The discovery of the FOXP2 transcription factor, and its implication in a rare severe human speech and language disorder, has led to two decades of empirical studies focused on uncovering its roles in the brain using a range of in vitro and in vivo methods. Here, we discuss what we have learned about the regulation of FOXP2, its downstream effectors, and its modes of action as a transcription factor in brain development and function, providing an integrated overview of what is currently known about the critical molecular networks
International audienceForkhead-box protein P2 is a transcription factor that has been associated wit...
Childhood syndromes disturbing language development are common and display high degrees of heritabil...
The signalling pathways controlling both the evolution and development of language in the human brai...
We previously discovered that mutations of the human FOXP2 gene cause a monogenic communication diso...
Mutations in FOXP2, a member of the forkhead family of transcription factor genes, are the only know...
Mutations in FOXP2, a member of the forkhead family of transcription factor genes, are the only know...
Forkhead-box protein P2 is a transcription factor that has been associated with intriguing aspects o...
Mutations of the FOXP2 gene cause a severe speech and language disorder, providing a molecular windo...
Disruption of FOXP2, a gene encoding a forkhead-domain transcription factor, causes a severe develop...
We previously discovered that mutations of the human FOXP2 gene cause a monogenic communication diso...
We previously discovered that mutations of the human FOXP2 gene cause a monogenic communication diso...
Disruptions of the FOXP2 gene cause a rare speech and language disorder, a discovery that has opened...
FOXP1 and FOXP2 are transcription factors with important roles in brain development. FOXP2 was the f...
FOXP transcription factors play important roles in neurodevelopment, but little is known about how t...
Developmental disorders affecting speech and language are highly heritable, but very little is curre...
International audienceForkhead-box protein P2 is a transcription factor that has been associated wit...
Childhood syndromes disturbing language development are common and display high degrees of heritabil...
The signalling pathways controlling both the evolution and development of language in the human brai...
We previously discovered that mutations of the human FOXP2 gene cause a monogenic communication diso...
Mutations in FOXP2, a member of the forkhead family of transcription factor genes, are the only know...
Mutations in FOXP2, a member of the forkhead family of transcription factor genes, are the only know...
Forkhead-box protein P2 is a transcription factor that has been associated with intriguing aspects o...
Mutations of the FOXP2 gene cause a severe speech and language disorder, providing a molecular windo...
Disruption of FOXP2, a gene encoding a forkhead-domain transcription factor, causes a severe develop...
We previously discovered that mutations of the human FOXP2 gene cause a monogenic communication diso...
We previously discovered that mutations of the human FOXP2 gene cause a monogenic communication diso...
Disruptions of the FOXP2 gene cause a rare speech and language disorder, a discovery that has opened...
FOXP1 and FOXP2 are transcription factors with important roles in brain development. FOXP2 was the f...
FOXP transcription factors play important roles in neurodevelopment, but little is known about how t...
Developmental disorders affecting speech and language are highly heritable, but very little is curre...
International audienceForkhead-box protein P2 is a transcription factor that has been associated wit...
Childhood syndromes disturbing language development are common and display high degrees of heritabil...
The signalling pathways controlling both the evolution and development of language in the human brai...