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

Nan, X; Hou, J; Maclean, A; Nasir, J; Lafuente, MJ; Shu, X; Kriaucionis, S; Bird, A (2007) Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 104 (8). 2709 - 2714 (6). ISSN 0027-8424 https://doi.org/10.1073/pnas.0608056104
SGUL Authors: Nasir, Jamal

Full text not available from this repository.
Item Type: Article
Additional Information: PubMed ID: 17296936
Keywords: Animals, Brain, Cells, Cultured, DNA, DNA Helicases, DNA Methylation, Humans, Intellectual Disability, Methyl-CpG-Binding Protein 2, Mice, Mutation, Nuclear Proteins, Protein Binding, Protein Transport, Two-Hybrid System Techniques, Science & Technology, Multidisciplinary Sciences, Science & Technology - Other Topics, DNA methylation, Rett syndrome, X-linked mental retardation, CPG-BINDING PROTEIN, RETT-SYNDROME, DNA METHYLATION, X SYNDROME, TRANSCRIPTIONAL REPRESSION, DEPENDENT PHOSPHORYLATION, NEURONAL MATURATION, HISTONE DEACETYLASE, CHROMOSOMAL PROTEIN, REMODELING COMPLEX, DNA methylation, Rett syndrome, X-linked mental retardation
SGUL Research Institute / Research Centre: Academic Structure > Institute of Medical & Biomedical Education (IMBE)
Academic Structure > Institute of Medical & Biomedical Education (IMBE) > Centre for Biomedical Education (INMEBE)
Journal or Publication Title: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
ISSN: 0027-8424
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Dates:
DateEvent
20 February 2007Published
Web of Science ID: WOS:000244511200028
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URI: https://openaccess.sgul.ac.uk/id/eprint/102
Publisher's version: https://doi.org/10.1073/pnas.0608056104

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