing ligands (EDLs)"

66 oelectronic characteristics of the Si/SiO(x) shell can be beneficial for various sensor architectures

67 or Galilean and Saturnian icy moons, the ice shell can undergo hemispheric symmetry breaking only if

68 These results indicate that oyster shells can be an effective sorbent for fluoride removal,

69 ly show that the curvature of self-assembled shells can produce close to optimal stiffness scaling wi

70 For CO(2) conversion, core-shell catalysts can provide distinctive advantages by ad

71 is, characterization, and evaluation of core-shell catalysts for such potential applications.

72 Furthermore, the valence shell charge concentrations (VSCCs) in the nonbonding re

73 ronic stabilization through the opening of a shell-closing gap at the top of the occupied manifold of

74 ter shell (NOS), the calcined natural oyster shell (CNOS), and biomolecules of the organic matrix ext

75 anding the intricate molecular regulation of shell color polymorphism and provide new insights into b

76 However, miRNAs and miRNA-targets underlying shell color polymorphism remain largely unknown in mollu

77 Using four shell colors full-sib families of the Pacific oyster Cra

78 LCST, formed hydrophobic cores around which shells composed of NIPAm, degradable crosslinker N, N'-b

79 A self-organized core-shell composite anode, comprising an outer sheath of lit

80 c properties that are inaccessible to closed-shell compounds.

81 ional harmonic potentials and prepare closed-shell configurations of 2, 6 and 12 fermionic atoms in t

82 an Ag(40) drum-like shell, while the Ag(25) shell consists of two Ag(10) S(10) P(10) Cl(5) rings and

83 rites and the evolved calcite, the perturbed shell contains two sets of carbonate species distinguish

84 onic characteristics of the porous Si/SiO(x) shell correlated to their chemical compositions.

85 the OS was heated to produce calcined oyster shell (COS).

86 ermined electrochemically in shrimp and soft-shell crab samples (20.63 and 6.59 mug g(-1), respective

87 These worms burrow into bivalve shells, creating unsightly mud blisters that are unappea

88 of different shell shapes against vertebrate shell-crushing predators.

89 ms(9-13) in that they possess tightly packed shells devoid of large apertures.

90 Quantitative modeling of multi-shell diffusion MRI data from 413 participants revealed

91 The calcified, hard-shelled dinosaur egg evolved independently at least thre

92 orates the organic composition of these soft-shelled dinosaur eggs, revealing a stratified arrangemen

93 t boron through a transition state with open-shell diradical character.

94 How the protein shell directs influx and efflux of molecules in an effec

95 In this work, we have used open-shell dispersion-corrected DFT calculations, quasi-class

96 ce of doublecortin expressing neurons in the shell division of the accessory basal nuclear cluster, a

97 ow that whilst there is little change to the shell domain of the capsid, the radiating protruding dom

98 nexpectedly bind to different regions of the shell domain, including receptor-binding domains.

99 and derivatives of the rostral zona limitans shell domain, respectively) were mapped across the preth

100 While the shell domains had homologous structures, the stabilizing

101 orn adults aged 25-27 years underwent single-shell DWI, from which a FD measure was derived using con

102 s bulk solvent viscosity and local hydration shell dynamics.

103 t the entirety of development, even when the shell edge exhibits significant irregularity due to inju

104 As modern crocodilians and birds lay hard-shelled eggs, this eggshell type has been inferred for n

105 rotation spectra were fitted with the double-shell ellipsoidal model, which considered varying cell w

106 Additionally, shell elongation from the umbo, a metric often overlooke

107 n the holistic assessment of nanoformulation shells' fate in soil and in the environment after releas

108 phenylhydrazine and the corresponding closed-shell [Fe(II)(eta(5)-Cp*)(dppe)CO](+) byproduct.

109 of agricultural biomass residues, including shell, fibre and soft peel, were incinerated at 900 +/-

110 Antibiotics loaded into core-shell fibrous platform effectively inhibit both gram-pos

111 incorporate desired enzymes into the protein shell for enhanced catalytic performance.

112 ses and functional partners within the empty shell for the production of hydrogen.

113 Actin perinuclear shells form each cell cycle and polygonal territories em

114 pport the findings of two distinct solvation shells formed by three chloroform molecules, where one t

115 k recovers and explains a large diversity of shell forms and highlights how parametric variations in

116 These increases may be due to a faster shell formulation, enabling PLGA microparticles to entra

117 the arms race that drives the predator-prey shell game.

118 The gCM shell genetically overexpressing SIRPalpha variants with

119 CdSe shell growth on the produced cores enhances their optica

120 etion site, which are required during normal shell growth, and repair.

121 Aim of the study is to present a fast multi-shell HARDI-ZOOMit dMRI protocol and validate its usabil

122 tinide series because its half-filled 5f (7) shell has lower energy than other 5f (n) configurations,

123 es in heteroallelic combinations, as well as SHELL heterodimerization and subcellular localization by

124 Furthermore, more BMSCs survived in the core-shell hydrogel group in vivo as compared to that in the

125 The data demonstrated that this core-shell hydrogel is an effective strategy for promoting tr

126 an injectable nanoparticle encapsulated core-shell hydrogel was fabricated for simultaneous iron over

127 venting functional disassembly of the capsid shell in infected cells.

128 r value of a EuSPION core-mesoporous silica shell in the presence of the AMF does not change, indica

129 obicity induced by cleavage of the procapsid shell in which it is embedded.

130 Electron diffraction verifies that all shells in the heterostructures are single crystals.

131 n the core and poly(lactic-co-glycolic acid) shell incorporating iron oxide nanocubes (IONCs).

132 have demonstrated that inhibition of the NAc shell induces voracious feeding, leading to the hypothes

133 unexpected PL increase (~ 540 nm) at the oil/shell interface.

134 we directly visualise an unsuspected 'single shelled' intermediate for a mammalian orthoreovirus in c

135 ses photoexcited lumiflavin to generate open-shell intermediates.

136 ctions of transient and highly reactive open-shell intermediates.

137 e nodes in the innermost [Formula: see text]-shells into a small number of communities.

138 L-shell ionisation and subsequent Coulomb explosion of ful

139 from a developmental point of view: When the shell is closed, the 2 valve edges meet each other in a

140 The Ag(24) shell is composed of a hitherto unknown sodalite-type si

141 connected DNA double helices, and the outer shell is composed of regularly arranged standing-up hair

142 nthesized Ag(2)S dots, on which a protective shell is grown by femtosecond laser irradiation.

143 rich WSe(2-2) (x) Te(2) (x) alloy, while the shell is the tellurium-poor WSe(2-2) (y) Te(2) (y) alloy

144 ollusks, produces an internal biomineralized shell, known as cuttlebone, which is an ultra-lightweigh

145 owing, repairing or remodelling the nacreous shell layer, whereas the second module orchestrates the

146 l cross-linked coating to functionalize core/shell lead sulfide/cadmium sulfide quantum dots (PbS/CdS

147 mutually exclusive markers, exhibit core or shell-like anatomical structure and have distinct electr

148 ons to organize their genomes into preformed shells, likely by a controlled process.

149 e with an Au(155) core protected by a ligand shell made of 24 monomeric [-S-Au-S-] and 6 dimeric [-S-

150 verall volume change, and the plastic carbon shell maintains the structural integrity of electrode ma

151 that an optimal fit between inner and outer shells maintains capsid function.

152 merical simulation shows that the engineered shell material with higher viscoelasticity improves the

153 h as open caps, cylindrical or ribbon-shaped shells may emerge, preventing the successful replication

154 tributed to the requirement for both an open-shell metal ion and a redox non-innocent ligand.

155 The observation of core-shell microstructures under certain conditions was hypot

156 Employing Pt(111) supported 2D Pt-core Au-shell model catalysts, we demonstrate that 2D core-shell

157 ic interpretation of the observed epithelial shell morphologies, highlighting the role of physical fa

158 ld be modulated by the particles' core-multi-shell morphology, suggesting a structural-chemical inter

159 sed intrinsically emitting shell of the core-shell MSN.

160 These sensing sutures, inspired by the "core-shell" multilayered structure of natural spider-silk fib

161 M(-1)s(-1)) containing key first and second-shell mutations found during evolution.

162 ns (D1-MSNs) in the nucleus accumbens medial shell (NAcmSh), and with lateral hypothalamus (LH)-proje

163 tical regions, such as the nucleus accumbens shell (NAcS) and basolateral amygdala, which encode posi

164 ans rats to test if phasic nucleus accumbens shell (NACs) dopamine dynamics are associated with risk-

165 gical manipulations of the nucleus accumbens shell (NAcSh) have repeatedly been demonstrated to incre

166 rgic synapses in the adult nucleus accumbens shell (NAcSh).

167 ype of raw materials derived from the oyster shell, namely the natural oyster shell (NOS), the calcin

168 Our work demonstrates that bimetallic core-shell nanocrystals are excellent probes for the local ph

169 s designed, using multilayered Pd-Ni-Pt core-shell nanocubes as precursors.

170 e reactions afford the synthesis of two open-shell nanographenes (1a and 1b) exhibiting different sce

171 Using core-shell nanoparticles (NPs) as a building block, the Pd-Fe

172 nsor, artificial nanozyme platinum/gold core-shell nanoparticles (Pt@Au NPs) as a signal probe, and a

173 no additional rotational motion of the core-shell nanoparticles is induced by the AMF, disproving th

174 ggregate-based FRET method, dye-core-polymer-shell nanoparticles showed two release processes intrace

175 This new approach mediated by core/shell nanostructure formation and conversion can be exte

176 Such porous Au@Rh core-shell nanostructures are expected to exhibit catalase-li

177 Hollow and yolk-shell nanostructures have been used to increase the cycl

178 a new bimetallic and biphasic Rh-based core-shell nanosystem (Au@Rh-ICG-CM) is developed to address

179 on of the first axial AlInN ultraviolet core-shell nanowire light-emitting diodes with highly stable

180 e for an originally non-biomineralized, soft-shelled nature of exceptionally preserved ornithischian

181 the oyster shell, namely the natural oyster shell (NOS), the calcined natural oyster shell (CNOS), a

182 Forming Co(2)P/MP(x) core/shell NRs and subsequently converting them into CoMP(x)

183 ks (yielding a "U-shape" in a histogram of k-shell occupancy) provide resilience against both local t

184 Intriguingly, we show that the ligand shell of Au(25) nanoclusters becomes more fragile and ri

185 enclosing the photosynthetic cells within a shell of bacterial cells undergoing aerobic respiration.

186 f viruses contain RNA genomes protected by a shell of capsid proteins.

187 number of waters within the first hydration shell of Cl(-) while it permeates the pore.

188 s of these events were shrouded by an opaque shell of dust and molecules(10), making it impossible to

189 a glutamate AMPA antagonist (DNQX) in medial shell of nucleus accumbens (NAc) can cause either intens

190 (gamma-Fe(2)O(3) NPs), and stabilized with a shell of poly(l-lysine) cationic polymer (PLL) for simul

191 and the silica-based intrinsically emitting shell of the core-shell MSN.

192 viewed and the range of TMCs employed in the shell of the hybrids are summarized, the one-phase, two-

193 Using the shell of the marine bivalve Atrina rigida as a model sys

194 ctions by studying the distribution of the k-shell of the underlying network.

195 d as [Au(3)@Au(23)@Au(63)]@Au(66) concentric shells of atoms.

196 th low melting temperature and quantum super-shells of clusters.

197 ter k-shells and low occupancy in the middle shells of financial and ecological networks (yielding a

198 tiple stages of infection.IMPORTANCE Protein shells of viruses (capsids) have evolved to undergo spec

199 oduced by MACE often show a porous Si/SiO(x) shell on crystalline pillar cores introduced by local el

200 )O(4) nanocube core that carries a Mn(3)O(4) shell on each facet.

201 The ice shell on Enceladus, an icy moon of Saturn, exhibits stro

202 ion via the highly programmable nucleic acid shell or a functional protein core.

203 The successful assembly of a closed protein shell (or capsid) is a key step in the replication of vi

204 Although various closed-shell organic molecules have been shown to behave as com

205 database (Rad-6) containing closed and open-shell organic molecules, along with an associated databa

206 Here, we build large, intact carboxysome shells (over 90 nm in diameter) in the industrial microo

207 zing unpaired spin in the ground state, open-shell pai-conjugated molecules can achieve optoelectroni

208 dvanced scatterer morphologies, such as core-shell particles or inverse photonic glasses-explaining r

209 tion of the infralimbic to nucleus accumbens shell pathway attenuates learned aversive responses in m

210 e approach to investigate and manipulate the shell permeability, with the intent of engineering BMC-b

211 tion of LSPR light trapping directly in core/shell PNCs for high-performance optoelectronics.

212 photodetectors using the AuCu/CsPbCl(3) core/shell PNCs, by more than 30 times as compared to the cou

213 re, a one-step strategy for fabricating core/shell poly(vinylidene difluoride) (PVDF)/dopamine (DA) n

214 to <=100 um particle size to produce oyster shell powder (OS).

215 the tooth cusps of Port Jackson sharks, hard-shelled prey specialists, possess unusual microarchitect

216 ical regions, whereas the dorsal and ventral shell project to the cortical motor system and temporal

217 n conchocelis, the release of HCO(3)(-) from shell promoted by carbonic anhydrase provides a source o

218 We obtain accurate stoichiometry of shell proteins and internal enzymes of the natural Pdu M

219 assembly that cannot be compensated by other shell proteins.

220 e present a system composed of CdSe/CdS core/shell QDs, covalently linked to naphthalenediimide (NDI)

221 Ultrabright PbS/CdS core/shell quantum dots (QDs) with dense polymer coating are

222 d CdSe/CdS@CdZnS core/crown@gradient-alloyed shell quantum wells.

223 Finally, using these gradient shelled quantum wells, we demonstrate a vertical cavity

224 45 eV in the core region and ~1.57 eV in the shell region.

225 erence in work function between the core and shell regions leads to a built-in electric field at the

226 ironmental calcium, which oysters enrich for shell repair and growth, regulates iam expression.

227 e transport of both ions and proteins to the shell secretion site, which are required during normal s

228 Both whole (i.e. in-shell) beans and shelled seeds (cotyledons) were analysed.

229 We develop strategies for enzyme activation, shell self-assembly, and cargo encapsulation to construc

230 While their shells serve as mechanical armor, bivalve shells also en

231 Therefore, bivalve shell shape is a critical determinant of how successfull

232 eir kind to isolate the influence of bivalve shell shape on strength and quantitatively demonstrate t

233 analyze the protective function of different shell shapes against vertebrate shell-crushing predators

234 etical study are consistent with examples of shell shapes that allow escape behaviors being mechanica

235 rocyclopentanediyl isomer represents an open-shell singlet biradical with interesting photochemical p

236 calculations, support assignment of an open-shell singlet electronic structure that maintains a form

237 CASSCF calculations reveal a closed-shell singlet ground state for 4 with a considerable dir

238 ilicon 1,3-cyclobutanediyls as stable closed-shell singlet species from the reversible reactions of c

239 ay be regarded as a rather unreactive closed-shell singlet species with one localized N=P and one C=P

240 crossing leads preferentially to the closed shell singlet zwitterion.

241 Dissolution of the Au shell slows down when both metals are exposed, which we

242 in a pendant electron donor, as well as core/shell SnO(2)/TiO(2) nanostructures, often prolong the li

243 Contrast enhanced ultrasound (CEUS) uses shell-stabilized gas bubbles to provide acoustic backsca

244 strength and quantitatively demonstrate that shell strength is derived from multiple shape parameters

245 ked, is shown to have significant effects on shell strength.

246 incorporation of the active moieties into a shell structure (e.g., protein, polysaccharide or lipid-

247 eO(x) NPs are transformed into a porous yolk-shell structure along with the formation of SMSIR upon t

248 SD/Ag78a shows a core-shell structure comprised of an all-metallic Ag(53) kern

249 The formation of a core-shell structure during CO(2) RR for FeAg NPs was inferre

250 The self-assembled core/shell structure is believed essential for the formation

251 the extent to which the [Formula: see text]-shell structure of the networks can be accounted for by

252 The coefficient A(v) for the NFO core/PZT shell structure was estimated to be - 1.92 kA/Vm (- 24 O

253 morphology of SMSI (fully-encapsulated core-shell structure) to obtain the intermediate state with d

254 an extended interpenetrating network or core-shell-structured gel beads-a rare example of a supramole

255 this work, monolayer ternary telluride core/shell structures are synthesized using a one-step chemic

256 ding porous particles, core-shell and hollow shell structures, and a unique 'fruits-on-a-vine' arrang

257 model catalysts, we demonstrate that 2D core-shell surfaces prepared under ultrahigh vacuum (UHV) con

258 ecursor to grow a strong, mesoporous capsule shell surrounding the droplets.

259 s of kT = 50 to 100 eV, accessible by double-shell-target implosions.

260 y slower water dynamics within the hydration shell than a similar beta-sheet protein, which may contr

261 t all modern specimens had up to 76% thinner shells than their historic counterparts.

262 ks have also convergently evolved a bivalved shell that displays an apparently mundane, yet striking

263 of the mantle, constrained both by the rigid shell that they secrete and by each other, we uncover th

264 droplets, which we named "anisosomes", have shells that exhibit birefringence, thus indicating liqui

265 nt on its permeability through the polymeric shell, the shell thickness, and the pressure gradient ac

266 Using the thin-shell theory of elasticity, we show how both the absolut

267 DI ligands is explored as a function of both shell thickness and number of NDIs per QD.

268 mispheric symmetry breaking only if the mean shell thickness is around 10 to 30 km.

269 ermeability through the polymeric shell, the shell thickness, and the pressure gradient across the sh

270 nagement when iron must traverse the protein shell through the disrupted four-fold pores (4FPs) gener

271 gradation property was selected as the outer shell to eliminate iron overload, and BMSCs implantation

272 for AMPA-blocking microinjections in medial shell to induce either positively-valenced 'desire' or n

273 ating the ecological function of this unique shell trait.

274 species, including that of the oldest fully shelled, Triassic stem-turtle Proganochelys, to evaluate

275 f antioxidants and polyphenols from chestnut shells using Response Surface Methodology (RSM).

276 In contrast, increasing CdS shell volume in the SQDs induces red-shift in the CdSe c

277 For RQDs, increasing the CdS shell volume through the length elongation has no effect

278 rtial depolymerization of chitin from shrimp shell waste (SSW), thereby offering water-soluble chitin

279 involves a pretreatment of chitin-containing shell waste and an enzymatic/fermentative bioprocess usi

280 However, the direct conversion of crustacean shell waste-derived chitin into a wide spectrum of nitro

281 an integrated biorefinery process to upgrade shell waste-derived chitin into two aromatic NCCs that c

282 cessible to humans in the form of crustacean shell waste.

283 lexibility occurs within a rigidly conserved shell, we determined the high-resolution cryo-electron m

284 he atomic order in the first Ca coordination shell, we determined the state of the calcium ions in ea

285 The fatty tissue and carbonate shells were assessed for accumulation of both inorganic

286 Discarded oyster shells were ground to <=100 um particle size to produce

287 Fibers with ferrite cores and PZT shells were prepared by electrospinning.

288 erythrocytes, the remnant erythrocyte ghost shells were prone to recognition and breakdown by RPMs.

289 e propose a mechanistic theory of epithelial shells which resemble small-organoid morphologies.

290 ts to water molecules in the first solvation shell, which affects access to exposed facets.

291 that K(+) ions maintain a complete hydration shell while passing between the transmembrane cavity and

292 no decahedron encaged by an Ag(40) drum-like shell, while the Ag(25) shell consists of two Ag(10) S(1

293 ions; this sandwich core is surrounded by a shell with lower concentration of substitutional defects

294 1.6 mM and 3.2 mM) to produce OS + P (oyster shell with phosphoric acid) and COS + P (calcined oyster

295 hosphoric acid) and COS + P (calcined oyster shell with phosphoric acid).

296 of carbonic anhydrase within the carboxysome shell with Rubisco, cyanobacteria are able to overcome t

297 (ssRNA) genomes with T=3 icosahedral protein shells with a maximum diameter of ~340 angstrom.

298 y epitaxial deposition of thin Hg(x)Cd(1-x)S shells with a small band gap.

299 demixing into intranuclear liquid spherical shells with liquid cores.

300 time-resolved femtosecond evolution of the K-shell X-ray emission spectra of iron during high intensi