Concepedia

Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase

Elisa Oppici, Alessandro Roncador, Riccardo Montioli, Silvia Bianconi, Barbara Cellini

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 2013 · 35 citations · 43 references

DOI

Concepts

References

43

Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

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

, , +16

Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment

Pierre Cochat, Sally A. Hulton, Cécile Acquaviva et al. · Nephrology Dialysis Transplantation · 2012 · 335 citations · Full text

, , +17

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

The crystal structure of human cytosolic serine hydroxymethyltransferase: a target for cancer chemotherapy

Suzanne Renwick, Keith Snell, Ulrich Baumann · Structure · 1998 · 177 citations · Full text

, , +14