Breaking the silence in Rett syndrome

被引:26
作者
Willard, HF [1 ]
Hendrich, BD
机构
[1] Case Western Reserve Univ, Dept Genet, Ctr Human Genet, Cleveland, OH 44106 USA
[2] Univ Hosp Cleveland, Cleveland, OH 44106 USA
[3] Univ Edinburgh, Inst Cell & Mol Biol, Edinburgh EH9 3JR, Midlothian, Scotland
关键词
D O I
10.1038/13751
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:127 / 128
页数:2
相关论文
共 15 条
  • [1] Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
    Amir, RE
    Van den Veyver, IB
    Wan, M
    Tran, CQ
    Francke, U
    Zoghbi, HY
    [J]. NATURE GENETICS, 1999, 23 (02) : 185 - 188
  • [2] Rett syndrome
    Clarke, A
    [J]. JOURNAL OF MEDICAL GENETICS, 1996, 33 (08) : 693 - 699
  • [3] Identification and characterization of a family of mammalian methyl-CpG binding proteins
    Hendrich, B
    Bird, A
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) : 6538 - 6547
  • [4] DNA methylation and imprinting: Why bother?
    Jaenisch, R
    [J]. TRENDS IN GENETICS, 1997, 13 (08) : 323 - 329
  • [5] Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting
    Lee, MP
    DeBaun, MR
    Mitsuya, K
    Galonek, HL
    Brandenburg, S
    Oshimura, M
    Feinberg, AP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (09) : 5203 - 5208
  • [6] PURIFICATION, SEQUENCE, AND CELLULAR-LOCALIZATION OF A NOVEL CHROMOSOMAL PROTEIN THAT BINDS TO METHYLATED DNA
    LEWIS, JD
    MEEHAN, RR
    HENZEL, WJ
    MAURERFOGY, I
    JEPPESEN, P
    KLEIN, F
    BIRD, A
    [J]. CELL, 1992, 69 (06) : 905 - 914
  • [7] MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin
    Nan, XS
    Campoy, FJ
    Bird, A
    [J]. CELL, 1997, 88 (04) : 471 - 481
  • [8] DNA methylation and chromatin modification
    Ng, HH
    Bird, A
    [J]. CURRENT OPINION IN GENETICS & DEVELOPMENT, 1999, 9 (02) : 158 - 163
  • [9] Imprinting in Prader-Willi and Angelman syndromes
    Nicholls, RD
    Saitoh, S
    Horsthemke, B
    [J]. TRENDS IN GENETICS, 1998, 14 (05) : 194 - 200
  • [10] Epilepsy and mental retardation limited to females: An X-linked dominant disorder with male sparing
    Ryan, SG
    Chance, PF
    Zou, CH
    Spinner, NB
    Golden, JA
    Smietana, S
    [J]. NATURE GENETICS, 1997, 17 (01) : 92 - 95