Veronique Brault

4PUBLICATIONS
27CO-AUTHORS
Neurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)Central nervous system
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Publications (4)

|Jul 09, 2025
Interneuron migration defects during corticogenesis contribute to Dyrk1a haploinsufficiency syndrome pathogenesis.

Maria Victoria Hinckelmann, Aline Dubos, Victorine Artot

|Jan 24, 2024
Increased dosage of DYRK1A leads to congenital heart defects in a mouse model of Down syndrome.

Eva Lana-Elola, Rifdat Aoidi, Miriam Llorian

|Dec 09, 2023
Stefin B Inhibits NLRP3 Inflammasome Activation via AMPK/mTOR Signalling.

Mojca Trstenjak-Prebanda, Monika Biasizzo, Klemen Dolinar

|Oct 11, 2017
Rodent models in Down syndrome research: impact and future opportunities.

Yann Herault, Jean M Delabar, Elizabeth M C Fisher

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