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Thursday I can't, I have Neuro'binar - April 2021

In this article find the video of the fourth edition which took place on April 29th, 2021, with Jean-Christophe Roux (MMG), Benoît Drouillas (INT) and Nicolas Hugues (INMED).

Estimated reading time : 4 min

For this fifth edition, we had the pleasure to welcome Jean-Christophe Roux (MMG), Benoît Drouillas (INT) and Nicolas Hugues (INMED). Benoît Drouillas and Nicolas Hugues introduced their respective Ph.D. in a cross-presentation. After a question session, Pierre-Yves JacobJean-Christophe Roux explained his research on the optimization of gene therapy in Rett Syndrome.

Format

A one-hour web conference in 2 parts: two PhD students will give a 10 min cross-presentation of their PhD work. After 5 min of questions, they will hand over to a researcher, a postdoc or an engineer from the neuroscience community who will present in 20 min an accessible version of their research. Once again, you will have the opportunity to ask questions, debate on the topic of the day or simply get to know your colleague better!

 

Neurobinar #7 with Jean-Christophe Roux (MMG), Benoît Drouillas (INT) and Nicolas Hugues (INMED)

Your "Zoomers" of this seventh edition

Learn more about Nicolas Hugues’s Ph.D. (INMED) presented by Benoît Drouillas (INT) and vice versa. The presentation of both theses is followed by the presentation of the work of Jean-Christophe Roux (MMG). You also have the opportunity to watch the previous Neurobinars on our Youtube channel.

jean-christophe-roux
jean-christophe-roux
Jean-Christophe Roux

Jean-Christophe ROUX (MMG) achieved his academic education at Claude Bernard University in Lyon (France), where he obtained a PhD in Physiology. As a postdoc at the Karolinska Institute, he participated in research on the development of respiratory control at birth and how environmental perturbations could affect it. In the human neurogenetics team led by Dr Laurent Villard, Jean-Christophe Roux is in charge of Rett Syndrome and associated pathologies since 2006. Rett syndrome is a devastating genetic disorder (Mecp2 mutation) leading to autonomic and cognitive deficits that worldwide represents the second most common genetic cause of severe intellectual disability in females. His group is studying mouse models of Mecp2 dysfunctions and his work led to the implementation of two clinical trials (phase 2a) with Rett patients. The first trial deals with the stimulation of the monoaminergic neurotransmission and the second with the trophic support. Recently, he has developed innovative approaches using gene therapy targeting the brain.

Team website
Nicolas Hugues

Almost 2 years ago, I gratuated a Master's degree in Human Movement Sciences from Marseille Sport Sciences Faculty. Since then, I'm carrying out my thesis project entitled "Impacts of various endurance exercise regimens and effects of their combination with cognitive training on neuroplasticity after cerebral ischemia". This project is supervised by Pr. Éric Berton and Jérôme Laurin at INMED (Mediterranean Neurobiology Institute).

Benoit drouillas
Benoit drouillas
Benoît Drouillas

Benoît Drouillas started a degree in genetics and discovered neurosciences during an optional course. He then decided to do a degree in cognitive neuroscience in Marseille. Curious about cellular mechanisms, he went on to do a master's degree in neurobiology, neurophysiology and neuropathology in Marseille, after which he started his thesis. He is currently in the 3rd year of his thesis at the Institut de Neurosciences de la Timone. Supervised by Frédéric Brocard in the P3M team (plasticity and physiopathology of rhythmic motor networks), he is interested in the spinal cord network responsible for the development of locomotion.

Ingrid Meucci Chargée de communication
Author

Après la validation d’un master en neuroscience et un master communication, je me suis spécialisée dans la communication neuroscientifique au service de l'institut NeuroMarseille. 

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