The Human Glycine Receptor Subunit α3
Authors:
- Bodo LaubeBLBodo Laube
- Ruthild G. WeberRWRuthild G. Weber
- Peter LichterPLPeter Lichter
- Petra KioschisPKPetra Kioschis
- Annemarie PoustkaAPAnnemarie Poustka
- Cornel MülhardtCMCornel Mülhardt
- Cord-Michael BeckerCBCord-Michael Becker
Open Access
- 1 July 1998
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 273 (31) , 19708-19714
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Structure of the human alpha 2 subunit gene of the glycine receptor--use of vectorette and Alu-exon PCR.Genome Research, 1996
- Mutational analysis of familial and sporadic hyperekplexiaAnnals of Neurology, 1995
- Review : Glycine Receptors: Molecular Heterogeneity and Implications for DiseaseThe Neuroscientist, 1995
- Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the α1 subunit of the inhibitory glycine receptorHuman Molecular Genetics, 1994
- Point mutation of glycine receptor α1 subunit in the spasmodic mouse affects agonist responsesFEBS Letters, 1994
- Organisation of the murine 5‐HT3 receptor gene and assignment tohuman chromosome 11FEBS Letters, 1994
- Distinct agonist- and antagonist-binding sites on the glycine receptorNeuron, 1992
- Mapping of the glycine receptor α2-subunit gene and the GABAA α3-subunit gene on the mouse X chromosomeGenomics, 1991
- Alternative splicing generates two isoforms of the α2 subunit of the inhibitory glycine receptorFEBS Letters, 1991
- Functional chloride channels by mammalian cell expression of rat glycine receptor subunitNeuron, 1989