Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain.
Mutations in FOXP2, a member of the forkhead family of transcription factor genes, are the only known cause of developmental speech and language disorders in humans. To date, there are no known targets of human FOXP2 in the nervous system. The identification of FOXP2 targets in the developing human...
Main Authors: | Spiteri, E, Konopka, G, Coppola, G, Bomar, J, Oldham, M, Ou, J, Vernes, S, Fisher, S, Ren, B, Geschwind, D |
---|---|
Formato: | Journal article |
Idioma: | English |
Publicado: |
2007
|
Títulos similares
-
High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders.
por: Vernes, S, et al.
Publicado: (2007) -
Singing mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and language.
por: White, SA, et al.
Publicado: (2006) -
FOXP2 as a molecular window into speech and language.
por: Fisher, S, et al.
Publicado: (2009) -
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.
por: MacDermot, K, et al.
Publicado: (2005) -
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.
por: Vernes, S, et al.
Publicado: (2011)