ライフサイエンスコーパス: icosahedral

1 pparent hexameric symmetry positioned on the icosahedral 2-fold axes.

2 positioned the betaA strand region under the icosahedral 2-fold axis rather than antiparallel to the

3 teractions act as "molecular staples" at the icosahedral 2-fold symmetry axis and significantly contr

4 her parvoviruses, such as depressions at the icosahedral 2-fold symmetry axis and surrounding the 5-f

5 uctures, the stabilizing interactions at the icosahedral 3-fold axes and the R domains differed great

6 The spikes on the icosahedral 3-fold axes and those in general positions a

7 et at the base of the protrusions around the icosahedral 3-fold axes of symmetry.

8 tributing to the protrusions surrounding the icosahedral 3-fold axes of the AAVs, is shorter in AAV5,

9 Steric hindrance around the icosahedral 3-fold axes prevents binding of a Fab to the

10 In addition, there are differences at the icosahedral 3-fold axes with regard to metal binding tha

11 t the base of capsid protrusions surrounding icosahedral 3-fold axes.

12 ow particle assembly via interactions at the icosahedral 3-fold axes.

13 the N termini of the three C subunits at the icosahedral 3-fold axes.

14 intersubunit beta-strand interactions at the icosahedral 3-fold axes.

15 onse focuses on the plateau epitope near the icosahedral 3-fold axes.

16 h destabilization of the beta-annulus at the icosahedral 3-fold axes.

17 a epitope to the protrusions surrounding the icosahedral 3-fold axis and the ADK1b and ADK5a epitopes

18 using cryo-electron microscopy to solve the icosahedral (3.0- angstrom resolution) and asymmetric (5

19 Poliovirus virions are nonenveloped icosahedral 30-nm particles with 60 copies of each of fo

20 ons: 12 pentameric turrets positioned on the icosahedral 5-fold axes and 30 turrets with apparent hex

21 nd sits slightly off-center from each of the icosahedral 5-fold axes.

22 Large-area icosahedral-AB(13)-type Pt-Pd binary superlattices (BNSL

23 Using a hitherto unexplored template, the icosahedral Ag-In-Yb quasicrystal, and various experimen

24 udy extend our knowledge on the stability of icosahedral AlCuFe at higher temperature and pressure th

25 tability at ambient temperature of synthetic icosahedral AlCuFe up to ~35 GPa, the simultaneous effec

26 n X-ray diffraction experiments on synthetic icosahedral AlCuFe using multianvil device to explore po

27 encephalitis virus (EEEV), a mosquito-borne icosahedral alphavirus found mainly in North America, ca

28 These icosahedral and capsular assemblies reveal at high-resol

29 The Khatyrka meteorite contains both icosahedral and decagonal quasicrystals.

30 tural order given by alternating layers with icosahedral and dodecahedral symmetries, while open netw

31 plets can be reversibly temperature-tuned to icosahedral and other faceted shapes, hitherto unreporte

32 ulk diffusivities of several near-spherical (icosahedral) and nonspherical (tailed) bacterial viruses

33 Many virus capsids are icosahedral, and assembly is thought to occur by the seq

34 Zika virions are enveloped and icosahedral, and contain a nonsegmented, single-stranded

35 mmetry averaging techniques that exploit the icosahedral architecture seen in many viruses.

36 show that 10 designs spanning three distinct icosahedral architectures form materials closely matchin

37 d protein containers with a wide spectrum of icosahedral architectures to protect their genetic mater

38 edral symmetry--tetrahedral, octahedral, and icosahedral--are the 5 Platonic polyhedra, the 13 Archim

39 apsid proteins (VP1 to VP3) adopt an altered icosahedral arrangement to open holes in the capsid at 2

40 case of an overarching design principle for icosahedral, as well as octahedral, architectures that c

41 kage one full-length RNA genome for every 11 icosahedral assemblies, similar to the best recombinant

42 ious rotavirus particles are triple-layered, icosahedral assemblies.

43 ng the four quasi-equivalent subunits in the icosahedral asymmetric unit.

44 opy (cryo-EM), showed only four proteins per icosahedral asymmetric unit: a dimer of the major capsid

45 between {111} and {110} facets grown on the icosahedral Au seeds, NCs with icosahedral, icosidodecah

46 10)Cl(8)]SbF(6) nanoclusters composed of two icosahedral Au(7)Ag(6) units by sharing one common Au ve

47 BT)50 structure with the recently discovered icosahedral Au133(p-TBBT)52 nanocluster (where p-TBBT =

48 much larger than the gap (0.9 eV) of the bi-icosahedral [Au38(SCH2CH2Ph)24].

49 e 5-fold and 2-fold but not along the 3-fold icosahedral axes.

50 hydrogen atoms, or hydrides from the stable icosahedral B(12)H(12)(2-) is investigated theoretically

51 We also show that a layer composed of icosahedral B12 is unfavorable on Cu and Ni but unexpect

52 ach can be utilized in other filamentous and icosahedral bacteriophages, and also in other biomolecul

53 ery of a family of at least seven rare earth icosahedral binary quasicrystals, i-R-Cd (R = Gd to Tm,

54 Icosahedral boranes, carboranes, and metallacarboranes a

55 Icosahedral boron cluster derivatives have been reviewed

56 iloxane and coordination polymers containing icosahedral boron clusters in the last few decades, whic

57 nthesizing crystals of C(60)(SnI(4))(2) from icosahedral buckminsterfullerene (C(60)) and tetrahedral

58 le model, the extraordinary abundance of the icosahedral C80 cage in EMFs can be easily understood.

59 ne complex containing two boron atoms of the icosahedral cage connected to a single exohedral metal c

60 ks are assembled to build a highly symmetric icosahedral cage.

61 d [PdH(2) ](2-) unit and its Cu(14) bicapped icosahedral cage.

62 two of the major particle compartments, the icosahedral capsid and the amorphous tegument, has been

63 where the interaction between heparin and an icosahedral capsid does not follow the symmetry elements

64 he product of gene 58, is assembled onto the icosahedral capsid lattice.

65 The large (90-nm) icosahedral capsid of bacteriophage T5 is composed of 77

66 oduced an atomic model for a continuous, T=3 icosahedral capsid shell.

67 icroscopy of this novel phage revealed a T=9 icosahedral capsid structure with the major capsid prote

68 ed in the family Siphoviridae because of its icosahedral capsid surrounded by head fibers and a non-c

69 yovirus KZ has a 270-kb genome within a T=27 icosahedral capsid that contains a large, unusual, and s

70 us (HBV) core protein (HBc) assemble into an icosahedral capsid that packages the viral pregenomic RN

71 are initiated via the attachment of the PCV2 icosahedral capsid to heparan sulfate (HS) and chondroit

72 transcribed and replicated in a specialized icosahedral capsid with a T=1 lattice consisting of 60 a

73 ortal complex that nucleates formation of an icosahedral capsid with capsid-associated tegument compl

74 glycans composing the fibers surrounding its icosahedral capsid, including the dideoxyhexose viosamin

75 racteristic particle structure comprising an icosahedral capsid, which contains the DNA genome and is

76 characterized by a highly pressurized pseudo-icosahedral capsid-with triangulation number (T) equal t

77 d an internal lipid membrane enclosed in the icosahedral capsid.

78 s encapsulated in an asymmetric T = 3 pseudo-icosahedral capsid.

79 rings at the special five-fold vertex of the icosahedral capsid.

80 f HAstV produced an atomic model for the T=3 icosahedral capsid.

81 ted by the L1 C terminus to constitute a T=7 icosahedral capsid.

82 uide the single-stranded DNA genome into the icosahedral capsid.

83 surface, merging seamlessly to complete the icosahedral capsid.

84 ic and asymmetric elements within the pseudo-icosahedral capsid.

85 ions required for productive assembly of the icosahedral capsid.

86 e hepatotropic enveloped DNA viruses with an icosahedral capsid.

87 three-fold and quasi-three-fold sites of the icosahedral capsid.

88 uble-stranded DNA genome, enclosed within an icosahedral capsid.

89 Viruses build icosahedral capsids of specific size and shape by regula

90 Icosahedral capsids of viruses are lattices of defined g

91 These viruses share structurally related icosahedral capsids that encase the double-stranded DNA

92 he major capsid protein, gp23, produced T=13 icosahedral capsids.

93 tinocytes containing densely packed 36-45-nm icosahedral capsids.

94 nserved number of transcription complexes in icosahedral capsids.

95 virus (RSV) CA-SP to assemble in vitro into icosahedral capsids.

96 sions surrounding the 3-fold axes of the T=1 icosahedral capsids.

97 copies of capsid protein comprising the T=3 icosahedral capsids.

98 single-stranded DNA genomes and nonenveloped icosahedral capsids.

99 Icosahedral carboranes in medicine are still an emerging

100 nce of individual building blocks within the icosahedral carboxysome.

101 17.51 nm is likely associated with the known icosahedral CBPV satellite (CBPVS).

102 While the icosahedral closo-[B(12)H(12)](2-) cluster does not disp

103 consistent with six-shell cuboctahedral and icosahedral clusters containing ~600 Pd atoms, where 45%

104 r clues to the driving forces underlying the icosahedral clusters that occur in Bergman-type quasicry

105 In vitro assembly of icosahedral complexes from independently purified compon

106 Given these results, we predict decreased icosahedral complexity (i.e. T <= 7) leads to a more sta

107 )ethane] nanoclusters both possess a 13-atom icosahedral core with 8 delocalized superatomic electron

108 on to confirming the theoretically predicted icosahedral-cored cluster, we also find samples with a t

109 We validate that Ag nanocrystals with icosahedral, decahedral, and single-crystal structures a

110 By combining a cell-targetable, icosahedral DNA-nanocapsule loaded with photoresponsive

111 We report a discovery that perfunctionalized icosahedral dodecaborate clusters of the type B12(OCH2Ar

112 In most icosahedral double-stranded (ds) DNA viruses, the viral

113 In contrast to tailed icosahedral double-stranded DNA (dsDNA) viruses infectin

114 IMPORTANCE Pacmanvirus is a newly discovered icosahedral double-stranded DNA virus that was isolated

115 d of 260 hexagonal units and 13 hexagons per icosahedral face.

116 ab bound only to epitopes located around the icosahedral five-fold vertex of the capsid.

117 he preformed capsid via a pore at one of its icosahedral fivefold axes.

118 small tilt of the core stack relative to the icosahedral fivefold axis and propose that this tilt ass

119 +) cation, attaching the N termini under the icosahedral fivefold symmetry axis, and forming a basket

120 rm bilayers that interact with PhiX174 at an icosahedral fivefold vertex and induce single-stranded (

121 irions, with molecules pushed inwards at the icosahedral fivefolds by ~100 angstrom, reminiscent of t

122 NCs with tetrahedral, cubic, octahedral, and icosahedral geometries have been chemically synthesized,

123 arison with interior 55-metal-atom two-shell icosahedral geometries observed within the multi-shell c

124 apsid of coliphage T5 is organized with T=13 icosahedral geometry and encloses a double-stranded DNA

125 , 60 protein subunits in total, with overall icosahedral geometry.

126 e carbon fullerenes and faceted viruses, the icosahedral Goldberg polyhedra are nearly spherical.

127 ; they have large genomes packaged within an icosahedral head and a long, contractile tail through wh

128 r motor assembled at the portal vertex of an icosahedral head.

129 Our results indicate that PVL phages with icosahedral heads, including Phi108PVL and PhiPVL, were

130 ith similar tail lengths (200 to 250 nm) and icosahedral heads.

131 L17 and pUL25 on the structural stability of icosahedral herpes simplex virus capsids.

132 rtices), whereas the outer (Ag(60)) shell is icosahedral (I(h)), a rhombicosidodecahedron (an Archime

133 grown on the icosahedral Au seeds, NCs with icosahedral, icosidodecahedral, and dodecahedral shapes

134 in the formation of TiLu2C@I(h)-C80 with an icosahedral Ih(7) carbon cage.

135 ese shapes represent a family of Au NCs with icosahedral (Ih) symmetry.

136 , we are able to identify the proportions of icosahedral (Ih), decahedral (Dh), and face-centered cub

137 sed transmission electron cryomicroscopy and icosahedral image reconstruction to examine the GLV viri

138 Using electron cryomicroscopy and icosahedral image reconstruction, we determined the viri

139 neral features with the previously described icosahedral large DNA viruses, the Pandoraviruses appear

140 The HPV capsid is an icosahedral lattice comprising 72 pentamers of the major

141 fic for the conjugative F-pilus, has a T = 3 icosahedral lattice of coat proteins assembled around it

142 d 89 coat protein dimers arranged in a T = 3 icosahedral lattice.

143 The 70-nm-diameter virion is built on a T=28 icosahedral lattice.

144 nd gp10 protein subunits that form the T = 7 icosahedral lattice.

145 otein has an HK97 fold arranged into a T = 4 icosahedral lattice.

146 g the major capsid protein (MCP) to build an icosahedral lattice.

147 s from thousands of individual proteins into icosahedral-like particles with a dense enzyme cargo enc

148 he rationale of our approach is to establish icosahedral local coordinates to estimate the statistica

149 heory of finite ideal gas reference state to icosahedral local coordinates.

150 We propose a series of icosahedral matryoshka clusters of A@B12@A20 (A = Sn, Pb

151 All of these icosahedral matryoshka clusters, including two previousl

152 cryo-electron microscopic structures of the icosahedral MCPyV capsid and analysis of its glycan inte

153 Also, an icosahedral membrane lies between the two protein layers

154 r viral genome encapsidation in the tailless icosahedral membrane-containing bacteriophage PRD1.

155 Tectiviridae comprises a group of tailless, icosahedral, membrane-containing bacteriophages that can

156 isolated from a hypersaline environment: an icosahedral, membrane-containing double-stranded DNA vir

157 e rare 8,1,2-closo-MC2B9 isomeric form of an icosahedral metallacarborane have been isolated as unexp

158 These include icosahedral Mimiviruses, amphora-shaped Pandoraviruses,

159 The new icosahedral mineral formed naturally and was discovered

160 dominated by the three-dimensional (3D) B12 icosahedral motifs,4 new forms of elemental boron are co

161 atonic dodecahedral Au NCs can be grown from icosahedral multiply twinned Au seeds.

162 conditions, we can eliminate completely all icosahedral nanoclusters, which are commonly found under

163 Among the Pt-M alloy icosahedral nanocrystals generated, Pt(3)Ni had an impre

164 ]-catenane composed of interlocked M(12)L(8) icosahedral nanometric cages (i.e., internal voids of 25

165 entire transformation process of strained Pt icosahedral nanoparticles (ICNPs) into larger FCC crysta

166 s components of tetrahedral, octahedral, and icosahedral nanoparticles, which were characterized by c

167 the Picornaviridae family, which consists of icosahedral, nonenveloped, single-stranded RNA viruses.

168 es represent new genera, the podoviruses and icosahedral, nontailed ssDNA phages were exceptional, wi

169 ssembly is finalized by the enclosure of the icosahedral nucleocapsid within a heterogeneous envelope

170 one, and a systematic, countable infinity of icosahedral ones, one for each Goldberg triangle.

171 the binary fluid into local structures with icosahedral or polytetrahedral symmetry prior to nucleat

172 etallic compounds and either of face-centred-icosahedral or primitive-icosahedral type, and the posit

173 a high cooling rate; and (ii) competition of icosahedral order against crystal order near the critica

174 molecule condensed by proteins (core) lacks icosahedral order characteristic of the virus protein co

175 he chemical origins of long- and short-range icosahedral order remain mysterious and a subject of deb

176 hat, in the presence of those perturbations, icosahedral packing is not the most stable arrangement f

177 protein (VP1) of all caliciviruses forms an icosahedral particle with two principal domains, shell (

178 positive-sense RNA genome packaged in a T=3 icosahedral particle.

179 taining double-stranded DNA virus--Salisaeta icosahedral phage 1 (SSIP-1) and its halophilic host bac

180 nal metals expand the stability range of the icosahedral phase and facilitate routine syntheses witho

181 The compositional range of the icosahedral phase is Al68-73Fe11-16Cu10-12Cr1-4Ni1-2 and

182 The chemistry of both the icosahedral phases was characterized by electron micropr

183 sized HER2-based cancer vaccines using three icosahedral plant viruses as carriers and evaluated the

184 f viral double-stranded DNA (dsDNA) into the icosahedral prohead shell is catalyzed by TerL, a motor

185 ocapsids, which are computationally designed icosahedral protein assemblies with positively charged i

186 protein-based molecular machines, including icosahedral protein cages that serve as scaffolds, enzym

187 he Tectiviridae family, has a 70 nm diameter icosahedral protein capsid that encapsulates a lipid mem

188 ntaining nucleoid surrounded by two distinct icosahedral protein capsids and two lipoprotein membrane

189 tic mottle virus (CCMV) forms highly elastic icosahedral protein capsids that undergo a characteristi

190 of co-assembling, two-component, 120-subunit icosahedral protein nanostructures with molecular weight

191 apsulate enzymes from the cytoplasm using an icosahedral protein shell that resembles viral capsids.

192 lf-assembly pathway of a most simple (T = 1) icosahedral protein shell.

193 viruses (AAV) are composed of nonenveloped, icosahedral protein shells that can be adapted to packag

194 single-stranded RNA (ssRNA) genomes with T=3 icosahedral protein shells with a maximum diameter of ~3

195 is the carboxysome, which is composed of an icosahedral proteinaceous shell encapsulating the key ca

196 s consisting of one, two, and three centered icosahedral Pt@Ag(12) units, respectively.

197 s with polytetrahedral symmetry, such as the icosahedral quasicrystal and the lambda-Al(13)Fe(4) phas

198 The Burgers vector of a dislocation in an icosahedral quasicrystal is a 6-dimensional vector, whic

199 We report the first occurrence of an icosahedral quasicrystal with composition Al62.0(8)Cu31.

200 Icosahedral quasicrystals (IQCs) are a form of matter th

201 Examples of stable binary icosahedral quasicrystals are relatively rare, and at pr

202 In our previous studies, icosahedral quasicrystals have been synthesized and reco

203 we clarify the shock synthesis mechanism of icosahedral quasicrystals through two new shock recovery

204 Five-component icosahedral quasicrystals with compositions in the range

205 erials, numerous micron-sized five-component icosahedral quasicrystals, average composition Al72Cu12F

206 Using electron cryomicroscopy and icosahedral reconstruction of mutants that express pUL17

207 058-nucleotide plus-strand RNA genome of the icosahedral satellite tobacco mosaic virus (STMV) using

208 The solid-state and gas-phase studies of the icosahedral Sb@M12@Sb20(n-/n+) ions show that the cluste

209 e space and supports the proposal that, like icosahedral Sc12Zn88, binary quasicrystalline phases may

210 Icosahedral seeds are used to dictate the growth of 3D e

211 0-A spherical procapsid condenses to a 400-A icosahedral-shaped capsid with associated specific auto-

212 determined that EncA self-assembles into an icosahedral shell 32 nm in diameter (26 nm internal diam

213 We computationally study how an icosahedral shell assembles around hundreds of molecules

214 180 envelope glycoproteins that make up the icosahedral shell.

215 rs and hexamers which assemble into a T = 43 icosahedral shell.

216 Bacteriophage capsids constitute icosahedral shells of exceptional stability that protect

217 However, the tail-less, icosahedral, single-stranded DNA PhiX174-like coliphages

218 surface while the shell domain forms a tight icosahedral sphere around the genome.

219 ns showed that the virus retains its overall icosahedral structure at this mildly acidic pH, except i

220 entional Au nanoparticles, as well as the bi-icosahedral structure of [Au38(SCH2CH2Ph)24].

221 The icosahedral structure, at 3.7-A resolution, resolves loo

222 ologs that self-assemble in space to form an icosahedral structure.

223 They also apply to other icosahedral structures in nature, and offer alternative

224 cages that self-assemble in vivo into stable icosahedral structures.

225 een known to progress from multiply twinned, icosahedral, structures in smaller molecular sizes to un

226 cupies positions beneath the vertices of the icosahedral surface shell, and the other is distributed

227 ain dimer formed by adjacent subunits on the icosahedral surface while the shell domain forms a tight

228 at it polymerizes according to two different icosahedral symmetries, causing the polypeptide chain to

229 other known naturally occurring mineral with icosahedral symmetry (though the latter composition had

230 sicrystalline phase displaying face-centered icosahedral symmetry and low phason strain.

231 ems such as spherical viruses, which utilize icosahedral symmetry as a guiding principle for the asse

232 The cage was constructed based on icosahedral symmetry by genetically fusing a trimeric pr

233 HAstV particles display T=3 icosahedral symmetry formed by 180 copies of the capsid

234 ween PCV2 and heparin does not adhere to the icosahedral symmetry of the capsid.

235 particle clusters with local tetrahedral or icosahedral symmetry that seed growth of the temporally

236 Orsay capsid has a T = 3 icosahedral symmetry with 60 trimeric surface spikes.

237 ions of the capsid are possible based on its icosahedral symmetry, but the surrounding tegument and e

238 Because of deviation from icosahedral symmetry, KSHV portal and tegument structure

239 building blocks, which are able to pack with icosahedral symmetry, we examine how stable these highly

240 k tightly to form a smooth protein coat with icosahedral symmetry.

241 riophage P22, reconstructed without imposing icosahedral symmetry.

242 atomic model of the alphavirus envelope with icosahedral symmetry.

243 codes further details of the molecule's rare icosahedral symmetry.

244 ike particles, which is characteristic of an icosahedral T = 1 symmetry.

245 intermediates comprising some 11 dimers, and icosahedral T = 3 capsids made up of 90 dimers.

246 tending from the capsid protein dimer to the icosahedral T = 4 capsid with 120 dimers.

247 15C5 and 11G1 engage the capsid loci at icosahedral three-fold and five-fold axes, respectively.

248 ke region of the AAV2 capsid adjacent to the icosahedral three-fold axis.

249 es (q3) and the 20 sites associated with the icosahedral threefold axes (i3).

250 Pores that are 7 A in diameter form around icosahedral threefold symmetry axes.

251 ough one of the large pores that open at the icosahedral twofold axes, and is transferred along a con

252 her of face-centred-icosahedral or primitive-icosahedral type, and the positions of their atoms have

253 bly intermediates, which become the capsid's icosahedral vertices.

254 tions that are ultimately occupied by 5-fold icosahedral vertices.

255 undetected protein was found to underlie the icosahedral vertices: this is tentatively assigned as a

256 erica serovar Typhimurium and is a model for icosahedral viral capsid assembly.

257 Icosahedral viral capsids are made of a large number of

258 Icosahedral viral capsids are obligated to perform a the

259 Icosahedral viral capsids must undergo conformational re

260 are important for the assembly of 3 types of icosahedral viral capsids: Adeno Associated Virus seroty

261 assemblies required for the formation of the icosahedral viral envelope.

262 rotein of norovirus VP1 assembles to form an icosahedral viral particle.

263 Iflaviruses have nonenveloped icosahedral virions containing single-stranded RNA genom

264 The Megaviridae exhibit pseudo-icosahedral virions up to 0.7 mum in diameter and adenin

265 e types of morphologically indistinguishable icosahedral virions with T=3 quasisymmetry.

266 s, tentatively named Metallosphaera turreted icosahedral virus (MTIV), that was isolated from an acid

267 l host cells infected by Sulfolobus turreted icosahedral virus (STIV) and Sulfolobus islandicus rod-s

268 Sulfolobus turreted icosahedral virus (STIV) was isolated in acidic hot spri

269 Sulfolobus turreted icosahedral virus (STIV), an archaeal virus that infects

270 Icosahedral virus assembly requires a series of concerte

271 ons at subnanometer (<10-A) resolution of an icosahedral virus assembly were obtained by cryogenic el

272 ly of hundreds of identical proteins into an icosahedral virus capsid is a remarkable feat of molecul

273 distribution of heparin on the surface of an icosahedral virus capsid.

274 ents for essential biochemical reactions and icosahedral virus capsids, which encapsidate and protect

275 lishment of a productive Sulfolobus turreted icosahedral virus infection.

276 that the archaeal virus Sulfolobus turreted icosahedral virus isolated from Yellowstone National Par

277 Icosahedral virus particles constitute paradigms to stud

278 een shown to assemble trimer-clustered T = 3 icosahedral virus particles.

279 elia capensis omega virus (NomegaV) is a T=4 icosahedral virus that undergoes a dramatic maturation i

280 llite tobacco mosaic virus (STMV) is a T = 1 icosahedral virus with a single-stranded RNA genome.

281 te and polynorbornene (PNB) when attached to icosahedral virus-like particles.

282 e to infection with the S ulfolobus turreted icosahedral virus.

283 visualization of the structure of DNA in an icosahedral virus.

284 with dimensions similar to those of a small icosahedral virus.

285 tions have implications for the evolution of icosahedral viruses and regulation of virus assembly.

286 Icosahedral viruses are under a micrometer in diameter,

287 STMV is among the simplest of the icosahedral viruses but, nonetheless, has an RNA genome

288 Noroviruses are nonenveloped, icosahedral viruses of global importance to human health

289 How icosahedral viruses regulate the release of viral RNA in

290 Two icosahedral viruses represented species in the family Po

291 nt head assembly gives guidance to how other icosahedral viruses reproducibly assemble into capsids w

292 The Parvovirinae are small nonenveloped icosahedral viruses that are important pathogens in many

293 ANCE The Parvovirinae are small nonenveloped icosahedral viruses that are important pathogens in many

294 ANCE The Parvovirinae are small nonenveloped icosahedral viruses that are important pathogens in many

295 Many icosahedral viruses use a specialized portal vertex to c

296 However, a mechanistic understanding of how icosahedral viruses utilize this process to transform im

297 es of the order Caudovirales and to tailless icosahedral viruses with the double jelly-roll capsid pr

298 For the icosahedral viruses, good agreement was also found betwe

299 ymmetric capsid vertex, is found in numerous icosahedral viruses, including tailed bacteriophages, he

300 dodecameric portal-a longstanding mystery in icosahedral viruses-and inform possible DNA-sequence rec