Allele-specific Characterization of Alanine: Glyoxylate Aminotransferase Variants Associated with Primary Hyperoxaluria

Gelijkaardige items

• In Vivo and in Vitro Examination of Stability of Primary Hyperoxaluria-associated Human Alanine:Glyoxylate Aminotransferase
  door: Hopper, Erin D., et al.
  Gepubliceerd in: (2008)
• Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I
  door: Cellini, Barbara, et al.
  Gepubliceerd in: (2010)
• Biochemical analyses are instrumental in identifying the impact of mutations on holo and/or apo-forms and on the region(s) of alanine:glyoxylate aminotransferase variants associated with Primary Hyperoxaluria Type I()
  door: Oppici, Elisa, et al.
  Gepubliceerd in: (2012)
• Crystal structure of the S187F variant of human liver alanine: Aminotransferase associated with primary hyperoxaluria type I and its functional implications
  door: Oppici, Elisa, et al.
  Gepubliceerd in: (2013)
• Molecular Insight into the Synergism between the Minor Allele of Human Liver Peroxisomal Alanine:Glyoxylate Aminotransferase and the F152I Mutation
  door: Cellini, Barbara, et al.
  Gepubliceerd in: (2009)