FoxP2 is a highly conserved vertebrate transcription factor known for its importance in
human speech and language production. Disruption of FoxP2 in several vertebrate models …

FOXP proteins form a subfamily of evolutionarily conserved transcription factors involved in
the development and functioning of several tissues, including the central nervous system. In …

The transcription factor FOXP2 has been linked to severe speech and language
impairments in humans. An analysis of the evolution of the FOXP2 gene has identified two …

The FOXP2 gene is important for the development of proper speech motor control in
humans. However, the role of the gene in general vocal behavior in other mammals …

Fundamental human traits, such as language and bipedalism, are associated with a range
of anatomical adaptations in craniofacial shaping and skeletal remodeling. However, it is …

Humans and songbirds are two of the rare animal groups that modify their innate
vocalizations. The identification of FOXP2 as the monogenetic locus of a human speech …

Genetic disruptions of the forkhead box transcription factor FOXP2 in humans cause an
autosomal-dominant speech and language disorder. While FOXP2 expression pattern are …

Learned vocal communication, including human speech, is a socially influenced behavior
limited to certain animals. This ability requires auditory feedback during vocalization, which …

Heterozygous disruptions of the Forkhead transcription factor FoxP2 impair acquisition of
speech and language. Experimental downregulation in brain region Area X of the avian …

Heterozygous mutations of the human FOXP2 gene are implicated in a severe speech and
language disorder. Aetiological mutations of murine Foxp2 yield abnormal synaptic plasticity …