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Identifying proteins bound to native mitotic ESC chromosomes reveals chromatin repressors are important for compaction.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-17823-z
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- Article
Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor.
- Published in:
- Nature Neuroscience, 2013, v. 16, n. 7, p. 898, doi. 10.1038/nn.3434
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- Article
CpG islands influence chromatin structure via the CpG-binding protein Cfp1.
- Published in:
- Nature, 2010, v. 464, n. 7291, p. 1082, doi. 10.1038/nature08924
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- Article
Exclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypes.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 20, p. 4389, doi. 10.1093/hmg/ddw269
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- Publication type:
- Article
The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndrome.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 3, p. 558, doi. 10.1093/hmg/ddv496
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- Article
Postnatal inactivation reveals enhanced requirement for MeCP2 at distinct age windows.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 17, p. 3806, doi. 10.1093/hmg/dds208
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- Article
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome.
- Published in:
- Nature Genetics, 2001, v. 27, n. 3, p. 322, doi. 10.1038/85899
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- Publication type:
- Article
Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 15, p. 2247, doi. 10.1093/hmg/ddi229
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- Publication type:
- Article
Morphological and functional reversal of phenotypes in a mouse model of Rett syndrome.
- Published in:
- Brain: A Journal of Neurology, 2012, v. 135, n. 9, p. 2699, doi. 10.1093/brain/aws096
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- Publication type:
- Article
Disease Modeling Using Embryonic Stem Cells: MeCP2 Regulates Nuclear Size and RNA Synthesis in Neurons.
- Published in:
- Stem Cells, 2012, v. 30, n. 10, p. 2128, doi. 10.1002/stem.1180
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- Article
A mutation-led search for novel functional domains in MeCP2.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 14, p. 2531, doi. 10.1093/hmg/ddy159
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- Publication type:
- Article