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1 dual compounds that adopt the most populated ternary 1:1:1 structure types (TiNiSi-, ZrNiAl-, PbFCl-,
2            We demonstrate binary (1 x 1) and ternary (1 x 2) Bcl-2 PPI analyses by imaging fluorescen
3  a segregation mechanism that is mediated by ternary AcrAB-TolC complex formation.
4     The corresponding Cf(III)-ligand-protein ternary adduct was characterized by X-ray diffraction an
5 tiated by the screening of simple binary and ternary admixtures of Pd/charcoal in combination with on
6                                           %) ternary alloy after laser surface remelting.
7 ty which is comparable to that of bulk InGaN ternary alloy.
8 mulation results suggest that the binary and ternary alloys exhibit higher radiation resistance than
9 s analyzing the element composition of these ternary alloys in all three spatial dimensions.
10 very versatile and can be applied to produce ternary and quaternary metal oxide onions with tunable s
11 ne and chloroform solvents and their binary, ternary and quaternary mixtures.
12 mparison of the apo, binary, open and closed ternary, and translocated product detail an ensemble of
13 cus SNPs, including widespread disruption of ternary androgen receptor (AR)-FOXA1 and AR-HOXB13 compl
14 hly efficient and stable solar cells using a ternary approach, wherein two non-fullerene acceptors ar
15  binding two CBs to form either 1:2 or 1:1:1 ternary assemblies despite consisting of a single cation
16 ults indicate that in simple Pu-NOM-goethite ternary batch systems, NOM will decrease Pu sorption to
17 random bit arrays are created that can offer ternary-bit architecture by determining the connection y
18             Probiotics encapsulated with the ternary blends incorporated in instant juice powder exhi
19                                        These ternary blends protected the probiotics and enhanced the
20                       Encapsulation with the ternary blends reduced particle size of the probiotic po
21 ighest performance reported for nonfullerene ternary blends.
22 ficant chemical inhomogeneities in all three ternary bronze alloys with profound local deviations fro
23 a neonates to Cd, Cu, Ni, or Zn alone and in ternary Cd-Cu-Ni and Cd-Ni-Zn combinations in standard 4
24 rophenyl rings, in addition to the diazepine ternary center and the side chain methylene moiety.
25 hat there is a degree of site masking in the ternary clay mineral-humic acid-bacteria composite.
26  the cleaved DNA strand in the drug-DNA-Top1 ternary cleavage complex, affect Top1 inhibitory activit
27     In this work, we report the synthesis of ternary cobalt manganese phosphide nanoparticles from th
28                                              Ternary complex (TC) and eIF4F complex assembly are the
29 ex (PIC) bearing the eIF2.GTP.Met-tRNAi(Met) ternary complex (TC) scans the mRNA for an AUG codon in
30 on complex (PIC) bearing Met-tRNAi(Met) in a ternary complex (TC) with eukaryotic initiation factor (
31 nds Met-tRNAi to form the eIF2-GTP*Met-tRNAi ternary complex (TC), which is recruited to the 40S ribo
32 D2 (BICD2) joins dynein with dynactin into a ternary complex (termed DDB) capable of processive movem
33 binding ability could stabilize a mismatched ternary complex and destabilize a matched ternary comple
34 ular interactions within the POT1-TPP1-ssDNA ternary complex and the conformational changes that cont
35                                          The ternary complex architecture explains how Rab11 vesicles
36 e CSD1 and the Sxl protein components in the ternary complex are revealed by the combination of NMR a
37 in acidic conditions enabled trapping of the ternary complex as a dominant population.
38 e TOCA HR1 domain to Cdc42 and the potential ternary complex between Cdc42 and the G protein-binding
39 ivery demonstrate that the two halves of the ternary complex between the MoFe protein and two reduced
40 ealing, we observe the formation of a stable ternary complex between U4 and U6 RNAs and Prp24, indica
41 re we structurally characterize the >100-kDa ternary complex by NMR and negative stain EM and show a
42     Here we solve the crystal structure of a ternary complex comprising full-length human papilloma v
43         The 1.85 A resolution structure of a ternary complex containing NADPH and a P5C/proline analo
44 transfer mapping of key residues within this ternary complex demonstrates that the protein substrate
45                    The two structures of the ternary complex ESA/Dic/Nps, obtained by competitive coc
46 ctor activity, focusing on the ERK-regulated ternary complex factor family of SRF partner proteins.
47                            The ERK-regulated ternary complex factors (TCFs) act with the transcriptio
48 mplications for the application of the CB[8] ternary complex for the formation of hydrogels, as these
49 ROTACs exhibited positive cooperativities of ternary complex formation and were more potent degraders
50  Pu sorption to goethite at pH 3, suggesting ternary complex formation or, in the case of humic acid,
51  with doxorubicin (DOX) prodrug 2 via hetero-ternary complex formation to yield 7.
52                               Mechanisms for ternary complex formation were characterized by Fourier
53 f 20-bp guide RNA:target DNA heteroduplex on ternary complex formation.
54 ting cleft adopts a "locked" conformation on ternary complex formation.
55 tributing to the RecA homology search before ternary complex formation.
56 ereospecificity during aldol addition, a key ternary complex formed by DHAP and d-G3P, comprising 2%
57                            In Arabidopsis, a ternary complex formed by MYB, bHLH transcription factor
58                   A notable exception is the ternary complex formed by proproteinase E, chymotrypsino
59                              We identified a ternary complex formed by TBP and the histone fold (HF)
60                    Crystal structures of the ternary complex formed by the extracellular domains reve
61 he TTR-Abeta interaction, as well as for the ternary complex formed in the presence of IDIF.
62                               No gH/UL116/gL ternary complex formed in transfected cells, suggesting
63 rization by the d-G3P aldehyde moiety in the ternary complex generates the active trans-isomer compet
64 action in PI3Kalpha activation involving the ternary complex in cell proliferation signaling by oncog
65  of Cu(I) with bathocuproine (BCP) to form a ternary complex in presence of sodium dodecyl sulfate (S
66 ecreased expression of any component of this ternary complex in RPE1 cells causes a defective recruit
67 ty (Ka = 1.3 x 10(4)) via the formation of a ternary complex in which one phosphate replaces both inn
68 dicate that the galectin-3-U1 snRNP-pre-mRNA ternary complex is a functional E complex and that U1 sn
69 in pathway to the IL-36R.IL-36alpha.IL-1RAcP ternary complex is through the IL-36R.IL-36alpha binary
70 in neural lineages and the lens by forming a ternary complex likely facilitated allosterically throug
71 sm of PglC, differing fundamentally from the ternary complex mechanisms of representative polytopic P
72                                         This ternary complex model may lead to development of novel M
73 n for mu-ORs, determined using an allosteric ternary complex model.
74 complex, extended ternary complex, and cubic ternary complex models for 7TMR function.
75 a bridge between the two enzymes to create a ternary complex named the transsulfursome.
76  In addition, the decreased stability of the ternary complex of 8-oxoG:dA extension results in furthe
77 CT(EC536) binary complex and the neutralized ternary complex of CysK/CdiA-CT/CdiI(EC536) CdiA-CT(EC53
78 nsfer to IsdB and growth of S. aureus, and a ternary complex of IsdB.Hb.Hp was observed.
79 ucing koff, indicating formation of a stable ternary complex of myosin:Xa:Va.
80 se a model of the conformationally protected ternary complex of nitrogenase.
81                      Here we report a stable ternary complex of Pol II, the replicative polymerase Po
82 ne to generate an AgmNAT*acetyl-CoA*agmatine ternary complex prior to catalysis.
83 and ASXH domains formed a cooperative stable ternary complex required for deubiquitination.
84 totypical Vbeta8.1(+) TCR-H-2D(b)-GAP5040-48 ternary complex revealed that germline-encoded complemen
85                     Crystal structure of the ternary complex reveals a noncanonical binding site for
86        The crystallographic structure of the ternary complex scFv LR-Cn2-scFv RU1 allowed us to ident
87 SP15SART3 makes a complex with USP4 and this ternary complex serves as a platform to deubiquitinate P
88 The crystal structure of the [CYP121(cYY)CN] ternary complex showed a rearrangement of the substrate
89 om DNA and formed a more stable intermediate ternary complex than that formed from IkappaBalpha(WT) b
90 ted a spectrum of occupancy by the BATF-IRF4 ternary complex that correlated with the sensitivity of
91 ex3 and RING-domain proteins, resulting in a ternary complex that was critical for the intra-ER sorti
92                                   The formed ternary complex was then revealed by the introduction of
93 two components of nitrogenase form a stable, ternary complex with a small [2Fe:2S] ferredoxin termed
94 orts, here we solve a structure of CCR2 in a ternary complex with an orthosteric (BMS-681) and allost
95                           First, aa-tRNAs in ternary complex with EF-Tu.GDP are selected in a step wh
96  by the messenger RNA programmed ribosome in ternary complex with elongation factor Tu (EF-Tu) and GT
97 t-specific tRNA-binding protein that forms a ternary complex with glutamyl-tRNA synthetase (GluRSc) a
98 ailoring by CblC, and it also stabilized the ternary complex with GSH.
99                             GIGANTEA forms a ternary complex with HSP90 and ZEITLUPE and its co-chape
100 the CDI toxin from Escherichia coli NC101 in ternary complex with its cognate immunity protein and el
101 uced in Arabidopsis protoplasts could form a ternary complex with NF-YC2 in vitro, providing a molecu
102 e VPS26 protomer and sequentially assemble a ternary complex with PTHR and SNX27.
103  displaces HIF-1alpha by forming a transient ternary complex with TAZ1 and HIF-1alpha and competing f
104                       In vitro, Mot1 forms a ternary complex with TBP and DNA and can use ATP hydroly
105 omplementary-tagged nucleotide forms a tight ternary complex with the primer/template and polymerase,
106 e crystal structure of human TDO (hTDO) in a ternary complex with the substrates L-Trp and O2 and in
107 tagonist that binds to syndecans and forms a ternary complex with the Wnt co-receptor Lipoprotein rec
108 ice sites of the major class of introns as a ternary complex with U2AF(65) and U2AF(35) splicing fact
109 ystems such as the ternary complex, extended ternary complex, and cubic ternary complex models for 7T
110 ed ternary complex and destabilize a matched ternary complex, and provided evidence with structures i
111 1, 36 formed a stable NDM-1:Zn(II):inhibitor ternary complex, as demonstrated by (1)H NMR, electron p
112 ntial for formation of the A1R/neurabin/RGS4 ternary complex, as well as for stable localization of R
113 s ways to build receptor systems such as the ternary complex, extended ternary complex, and cubic ter
114 ither CRY1 or CLOCK disrupt formation of the ternary complex, highlighting the importance of this int
115 ntigen (PfCyRPA) is a crucial component of a ternary complex, including Reticulocyte binding-like Hom
116                          On formation of the ternary complex, ligand efficacy determines the quality
117 lecule in a neurabin homo-oligomer to form a ternary complex, representing a novel mode of regulation
118 bly of these tubulin binding proteins into a ternary complex, the concentration-dependent formation o
119           Consistent with the formation of a ternary complex, we find that the inhibitory peptide is
120  K188 and K189 to recruit NACK to the Notch1 ternary complex, which results in the recruitment of RNA
121 her hand, the CDV IRES forms a 40S/eIF3/IRES ternary complex, with multiple points of contact.
122 nting the dominant population trapped in the ternary complex, would lead to re-face attack on the ald
123  previously disclosed 3-CRBN-GSPT1 cocrystal ternary complex.
124 t, H11, which enabled crystallization of the ternary complex.
125 membrane, organizing a K-Ras4B-CaM-PI3Kalpha ternary complex.
126 that joins dynein and dynactin into a stable ternary complex.
127 idence that HS, OPG, and RANKL form a stable ternary complex.
128 nd UvsY and gp32 independently and also as a ternary complex.
129 ycling of RNAP by releasing the RNA from the ternary complex.
130 E when compared with the TRBV14(+) TCR-HLA-E ternary complex.
131 r of Notch signaling and binds to the Notch1 ternary complex.
132 s product requires the binding of the other (ternary-complex mechanism).
133 ther layer of regulation in the classic GPCR ternary-complex model, with broad implications for the m
134       With Fe/CA molar ratios from 2 to 0.5, ternary complexation of CA to kaolinite via a five-coord
135 wed the important contribution of Fe-bridged ternary complexation on CA retention.
136 he enhancement in adsorption associated with ternary complexation.
137 ting the levels of active eIF2-GTP/Met-tRNAi ternary complexes (TC).
138 ling suggest that varied competition between ternary complexes and release factors perturbs the UGA r
139 WY 14,643) and reduced (hAR*NADPH*WY 14,643) ternary complexes are comparable to each other.
140                     NACK is recruited to the ternary complexes containing Maml1 and Maml3, but not Ma
141                             We show that the ternary complexes containing proliferating cell nuclear
142 dy of Thermus thermophilus Argonaute (TtAgo) ternary complexes containing single-base bulges position
143  6.5, and then extraction of the hydrophobic ternary complexes formed in presence of cetyltrimethylam
144 ults suggest the existence of Kv4/KChIP/DPPL ternary complexes in ISA -expressing nociceptors and pai
145 ling that includes formation constants for U ternary complexes reveals that the aqueous concentration
146 the assembly of temporary Fcho1/2Eps15/RAP-2 ternary complexes to facilitate conformational activatio
147 sely, the dissociation rate constants of the ternary complexes varied dramatically with the guest str
148 nt polymers captured in the nanopore in such ternary complexes were clearly distinguishable and seque
149    Five x-ray crystal structures of hpol eta ternary complexes were determined, three at the insertio
150 Pu with TBP and DBP yielded the formation of ternary complexes whose stoichiometry was directly relat
151 ormula: see text] and its various binary and ternary complexes with DNA and the inhibitor IkappaB.
152 of this human enzyme as the holo form and as ternary complexes with estrone and with the first potent
153 e end of SecA allowed us to efficiently form ternary complexes with SecYEG for spectroscopic studies.
154 ectron-rich aromatic moieties forming hetero-ternary complexes with the macrocycle cucurbit[8]uril (C
155                Structural comparison of C2c1 ternary complexes with their Cas9 and Cpf1 counterparts
156 mic acid rather than due to the formation of ternary complexes, except at very low TC concentrations.
157 -Ts promotes the formation of GTP.EF-Tu.tRNA ternary complexes, thereby accelerating substrate turnov
158 metic nanobody, between more and less active ternary complexes.
159 interacted with the salivary protein to form ternary complexes.
160 R-SCR binary and JACKDAW (JKD)/IDD10-SHR-SCR ternary complexes.
161 , and Klebsiella pneumonia SlmA-DNA-FtsZ CTD ternary complexes.
162 early symmetric for PR20, as dimer-inhibitor ternary complexes.
163 em with the previous nucleic acid-associated ternary complexes.
164 ic phases and at least two subpopulations of ternary complexes.
165 ext of translationally active GTP.EF-Tu.tRNA ternary complexes.
166                      Because of this, in the ternary composite, Cd preferentially binds to the higher
167                         Specifically, in the ternary composite, the coexistence of HA and bacteria in
168  predict the crystal structure of equiatomic ternary compositions based only on the constituent eleme
169 (TIs; refs ,,,), followed by closely related ternary compounds and predictions of several weak TIs.
170 ties of the relatively unexplored rare-earth ternary compounds La3Cu3X4 (X = Bi, Sb, As, and P) using
171 r studies into additional solid solutions or ternary compounds taking this structure type.
172 ggest that TSSs may be found in half-Heusler ternary compounds.
173 ing seen in other studies, the pre-catalytic ternary crystal structures of hPolbeta, DNA and L-dCTP o
174                    The comparison of the two ternary crystal structures, AmbP3-DMSPP/hapalindole U an
175 obe the spatial element composition of three ternary Cu-Sn-Pb model bronze alloys (lead bronzes: CuSn
176 or modeling, lanthanoid ratios, and La-Ce-Sm ternary diagrams pointed to petroleum refineries as bein
177 tive and quantitative analysis of binary and ternary edible oil mixtures.
178              This study demonstrates a novel ternary electrocatalyst of porous cobalt phosphoselenide
179  low voltage of 1.64 V is achieved using the ternary electrode as both the anode and cathode, and the
180 ross-links RNA in an RNA:DNA hybrid within a ternary elongation complex (TEC).
181 termined structures of Escherichia coli RNAP ternary elongation complexes (TECs) with and without Nun
182 ifference in the thermodynamic properties of ternary FeSexTe1-x, based on first principle calculation
183 by nuclear magnetic resonance formation of a ternary FLI1-DNA-MTM complex on a single GGAA FLI1/MTM b
184                        It was shown that the ternary formulations showed higher PY, S and RTA than th
185 BA and basal activity employing concatemeric ternary GABAA receptors expressed in Xenopus oocytes.
186 main migration is observed on the surface of ternary giant unilamellar vesicles held in a temperature
187 in lengths of 10-14 carbons decrease Tmix in ternary GUVs of dioleoyl-PC/dipalmitoyl-PC/cholesterol,
188 ments results are exhibited as pseudo colour ternary heat maps.
189 contacts and the central ligand cements this ternary interaction.
190 carcity of techniques capable of identifying ternary interactions, we developed tricolor heterospecie
191 molecular event involving the formation of a ternary ligand-GPCR-G-protein complex.
192 determine the ability of PROTACs to form the ternary ligase-PROTAC-target protein complex and a MSD a
193 aration and communication across leaflets in ternary lipid bilayers, including saturated lipids with
194 e separation and domain formation in GUVs of ternary lipid mixtures composed of egg sphingomyelin, ch
195      The condensing effect of cholesterol in ternary lipid mixtures was evaluated in terms of phospha
196 omposed together to build band-pass filters, ternary logic systems and multi-level analogue-to-digita
197 stants, and can follow either a ping-pong or ternary mechanism.
198                                              Ternary metal chalcogenide nanocrystals (NCs) offer exci
199 s for water oxidation, our study establishes ternary metal vanadates as a prolific class of photoanod
200 toxicity-controlling mechanisms can occur in ternary-metal mixtures but might be predicted by mechani
201                         A sequential-casting ternary method is developed to create stratified bulk he
202 is of NTs from chalcogenide- and oxide-based ternary misfit layered compounds, as well as their struc
203 {M(2+)} in solution) were conducted to study ternary mixture (Ni, Cu, Cd) chronic toxicity to Lemna m
204  phases were systematically investigated for ternary mixture lipid multilayers consisting of 1:1 1,2-
205 s can appear in lipid bilayers composed of a ternary mixture of a low-melting temperature lipid, a hi
206 r, a binary mixture of Cu(2+) and Fe(3+) and ternary mixture of Cd(2+), Ni(2+), and Pb(2+) were measu
207                                      Using a ternary mixture of lipids, the modulated-intensity profi
208                        We use a binary and a ternary mixture: a saturated and an unsaturated lipid, o
209    Here, we find that when GUVs of canonical ternary mixtures are formed in aqueous solutions of shor
210 e stability of microemulsions in homogeneous ternary mixtures based on cosolvents.
211 ly affected through heteroaggregation in the ternary mixtures because of the limited availability of
212    Here we show that the evaporation of such ternary mixtures can trigger a phase transition and the
213 iant unilamellar vesicles (GUVs) composed of ternary mixtures of a lipid with a low melting temperatu
214 s on MnO2 reactivity, the MnO2 reactivity in ternary mixtures of Al2O3, MnO2, and NOM was mostly enha
215 mixtures of bacterial species was shown with ternary mixtures of Bacillus licheniformis, Escherichia
216 study the spray drying of jussara pulp using ternary mixtures of gum Arabic (GA) and modified starch
217 ver the past two decades, the evaporation of ternary mixtures of liquids with different volatilities
218       For the effect of Al ions, we examined ternary mixtures of MnO2, Al ions, and NOM.
219 rent work was to investigate interactions in ternary mixtures of MnO2, Al2O3, and NOM and how the int
220                                           In ternary mixtures of MnO2, Al2O3, and NOM, NOM inhibited
221  vertices, binary mixtures at the edges, and ternary mixtures on the faces of a tetrahedron.
222 e analysis was applied to several binary and ternary mixtures which mimic the composition of milk rep
223 ract (binary mixtures) or with both of them (ternary mixtures) was also assessed.
224        For the organic liquids in binary and ternary mixtures, Dw depends on relative humidity and fo
225                                     In these ternary mixtures, two metals were held constant, while t
226 thyl acetate), used as pure or in binary and ternary mixtures, was studied for the extraction of seed
227  of 650 degrees C by using low-melting-point ternary molten salts CaCl2 -MgCl2 -NaCl, which still ret
228 is observed for the binary Mont-bacteria and ternary Mont-HA-bacteria composite, respectively.
229 We then purified Spc29 and reconstituted the ternary Mps2-Bbp1-Spc29 complex, proving that Bbp1 can s
230  PEGylation density) and identification of a ternary nanomedicine optimized to overcome important siR
231  on ultrasmall ( approximately 5 nm) Pd-Ni-P ternary nanoparticles for ethanol electrooxidation.
232 ric conductivity and large surface area, the ternary nanosheets supported on electrochemically exfoli
233                 Moreover, the integration of ternary nanosheets with macroporous silicon enables high
234          Inspired by nacre's architecture, a ternary nanostructured composite has been developed, whe
235  phosphosulfide for Li2S impregnation, using ternary nickel phosphosulphide as a highly conductive co
236 ial to allow formation of a range of binary, ternary, or higher-ordered compounds to be synthesized i
237                                            A ternary organic semiconducting blend composed of a small
238 tors and one copolymer are used to fabricate ternary organic solar cells (OSCs).
239                                Of these, the ternary Par3-atypical protein kinase C-Par6 polarity com
240 a coupled cavity arrangement-specifically, a ternary, parity-time-symmetric photonic laser molecule-w
241 heath-free separation of both a binary and a ternary particle mixture in viscoelastic polymer solutio
242                        The new generation of ternary Pb(In1/2Nb1/2)O3-Pb(Mg1/3Nb2/3)O3-PbTiO3 ferroel
243 ing trace amounts of gold in palladium-based ternary (Pd6CoCu) nanocatalysts, the durability of the c
244 he ordering of the observed OH overlayers.As ternary perovskite-type oxides are increasingly used in
245                                   As complex ternary perovskite-type oxides are increasingly used in
246                              Manganese-based ternary phosphides represent a promising new system to e
247 dence of the glass transition temperature of ternary polymer/fullerene blend thin films and their con
248                                          The ternary product-related VioA structure indicated involve
249   Here we have demonstrated that HTT forms a ternary protein complex with the scaffolding protein DIS
250 at unmodified UNG2, PCNA, and RPA can form a ternary protein complex.
251 analysis to explore the interactions of this ternary protein system.
252          Here, we refined the structure of a ternary protein-protein-RNA complex comprising three dom
253 e influence of multicomponent diffusion in a ternary protein-salt-water system on protein diffusion a
254 B does not appear to facilitate formation of ternary Pu-DFOB-goethite complexes.
255 rent catalysts/initiators are explored using ternary reactions between two Michael acceptors and a si
256                         The results from the ternary reactions provide a platform from which sequenti
257 ol-Michael reactions through a series of 270 ternary reactions using (1)H NMR spectroscopy to quantif
258                                       In the ternary receptor, there are predicted to be two copies o
259                      The use of a reversible ternary redox switch enables us to set the pKa to three
260  validated in human cell lines, and formed a ternary regulatory complex with GRB2-associated-binding
261 osited on (0 1 1)-oriented domain-engineered ternary relaxor ferroelectric single crystals with exten
262 ons, e.g., NSN(2-) and SSNSS(-), and related ternary S,N,O anions such as the structural isomers NSO(
263                                            A ternary SAM (T-SAM) configuration, which included a PEG-
264 reporter, and deposited on an electrode as a ternary SAM configuration, is a suitable platform to dev
265 d to Cd and/or Hg surface atoms of II/VI and ternary SC NC and to gold and silver nanoparticles.
266 where, quadratic residue, primitive root and ternary sequence diffusers are mimicked by metadiffusers
267             A rationally-designed library of ternary siRNA polyplexes was developed and screened for
268                                              Ternary siRNA polyplexes were assembled with varied amou
269  linker region induced by Munc13-1 initiates ternary SNARE complex formation in the neuronal system.
270  The complexin-1 induced conformation of the ternary SNARE complex may be related to a conformation t
271  the membrane-proximal C-terminal end of the ternary SNARE complex that specifically depends on the N
272 mplexin-1 can simultaneously interact with a ternary SNARE complex via the central domain and a binar
273 ains associated with mature MDVs and forms a ternary SNARE complex with SNAP29 and VAMP7 to mediate M
274 wo conformations of complexin-1 bound to the ternary SNARE complex.
275 n from a closed complex with Munc18 into the ternary SNARE complex.
276 g to synaptobrevin-2 and SNAP-25 to form the ternary SNARE complex.
277 evin subconfiguration during assembly of the ternary SNARE complex.
278 xes have shown that Gbetagamma binds to both ternary SNARE complexes, t-SNARE heterodimers, and monom
279 ndependent variables in composition of these ternary solid solution crystals.
280                                              Ternary solutions containing one hydrotrope (such as eth
281 nterfacial tension over a period of 48 h for ternary solutions of both methylglyoxal and formaldehyde
282 r-octanol as a simple model of such kinds of ternary solutions.
283 ect balance of TMAO and urea interactions in ternary solutions.
284  inspection of the active site in the closed ternary structure reveals a sub-optimal binding geometry
285 ide binding conformation in the precatalytic ternary structures (hPolbeta.DNA.dNTP) for both extensio
286 the basis of this selectivity, we determined ternary structures of Poliota bound to template 1-MeA an
287                                              Ternary structures showed that induced-fit molecular mim
288 ompetitive processes: solution complexation, ternary surface complexation, and surface site competiti
289                                              Ternary surface complexes were not needed to explain the
290 inity are due to the formation of Ni-oxalate ternary surface complexes.
291                                          The ternary system containing aqueous U(VI), aqueous phospha
292 ay to biomedical applications of this simple ternary system.
293                                 Phospholipid ternary systems are useful model systems for understandi
294  sequence of different compositions in these ternary systems have been determined with increasing ele
295   We demonstrate this for a high temperature ternary Ti-Pd-Cr SMA by achieving both a small DeltaT an
296         The 'MAlB' phases are nanolaminated, ternary transition metal borides that consist of a trans
297 ive description of the phase behavior of the ternary unsaturated phospholipid/Chol/GlcCer mixture is
298 nts in an integrated workflow, we find eight ternary vanadate oxide photoanodes in the target band-ga
299 ructures of the binary VioA.FADH2 and of the ternary VioA.FADH2.2-(1H-indol-3-ylmethyl)prop-2-enoic a
300                                    The novel ternary Zintl phase Li3NaGe2 comprises alkali-metal cati

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