Concepedia

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

Elisa Oppici, Riccardo Montioli, Antonio Lorenzetto, Silvia Bianconi, Carla Borri Voltattorni, Barbara Cellini

Molecular Genetics and Metabolism · 2011 · 41 citations · 32 references

DOI

Concepts

References

32

The PyMOL Molecular Graphics System

Warren L. DeLano · Medical Entomology and Zoology · 2002 · 18.1K citations

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The use of differential scanning fluorimetry to detect ligand interactions that promote protein stability

F. Niesen, H. Berglund, Masoud Vedadi · Nature Protocols · 2007 · 2.4K citations

, , +14

Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

Christopher J. Danpure, Patricia R. Jennings · FEBS Letters · 1986 · 347 citations

, , +16

Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1.

P. Edward Purdue, Yoshikazu Takada, Christopher J. Danpure · The Journal of Cell Biology · 1990 · 233 citations · Full text

, , +17

Pyridoxine effect in type I primary hyperoxaluria is associated with the most common mutant allele

Carla G. Monico, Sandro Rossetti, Julie B. Olson et al. · Kidney International · 2005 · 184 citations · Full text

, , +9