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1 ithout atomic coordinates such as those from cryo-electron microscopy.
2 and two RNAs and determined its structure by cryo-electron microscopy.
3 tionally reconstituted in lipids optimal for cryo-electron microscopy.
4 d on crystallography, x-ray diffraction, and cryo-electron microscopy.
5 e of mouse cGAS bound to human nucleosome by cryo-electron microscopy.
6  angstrom resolution using fiducial-assisted cryo-electron microscopy.
7 ) receptor, captured in an inactive state by cryo-electron microscopy.
8 eraction we structurally characterized using cryo-electron microscopy.
9 d form of the SARS-CoV-2 spike protein using cryo-electron microscopy.
10 of approximately 3.5 angstrom, determined by cryo-electron microscopy.
11 ex, poised for intramembrane proteolysis, by cryo-electron microscopy.
12 bscessus AftD, determined by single-particle cryo-electron microscopy.
13 e presence and absence of hepcidin solved by cryo-electron microscopy.
14 ng prophage AFP from Serratia entomophila by cryo-electron microscopy.
15 actors, nsp7 and nsp8, using single particle cryo-electron microscopy.
16 igami whose structure has been determined by cryo-electron microscopy.
17 tion with other experimental approaches like cryo-electron microscopy.
18 age structural changes using single-particle cryo-electron microscopy.
19 ttering, targeted protein cross-linking, and cryo-electron microscopy.
20 ture of Saccharomyces cerevisiae THO-Sub2 by cryo-electron microscopy.
21 r high-resolution structure determination by cryo-electron microscopy.
22 ucture of the C9orf72-SMCR8-WDR41 complex by cryo-electron microscopy.
23 y, for example with x-ray crystallography or cryo-electron microscopy.
24 structure, at 2.6-angstrom resolution, using cryo-electron microscopy.
25 romolecular crystallography, and recently in Cryo-electron microscopy.
26 S proteins have been studied in detail using cryo-electron microscopy(2,7,9-12), but the structure an
27         Recent advances have made cryogenic (cryo) electron microscopy a key technique to achieve nea
28                                              Cryo-electron microscopy allowed the construction of an
29                           Here we report the cryo-electron microscopy analysis of synaptic mini-filam
30 of the active Hrd1 complex, as determined by cryo-electron microscopy analysis of two subcomplexes.
31  structure and properties of ferritins using cryo-electron microscopy and a range of functional analy
32 l nanoparticles, which were characterized by cryo-electron microscopy and assessed for their ability
33                                        Using cryo-electron microscopy and binding assays, we show tha
34                                        Using cryo-electron microscopy and forcefield-based refinement
35                           Here, we have used cryo-electron microscopy and functional assays to addres
36                                 Here, we use cryo-electron microscopy and functional studies to inves
37  AAV isolate complexed with antibodies using cryo-electron microscopy and harness this structural inf
38  clinical vectors at atomic resolution using cryo-electron microscopy and image reconstruction for co
39 ngstrom and 2.9 angstrom, respectively, with cryo-electron microscopy and image reconstruction method
40                                 Here, we use cryo-electron microscopy and mass spectrometry to show t
41                                        Using cryo-electron microscopy and molecular characterization,
42                              Here we present cryo-electron microscopy and single-molecule characteriz
43 o receptor structures recently determined by cryo-electron microscopy and site-directed mutagenesis a
44 AVrh.10 and AAVrh.39 have been determined by cryo-electron microscopy and three-dimensional image rec
45                                              Cryo-electron microscopy and three-dimensional image rec
46 gh-resolution cellular ultra-structures from cryo-electron microscopy and tomography (cryoEM/ET).
47                              Here we applied cryo-electron microscopy and tomography to image intact
48                 In this study, we determined cryo-electron microscopy and x-ray crystal structures of
49 orylated Ric-8A at near atomic resolution by cryo-electron microscopy and X-ray crystallography.
50                       X-ray crystallography, cryo-electron microscopy, and hydrogen-deuterium exchang
51 ds including macromolecular crystallography, cryo-electron microscopy, and integrative methods.
52 se a combined quantitative mass spectrometry/cryo-electron microscopy approach to detail the protein
53 Here, we use correlative FIB-SEM, light- and cryo-electron microscopy approaches to elucidate the str
54                                  Advances in cryo-electron microscopy are enabling increasingly elabo
55 e describe the structure of ENaC resolved by cryo-electron microscopy at 3 angstrom.
56 ructure of the GCGR-G(s) complex by means of cryo-electron microscopy at 3.1-angstrom resolution.
57 FIIH core complex, determined by phase-plate cryo-electron microscopy at 3.7 angstrom resolution.
58 e-bound O-acyltransferase (MBOAT) family, by cryo-electron microscopy at approximately 3.0 angstrom r
59                    Here, we demonstrate that cryo-electron microscopy can routinely resolve maps of R
60 endent changes in morphology, as observed by cryo-electron microscopy (cEM).
61 ver, only recently, due to the revolution in cryo-electron microscopy, could pseudoatomic structures
62                                              Cryo electron microscopy (cryo-EM), a key method for str
63                                        Using cryo-electron microscopy (cryo-EM) and biochemical appro
64 logical improvements in both single particle cryo-electron microscopy (cryo-EM) and hydrogen/deuteriu
65 he WHV capsid to 4.5- angstrom resolution by cryo-electron microscopy (cryo-EM) and of the WHV Cp dim
66 ere, we apply methods for analyzing filament cryo-electron microscopy (cryo-EM) data at the single su
67 s are sparse, this information is present in cryo-electron microscopy (cryo-EM) density maps and it h
68         We present an approach for preparing cryo-electron microscopy (cryo-EM) grids to study short-
69                                              Cryo-electron microscopy (cryo-EM) has become a leading
70                                              Cryo-electron microscopy (cryo-EM) has become an indispe
71 n and symmetry relaxation methods to process cryo-electron microscopy (cryo-EM) images of HSV-1 virio
72                                              Cryo-electron microscopy (cryo-EM) images show that new
73                        The rapid progress of cryo-electron microscopy (cryo-EM) in structural biology
74                                              Cryo-electron microscopy (Cryo-EM) is widely used in the
75                           Here, we present a cryo-electron microscopy (cryo-EM) reconstruction of a h
76 f the simulation results with the results of cryo-electron microscopy (cryo-EM) reconstruction of mul
77 econstruction of macromolecular structure by cryo-electron microscopy (cryo-EM) relies on accurate de
78 crographs of frozen hydrated biomolecules by cryo-electron microscopy (cryo-EM) represents a major pr
79                                              Cryo-electron microscopy (cryo-EM) revealed that one nan
80                                              Cryo-electron microscopy (cryo-EM) showed that the desig
81 alytically from experimental single-particle cryo-electron microscopy (cryo-EM) snapshots of ryanodin
82 smolality in Arabidopsis Here, we report the cryo-electron microscopy (cryo-EM) structure and functio
83                     Moreover, a 3.4 angstrom cryo-electron microscopy (cryo-EM) structure of a neutra
84                  We therefore determined the cryo-electron microscopy (cryo-EM) structure of alpha-sy
85             Reported here is a 3.8- angstrom cryo-electron microscopy (cryo-EM) structure of CDT, a b
86                          Here, we report the cryo-electron microscopy (cryo-EM) structure of Homo sap
87                           Here, we present a cryo-electron microscopy (cryo-EM) structure of the Esch
88             Based on a recent low-resolution cryo-electron microscopy (cryo-EM) structure of this lar
89                              Here, we report cryo-electron microscopy (cryo-EM) structures of an inta
90 ved shell, we determined the high-resolution cryo-electron microscopy (cryo-EM) structures of cucumbe
91                              Here, we report cryo-electron microscopy (cryo-EM) structures of DNA-bou
92                              Here we present cryo-electron microscopy (cryo-EM) structures of human p
93                               Here we report cryo-electron microscopy (cryo-EM) structures of the nuc
94  2015 and highlight multiple high-resolution cryo-electron microscopy (cryo-EM) structures of the pol
95                             Here, we present cryo-electron microscopy (cryo-EM) structures of transla
96                                 Here, we use cryo-electron microscopy (cryo-EM) to characterize J-C b
97                                 Here, we use cryo-electron microscopy (cryo-EM) to determine the stru
98            The dramatic growth in the use of cryo-electron microscopy (cryo-EM) to generate high-reso
99 ilized molecular genetics, biochemistry, and cryo-electron microscopy (cryo-EM) to investigate the fu
100                                 We have used cryo-electron microscopy (cryo-EM) to solve the atomic s
101                    Here, we use genetics and cryo-electron microscopy (cryo-EM) to study the high-res
102 mic resolution are now routinely reported by cryo-electron microscopy (cryo-EM), many density maps ar
103                                        Using cryo-electron microscopy (cryo-EM), we determined the st
104                                        Using cryo-electron microscopy (cryo-EM), we determined the st
105 l-angle x-ray scattering and single-particle cryo-electron microscopy (cryo-EM), we present evidence
106                        Using single particle cryo-electron microscopy (cryo-EM), we report reconstruc
107  CALHM1 and human CALHM2, by single-particle cryo-electron microscopy (cryo-EM), which show novel ass
108                   Data from a combination of cryo-electron microscopy (cryo-EM), x-ray crystallograph
109 nction, and determined their structure using cryo-electron microscopy (cryo-EM).
110 techniques such as x-ray crystallography and cryo-electron microscopy (cryo-EM).
111 esensitized conformations by single-particle cryo-electron microscopy (cryo-EM).
112 nsity map with 2.62 angstrom resolution from cryo-electron microscopy (cryo-EM).
113 ec71-Sec72) from Saccharomyces cerevisiae by cryo-electron microscopy (cryo-EM).
114 tact virions prompted structural analysis by cryo-electron microscopy (cryo-EM).
115 mics approach whereby near-atomic-resolution cryo electron microscopy (cryoEM) maps are reconstructed
116                                              Cryo-electron microscopy (cryoEM) is becoming the prefer
117                             Here we report a cryo-electron microscopy (cryoEM) structure of PDE6 comp
118                          Here we present the cryo-electron microscopy (cryoEM) structure of the hnRNP
119                          Our high-resolution cryo-electron microscopy (cryoEM) studies of B41 in comp
120                                  Here, using cryo-electron microscopy (cryoEM), we analyzed the size
121             Combining structural analyses of cryo-electron microscopy data with molecular dynamic sim
122 ction has advanced greatly, particularly via cryo-electron microscopy data.
123 gle X-ray and neutron scattering, as well as cryo-electron microscopy, demonstrate that these assembl
124                                          Per cryo-electron microscopy, each troponin is highly extend
125                              Here we present cryo-electron microscopy (EM) data resolving the EC1 and
126 even quite impure samples in single-particle cryo-electron microscopy (EM).
127                                 By employing cryo-electron microscopy for the first time to study spe
128 ce imaging at sub-nanometre resolution using cryo-electron microscopy has provided key insights into
129                                  Advances in cryo-electron microscopy have enabled high-resolution st
130                    X-ray crystallography and cryo-electron microscopy have revealed features not prev
131  structure data from electron tomography and cryo-electron microscopy, here we map and classify three
132 by X-ray crystallography and single-particle cryo-electron microscopy in distinct conformational stat
133                                     Further, cryo-electron microscopy in the presence of Ca(2+) revea
134                                              Cryo-electron microscopy is a popular method for the det
135                                              Cryo-electron microscopy is an essential tool for high-r
136                                          Our cryo electron microscopy map reveals structural transiti
137                            The 3.6- angstrom cryo-electron microscopy map of the heterotrimer assembl
138                                Moreover, the cryo-electron microscopy map reveals that the C-edge of
139                                          The cryo-electron microscopy maps enabled de novo modelling
140                                  We combined cryo-electron microscopy, molecular dynamics, and bioche
141                      Cysteine-cross-linking, cryo-electron microscopy multivariate analysis and molec
142 e determination by X-ray crystallography and cryo-electron microscopy not only confirms that IrtAB ha
143                                 Furthermore, cryo-electron microscopy of PUUV-like particles in the p
144       Structural analysis by single-particle cryo-electron microscopy performed on the BG505 SOSIP mu
145 to an overall resolution of 3.4 angstroms by cryo-electron microscopy, permitting building of a nearl
146 ltransferase-deficient archaeal ribosomes by cryo-electron microscopy provided structural insights in
147 tal approaches such as fiber diffraction and cryo-electron microscopy reconstruction have defined reg
148                             Here we report a cryo-electron microscopy reconstruction that shows the r
149                                              Cryo-electron microscopy reconstructions of one antibody
150                                              Cryo-electron microscopy reconstructions of two highly n
151                             Here, we present cryo-electron microscopy reconstructions, native mass sp
152 lecular dynamics simulations based on recent cryo-electron microscopy reconstructions, we studied the
153  the Vibrio cholerae Tn6677 transposon using cryo-electron microscopy, revealing the mechanistic basi
154 complex with a monoclonal antibody (mAb5) by cryo-electron microscopy, revealing the tertiary and qua
155                                              Cryo-electron microscopy reveals a large assembly at the
156                                              Cryo-electron microscopy reveals how ubiquitination prom
157                     We used a combination of cryo-electron microscopy, ribosome profiling, and mRNA s
158        Assessment of the S protein trimer by cryo-electron microscopy showed that D614G disrupts an i
159 irus-like particles (VLPs), determined using cryo-electron microscopy, showed similarities to rodent
160             Here we show through a series of cryo-electron microscopy single particle reconstructions
161 on between heparin and the PCV2 capsid using cryo-electron microscopy single-particle analysis, symme
162                 By contrast, single-particle cryo-electron microscopy (SP-cryo-EM) routinely reaches
163          Here we present the high-resolution cryo electron microscopy structure of the GFLV-Nb23 comp
164 ion factor-nucleosome interaction to empower cryo-electron microscopy structure determination of the
165                           Here we report the cryo-electron microscopy structure of a chemically trapp
166             Here we present the 3.3-angstrom cryo-electron microscopy structure of a human postcataly
167                           Here we report the cryo-electron microscopy structure of a membrane-embedde
168            Here, we present the 2.8 angstrom cryo-electron microscopy structure of a Mycobacterium sm
169                          Here we present the cryo-electron microscopy structure of a ternary complex
170                               A 3.5 angstrom cryo-electron microscopy structure of Ab1485 in complex
171 Es), we determined a 3.2-angstrom resolution cryo-electron microscopy structure of ABE8e in a substra
172                                     A second cryo-electron microscopy structure of ALG6 bound to an a
173                         Here, we present the cryo-electron microscopy structure of an export gate con
174                            Here we present a cryo-electron microscopy structure of beta-arrestin 1 (b
175          We report a 3.3-angstrom-resolution cryo-electron microscopy structure of cGAS in complex wi
176        Here, we determined a single-particle cryo-electron microscopy structure of Crl-sigma(S)-RNAP
177                             Here we show the cryo-electron microscopy structure of Etx pore assembled
178                             Here we report a cryo-electron microscopy structure of full-length human
179                                            A cryo-electron microscopy structure of HexaPro at a resol
180                          Here we present the cryo-electron microscopy structure of human ACAT1 as a d
181                             Here we report a cryo-electron microscopy structure of human ACAT1 in com
182             Here, we report the 3.0-angstrom cryo-electron microscopy structure of human CST bound to
183                          Here we present the cryo-electron microscopy structure of human DGAT1 in com
184                          Here we present the cryo-electron microscopy structure of human TBK1 in comp
185                             Here we report a cryo-electron microscopy structure of human VIP1R bound
186 in-swapped K(v) channels on the basis of the cryo-electron microscopy structure of KAT1, the hyperpol
187  the 3.3 angstrom resolution single-particle cryo-electron microscopy structure of Mycobacterium smeg
188                                          Our cryo-electron microscopy structure of RagA/RagC in compl
189                                We report the cryo-electron microscopy structure of rat VGLUT2 at 3.8-
190                           Here we report the cryo-electron microscopy structure of Saccharomyces cere
191                          Here we present the cryo-electron microscopy structure of SAGA from the yeas
192                            Our 2.85-angstrom cryo-electron microscopy structure of SARS-CoV-2 spike (
193                             Here we report a cryo-electron microscopy structure of shutdown smooth mu
194                                          The cryo-electron microscopy structure of SidJ in complex wi
195                                            A cryo-electron microscopy structure of the 16-helix trans
196 ent, we determined a 3.5-angstrom-resolution cryo-electron microscopy structure of the 2019-nCoV S tr
197 Here we describe the 3.8-angstrom-resolution cryo-electron microscopy structure of the activated ROQ1
198 have determined the 3.2- angstrom resolution cryo-electron microscopy structure of the ATPgammaS-boun
199 or arrestin coupling, here we determined the cryo-electron microscopy structure of the beta(1)AR-beta
200  Here we report the first, to our knowledge, cryo-electron microscopy structure of the eukaryotic EMC
201                        Here, we describe the cryo-electron microscopy structure of the F-actin-bound
202                         Here, we provide the cryo-electron microscopy structure of the full-length Wz
203                          Here we report a 3D cryo-electron microscopy structure of the human 17S U2 s
204                                       In the cryo-electron microscopy structure of the human cGAS-nuc
205             Here, we present a 3.3- angstrom cryo-electron microscopy structure of the human chemokin
206                          Here, we report the cryo-electron microscopy structure of the human THO-UAP5
207                             Here we report a cryo-electron microscopy structure of the monoubiquitina
208                          Here, we report the cryo-electron microscopy structure of the PEDV S protein
209                         Here, we present the cryo-electron microscopy structure of the ribosome from
210      We report here a 4- angstrom-resolution cryo-electron microscopy structure of the ZIKV virion in
211  the 3.9 angstrom resolution single-particle cryo-electron microscopy structure of their complex and
212                          Here we present the cryo-electron microscopy structure of yeast ALG6 at 3.0
213                                        Using cryo-electron microscopy, structure-guided mutagenesis,
214                       We also report related cryo-electron microscopy structures (3.7 to 4.4 angstrom
215                          Here, we report two cryo-electron microscopy structures derived from a prepa
216       Here we present near-atomic-resolution cryo-electron microscopy structures for feline calicivir
217       Here we report several high-resolution cryo-electron microscopy structures in which the full-le
218                                              Cryo-electron microscopy structures of a +3 extended RTI
219                             Here, we present cryo-electron microscopy structures of a MscS homolog fr
220               Here we report high-resolution cryo-electron microscopy structures of actin filaments w
221               Here, I report high-resolution cryo-electron microscopy structures of AMPAR in complex
222                               Here we report cryo-electron microscopy structures of both DNA-free and
223                                              Cryo-electron microscopy structures of both proteins bou
224                           Here we report the cryo-electron microscopy structures of Danio rerio TRPM2
225                                    We report cryo-electron microscopy structures of eIF2 bound to eIF
226                              Here, we report cryo-electron microscopy structures of Escherichia coli
227                           Here we report the cryo-electron microscopy structures of full-length SARM1
228                              Here we present cryo-electron microscopy structures of full-length STING
229                              Here we present cryo-electron microscopy structures of GABA(A) receptors
230                           Here we report the cryo-electron microscopy structures of GPBAR-G(s) comple
231                              Here we present cryo-electron microscopy structures of heterodimeric and
232             Here, we present high-resolution cryo-electron microscopy structures of HIV intasomes bou
233                   Here we report near-atomic cryo-electron microscopy structures of HsCKK- and NgCKK-
234                          Here, we report two cryo-electron microscopy structures of human CFTR in com
235                          Here we present two cryo-electron microscopy structures of human PAC in a hi
236                    Here we describe multiple cryo-electron microscopy structures of human TRPV3 recon
237                               Here we report cryo-electron microscopy structures of influenza C virus
238             Here, we present and compare the cryo-electron microscopy structures of M1R in complex wi
239                          Here, we report the cryo-electron microscopy structures of murine SIgA and d
240             Here, we present single-particle cryo-electron microscopy structures of Mus musculus LRRC
241                              Here we present cryo-electron microscopy structures of Mus musculus TASK
242                            Here we solve the cryo-electron microscopy structures of NSD2 and NSD3 bou
243                           Here we report the cryo-electron microscopy structures of purified VZV A-ca
244                      Here we present in situ cryo-electron microscopy structures of rotavirus dsRNA-d
245                                              Cryo-electron microscopy structures of Saccharomyces cer
246                         Here, beginning with cryo-electron microscopy structures of the amphioxus Pro
247                               Here we report cryo-electron microscopy structures of the DNA-binding d
248                                          The cryo-electron microscopy structures of the EV71 virion i
249                         Here we present four cryo-electron microscopy structures of the human full-le
250                           We report here the cryo-electron microscopy structures of the ribosome of a
251                       Here, we report on the cryo-electron microscopy structures of the RNAP, RNAP-TF
252 including new information provided by recent cryo-electron microscopy structures of the spliceosomal
253                                              Cryo-electron microscopy structures of these minibinders
254 ere we report one crystal structure and five cryo-electron microscopy structures of Transib(4,5), a R
255                    We determined a series of cryo-electron microscopy structures portraying the hexam
256                                              Cryo-electron microscopy structures reveal the opening o
257                                              Cryo-electron microscopy structures show that S2E12 and
258  of channel activity has been illuminated by cryo-electron microscopy structures that reveal the atom
259  pH affect spike conformation, we determined cryo-electron microscopy structures-at serological and e
260                                        Using cryo-electron microscopy, structures for the p53 monomer
261                              Single-particle cryo-electron microscopy studies confirmed that B41- and
262 dels of MT assembly is suggested by a recent cryo-electron microscopy study of microtubules (MTs).
263                            Here we present a cryo-electron microscopy study of the protozoans Leishma
264 ctures of human and frog PANX1 determined by cryo-electron microscopy that revealed a heptameric chan
265 rt the structure of this complex by means of cryo-electron microscopy to 3.6-angstrom resolution, all
266 i cytochrome bd-I oxidase by single-particle cryo-electron microscopy to a resolution of 2.7 angstrom
267                                  Here we use cryo-electron microscopy to analyse the structures of ta
268 better understand how CDT functions, we used cryo-electron microscopy to define the structure of CDTb
269  understand the mechanisms involved, we used cryo-electron microscopy to determine the structure of a
270 se X-ray crystallography and single-particle cryo-electron microscopy to determine the structure of t
271                                      We used cryo-electron microscopy to determine the structures of
272                                 Here we used cryo-electron microscopy to elucidate the structure of a
273                                  Here we use cryo-electron microscopy to identify the molecular gatin
274                                 Here, we use cryo-electron microscopy to obtain structures of Escheri
275                              Here, we employ cryo-electron microscopy to reveal how FAK associates wi
276                                       We use cryo-electron microscopy to reveal how the solvent-expos
277                                  Here we use cryo-electron microscopy to reveal the structure of KBP
278              In this study, we used cellular cryo-electron microscopy to visualize a molecular pore c
279                                 Here, we use cryo-electron microscopy to visualize the HTLV-1 intasom
280                      We used single-particle cryo-electron microscopy to visualize the mode of action
281  outcomes are in good agreement with current cryo-electron microscopy topology and consistent with lo
282  time-resolved sample preparation method for cryo-electron microscopy (trEM) using a modular microflu
283 form helical filaments, which we analyzed by cryo-electron microscopy using helical reconstruction.
284                                        Using cryo-electron microscopy we show that antibody binding r
285                                        Using cryo-electron microscopy, we determine the structures of
286 m of RAG1 with methionine at residue 848 and cryo-electron microscopy, we determined structures that
287                                        Using cryo-electron microscopy, we determined the atomic organ
288                                        Using cryo-electron microscopy, we determined the structures o
289             Using biochemical approaches and cryo-electron microscopy, we have determined how three c
290                                  Here, using cryo-electron microscopy, we show that alpha-synuclein i
291                                        Using cryo-electron microscopy, we show that human LIS1 binds
292 d solid-state nuclear magnetic resonance and cryo-electron microscopy, we show that thiol groups of c
293                        Using single particle cryo-electron microscopy, we solved the structure of Pf2
294 with one of these inhibitors (NDI-091143) by cryo-electron microscopy, which reveals an unexpected me
295                          Users familiar with cryo-electron microscopy who get basic training in dual-
296                                              Cryo-electron microscopy with a two-domain receptor frag
297                                        Using cryo-electron microscopy with electron energy loss spect
298                                      We used cryo-electron microscopy with single-particle analysis,
299 the structure of smooth muscle 10S myosin by cryo-electron microscopy with sufficient resolution to e
300 uilding on the static structures found using cryo-electron microscopy, x-ray crystallography, and oth

 
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