Crystal structure of the S187F variant of human liver alanine: Aminotransferase associated with primary hyperoxaluria type I and its functional implications

Eitemau Tebyg

• Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I
  gan: Cellini, Barbara, et al.
  Cyhoeddwyd: (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()
  gan: Oppici, Elisa, et al.
  Cyhoeddwyd: (2012)
• Human wild-type alanine:glyoxylate aminotransferase and its naturally occurring G82E variant: functional properties and physiological implications
  gan: Cellini, Barbara, et al.
  Cyhoeddwyd: (2007)
• Molecular Requirements for Peroxisomal Targeting of Alanine-Glyoxylate Aminotransferase as an Essential Determinant in Primary Hyperoxaluria Type 1
  gan: Fodor, Krisztián, et al.
  Cyhoeddwyd: (2012)
• Molecular Insight into the Synergism between the Minor Allele of Human Liver Peroxisomal Alanine:Glyoxylate Aminotransferase and the F152I Mutation
  gan: Cellini, Barbara, et al.
  Cyhoeddwyd: (2009)