Molecular and Clinical Heterogeneity in Primary Hyperoxaluria Type 1

The Metabolic Basis of Inherited Disease.

Annals of Internal Medicine · 1983 · 2.7K citations

Life Sciences, Genetics, Molecular Genetics +13

Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

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

Life Sciences, Biochemistry, Biochemical Genetics +16

ENZYMOLOGICAL DIAGNOSIS OF PRIMARY HYPEROXALURIA TYPE 1 BY MEASUREMENT OF HEPATIC ALANINE: GLYOXYLATE AMINOTRANSFERASE ACTIVITY

ChristopherJ. Danpure, PatriciaR. Jennings, RichardW.E. Watts · The Lancet · 1987 · 174 citations

Life Sciences, Biochemistry, Enzymology +12

An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: peroxisomal alanine/glyoxylate aminotransferase rerouted to mitochondria.

Christopher J. Danpure, P. J. Cooper, P. J. Wise et al. · The Journal of Cell Biology · 1989 · 164 citations · Full text

Life Sciences, Biochemistry, Pathobiology +16

Human peroxisomal <scp>l</scp>-alanine: glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codon

Yoshikazu Takada, Naomi Kaneko, Hiroyasu Esumi et al. · Biochemical Journal · 1990 · 111 citations · Full text

Life Sciences, Genetics, Molecular Biology +15