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1 correlated with the bridge barrier E(F) - E(HOMO).
2 2D/G12D bone marrow cells develop TALL (TALL-homo).
3 s determined by the bridge barrier, E(F) - E(HOMO).
5 d the analogous longer chain substrates cis-(homo)(2)aconitate, cis-(homo)(3)aconitate, and cis-(homo
6 hain substrates cis-(homo)(2)aconitate, cis-(homo)(3)aconitate, and cis-(homo)(4)aconitate, all with
9 y higher highest occupied molecular orbital (HOMO) (-5.43 eV) and lowest unoccupied molecular orbital
10 (-3.80 eV) energy levels relative to ITIC1 (HOMO: -5.48 eV; LUMO: -3.84 eV), and higher electron mob
12 both the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) of
13 ween the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO)
14 and frontier orbitals of the aromatic donor (HOMO) and the NO(+) acceptor (LUMO) clearly suggests an
15 eems to have varied little through the genus Homo, and it should not be used to account for other asp
16 met Neandertals, Denisovans, mid-Pleistocene Homo, and possibly H. floresiensis, with some degree of
17 best for additional bonding overlaps in the HOMO, and this amidine effect predicts lower N-inversion
19 or styrenic monomers during the synthesis of homo- and block copolymers as the stability and reactivi
21 nces, and architectures of a wide variety of homo- and copolymeric materials, including multicomponen
22 into the ROMP mechanism, monomer design, and homo- and copolymerization rate trends offer a general s
23 ilding blocks (1-12) and their corresponding homo- and copolymers (P1-P14), and examine in detail the
24 erous strategies have been developed for the homo- and cross coupling of alkynes to enynes via transi
25 The role of gold as the organizing metal in homo- and cross-coupling reactions is explored in this p
26 on including inactivation of HK activity via homo- and hetero oligomerization, and cross-phosphorylat
27 n epithelial cells, as well as organizes the homo- and hetero-association of these cell surface prote
28 between cytoplasmic regulatory domains (both homo- and hetero-connexin) could be important for the re
29 only allows the production of angstrom-sized homo- and hetero-crystals, but also provides new experim
32 interactions of murine GBPs (mGBP1/2/3/5/6), homo- and hetero-multimerization properties of mGBP2 and
35 istributive, leading to the synthesis of DNA homo- and hetero-oligomeric and -polymeric ladders rangi
36 in 1 (RHL1) and RHL2] can assemble into both homo- and hetero-oligomeric complexes, displaying three
37 FHR1, FHR2, and FHR5 circulate in plasma as homo- and hetero-oligomeric complexes, the formation of
38 and recognition, conformational changes, and homo- and hetero-oligomeric interactions within the supr
41 the pentraxin domain that is involved in the homo- and hetero-oligomerization of NPTX2 and NPTXR.
42 mical studies suggest formation of flotillin homo- and hetero-oligomers in other cell types, but so f
46 ar-atomic resolution provides a template for homo- and hetero-PYD/PYD associations, as confirmed by s
47 RHA) showed aggregation enhancement for both homo- and hetero-systems, in presence of divalent Ca(2+)
49 riments showed the presence of Rds mainly as homo- and hetero-tetramers with Rom-1 in the photorecept
50 e that Rds traffics from the IS to the OS as homo- and hetero-tetramers, with subsequent disulfide-li
52 ing strategy for the synthesis of oligomeric homo- and hetero[n]rotaxanes with precise control over t
53 analyses, we could assess the extent of both homo- and heteroagglomeration as well as particle sedime
58 thod relies on characterizing an ensemble of homo- and heteroaggregates using (6)Li NMR spectroscopy.
59 n chemistry that determines NPs dissolution, homo- and heteroaggregation, and co- and competitive-ret
60 o-biaryl substituted alkynes into polycyclic homo- and heteroarenes of different size, shape, and cur
62 ntroduced that enables the isolation of both homo- and heterobimetallic complexes of divalent first-r
63 ks have motivated the synthesis and study of homo- and heterobinuclear conjugates as light-harvesting
64 and excited-state features of many of these homo- and heterobinuclear phthalocyanine and/or porphyri
65 preparation of covalent and supramolecular, homo- and heterobinuclear systems based on phthalocyanin
72 ergies (overall average and per residue) for homo- and heterodimer pairs of CXC (CXCL4/PF4, CXCL8/IL8
73 with lapatinib and trastuzumab to block all homo- and heterodimer signaling as well as by blockade o
74 omers (2R,7R)- and (2S,7S)-2 and a series of homo- and heterodimeric analogues in which octanedioic a
75 y, the contrast between the functions of the homo- and heterodimeric forms of proteins deserves the a
77 IM) domains (PAS-A and PAS-B), which mediate homo- and heterodimeric mPER-mPER interactions as well a
80 e is general and can be applied to study the homo- and heterodimerization of GPCRs and other transmem
85 and EHD3 have 86% amino acid identity; they homo- and heterodimerize and partially co-localize to TR
88 oforms that determines the relative ratio of homo- and heterodimers (active or inactive) in a spatial
89 re obtained via implicit solvent modeling of homo- and heterodimers and analysis of interactions in t
90 , we report that both ATase1 and ATase2 form homo- and heterodimers and associate with members of the
91 The results show that all combinations of homo- and heterodimers are formed, but with varying degr
92 Cys mutants, which purified as a mixture of homo- and heterodimers at volumes consistent with a tetr
93 and purified, the resulting acyl-CoA oxidase homo- and heterodimers displayed different side-chain le
94 tereocontrolled synthesis of ribonucleosidic homo- and heterodimers has been achieved from inexpensiv
97 urther, the D200N- and D18N-containing TREX1 homo- and heterodimers inhibit the dsDNA degradation act
98 ata demonstrate for the first time that both homo- and heterodimers of ABCD1 and ABCD2 are functional
99 ically analyze dimerization of 18 TM helical homo- and heterodimers of different bitopic proteins, in
101 , we describe the synthesis of a full set of homo- and heterodimers of three intact structures of dif
102 These findings uncover a novel network of homo- and heterodimers of ZnTs with distinct subcellular
104 X-seq) on several floral MADS domain protein homo- and heterodimers to measure their DNA binding spec
105 cation of Intact Glycopeptides", noncovalent homo- and heterodimers were mis-identified as glycopepti
106 We report that 5-HT2 receptors can form homo- and heterodimers when expressed alone or co-expres
107 eta-oxidation cycles, form different protein homo- and heterodimers with distinct substrate preferenc
108 ar regions and promote formation of specific homo- and heterodimers with enhanced tyrosine kinase act
111 PCR dimerization, functional consequences of homo- and heterodimers, and approaches of medicinal chem
114 optosome mediates the formation of caspase-9 homo- and heterodimers, both of which are impacted by cl
115 pase-9-p35/p12 inhibited its ability to form homo- and heterodimers, but feedback cleavage by caspase
116 heterodimers, and that many GPCRs form both homo- and heterodimers, has led to speculation that GPCR
117 B2- and betaA3-crystallins form a mixture of homo- and heterodimers, mixed betaB1- and betaA3-crystal
124 rikingly different reactivity of a series of homo- and heterodinuclear [(M(III) )(mu-O)2 (M(III) )'](
125 ily coordinate a second metal center to form homo- and heterodinuclear complexes, namely {[S4CalixBut
131 his study, we show how the interplay between homo- and heteroion pairing influences protein stability
132 sized a series of chlorophosphines utilizing homo- and heteroleptic (dianionic)guanidinates and have
135 e of PhTX-74 and related polyamine toxins at homo- and heteromeric AMPARs in the presence and absence
137 ology and membrane anchor domains and blocks homo- and heteromeric CerS2/6 complex formation and acti
138 f the immunocomplex, we show the presence of homo- and heteromeric complexes for human TPC1 and TPC2.
139 D(2) receptors (A(2A) and D(2)) associate in homo- and heteromeric complexes in the striatum, providi
140 hich indicates that AdipoR1 and AdipoR2 form homo- and heteromeric complexes under resting conditions
141 her in a single genetic pathway, possibly in homo- and heteromeric complexes, to promote carbon expor
144 if (TIFF/YXG) within the ZIM domain mediates homo- and heteromeric interactions between most Arabidop
147 rane spanning (7TM) receptors/GPCRs can form homo- and heteromers and initiate distinct signaling pat
148 rmal Xenopus development and Smad2 and Smad4 homo- and heteromers in isolated Xenopus blastomeres.
149 d to simultaneously visualize A(2A) and D(2) homo- and heteromers in living cells and to examine drug
150 dings indicate that AdipoR1 and AdipoR2 form homo- and heteromers that present unique interaction beh
151 level, the portion of receptors engaging in homo- and heteromers, as well as the effect of persisten
153 xt of using a series of strongly oxo-coupled homo- and heterometallic poly(f-block) chains to better
158 two-dimensional NMR approaches based on both homo- and heteronuclear couplings ((1)H-(1)H COSY; (1)H-
159 abolite content, leading to remarkably clean homo- and heteronuclear NMR spectra of the serum metabol
161 y transfer to characterize the energetics of homo- and heterooligomer interactions between the Vpu TM
162 that Ca(v)beta subunits form multimolecular homo- and heterooligomeric complexes in human vascular s
163 on paramagnetic resonance (EPR) to probe the homo- and heterooligomeric interactions of reconstituted
165 of ARF and Aux/IAA proteins facilitate their homo- and heterooligomerization, the molecular basis for
168 h MDMX, the function and regulation of these homo- and heterooligomers in vivo remain incompletely un
169 hesion molecules (SynCAMs) 1 and 2 engage in homo- and heterophilic interactions and bridge the synap
170 these Delta proteins can bind to one another homo- and heterophilically, and to study the localisatio
176 ing with influenza viruses of both H1 and H3 homo- and heterosubtypes protected against lethal CA/E3/
179 de evidence that vaccinations stimulate both homo- and heterosubtypic immune responses in young and m
181 as a homotetramer channel, in astrocytes as homo- and heterotetramer channels together with KIR5.1.
182 dividual IP3R monomers are assembled to form homo- and heterotetrameric channels that mediate Ca(2+)
183 nstrate that both transporters exist as both homo- and heterotetramers, with a predominance of homote
186 in confocal images indicated segregation of homo- and heterotrimers at a subfibrillar level througho
187 ith 3D confocal imaging of fibrils, in which homo- and heterotrimers were labeled with different fluo
188 tion and reassociation of the pepsin-treated homo- and heterotrimers, but this remixing did not signi
189 or modeling lies in capturing the panoply of homo- and heterotypic cellular interactions within the c
190 igomerized with comparable efficiency in all homo- and heterotypic combinations, but only the homotyp
191 ultidomain transmembrane proteins possessing homo- and heterotypic contact sites in their ectodomains
192 ue-ECM boundary, rather than by differential homo- and heterotypic energies of cell-cell interaction.
193 and, residues in the C'C" loop necessary for homo- and heterotypic interactions are dispensable for M
194 hod may find utility in the analysis of weak homo- and heterotypic interactions involved in other bio
195 9 system enables the generation of transient homo- and heterozygous deletion libraries and allows for
196 ntaining a diverse set of glycans, including homo- and mixed N-glycans (high-mannose, hybrid and comp
199 with both MDM2 and MDMX by inhibitor-driven homo- and/or heterodimerization of MDM2 and MDMX protein
200 stress, MRs and GRs seem to bind to GREs as homo- and/or heterodimers in a gene-dependent manner.
203 hat the highest occupied molecular orbitals (HOMOs) are localized (24-99%) in all cruciforms, in cont
206 he aniline nitrogen lowers the energy of the HOMO (but not of the LUMO), leading to a blue-shifted em
207 f indole highest occupied molecular orbital (HOMO) charge density toward the cation with a subsequent
208 us with derived morphology observed in later Homo, confirming that dentognathic departures from the a
209 (dA) strands, we constructed 40 hypothetical homo-(dA) anti-parallel duplexes and docked coralyne int
210 xperiments predict that the coralyne-induced homo-(dA) duplex structure adopts the transWH geometry.
213 cerns the fate of archaic forms of the genus Homo: did they go extinct without interbreeding with ana
214 r similarity and ability to form hetero (and homo) dimers, DDX5 and DDX17 are used by HIV in differen
218 pshifted highest occupied molecular orbital (HOMO) energy level mainly due to the additional octyl on
220 y compresses polymer bandgaps and lowers the HOMOs--essential to maximize power conversion efficiency
222 e show that reduction in molar size in early Homo (H. habilis and H. rudolfensis) is explicable by ph
223 that the highest occupied molecular orbital (HOMO) has mixed metal-ligand character rather than being
224 ance comes from the highest filled orbitals (HOMO, HOMO-1, and HOMO-2) of individual bases, with a ra
225 genera Australopithecus, Kenyanthropus, and Homo; however, Theropithecus and Paranthropus have simil
227 a deeper highest occupied molecular orbital (HOMO) level for obtaining polymer solar cells with a hig
229 a higher highest occupied molecular orbital (HOMO) level, a lower lowest unoccupied molecular orbital
231 ral modifications could be used to alter the HOMO, LUMO, and band gap over a range of 1.0, 0.5, and 0
233 and electrochemical studies show that their HOMOs, LUMOs, and energy gaps can be easily modified or
234 ve of a strong dependence upon energy of the HOMO: measured rates of protonation vary over 6 orders o
235 donor molecules with relatively high energy HOMO, molecules with high HOMO-LUMO gaps and acceptor mo
236 ween the highest occupied molecular orbital (HOMO) of N,N'-bis(1-naphthyl)N,N'-diphenyl-1,1'-biphenyl
237 e between the highest occupied energy level (HOMO) of the metal and the lowest unoccupied energy leve
238 .e., the highest occupied molecular orbital (HOMO) or HOMO-n (n >/= 0) when the HOMO is not located o
239 bditis elegans PKD, DKF-2A, are exclusively (homo- or hetero-) dimers in cell extracts and intact cel
240 and PopD insert pores into membranes forming homo- or hetero-complexes of undetermined stoichiometry.
241 owth-factor ligands typically signal through homo- or hetero-dimeric cell surface receptors via Janus
242 at formation of one or more disulfide-linked homo- or hetero-dimeric proteins might signal photorecep
246 odate a large variety of organic ligands and homo- or hetero-metallic clusters, which allows for extr
247 oteins frequently assemble into higher order homo- or hetero-oligomers within their natural lipid env
248 t a large portion of nanoparticles will form homo- or heteroagglomerates when released into environme
249 background of SDE is a dynamic formation of homo- or heterochiral dimeric or oligomeric aggregates o
250 h it is well known that Ascl1 binds DNA as a homo- or heterodimer via its basic helix-loop-helix (bHL
251 here the hypothesis that ALX might exist as homo- or heterodimer with FPR1 or FPR3 (the two other fa
253 ponse of N. crassa and indicate that LOV-LOV homo- or heterodimerization may be a mechanism for regul
257 ) and U1-70K revealed that U2AF(35) can form homo- or heterodimers and that U2AF(35) proteins can ass
260 to one or more targets are co-synthesized as homo- or heterodimers or multimers via phosphodiester li
262 HLH122 and bHLH51 act sequentially as either homo- or heterodimers to choreograph tapetal development
263 ) signaling is affected by formation of GPCR homo- or heterodimers, but GPCR regulation by other cell
269 ADO can use a diiron cofactor (rather than a homo- or heterodinuclear cluster involving another trans
272 from Xenopus oocytes expressing recombinant homo- or heteromeric combinations of GluA1, GluA2, and G
275 be subsequently trapped via coordination of homo- or heterometal adatoms, which may also play a role
277 logical signals and systems and are found in homo- or heteromultimerization of signaling molecules as
281 ents were hyperresponsive and failed to show homo- or heterotolerance to TLR ligands, manifested by e
285 ins and suggest that substrate dimerization (homo- or possibly heterodimerization) might represent a
286 Instead, an excited state formed by a Ph-NN (HOMO) --> Ph-NN (LUMO) one-electron promotion configurat
288 elow the highest occupied molecular orbital (HOMO) should contribute to laser-driven high harmonic ge
290 odied (i.e., well within the range of living Homo) specimen that, at 3.58 Ma, also substantially ante
292 k Fermi level pinning (UPS revealed E(F) - E(HOMO) varied only weakly with Phi), but R(0) varies stro
294 ples the highest occupied molecular orbital (HOMO, which is localized on the carboxylate group) from
295 s from the unsymmetrical distribution of the HOMO, which shows decreased orbital coefficients on the
297 via the highest occupied molecular orbital (HOMO) with a rectification ratio R = 99, but junctions w
298 uitable highest occupied molecular orbitals (HOMO) with respect to the valence band level of the pero
299 volving hole transport through the molecular HOMO, with a decay constant beta = 3.4 +/- 0.1 nm(-1) an
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