Concepedia

Primary hyperoxaluria type I due to a point mutation of T to C in the coding region of the serine:pyruvate aminotransferase gene

Kozo Nishiyama, Tsuneyoshi Funai, Ritsuko Katafuchi, Kaoru Onoyama, Arata Ichiyama

Biochemical and Biophysical Research Communications · 1991 · 47 citations · 14 references

DOI

Concepts

References

14

Studies on transformation of Escherichia coli with plasmids

Douglas Hanahan · Journal of Molecular Biology · 1983 · 11.3K citations

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Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

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

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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

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Rapid isolation of eukaryotic DNA

David D.L. Bowtell · Analytical Biochemistry · 1987 · 213 citations

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Purification and characterization of the principal inhibitor of calcium oxalate monohydrate crystal growth in human urine.

Yasushi Nakagawa, Veronika Abram, Ferenc J. Kézdy et al. · Journal of Biological Chemistry · 1983 · 208 citations · Full text

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