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Literature Workspace

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References
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1 reference

Research article 2023 Reviewed MVA Hackathon 2026 — BUB1B

Amlexanox: Readthrough Induction and Nonsense-Mediated mRNA Decay Inhibition in a Charcot–Marie–Tooth Model of hiPSCs-Derived Neuronal Cells Harboring a Nonsense Mutation in GDAP1 Gene

Nesrine Benslimane, Federica Miressi, Camille Loret and 7 more Pharmaceuticals

Nonsense mutations are involved in multiple peripheral neuropathies. These mutations induce the presence of a premature termination codon (PTC) at the mRNA level. As a result, a dysfunctional or truncated protein is synt… abstract via Crossref

Evidence snapshot note: Amlexanox in GDAP1 neuronal progenitors. Model: Human iPSC-derived neuronal progenitors with GDAP1 p.Ser194* (UGA). Where: Figures 2-4 · cited by MVA-AMLEXANOX-010

  • Cmt Disease
  • Nonsense Mutation
  • Premature Termination Codon (Ptc)
  • Nonsense-mediated Decay (Nmd)

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KBot · Guía de investigación

Respuestas preescritas · Evidencia enlazada

KBot

Hola, soy KBot, la guía de investigación de BioLab. Puedo explicar los casos de investigación, el Literature Workspace, el grafo de evidencia y las herramientas de análisis, y dónde termina cada uno. Elige un tema abajo. Son explicaciones preescritas, no una consulta de IA en vivo.

Información de investigación, no consejo médico individual. No se envía ni se guarda ningún mensaje.