scholarly article | Q13442814 |
P819 | ADS bibcode | 2013PLoSO...859411R |
P356 | DOI | 10.1371/JOURNAL.PONE.0059411 |
P932 | PMC publication ID | 3605439 |
P698 | PubMed publication ID | 23555667 |
P5875 | ResearchGate publication ID | 236106521 |
P50 | author | Milos Rokic | Q59687585 |
Vendula Tvrdonova | Q59707085 | ||
P2093 | author name string | Hana Zemkova | |
Pavlo Kuzyk | |||
Stanko S Stojilkovic | |||
Vojtech Vavra | |||
P2860 | cites work | Histidine 140 plays a key role in the inhibitory modulation of the P2X4 nucleotide receptor by copper but not zinc | Q24306094 |
ATP- and adenosine-mediated signaling in the central nervous system: chronic pain and microglia: involvement of the ATP receptor P2X4 | Q24311307 | ||
P2X1 and P2X3 receptors form stable trimers: a novel structural motif of ligand-gated ion channels | Q24533248 | ||
Molecular and functional properties of P2X receptors--recent progress and persisting challenges | Q24617046 | ||
Ion access pathway to the transmembrane pore in P2X receptor channels | Q24629121 | ||
Mechanism of ivermectin facilitation of human P2X4 receptor channels | Q24644507 | ||
Polar residues in the second transmembrane domain of the rat P2X2 receptor that affect spontaneous gating, unitary conductance, and rectification | Q24648191 | ||
Crystal structure of the ATP-gated P2X(4) ion channel in the closed state | Q24657193 | ||
Molecular mechanism of ATP binding and ion channel activation in P2X receptors | Q27678739 | ||
Allosteric control of gating and kinetics at P2X(4) receptor channels | Q28142880 | ||
Molecular physiology of P2X receptors | Q28203477 | ||
Identification of a non-canonical tyrosine-based endocytic motif in an ionotropic receptor | Q28213523 | ||
Signaling at purinergic P2X receptors | Q28296741 | ||
Gain and loss of channel function by alanine substitutions in the transmembrane segments of the rat ATP-gated P2X2 receptor | Q28564289 | ||
Identification of an intersubunit cross-link between substituted cysteine residues located in the putative ATP binding site of the P2X1 receptor | Q28569271 | ||
A point mutation in the ectodomain-transmembrane 2 interface eliminates the inhibitory effects of ethanol in P2X4 receptors | Q33601789 | ||
Gated access to the pore of a P2X receptor: structural implications for closed-open transitions. | Q33744436 | ||
Neuromodulation by extracellular ATP and P2X receptors in the CNS. | Q33781729 | ||
Identification of P2X4 receptor-specific residues contributing to the ivermectin effects on channel deactivation | Q34562779 | ||
Structural Insights into the Function of P2X4: An ATP-Gated Cation Channel of Neuroendocrine Cells | Q34588858 | ||
Regulation of P2X4 receptors by lysosomal targeting, glycan protection and exocytosis | Q34701623 | ||
Activation and regulation of purinergic P2X receptor channels | Q35122793 | ||
Preferential use of unobstructed lateral portals as the access route to the pore of human ATP-gated ion channels (P2X receptors). | Q35170819 | ||
Allosteric modulation of Ca2+ flux in ligand-gated cation channel (P2X4) by actions on lateral portals | Q35801949 | ||
Gating mechanism of a P2X4 receptor developed from normal mode analysis and molecular dynamics simulations | Q35837037 | ||
Cysteine substitution mutants give structural insight and identify ATP binding and activation sites at P2X receptors | Q36166147 | ||
Acidic amino acids impart enhanced Ca2+ permeability and flux in two members of the ATP-gated P2X receptor family | Q36295984 | ||
Pathophysiology and therapeutic potential of purinergic signaling | Q36409590 | ||
Secondary structure and gating rearrangements of transmembrane segments in rat P2X4 receptor channels | Q36412653 | ||
Contribution of extracellular negatively charged residues to ATP action and zinc modulation of rat P2X2 receptors | Q36951788 | ||
Purinergic regulation of hypothalamopituitary functions | Q37397335 | ||
An antagonist-insensitive P2X receptor expressed in epithelia and brain | Q38362921 | ||
Cysteine scanning mutagenesis (residues Glu52-Gly96) of the human P2X1 receptor for ATP: mapping agonist binding and channel gating | Q38673214 | ||
Functional relevance of aromatic residues in the first transmembrane domain of P2X receptors | Q39854925 | ||
On the role of the first transmembrane domain in cation permeability and flux of the ATP-gated P2X2 receptor | Q40042581 | ||
An intracellular P2X receptor required for osmoregulation in Dictyostelium discoideum | Q40108297 | ||
Participation of the Lys313-Ile333 sequence of the purinergic P2X4 receptor in agonist binding and transduction of signals to the channel gate | Q40235376 | ||
Contribution of transmembrane regions to ATP-gated P2X2 channel permeability dynamics | Q40489469 | ||
Contribution of calcium ions to P2X channel responses. | Q40571393 | ||
P2X receptor trafficking in neurons is subunit specific. | Q40723365 | ||
Amino acid residues involved in gating identified in the first membrane-spanning domain of the rat P2X(2) receptor | Q40816581 | ||
Pore dilation of neuronal P2X receptor channels | Q40960421 | ||
Identification of amino acid residues contributing to the pore of a P2X receptor | Q41106961 | ||
Neuronal P2X transmitter-gated cation channels change their ion selectivity in seconds. | Q41646184 | ||
Zinc enhances long-term potentiation through P2X receptor modulation in the hippocampal CA1 region | Q42972142 | ||
ATP binding at human P2X1 receptors. Contribution of aromatic and basic amino acids revealed using mutagenesis and partial agonists | Q44709204 | ||
Contribution of conserved glycine residues to ATP action at human P2X1 receptors: mutagenesis indicates that the glycine at position 250 is important for channel function | Q46762841 | ||
Contribution of conserved polar glutamine, asparagine and threonine residues and glycosylation to agonist action at human P2X1 receptors for ATP. | Q46863050 | ||
Facilitation of glutamate and GABA release by P2X receptor activation in supraoptic neurons from freshly isolated rat brain slices. | Q54372782 | ||
Identification of Amino Acid Residues Contributing to the ATP-binding Site of a Purinergic P2X Receptor | Q56828299 | ||
Ethanol inhibition of adenosine 5'-triphosphate-activated current in freshly isolated adult rat hippocampal CA1 neurons | Q73222592 | ||
Glycine rescue of β-sheets from cis-proline | Q84990063 | ||
P275 | copyright license | Creative Commons CC0 License | Q6938433 |
P6216 | copyright status | copyrighted, dedicated to the public domain by copyright holder | Q88088423 |
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | e59411 | |
P577 | publication date | 2013-03-21 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Multiple roles of the extracellular vestibule amino acid residues in the function of the rat P2X4 receptor | |
P478 | volume | 8 |
Q35920298 | Allosteric regulation of the P2X4 receptor channel pore dilation |
Q34295303 | Basolateral P2X₄channels stimulate ENaC activity in Xenopus cortical collecting duct A6 cells |
Q34514344 | Identification of functionally important residues of the rat P2X4 receptor by alanine scanning mutagenesis of the dorsal fin and left flipper domains |
Q26771359 | Insights into the channel gating of P2X receptors from structures, dynamics and small molecules |
Q47611830 | Ivermectin and its target molecules: shared and unique modulation mechanisms of ion channels and receptors by ivermectin |
Q38273638 | Key sites for P2X receptor function and multimerization: overview of mutagenesis studies on a structural basis |
Q39390185 | P2X Receptor Activation |
Q33718454 | P2X4 Receptor Function in the Nervous System and Current Breakthroughs in Pharmacology. |
Q34509716 | Plasma membrane cholesterol as a regulator of human and rodent P2X7 receptor activation and sensitization |
Q35587851 | Roles of the lateral fenestration residues of the P2X₄ receptor that contribute to the channel function and the deactivation effect of ivermectin |
Q37526362 | Structural and functional properties of the rat P2X4 purinoreceptor extracellular vestibule during gating. |
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