ATRX, a guardian of chromatin
Author:
Funder
European Research Council
Ministerio de Ciencia e Innovación
European Social Fund
Junta de Andalucía
Gobierno de España Ministerio de Ciencia e Innovación
Publisher
Elsevier BV
Subject
Genetics
Reference135 articles.
1. ATRX encodes a novel member of the SNF2 family of proteins: Mutations point to a common mechanism underlying the ATR-X syndrome;Picketts;Hum. Mol. Genet.,1996
2. Mutations in a putative global transcriptional regulator cause X-linked mental retardation with a-thalassemia (ATR-X syndrome);Gibbons;Cell,1995
3. A newly defined X linked mental retardation syndrome associated with a thalassaemia;Gibbons;J. Med. Genet.,1991
4. The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis;Bérubé;J. Clin. Invest.,2005
5. Atrx deficiency induces telomere dysfunction, endocrine defects, and reduced life span;Watson;J. Clin. Invest.,2013
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