Mutations in the Glucose-6-Phosphatase-α (G6PC) Gene that Cause Type Ia Glycogen Storage Disease

Lignende værker

• Hepatic glucose-6-phosphatase-α deficiency leads to metabolic reprogramming in glycogen storage disease type Ia
  af: Cho, Jun-Ho, et al.
  Udgivet: (2018)
• An evolutionary approach to optimizing glucose-6-phosphatase-α enzymatic activity for gene therapy of glycogen storage disease type Ia
  af: Zhang, Lisa, et al.
  Udgivet: (2019)
• The Upstream enhancer elements of the G6PC promoter are critical for optimal G6PC expression in murine glycogen storage disease type Ia
  af: Lee, Young Mok, et al.
  Udgivet: (2013)
• Minimal hepatic glucose-6-phosphatase-α activity required to sustain survival and prevent hepatocellular adenoma formation in murine glycogen storage disease type Ia
  af: Lee, Young Mok, et al.
  Udgivet: (2015)
• Complete Normalization of Hepatic G6PC Deficiency in Murine Glycogen Storage Disease Type Ia Using Gene Therapy
  af: Yiu, Wai Han, et al.
  Udgivet: (2010)