Cytosolic compartmentalization of hepatic alanine: Glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism

Autor: Danpure, C. J., Fryer, P., Griffiths, S., Guttridge, K. M., Jennings, P. R., Allsop, J., Moser, A. B., Naidu, S., Moser, H. W., MacCollin, M., DeVivo, D. C.

Publikováno v: Journal of Inherited Metabolic Disease; January 1994, Vol. 17 Issue: 1 p27-40, 14p

Immunoelectron microscopic localization of alanine-glyoxylate aminotransferase in normal human liver and type 1 hyperoxaluric liver

Autor: COOPER, P. J., DANPURE, C. J., WISE, P. J., GUTTRIDGE, K. M.

Publikováno v: Biochemical Society Transactions; August 1988, Vol. 16 Issue: 4 p627-628, 2p

Enzymological and mutational analysis of a complex primary hyperoxaluria type 1 phenotype involving alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting and intraperoxisomal aggregation.

Autor: Danpure CJ; Biochemical Genetics Research Group, Medical Research Council Clinical Research Centre, Harrow, Middlesex, United Kingdom., Purdue PE, Fryer P, Griffiths S, Allsop J, Lumb MJ, Guttridge KM, Jennings PR, Scheinman JI, Mauer SM, et. al.

Publikováno v: American journal of human genetics [Am J Hum Genet] 1993 Aug; Vol. 53 (2), pp. 417-32.

Differentiation of the myocardial rudiment of mouse embryos: an ultrastructural study including freeze-fracture replication.

Autor: Navaratnam V; Department of Anatomy, University of Cambridge., Kaufman MH, Skepper JN, Barton S, Guttridge KM

Publikováno v: Journal of anatomy [J Anat] 1986 Jun; Vol. 146, pp. 65-85.