نتایج جستجو برای: foxp2
تعداد نتایج: 433 فیلتر نتایج به سال:
The discovery and description of the affected members of the KE family (aKE) initiated research on how genes enable the unique human trait of speech and language. Many aspects of this genetic influence on speech-related cognitive mechanisms are still elusive, e.g. if and how cognitive processes not directly involved in speech production are affected. In the current study we investigated the eff...
INTRODUCTION Genetic analysis of specific language disorders is of major interest for both clinical research and linguistic theory. However, the results of this analysis almost always do not show any univocal and compulsory relationships between particular gene mutations and particular disorders or a casual link between the genotype and the phenotype. OBJECTIVES This paper will review this ty...
Previous evidence suggests that language function is modulated by genetic variants on chromosome 7q31-36. However, it is unclear whether this region harbors loci that contribute to speech delay in autism. We previously reported that the WNT2 gene located on 7q31 was associated with the risk of autism. Additionally, two other genes on 7q31-36, FOXP2 and the EN2 genes are also found to play a rol...
The mammalian main olfactory bulb (OB) has a large population of GABAergic inhibitory interneurons that contains several subtypes defined by the co-expression other neurotransmitters and calcium binding proteins. The three most commonly studied OB interneuron subtypes co-express either Calretinin, Calbindin, or Tyrosine hydroxylase (Th). Combinations of transcription factors used to specify the...
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