cysteine and Congenital Myasthenia

cysteine has been researched along with Congenital Myasthenia in 3 studies

Research

Studies (3)

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

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

Reviews

1 review(s) available for cysteine and Congenital Myasthenia

Article	Year
Recent advances in Cys-loop receptor structure and function. Nature, 2006, Mar-23, Volume: 440, Issue:7083 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

Other Studies

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. Human molecular genetics, 2002, Nov-15, Volume: 11, Issue:24 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. The Journal of clinical investigation, 2003, Volume: 111, Issue:4 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

Article

Year

Mutations in congenital myasthenic syndromes reveal an epsilon subunit C-terminal cysteine, C470, crucial for maturation and surface expression of adult AChR.

Human molecular genetics, 2002, Nov-15, Volume: 11, Issue:24

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.

The Journal of clinical investigation, 2003, Volume: 111, Issue:4

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