Cytosolic compartmentalization of hepatic alanine: Glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism-Reference-Cited by-同舟云学术

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

Published:1994 Issue:1 Volume:17 Page:27-40
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

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.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://www.springerlink.com/index/pdf/10.1007/BF00735393

Reference32 articles.

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2. Carlemalm E, Garavito RM, Villiger W (1982) Resin development for electron microscopy and an analysis of embedding at low temperature.J Microsc 126: 123?143.

3. Cooper PJ, Danpure CJ, Wise PJ, Guttridge KM (1988) Immunocytochemical localization of human hepatic alanine: glyoxylate aminotransferase in control subjects and patients with primary hyperoxaluria type 1.J Histochem Cytochem 36: 1285?1294.

4. Danpure CJ (1989) Recent advances in the understanding, diagnosis and treatment of primary hyperoxaluria type 1.J Inher Metab Dis 12: 210?224.

5. Danpure CJ, Jennings PR (1986) Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type 1.FEBS Lett 201: 20?24.

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