Evolutionary accessibility of mutational pathways von Franke, Jasper, Klözer, Alexander, de Visser, J Arjan G M, Krug, Joachim

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Initial mutations direct alternative pathways of protein evolution von Salverda, Merijn L M, Dellus, Eynat, Gorter, Florien A, Debets, Alfons J M, van der Oost, John, Hoekstra, Rolf F, Tawfik, Dan S, de Visser, J Arjan G M

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Nanowire sensors monitor bacterial growth kinetics and response to antibiotics von Ibarlucea, B, Rim, T, Baek, C. K, de Visser, J. A. G. M, Baraban, L, Cuniberti, G

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The evolution of sex: empirical insights into the roles of epistasis and drift von de Visser, J. Arjan G. M, Elena, Santiago F

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RYR1-related myopathies: a wide spectrum of phenotypes throughout life von Snoeck, M., van Engelen, B. G. M., Küsters, B., Lammens, M., Meijer, R., Molenaar, J. P. F., Raaphorst, J., Verschuuren-Bemelmans, C. C., Straathof, C. S. M., Sie, L. T. L., de Coo, I. F., van der Pol, W. L., de Visser, M., Scheffer, H., Treves, S., Jungbluth, H., Voermans, N. C., Kamsteeg, E.-J.

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Quantifying the adaptive potential of an antibiotic resistance enzyme von Schenk, Martijn F, Szendro, Ivan G, Krug, Joachim, de Visser, J Arjan G M

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PERSPECTIVE:EVOLUTION AND DETECTION OF GENETIC ROBUSTNESS von de Visser, J. Arjan G M, Hermisson, Joachim, Wagner, Günter P, Meyers, Lauren Ancel, Bagheri-Chaichian, Homayoun, Blanchard, Jeffrey L, Chao, Lin, Cheverud, James M, Elena, Santiago F, Fontana, Walter, Gibson, Greg, Hansen, Thomas F, Krakauer, David, Lewontin, Richard C, Ofria, Charles, Rice, Sean H, von Dassow, George, Wagner, Andreas, Whitlock, Michael C

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Lineage Tracking for Probing Heritable Phenotypes at Single-Cell Resolution von Cottinet, Denis, Condamine, Florence, Bremond, Nicolas, Griffiths, Andrew D, Rainey, Paul B, de Visser, J Arjan G M, Baudry, Jean, Bibette, Jérôme

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Responsiveness and meaningful thresholds of PROMIS pain interference, fatigue, and physical function forms in adults with idiopathic inflammatory myopathies: Report from the OMERAC... von Saygin, D, DiRenzo, D, Raaphorst, J, de Groot, I, Bingham, C O, Lundberg, I E, Regardt, M, Sarver, C, de Visser, M, Maxwell, L J, Beaton, D, Kim, J Y, Needham, M, Alexanderson, H, Christopher-Stine, L, Mecoli, C A, Park, J K

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causes of epistasis von de Visser, J. Arjan G. M, Cooper, Tim F, Elena, Santiago F

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Natural evolution of TEM-1 β-lactamase: experimental reconstruction and clinical relevance von Salverda, Merijn L.M, de Visser, J. Arjan G.M, Barlow, Miriam

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High-Throughput Gel Microbeads as Incubators for Bacterial Competition Study von Nguyen-Le, Trang Anh, Zhao, Xinne, Bachmann, Michael, Ruelens, Philip, Visser, J Arjan G M de, Baraban, Larysa

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Power provides protection: Genetic robustness in yeast depends on the capacity to generate energy von Plech, Marcin, Tomala, Katarzyna, Tutaj, Hanna, Piwcewicz, Dominika Ewa, de Visser, J Arjan G M, Korona, Ryszard

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Effect of donor-recipient relatedness on the plasmid conjugation frequency: a meta-analysis von Alderliesten, Jesse B, Duxbury, Sarah J N, Zwart, Mark P, de Visser, J Arjan G M, Stegeman, Arjan, Fischer, Egil A J

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Local and systemic inflammatory lipid profiling in a rat model of osteoarthritis with metabolic dysregulation von de Visser, H M, Mastbergen, S C, Ravipati, S, Welsing, P M J, Pinto, F C, Lafeber, F P J G, Chapman, V, Barrett, D A, Weinans, H

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Controlled release of celecoxib inhibits inflammation, bone cysts and osteophyte formation in a preclinical model of osteoarthritis von Tellegen, A. R., Rudnik-Jansen, I., Pouran, B., de Visser, H. M., Weinans, H. H., Thomas, R. E., Kik, M. J. L., Grinwis, G. C. M., Thies, J. C., Woike, N., Mihov, G., Emans, P. J., Meij, B. P., Creemers, L. B., Tryfonidou, M. A.

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Classification of myositis von Lundberg, Ingrid E., de Visser, Marianne, Werth, Victoria P.

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Clonal Interference and the Periodic Selection of New Beneficial Mutations in Escherichia coli von de Visser, J. Arjan G. M, Rozen, Daniel E

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EFNS guideline on diagnosis and management of post-polio syndrome. Report of an EFNS task force von Farbu, E., Gilhus, N. E., Barnes, M. P., Borg, K., De Visser, M., Driessen, A., Howard, R., Nollet, F., Opara, J., Stalberg, E.

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Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency von Pintao, Maria C, Garcia, A. A, Borgel, D, Alhenc-Gelas, M, Spek, C. A, de Visser, M. C. H, Gandrille, S, Reitsma, Pieter H

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