The Human Glycine Receptor Subunit α3

This publication has 39 references indexed in Scilit:

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  Genome Research, 1996
• Mutational analysis of familial and sporadic hyperekplexia
  Annals of Neurology, 1995
• Review : Glycine Receptors: Molecular Heterogeneity and Implications for Disease
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• Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the α₁ subunit of the inhibitory glycine receptor
  Human Molecular Genetics, 1994
• Point mutation of glycine receptor α1 subunit in the spasmodic mouse affects agonist responses
  FEBS Letters, 1994
• Organisation of the murine 5‐HT₃ receptor gene and assignment tohuman chromosome 11
  FEBS Letters, 1994
• Distinct agonist- and antagonist-binding sites on the glycine receptor
  Neuron, 1992
• Mapping of the glycine receptor α2-subunit gene and the GABAA α3-subunit gene on the mouse X chromosome
  Genomics, 1991
• Alternative splicing generates two isoforms of the α2 subunit of the inhibitory glycine receptor
  FEBS Letters, 1991
• Functional chloride channels by mammalian cell expression of rat glycine receptor subunit
  Neuron, 1989