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GCN2 inhibition reduces mutant SOD1 clustering and toxicity and delays disease progression in an amyotrophic lateral sclerosis mouse model.

Didio Alberto OrtizNuria PeregrínMiguel ValenciaRodrigo Vinueza-GavilanesElisa Marín-OrdovasRoberto FerreroMaría Jesús NicolásGloria González-AseguinolazaMontserrat ArrasateTomás Aragón
Published in: Translational neurodegeneration (2024)
Keyphrases
  • amyotrophic lateral sclerosis
  • mouse model
  • single cell
  • oxidative stress
  • rna seq
  • wild type
  • oxide nanoparticles