Adenoviral-mediated correction of methylmalonyl-CoA mutase deficiency in murine fibroblasts and human hepatocytes

Samankaltaisia teoksia

• Pre-clinical efficacy and dosing of an AAV8 vector expressing human methylmalonyl-CoA mutase in a murine model of methylmalonic acidemia (MMA)
  Tekijä: Chandler, Randy J., et al.
  Julkaistu: (2012)
• Inherited Methylmalonyl CoA Mutase Apoenzyme Deficiency in Human Fibroblasts: EVIDENCE FOR ALLELIC HETEROGENEITY, GENETIC COMPOUNDS, AND CODOMINANT EXPRESSION
  Tekijä: Willard, Huntington F., et al.
  Julkaistu: (1980)
• Functional Characterization and Categorization of Missense Mutations that Cause Methylmalonyl‐CoA Mutase (MUT) Deficiency
  Tekijä: Forny, Patrick, et al.
  Julkaistu: (2014)
• Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency
  Tekijä: Luciani, Alessandro, et al.
  Julkaistu: (2020)
• Immunochemical studies of fibroblasts from patients with methylmalonyl-CoA mutase apoenzyme deficiency: detection of a mutation interfering with mitochondrial import.
  Tekijä: Fenton, W A, et al.
  Julkaistu: (1987)