Compromised Structure and Function of HDAC8 Mutants Identified in Cornelia de Lange Syndrome Spectrum Disorders

Lignende værker

• Biochemical and Structural Characterization of HDAC8 Mutants Associated with Cornelia de Lange Syndrome Spectrum Disorders
  af: Decroos, Christophe, et al.
  Udgivet: (2015)
• Structural aspects of HDAC8 mechanism and dysfunction in Cornelia de Lange syndrome spectrum disorders
  af: Deardorff, Matthew A., et al.
  Udgivet: (2016)
• Structural Analysis of Histone Deacetylase 8 Mutants Associated with Cornelia de Lange Syndrome Spectrum Disorders
  af: Osko, Jeremy D., et al.
  Udgivet: (2020)
• HDAC8 mutations in Cornelia de Lange Syndrome affect the cohesin acetylation cycle
  af: Deardorff, Matthew A., et al.
  Udgivet: (2012)
• Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance
  af: Kaiser, Frank J., et al.
  Udgivet: (2014)