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Patients, clinicians and researchers: a winning trio serving therapeutic innovation
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Stem- and iPS-cell therapy in the CNS
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Neuronal structure and function
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Neuroinflammation, a process common to many CNS diseases
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Understanding life’s rhythms
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Molecular shuttles to transport drugs into the CNS

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The Institute of Neurophysiopathology

Our research unit (UMR-7051)  is a center of excellence for training and research, combining basic and transactional research to understand brain function and develop innovative treatments. At INP we study the organization, function and interaction of neural cells, the molecular and cellular basis of major brain diseases, and the development of innovative cellular and molecular therapy strategies.

Latest news from the lab

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Team leaders

Eq 4. Oligodendroglial Cell Lineage in Aging and in Disease

PFNT Facilities

NICS facility

PFNT - NCIS/PImaNT

PETRA facility

PFNT - PETRA“TECH”

PINT facility

PFNT - PINT

PFNT - SCeNT

BIOINFO facility

BioInformatique

Our publications provide insight into our research progress

Upcoming events

Galette des Rois

Très Bonne Année à tou.te.s!!!

Happy new year to all !!
 

Des recettes de galettes des rois traditionnelles pour l'épiphanie 2025

Afin d'entamer la nouvelle année sur une note gourmande, nous vous donnons rendez-vous vendredi 10 janvier à 13h30en salle de convivialité pour déguster la traditionnelle galette des rois.
A très bientôt.
 
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To start the New Year on a greedy note, we invite you to join us on Friday 10 January at 1.30pm in the social room for the traditional "galette des rois".

We look forward to seeing you there.

 
INP Animation Team
 
 
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salle de convivialité
salle de convivialité

Septins and Microtubules, Conveyors from Cytoskeleton in Cancer cells to Cytoskeleton in Neurons
 

amphi 7
amphi 7

Pascal Verdier-Pinard CRCN Inserm (invité équipe 7)

Therapeutic resistance is the leading cause of cancer-related mortalities, thus urging the development of more effective treatments for refractory tumors. Drug repurposing, which consists in using existing drugs for new medical indications represents a promising strategy to fast-track novel drug combinations in cancer. However, to increase the success rate in clinical trial of novel therapeutic options, it is essential to fully unravel their molecular mechanisms ofaction. We recently developed an innovative approach, termed reverse molecular pharmacology, which consists in deciphering the poly-pharmacology of existing drugs (either approved or in clinical development) to unveil disease-relevant targetable vulnerabilities. This strategy is based on pharmaco-proteomics to reveal the interactome of drugs within tumor cells. We applied our original method to beta-blockers in the pediatric cancer, neuroblastoma, and to anti-helminthics in brain tumors. This revealed the unsuspected role of the heme biosynthesis pathway in neuroblastoma chemoresistance and that of the methylosome in glioblastoma. Our integrated approach thus highlighted novel targetable vulnerabilities in these hard-to-treat cancers, thus opening potential avenues to improve treatments and patient outcome.

amphi 7
amphi 7

Dr Eddy Pasquier