Marion Guillon on Muck Rack

Marion Guillon

As seen in: Stem Cell Reports
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Articles

MECP2 mutations rewire human ESC fate and bias cortical lineage commitment

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By Laetitia Laurent, Alexia Bernard, Yi Liu, Anthony Flamier, Marion Guillon, Margaux Brin, Elodie Gabet, Justine Gromaire, Mathéa Bernard, Théo Rabin, Lisa Bianchin, Marie Veziano, Julie Kloda, Laila Asali
| Stem Cell Reports Verified
Keywords MECP2 Rett syndrome pluripotency EMX1 transcriptomics neurodevelopment cerebral organoids lineage specification stem cell differentiation Introduction Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder that affects ≈1 in 10,000 girls worldwide and, in rare surviving males, presents with an even more severe encephalopathy (Liu et al., 2025b; Petriti et al., 2023).
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