Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation

Keyphrases

• Intellectual Disability 100%
• Chromatin-associated Proteins 100%
• Methyl-CpG-binding Protein 2 (MeCP2) 100%
• Rett Syndrome 33%
• X-linked Mental Retardation 33%
• Null Mice 16%
• Heterochromatic 16%
• Protein-coding Genes 16%
• Ligand-binding Domain 16%
• Point mutation 16%
• Mouse Cells 16%
• ATP Synthase 16%
• DNA Helicase 16%
• Thalassemia 16%
• Aged Mice 16%
• Neurological Disorders 16%
• X-linked 16%
• Pathological Changes 16%
• Helicase Domain 16%
• DNA Methylation (DNAm) 16%
• Methyl-binding Proteins 16%
• SnF2 16%
• ATR-X Syndrome 16%
• Methyl-CpG 16%

Biochemistry, Genetics and Molecular Biology

• Alpha Thalassemia/Mental Retardation X-Linked 100%
• MECP2 100%
• Helicase 28%
• Rett Syndrome 28%
• Knockout Mouse 14%
• Binding Protein 14%
• Binding Domain 14%
• Point Mutation 14%
• ATPase 14%
• DNA Methylation 14%