Compounds > cysteine

cysteine and Leigh Disease

cysteine has been researched along with Leigh Disease in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's0 (0.00)29.6817
2010's2 (50.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Ganetzky, R; Loomes, KM; Monteil, D; Murali, CN; Padilla, CD; Scaglia, F; Shah, AA; Soler-Alfonso, C1
Boneh, A; Ferdinandusse, S; Peters, H; Pitt, J; Ruiter, JP; Wanders, RJ1
Baatz, JE; Clapper, AC; Frizzell, N; Manuel, AM; Palmiter, RD; Piroli, GG; Quintana, A; Walla, MD1
Bertini, E; De Meirleir, L; Dionisi-Vici, C; Fariello, G; Rimoldi, M; Seneca, S; Zeviani, M1

Other Studies

4 other study(ies) available for cysteine and Leigh Disease

ArticleYear
TRMU deficiency: A broad clinical spectrum responsive to cysteine supplementation.
    Molecular genetics and metabolism, 2021, Volume: 132, Issue:2

    Topics: Acetylcysteine; Acidosis; Cysteine; DNA, Mitochondrial; Female; Humans; Infant; Leigh Disease; Liver Failure; Liver Transplantation; Male; Mitochondria; Mitochondrial Proteins; Protein Biosynthesis; RNA, Transfer; tRNA Methyltransferases

2021
Metabolite studies in HIBCH and ECHS1 defects: Implications for screening.
    Molecular genetics and metabolism, 2015, Volume: 115, Issue:4

    Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Child; Cysteine; Enoyl-CoA Hydratase; Female; Fibroblasts; Glutathione; Humans; Infant; Leigh Disease; Mass Screening; Mutation; Prognosis; Thiolester Hydrolases; Valine

2015
Succination is Increased on Select Proteins in the Brainstem of the NADH dehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) Knockout Mouse, a Model of Leigh Syndrome.
    Molecular & cellular proteomics : MCP, 2016, Volume: 15, Issue:2

    Topics: Animals; Brain Stem; Citric Acid Cycle; Cysteine; Disease Models, Animal; Electron Transport Complex I; Fumarates; Humans; Leigh Disease; Mice; Mice, Knockout; Mitochondria; Protein Processing, Post-Translational; Proteomics; Succinates; Tandem Mass Spectrometry

2016
Fulminant Leigh syndrome and sudden unexpected death in a family with the T9176C mutation of the mitochondrial ATPase 6 gene.
    Journal of inherited metabolic disease, 1998, Volume: 21, Issue:1

    Topics: Adenosine Triphosphatases; Cysteine; DNA, Mitochondrial; Humans; Infant; Leigh Disease; Male; Mitochondria; Pedigree; Point Mutation; Radiography; Sudden Infant Death; Threonine; Tomography Scanners, X-Ray Computed

1998