CHD7 targets active gene enhancer elements to modulate ES cell-specific gene expression.
CHD7 is one of nine members of the chromodomain helicase DNA-binding domain family of ATP-dependent chromatin remodeling enzymes found in mammalian cells. De novo mutation of CHD7 is a major cause of CHARGE syndrome, a genetic condition characterized by multiple congenital anomalies. To gain insight...
Saved in:
| Main Authors: | Michael P Schnetz, Lusy Handoko, Batool Akhtar-Zaidi, Cynthia F Bartels, C Filipe Pereira, Amanda G Fisher, David J Adams, Paul Flicek, Gregory E Crawford, Thomas Laframboise, Paul Tesar, Chia-Lin Wei, Peter C Scacheri |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2010-07-01
|
| Series: | PLoS Genetics |
| Online Access: | https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1001023&type=printable |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Duplication of the autism-related gene Chd8 leads to behavioral hyperactivity and neurodevelopmental defects in mice
by: Atsuki Kawamura, et al.
Published: (2025-05-01) -
Evaluation of molecular primers for sexing the magpie robin and green cucak via CHD1 gene amplification
by: Khilmi Fuadah, et al.
Published: (2025-06-01) -
Enrichment of tandem repeat element variants near CHD genes identified by short- and long-read genome sequencing
by: Abhilash Suresh, et al.
Published: (2025-07-01) -
CHD5, a brain-specific paralog of Mi2 chromatin remodeling enzymes, regulates expression of neuronal genes.
by: Rebecca Casaday Potts, et al.
Published: (2011-01-01) -
FIRST RESULTS OF CHD PROGNOSIS STUDY
by: E. A. Gofman, et al.
Published: (2014-07-01)