Found: 25
Select item for more details and to access through your institution.
Epigenetics in the Nervous System.
- Published in:
- Journal of Neuroscience, 2008, v. 28, n. 46, p. 11753, doi. 10.1523/JNEUROSCI.3797-08.2008
- By:
- Publication type:
- Article
Investigation of modifier genes within copy number variations in Rett syndrome.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 5, p. 342, doi. 10.1038/jhg.2012.30
- By:
- Publication type:
- Article
Investigation of modifier genes within copy number variations in Rett syndrome.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 7, p. 508, doi. 10.1038/jhg.2011.50
- By:
- Publication type:
- Article
Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6695, doi. 10.1093/hmg/ddu496
- By:
- Publication type:
- Article
MeCP2 regulates activity-dependent transcriptional responses in olfactory sensory neurons.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 23, p. 6366, doi. 10.1093/hmg/ddu358
- By:
- Publication type:
- Article
Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 9, p. 2447, doi. 10.1093/hmg/ddt640
- By:
- Publication type:
- Article
A Prader–Willi locus lncRNA cloud modulates diurnal genes and energy expenditure.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 21, p. 4318, doi. 10.1093/hmg/ddt281
- By:
- Publication type:
- Article
Long-lived epigenetic interactions between perinatal PBDE exposure and Mecp2308 mutation.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 11, p. 2399, doi. 10.1093/hmg/dds046
- By:
- Publication type:
- Article
15q11.2–13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4311, doi. 10.1093/hmg/ddr357
- By:
- Publication type:
- Article
Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 19, p. 3798, doi. 10.1093/hmg/ddr298
- By:
- Publication type:
- Article
Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 3, p. 525, doi. 10.1093/hmg/ddn380
- By:
- Publication type:
- Article
15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 6, p. 691, doi. 10.1093/hmg/ddm014
- By:
- Publication type:
- Article
Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 12, p. 2003, doi. 10.1093/hmg/ddl124
- By:
- Publication type:
- Article
Homologous pairing of 15q11–13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 6, p. 785, doi. 10.1093/hmg/ddi073
- By:
- Publication type:
- Article
Sequence features accurately predict genome-wide MeCP2 binding in vivo.
- Published in:
- Nature Communications, 2016, v. 7, n. 3, p. 11025, doi. 10.1038/ncomms11025
- By:
- Publication type:
- Article
MECP2 promoter methylation and X chromosome inactivation in autism.
- Published in:
- Autism Research: Official Journal of the International Society for Autism Research, 2008, v. 1, n. 3, p. 169, doi. 10.1002/aur.24
- By:
- Publication type:
- Article
Editorial: Epigenetic Mechanisms and Their Involvement in Rare Diseases.
- Published in:
- 2021
- By:
- Publication type:
- Editorial
The Molecular Functions of MeCP2 in Rett Syndrome Pathology.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.624290
- By:
- Publication type:
- Article
Snord116-dependent diurnal rhythm of DNA methylation in mouse cortex.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-03676-0
- By:
- Publication type:
- Article
Sex disparate gut microbiome and metabolome perturbations precede disease progression in a mouse model of Rett syndrome.
- Published in:
- Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02915-3
- By:
- Publication type:
- Article
MeCP2 modulates gene expression pathways in astrocytes.
- Published in:
- Molecular Autism, 2013, v. 4, n. 1, p. 1, doi. 10.1186/2040-2392-4-3
- By:
- Publication type:
- Article
Placental DNA methylation levels at CYP2E1 and IRS2 are associated with child outcome in a prospective autism study.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2659, doi. 10.1093/hmg/ddz084
- By:
- Publication type:
- Article
MeCP2 isoform e1 mutant mice recapitulate motor and metabolic phenotypes of Rett syndrome.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 23, p. 4077, doi. 10.1093/hmg/ddy301
- By:
- Publication type:
- Article
Prader–Willi locus Snord116 RNA processing requires an active endogenous allele and neuron-specific splicing by Rbfox3/NeuN.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 23, p. 4051, doi. 10.1093/hmg/ddy296
- By:
- Publication type:
- Article
Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 15, p. 3284, doi. 10.1093/hmg/ddw178
- By:
- Publication type:
- Article