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209 related items for PubMed ID: 7925268
1. Decreased agonist affinity and chloride conductance of mutant glycine receptors associated with human hereditary hyperekplexia. Langosch D, Laube B, Rundström N, Schmieden V, Bormann J, Betz H. EMBO J; 1994 Sep 15; 13(18):4223-8. PubMed ID: 7925268 [Abstract] [Full Text] [Related]
2. Properties of human glycine receptors containing the hyperekplexia mutation alpha1(K276E), expressed in Xenopus oocytes. Lewis TM, Sivilotti LG, Colquhoun D, Gardiner RM, Schoepfer R, Rees M. J Physiol; 1998 Feb 15; 507 ( Pt 1)(Pt 1):25-40. PubMed ID: 9490812 [Abstract] [Full Text] [Related]
3. The startle disease mutation Q266H, in the second transmembrane domain of the human glycine receptor, impairs channel gating. Moorhouse AJ, Jacques P, Barry PH, Schofield PR. Mol Pharmacol; 1999 Feb 15; 55(2):386-95. PubMed ID: 9927632 [Abstract] [Full Text] [Related]
4. Mutation of an arginine residue in the human glycine receptor transforms beta-alanine and taurine from agonists into competitive antagonists. Rajendra S, Lynch JW, Pierce KD, French CR, Barry PH, Schofield PR. Neuron; 1995 Jan 15; 14(1):169-75. PubMed ID: 7826634 [Abstract] [Full Text] [Related]
5. Hyperekplexia mutations of the glycine receptor unmask the inhibitory subsite for beta-amino-acids. Laube B, Langosch D, Betz H, Schmieden V. Neuroreport; 1995 Apr 19; 6(6):897-900. PubMed ID: 7542038 [Abstract] [Full Text] [Related]
6. Glycine receptor knock-in mice and hyperekplexia-like phenotypes: comparisons with the null mutant. Findlay GS, Phelan R, Roberts MT, Homanics GE, Bergeson SE, Lopreato GF, Mihic SJ, Blednov YA, Harris RA. J Neurosci; 2003 Sep 03; 23(22):8051-9. PubMed ID: 12954867 [Abstract] [Full Text] [Related]
7. Propofol restores the function of "hyperekplexic" mutant glycine receptors in Xenopus oocytes and mice. O'Shea SM, Becker L, Weiher H, Betz H, Laube B. J Neurosci; 2004 Mar 03; 24(9):2322-7. PubMed ID: 14999083 [Abstract] [Full Text] [Related]