ライフサイエンスコーパス: cryoelectron microscopy

1 l structures of both GCRV core and virion by cryoelectron microscopy.

2 n in a "D6 barrel" cage assembly measured by cryoelectron microscopy.

3 of a filamentous virus, bacteriophage fd, by cryoelectron microscopy.

4 hedral plant virus, was resolved to 8.5 A by cryoelectron microscopy.

5 esence of four gold clusters was verified by cryoelectron microscopy.

6 tre-LH1-PufX complexes have been analysed by cryoelectron microscopy.

7 e FKBP12.6-binding site mapped previously by cryoelectron microscopy.

8 imilar to the ribosome-bound RF2 observed by cryoelectron microscopy.

9 ed by either x-ray crystallographic study or cryoelectron microscopy.

10 receptor (PVR or CD155), were determined by cryoelectron microscopy.

11 sid protein and nucleic acid were studied by cryoelectron microscopy.

12 multicomponent death machine, deciphered by cryoelectron microscopy.

13 mmine cobalt (III) have been investigated by cryoelectron microscopy.

14 pase-8 tDED filament structure determined by cryoelectron microscopy.

15 using site-specific mutagenesis, followed by cryoelectron microscopy.

16 (KSHV) was visualized at 24-A resolution by cryoelectron microscopy.

17 heir identity as procapsids was confirmed by cryoelectron microscopy.

18 s and imaged in the frozen-hydrated state by cryoelectron microscopy.

19 density, and particle morphology by scanning cryoelectron microscopy.

20 n studied by means of three-dimensional (3D) cryoelectron microscopy.

21 D structure of bR from x-ray diffraction and cryoelectron microscopy.

22 thermophilus ribosome has been determined by cryoelectron microscopy.

23 homo-tetrameric structure has been solved by cryoelectron microscopy.

24 in high-resolution structural information by cryoelectron microscopy.

25 ight of structural data recently obtained by cryoelectron microscopy.

26 ay mass spectrometry, and negative stain and cryoelectron microscopy.

27 pected "fan blade" motifs when visualized by cryoelectron microscopy.

28 zed the structure of the furin precursor, by cryoelectron microscopy.

29 in the GR:Hsp70:Hsp90:Hop complex imaged by cryoelectron microscopy.

30 uited to two-dimensional class averages from cryoelectron microscopy.

31 and peripentonal triplexes as visualized by cryoelectron microscopy.

32 complexed with Fab fragments of CR4354 using cryoelectron microscopy.

33 cking gp17, gp50, or gp65 were determined by cryoelectron microscopy.

34 A cryoelectron microscopy 8.5 A resolution map of the 1,90

35 supports the results of a previous report of cryoelectron microscopy analysis.

36 By direct electron-counting cryoelectron microscopy and asymmetric reconstruction, w

37 Cryoelectron microscopy and biochemical analyses show th

38 In this study, cryoelectron microscopy and computer modeling provide ev

39 By using cryoelectron microscopy and correlation averaging, diffe

40 as been determined by using a combination of cryoelectron microscopy and fitting of the known structu

41 We also used cryoelectron microscopy and helical image analysis to de

42 xtending previous observations, we have used cryoelectron microscopy and helical image analysis to ge

43 Here, we use cryoelectron microscopy and helical image analysis to vi

44 Using the techniques of cryoelectron microscopy and helical image analysis we ha

45 ion of the stacked disk obtained by means of cryoelectron microscopy and helical image processing.

46 By using cryoelectron microscopy and helical image reconstruction

47 otide-dependent conformational changes using cryoelectron microscopy and image analysis.

48 Cryoelectron microscopy and image averaging of the compl

49 ional structure of isoform 3 was obtained by cryoelectron microscopy and image enhancement techniques

50 ructure of the mutant RNAP was determined by cryoelectron microscopy and image processing of frozen-h

51 We have used cryoelectron microscopy and image processing to study th

52 Cryoelectron microscopy and image reconstruction analysi

53 he particle structure was also determined by cryoelectron microscopy and image reconstruction methods

54 Transmission cryoelectron microscopy and image reconstruction of r-co

55 to 16 and 25 A resolution, respectively, by cryoelectron microscopy and image reconstruction techniq

56 In this study, we used cryoelectron microscopy and image reconstruction to show

57 We have used cryoelectron microscopy and image reconstruction to stud

58 The CRPV structure determined by cryoelectron microscopy and image reconstruction was sim

59 ) and visualized at 24-A resolution by using cryoelectron microscopy and image reconstruction.

60 eaved lambda2 were subjected to transmission cryoelectron microscopy and image reconstruction.

61 ave visualized its precursor, Prohead-II, by cryoelectron microscopy and modeled the conformational c

62 ganded) and CD4-induced (liganded) states by cryoelectron microscopy and molecular modeling.

63 Using cryoelectron microscopy and other biophysical and bioche

64 Cryoelectron microscopy and reconstruction localized the

65 nce microscopy, atomic force microscopy, and cryoelectron microscopy and review recent studies that u

66 Using ATP-stabilised p53, we have employed cryoelectron microscopy and single particle analysis to

67 ee-dimensional (3D) structure, determined by cryoelectron microscopy and single particle analysis to

68 nt with a dimeric subunit stoichiometry, and cryoelectron microscopy and single particle analysis wit

69 Cryoelectron microscopy and single-particle analysis rev

70 se complex at 12 A resolution as obtained by cryoelectron microscopy and single-particle image recons

71 Cryoelectron microscopy and single-particle image recons

72 We have used cryoelectron microscopy and three-dimensional (3D) recon

73 ufficient for structural characterization by cryoelectron microscopy and three-dimensional (3D) recon

74 We used cryoelectron microscopy and three-dimensional image anal

75 We have used cryoelectron microscopy and three-dimensional image reco

76 We have used cryoelectron microscopy and three-dimensional image reco

77 i 70S ribosome were visualized directly with cryoelectron microscopy and three-dimensional reconstruc

78 Cryoelectron microscopy and tomography analyses revealed

79 Cryoelectron microscopy and tomography have been applied

80 fixation, thus exemplifying the potential of cryoelectron microscopy and tomography to reveal structu

81 Cryoelectron microscopy and X-ray crystallography have r

82 RyR2 by green fluorescent protein insertion, cryoelectron microscopy, and single-particle image proce

83 We have used cryoelectron microscopy at approximately 11-A resolution

84 the Qbeta-MurA complex using single-particle cryoelectron microscopy, at 4.7-A, 3.3-A, and 6.1-A reso

85 A 7-A cryoelectron microscopy-based reconstruction of Sindbis

86 integrated structure-function approach using cryoelectron microscopy, biochemical kinetics, and force

87 t, as observed previously by single-particle cryoelectron microscopy, blocks 80S formation at a later

88 Cryoelectron microscopy can image pleomorphic structures

89 Crystallography and cryoelectron microscopy can reveal the structural relati

90 Cryoelectron microscopy (cryo-EM) analyses have shown th

91 NSP5 and RNA, we carried out single-particle cryoelectron microscopy (cryo-EM) analysis of NSP2 alone

92 tures derived from X-ray crystallography and cryoelectron microscopy (cryo-EM) for the 1095 strain of

93 gh-resolution structures into low-resolution cryoelectron microscopy (cryo-EM) maps is presented.

94 Here, we present cryoelectron microscopy (cryo-EM) maps of 80SCrPV-STOP e

95 tures and experimental electron density from cryoelectron microscopy (cryo-EM) measurements is then c

96 Here a subnanometer asymmetric cryoelectron microscopy (cryo-EM) reconstruction of a co

97 In this study, we present a cryoelectron microscopy (cryo-EM) reconstruction of the

98 In addition, cryoelectron microscopy (cryo-EM) reconstructions of vir

99 Cryoelectron microscopy (cryo-EM) single-particle analys

100 Here, we present the cryoelectron microscopy (cryo-EM) structure of a KCNQ1/c

101 Here, we use cryoelectron microscopy (cryo-EM) to determine the quate

102 Here, we used cryoelectron microscopy (cryo-EM) to visualize the inter

103 on, determined to subnanometer resolution by cryoelectron microscopy (cryo-EM), showed only four prot

104 Using cryoelectron microscopy (cryo-EM), we show that the bind

105 n microscopy (TEM), scanning TEM (STEM), and cryoelectron microscopy (cryo-EM).

106 in the ribosome-bound form against data from cryoelectron microscopy (cryo-EM).

107 termined at approximately 21-A resolution by cryoelectron microscopy (cryo-EM).

108 calculations, and electron scattering using cryoelectron microscopy (cryo-EM).

109 Cryoelectron microscopy (cryoEM) and single-particle ima

110 as determined to 13 A resolution by means of cryoelectron microscopy (cryoEM) and three-dimensional i

111 e have constructed a first-of-its-kind BSL-3 cryoelectron microscopy (cryoEM) containment facility.

112 Automatic modeling methods using cryoelectron microscopy (cryoEM) density maps as constra

113 The cryoelectron microscopy (cryoEM) image reconstruction of

114 d with ICAM-1Kilifi, have been determined by cryoelectron microscopy (cryoEM) image reconstruction to

115 rus was determined to a resolution of 6 A by cryoelectron microscopy (cryoEM) single-particle image r

116 empty wild-type particles were determined by cryoelectron microscopy (cryoEM) to 7.5-A and 11.3-A res

117 In this paper, we used cryoelectron microscopy (cryoEM) to visualize destabiliz

118 tate nuclear magnetic resonance (SSNMR), and cryoelectron microscopy (cryoEM), have enabled high-reso

119 Using gel electrophoresis and cryoelectron microscopy (cryoEM), the ability of the rec

120 osphatidylcholine vesicles, and imaged using cryoelectron microscopy (cryoEM).

121 ating restraints derived from 9-A resolution cryoelectron microscopy data, and from mutagenesis data

122 ons of, for example, structures derived from cryoelectron microscopy data.

123 The structure of CsgE fits well into the cryoelectron microscopy density map of the CsgG-CsgE com

124 ctures, our new atomic model can be fit into cryoelectron microscopy density maps of the motor attach

125 e of the E1 glycoprotein was fitted into the cryoelectron microscopy density, in part by using the kn

126 lization of these peptides as bulk labels in cryoelectron microscopy-derived difference maps.

127 Frank, and Richard Henderson for "developing cryoelectron microscopy for the high-resolution structur

128 Cryoelectron microscopy had shown that the tail is folde

129 Cryoelectron microscopy has recently identified the EB b

130 Recent advances in cryoelectron microscopy have accelerated structure-funct

131 ral studies with protein crystallography and cryoelectron microscopy have shed light on the residues

132 4 crystal structure into a three-dimensional cryoelectron microscopy image reconstruction of the viru

133 A 5-fold symmetric, 3D reconstruction using cryoelectron microscopy images has now shown that the qu

134 In addition, cryoelectron microscopy images of actomyosin VI show the

135 rid approach combining spin labeling EPR and cryoelectron microscopy imaging at 10A resolution reveal

136 rom rabbit skeletal muscle was determined by cryoelectron microscopy in combination with homology mod

137 Here, we used cryoelectron microscopy in conjunction with electron par

138 se in the E1 state to a new 6 A structure by cryoelectron microscopy in the E2 state.

139 Images obtained from cryoelectron microscopy indicate that R120G alphaB-cryst

140 Cryoelectron microscopy indicates large conformational c

141 New results obtained by cryoelectron microscopy, interpreted in the light of x-r

142 of biochemistry, single-molecule assays, and cryoelectron microscopy-led to the surprising discovery

143 f component proteins into an 11-A resolution cryoelectron microscopy map.

144 Our cryoelectron microscopy maps of Hsp104 hexamers reveal s

145 Here, we present subnanometer resolution cryoelectron microscopy maps of the mammalian 80S riboso

146 We have significantly revised the recent cryoelectron microscopy models for proteins IIIa and IX

147 Recent results obtained by cryoelectron microscopy of "naked" ribosomes and ribosom

148 Cryoelectron microscopy of 2D crystals yielded a project

149 Cryoelectron microscopy of AQP1 previously revealed the

150 Cryoelectron microscopy of capsids, now attaining resolu

151 Cryoelectron microscopy of cardiolipin-liposomes reveale

152 Cryoelectron microscopy of chicken granulocyte chromatin

153 Now, using cryoelectron microscopy of frozen hydrated reconstituted

154 Recently, cryoelectron microscopy of isolated macromolecular compl

155 Cryoelectron microscopy of LDL quick-frozen from 10 (cor

156 Cryoelectron microscopy of purified RyR2s showed structu

157 Cryoelectron microscopy of reconstituted AQP1 membrane c

158 Cryoelectron microscopy of RyR2 so prepared yielded imag

159 s responsible for receptor recognition using cryoelectron microscopy of the SVV-ANTXR1-Fc complex.

160 Cryoelectron microscopy of triglyceride-rich LDL prepare

161 rom co-crystals of PLB with Ca(2+)-ATPase by cryoelectron microscopy of tubular co-crystals at 8--10

162 died the structural effects of TG binding by cryoelectron microscopy of tubular crystals, which have

163 al properties of this phosphoenzyme, we used cryoelectron microscopy of two-dimensional crystals form

164 Using cryoelectron microscopy of vitreous sections, we investi

165 Using cryoelectron microscopy on ribosomes with a P-loop mutat

166 and lengths of helices from crystallography, cryoelectron microscopy, or in vivo crosslinking and che

167 er vesicles, and its direct visualization by cryoelectron microscopy pave the way for more detailed s

168 been explored with X-ray crystallography and cryoelectron microscopy procedures.

169 cture of RNA polymerase-Spt4/5 complex using cryoelectron microscopy reconstruction and single partic

170 es remarkably similar to those observed in a cryoelectron microscopy reconstruction image of a human

171 Here, we report cryoelectron microscopy reconstruction of a functional C

172 rmined to 2.2-A resolution and fitted into a cryoelectron microscopy reconstruction of a rhinovirus-I

173 A cryoelectron microscopy reconstruction of a variant of C

174 omology model of T4 Soc were fitted into the cryoelectron microscopy reconstruction of the T4 capsid.

175 pili, the F and pED208 pili, generated from cryoelectron microscopy reconstructions at 5.0 and 3.6 A

176 Here we present cryoelectron microscopy reconstructions of bacterial RNA

177 Cryoelectron microscopy reconstructions of free and DNA-

178 his study, we report subnanometer resolution cryoelectron microscopy reconstructions of microtubule-b

179 ng molecular homology modeling for Tob55 and cryoelectron microscopy reconstructions of the TOB compl

180 d fitted into approximately 8.5-A resolution cryoelectron microscopy reconstructions of the virus-rec

181 Statistical analysis of rings imaged by cryoelectron microscopy revealed 16-fold symmetry, corre

182 cursor were not affected by these mutations, cryoelectron microscopy revealed a loss of virion matura

183 Cryoelectron microscopy revealed structured termini not

184 Immunofluorescence and cryoelectron microscopy revealed that PNT1 localizes to

185 High-resolution cryoelectron microscopy revealed the protofilament bound

186 nance spectroscopy, X-ray fiber diffraction, cryoelectron microscopy, scanning transmission electron

187 Cryoelectron microscopy showed that UNC-60B changed the

188 Cryoelectron microscopy shows that the protein occupies

189 We used cryoelectron microscopy single-particle analysis to obta

190 The cryoelectron microscopy structure of ASC(PYD) filament a

191 Here, we present a cryoelectron microscopy structure of the complete 1.4-me

192 Presented here are the cryoelectron microscopy structures of an MNV virion and

193 Modeling of Nas6 into cryoelectron microscopy structures of the proteasome sug

194 between VP19C and VP23 was inferred by yeast cryoelectron microscopy studies and subsequently confirm

195 Cryoelectron microscopy studies have identified distinct

196 Recent cryoelectron microscopy studies have revealed that herpe

197 Three-dimensional cryoelectron microscopy studies of Ag-Ab complexes revea

198 Previous cryoelectron microscopy studies of the mature DENV showe

199 esonance experiments on cysteine mutants and cryoelectron microscopy studies.

200 onsistent with the predictions of a previous cryoelectron microscopy study and strongly supports the

201 Here we show, using cryoelectron microscopy, that the structure of immature

202 d crystal structures of the P dimer into the cryoelectron microscopy three-dimensional (3D) image rec

203 Cryoelectron microscopy three-dimensional reconstruction

204 Using cryoelectron microscopy, three-dimensional image reconst

205 ructurally intact by both negative stain and cryoelectron microscopy, three-dimensional reconstructio

206 lated, ATP-bound conformation, determined by cryoelectron microscopy to 3.4 A resolution.

207 We have used cryoelectron microscopy to characterize interactions of

208 ate its role in membrane remodeling, we used cryoelectron microscopy to characterize structural chang

209 We used cryoelectron microscopy to derive 8-9 A-resolution maps

210 We used cryoelectron microscopy to determine a 13-A resolution s

211 Here, we used single particle cryoelectron microscopy to determine the quaternary arra

212 We have studied this interaction by using cryoelectron microscopy to determine the structure, at 2

213 We used cryoelectron microscopy to generate a 9-A resolution thr

214 Here, we have used cryoelectron microscopy to produce an 11-A density map o

215 ty of GTP-bound FtsZ protofilaments by using cryoelectron microscopy to sample their bending fluctuat

216 precursor could be isolated and analyzed by cryoelectron microscopy to yield a 3D structure at 22 A

217 We applied cryoelectron microscopy tomography to define ultrastruct

218 Cryoelectron microscopy was used to obtain a 3-D image a

219 onation, analytical ultracentrifugation, and cryoelectron microscopy, was found to increase systemati

220 Using cryoelectron microscopy we could localize golgin-84 to t

221 Using cryoelectron microscopy, we demonstrate that amelogenin

222 taining the alternative sigma(54) factor and cryoelectron microscopy, we determined structures of RPc

223 Using single-particle cryoelectron microscopy, we have determined the structur

224 Using cryoelectron microscopy, we present here a three-dimensi

225 Using cryoelectron microscopy, we show that although the virus

226 Utilizing small-angle X-ray scattering and cryoelectron microscopy, we underpin three crucial facto

227 anism of these transitions via time-resolved cryoelectron microscopy, whereas the predictions of prev

228 ructural data from x-ray crystallography and cryoelectron microscopy with functional measurements of

229 of these two molecules have been studied by cryoelectron microscopy, with helical crystals in the ca

230 y an integrative approach based on data from cryoelectron microscopy, X-ray crystallography, residue-