Brain assembloids decode human cortical networks in Rett syndrome.
Cell reports, 44(12): 116709 PMID 41389206 DOI 10.1016/j.celrep.2025.116709
Аннотация
Tenreiro et al.1 employ human cerebral organoids and telencephalic assembloids to reveal that MeCP2 deficiency leads to multiple defects in the formation of cortical neuronal networks during early prenatal brain development, offering new insights into the pathology of Rett syndrome.