Page last updated: 2024-09-03

s-sulphocysteine and Metal Metabolism, Inborn Errors

s-sulphocysteine has been researched along with Metal Metabolism, Inborn Errors in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's5 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
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, A1
Atwal, PS; Scaglia, F1
Brueck, W; Burfeind, P; Hakroush, S; Jakubiczka-Smorag, J; Kumar, A; Metz, I; Reiss, J; Santamaria-Araujo, JA; Schwarz, G; Smorag, L1
Ceyhan, S; Clayton, PT; Footitt, EJ; Jakobs, C; Mills, PB; Struys, EA; Waters, PJ1
Belaidi, AA; Schwarz, G1

Reviews

1 review(s) available for s-sulphocysteine and Metal Metabolism, Inborn Errors

ArticleYear
Molybdenum cofactor deficiency.
    Molecular genetics and metabolism, 2016, Volume: 117, Issue:1

    Topics: Aldehyde Oxidase; Cysteine; Humans; Metal Metabolism, Inborn Errors; Organophosphorus Compounds; Oximes; Pterins; Sulfite Oxidase; Sulfites; Thiosulfates; Xanthine Dehydrogenase

2016

Other Studies

4 other study(ies) available for s-sulphocysteine and Metal Metabolism, Inborn Errors

ArticleYear
S-sulfocysteine/NMDA receptor-dependent signaling underlies neurodegeneration in molybdenum cofactor deficiency.
    The Journal of clinical investigation, 2017, 12-01, Volume: 127, Issue:12

    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.
    Human genetics, 2016, Volume: 135, Issue:7

    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.
    Journal of inherited metabolic disease, 2012, Volume: 35, Issue:6

    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.
    Advances in experimental medicine and biology, 2013, Volume: 776

    Topics: Case-Control Studies; Chromatography, High Pressure Liquid; Cysteine; Humans; Metal Metabolism, Inborn Errors; Molybdoferredoxin; Taurine

2013