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7 in total

1. A new type of hyperlysinaemia due to a transport defect of lysine into mitochondria.

Authors: K Oyanagi; T Aoyama; A Tsuchiyama; T Nakao; N Uetsuji; K Wagatsuma; S Tsugawa
Journal: J Inherit Metab Dis Date: 1986 Impact factor: 4.982

2. Familial hyperlysinemias--multiple enzyme deficiencies associated with the bifunctional aminoadipic semialdehyde synthase.

Authors: R P Cox; P J Markovitz; D T Chuang
Journal: Trans Am Clin Climatol Assoc Date: 1986

3. Familial hyperlysinaemia due to L-lysine alpha-ketoglutarate reductase deficiency: results of attempted treatment.

Authors: C vd Heiden; M Brink; P K de Bree; F J v Sprang; S K Wadman; J M de Pater; J P van Biervliet
Journal: J Inherit Metab Dis Date: 1978 Impact factor: 4.982

4. Identification of L-amino acid/L-lysine alpha-amino oxidase in mouse brain.

Authors: S N Murthy; M K Janardanasarma
Journal: Mol Cell Biochem Date: 1999-07 Impact factor: 3.396

Review 5. Lysine metabolism in mammalian brain: an update on the importance of recent discoveries.

Authors: André Hallen; Joanne F Jamie; Arthur J L Cooper
Journal: Amino Acids Date: 2013-09-17 Impact factor: 3.520

6. Familial hyperlysinemia: enzyme studies, diagnostic methods, comments on terminology.

Authors: J Dancis; J Hutzler; R P Cox
Journal: Am J Hum Genet Date: 1979-05 Impact factor: 11.025

Review 7. Reciprocal Control of Thyroid Binding and the Pipecolate Pathway in the Brain.

Authors: André Hallen; Arthur J L Cooper
Journal: Neurochem Res Date: 2016-08-12 Impact factor: 3.996

7 in total