Michèle Studer

The paper identifies an NR2F1-dependent retinoic acid network in mice that regulates retinal specialization and links its disruption to foveal hypoplasia in BBSOAS patients.

This study develops a human cortico-endothelial assembloid model to investigate glioblastoma cell tropism, identifying CELF2 and AHNAK as key regulators of neuronal versus endothelial invasion.

The paper identifies SOX2 and NR2F1 as regulators of gene expression in the early postnatal visual thalamus, showing their shared target genes and regulatory mechanisms.

The paper investigates NR2F1 nucleolar localization using multiple antibodies in vitro and in vivo, finding it artificial and non-functional, and recommends optimal antibody use.

This study shows FGF8 signaling influences regional identity and cellular diversity in human cerebral organoids, affecting neural progenitor fate and genes linked to neurodevelopmental disorders.

This study shows Nr2f1 regulates mitochondrial dynamics in adult-born hippocampal neurons, linking it to BBSOAS pathogenesis.

This study identifies dB2 neurons as causative of CCHS by showing their role in respiratory functions and neonatal survival using genetic and functional approaches.

The paper shows that Nr2f1 gene expression in postmitotic neurons controls corticopontine topographic mapping, while its expression in progenitor cells affects the ratio of corticopontine to corticospinal fibers.

This study shows that Nr2f1 regulates neuronal activity and morphology in the developing somatosensory cortex, impacting network synchronization and excitability.