A Specific Enzyme Defect in Gyrate Atrophy
- 1 February 1978
- journal article
- research article
- Published by Elsevier in American Journal of Ophthalmology
- Vol. 85 (2) , 200-204
- https://doi.org/10.1016/s0002-9394(14)75948-3
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Stimulation of DNA synthesis, cell multiplication, and ornithine decarboxylase in 3T3 cells by multiplication stimulating activity (MSA)Journal of Cellular Physiology, 1976
- Type II hyperprolinemia. Delta1-pyrroline-5-carboxylic acid dehydrogenase deficiency in cultured skin fibroblasts and circulating lymphocytes.Journal of Clinical Investigation, 1976
- Plasma amino-acids in hereditary retinal disease. Ornithine, lysine, and taurine.British Journal of Ophthalmology, 1976
- Gyrate Atrophy of the Choroid and Retina with HyperornithinemiaAmerican Journal of Ophthalmology, 1975
- Increased sensitivity of lymphocyte Δ1pyrroline-5-carboxylate reductase to inhibition by proline with transformationNature, 1975
- Genetic aspects in gyrate atrophy of the choroid and retina with hyperornithinaemia.British Journal of Ophthalmology, 1974
- A radioisotopic assay for ornithine-δ-transaminaseAnalytical Biochemistry, 1973
- RAISED PLASMA-ORNITHINE AND GYRATE ATROPHY OF THE CHOROID AND RETINAThe Lancet, 1973
- Localisation of proline oxidase and Δ‐pyrroline‐5‐carboxylic acid dehydrogenase in rat liverFEBS Letters, 1969
- Purification and Properties of Rat Liver Ornithine δ-TransaminaseJournal of Biological Chemistry, 1965