Cockayne syndrome group B protein-null fibroblast rescue (HG-U133B)
Summary:
Analysis of Cockayne syndrome group B (CSB) protein-null fibroblasts rescued by expression of CSB cDNA. CS, a neurodegenerative disorder, arises mostly from CSB defects. Results provide insight into how CSB defects cause CS.
GPL97:
[HG-U133B] Affymetrix Human Genome U133B Array
Citation:
Newman JC, Bailey AD, Weiner AM. Cockayne syndrome group B protein (CSB) plays a general role in chromatin maintenance and remodeling. Proc Natl Acad Sci U S A 2006 Jun 20;103(25):9613-8. PMID: 16772382
