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2461por Sahtoe, Danny D., Praetorius, Florian, Courbet, Alexis, Hsia, Yang, Wicky, Basile I.M., Edman, Natasha I., Miller, Lauren M., Timmermans, Bart J. R., Decarreau, Justin, Morris, Hana M., Kang, Alex, Bera, Asim K., Baker, David“…We construct linearly arranged hetero-oligomers with up to 6 unique components, branched hetero-oligomers, closed C4-symmetric two-component rings, and hetero-oligomers assembled on a cyclic homo-oligomeric central hub, and demonstrate such complexes can readily reconfigure through subunit exchange. …”
Publicado 2022
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2462por Perissinotti, Laura L., De Biase, Pablo M., Guo, Jiqing, Yang, Pei-Chi, Lee, Miranda C., Clancy, Colleen E., Duff, Henry J., Noskov, Sergei Y.“…There is little doubt now that hERG-related component of I(Kr) in the heart depends on the tetrameric (homo- or hetero-) channels formed by two alternatively processed isoforms of hERG, termed hERG1a and hERG1b. …”
Publicado 2018
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2463Publicado 1985Tabla de Contenidos: “…Bacche, bene venies (CB 200) (2:58) -- Virent prata hiemata (CB 151) (1:49) -- Nonem a sollempnibus (CB 52) (2:11) -- Alte clamat Epicurus (CB 211) ; Nu lebe ich (CB 211a) (7:05) -- Vite perdite II (CB 31) (1:34) -- Vacillantis trutine (CB 108) (4:41) -- In taberna quando sumus (CB 196) (2:42) -- Iste mundus furibundus (CB 24) (1:39) -- Axe Phebus aurea (CB 71) (2:53) --Dulce solum natatlis patrie (CB 119) (8:19) --Procurans odium (CB 12) (2:42) -- Vite perdite I (CB 31) (1:04) -- Sic mea fata canendo solo (CB 116) (3:24) -- Ich was ein chint so wolgetan (CB 185) (3:33) -- Deduc Syon, uberrimas (CB 34) (2:50) -- Ecce torpet probitas (CB 3) (2:18) -- In terra summus rex (CB 11) (3:01) -- Fas et nefas ambulant (CB 19) (1:51) -- Flete flenda (CB 5) (1:08) -- Homo qui vigeas (CB 22) (2:36)…”
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2464por Fehr, Julia M., Myrthil, Nathalie, Garrison, Anna L., Price, Tavis W., Lopez, Steven A., Jasti, Ramesh“…These molecules are strained alkyne-containing cycloparaphenylenes (or [n+1]CPPs), which have been shown to possess size-dependent reactivity as well as the classic characteristics of the unfunctionalized parent CPP, such as a tunable HOMO–LUMO gap and bright fluorescence for large sizes. …”
Publicado 2023
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2465por Kurbanova, Malahat Musrat, Faizi, Md. Serajul Haque, Cinar, Emine Berrin, Jamal, Asif, Çemberci, Mustafa, Sadigova, Arzu, Askerov, Rizvan, Dege, Necmi, Nabi, Tahera“…From DFT calculations, the LUMO–HOMO energy gap of the molecule is 0.827 eV.…”
Publicado 2023
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2466“…Steady‐state spectroscopy and photokinetics experiments under UV or visible irradiation indicated the presence of intramolecular energy transfer processes among the DCM units. Homo‐ and hetero‐energy transfer processes between adjacent chromophores were confirmed by fluorescence anisotropy and decays. …”
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2467por Bayach, Imene, Sarfaraz, Sehrish, Sheikh, Nadeem S., Alamer, Kawther, Almutlaq, Nadiah, Ayub, Khurshid“…The highest reduction in the HOMO–LUMO energy gap compared to the bare nanobelt is seen in the case of the Zn@NB catalyst (4.76 eV). …”
Publicado 2023
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2468por Tay, Hui Min, Tse, Yuen Cheong, Docker, Andrew, Gateley, Christian, Thompson, Amber L., Kuhn, Heike, Zhang, Zongyao, Beer, Paul D.“…The first examples of halogen bonding (XB) heteroditopic homo[2]catenanes were prepared by discrete Na(+) template‐directed assembly of oligo(ethylene glycol) units derived from XB donor‐containing macrocycles and acyclic bis‐azide precursors, followed by a Cu(I)‐mediated azide‐alkyne cycloaddition macrocyclisation reaction. …”
Publicado 2022
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2469“…XRD, NMR and computational data suggest that homo-oligomers adopt an extended right-handed helix with a pitch of over 30 Å, approximately that of B-DNA. …”
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2470por Kerketta, Romica, Erasmus, M. Frank, Wilson, Bridget S., Halász, Ádám M., Edwards, Jeremy S.“…This low level, ligand-independent signaling is likely achieved through frequent, but short-lived, homo interactions. Tonic signaling is also central in the pathology of precursor B acute lymphoblastic leukemia (B-ALL). …”
Publicado 2023
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2471“…We show this is the case within the proteomes of five model organisms: Homo sapiens, Saccharomyces cerevisiae, Drosophila melanogaster, Caenorhabditis elegans, and Arabidopsis thaliana. …”
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2472por Savina, Ekaterina A., Shumilina, Tatiana G., Tumanyan, Vladimir G., Anashkina, Anastasia A., Il’icheva, Irina A.“…In this work, we have analyzed the POL II core promoters of the precursors of lncRNAs in Homo sapiens and Mus musculus genomes. Structural analysis of nucleotide sequences in positions −50, +30 bp in relation to the TSS have shown the extremely heterogeneous 3D structure that includes two singular regions - hexanucleotide “INR” around the TSS and octanucleotide “TATA-box” at around ~−28 bp upstream. …”
Publicado 2023
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2473por Kim, Sangin, Kim, Yeongjae, Kim, Youyoung, Yoon, Suhyeon, Lee, Kyoo-young, Lee, Yoonsung, Kang, Sukhyun, Myung, Kyungjae, Oh, Chang-Kyu“…PCNA(ΔSL47) shows a defective interaction with PCNA(WT) leading to defects in homo-trimerization in vitro. PCNA(ΔSL47) is defective in the FEN1 and LIG1 interaction. …”
Publicado 2023
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2474por Winterhalter, Charles, Stevens, Daniel, Fenyk, Stepan, Pelliciari, Simone, Marchand, Elie, Soultanas, Panos, Ilangovan, Aravindan, Murray, Heath“…Systematic characterization of the essential initiation protein DnaD revealed distinct protein interfaces required for homo-oligomerization, interaction with the master initiator protein DnaA, and interaction with the helicase co-loader protein DnaB. …”
Publicado 2022
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2475“…In this work, we critically assess the linear dependence of the anodic limit from the HOMO level of 27 anions, whose performances have been experimentally investigated in the previous literature. …”
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2476“…Compared to pristine GQD model C96 (with a maximum absorption peak at 592 nm), the absorption spectra of 6 defective C96 exhibit blue shifts ranging from 554 to 591 nm, while 12 defective C96 lead to red shifts (598–668 nm). The HOMO–LUMO gaps vary from 0.62 to 2.04 eV (2.10 eV for pristine C96). …”
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2477“…OSBPs have been extensively investigated in human and yeast cells where 12 have been identified in Homo sapiens and 7 in Saccharomyces cerevisiae. The evolutionary relationship between these well-characterized OSBPs is still unclear. …”
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2478“…The energy gap (E(g)) between the highest occupied and lowest unoccupied molecular orbitals (HOMO and LUMO, respectively) of PNS remains constant after the adsorption process. …”
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2479“…Complex coacervate prepared from the series of reduced-σ polyanions and the polycation, homo-poly-l-lysine, could act as a scaffold that sequestered various globular proteins with high encapsulation efficiency (>80%), which sometimes involved further agglomerations in the coacervates. …”
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2480por Zhang, Shasha, Yang, Wenfang, Lu, Xiao, Zhang, Xinyi, Pan, Zhichao, Qu, Da-Hui, Mei, Dong, Mei, Ju, Tian, He“…Herein, three AIE-active PSs with D–π–A structures are rationally designed to realize efficient (1)O(2) generation, by reducing the electron–hole distribution overlap, enlarging the difference on the electron-cloud distribution at the HOMO and LUMO, and decreasing the ΔE(ST). The design principle has been expounded with the aid of time-dependent density functional theory (TD-DFT) calculations and the analysis of electron–hole distributions. …”
Publicado 2023
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