Forkhead box protein P2 (FOXP2) is a protein that, in humans, is encoded by the FOXP2 gene. FOXP2 is a member of the forkhead box family of transcription factors, proteins that regulate …

Foxp2基因（Forkhead box p2）即叉头框P2基因，是控制语言能力发展的基因。 在人类，FOXP2基因位于第7对染色体上。 它是在许多其它具有复杂发声、及发声学习能力的动物， …

FOXP2 （Forkhead box protein P2）基因，即 叉头框P2 基因，是一个与 言语 功能的 发育 有关的 基因。 在人类，FOXP2基因為 體染色體 顯，位于 7号染色体 上。 FOXP2基因在许多其它具 …

2024年12月25日 · FOXP2 (Forkhead Box P2) is a Protein Coding gene. Diseases associated with FOXP2 include Isolated Childhood Apraxia Of Speech and Language Disorder. Among its …

2002年8月14日 · FOXP2 is the first gene relevant to the human ability to develop language 2. A point mutation in FOXP2 co-segregates with a disorder in a family in which half of the …

The FOXP2 gene provides instructions for making a protein that acts as a transcription factor, which means that it controls the activity of other genes. It attaches (binds) to the DNA of these …

2016年6月23日 · The core phenotype of FOXP2- SLD is childhood apraxia of speech (CAS), a disorder of speech motor programming or planning that affects the production, sequencing, …

2025年2月8日 · Human FOXP2 contains changes in amino-acid coding and a pattern of nucleotide polymorphism, which strongly suggest that this gene has been the target of …

The forkhead box P2 gene, designated FOXP2, is the first gene implicated in a speech and language disorder. Since its discovery, many studies have been carried out in an attempt to …

2005年2月1日 · FOXP2 encodes a transcription factor that is expressed in the brain, lungs, heart and gut. In the brain, it is widely expressed in sensory, limbic and motor structures. The effects …