Analysis of the interplay between MeCP2 and histone H1 during <i>in vitro</i> differentiation of human ReNCell neural progenitor cells-Reference-Cited by-同舟云学术

Analysis of the interplay between MeCP2 and histone H1 during in vitro differentiation of human ReNCell neural progenitor cells

Published:2023-11-17 Issue:1 Volume:18 Page:
ISSN:1559-2294
Container-title:Epigenetics
language:en
Short-container-title:Epigenetics

Author:

Siqueira Edilene¹²^ORCID,Kim Bo-Hyun³^ORCID,Reser Larry⁴^ORCID,Chow Robert⁵^ORCID,Delaney Kerry⁵^ORCID,Esteller Manel¹⁶⁷^ORCID,Ross Mark M.⁴,Shabanowitz Jeffrey⁴^ORCID,Hunt Donald F.⁴⁸^ORCID,Guil Sonia¹⁹^ORCID,Ausió Juan³^ORCID

Affiliation:

1. Josep Carreras Leukaemia Research Institute (IJC), Badalona, Barcelona, Catalonia, Spain

2. National Council for Scientific and Technological Development (CNPq), Brasilia, Federal District, Brazil

3. Department of Biochemistry and Microbiology, University of Victoria, Victoria, BC, Canada

4. Department of Chemistry, University of Virginia, Charlottesville, Virginia, USA

5. Department of Biology, University of Victoria, Victoria, BC, Canada

6. Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, Catalonia, Spain

7. Physiological Sciences Department, School of Medicine and Health Sciences, University of Barcelona (UB), Barcelona, Catalonia, Spain

8. Department of Pathology, University of Virginia, Charlottesville, Virginia, USA

9. GermansTrias i Pujol Health Science Research Institute, Badalona, Barcelona, Catalonia, Spain

Funder

National Institutes of Health

Ontario Rett Syndrome Association

Catalan and Spanish Associations for Rett Syndrome

Publisher

Informa UK Limited

Subject

Cancer Research,Molecular Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/15592294.2023.2276425

Reference95 articles.

1. MeCP2 and the enigmatic organization of brain chromatin. Implications for depression and cocaine addiction

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

3. [On a unusual brain atrophy syndrome in hyperammonemia in childhood];Rett A;Wien Med Wochenschr,1966

4. Rett Syndrome: A Prototypical Neurodevelopmental Disorder

5. van Holde KE. Chromatin. NY: Springer-Verlag; 1988.

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