ライフサイエンスコーパス: sheet

1 discharge from the surrounding grounded ice sheet.

2 ds, can contain a significant amount of beta-sheet.

3 antized triangular nanopores through an h-BN sheet.

4 elerated future retreat of the Antarctic Ice Sheet.

5 eractions with proteases at the end of the A-sheet.

6 ase (matrix phase) in a pre-stretched Nafion sheet.

7 thic two- or three- strand antiparallel beta sheet.

8 (CASE) Index, alongside the background data sheet.

9 te as an extra beta-strand in a central beta-sheet.

10 ysis biomechanics in peptide aptamers and GO sheets.

11 ulated interconnected network of tubules and sheets.

12 nanoparticles encapsulated by large graphene sheets.

13 M, which indicated attachment of NR on po-Gr sheets.

14 twist angle in bilayer and trilayer graphene sheets.

15 crobial sanitization with scalable, flexible sheets.

16 the fibril axis into tight self-associating sheets.

17 particles directionally sintered into porous sheets.

18 uds (cellular aggregates) to epithelial cell sheets.

19 outhern Ocean as a consequence of larger ice sheets.

20 usions specifically enriched in amyloid beta-sheets.

21 f electron delocalization through the 2D COF sheets.

22 gment, 15-25 WT, forms non-toxic labile beta-sheets.

23 rticles on the 2D carbon nanomaterial planar sheets.

24 ntrollable, antibiotic-releasing nanofibrous sheets.

25 ystalline powders and exfoliated micron-size sheets.

26 ucture when interacting with extended silica sheets.

27 )), H-bonded parallel- and antiparallel-beta-sheets (1690cm(-1)) and H-bonded beta-turns (1664cm(-1))

28 milarly, reactive center loop insertion into sheet A decreased heparin binding because it disturbs th

29 o assess relationships between Antarctic ice-sheet (AIS) dynamics, climate change and sea level.

30 -bonded molecules stacked in an antiparallel sheet alignment.

31 [URE3] are folded in-register parallel beta-sheet amyloids of Sup35p and Ure2p, respectively.

32 ices act as a transient intermediate to beta-sheet and fibril formation of pEAbeta (3-42).

33 We used lattice light-sheet and quantum dot-enabled synaptic contact mapping m

34 ical in the cytosol and acquires a more beta-sheet and random coil character in the nucleus.

35 stitching image columns, pivoting the light-sheet and sectioning the heart mechanically, we establis

36 rt survey composed of the respondent profile sheet and the Social Skills Inventory.

37 conjugation into the combined graphene oxide sheets and are responsible for the highly conductive nat

38 cated icosahedron and fabricated on flexible sheets and further folded either into a concave or conve

39 es (ca. 3 nm in size), together with the rGO sheets and in situ generated amorphous carbon that serve

40 FAM134B, responsible for the turnover of ER sheets and SEC62 that regulates ER recovery following st

41 ive proteins are often formed by curved beta sheets, and the ability to control beta-sheet curvature

42 phase shift of the perfectly modulated light sheet are demonstrated.

43 scopy and X-ray analyses have shown that the sheets are crystalline.

44 Graphene oxide (GO) sheets are mixed with the aptamer-QDs.

45 trate this concept, planar and 3D-structured sheets are preprogrammed to evolve into bio-inspired sha

46 tional angles in a freestanding bilayer MoS2 sheet as directly observed using an aberration-corrected

47 engraving of polymethyl methacrylate (PMMA) sheet as off surface matrix was integrated in very close

48 nsitive to the history of the Laurentide Ice Sheet as the coastline lies along the ice sheet's periph

49 an electrochemical immunosensor employing Au sheet as working electrode, Fe3O4 magnetic nanoparticles

50 allography reveals that the macrocyclic beta-sheet assembles to form double-walled nanotubes, with an

51 vide non-covalent cross-linking through beta-sheet assembly, reinforced with a polymer backbone to im

52 The respondent profile sheet assessed demographic profile and social media use

53 sheets were deposited on 1.00mm thick copper sheet at 850 degrees C using acetylene (C2H2) as carbon

54 protein that folds into an antiparallel beta-sheet at the A/W interface and presents strong intermole

55 the melting history of the Fennoscandian Ice Sheet at the end of the last deglaciation ( approximatel

56 t) anomaly was reported in the Greenland ice sheet at the Younger Dryas boundary (YDB) (12,800 Cal B.

57 ermining the relative stability of different sheets at a given doping level.

58 of the nanostructures or their internal beta-sheet backbone, but must involve accessible adaptive con

59 Light-sheet-based fluorescence microscopy (LSFM) features opti

60 proximately 345 K, above which the Te square sheets become disordered with no q-vector.

61 atterns, in which crease folding requires no sheet bending, and random patterns with high-energy fold

62 terns with high-energy folding, in which the sheet bends as much as creases fold.

63 via the formation of an intermolecular beta-sheet between the membrane-proximal (third) Fibronectin

64 stable clothes by inserting the bent polymer sheets between two fabrics.

65 the peptide in its active form within silica sheets by interface-specific vibrational spectroscopy in

66 obility exceeding 2000 cm(2) V(-1) s(-1) and sheet carrier density above 1.07 x 10(13) cm(-2) .

67 Cultured epidermal cell sheets (CES) containing undifferentiated cells are usefu

68 argeted helix-(pi-sheet)-helix and helix-(pi-sheet)-coil assemblies occur without compromising intrin

69 assemblies, a mix of sequence-defined helix-sheet-coil and helix-sheet-helix architectures, are Natu

70 accurate coupling between atmosphere and ice sheet components in climate models.

71 apeptides transform from alpha-helix to beta-sheet conformation.

72 Stable bent-sheet conformations were shown to prevail in chlorinated

73 ing a beta hairpin and an anti-parallel beta sheet consisting of strands from the top and bottom mole

74 y and variable levels of intermolecular beta-sheet content in their protein shells.

75 25 degrees C for 18min exhibited higher beta-sheet contents and more chemical bonds such as hydrophob

76 The alpha-helix and beta-sheet contents decreased, while aggregated beta-sheet, t

77 modeling studies have suggested that the ice sheet contribution to future sea level rise could have b

78 ese oligomers undergo an alpha-helix to beta-sheet conversion catalyzed by lipid vesicles and disrupt

79 due to the ability of the non-covalent beta-sheet cross-links to reassemble, the hydrogels can self-

80 ange from multi-beta-strand barrels, to beta-sheet cups and baskets covered by alpha-helical lids, to

81 investigated the mechanisms controlling beta-sheet curvature by studying the geometry of beta sheets

82 the computational models, showing that beta-sheet curvature can be controlled with atomic-level accu

83 beta sheets, and the ability to control beta-sheet curvature would allow design of binding proteins w

84 Moreover, the graphene sheets dampen capillary waves such that rotational aniso

85 e, we report the synthesis of MoS2 monolayer sheets decorated with isolated Co atoms that bond covale

86 odulation spectroscopy to reveal a bipolaron sheet density >10(10) cm(-2) at the interface between an

87 ra were erupted though the center of the ice sheet, deposited near WAIS Divide and preserved in the W

88 ted beta-sheets with an increased inter-beta-sheet distance and a higher solvent exposure than WT-alp

89 mical measurements in the West Antarctic Ice Sheet Divide, Byrd, and other ice cores to document a un

90 ic interactions between residues in the beta-sheet domain that reduce the width of the cavity.

91 in regions between the alpha-helix and beta-sheet domains.

92 entary Fe sources, such as the Antarctic ice sheet, due to the difficulty of locating and interrogati

93 andmasses were covered by the Laurentide ice sheet during the Last Glacial Maximum (18,000 years befo

94 st vulnerable part of the West Antarctic Ice Sheet, during the Holocene epoch (from 11.7 thousand yea

95 hat the MPT was initiated by a change in ice sheet dynamics and that longer and deeper post-MPT ice a

96 We argue that neither ice sheet dynamics nor CO2 change in isolation can explain t

97 loess sedimentation rate, Fennoscandian ice sheet dynamics, and sea level changes is proposed.

98 y (and then possible feedback) and ocean-ice sheet dynamics, respectively, rather than simple propaga

99 posite direction to the movement of a single sheet electron beam bunch in the experiment.

100 w, and present a challenge for modelling ice-sheet evolution and projecting global sea-level rise fro

101 s is in contrast to the expectation that ice sheets expand in colder climates and shrink in warmer cl

102 Loss of HSP hairpin proteins causes ER sheet expansion, partial loss of ER from distal motor ax

103 Light-sheet fluorescence microscopy (LSFM) serves to advance d

104 Light-sheet fluorescence microscopy and optical projection tom

105 Multicolour light sheet fluorescence microscopy provided information about

106 ic microparticles, in both cases using light-sheet fluorescence microscopy to optically access the in

107 esign can be manufactured using origami-like sheet folding and bonding methods.

108 ne aminated peptides that readily adopt beta-sheet folds.

109 try.With the use of the FAOSTAT food balance sheets for Australia, the per capita availability of add

110 odified titanium with and without epithelial sheet formation.

111 es cluster on the inner strands of both beta-sheets forming the fibronectin domains.

112 t a six-helix bundle and a six-stranded beta-sheet, forms a genome-delivery apparatus and joins 89 co

113 their main role is to protect the epithelial sheet from external mechanical strain, how HDs respond t

114 Transplantation of limbal epithelial sheets from explant cultures is one of the standard trea

115 offshore Svalbard to constrain a coupled ice sheet/gas hydrate model, we identify distinct phases of

116 To determine whether cell sheets generated with long-term passaged (P10) aging hum

117 tive biosensor employing graphene oxide nano-sheets (GO), multiwalled carbon nanotubes (MWCNTs), and

118 of the chondriod callus in the aged P10 MSC sheet groups was significantly larger than in P3 MSC she

119 oups was significantly larger than in P3 MSC sheet groups.

120 sibly associated to hot spots or whole Fermi sheets) has a strong mass enhancement at the QCP, and th

121 We demonstrate that targeted helix-(pi-sheet)-helix and helix-(pi-sheet)-coil assemblies occur

122 sequence-defined helix-sheet-coil and helix-sheet-helix architectures, are Nature-inspired synthetic

123 degree of regioselectivity, leading to a low sheet homogeneity (Hsheet).

124 The space was divided into sheets (i.e., space between two parallel membranes) and

125 the ventricle from high resolution 4-D light sheet image data.

126 Here, we introduce lattice-light sheet imaging of MDA-MB-231 human breast cancer cells ge

127 ping zebrafish embryos by coupling 4-D light sheet imaging with a stabilized finite element flow solv

128 ential partial collapse of the Antarctic ice sheet in assessing future coastal inundation.

129 Heinrich events, but also suggests that ice sheets in contact with warming oceans may be vulnerable

130 t curvature by studying the geometry of beta sheets in naturally occurring protein structures and fol

131 the mutant proteins assembled into tubes or sheets instead of capsids.

132 We used confocal and lattice light sheet instrumentation and an imaging informatics pipelin

133 cylindrical sheet into a flower, and a flat sheet into a complex canyon-like structure.

134 numerically simulating the growth of a flat sheet into a face, a cylindrical sheet into a flower, an

135 h of a flat sheet into a face, a cylindrical sheet into a flower, and a flat sheet into a complex can

136 te that the distal end of the antithrombin A-sheet is crucial for the last steps of protease inhibiti

137 The West Antarctic Ice Sheet is one of the largest potential sources of rising

138 the volume of the present East Antarctic Ice Sheet is required to explain many of the approximately 1

139 The most unique feature of the sheets is DNA-directed surface addressability, which is

140 ite in agitated solutions, the size of these sheets is generally limited due to fragmentation along f

141 and of nAu and pi* continuum of polyaromatic sheets is likely to dominate on 700 degrees C biochar.

142 by altering the geometry and topology of the sheet itself.

143 persisting up to and beyond a 100-nanometer sheet length.

144 their C-terminal, self-assemble to form beta-sheet like structures upon mixing.

145 ated, and some connected to needle-shaped or sheet-like cholesterol crystals.

146 To engineer heterotelechelic PPVs in a sheet-like design, we engineer an iterative one-pot cros

147 characteristic novel phenotype consisting of sheet-like invaginations of the sarcolemma.

148 le, where the oil remained connected in thin sheet-like layers in the narrower regions of the pore sp

149 -COF, with a hexagonal layered structure and sheet-like morphology, is synthesized.

150 d structures, in particular, those emulating sheet-like structural aspects using poly(p-phenyleneviny

151 Their sheet-like structure derives from two independent polyme

152 y, while both parallel and antiparallel beta-sheet-like structures are realized.

153 nd projecting global sea-level rise from ice-sheet loss.

154 se to an earlier perturbation in driving ice-sheet loss.

155 alcites from close to the East Antarctic Ice-Sheet margin, which together suggest that volcanically-i

156 ximately 25% increase in total Greenland ice sheet mass loss ( approximately 1.4 m sea-level equivale

157 and predicting the impacts of Antarctic Ice Sheet melting concerns the vertical distribution of the

158 We demonstrate the first light sheet microscope using propagation invariant, accelerati

159 l expression of GCaMP6s, combined with light sheet microscopy and a novel image processing pipeline,

160 lism was visualized by multiphoton and light sheet microscopy in cultured bovine hair follicles and p

161 This implementation for light sheet microscopy opens up new possibilities across a wid

162 on-uniform refractive index, extending light-sheet microscopy to partially cleared samples.

163 We therefore employed lattice light sheet microscopy to perform three-dimensional, time-laps

164 C-DSLM (cleared tissue digital scanned light-sheet microscopy) as a low-cost method intended to autom

165 mbination of 1) single-objective based light-sheet microscopy, 2) photoconvertible proteins, and 3) f

166 Using light-sheet microscopy, early neural development is here follo

167 By quantitative fluorescence lattice light-sheet microscopy, we have shown that ESCRT-III subunits

168 o neighboring patches embedded in a cortical sheet, mimicking the two digit regions, were costimulate

169 Using a standard 3-stranded beta-sheet model, the WW domain, it was found that the pH swi

170 Earth-system and ice-sheet modelling suggests these contrasting trends were l

171 However, most ice-sheet models estimate basal traction from satellite-deri

172 lower-resolution data currently used for ice-sheet models, these data show a contrasting topography a

173 in the predictive capability of current ice-sheet models.

174 two complementary pentapeptides from a beta-sheet motif of a protein, being connected to an aromatic

175 no acid interactions in an antiparallel beta-sheet motif.

176 Each cell within a polarized epithelial sheet must align and correctly position a wide range of

177 adable carbon-based electrodes onto a single sheet of paper, and demonstrate its use as a shock senso

178 mensional molecular aggregate (2DMA), a thin sheet of strongly interacting dipole molecules self-asse

179 ells connect via cell-cell junctions to form sheets of cells with separate cellular compartments.

180 curvatures, which shape growing volumes and sheets of cells.

181 es and cell stiffness both in cell pairs and sheets of cells.

182 acrophyte Fucus vesiculosus with laser light sheets of defined spectral composition, while imaging va

183 f slices were wrapped in special three-layer sheets of packaging material, some with a coating of REO

184 Basement membranes (BMs) are thin, dense sheets of specialized, self-assembled extracellular matr

185 om coil structure, evolves into ordered beta-sheet oligomers containing at least 5 strands, and then

186 cial physicochemical features, including the sheet-on-sheet sandwich-like structure, ultrathin nanosh

187 baseline intervention forms and 274 outcome sheets one year later (31%).

188 Fe(II) into predominantly-Fe(III) octahedral sheets or through the adsorption of Fe(II) onto the mine

189 sessed how Fe(II) residing in the octahedral sheets, or Fe(II) adsorbed at the edge sites alters redo

190 om thin peptide films shows features of beta-sheet ordering for both peptides, along with evidence fo

191 d reporter assay in Drosophila ovary somatic sheet (OSS) cells [1].

192 We propose that the appearance of larger ice sheets over the past million years was a consequence of

193 he experimentally observed antiparallel beta-sheet packing.

194 ircuit model is established and the graphene-sheet pattern is designed optimally for maximizing the r

195 By altering the beta-sheet peptide graft density and concentration, we can ta

196 This self-healing polymer-beta-sheet peptide hybrid hydrogel with tailorable mechanical

197 17 of IAPP (RLANFLV) into a macrocyclic beta-sheet peptide results in a monomeric peptide that does n

198 onalization of its repeating units with beta-sheet peptides to form a hydrogel, it can easily be modi

199 ross-linked via grafted self-assembling beta-sheet peptides to provide non-covalent cross-linking thr

200 Ice sheets play a more important role in the global silicon

201 vity, we treated partially oxidized graphene sheets (po-Gr) with NR to obtain po-Gr-NR dispersion by

202 eta-sandwich fold, with the face of one beta-sheet possessing the beta-1,3-glucan-binding surface.

203 Pt anomaly is consistent with Greenland Ice Sheet Project 2 (GISP2) data that indicated atmospheric

204 l hydration network are observed in the beta-sheet protein.

205 , pi-stacking interactions with the graphene sheets provide further pi-delocalization that improves t

206 oduction of a disulfide bond in the bridging sheet region further stabilized the closed conformation

207 se results reveal the importance of the beta-sheet region of lysozyme for initiating self-assembly in

208 s (I476 and V482) were within coiled or beta-sheet regions in domain B distant to the active site.

209 e material in which the alpha-helix and beta-sheet regions of the protein are similar to crystal grai

210 A 28-nanometer-thick gold foil with a sheet resistance of 7 ohms per square showed only a 4% i

211 The resulting fibres display sheet resistance values as low as 600 Omegasq(-1), demon

212 eport on angle-dependent measurements of the sheet resistances and Hall coefficients of electron liqu

213 etreat may have been a highly non-linear ice sheet response to relatively continuous external forcing

214 th of both NiFe-LDH and carbon in one single sheet results in fully integrated amorphous NiFe-LDH/C n

215 At 3 weeks after transplantation of MSC sheets, results showed more bony callus formed between a

216 We infer rapid and sustained ice-sheet retreat driven by MICI, commencing around 12,300 y

217 ervational evidence that rapid deglacial ice-sheet retreat into Pine Island Bay proceeded in a simila

218 sequestration and subsequent release on ice sheet retreat that led to the formation of a suite of se

219 native-like properties and convert into beta-sheet-rich amyloid-like structures, as indicated by thei

220 ordered, monomeric alpha-synuclein into beta-sheet-rich oligomers and fibrils is associated with mult

221 We suggest that enhanced ice sheet runoff is primarily associated with albedo effects

222 ce Sheet as the coastline lies along the ice sheet's peripheral bulge.

223 icochemical features, including the sheet-on-sheet sandwich-like structure, ultrathin nanosheets with

224 C), inflowing warm Atlantic Layer water, ice sheet, sea-ice and ice-shelf feedbacks, and sensitivity

225 haracteristic 2D IR features of amyloid beta-sheet secondary structure are created by as few as four

226 cited antibodies to the peptide and the beta-sheet secondary structure conformation.

227 selected to specifically react with the beta-sheet secondary structure of pathological oligomeric con

228 of which reflects the curvature of the beta-sheet segment.

229 The beta-sheet self-assembles to form long fibrils with the hydro

230 n vitro and is a major signal for cross-beta-sheet self-association of the 49-mer Phe521Leufs peptide

231 el prefers alpha-helical sequences over beta-sheet sequences.

232 ealed that this protein contained three beta-sheets, seven alpha-helices, and coils.

233 The sheet size is on the order of 5 x 5 mum(2).

234 the last glacial period, the Laurentide Ice Sheet sporadically discharged huge numbers of icebergs t

235 mphasize the importance of the ocean for ice sheet stability under the current changing climate.

236 c reticulum (ER) is a network of tubules and sheets stretching throughout the eukaryotic cells.

237 dic region of Ng peptide pries open the beta-sheet structure between the Ca(2+) binding loops particu

238 stinct from the intermolecular parallel beta-sheet structure observed in mature fibrils.

239 ze that NUCB1 binds to the common cross-beta-sheet structure of protofibril aggregates to "cap" and s

240 face region and the extended two-dimensional sheet structure within the nanoframe that minimizes the

241 As a result of their distinct beta-sheet structure, 1-108-alphaS fibrils resist incorporati

242 hydrogen bonding, including an extended beta-sheet structure, as well as aromatic interactions.

243 eracts with the stalk to form a compact beta-sheet structure.

244 sitely charged ionic segments that form beta-sheet-structured hydrogel assemblies via polyion complex

245 ortionation with structural Mn(IV) may alter sheet structures by forming larger and distorted Mn(III)

246 ics in general are more retarded around beta-sheet structures than alpha-helical motifs.

247 urn-helix architectures in which helical and sheet subcomponents conserve their respective integrity.

248 re proteins consist of three sequential beta-sheet subdomains that bind to specific carbohydrates to

249 y different approach to produce nanopores in sheet substrates under dry, ambient conditions, using na

250 with peptides aligned perpendicularly to the sheet surfaces.

251 elop an ultra compact, high resolution light sheet system without beam scanning.

252 se who wish to develop and use bespoke light-sheet systems and to assist in identifying the best appr

253 hin the eastern sector of the Laurentide Ice Sheet than traditional reconstructions for this interval

254 plex 3D structures starts with an epithelial sheet that is patterned by inductive cues that control t

255 ly for the crafting of high aspect ratio, 2D sheets that are densely surface-decorated with DNA.

256 The peptide forms amphiphilic parallel beta-sheets that assemble into stacked bilayers with alternat

257 evealed altered packing arrangements of beta-sheets that encompass residues 139 and 186 of PrP(Sc).

258 ontrol two counterpropagating coherent light sheets that generate excitation patterns in the focal pl

259 to be composed of thin (<0.75 microm), flat sheets that sometimes interleave to form rosettes.

260 hrough intermolecular hydrogen bonds to beta-sheets thereby placing the azide and alkyne motifs in pr

261 of the largest glaciers of the Greenland Ice Sheet; these have been major contributors to ice loss in

262 ice-shelf collapse may have caused rapid ice-sheet thinning further upstream-and since the 1940s.

263 When placed into the turn of a beta-sheet, this leads to a pH switch of folding.

264 e of meltwater across the surface of the ice sheet through surface streams and ponds (hereafter 'surf

265 ates and shells, we constrained flat elastic sheets to adopt fixed curvature profiles.

266 trated in this article, the redesign of beta-sheets to contain a global, or local, pH-dependent confo

267 y, the aptamer-conjugated QDs bind to the GO sheets to form a GO/aptamer-QDs ensemble.

268 unit interface, altering the packing of beta-sheets to induce changes that lead to asynchronous pore-

269 used so far for modification of 2-D graphene sheets to make is three-dimensional.

270 The sensitivity of past ice sheets to volcanic ashfall highlights the need for an ac

271 highlighting the sensitivity of ancient ice sheets to volcanism is scarce.

272 sheets with a previously unobserved silicate sheet topology that contains the uncommon cyclic Si3O9 t

273 et contents decreased, while aggregated beta-sheet, turns and random coil contents increased as tempe

274 roscopy can identify the highly ordered beta-sheets typical of amyloid secondary structure even if th

275 d superconducting symmetrically bonded AuHAu sheets under compression.

276 ed the effect of bending aromatic amide beta-sheets using building blocks that impart curvature.

277 rect electropolymerization of graphene oxide sheets via oxidation of the phenol edge groups on graphe

278 ogical data show that the West Antarctic Ice Sheet (WAIS) advanced to the eastern Ross Sea shelf edge

279 The West Antarctic ice sheet (WAIS) is highly vulnerable to collapsing because

280 ilar to that observed beneath the extant ice sheet, was also active during the last glacial period.

281 gments flanking a central bent aromatic beta-sheet were then synthesized and shown to form well-defin

282 The graphene sheets were deposited on 1.00mm thick copper sheet at 85

283 ubglacial basin before continental-scale ice sheets were established about 34 million years ago.

284 d monomers to alpha-helices and then to beta-sheets when the proteins encounter the cell membrane, an

285 abilized by apolar side chains from adjacent sheets, whereas the hydrated polar interface houses the

286 chelic PPVs is used to realize a parallel pi-sheet, wherein further orthogonal assembly with helical

287 e in the major groove while inserting a beta sheet 'wing' into the adjacent minor groove.

288 igned based on decorated graphene oxide (GO) sheet with alumina (Al2O3) nanocrystals.

289 hrough the decoration of either faces of the sheet with gold nanoparticles through sequence-specific

290 molecular dynamics simulations of perforated sheets with a dense periodic array of holes and observe

291 EO6 and REO2F4 polyhedra connected by Si4O10 sheets with a previously unobserved silicate sheet topol

292 Programmable stiff sheets with a single low-energy folding motion have been

293 We combined graphene oxide (GO) sheets with a specific peptide aptamer to create a novel

294 haS fibrils consist of strongly twisted beta-sheets with an increased inter-beta-sheet distance and a

295 The design of protein sheets with architecture and physical properties suitabl

296 s were electrospun to form elastic polymeric sheets with fiber diameters ranging from 350 to 1100 nm

297 rbon stacks is composed of well-preserved 2D sheets with highly accessible interlayer macropores, nar

298 nd Sc atoms, we show evidence for 2D Mo1.33C sheets with ordered metal divacancies and high electrica

299 he materials and verify the presence of beta-sheets within the hybrid hydrogels.

300 e ends in both young P3 MSC and aged P10 MSC sheet-wrapped groups when compared to allograft alone.