Phosphatidylserine improves axonal transport by inhibition of HDAC and has potential in treatment of

• 作 者: Shiran Naftelberg Gil Ast Eran
• 机 构: DepartmentofHumanMolecularGeneticsandBiochemistry,DepartmentofPhysiologyandPharmacology
• 出 处: 中国神经再生研究：英文版
• 发表日期: 2017年4期
• 基金项目: National Network of Excellence in Neuroscience （NNE） [1234944]. E.P. was supported by grants from the Isr,the European Research Council （ERC） [309377]. S.N. was supported by grants from Teva Pharmaceu

Familial dysautonomia(FD) is a rare children neurodegenerative disease caused due to a point mutation in the IKBKAP gene that results in decreased IKK complex-associated protein(IKAP) protein production. The disease affects mostly the dorsal root ganglion