Publications and communications of Laurie Medard

Gilsoul, M., Medard, L., Coumans, B., Delgado-Escueta, A., de Nijs, L., & Lakaye, B. (July 2018). EFHC1, a protein mutated in Juvenile Myoclonic Epilepsy, interacts with TTLL6 and modulates the level of tubulin polyglutamylation [Poster presentation]. FENS - 11th edition, Berlin, Germany.

Medard, L., Coumans, B., Lakaye, B., De Nijs, L., & Godin, J. (Other coll.). (June 2016). Myoclonin-1 modulates the post-translational modification of microtubules [Poster presentation]. EMBO | EMBL Symposium: Microtubules: From Atoms to Complex Systems, Heidelberg, Germany.

Medard, L. (25 April 2016). Study of the interaction between EFHC1and TTLL6, and its functional implication [Paper presentation]. Séminaire Giga Neurosciences.

Medard, L., Godin, J. (Other coll.), Coumans, B. (Other coll.), GRISAR, T. (Other coll.), Delgado-Escueta, A. (Other coll.), Lakaye, B. (Other coll.), & de Nijs, L. (Other coll.). (December 2015). EFHC1/Myoclonin-1 modulates the post-translational modification of microtubules [Poster presentation]. 69th Annual Meeting American Epilepsy Society, Philadelphie, United States.

Medard, L. (28 September 2015). Study of the interaction between EFHC1and TTLL6, and its functional implication [Paper presentation]. Séminaire Giga Neurosciences.

Medard, L. (12 January 2015). Study of the interaction between EFHC1, a protein mutated in juvenile myoclonic epilepsy, and the TTLL6 glutamylase. Analysis of its functional consequences [Paper presentation]. Séminaire Giga Neurosciences.

Medard, L., Lakaye, B., Godin, J. (Other coll.), Coumans, B. (Other coll.), & de Nijs, L. (Other coll.). (2015). Myoclonin 1 modulates the post-translational modification of microtubules [Poster presentation]. BSCDB SPRING MEETING 2015, Liège, Belgium.

Medard, L. (24 April 2014). Study of the interaction between EFHC1and TTLL6, and its functional implication [Paper presentation]. Séminaire Giga Neursciences.

Medard, L. (07 October 2013). Study of the interaction between EFHC1, a protein mutated in juvenile myoclonic epilepsy, and the TTLL6 glutamylase. Analysis of its functional consequences [Paper presentation]. Monday Meeting Giga Neurosciences.