Artykuły w czasopismach: „Chautauqua Assembly (N.Y.)”

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ANITA C. DANKER. "“Redeeming the Time”: Learning Vacations at the New England Chautauqua Assembly". Massachusetts Historical Review 17 (2015): 67. http://dx.doi.org/10.5224/masshistrevi.17.1.0067.

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Dawe, Louise N., Konstantin V. Shuvaev i Laurence K. Thompson. "Magnetic [n×n] (n= 2−5) Grids by Directed Self-Assembly". Inorganic Chemistry 48, nr 8 (20.04.2009): 3323–41. http://dx.doi.org/10.1021/ic801078h.

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Ashton, Peter R., Douglas Philip, Neil Spencer i J. Fraser Stoddart. "The self-assembly of [n]pseudorotaxanes". Journal of the Chemical Society, Chemical Communications, nr 23 (1991): 1677. http://dx.doi.org/10.1039/c39910001677.

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Xu, Wei, i Jian-Li Lin. "Dichloridobis(1,10-phenanthroline-κ2 N,N′)tungsten(II)". Acta Crystallographica Section E Structure Reports Online 63, nr 3 (28.02.2007): m859—m861. http://dx.doi.org/10.1107/s1600536807008148.

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In the title compound, [WCl2(C12H8N2)2], the W atom has a distorted six-coordinate octahedral geometry. There are some π–π stacking interactions in the structure, which are responsible for the supramolecular assembly.

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Singh, Pushpendra, Harkesh B. Singh i Ray J. Butcher. "{N 1-[2-(Butylselanyl)benzyl]-N 2,N 2-dimethylethane-1,2-diamine}dichloridomercury(II)". Acta Crystallographica Section E Crystallographic Communications 74, nr 8 (27.07.2018): 1151–54. http://dx.doi.org/10.1107/s2056989018010423.

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In the title compound, [HgCl2(C16H28N2Se)], the primary geometry around the Se and Hg atoms is distorted trigonal–pyramidal and distorted square-pyramidal, respectively. The distortion of the molecular geometry in the complex is caused by the steric demands of the ligands attached to the Se atom. The Hg atom is coordinated through two chloride anions, an N atom and an Se atom, making up an unusual HgNSeCl2 coordination sphere with an additional long Hg...N interaction. Intermolecular C—H...Cl interactions are the only identified intermolecular hydrogen-bonding interactions that seem to be responsible for the self assembly. These relatively weak C—H...Cl hydrogen bonds possess the required linearity and donor–acceptor distances. They act as molecular associative forces that result in a supramolecular assembly along the b-axis direction in the solid state of the title compound.

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Jia, Qianfa, i Jian Wang. "N-Heterocyclic Carbene-Catalyzed Convenient Benzonitrile Assembly". Organic Letters 18, nr 9 (15.04.2016): 2212–15. http://dx.doi.org/10.1021/acs.orglett.6b00844.

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Kerékgyártó, János, László Kalmár, Zoltán Szurmai, Orsolya Hegyi i Gábor K. Tóth. "Synthesis of N-Glycopeptides by Convergent Assembly". International Journal of Peptide Research and Therapeutics 18, nr 1 (27.09.2011): 1–5. http://dx.doi.org/10.1007/s10989-011-9271-y.

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BELOHRADSKY, M., D. PHILP, F. M. RAYMO i J. F. STODDART. "ChemInform Abstract: Self-Assembly of (n)Rotaxanes". ChemInform 26, nr 43 (17.08.2010): no. http://dx.doi.org/10.1002/chin.199543297.

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Lavine, M. S. "Nonequilibrium transient self-assembly". Science 349, nr 6252 (3.09.2015): 1066–68. http://dx.doi.org/10.1126/science.349.6252.1066-n.

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Zhou, Qi-hua, Zhi-yun Li, Hua-qing Liang, Yong-jiang Long, Qing Wu, Hai-yang Gao, Guo-dong Liang i Fang-ming Zhu. "Crystallization-driven self-assembly of isotactic polystyrene in N, N-dimethylformamide". Chinese Journal of Polymer Science 33, nr 4 (11.02.2015): 646–51. http://dx.doi.org/10.1007/s10118-015-1615-1.

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Isaia, Francesco, M. Carla Aragoni, Massimiliano Arca, Francesco Demartin, Francesco A. Devillanova, Guido Ennas, Alessandra Garau, Vito Lippolis, Annalisa Mancini i Gaetano Verani. "Molecular Iodine Stabilization in an Extended N···I-I···N Assembly". European Journal of Inorganic Chemistry 2009, nr 24 (sierpień 2009): 3667–72. http://dx.doi.org/10.1002/ejic.200900429.

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Dos Santos, Patricia C., Archer D. Smith, Jeverson Frazzon, Valerie L. Cash, Michael K. Johnson i Dennis R. Dean. "Iron-Sulfur Cluster Assembly". Journal of Biological Chemistry 279, nr 19 (1.03.2004): 19705–11. http://dx.doi.org/10.1074/jbc.m400278200.

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The NifU protein is a homodimer that is proposed to provide a molecular scaffold for the assembly of [Fe-S] clusters uniquely destined for the maturation of the nitrogenase catalytic components. There are three domains contained within NifU, with the N-terminal domain exhibiting a high degree of primary sequence similarity to a related family of [Fe-S] cluster biosynthetic scaffolds designated IscU. The C-terminal domain of NifU exhibits sequence similarity to a second family of proposed [Fe-S] cluster biosynthetic scaffolds designated Nfu. Genetic experiments described here involving amino acid substitutions within the N-terminal and C-terminal domains of NifU indicate that both domains can separately participate in nitrogenase-specific [Fe-S] cluster formation, although the N-terminal domain appears to have the dominant function. Thesein vivoexperiments were supported byin vitro[Fe-S] cluster assembly and transfer experiments involving the activation of an apo-form of the nitrogenase Fe protein.

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Mathias, Jenny-Lee, Himanshu Arora, Ronit Lavi, Hervé Vezin, Dmitry Yufit, Maylis Orio, Núria Aliaga-Alcade i Laurent Benisvy. "Redox-switchable tetra-copper assembly of N,N-, N,O-phenolate-phenanthroimidazolate bridging ligands". Dalton Transactions 42, nr 7 (2013): 2358. http://dx.doi.org/10.1039/c2dt32585c.

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Pham, Chien Thang, Maximilian Roca Jungfer i Ulrich Abram. "Indium(iii) {2}-metallacryptates assembled from 2,6-dipicolinoyl-bis(N,N-diethylthiourea)". New Journal of Chemistry 44, nr 9 (2020): 3672–80. http://dx.doi.org/10.1039/c9nj06420f.

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Łukaszyk, Szymon, i Wawrzyniec Bieniawski. "Assembly Theory of Binary Messages". Mathematics 12, nr 10 (20.05.2024): 1600. http://dx.doi.org/10.3390/math12101600.

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Using assembly theory, we investigate the assembly pathways of binary strings (bitstrings) of length N formed by joining bits present in the assembly pool and the bitstrings that entered the pool as a result of previous joining operations. We show that the bitstring assembly index is bounded from below by the shortest addition chain for N, and we conjecture about the form of the upper bound. We define the degree of causation for the minimum assembly index and show that, for certain N values, it has regularities that can be used to determine the length of the shortest addition chain for N. We show that a bitstring with the smallest assembly index for N can be assembled via a binary program of a length equal to this index if the length of this bitstring is expressible as a product of Fibonacci numbers. Knowing that the problem of determining the assembly index is at least NP-complete, we conjecture that this problem is NP-complete, while the problem of creating the bitstring so that it would have a predetermined largest assembly index is NP-hard. The proof of this conjecture would imply P ≠ NP since every computable problem and every computable solution can be encoded as a finite bitstring. The lower bound on the bitstring assembly index implies a creative path and an optimization path of the evolution of information, where only the latter is available to Turing machines (artificial intelligence). Furthermore, the upper bound hints at the role of dissipative structures and collective, in particular human, intelligence in this evolution.

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Dai, Lin-Xiu, Xin-Yu Wang, Xiao-Yu Zheng i Ya-Wen Zhang. "Pt and Pt–Rh supercrystals self-assembled in N,N-dimethylformamide". Chemical Communications 52, nr 28 (2016): 5023–26. http://dx.doi.org/10.1039/c6cc01110a.

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N,N-Dimethylformamide (DMF) serves as the facet-specific agent for the formation of a cubic shape and the structure-directing agent for the self-assembly of Pt and Pt–Rh building blocks of the supercrystals.

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Govindarajan, Rajgopal, Souvik Chakraborty, Kristen E. Johnson, Matthias M. Falk, Margaret J. Wheelock, Keith R. Johnson i Parmender P. Mehta. "Assembly of Connexin43 into Gap Junctions Is Regulated Differentially by E-Cadherin and N-Cadherin in Rat Liver Epithelial Cells". Molecular Biology of the Cell 21, nr 23 (grudzień 2010): 4089–107. http://dx.doi.org/10.1091/mbc.e10-05-0403.

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Cadherins have been thought to facilitate the assembly of connexins (Cxs) into gap junctions (GJs) by enhancing cell–cell contact, however the molecular mechanisms involved in this process have remained unexplored. We examined the assembly of GJs composed of Cx43 in isogenic clones derived from immortalized and nontransformed rat liver epithelial cells that expressed either epithelial cadherin (E-Cad), which curbs the malignant behavior of tumor cells, or neuronal cadherin (N-Cad), which augments the invasive and motile behavior of tumor cells. We found that N-cad expression attenuated the assembly of Cx43 into GJs, whereas E-Cad expression facilitated the assembly. The expression of N-Cad inhibited GJ assembly by causing endocytosis of Cx43 via a nonclathrin-dependent pathway. Knock down of N-Cad by ShRNA restored GJ assembly. When both cadherins were simultaneously expressed in the same cell type, GJ assembly and disassembly occurred concurrently. Our findings demonstrate that E-Cad and N-Cad have opposite effects on the assembly of Cx43 into GJs in rat liver epithelial cells. These findings imply that GJ assembly and disassembly are the down-stream targets of the signaling initiated by E-Cad and N-Cad, respectively, and may provide one possible explanation for the disparate role played by these cadherins in regulating cell motility and invasion during tumor progression and invasion.

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McIlhinney, R. A. J., E. Philipps, B. Le Bourdelles, S. Grimwood, K. Wafford, S. Sandhu i P. Whiting. "Assembly of N-methyl-d-aspartate (NMDA) receptors". Biochemical Society Transactions 31, nr 4 (1.08.2003): 865–68. http://dx.doi.org/10.1042/bst0310865.

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The N-methyl-d-aspartate receptor (NMDAR) requires both NR1 and NR2 subunits to form a functional ion channel. Despite the recent advances in our understanding of the contributions of these different subunits to both the function and pharmacology of the NMDAR, the precise subunit stoichiometry of the receptor and the regions of the subunits governing subunit interactions remain unclear. Since NR2 subunits are not transported to the cell surface unless they associate with NR1 subunits, cell-surface expression of NR2A can be used to monitor the association of the different subunits in cells transfected with N- and C-terminally truncated NR1 subunits. By combining measurements of cell-surface expression of NR2A with co-immunoprecipitation experiments, and by using Blue Native gel electrophoresis to determine the oligomerization status of the subunits, we have shown that regions of the N-terminus of NR1 are critical for subunit association, whereas the truncation of the C-terminus of NR1 before the last transmembrane region has no effect on the association of the subunits. Evidence from the Blue Native gels, sucrose-gradient centrifugation and size exclusion of soluble NR1 domains suggests that NR1 subunits alone can form stable dimers. Using a cell line, which can be induced to express the NMDAR following exposure to dexamethasone, we have shown that NMDARs can be expressed at the cell surface within 5 h of the recombinant gene induction, and that there appears to be a delay between the first appearance of the subunits and their stable association.

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Nayak, Prakash S., Jerry P. Jasinski, James A. Golen, Badiadka Narayana, Manpreet Kaur, Hemmige S. Yathirajan i Christopher Glidewell. "HalogenatedC,N-diarylacetamides: molecular conformations and supramolecular assembly". Acta Crystallographica Section C Structural Chemistry 70, nr 9 (23.08.2014): 889–94. http://dx.doi.org/10.1107/s2053229614018713.

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The structures of four halogenatedN,2-diarylacetamides are reported and compared with a range of analogues.N-(4-Chloro-3-methylphenyl)-2-phenylacetamide, C15H14ClNO, (I), andN-(4-bromo-3-methylphenyl)-2-phenylacetamide, C15H14BrNO, (II), are isostructural in the space groupP\overline{1}. The molecules of (I) and (II) are linked into chains of rings by a combination of N—H...O and C—H...π(arene) hydrogen bonds. The molecules ofN-(4-chloro-3-methylphenyl)-2-(2,4-dichlorophenyl)acetamide, C15H12Cl3NO, (III), andN-(4-bromo-3-methylphenyl)-2-(2-chlorophenyl)acetamide, C15H13BrClNO, (IV), are linked into simpleC(4) chains by N—H...O hydrogen bonds, but significant C—H...π(arene) interactions are absent. TheN-aryl groups in compounds (III) and (IV) adopt a different orientation, byca180°, from that of the corresponding groups in compounds (I) and (II), but otherwise the conformations of (I)–(IV) are very similar. Comparisons are drawn between compounds (I) and (IV) and a range of analogues of the typeR1CH2CONHR2, whereR2represents a halogenated aryl ring andR1represents either another halogenated aryl ring or a naphthalen-1-yl unit.

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Kovacs, E. M. "Tuba stimulates intracellular N-WASP-dependent actin assembly". Journal of Cell Science 119, nr 13 (6.06.2006): 2715–26. http://dx.doi.org/10.1242/jcs.03005.

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Amabilino, David B., Peter R. Ashton, Christopher L. Brown, Emilio Cordova, Luis A. Godinez, Timothy T. Goodnow, Angel E. Kaifer, Simon P. Newton i Marek Pietraszkiewicz. "Molecular Meccano. 2. Self-Assembly of [n]Catenanes". Journal of the American Chemical Society 117, nr 4 (luty 1995): 1271–93. http://dx.doi.org/10.1021/ja00109a011.

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Terranova, M. L., D. Manno, M. Rossi, A. Serra, E. Filippo, S. Orlanducci i E. Tamburri. "Self-Assembly of n-Diamond Nanocrystals Into Supercrystals". Crystal Growth & Design 9, nr 3 (4.03.2009): 1245–49. http://dx.doi.org/10.1021/cg800352n.

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Amabilino, David B., Peter R. Ashton, Vincenzo Balzani, Christopher L. Brown, Alberto Credi, Jean M. J. Fréchet, Jeffrey W. Leon i in. "Self-Assembly of [n]Rotaxanes Bearing Dendritic Stoppers⊥". Journal of the American Chemical Society 118, nr 48 (styczeń 1996): 12012–20. http://dx.doi.org/10.1021/ja962113h.

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Zhu, Aiping, Yan Lu, Yingnan Pan, Sheng Dai i Hao Wu. "Self-assembly of N-maleoylchitosan in aqueous media". Colloids and Surfaces B: Biointerfaces 76, nr 1 (marzec 2010): 221–25. http://dx.doi.org/10.1016/j.colsurfb.2009.10.040.

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Jiao, Tianyu, Guangcheng Wu, Yang Zhang, Libo Shen, Ye Lei, Cai‐Yun Wang, Albert C. Fahrenbach i Hao Li. "Self‐Assembly in Water with N‐Substituted Imines". Angewandte Chemie International Edition 59, nr 42 (3.06.2020): 18350–67. http://dx.doi.org/10.1002/anie.201910739.

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Shao, Hui, James Seifert, Natalie C. Romano, Min Gao, Jonathan J. Helmus, Christopher P. Jaroniec, David A. Modarelli i Jon R. Parquette. "Amphiphilic Self-Assembly of an n-Type Nanotube". Angewandte Chemie International Edition 49, nr 42 (6.09.2010): 7688–91. http://dx.doi.org/10.1002/anie.201003415.

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Chen, Zhongrui, Rose Haddoub, Jérôme Mahé, Gabriel Marchand, Denis Jacquemin, Judicaelle Andeme Edzang, Gabriel Canard i in. "N-Substituted Azacalixphyrins: Synthesis, Properties, and Self-Assembly". Chemistry - A European Journal 22, nr 49 (11.10.2016): 17820–32. http://dx.doi.org/10.1002/chem.201602288.

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Shao, Hui, James Seifert, Natalie C. Romano, Min Gao, Jonathan J. Helmus, Christopher P. Jaroniec, David A. Modarelli i Jon R. Parquette. "Amphiphilic Self-Assembly of an n-Type Nanotube". Angewandte Chemie 122, nr 42 (6.09.2010): 7854–57. http://dx.doi.org/10.1002/ange.201003415.

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Krekić, Kristijan, Natascha F. Hurkes, Clemens Bruhn, Ferdinand Belaj i Rudolf Pietschnig. "Silanol Mediated π-Assembly of Extended N-Heterocycles". Zeitschrift für anorganische und allgemeine Chemie 642, nr 4 (luty 2016): 302–5. http://dx.doi.org/10.1002/zaac.201500816.

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He, Jin Hua, Cui Hua Li, Lian An Qian, Jian Hong Liu i Qian Ling Zhang. "Self-Assembly Behavior of N-Methly-N-Hexadecyl-Pyrrolidinium Bromide in Water". Advanced Materials Research 557-559 (lipiec 2012): 611–14. http://dx.doi.org/10.4028/www.scientific.net/amr.557-559.611.

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N-methyl-N-hexadecylpyrrolidinium bromide (IL) was synthesized for the design of ionic liquid crystals which is a fascinating class of molecular materials, offering the combination of order and mobility. In binary mixtures with water, lyotropic liquid crystalline phase appears in the range of IL content from 35% to 70% and the temperature range from -1.1 to 24 °C in the heating run. The SAXS curves explored the self-assembly processes and hexagonal phase of the IL apparent sol. The saturated aliphatic ionic liquid in water assemble less tightly compared with aromatic ionic liquid based on imidazolium in water, which is due to the absence of aromatic package effect.

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Bertolasi, Valerio, Paola Gilli, Valeria Ferretti, Gastone Gilli i Cristina Fernàndez-Castaño. "Self-assembly of NH-pyrazoles via intermolecular N—H...N hydrogen bonds". Acta Crystallographica Section B Structural Science 55, nr 6 (1.12.1999): 985–93. http://dx.doi.org/10.1107/s0108768199004966.

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The crystal structures of two NH-pyrazole derivatives forming intermolecular N—H...N hydrogen bonds are reported: 5-methyl-4-(3-methylpyrazol-5-yl)pyrazol-3-ol, C8H10N4O (P1), and 3-methyl-5-dihydro-1H-naphtho[1,2-d]pyrazole hemihydrochloride, C12H12N2.-C12H13N_{2}^{+}.Cl− (P2). 26 other structures are surveyed in order to obtain a deeper insight into the ways NH-pyrazoles self-assemble by means of intermolecular N—H...N hydrogen bonds in molecular crystals. A limited number of compounds form chains or dimers via homonuclear N+—H...N positive-charge-assisted hydrogen bonds, typical of proton sponges, which can be remarkably short [e.g. N...N 2.714 (3), N—H 1.09 (3), H...N 1.63 (3) Å, N—H...N 169 (3)° in (P2)]. Most pyrazoles, however, pack via neutral N—H...N bonds which are formally assisted by resonance (resonance-assisted hydrogen bond, RAHB) through the ...N=C—C=C—NH... iminoenamine fragment, contained in the ring, giving rise to dimers, trimers, tetramers and infinite chains of pyrazole molecules. Surprisingly, the resonance does not appear to shorten the N—H...N bond with respect to the accepted mean value N...N 2.97 (10) Å for non-resonant N—H...N bonds. It is shown that this is due to the internal π-delocalization of the pyrazole ring, which can be hardly increased by the hydrogen-bond interaction, except in symmetrically 3,5-substituted pyrazoles which display N...N distances as short as 2.82 Å, identical C—C and C—N distances in the two halves of the pyrazole molecule, and typical phenomena of N—H...N dynamical proton disorder, detectable by 15N-CP/MAS solid-state NMR.

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Vincent, Séverine, Denis Gerlier i Serge N. Manié. "Measles Virus Assembly within Membrane Rafts". Journal of Virology 74, nr 21 (1.11.2000): 9911–15. http://dx.doi.org/10.1128/jvi.74.21.9911-9915.2000.

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ABSTRACT During measles virus (MV) replication, approximately half of the internal M and N proteins, together with envelope H and F glycoproteins, are selectively enriched in microdomains rich in cholesterol and sphingolipids called membrane rafts. Rafts isolated from MV-infected cells after cold Triton X-100 solubilization and flotation in a sucrose gradient contain all MV components and are infectious. Furthermore, the H and F glycoproteins from released virus are also partly in membrane rafts (S. N. Manié et al., J. Virol. 74:305–311, 2000). When expressed alone, the M but not N protein shows a low partitioning (around 10%) into rafts; this distribution is unchanged when all of the internal proteins, M, N, P, and L, are coexpressed. After infection with MGV, a chimeric MV where both H and F proteins have been replaced by vesicular stomatitis virus G protein, both the M and N proteins were found enriched in membrane rafts, whereas the G protein was not. These data suggest that assembly of internal MV proteins into rafts requires the presence of the MV genome. The F but not H glycoprotein has the intrinsic ability to be localized in rafts. When coexpressed with F, the H glycoprotein is dragged into the rafts. This is not observed following coexpression of either the M or N protein. We propose a model for MV assembly into membrane rafts where the virus envelope and the ribonucleoparticle colocalize and associate.

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Lanman, Jason, Jennifer Sexton, Michael Sakalian i Peter E. Prevelige,. "Kinetic Analysis of the Role of Intersubunit Interactions in Human Immunodeficiency Virus Type 1 Capsid Protein Assembly In Vitro". Journal of Virology 76, nr 14 (15.07.2002): 6900–6908. http://dx.doi.org/10.1128/jvi.76.14.6900-6908.2002.

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ABSTRACT The human immunodeficiency virus type 1 (HIV-1) capsid protein (CA) plays a crucial role in both assembly and maturation of the virion. Numerous recent studies have focused on either the soluble form of CA or the polymer end product of in vitro CA assembly. The CA polymer, in particular, has been used to study CA-CA interactions because it is a good model for the CA interactions within the virion core. However, analysis of the process of in vitro CA assembly can yield valuable insights into CA-CA interactions and the mechanism of core assembly. We describe here a method for the analysis of CA assembly kinetics wherein the progress of assembly is monitored by using turbidity. At pH 7.0 the addition of either of the isolated CA domains (i.e., the N or the C domain) to an assembly reaction caused a decrease in the assembly rate by competing for binding to the full-length CA protein. At pH 8.0 the addition of the isolated C domain had a similar inhibitory affect on CA assembly. However, at pH 8.0 the isolated N domain had no affect on the rate of CA assembly but, when mixed with the C domain, it alleviated the C-domain inhibition. These data provide biochemical evidence for a pH-sensitive homotypic N-domain interaction, as well as for an N- and C-domain interaction.

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Meddows, Elisabeth, Beatrice LeBourdellès, Paul J. Whiting i R. A. Jeffrey McIlhinney. "Identification of determinants important for the assembly of N-methyl-D-aspartate (NMDA) receptor assembly". Biochemical Society Transactions 27, nr 3 (1.06.1999): A119. http://dx.doi.org/10.1042/bst027a119a.

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Gao, Yang, Jianhong Nie, Yanping Huo i Xiao-Qiang Hu. "Anthranils: versatile building blocks in the construction of C–N bonds and N-heterocycles". Organic Chemistry Frontiers 7, nr 9 (2020): 1177–96. http://dx.doi.org/10.1039/d0qo00163e.

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This review article provides an overview of the recent progress in the transformations of anthranils, which have emerged as versatile building blocks in the assembly of various C–N bonds and medicinally active heterocyclic systems.

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Zábranský, Aleš, Peter Hoboth, Romana Hadravová, Jitka Štokrová, Michael Sakalian i Iva Pichová. "The Noncanonical Gag Domains p8 and n Are Critical for Assembly and Release of Mouse Mammary Tumor Virus". Journal of Virology 84, nr 21 (25.08.2010): 11555–59. http://dx.doi.org/10.1128/jvi.00652-10.

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ABSTRACT The mouse mammary tumor virus (MMTV) Gag contains the unique domains pp21, p3, p8, and n. We investigated the contribution of these domains to particle assembly and found that the region spanning the p8 and n domains is critical for shape determination and assembly. Deletion of pp21 and p3 reduced the number of released particles, but deletion of the n domain resulted in frequent formation of aberrant particles, while deletion of p8 severely impaired assembly. Further investigation of p8 revealed that both the basic and the proline-rich motifs within p8 contribute to MMTV assembly.

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Dawe, Louise N., Konstantin V. Shuvaev i Laurence K. Thompson. "Polytopic ligand directed self-assembly—polymetallic [n×n] grids versus non-grid oligomers". Chemical Society Reviews 38, nr 8 (2009): 2334. http://dx.doi.org/10.1039/b807219c.

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Pardin, Christophe, Loïc Leclercq i Andreea R Schmitzer. "N,N′-Methylenediimidazolium Salts: From Self-Assembly to an Efficient DNAse Protection System". Chemistry - A European Journal 16, nr 15 (19.04.2010): 4686–92. http://dx.doi.org/10.1002/chem.200902794.

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Khimani, M., S. Yusa, A. Nagae, R. Enomoto, V. K. Aswal, E. Kesselman, D. Danino i P. Bahadur. "Self-assembly of multi-responsive poly(N-isopropylacrylamide)-b-poly(N,N-dimethylaminopropylacrylamide) in aqueous media". European Polymer Journal 69 (sierpień 2015): 96–109. http://dx.doi.org/10.1016/j.eurpolymj.2015.05.027.

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Chen, Gong-Jun, Feng-Xian Gao, Fu-Ping Huang, Jin-Lei Tian, Wen Gu, Xin Liu, Shi-Ping Yan i Dai-Zheng Liao. "Sodium-Mediated Self-Assembly: Three Novel 2D Coordination Aggregates of 1,4,7-Triazacyclononane-N,N′,N′′-tripropionate". Crystal Growth & Design 9, nr 6 (3.06.2009): 2662–67. http://dx.doi.org/10.1021/cg801227e.

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Wu, Jincheng, Liang Zhao, Dexian Wang i Meixiang Wang. "Synthesis, Structure and Coordination Self-Assembly of Azacalix[4-n]pyridine[n]pyrazines (n=1-3)". Chinese Journal of Chemistry 31, nr 5 (3.04.2013): 589–97. http://dx.doi.org/10.1002/cjoc.201300078.

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Lu, Cong, Deng-Sheng Huo i Zi-Yue Wang. "Assembly variation analysis of the aircraft panel in multi-stage assembly process with N-2-1 locating scheme". Proceedings of the Institution of Mechanical Engineers, Part C: Journal of Mechanical Engineering Science 233, nr 19-20 (13.08.2019): 6754–73. http://dx.doi.org/10.1177/0954406219869040.

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The flexible aircraft panel parts are easy to deform during the assembly process, the deformation can directly affect the assembly accuracy of the aircraft panel, and further affect the assembly quality of the aircraft fuselage. In order to evaluate the assembly accuracy of the aircraft panel in multi-stage assembly process with N-2-1 locating scheme, this paper proposes an assembly variation analyzing approach, considering the effect of the contact force between the panel skin and the fixture components on the deformation of the panel in the assembly process. The mathematical models are established to conclude the contact force between the panel skin and the fixture components in multi-stage assembly process of the panel with N-2-1 locating scheme, and the effect of the contact force between the skin and the fixture components on the deformation of the panel in assembly is investigated. An assembly variation model is built for the aircraft panel considering the variation sources including the manufacturing error of the flexible panel parts, fixture error, and the deformation of the panel in multi-stage assembly process considering the effect of the contact force. Finally, the proposed assembly variation analyzing approach for the aircraft panel is tested with a case study.

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Banach, Ewa, Christian Invernizzi, Mathieu Baudin, Reinhard Neier i Diego Carnevale. "Columnar self-assembly of N,N′,N′′-trihexylbenzene-1,3,5-tricarboxamides investigated by means of NMR spectroscopy and computational methods in solution and the solid state". Physical Chemistry Chemical Physics 19, nr 7 (2017): 5525–39. http://dx.doi.org/10.1039/c6cp05598b.

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Feng, Ya-Xiong, Tong Li, Stephen Campbell i Alan Rein. "Reversible Binding of Recombinant Human Immunodeficiency Virus Type 1 Gag Protein to Nucleic Acids in Virus-Like Particle Assembly In Vitro". Journal of Virology 76, nr 22 (15.11.2002): 11757–62. http://dx.doi.org/10.1128/jvi.76.22.11757-11762.2002.

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ABSTRACT Recombinant human immunodeficiency virus type 1 (HIV-1) Gag protein can assemble into virus-like particles (VLPs) in suitable buffer conditions with nucleic acid. We have explored the role of nucleic acid in this assembly process. HIV-1 nucleocapsid protein, a domain of Gag, can bind to oligodeoxynucleotides with the sequence d(TG)n with more salt resistance than to d(A)n oligonucleotides. We found that assembly of VLPs on d(TG)n oligonucleotides was more salt resistant than assembly on d(A)n; thus, the oligonucleotides do not simply neutralize basic residues in Gag but provide a binding surface upon which Gag molecules assemble into VLPs. We also found that Gag molecules could be “trapped” on internal d(TG)n sequences within 40-base oligonucleotides, rendering them unable to take part in assembly. Thus, assembly on oligonucleotides requires that Gag proteins bind near the ends of the nucleic acid, and binding of Gag to internal d(TG)n sequences is apparently cooperative. Finally, we showed that nucleic acids in VLPs can exchange with nucleic acids in solution; there is a hierarchy of preferences in these exchange reactions. The results are consistent with an equilibrium model of in vitro assembly and may help to explain how Gag molecules in vivo select genomic RNA despite the presence in the cell of a vast excess of cellular mRNA molecules.

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Gong, Bing, Chong Zheng, Huaqiang Zeng i Jin Zhu. "Polar Assembly ofN,N‘-Bis(4-substituted benzyl)sulfamides". Journal of the American Chemical Society 121, nr 41 (październik 1999): 9766–67. http://dx.doi.org/10.1021/ja992432j.

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Lin, Ya-Fan, Chih-Hsun Liu, Chung-Hao Hu i Ching-Wen Chiu. "Non-chelating polydentate N-heterocyclic carbenes through assembly approaches". Phosphorus, Sulfur, and Silicon and the Related Elements 191, nr 4 (2.04.2016): 613–17. http://dx.doi.org/10.1080/10426507.2015.1128918.

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Yin, Zhenming, Yanhua Zhang, Jiaqi He i Jin-Pei Cheng. "Hydrogen bond assisted helical self-assembly into [n]catenane". Chemical Communications, nr 25 (2007): 2599. http://dx.doi.org/10.1039/b703591h.

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Morimoto, Nobuyuki, Françoise M. Winnik i Kazunari Akiyoshi. "Botryoidal Assembly of Cholesteryl−Pullulan/Poly(N-isopropylacrylamide) Nanogels†". Langmuir 23, nr 1 (styczeń 2007): 217–23. http://dx.doi.org/10.1021/la0616045.

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Jin, Seon-Pil, Jang-Hee Oh, Eun Young Seo i Jin Ho Chung. "N-glycosylation in desmoglein is required for desmosome assembly". Journal of Dermatological Science 84, nr 1 (październik 2016): e134. http://dx.doi.org/10.1016/j.jdermsci.2016.08.400.

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Ashton, Peter R., Roberto Ballardini, Vincenzo Balzani, Martin Bělohradský, Maria Teresa Gandolfi, Douglas Philp, Luca Prodi i in. "Self-Assembly, Spectroscopic, and Electrochemical Properties of [n]Rotaxanes1". Journal of the American Chemical Society 118, nr 21 (styczeń 1996): 4931–51. http://dx.doi.org/10.1021/ja954334d.

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