Abstract The transcription factor FoxP2 is involved in setting up the neuronal circuitry for vocal learning in mammals and birds and is thought to have played a special role in the evolution of human speech and language. It has been shown that an allele with a humanized version of the murine Foxp2 gene changes the ultrasonic vocalization of mouse pups compared to pups of the wild-type inbred strain. Here we tested if this humanized allele would also affect the ultrasonic vocalization of adult female and male mice. In a previous study, in which only male vocalization was considered and the mice were recorded under a restricted spatial and temporal regime, no difference in adult vocalization between genotypes was found. Here, we use a differe...
It has been proposed that two amino acid substitutions in the transcription factor FOXP2 have been p...
Disruptions of the FOXP2 gene cause a rare speech and language disorder, a discovery that has opened...
The mysterious human propensity for acquiring speech and language has fascinated sci-entists for dec...
Development of proficient spoken language skills is disrupted by mutations of the FOXP2 transcriptio...
Adult mouse ultrasonic vocalizations (USVs) occur in multiple behavioral and stimulus contexts assoc...
Comparisons of human and ape genomes generate hypotheses about the molecular basis of human-specific...
Heterozygous mutations of the human FOXP2 gene are implicated in a severe speech and language disord...
FOXP2 has been identified as a gene related to speech in humans, based on rare mutations that yield ...
Heterozygous mutations of the human FOXP2 gene are implicated in a severe speech and language disord...
Heterozygous mutations of the human FOXP2 gene are implicated in a severe speech and language disord...
In 2001, a point mutation in the forkhead box P2 (FOXP2) coding sequence was identified as the basis...
SummaryIt has been proposed that two amino acid substitutions in the transcription factor FOXP2 have...
It has been proposed that two amino acid substitutions in the transcription factor FOXP2 have been p...
Contains fulltext : 161830.pdf (publisher's version ) (Open Access
It has been proposed that two amino acid substitutions in the transcription factor FOXP2 have been p...
It has been proposed that two amino acid substitutions in the transcription factor FOXP2 have been p...
Disruptions of the FOXP2 gene cause a rare speech and language disorder, a discovery that has opened...
The mysterious human propensity for acquiring speech and language has fascinated sci-entists for dec...
Development of proficient spoken language skills is disrupted by mutations of the FOXP2 transcriptio...
Adult mouse ultrasonic vocalizations (USVs) occur in multiple behavioral and stimulus contexts assoc...
Comparisons of human and ape genomes generate hypotheses about the molecular basis of human-specific...
Heterozygous mutations of the human FOXP2 gene are implicated in a severe speech and language disord...
FOXP2 has been identified as a gene related to speech in humans, based on rare mutations that yield ...
Heterozygous mutations of the human FOXP2 gene are implicated in a severe speech and language disord...
Heterozygous mutations of the human FOXP2 gene are implicated in a severe speech and language disord...
In 2001, a point mutation in the forkhead box P2 (FOXP2) coding sequence was identified as the basis...
SummaryIt has been proposed that two amino acid substitutions in the transcription factor FOXP2 have...
It has been proposed that two amino acid substitutions in the transcription factor FOXP2 have been p...
Contains fulltext : 161830.pdf (publisher's version ) (Open Access
It has been proposed that two amino acid substitutions in the transcription factor FOXP2 have been p...
It has been proposed that two amino acid substitutions in the transcription factor FOXP2 have been p...
Disruptions of the FOXP2 gene cause a rare speech and language disorder, a discovery that has opened...
The mysterious human propensity for acquiring speech and language has fascinated sci-entists for dec...