lysine has been researched along with Adrenoleukodystrophy in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Duval, C; Ferrer, I; Fourcade, S; Galino, J; Jove, M; Kemp, S; López-Erauskin, J; Naudi, A; Pamplona, R; Portero-Otin, M; Pujol, A; Villarroya, F | 1 |
Aubourg, P; Cartier, N; Douar, AM; Mandel, JL; Mosser, J; Sarde, CO | 1 |
2 other study(ies) available for lysine and Adrenoleukodystrophy
Article | Year |
---|---|
Early oxidative damage underlying neurodegeneration in X-adrenoleukodystrophy.
Topics: Adrenoleukodystrophy; Animals; Catalase; Chemokine CCL22; Chromans; Fatty Acids; Fibroblasts; Humans; In Vitro Techniques; Lysine; Malondialdehyde; Membrane Potential, Mitochondrial; Mice; Mice, Inbred C57BL; Motor Neurons; Oxidation-Reduction; Oxidative Stress; Spinal Cord; Superoxide Dismutase | 2008 |
Abnormal messenger RNA expression and a missense mutation in patients with X-linked adrenoleukodystrophy.
Topics: Adrenoleukodystrophy; Amino Acid Sequence; ATP-Binding Cassette Transporters; Base Sequence; Blotting, Northern; Cloning, Molecular; Conserved Sequence; DNA Probes; Exons; Female; Fibroblasts; Glutamates; Glutamic Acid; Humans; Lysine; Male; Membrane Proteins; Microbodies; Molecular Sequence Data; Pedigree; Point Mutation; RNA, Messenger; Sequence Deletion; Transcription, Genetic; X Chromosome | 1993 |