Novel MeCP2 Isoform-Specific Antibody Reveals the Endogenous MeCP2E1 Expression in Murine Brain, Primary Neurons and Astrocytes
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Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference44 articles.
1. Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA;RR Meehan;Nucleic Acids Res,1992
2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;RE Amir;Nat Genet,1999
3. Rett’s syndrome: prevalence and impact on progressive severe mental retardation in girls;B Hagberg;Acta Paediatr Scand,1985
4. Linking Epigenetics to Human Disease and Rett Syndrome: The Emerging Novel and Challenging Concepts in MeCP2 Research,;RM Zachariah;Neural Plasticity,2012
5. The story of Rett syndrome: from clinic to neurobiology;M Chahrour;Neuron,2007
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