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Esco2 and cohesin regulate CRL4 ubiquitin ligase ddb1 expression and thalidomide teratogenicity
- Authors
- M. Kathryn IovineRobert Skibbens
- Description
Cornelia de Lange syndrome (CdLS) and Roberts syndrome (RBS) are severe developmental maladies that arise from mutation of cohesin (including SMC3, CdLS) and ESCO2 (RBS). Though ESCO2 activates cohesin, CdLS and RBS etiologies are currently considered non-synonymous and for which pharmacological treatments are unavailable. Here, we identify a unifying mechanism that integrates these genetic maladies...
- Subject
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Abnormalities, HumanCongenital AbnormalitiesCRL4 E3 ubiquitin ligase complex, humanDe Lange SyndromeRoberts SyndromeThalidomide
- Access Rights
- Free to All
- Local Expert
- Robert Skibbens