During cortical development, human basal radial glial cells (bRGCs) are highly capable of
sustained self-renewal and neurogenesis. Selective pressures on this cell type may have …

The laminar architecture of the mammalian neocortex depends on the orderly generation of
distinct neuronal subtypes by apical radial glia (aRG) during embryogenesis. Here, we …

Forkhead Box G1 (FOXG1) is a member of the Forkhead family of genes with non-redundant
roles in brain development, where alteration of this gene's expression significantly affects …

Neocortical astrogenesis follows neuronogenesis and precedes oligogenesis. Among key
factors dictating its temporal articulation, there are progression rates of pallial stem cells …

Mutations of the transcription factor FOXP2 in humans cause a severe speech and language
disorder. Disruption of Foxp2 in songbirds or mice also leads to deficits in song learning or …

The transcription factor FoxP2 has been associated with the development of human speech
but the underlying cellular function of FoxP2 is still unclear. Here we provide evidence that …

The cortex consists of 100s of neuronal subtypes that are organized into distinct functional
regions; however, the mechanisms underlying cell fate determination remain unclear. Foxg1 …

FOXP1 is a member of FOXP subfamily transcription factors. Mutations in FOXP1 gene have
been found in various development-related cognitive disorders. However, little is known …

Forkhead-box protein P2 is a transcription factor that has been associated with intriguing
aspects of cognitive function in humans, non-human mammals, and song-learning birds …

Heterozygous loss-of-function mutations in Forkhead box G1 (FOXG1), a uniquely brain-
expressed gene, cause microcephaly, seizures, and severe intellectual disability, whereas …