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1 steric changes in AMA1 that are not observed crystallographically.
2 e., H(2)O.4H(2)O or F(-).4H(2)O, as observed crystallographically.
3  precursors, and elucidated germline binding crystallographically.
4 examined kinetically, spectroscopically, and crystallographically.
5 chieve final poses matching those determined crystallographically.
6 y the "inactive-like" configuration observed crystallographically.
7 n treatment with CO(2) and was characterized crystallographically.
8 P2 in complex with Rab11 that was determined crystallographically.
9 be followed optically, spectroscopically and crystallographically.
10 ey are disordered and therefore undetectable crystallographically.
11 BF4 were characterized spectroscopically and crystallographically.
12 nyl analogue of which has been characterized crystallographically.
13 ogically and on protein structure determined crystallographically.
14  2*bipy, and 2*tmeda have been characterized crystallographically.
15 o the 3-phosphoglycerate molecule identified crystallographically.
16 2C2H4)(mu-CO)(CN)2(PPh3)2(CO)2, as confirmed crystallographically.
17 nt with the pentamer-of-dimers assembly seen crystallographically.
18 some of the higher-order assemblies observed crystallographically.
19 ational fluctuations that have been observed crystallographically.
20 nions in [Cs(C21 H11(-) )2 ](-) was revealed crystallographically.
21 ary reactants and subsequently characterized crystallographically.
22 haracterized this virus-receptor interaction crystallographically.
23 ate NMR and biochemical techniques but never crystallographically.
24 h symmetry of the His6 binding site observed crystallographically.
25 e unpaired base of the DNA template observed crystallographically (-11C) could also be removed withou
26 Br(2) allowed us to isolate and characterize crystallographically a very unusual mononuclear, paramag
27                      The nanocrystals became crystallographically aligned early in the overall self-a
28 of dislocations through the interiors of the crystallographically aligned grains.
29 is minimized by the use of relatively large, crystallographically aligned grains.
30 tals are composed of spatially separated and crystallographically aligned nanocrystals.
31                              We characterize crystallographically an early intermediate along the rea
32  of two stereoisomers, the one characterized crystallographically and a contribution of about 10% fro
33 e, the SSB-binding site on chi is identified crystallographically and biochemical and cellular studie
34 ne (Y215F, Y215H) were analyzed kinetically, crystallographically and by molecular dynamics simulatio
35 ap clusters appear at the interfaces between crystallographically and compositionally distinct entiti
36                One of these is characterized crystallographically and contains a C4 ligand oxygen bou
37 is also square-planar, and was characterized crystallographically and has tau4=0.13.
38                                 Here we show crystallographically and in solution that the ATP-depend
39 his process can be traced in the solid state crystallographically and in solution using dynamic light
40 cular and metallic characteristics, explored crystallographically and optically and modeled theoretic
41 ed of highly crystalline hydroxyapatite that crystallographically and structurally differs from bone
42 erichia coli, has been structurally resolved crystallographically and subjected to intensive mutagene
43     These results corroborate those obtained crystallographically and, importantly, provide structura
44 a5-C5H5)Br2(R,R-phospholane)] (characterized crystallographically) and [Rh(eta5-C5H5)(H)2(R,R-phospho
45           These compounds were characterized crystallographically, and also by NMR, EPR, electrochemi
46 was confirmed spectroscopically, chemically, crystallographically, and analytically.
47 iolato hydride, [3H]BF(4), was characterized crystallographically: as anticipated by biophysical stud
48 ominally disordered inverse structure orders crystallographically at low T, and (ii) at finite temper
49 We present results of the restoration of all crystallographically available intra- and extracellular
50 However, few of them have been characterized crystallographically, because they are either too reacti
51      Although neither THF nor Ph(3)PO formed crystallographically characterizable (C(5)Me(5))(3)LaL(x
52                                    The first crystallographically characterizable complex of Sc(2+) ,
53                        The first examples of crystallographically characterizable complexes of Tb(2+)
54 ghly reactive due to steric crowding and few crystallographically characterizable Th(3+) complexes ar
55  KC(8) or Li in THF forms a new example of a crystallographically characterizable Th(III) complex in
56 trate analogue, we were now able to trap and crystallographically characterize various stages in the
57 Addition of Me(3)CCN to 1 produced the first crystallographically characterized (C(5)Me(5))(3)ML(2) c
58  (mu-H) and the proton of the (mu-NH) of the crystallographically characterized 3 show the proposed s
59                                         This crystallographically characterized 6-isocyano-2-formamid
60                       In particular, we have crystallographically characterized a diamagnetic arylnic
61  via the primary amine moiety, affording the crystallographically characterized adduct [(L1)Pd(p-toly
62 ver complexes 3a and 3b are rare examples of crystallographically characterized Ag(I) cyclopentadieny
63                                            A crystallographically characterized analog (Et4N)2[Co(L)C
64 obalt catalyst, 6-(H)2BPin, was prepared and crystallographically characterized and proved inactive f
65                       The two compounds were crystallographically characterized and studied by absorp
66 dral Zintl ion [Fe@Ge(10)](3-) (1) which was crystallographically characterized as a [K(2,2,2-crypt)]
67 he unusual catalytic CODH C-cluster has been crystallographically characterized as either a NiFe(4)S(
68 ) (4) ] (MAA=methyl 2-acetamidoacrylate) was crystallographically characterized as the opposite diast
69 whose individual catalytic domains have been crystallographically characterized at high resolution.
70 ded contact distance is the shortest for any crystallographically characterized compound.
71 nt study probes this issue by examining four crystallographically characterized Cu/aminoxyl halide co
72 nds are significantly shorter than any other crystallographically characterized d-f-block bimetallic,
73 vity of 2 with that of a more electron-rich, crystallographically characterized derivative, [Fe(III)S
74     Compounds 1-3 represent a rare series of crystallographically characterized diphosphenes bearing
75 or-arrested inclusion complexes, including a crystallographically characterized encapsulated Au(III)
76                          We report the first crystallographically characterized examples of molecular
77 wn to reductively trimerize CO to yield rare crystallographically characterized examples of the plana
78 y scattering (SAXS) and compared to existing crystallographically characterized Fe protein conformati
79                                              Crystallographically characterized GADIPY displays inten
80 the [Au18(SC6H11)14] cluster is the smallest crystallographically characterized gold cluster protecte
81 ond" cores, including the first example of a crystallographically characterized heterobimetallic bis(
82         Compound 2 is the first example of a crystallographically characterized hydride complex in wh
83 (CH(2)CH(CH(2))(2))](2-), respectively, were crystallographically characterized in compounds with [K-
84            These results represent the first crystallographically characterized magnesium and zinc ca
85                            A series of seven crystallographically characterized Mn monomers and dimer
86 (2)NBn](CO)(4)(dppn)](+) ([2](+)), the first crystallographically characterized model for the H(ox) s
87    This is a rare example of an isolable and crystallographically characterized phenoxyl radical and
88 ly nonplanar solid-state structures of three crystallographically characterized PMPs containing an ei
89                     Here we report the first crystallographically characterized porphyrin-binding pro
90 m addition of a suitable amine-borane to the crystallographically characterized precursor [Rh(eta(6)-
91 n structures previously observed for over 40 crystallographically characterized rare-earth metal (N h
92                       Isolation of the first crystallographically characterized REMB complex with sub
93 rylamine) "bipolarons": we have isolated and crystallographically characterized salts of the dication
94                           We report herein a crystallographically characterized synthetic Cu(II)2(mu-
95 (DO2A)(DPA)(-) complex solutions (1.0 microM crystallographically characterized TBA x Eu(DO2A)(DPA))
96 (BF(4))(2) represents the first example of a crystallographically characterized terminal hydride prod
97                                            A crystallographically characterized three-coordinate, for
98 xplains why SznF was previously purified and crystallographically characterized without its cofactor.
99 ilized methylidenes candium complex has been crystallographically characterized, and its bonding sche
100 enium oxyanion complexes have been prepared, crystallographically characterized, and screened for the
101      Both Ge(TPP) and Ge(TPP)(py)2 have been crystallographically characterized, and the antiaromatic
102                           Both products were crystallographically characterized, and the latter react
103         The series of zinc alkylperoxides is crystallographically characterized, and the structures s
104 ds along the cyclic pathway are isolated and crystallographically characterized, and their reactivity
105 conocene sandwich yields a rare example of a crystallographically characterized, base-free eta5,eta5-
106                 The AgOTf complex, which was crystallographically characterized, exhibits a structure
107 exes nor their fleeting precursors have been crystallographically characterized, hindering direct exp
108 s of the quinoline-annulated porphyrins were crystallographically characterized, proving their connec
109 etic complex 3 [Ni(Ph)(PN(P)N(H))], which is crystallographically characterized.
110 d Cu(II) complexes have been synthesized and crystallographically characterized.
111 hthylpurine derivative has been obtained and crystallographically characterized.
112 N]Mo(NB(C6F5)3) complexes (n = 1 and 3) were crystallographically characterized.
113 ity, several large PAHs were synthesized and crystallographically characterized.
114 duct [Fe(II)(N3PySO(2))(NCS)] (2), which was crystallographically characterized.
115 ranium vinyl complexes that are reported and crystallographically characterized.
116 ate and resulting Pd-alkyl species have been crystallographically characterized.
117                    All of these systems were crystallographically characterized.
118 NH(2)-BH(3))Cl(2)(thf)(3), 3, which has been crystallographically characterized.
119  of a carbon-carbon bond, is synthesized and crystallographically characterized.
120  were sufficiently stable to be isolated and crystallographically characterized.
121  zincate has also been spectroscopically and crystallographically characterized.
122 2))(P(i)Bu(3))(2)][BAr(F)(4)] have also been crystallographically characterized.
123 .NHMe(2))][BAr(F)(4)], has been isolated and crystallographically characterized.
124 gen compounds were isolated and in one case, crystallographically characterized.
125 ) that have been isolated in good yields and crystallographically characterized.
126  which was isolated as the triflate salt and crystallographically characterized.
127 nd {K(18-crown-6)THF(2) }(+) counterions and crystallographically characterized.
128 nic species, and the latter was isolated and crystallographically characterized.
129 activated intermediate has been isolated and crystallographically characterized.
130 g products, which were spectroscopically and crystallographically characterized.
131 talloindene complexes have been isolated and crystallographically characterized.
132 es were also synthesized, and the latter was crystallographically characterized.
133  the monomeric (IPr**)AgH complex, which was crystallographically characterized.
134 salts, which have been spectroscopically and crystallographically characterized.
135 )] and Cs3[U(III---)-N-(---U(III)] have been crystallographically characterized.
136 lPhos, L2) was prepared in 63% yield and was crystallographically characterized; the [Pd(cinnamyl)Cl]
137 periodically layered zig-zag architecture of crystallographically co-oriented calcite lamellae.
138 del system that has been fully characterized crystallographically, computationally and kinetically.
139                          Pironetin, the only crystallographically confirmed natural product to target
140 space in the presence and absence of several crystallographically conserved and buried water molecule
141 mpetent to bind the inhibitor BIRB796 in the crystallographically correct position and with docked en
142  large external cleft, the cleft itself, the crystallographically defined binding pocket, and the gat
143 ecular dynamics study in which we analyzed a crystallographically defined complex that involves the H
144 d to define the electronic structures of two crystallographically defined Cu(II)-phenolate complexes.
145 cytochrome c peroxidase (rCcP), in which the crystallographically defined cytochrome c binding site i
146 le receptors active in cells verify that the crystallographically defined HAMP conformers are maintai
147                                          The crystallographically defined interface is shown to be co
148  protein designed to disrupt contacts in the crystallographically defined interface.
149 omote arrestin-2 oligomerization via the two crystallographically defined ligand-binding locations.
150  to directly calculate the EXAFS spectrum of crystallographically defined model complexes.
151 00000 compounds for predicted binding to the crystallographically defined nucleotide binding region o
152 ar perovskite structure evolves to construct crystallographically defined quantum wells (QWs).
153 relaxation measurements, we demonstrate that crystallographically defined superatomic solids assemble
154 imilar position in the bovine structure, the crystallographically defined, conserved steroid binding
155 is greatly enhanced by residues flanking the crystallographically-defined recognition motif, apparent
156 an that of DeltaGly-141, consistent with its crystallographically demonstrated more rigid loop.
157 ial diastereomers, lending strong support to crystallographically derived models of aminoglycoside-ri
158  Data Bank entries 1EHK and 1XME ), having a crystallographically detectable water between the Cu(B)
159                            We also show that crystallographically determined binding site locations r
160 forming a complex virtually identical to the crystallographically determined bound structure.
161 quality of these maps allowed us to build in crystallographically determined conformations of kinesin
162 esence of side-chain residues fixed at their crystallographically determined coordinates.
163 (30) (x approximately 60), 2, as the largest crystallographically determined discrete transition meta
164  a coarse-grained dynamics method comes to a crystallographically determined intermediate structure w
165 h a set of five proteins with at least three crystallographically determined on-pathway high-resoluti
166  to generate ligand conformations similar to crystallographically determined protein/ligand complex s
167       The release of one sodium ion from the crystallographically determined sodium binding site Na2
168 abilized Et(3)BNH(2)BH(3)(-) anion, with the crystallographically determined structure of the [Et(3)B
169                                    While the crystallographically determined structure of the enzyme
170 hiolate-protected Au nanoparticle that has a crystallographically determined structure.
171                               By fitting the crystallographically determined structures of these Fab
172  for {ES-NO}7 are in good agreement with the crystallographically determined substrate-bound active s
173                       In this study, we have crystallographically determined the 3D structure of the
174                                              Crystallographically determined, apparent dissociation c
175 e conformational-change pathways linking the crystallographically-determined effector-free and bound-
176 teracting with one or more Ge atoms in three crystallographically different molecules in the structur
177 tes that have identical hole density but are crystallographically different outside of the CuO(2) pla
178 -pair salt isolated as K(L(C))(+)//DNB(-) is crystallographically differentiated from the "contact" i
179 g the conformations of a mobile loop that is crystallographically disordered in both prior crystal st
180 ion of the primary sequence corresponds to a crystallographically disordered loop adjacent to the act
181                          These materials are crystallographically disordered on the atomic scale, but
182 ique information regarding the function of a crystallographically disordered segment of the loop near
183 ut that 214 residues, including the NTD, are crystallographically disordered.
184 compounds of the type [CuLCl](2), identified crystallographically, dissociate in solution to give mon
185 aces is linked to simultaneous growth of the crystallographically distinct (001) basal plane.
186 forms islands that are compact in shape with crystallographically distinct boundaries that have essen
187 phase to be Mn(19)Si(33), one of a series of crystallographically distinct higher manganese silicides
188                  The complex studied has two crystallographically distinct iron sites; one site has a
189 hese two polymorphs of NaNbO(3) contains two crystallographically distinct Na sites.
190  S = 1/2 kagome layer that exhibits only one crystallographically distinct Ti(3+), d(1) site, and one
191 g salts of [1]+, which were characterized by crystallographically, EPR, and elemental analyses.
192  absence of dynamics but the boron pairs are crystallographically equivalent or (2) the boron pairs a
193 tides form parallel-stranded duplexes with a crystallographically equivalent strand, resulting in the
194 tensive single amino acid mutagenesis within crystallographically established domains, manipulation o
195                          The total number of crystallographically estimated Pt atoms, 8 +/- 3, which
196 formations of EGFR kinase have been resolved crystallographically, experimental characterization of t
197 ahedral and icosahedral symmetry, exhibiting crystallographically forbidden five-fold symmetry elemen
198 ty due to the Sn(2+) s(2) lone pair causes a crystallographically hidden, locally distorted state to
199 l four unique iron(II) ions in the cages are crystallographically high-spin at 250 K, but they underg
200 environments, and the divalent metal site is crystallographically identified and has a Phpy ligand at
201 of phosphatidyl-4,5-bisphosphate (PIP2) at a crystallographically identified binding site, but an add
202                              On the basis of crystallographically identified cation-binding sites at
203 are consistent with one another and with the crystallographically identified contact residues.
204 ments between LeuT and vSGLT reveal that the crystallographically identified galactose-binding site i
205                             Mutations of the crystallographically identified metal-binding residues h
206 recluded correlation of EPR signals with the crystallographically identified monocopper and dicopper
207 t(2) )Li(OEt(2) )(2) UMe(7) Li}(n) were both crystallographically identified.
208 modimer, previous structures have captured a crystallographically-imposed symmetric state.
209 ocktails, four compounds could be identified crystallographically in the active site.
210      A dimeric structure has been determined crystallographically in which the K(+) cations interact
211                                         Five crystallographically independent 1D channels including t
212                          A comparison of two crystallographically independent flexizyme conformations
213                                      The two crystallographically independent ligand molecules adopt
214 embly-competent CA hexamers and derived four crystallographically independent models that define the
215 nd-to-end twist of 144 degrees , and the two crystallographically independent molecules of 2m have tw
216 c showed that the structures consist of four crystallographically independent molecules, A, B, C, and
217 coordination sphere of the metals in the two crystallographically independent orientations is identic
218 ad-to-tail overlap complexes in four of five crystallographically independent parallel dimers.
219 ray diffraction indicated that one out of 15 crystallographically independent phosphorus atoms appear
220                                          Two crystallographically independent views reveal that the c
221 d along the chain due to the presence of two crystallographically independent {Mn2(saltmen)2} units,
222 nium ion or N-acetylgalactal form, which are crystallographically indistinguishable at the present re
223 ically equivalent or (2) the boron pairs are crystallographically inequivalent but are rendered magne
224 tra yield isotropic chemical shifts for each crystallographically inequivalent carbon and spin-lattic
225 ure superconductors (HTSCs) that possess two crystallographically inequivalent CuO(2) planes in the u
226  the successful, prospective optimization of crystallographically intractable fragment hits into more
227 re of the rat endophilin A1 dimer determined crystallographically is maintained under predominantly v
228 structure is confirmed spectroscopically and crystallographically, is investigated by DFT calculation
229 25(SCH 2CH 2Ph) 18 nanoparticle structure is crystallographically known to consist of a centered Au 1
230                         Channels filled with crystallographically located water and acidic groups are
231  molecular layer of dodecane trapped between crystallographically misaligned dry surfaces.
232  the soluble region of pmoB at the site of a crystallographically modeled dicopper center.
233 NA glycosylase AlkD from Bacillus cereus, we crystallographically monitored excision of an alkylpurin
234 osphine (SP)-PMeIs(p-MeOC6H4) was determined crystallographically; NMR studies and comparison to the
235 nodes and seven tricarboxylate ligands (both crystallographically nonequivalent), resulting in a 173.
236  two end facets of wurtzite CdS nanorods are crystallographically nonequivalent, asymmetric heterostr
237   This observation suggests that some of the crystallographically observed allosteric effects that re
238 ere interpreted as being consistent with the crystallographically observed ARD structure.
239                                          The crystallographically observed binding interface was conf
240             Finally, we demonstrate that the crystallographically observed conformation of the mobile
241 pontaneously from the active to the inactive crystallographically observed conformation.
242 h the isotropic thermal fluctuations and the crystallographically observed conformational changes wit
243 lated conformation of 2 agreed well with the crystallographically observed conformations of 1 and 2.
244 ree nucleotide states could sample the major crystallographically observed conformations.
245                       We also confirm that a crystallographically observed disorder to order transiti
246  observed crystal structure but maintain key crystallographically observed hydrogen bonds still have
247 as of Get3 open and closed structures in the crystallographically observed no-nucleotide, two ATP, an
248 orientation is very close (<1 A RMSD) to the crystallographically observed orientation in most cases,
249  rather than C-8, indicating that the second crystallographically observed orientation is significant
250                                              Crystallographically observed structural changes (e.g.,
251 e actinyl tetrahalide dianions and reconcile crystallographically observed structural motifs and non-
252  or requires an extension of the lever arms' crystallographically observed structure.
253 rameworks are covalently functionalized with crystallographically ordered pendant metal clusters have
254 ially nanocrystalline Au films gain texture, crystallographically orient with the 2D crystal overlaye
255 dynamics at the nanoscale, where identically crystallographically-oriented facets are qualitatively d
256                            The only previous crystallographically proven 26- and 29-atom DI members a
257 pret such data in terms of a small number of crystallographically refinable, time-independent structu
258                                          The crystallographically refined crystal structures using si
259                                          The crystallographically refined occupancies of these confor
260                              Both phases are crystallographically related to the parent beta (BCC) ma
261 ng kinetic model at two levels: first, using crystallographically relevant internal cavities and thei
262 eta(2)-side S,O-bound (MS2) photoisomers are crystallographically resolved by probing a light-induced
263 rmational transition pathways connecting the crystallographically resolved conformations.
264                                 We find that crystallographically resolved Ti17O24(OPr(i))20 nanopart
265 ructure of these Lewis pairs was established crystallographically, revealing an additional Ru-Al inte
266 ay scattering studies confirm the state seen crystallographically, showing that the DnaB ATPase domai
267 slippage in boron nitride nanotubes that are crystallographically similar to carbon nanotubes, but el
268  [K(2.2.2-cryptand)][Cp'3UH], which could be crystallographically similar, the hydride complex was sy
269                          We survey 118 X-ray crystallographically solved structures of homo-oligomeri
270 ), M = Mg, Zn, Fe, and Co) and characterized crystallographically, spectroscopically, electrochemical
271 e, or l-cysteine-l-phosphotyrosine formed on crystallographically textured films of gold, we conclude
272 r high temperature properties without HRE, a crystallographically textured nanoscale grain structure
273                                 We determine crystallographically that NurA folds in a toroidal dimer
274 on of the human EGFR dimer has been resolved crystallographically, the crystal structures do not reve
275 ncluding the transmembrane pocket identified crystallographically, the extracellular (EC) domain, and
276 fusion hairpin forms have been characterized crystallographically, the transiently extended prehairpi
277 nel is the "mobile" Glu(292), which was seen crystallographically to adopt distinct positions up and
278  the most soluble, with a paratope we showed crystallographically to be virtually identical to that o
279 isons among all the multi-domain NRs studied crystallographically to date show significant variations
280 the longest 3(10) helical structure observed crystallographically to date.
281 r(f)(4)](-) (9) can be synthesized and shown crystallographically to feature a terminally bound GaI l
282 K1 structural model, which has thus far been crystallographically unattainable, a potential alternate
283 um Neisseria meningitidis (NmHO) possesses a crystallographically undetected C-terminal fragment that
284 l 2-fold and mirror symmetry, exhibits three crystallographically unique one-dimensional channels as
285              The two structures contain five crystallographically unique subunits of MntR, providing
286                         The overlay of eight crystallographically unique U3S molecules reveals a huge
287 vel, because such boundary is, in principle, crystallographically unobservable.
288  dynamics (MD) simulations, we show that the crystallographically unresolved C2 loop plays a crucial
289          These findings demonstrate that the crystallographically unresolved loops of membrane protei
290           Examples for n = 1 and 3 have been crystallographically verified for R = 2,6-iPr2C6H3 (Dipp
291 carbamic acid pairs, the latter of which are crystallographically verified for the first time in a po
292 y establish a FeCO vibrational signature for crystallographically verified pentacoordination.
293 n one case, the B-H bond activation step was crystallographically verified, a snapshot of the sigma-b
294 y example in which the parent phenol is also crystallographically well-defined.
295 licational endeavours, they may also present crystallographically well-oriented nano-templates of bul
296 e structures of Fab fragments not determined crystallographically were predicted by homology modeling
297 o "open/closed" states previously identified crystallographically, were indicated to have direct effe
298              GlcN6P binding becomes apparent crystallographically when the pH is raised to 8.5, where
299 ly resembles the CFeSP/MeTr complex observed crystallographically with 2:1 protein stoichiometry, whi
300             This could in theory be achieved crystallographically with a structure whose three-dimens

 
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