HAL (France)
open access
Propagation et toxicité de la superoxide dismutase 1 dans la Sclérose Latérale Amyotrophique modélisée par des neurones moteurs dérivés de cellules souches pluripotentes induites
La sclérose latérale amyotrophique (SLA) est une maladie neurodégénérative rapidement fatale et sans traitement curatif, qui entraîne la mort des neurones moteurs (MN) via des mécanismes encore mal identifiés. La dégénérescence des MN provoque une paralysie progressive, qui débute localement avant d
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- Excitotoxicity as a target against neurodegenerative processes#935902
- Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice#1290896
- Propagation et toxicité de déterminants de la sclérose latérale amyotrophique#330019
- In-situ Cytokines Expression in the CNS in Amyotrophic Lateral Sclerosis (ALS)#890185
- Exploring neuronal circuitry in neurodegenerative diseases: from traditional models to cutting-edge techniques#274697
Record · ID 1328946
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive