PUBLICATIONS

Last update : 10/10/2026
  • Robert-Paganin, J., Auguin, D., Houdusse, A. "Hypertrophic cardiomyopathy disease results from disparate impairments of cardiac myosin function and auto-inhibition" Nature Communications., 9: art.n° 4019. (2018).
  • Samson, C., Petitalot, A., Celli, F., Herrada, I., Ropars, V., Le Du, M.H., Nhiri, N., Jacquet, E., Arteni, A.A., Buendia, B., Zinn-Justin, S. "Structural analysis of the ternary complex between lamin A/C, BAF and emerin identifies an interface disrupted in autosomal recessive progeroid diseases" Nucleic Acids Research., 46(19): 10460–10473. (2018).
  • Lam, W.H., Sze, K.H., Ke, Y., Tse, M.K., Zhang, H., Woo, P.C.Y., Lau, S.K.P., Lau, C.C.Y., Xu, S., Lai, P.M., Zhou, T., Antonyuk, S.V., Kao, R.Y.T., Yuen, K.Y., Hao, Q. "Talaromyces marneffei Mp1 Protein, a Novel Virulence Factor, Carries Two Arachidonic Acid-Binding Domains To Suppress Inflammatory Responses in Hosts" Infection and Immunity., 87(4): art.n° e00679-18. (2019).
  • Nguyen, T.Q., Aumont-Nicaise, M., Andreani, J., Velours, C., Chenon, M., Vilela, F., Geneste, C., Varela, P.F., Llinas, P., Ménétrey, J. "Characterization of the binding mode of JNK-interacting protein 1 (JIP1) to kinesin-light chain 1 (KLC1)" Journal of Biological Chemistry., 293(36): 13946-13960. (2018).
  • Liénart, S., Merceron, R., Vanderaa, C., Lambert, F., Colau, D., Stockis, J., van der Woning, B., De Haard, H., Saunders, M., Coulie, P.G., Savvides, S.N., Lucas, S. "Structural basis of latent TGF-β1 presentation and activation by GARP on human regulatory T cells" Science., 362(6417): 952-956. (2018).
  • Landeras-Bueno, S., Oda, S.I., Norris, M.J., Salie, Z.L., Guenaga, J., Wyatt, R.T., Saphire, E.O. "Sudan Ebolavirus VP35-NP Crystal Structure Reveals a Potential Target for Pan-Filovirus Treatment" mBio., 10(4): art.n° e00734-19. (2019).
  • Maurice, F., Pérébaskine, N., Thore, S., Fribourg, S. "In vitro dimerization of human RIO2 kinase" RNA Biology., 16(11): 1633-1642. (2019).
  • Arrondel, C., Missoury, S., Snoek, R., Patat, J., Menara, G., Collinet, B., Liger, D., Durand, D., Gribouval, O., Boyer, O., Buscara, L., Martin, G., Machuca, E., Nevo, F., Lescop, E., Braun, D.A., Boschat, A.C., Sanquer, S., Guerrera, I.C., Revy, P., Parisot, M., Masson, C., Boddaert, N., Charbit, M., Decramer, S., Novo, R., Macher, M.A., Ranchin, B., Bacchetta, J., Laurent, A., Collardeau-Frachon, S., van Eerde, A.M., Hildebrandt, F., Magen, D., Antignac, C., van Tilbeurgh, H., Mollet, G. "Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome" Nature Communications., 10: art.n° 3967. (2019).
  • Collie, G.W., Koh, C.M., O’Neill, D.J., Stubbs, C.J., Khurana, P., Eddershaw, A., Snijder, A., Mauritzson, F., Barlind, L., Dale, I.L., Shaw, J., Phillips, C., Hennessy, E.J., Cheung, T., Narvaez, A.J. "Structural and Molecular Insight into Resistance Mechanisms of First Generation cMET Inhibitors" ACS Medicinal Chemistry Letters., 10(9): 1322-1327. (2019).
  • Holzer, S., Rzechorzek, N.J., Short, I.R., Jenkyn-Bedford, M., Pellegrini, L., Kilkenny, M.L. "Structural basis for inhibition of human primase by arabinofuranosyl nucleoside analogues fludarabine and vidarabine" ACS Chemical Biology., 14(9): 1904-1912. (2019).