Building New Function Into Glycine Receptors: A Structural Model for the Activation of the Glycine‐gated Chloride Channel

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Acetylcholine Receptor Channel Structure Probed in Cysteine-Substitution Mutants1992 · 672 citations
2. 2Hyperekplexia mutations of the glycine receptor unmask the inhibitory subsite for β-amino-acids1995 · 43 citations
3. 3Modulation by zinc ions of native rat and recombinant human inhibitory glycine receptors.1995 · 181 citations
4. 4Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the α1 subunit of the inhibitory glycine receptor1994 · 141 citations
5. 5Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis.1996 · 75 citations