Michele Bertacchi
Nice, France
Last Updated: 09/26/2026
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Found 25 publications
Genetic code expansion: Bridging synthetic biology precision and cellular complexity to decipher molecular mechanisms of diseases.
Journal: Current opinion in chemical biology
Published: January 31, 2026
Models of Bosch-Boonstra-Schaaf optic atrophy syndrome reveal genotype-phenotype correlations in brain structure and behavior.
Journal: Disease models & mechanisms
Published: April 17, 2025
Unravelling the conundrum of nucleolar NR2F1 localization using antibody-based approaches in vitro and in vivo.
Journal: Communications biology
Published: October 14, 2024
FGF8-mediated gene regulation affects regional identity in human cerebral organoids.
Journal: eLife
Published: March 31, 2024
Disrupted protein interaction dynamics in a genetic neurodevelopmental disorder revealed by structural bioinformatics and genetic code expansion.
Journal: Protein science : a publication of the Protein Society
Published: October 11, 2023
Pathophysiological Heterogeneity of the BBSOA Neurodevelopmental Syndrome.
Journal: Cells
Published: February 03, 2022
Structural and Functional Aspects of the Neurodevelopmental Gene NR2F1: From Animal Models to Human Pathology.
Journal: Frontiers in molecular neuroscience
Published: August 31, 2021
Pathogenic NR2F1 variants cause a developmental ocular phenotype recapitulated in a mutant mouse model.
Journal: Brain communications
Published: May 10, 2021
Dynamic expression of NR2F1 and SOX2 in developing and adult human cortex: comparison with cortical malformations.
Journal: Brain structure & function
Published: September 03, 2020
Optimized Immunostaining of Embryonic and Early Postnatal Mouse Brain Sections.
Journal: Bio-protocol
Published: July 29, 2020
Last Updated: 09/26/2026