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

অনুরূপ উপাদানগুলি

• In Vivo and in Vitro Examination of Stability of Primary Hyperoxaluria-associated Human Alanine:Glyoxylate Aminotransferase
  অনুযায়ী: Hopper, Erin D., অন্যান্য
  প্রকাশিত: (2008)
• Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I
  অনুযায়ী: Cellini, Barbara, অন্যান্য
  প্রকাশিত: (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()
  অনুযায়ী: Oppici, Elisa, অন্যান্য
  প্রকাশিত: (2012)
• Crystal structure of the S187F variant of human liver alanine: Aminotransferase associated with primary hyperoxaluria type I and its functional implications
  অনুযায়ী: Oppici, Elisa, অন্যান্য
  প্রকাশিত: (2013)
• Molecular Insight into the Synergism between the Minor Allele of Human Liver Peroxisomal Alanine:Glyoxylate Aminotransferase and the F152I Mutation
  অনুযায়ী: Cellini, Barbara, অন্যান্য
  প্রকাশিত: (2009)