Page last updated: 2024-08-17

lysine and Adrenoleukodystrophy

lysine has been researched along with Adrenoleukodystrophy in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
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, F1
Aubourg, P; Cartier, N; Douar, AM; Mandel, JL; Mosser, J; Sarde, CO1

Other Studies

2 other study(ies) available for lysine and Adrenoleukodystrophy

ArticleYear
Early oxidative damage underlying neurodegeneration in X-adrenoleukodystrophy.
    Human molecular genetics, 2008, Jun-15, Volume: 17, Issue:12

    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.
    Human molecular genetics, 1993, Volume: 2, Issue:11

    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