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Hybrid h-BN–graphene monolayer with B–C boundaries on a lattice-matched surface
Bokai, K. A., Tarasov, A. V., Shevelev, V. O., Vilkov, O. Y., Makarova, A. A., Marchenko, D., … Usachov, D. Y. (2020). Hybrid h-BN–graphene monolayer with B–C boundaries on a lattice-matched surface. Chemistry of Materials, 32(3), 1172-1181. https://doi.org/10.1021/acs.chemmater.9b04207
Identification of FAM181A and FAM181B as new interactors with the TEAD transcription factors
Bokhovchuk, F., Mesrouze, Y., Delaunay, C., Martin, T., Villard, F., Meyerhofer, M., … Chène, P. (2020). Identification of FAM181A and FAM181B as new interactors with the TEAD transcription factors. Protein Science, 29(2), 509-520. https://doi.org/10.1002/pro.3775
'Drc', a structurally novel ssDNA-binding transcription regulator of N4-related bacterial viruses
Boon, M., De Zitter, E., De Smet, J., Wagemans, J., Voet, M., Pennemann, F. L., … Lavigne, R. (2020). 'Drc', a structurally novel ssDNA-binding transcription regulator of N4-related bacterial viruses. Nucleic Acids Research, 48(1), 445-459. https://doi.org/10.1093/nar/gkz1048
Structure of <em>Drosophila melanogaster</em> ARC1 reveals a repurposed molecule with characteristics of retroviral Gag
Cottee, M. A., Letham, S. C., Young, G. R., Stoye, J. P., & Taylor, I. A. (2020). Structure of Drosophila melanogaster ARC1 reveals a repurposed molecule with characteristics of retroviral Gag. Science Advances, 6(1), eaay6354 (12 pp.). https://doi.org/10.1126/sciadv.aay6354
Hybrid histidine kinase activation by cyclic di-GMP-mediated domain liberation
Dubey, B. N., Agustoni, E., Böhm, R., Kaczmarczyk, A., Mangia, F., von Arx, C., … Schirmer, T. (2020). Hybrid histidine kinase activation by cyclic di-GMP-mediated domain liberation. Proceedings of the National Academy of Sciences of the United States of America PNAS, 117(2), 1000-1008. https://doi.org/10.1073/pnas.1911427117
Anion binding and oxidative modification at the molybdenum cofactor of formate dehydrogenase from<em> Rhodobacter capsulatus </em>studied by X-ray absorption spectroscopy
Duffus, B. R., Schrapers, P., Schuth, N., Mebs, S., Dau, H., Leimkühler, S., & Haumann, M. (2020). Anion binding and oxidative modification at the molybdenum cofactor of formate dehydrogenase from Rhodobacter capsulatus studied by X-ray absorption spectroscopy. Inorganic Chemistry, 59(1), 214-225. https://doi.org/10.1021/acs.inorgchem.9b01613
Recognition of different base tetrads by RHAU (DHX36): X-ray crystal structure of the G4 recognition motif bound to the 3′-end tetrad of a DNA G-quadruplex
Heddi, B., Cheong, V. V., Schmitt, E., Mechulam, Y., & Phan, A. T. (2020). Recognition of different base tetrads by RHAU (DHX36): X-ray crystal structure of the G4 recognition motif bound to the 3′-end tetrad of a DNA G-quadruplex. Journal of Structural Biology, 209(1), 107399 (8 pp.). https://doi.org/10.1016/j.jsb.2019.10.001
Crystal structure of the translation recovery factor Trf from <em>Sulfolobus solfataricus</em>
Kaiser, M., Wurm, J. P., Märtens, B., Bläsi, U., Pogoryelov, D., & Wöhnert, J. (2020). Crystal structure of the translation recovery factor Trf from Sulfolobus solfataricus. FEBS Open Bio, 10(2), 221-228. https://doi.org/10.1002/2211-5463.12772
Stereoselective activity of 1-propargyl-4-styrylpiperidine-like analogues that can discriminate between monoamine oxidase isoforms A and B
Knez, D., Colettis, N., Iacovino, L. G., Sova, M., Pišlar, A., Konc, J., … Gobec, S. (2020). Stereoselective activity of 1-propargyl-4-styrylpiperidine-like analogues that can discriminate between monoamine oxidase isoforms A and B. Journal of Medicinal Chemistry. https://doi.org/10.1021/acs.jmedchem.9b01886
Design, synthesis and identification of novel, orally bioavailable non-covalent Nrf2 activators
Ma, B., Lucas, B., Capacci, A., Lin, E. Y. S., Jones, J. H., Dechantsreiter, M., … Richter, K. (2020). Design, synthesis and identification of novel, orally bioavailable non-covalent Nrf2 activators. Bioorganic and Medicinal Chemistry Letters, 30(4), 126852 (8 pp.). https://doi.org/10.1016/j.bmcl.2019.126852
Ancestral-sequence reconstruction unveils the structural basis of function in mammalian FMOs
Nicoll, C. R., Bailleul, G., Fiorentini, F., Mascotti, M. L., Fraaije, M. W., & Mattevi, A. (2020). Ancestral-sequence reconstruction unveils the structural basis of function in mammalian FMOs. Nature Structural and Molecular Biology, 27(1), 14-24. https://doi.org/10.1038/s41594-019-0347-2
Examination of crystal dissolution in 3D: a way to reconcile dissolution rates in the laboratory?
Noiriel, C., Oursin, M., & Daval, D. (2020). Examination of crystal dissolution in 3D: a way to reconcile dissolution rates in the laboratory? Geochimica et Cosmochimica Acta. https://doi.org/10.1016/j.gca.2020.01.003
Comparison of orexin 1 and orexin 2 ligand binding modes using X-ray crystallography and computational analysis
Rappas, M., Ali, A. A. E., Bennett, K. A., Brown, J. D., Bucknell, S. J., Congreve, M., … Christopher, J. A. (2020). Comparison of orexin 1 and orexin 2 ligand binding modes using X-ray crystallography and computational analysis. Journal of Medicinal Chemistry. https://doi.org/10.1021/acs.jmedchem.9b01787
Clathrin's adaptor interaction sites are repurposed to stabilize microtubules during mitosis
Rondelet, A., Lin, Y. C., Singh, D., Porfetye, A. T., Thakur, H. C., Hecker, A., … Bird, A. W. (2020). Clathrin's adaptor interaction sites are repurposed to stabilize microtubules during mitosis. Journal of Cell Biology, 219(2), e201907083. https://doi.org/10.1083/jcb.201907083
Discovery of novel inhibitors of LpxC displaying potent in vitro activity against Gram-negative bacteria
Surivet, J. P., Panchaud, P., Specklin, J. L., Diethelm, S., Blumstein, A. C., Gauvin, J. C., … Rueedi, G. (2020). Discovery of novel inhibitors of LpxC displaying potent in vitro activity against Gram-negative bacteria. Journal of Medicinal Chemistry, 63(1), 66-87. https://doi.org/10.1021/acs.jmedchem.9b01604
<em>In situ</em> oxidation studies of Cu thin films: growth kinetics and oxide phase evolution
Unutulmazsoy, Y., Cancellieri, C., Chiodi, M., Siol, S., Lin, L., & Jeurgens, L. P. H. (2020). In situ oxidation studies of Cu thin films: growth kinetics and oxide phase evolution. Journal of Applied Physics, 127(6), 065101 (11 pp.). https://doi.org/10.1063/1.5131516
Thallium stable isotope ratios in naturally Tl-rich soils
Vaněk, A., Voegelin, A., Mihaljevič, M., Ettler, V., Trubač, J., Drahota, P., … Holubík, O. (2020). Thallium stable isotope ratios in naturally Tl-rich soils. Geoderma, 364, 114183 (7 pp.). https://doi.org/10.1016/j.geoderma.2020.114183
Conformational changes in apolipoprotein N-acyltransferase (Lnt)
Wiseman, B., & Högbom, M. (2020). Conformational changes in apolipoprotein N-acyltransferase (Lnt). Scientific Reports, 10(1), 639 (11 pp.). https://doi.org/10.1038/s41598-020-57419-7
Flexible fragment growing boosts potency of quorum-sensing inhibitors against <em>Pseudomonas aeruginosa </em>virulence
Zender, M., Witzgall, F., Kiefer, A., Kirsch, B., Maurer, C. K., Kany, A. M., … Empting, M. (2020). Flexible fragment growing boosts potency of quorum-sensing inhibitors against Pseudomonas aeruginosa virulence. ChemMedChem, 15(2), 188-194. https://doi.org/10.1002/cmdc.201900621
Discovery and optimization of heteroaryl piperazines as potent and selective PI3Kδ inhibitors
Zhou, H., McGowan, M. A., Lipford, K., Christopher, M., Fradera, X., Witter, D., … Katz, J. D. (2020). Discovery and optimization of heteroaryl piperazines as potent and selective PI3Kδ inhibitors. Bioorganic and Medicinal Chemistry Letters, 30(1), 126715 (8 pp.). https://doi.org/10.1016/j.bmcl.2019.126715
 

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