cysteine has been researched along with Congenital Myasthenia in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Abdelgany, A; Beeson, D; Brownlow, S; Ealing, J; Muntoni, F; Oosterhuis, H; Vaux, DJ; Vincent, A; Webster, R | 1 |
Brengman, JM; Engel, AG; Gingold, M; Ohno, K; Shen, XM; Sine, SM; Tsujino, A | 1 |
Engel, AG; Sine, SM | 1 |
1 review(s) available for cysteine and Congenital Myasthenia
Article | Year |
---|---|
Recent advances in Cys-loop receptor structure and function.
Topics: Acetylcholine; Animals; Cysteine; Humans; Ion Channel Gating; Myasthenic Syndromes, Congenital; Neurotransmitter Agents; Nicotinic Agonists; Protein Conformation; Receptors, Nicotinic; Structure-Activity Relationship; Synapses; Synaptic Transmission | 2006 |
2 other study(ies) available for cysteine and Congenital Myasthenia
Article | Year |
---|---|
Mutations in congenital myasthenic syndromes reveal an epsilon subunit C-terminal cysteine, C470, crucial for maturation and surface expression of adult AChR.
Topics: Cysteine; DNA Mutational Analysis; Green Fluorescent Proteins; Humans; Luminescent Proteins; Mutation; Myasthenic Syndromes, Congenital; Receptors, Cholinergic; Recombinant Fusion Proteins; Sequence Deletion | 2002 |
Mutation causing severe myasthenia reveals functional asymmetry of AChR signature cystine loops in agonist binding and gating.
Topics: Acetylcholine; Amino Acid Sequence; Case-Control Studies; Cell Line; Child, Preschool; Cysteine; Female; Humans; In Vitro Techniques; Ion Channel Gating; Kinetics; Male; Models, Molecular; Molecular Sequence Data; Myasthenic Syndromes, Congenital; Phenotype; Point Mutation; Protein Subunits; Receptors, Cholinergic; Recombinant Proteins; Sequence Homology, Amino Acid | 2003 |