ATRX and the replication of structured DNA
Author:
Funder
Medical Research Council
University of Oxford
Publisher
Elsevier BV
Subject
Developmental Biology,Genetics
Reference35 articles.
1. Syndromal mental retardation due to mutations in a regulator of gene expression;Gibbons;Hum Mol Genet,1995
2. Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation;Gibbons;Nat Genet,2000
3. Loss of ATRX leads to chromosome cohesion and congression defects;Ritchie;J Cell Biol,2008
4. ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes;De La Fuente;Dev Biol,2004
5. ATRX interacts with H3.3 in maintaining telomere structural integrity in pluripotent embryonic stem cells;Wong;Genome Res,2010
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1. ATRX restricts Human Cytomegalovirus (HCMV) viral DNA replication through heterochromatinization and minimizes unpackaged viral genomes;PLOS Pathogens;2024-09-05
2. The Chromatin Remodeler ATRX: Role and Mechanism in Biology and Cancer;Cancers;2023-04-10
3. pilE G-Quadruplex Is Recognized and Preferentially Bound but Not Processed by the MutL Endonuclease from Neisseria gonorrhoeae Mismatch Repair Pathway;International Journal of Molecular Sciences;2023-03-24
4. ATRX loss in glioma results in dysregulation of cell-cycle phase transition and ATM inhibitor radio-sensitization;Cell Reports;2022-01
5. Neuroblastoma—Telomere maintenance, deregulated signaling transduction and beyond;International Journal of Cancer;2021-10-26
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