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• W3048862743 abstract "The ability to determine the genetic etiology of intellectual disability (ID) and neurodevelopmental disorders (NDD) has improved immensely over the last decade. One prevailing metric from these studies is the large percentage of genes encoding epigenetic regulators, including many members of the ATP-dependent chromatin remodeling enzyme family. Chromatin remodeling proteins can be subdivided into 5 classes that include SWI/SNF, ISWI, CHD, INO80, and ATRX. These proteins utilize the energy from ATP hydrolysis to alter nucleosome positioning to mediate most cellular processes. As such, defining their precise roles and contributions to brain development and disease pathogenesis has proven to be complex. In this review, we illustrate that complexity by reviewing the roles of ATRX on genome stability, replication, and transcriptional regulation and how these mechanisms provide keys to the phenotype of ATR-X patients." @default.
• W3048862743 created "2020-08-18" @default.
• W3048862743 creator A5004213424 @default.
• W3048862743 creator A5011572563 @default.
• W3048862743 date "2020-08-11" @default.
• W3048862743 modified "2023-10-01" @default.
• W3048862743 title "Neurodevelopmental Disorders Caused by Defective Chromatin Remodeling: Phenotypic Complexity Is Highlighted by a Review of ATRX Function" @default.
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