s-sulphocysteine has been researched along with Metal Metabolism, Inborn Error in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 5 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Arjune, S; Ayton, S; Belaidi, AA; Bush, AI; Dejanovic, B; Fusca, D; Hetsch, F; Kloppenburg, P; Kumar, A; Meier, JC; Santamaria-Araujo, JA; Schwarz, G; Semtner, M; Winkelmann, A | 1 |
| Atwal, PS; Scaglia, F | 1 |
| Brueck, W; Burfeind, P; Hakroush, S; Jakubiczka-Smorag, J; Kumar, A; Metz, I; Reiss, J; Santamaria-Araujo, JA; Schwarz, G; Smorag, L | 1 |
| Ceyhan, S; Clayton, PT; Footitt, EJ; Jakobs, C; Mills, PB; Struys, EA; Waters, PJ | 1 |
| Belaidi, AA; Schwarz, G | 1 |
1 review(s) available for s-sulphocysteine and Metal Metabolism, Inborn Error
| Article | Year |
|---|---|
Molybdenum cofactor deficiency.
Topics: Aldehyde Oxidase; Cysteine; Humans; Metal Metabolism, Inborn Errors; Organophosphorus Compounds; Oximes; Pterins; Sulfite Oxidase; Sulfites; Thiosulfates; Xanthine Dehydrogenase | 2016 |
4 other study(ies) available for s-sulphocysteine and Metal Metabolism, Inborn Error
| Article | Year |
|---|---|
S-sulfocysteine/NMDA receptor-dependent signaling underlies neurodegeneration in molybdenum cofactor deficiency.
Topics: Animals; Calcium Signaling; Cysteine; Disease Models, Animal; GABAergic Neurons; HEK293 Cells; Humans; Memantine; Metal Metabolism, Inborn Errors; Mice; Neurodegenerative Diseases; Organophosphorus Compounds; Pterins; Receptors, N-Methyl-D-Aspartate; Synapses; Tungsten Compounds | 2017 |
Mouse model for molybdenum cofactor deficiency type B recapitulates the phenotype observed in molybdenum cofactor deficient patients.
Topics: Animals; Apoptosis; Carbon-Carbon Lyases; Coenzymes; Cysteine; Disease Models, Animal; Gene Expression; Humans; Hypoxanthine; Metal Metabolism, Inborn Errors; Metalloproteins; Mice; Mice, Knockout; Molybdenum Cofactors; Mutation; Nuclear Proteins; Phenotype; Pteridines; Xanthine | 2016 |
Urinary AASA excretion is elevated in patients with molybdenum cofactor deficiency and isolated sulphite oxidase deficiency.
Topics: 2-Aminoadipic Acid; Adolescent; Amino Acid Metabolism, Inborn Errors; Child; Coenzymes; Cysteine; Humans; Infant, Newborn; L-Aminoadipate-Semialdehyde Dehydrogenase; Lysine; Metabolic Networks and Pathways; Metal Metabolism, Inborn Errors; Metalloproteins; Models, Biological; Molybdenum Cofactors; Molybdoferredoxin; Oxidoreductases Acting on Sulfur Group Donors; Pteridines; Sulfite Oxidase; Sulfites | 2012 |
Molybdenum cofactor deficiency: metabolic link between taurine and S-sulfocysteine.
Topics: Case-Control Studies; Chromatography, High Pressure Liquid; Cysteine; Humans; Metal Metabolism, Inborn Errors; Molybdoferredoxin; Taurine | 2013 |