Diminished prevalence but preserved synaptic distribution of N-methyl-d-aspartate receptor subunits in the methyl CpG binding protein 2(MeCP2)-null mouse brain

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Ruthie E. Amir, Ignatia B. Van den Veyver, Mimi Wan et al. · Nature Genetics · 1999 · 5K citations

Life Sciences, Genetics, Molecular Genetics +9

Developmental and regional expression in the rat brain and functional properties of four NMDA receptors

Hannah Monyer, Nail Burnashev, David Laurie et al. · Neuron · 1994 · 3.5K citations

Life Sciences, Neurobiology, Neuroscience +15

MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription

Maria H. Chahrour, Sung Yun Jung, Chad A. Shaw et al. · Science · 2008 · 1.8K citations

Life Sciences, Genetics, Neuroscience +17

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

Jacky Guy, Brian Hendrich, Megan C. Holmes et al. · Nature Genetics · 2001 · 1.6K citations

Life Sciences, Genetics, Neuroscience +14

DNA Methylation-Related Chromatin Remodeling in Activity-Dependent <i>Bdnf</i> Gene Regulation

Keri Martinowich, Daisuke Hattori, Hao Wu et al. · Science · 2003 · 1.4K citations

Life Sciences, Molecular Biology, Neuroscience +14