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基因在许多其它具有复 …

2025年3月30日 · FOXP2 (Forkhead Box P2) is a Protein Coding gene. Diseases associated with FOXP2 include Childhood Apraxia Of Speech and Isolated Childhood Apraxia Of Speech. …

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 …

2025年2月8日 · Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review. FOXP2 suppresses the proliferation, invasion, and …

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 …

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 …

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, …

2021年7月14日 · FOXP2 was discovered 20 years ago to be required for human speech and language development. This review discusses molecular networks of FOXP2 regulation, …