A novel DNA-binding feature of MeCP2 contributes to Rett syndrome

Gelijkaardige items

• MeCP2_e2 partially compensates for lack of MeCP2_e1: A male case of Rett syndrome
  door: Ryo Takeguchi, et al.
  Gepubliceerd in: (2020-02-01)
• The Molecular Functions of MeCP2 in Rett Syndrome Pathology
  door: Osman Sharifi, et al.
  Gepubliceerd in: (2021-04-01)
• MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett Syndrome
  door: Xu-Rui Jin, et al.
  Gepubliceerd in: (2017-10-01)
• Rett-causing mutations reveal two domains critical for MeCP2 function and for toxicity in MECP2 duplication syndrome mice
  door: Laura Dean Heckman, et al.
  Gepubliceerd in: (2014-06-01)
• Manipulations of MeCP2 in glutamatergic neurons highlight their contributions to Rett and other neurological disorders
  door: Xiangling Meng, et al.
  Gepubliceerd in: (2016-06-01)