Investigating MeCP2 isoform-specific functions in neurons; Insights on the role of MeCP2 in Rett Syndrome

被引：0
|
作者：
Zachariah, Robby M. [1 ]
Rastegar, Mojgan [1 ]
机构：
[1] Univ Manitoba, Regenerat Med Program, Fac Med, Dept Biochem & Med Genet, Winnipeg, MB R3T 2N2, Canada
来源：
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE | 2015年 / 47卷
关键词：
D O I：
10.1016/j.ijdevneu.2015.04.174
中图分类号：
Q [生物科学];
学科分类号：
07 ; 0710 ; 09 ;
摘要：
引用
收藏
页码：62 / 62
页数：1
相关论文
共 50 条
  • [41] Survey of MeCP2 in the Rett syndrome and the non-Rett syndrome brain
    Armstrong, DD
    Deguchi, M
    Antallfy, B
    JOURNAL OF CHILD NEUROLOGY, 2003, 18 (10) : 683 - 687
  • [42] Magnetic resonance spectroscopy and analysis of MECP2 in Rett syndrome
    Khong, PL
    Lam, CW
    Ooi, CGC
    Ko, CH
    Wong, VCN
    PEDIATRIC NEUROLOGY, 2002, 26 (03) : 205 - 209
  • [43] Deleterious mutations in exon 1 of MECP2 in Rett syndrome
    Quenard, Aline
    Yilmaz, Saliha
    Fontaine, Herve
    Bienvenu, Thierry
    Moncla, Anne
    des Portes, Vincent
    Rivier, Francois
    Mathieu, Michele
    Raux, Gregory
    Jonveaux, Philippe
    Philippe, Christophe
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2006, 49 (04) : 313 - 322
  • [44] Impact of Rett Syndrome Mutations on MeCP2 MBD Stability
    Kucukkal, Tugba G.
    Yang, Ye
    Uvarov, Olga
    Cao, Weiguo
    Alexov, Emil
    BIOCHEMISTRY, 2015, 54 (41) : 6357 - 6368
  • [45] Ckassic Rett syndrome in a boy with MECP2 mutation.
    Kondo, I
    Masuyama, T
    Matsuo, S
    Kitsuki, K
    Kan, Y
    Ishii, K
    Yamagata, H
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 258 - 258
  • [46] Spectrum of MECP2 mutations in Vietnamese patients with RETT syndrome
    Huong Le Thi Thanh
    Trinh Do Thi Diem
    Chinh Vu Duy
    Ha Ly Thi Thanh
    Hoa Bui Thi Phuong
    Liem Nguyen Thanh
    BMC MEDICAL GENETICS, 2018, 19
  • [47] Rett syndrome:: Clinical manifestations in males with MECP2 mutations
    Ben Zeev, B
    Yaron, Y
    Schanen, NC
    Wolf, H
    Brandt, N
    Ginot, N
    Shomrat, R
    Orr-Urtreger, A
    JOURNAL OF CHILD NEUROLOGY, 2002, 17 (01) : 20 - 24
  • [48] Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgene
    Pitcher, Meagan R.
    Herrera, Jose A.
    Buffington, Shelly A.
    Kochukov, Mikhail Y.
    Merritt, Jonathan K.
    Fisher, Amanda R.
    Schanen, N. Carolyn
    Costa-Mattioli, Mauro
    Neul, Jeffrey L.
    HUMAN MOLECULAR GENETICS, 2015, 24 (09) : 2662 - 2672
  • [49] MECP2 germline mosaicism plays an important part in the inheritance of Rett syndrome: a study of MECP2 germline mosaicism in males
    Yongxin Wen
    Jiaping Wang
    Qingping Zhang
    Xiaoxu Yang
    Liping Wei
    Xinhua Bao
    BMC Medicine, 21
  • [50] Homozygosity for MECP2 gene in a girl with classical Rett syndrome
    Karall, Daniela
    Haberlandt, Edda
    Scholl-Burgi, Sabine
    Baumgartner, Sara
    Naudo, Montserrat
    Martorell, Loreto
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2007, 50 (06) : 465 - 468
12345