A small-molecule screen reveals novel modulators of MeCP2 and X-chromosome inactivation maintenance
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1866-1955
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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A small-molecule screen reveals novel modulators of MeCP2 and X-chromosome inactivation maintenance ; volume:12 ; number:1 ; day:10 ; month:11 ; year:2020 ; pages:1-11 ; date:12.2020
Journal of neurodevelopmental disorders ; 12, Heft 1 (10.11.2020), 1-11, 12.2020
- Creator
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Lee, Hyeong-Min
Kuijer, M. Bram
Ruiz Blanes, Nerea
Clark, Ellen P.
Aita, Megumi
Galiano Arjona, Lorena
Kokot, Agnieszka
Sciaky, Noah
Simon, Jeremy M.
Bhatnagar, Sanchita
Philpot, Benjamin D.
Cerase, Andrea
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s11689-020-09332-3
- URN
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urn:nbn:de:101:1-2020122122594921804173
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:36 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Lee, Hyeong-Min
- Kuijer, M. Bram
- Ruiz Blanes, Nerea
- Clark, Ellen P.
- Aita, Megumi
- Galiano Arjona, Lorena
- Kokot, Agnieszka
- Sciaky, Noah
- Simon, Jeremy M.
- Bhatnagar, Sanchita
- Philpot, Benjamin D.
- Cerase, Andrea
- SpringerLink (Online service)
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Interplay between MeCP2 and BDNF in Rett Syndrome
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Chromatin-dependent allosteric regulation of DNMT3A activity by MeCP2
Expression, Purification, Characterization and Cellular Uptake of MeCP2 Variants
Proteininteraktionspartner des humanen Methyl-CpG-Bindungsproteins 2 (MeCP2)
MeCP2 and Chromatin Compartmentalization
Regulation of MeCP2 induced heterochromatin remodeling
Regulation of MeCP2 induced heterochromatin remodeling
Epigenetik der chronischen Herzinsuffizienz: Bedeutung von MeCP2
Interplay between MeCP2 and BDNF in Rett Syndrome
Heterochromatin composition, organization and MeCP2 post-translational modifications
Proteininteraktionspartner des humanen Methyl-CpG-Bindungsproteins 2 (MeCP2)
MeCP2 mutations: progress towards understanding and treating Rett syndrome
MeCP2 phosphorylation in the brain: from transcription to behavior
Chromatin-dependent allosteric regulation of DNMT3A activity by MeCP2
Expression, Purification, Characterization and Cellular Uptake of MeCP2 Variants