The transmitter-gated channels: a range of receptor types and structures.

[1]  D. Osguthorpe,et al.  Modeling of agonist binding to the ligand‐gated ion channel superfamily of receptors , 1990, Proteins.

[2]  M. Kavanaugh,et al.  An excitatory amino-acid transporter with properties of a ligand-gated chloride channel , 1995, Nature.

[3]  P. Smith,et al.  Cloning and functional expression of the cDNA encoding a novel ATP‐sensitive potassium channel subunit expressed in pancreatic β‐cells, brain, heart and skeletal muscle , 1995 .

[4]  M. Hediger,et al.  A new family of neurotransmitter transporters: the high‐affinity glutamate transporters , 1993, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[5]  Y. Jan A superfamily of ion channels , 1990, Nature.

[6]  A. Nairn,et al.  Coupling of CFTR Cl− channel gating to an ATP hydrolysis cycle , 1994, Neuron.

[7]  A. Miyawaki,et al.  Cloning and characterization of human type 2 and type 3 inositol 1,4,5-trisphosphate receptors. , 1994, Receptors & channels.

[8]  M. Lazdunski,et al.  Cloning of the amiloride-sensitive FMRFamide peptide-gated sodium channel , 1995, Nature.

[9]  S. Siegelbaum,et al.  Molecular mechanism of cyclic-nucleotide-gated channel activation , 1994, Nature.

[10]  M. Lazdunski,et al.  Molecular Properties of Neuronal G-protein-activated Inwardly Rectifying K+ Channels (*) , 1995, The Journal of Biological Chemistry.

[11]  Raymond Dingledine,et al.  Topology profile for a glutamate receptor: Three transmembrane domains and a channel-lining reentrant membrane loop , 1995, Neuron.

[12]  M. Welsh,et al.  The amino-terminal portion of CFTR forms a regulated CI− channel , 1994, Cell.

[13]  J. Inazawa,et al.  Reconstitution of IKATP: An Inward Rectifier Subunit Plus the Sulfonylurea Receptor , 1995, Science.

[14]  N. Nayeem,et al.  Quaternary Structure of the Native GABAA Receptor Determined by Electron Microscopic Image Analysis , 1994, Journal of neurochemistry.

[15]  R. North,et al.  Cloning OF P2X5 and P2X6 receptors and the distribution and properties of an extended family of ATP-gated ion channels , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  A. Karlin,et al.  Toward a structural basis for the function of nicotinic acetylcholine receptors and their cousins , 1995, Neuron.

[17]  R. Beroukhim,et al.  Ultrastructure of the 5‐Hydroxytryptamine3 Receptor , 1995, Journal of neurochemistry.

[18]  Michael Hollmann,et al.  N-glycosylation site tagging suggests a three transmembrane domain topology for the glutamate receptor GluR1 , 1994, Neuron.

[19]  D. Vassilatis,et al.  Cloning of an avermectin-sensitive glutamate-gated chloride channel from Caenorhabditis elegans , 1994, Nature.

[20]  E. Kawashima,et al.  The Cytolytic P2Z Receptor for Extracellular ATP Identified as a P2X Receptor (P2X7) , 1996, Science.

[21]  M. Kavanaugh,et al.  Ion fluxes associated with excitatory amino acid transport , 1995, Neuron.

[22]  H. Lester,et al.  The inward rectifier potassium channel family , 1995, Current Opinion in Neurobiology.

[23]  A. Karlin,et al.  Acetylcholine receptor binding site contains a disulfide cross-link between adjacent half-cystinyl residues. , 1986, The Journal of biological chemistry.

[24]  L. Schild,et al.  Amiloride-sensitive epithelial Na+ channel is made of three homologous subunits , 1994, Nature.

[25]  M. Lazdunski,et al.  Expression cloning of an epithelial amiloride‐sensitive Na+ channel , 1993, FEBS letters.

[26]  S. Siegelbaum,et al.  Exposure of Residues in the Cyclic Nucleotide–Gated Channel Pore: P Region Structure and Function in Gating , 1996, Neuron.

[27]  E. Barnard,et al.  Receptor classes and the transmitter-gated ion channels. , 1992, Trends in biochemical sciences.

[28]  M. Welsh,et al.  Cloning and Expression of a Novel Human Brain Na Channel (*) , 1996, The Journal of Biological Chemistry.

[29]  N. Unwin,et al.  Neurotransmitter action: Opening of ligand-gated ion channels , 1993, Cell.

[30]  M. Lazdunski,et al.  The receptor for antidiabetic sulfonylureas controls the activity of the ATP-modulated K+ channel in insulin-secreting cells. , 1987, The Journal of biological chemistry.

[31]  M. Lazdunski,et al.  The Mammalian Degenerin MDEG, an Amiloride-sensitive Cation Channel Activated by Mutations Causing Neurodegeneration in Caenorhabditis elegans(*) , 1996, The Journal of Biological Chemistry.

[32]  D. Strickland,et al.  Ldl Receptor-related Protein: a Multiligand Receptor for Lipoprotein and Proteinase Catabolism the Ldl Receptor Family Table 1. Ligands for Lrp Secretion-recapture Model for Remnant Metabolism , 2022 .

[33]  Jean-Luc Galzi,et al.  Neurotransmitter-gated ion channels as unconventional allosteric proteins , 1994 .

[34]  M. Lazdunski,et al.  Biochemical analysis of the membrane topology of the amiloride-sensitive Na+ channel. , 1994, The Journal of biological chemistry.

[35]  P. Seeburg,et al.  Molecular biology of the GABAA receptor: the receptor/channel superfamily , 1987, Trends in Neurosciences.