Expression Pattern of the Rett Syndrome Gene MeCP2 in Primate Prefrontal Cortex

This publication has 23 references indexed in Scilit:

• A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
  Nature Genetics, 2001
• Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
  Nature Genetics, 2001
• Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation
  Nature Genetics, 2000
• Methylation-Induced Repression— Belts, Braces, and Chromatin
  Published by Elsevier ,1999
• Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
  Nature Genetics, 1999
• A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3"-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression
  Human Molecular Genetics, 1999
• Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells
  Nature Genetics, 1999
• Histone macroH2A1 is concentrated in the inactive X chromosome of female mammals
  Nature, 1998
• Pervasive neuroanatomic abnormalities of the brain in three cases of Rett's syndrome
  Neurology, 1995
• Monoclonal antibody to neurofilament protein (SMI‐32) labels a subpopulation of pyramidal neurons in the human and monkey neocortex
  Journal of Comparative Neurology, 1989