ライフサイエンスコーパス: homo-

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).

4 The resulting trishomocyclopropyl HOMO{-1} is a three-center two-electron bond responsible

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

7 )aconitate, cis-(homo)(3)aconitate, and cis-(homo)(4)aconitate, all with similar specificities.

8 hole injection and transport ceases when the HOMO < -5.6 eV.

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

11 These associate in vivo to form homo- (alpha(2)) and heterodimers (alpha.beta) with litt

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

18 Several lines of evidence from both homo- and block copolymerization results have demonstrat

19 or styrenic monomers during the synthesis of homo- and block copolymers as the stability and reactivi

20 applications of synthetic stimuli-responsive homo- and block polypeptides are reviewed.

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

30 Competitive homo- and hetero-dimerization of their amino-terminal do

31 The encoded proteins form multiple homo- and hetero-interactions and localize within secret

32 interactions of murine GBPs (mGBP1/2/3/5/6), homo- and hetero-multimerization properties of mGBP2 and

33 All of these homo- and hetero-NCDs could be successively formed by se

34 stions on the functional differences between homo- and hetero-oligomeric AAA proteases.

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

39 Homo- and hetero-oligomeric proteolytic complexes exist,

40 Using this pair, we measure homo- and hetero-oligomerization interactions in living

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

43 All AtHIR proteins could form homo- and hetero-oligomers in vivo and were enriched in

44 ce showing that IFITM family members work as homo- and hetero-oligomers to modulate virus entry.

45 Here, we show that HDAC4 and HDAC5 form homo- and hetero-oligomers via a conserved coiled-coil d

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+)

48 Rds also forms noncovalent homo- and hetero-tetramers with its nonglycosylated homo

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

51 There are homo- and hetero-trimeric types of collagen consisting o

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

54 Over time, CeO2-NPs tend to homo- and heteroaggregate and to accumulate on the surfi

55 Ensembles of homo- and heteroaggregated enolates are generated by mix

56 The strategy relies on forming ensembles of homo- and heteroaggregated enolates.

57 tegy relies on the formation of ensembles of homo- and heteroaggregated phenolates.

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

61 These include homo- and heteroarenes, rings of five to six atoms, and

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

66 ists to target these receptor complexes with homo- and heterobivalent ligands.

67 ugh a complex mechanism, where both receptor homo- and heterocomplexes are formed.

68 PMD1 and PMD2 can form homo- and heterocomplexes.

69 Halogenated homo- and heterocyclic aromatics including disinfectants

70 etraspanins can physically interact, forming homo- and heterodimer complexes.

71 Moreover, they suggest that homo- and heterodimer formation poise C/EBPbeta to execu

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

76 Interestingly, the role of ABCD2 (in homo- and heterodimeric forms) in the metabolism of poly

77 IM) domains (PAS-A and PAS-B), which mediate homo- and heterodimeric mPER-mPER interactions as well a

78 erbB3 homo- and heterodimerization events were captured in rea

79 Recent development suggests that homo- and heterodimerization of APP and APP-like protein

80 e is general and can be applied to study the homo- and heterodimerization of GPCRs and other transmem

81 To study the consequences of homo- and heterodimerization of wild-type and mutant PTE

82 The regulation of MST1/2 includes both homo- and heterodimerization, mediated by helical SARAH

83 ated in many biological processes mainly via homo- and heterodimerization.

84 Although homo- and heterodimerizations of G protein-coupled recep

85 and EHD3 have 86% amino acid identity; they homo- and heterodimerize and partially co-localize to TR

86 NKD1 and NKD2 can homo- and heterodimerize through their ID domains.

87 Given that NAC53 and NAC78 homo- and heterodimerize, we propose that they work as a

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

95 Meq homo- and heterodimers have different DNA binding affini

96 These receptors form homo- and heterodimers in response to ligand with ErbB2

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

100 Homo- and heterodimers of E2F7 and E2F8 were found on ta

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

103 The archaeal histones are homo- and heterodimers that pair on DNA to form tetrasom

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

109 bZIP28 forms homo- and heterodimers with other bZIP TF family members

110 (A)) and B (ET(B)) receptors, which may form homo- and heterodimers with unknown function.

111 PCR dimerization, functional consequences of homo- and heterodimers, and approaches of medicinal chem

112 HDAC1 and -2 form homo- and heterodimers, and their activity is dependent

113 They form homo- and heterodimers, and then collaboratively regulat

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

118 ed, thus demonstrating functionality of both homo- and heterodimers.

119 ) and large (L), which form disulfide-bonded homo- and heterodimers.

120 cells, and Hook proteins were found to form homo- and heterodimers.

121 mechanisms of binding and stripping for both homo- and heterodimers.

122 zipper region of Meq allows the formation of homo- and heterodimers.

123 hing cellular responses to IL-17A and IL-17F homo- and heterodimers.

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

126 In this approach, unprotected homo- and heterodipeptides (including aromatic, aliphati

127 Homo- and heterodivalent crown-ammonium pseudorotaxanes

128 Homo- and heterofunctionalized glycoclusters with galact

129 ross sections, and composite structures with homo- and heterogeneous components.

130 s and enables a superior characterization of homo- and heterogenic systems.

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

133 Live FRET imaging suggested that both homo- and heteromeric AdipoR complexes dissociate in res

134 biogenesis of functionally diverse pools of homo- and heteromeric AMPAR tetramers.

135 e of PhTX-74 and related polyamine toxins at homo- and heteromeric AMPARs in the presence and absence

136 How cells regulate the formation of diverse homo- and heteromeric AMPARs is unknown.

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

142 therefore, on the steady-state proportion of homo- and heteromeric complexes.

143 ha1(Q-26'E)) enhances receptor activation in homo- and heteromeric glycine receptors.

144 if (TIFF/YXG) within the ZIM domain mediates homo- and heteromeric interactions between most Arabidop

145 durations and reduced channel conductance in homo- and heteromeric receptors.

146 Homo- and heteromerization were confirmed by a FRET stud

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

152 n the endoplasmic reticulum (ER) and to form homo- and heteromers.

153 xt of using a series of strongly oxo-coupled homo- and heterometallic poly(f-block) chains to better

154 sions of beta-crystallins may influence both homo- and heteromolecular interactions.

155 HeT-A and TART Gags form homo- and heteromultimers using a region containing majo

156 Multidimensional homo- and heteronuclear correlation spectra of CA assemb

157 a combination of two- and three-dimensional homo- and heteronuclear correlation spectra.

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

160 The relevant homo- and heteronuclear spin-spin couplings are reported

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

164 6-Phosphofructokinases (Pfk) are homo- and heterooligomeric, allosteric enzymes that cata

165 of ARF and Aux/IAA proteins facilitate their homo- and heterooligomerization, the molecular basis for

166 GFP assays indicate that Arabidopsis SWEETs homo- and heterooligomerize.

167 ORMDL proteins formed homo- and heterooligomers and displayed similar patterns

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

171 Spirocyclic adducts, in both homo- and heteropolymer background single-stranded DNA s

172 Homo- and heteropolymeric tracts of A and T demarcate nu

173 epare multiple two-loop structures with both homo- and heterosequences.

174 Homo- and heterospectral correlation analysis are powerf

175 of the cooperative effect of substituents in homo- and heterosubstituted oligomers.

176 ing with influenza viruses of both H1 and H3 homo- and heterosubtypes protected against lethal CA/E3/

177 To determine the prevalence for human homo- and heterosubtypic antibody responses, we scrutini

178 responses that contribute to protection from homo- and heterosubtypic IAV infections.

179 de evidence that vaccinations stimulate both homo- and heterosubtypic immune responses in young and m

180 es and conferred complete protection against homo- and heterosubtypic lethal virus challenges.

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

184 Comparative analysis of the homo- and heterotrimer cleavage kinetics revealed that M

185 Independent homo- and heterotrimer solubility measurements in mixtur

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

197 ur structure revision, but the structures of homo- and nor-plakotenin must also be revised.

198 Furthermore, a series of TPD homo- and pseudohomopolymers bearing various alkyl chain

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.

201 Rs) associate in the plasma membrane to form homo- and/or heteromers.

202 BTI units leads to polymers with a low-lying HOMOs ( approximately -5.6 eV).

203 hat the highest occupied molecular orbitals (HOMOs) are localized (24-99%) in all cruciforms, in cont

204 ssed in lung epithelial A549 cells, can form homo- as well as heteromers.

205 ar machine capable of sequence-specific beta-homo (beta(3)) peptide synthesis.

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.

211 substitutions (dA-->7) were engineered into homo-(dA) sequences.

212 he thermal stability of the coralyne-induced homo-(dA) structure.

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

215 Children less than 3 years old in Abu Homos, Egypt, had approximately five diarrheal episodes

216 range of highest occupied molecular orbital (HOMO) energies as determined by cyclovoltammetry.

217 orbates' highest occupied molecular orbital (HOMO) energies.

218 pshifted highest occupied molecular orbital (HOMO) energy level mainly due to the additional octyl on

219 d to the highest occupied molecular orbital (HOMO) energy levels of their fluorophores.

220 y compresses polymer bandgaps and lowers the HOMOs--essential to maximize power conversion efficiency

221 Whereas a simple HOMO-->LUMO-type single substitution perfectly accounts

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

226 However, in species of Homo, including modern humans, there is a tight link bet

227 a deeper highest occupied molecular orbital (HOMO) level for obtaining polymer solar cells with a hig

228 ring the highest occupied molecular orbital (HOMO) level of the nanofiber building blocks.

229 a higher highest occupied molecular orbital (HOMO) level, a lower lowest unoccupied molecular orbital

230 e of the highest occupied molecular orbital (HOMO) localized on the six-atom Sc(4)O(2) cluster.

231 ral modifications could be used to alter the HOMO, LUMO, and band gap over a range of 1.0, 0.5, and 0

232 polar transport prevails when molecules have HOMO/ LUMO levels within the aforementioned range.

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

243 The coiled-coil motif that mediates homo- or hetero-dimerization of the bZIP proteins has be

244 ose and can be linked to create single-chain homo- or hetero-ligands of defined stoichiometry.

245 ium binding C2A domain that mediates protein homo- or hetero-meric interactions.

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

252 Here, we focus on antiparallel homo- or heterodimeric small multidrug resistance protei

253 ponse of N. crassa and indicate that LOV-LOV homo- or heterodimerization may be a mechanism for regul

254 eptor (TIR) domains of the receptors undergo homo- or heterodimerization.

255 may modulate cell survival and death through homo- or heterodimerization.

256 S proteins that are likely involved in their homo- or heterodimerization.

257 ) and U1-70K revealed that U2AF(35) can form homo- or heterodimers and that U2AF(35) proteins can ass

258 ATDC has been proposed to form homo- or heterodimers and to bind nucleic acids.

259 However, certain covalent homo- or heterodimers eliminated twitching motility, sug

260 to one or more targets are co-synthesized as homo- or heterodimers or multimers via phosphodiester li

261 These receptors can function as homo- or heterodimers such as TR:9-cis retinoic acid rec

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

264 Furthermore, SGR1 and SGR2 formed homo- or heterodimers, strongly suggesting a role for SG

265 regulate the preferential formation of Hax-1 homo- or heterodimers.

266 rs by expressing chimeric proteins mimicking homo- or heterodimers.

267 th other leucine zippers to form coiled-coil homo- or heterodimers.

268 ut nearly 200 of these peptides are found as homo- or heterodimers.

269 ADO can use a diiron cofactor (rather than a homo- or heterodinuclear cluster involving another trans

270 s (4-alkylidene-2-oxetanones) available from homo- or heteroketene dimerization.

271 AMPARs are tetramers formed by homo- or heteromeric assembly of GluA1-4 subunits to pro

272 from Xenopus oocytes expressing recombinant homo- or heteromeric combinations of GluA1, GluA2, and G

273 The switch between homo- or heteromeric DLK-1 complexes is influenced by Ca

274 Functional receptors are homo- or heteromeric tetramers with each subunit contrib

275 be subsequently trapped via coordination of homo- or heterometal adatoms, which may also play a role

276 ed PKD polypeptides may interact to generate homo- or heteromultimeric regulatory complexes.

277 logical signals and systems and are found in homo- or heteromultimerization of signaling molecules as

278 of the nature of the spacer used or whether homo- or heteroprotein dimers are targeted.

279 exogenously expressed human Kv7.4 and Kv7.5 homo- or heterotetrameric channels in A7r5 cells.

280 Kv7 (KCNQ) channels, formed as homo- or heterotetramers of Kv7.4 and Kv7.5 alpha-subuni

281 ents were hyperresponsive and failed to show homo- or heterotolerance to TLR ligands, manifested by e

282 Homo- or heterozygosity at Ars1127354 or Crs7270101 , en

283 Homo- or heterozygous presence of the frequent [C] allel

284 nditions with various organic substrates and homo- or mixed-sequenced ODNs.

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

287 rons occupying the orbital just below the N2 HOMO, referred to as the HOMO-1.

288 elow the highest occupied molecular orbital (HOMO) should contribute to laser-driven high harmonic ge

289 d beta-activation of carbonyl compounds, via HOMO, SOMO or LUMO activation pathways.

290 odied (i.e., well within the range of living Homo) specimen that, at 3.58 Ma, also substantially ante

291 nfluence: bulky substituents destabilize the HOMO, thereby increasing the rate of protonation.

292 k Fermi level pinning (UPS revealed E(F) - E(HOMO) varied only weakly with Phi), but R(0) varies stro

293 ability of estrogenic ligands to promote ER homo- vs. heterodimerization.

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

296 d is the highest occupied molecular orbital (HOMO) with a "bent" geometry.

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

300 s to the highest occupied molecular orbital (HOMO)-with a Ge-centred lone pair as the HOMO-1.