搜索结果: 1-6 共查到“实验语言学 Foxp2”相关记录6条 . 查询时间(0.046 秒)
Assessing the effects of common variation in the FOXP2 gene on human brain structure
FOXP2 imaging genetics language transcription factor MRI brain anatomy VBM
2015/5/5
The FOXP2 transcription factor is one of the most well-known genes to have been implicated in developmental speech and language disorders. Rare mutations disrupting the function of this gene have been...
Disruptions of the FOXP2 gene cause a rare speech and language disorder, a discovery that has opened up novel avenues for investigating the relevant neural pathways. FOXP2 shows remarkably high conser...
FOXP2 Targets Show Evidence of Positive Selection in European Populations
FOXP2 Evidence of Positive Selection European Populations
2015/4/24
Forkhead box P2 (FOXP2) is a highly conserved transcription factor that has been implicated in human speech and language disorders and plays important roles in the plasticity of the developing brain. ...
Foxp2 Mutations Impair Auditory-Motor Association Learning
Foxp2 Auditory-Motor Association Learning
2015/4/20
Heterozygous mutations of the human FOXP2 transcription factor gene cause the best-described examples of monogenic speech and language disorders. Acquisition of proficient spoken language involves aud...
An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
Foxp2 in vivo recording KE family motor-skill learning speech and language striatum
2015/4/20
Mutations in the human FOXP2 gene cause impaired speech development and linguistic deficits, which have been best characterised in a large pedigree called the KE family. The encoded protein is highly ...