Work

MeCP2 links heterochromatin condensates and neurodevelopmental disease

Year: 2020

Type: article

Source: Nature

DOI: 10.1038/s41586-020-2574-4

Institutions: Whitehead Institute for Biomedical Research, Massachusetts Institute of Technology, Massachusetts General Hospital, University Medical Center Utrecht, Columbia University Irving Medical Center, Columbia University, New York University

Language: English

Topic: Genetics and Neurodevelopmental Disorders

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: National Institutes of Health, National Institute of Mental Health, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Diabetes and Digestive and Kidney Diseases

Awards: G1582611089, Graduate Training in Computational and Systems Biology, Transcriptional regulatory networks in living cells, Transcriptional condensates, epigenetic editing and Rett Syndrome, G4482077051, Pre-Doctoral Training in Biological Sciences, G8092220031, Role of the Rett Syndrome-causing gene MeCP2 in 3D chromosomal organization and rescue of cellular disease phenotypes, G9000177868

OpenAlex ID: W3045466751

FWCI: 13.22

Cites: 52

Cited by: 197

Related to: 10