Rett mutations attenuate phase separation of MeCP2

被引:22
|
作者
Fan, Chunyan [1 ]
Zhang, Honglian [1 ]
Fu, Liangzheng [1 ,2 ]
Li, Yuejiao [1 ,2 ]
Du, Yi [1 ,2 ]
Qiu, Zilong [2 ,3 ,4 ]
Lu, Falong [1 ,2 ,5 ]
机构
[1] Chinese Acad Sci, State Key Lab Mol Dev Biol, Inst Genet & Dev Biol, Beijing 100101, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Ctr Excellence Brain Sci & Intelligence Technol, Shanghai 200031, Peoples R China
[4] Chinese Acad Sci, State Key Lab Neurosci, Inst Neurosci, Shanghai 200031, Peoples R China
[5] Chinese Acad Sci, Innovat Acad Seed Design, Beijing 100101, Peoples R China
基金
中国国家自然科学基金;
关键词
SELF-RENEWAL; BINDING; PROTEIN; SEQUENCE; NEURONS; DNA;
D O I
10.1038/s41421-020-0172-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
引用
收藏
页数:4
相关论文
共 50 条
  • [1] Rett mutations attenuate phase separation of MeCP2
    Chunyan Fan
    Honglian Zhang
    Liangzheng Fu
    Yuejiao Li
    Yi Du
    Zilong Qiu
    Falong Lu
    Cell Discovery, 6
  • [2] Spectrum of MECP2 mutations in Rett syndrome
    Bienvenu, T
    Villard, L
    De Roux, N
    Bourdon, V
    Fontes, M
    Beldjord, C
    Tardieu, M
    Jonveaux, P
    Chelly, J
    GENETIC TESTING, 2002, 6 (01): : 1 - 6
  • [3] Mutations of the MECP2 gene in Rett syndrome
    Hampson, K
    Latif, F
    Woods, CG
    Webb, T
    JOURNAL OF MEDICAL GENETICS, 2000, 37 : S73 - S73
  • [4] Spectrum of MECP2 mutations in Rett syndrome
    Lee, SSJ
    Wan, MM
    Francke, U
    BRAIN & DEVELOPMENT, 2001, 23 : S138 - S143
  • [5] MECP2 mutations in Swedish Rett syndrome clusters
    Xiang, FQ
    Stenbom, Y
    Anvret, M
    CLINICAL GENETICS, 2002, 61 (05) : 384 - 385
  • [6] MECP2 Mutations in People Without Rett Syndrome
    Suter, B.
    Treadwell-Dearing, D.
    Zoghbi, H.
    Glaze, D.
    Neul, J. L.
    ANNALS OF NEUROLOGY, 2010, 68 (04) : S98 - S99
  • [7] MeCP2 mutations and gastrointestinal phenotype in Rett Syndrome
    Bibat, G
    Cuffari, C
    Naidu, S
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 272 - 272
  • [8] MECP2 mutations in Malaysian Rett syndrome patients
    Fong, C. B.
    Thong, M. K.
    Sam, C. K.
    Noor, Mohamed M. N.
    Ariffin, R.
    SINGAPORE MEDICAL JOURNAL, 2009, 50 (05) : 529 - 533
  • [9] MECP2 mutations in Serbian Rett syndrome patients
    Djarmati, A.
    Dobricic, V.
    Kecmanovic, M.
    Marsh, P.
    Jancic-Stefanovic, J.
    Klein, C.
    Djuric, M.
    Romac, S.
    ACTA NEUROLOGICA SCANDINAVICA, 2007, 116 (06): : 413 - 419
  • [10] Rett Syndrome and MeCP2
    Liyanage, Vichithra R. B.
    Rastegar, Mojgan
    NEUROMOLECULAR MEDICINE, 2014, 16 (02) : 231 - 264