Results 211 to 220 of about 2,731,322 (279)
Selective potentiation of alpha 1 glycine receptors by ginkgolic acid. [PDF]
Maleeva G, Buldakova S, Bregestovski P.
europepmc +1 more source
Signaling mechanism for modulation by ATP of glycine receptors on rat retinal ganglion cells. [PDF]
Zhang PP +5 more
europepmc +1 more source
Cadmium opens GluK2 kainate receptors with cysteine substitutions at the M3 helix bundle crossing [PDF]
Huettner, James E, Wilding, Timothy J
core +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Encyclopedia of Biological Chemistry III, 2021
T. Lynagh, B. Laube, J. Schaffer
semanticscholar +2 more sources
T. Lynagh, B. Laube, J. Schaffer
semanticscholar +2 more sources
Encyclopedia of Molecular Pharmacology, 2021
Gustavo Moraga-Cid, L. Aguayo
semanticscholar +2 more sources
Gustavo Moraga-Cid, L. Aguayo
semanticscholar +2 more sources
Glycine binding primes NMDA receptor internalization
Nature, 2003NMDA (N-methyl-d-aspartate) receptors (NMDARs) are a principal subtype of excitatory ligand-gated ion channel with prominent roles in physiological and disease processes in the central nervous system. Recognition that glycine potentiates NMDAR-mediated currents as well as being a requisite co-agonist of the NMDAR subtype of 'glutamate' receptor ...
Lorraine V Kalia +2 more
exaly +3 more sources
Excitatory glycine receptors containing the NR3 family of NMDA receptor subunits
Nature, 2002J. Chatterton +12 more
exaly +2 more sources
Pharmacology & Therapeutics, 1997
The inhibitory glycine receptor (GlyR) is a member of the ligand-gated ion channel receptor superfamily. The GlyR comprises a pentameric complex that forms a chloride-selective transmembrane channel, which is predominantly expressed in the spinal cord and brain stem. We review the pharmacological and physiological properties of the GlyR and relate this
Rajendra, S, Lynch, JW, Schofield, PR
openaire +3 more sources
The inhibitory glycine receptor (GlyR) is a member of the ligand-gated ion channel receptor superfamily. The GlyR comprises a pentameric complex that forms a chloride-selective transmembrane channel, which is predominantly expressed in the spinal cord and brain stem. We review the pharmacological and physiological properties of the GlyR and relate this
Rajendra, S, Lynch, JW, Schofield, PR
openaire +3 more sources
General Pharmacology: The Vascular System, 1978
Abstract 1. Recent studies aimed at elucidating synaptic glycine-receptors have been reviewed. 2. Biochemical and iontophoretic findings have revealed that such receptors exist in several regions of the vertebrate CNS. 3. Subcellular studies with labelled strychnine and glycine have revealed that strychnine does not interact directly with glycine ...
openaire +2 more sources
Abstract 1. Recent studies aimed at elucidating synaptic glycine-receptors have been reviewed. 2. Biochemical and iontophoretic findings have revealed that such receptors exist in several regions of the vertebrate CNS. 3. Subcellular studies with labelled strychnine and glycine have revealed that strychnine does not interact directly with glycine ...
openaire +2 more sources

