scholarly article | Q13442814 |
P50 | author | Lin-Hua Jiang | Q39064563 |
P2093 | author name string | Francois Rassendren | |
R Alan North | |||
Annmarie Surprenant | |||
Yi-Hong Zhang | |||
Amanda Mackenzie | |||
P2860 | cites work | Mitogen-activated protein kinase and caspase signaling pathways are required for P2X7 receptor (P2X7R)-induced pore formation in human THP-1 cells | Q44666463 |
Density-dependent changes of the pore properties of the P2X2 receptor channel | Q44859237 | ||
The P2X(7) receptor from Xenopus laevis: formation of a large pore in Xenopus oocytes | Q48865628 | ||
Differential assembly of rat purinergic P2X7 receptor in immune cells of the brain and periphery | Q48907038 | ||
P2X7 purinoceptor expression in Xenopus oocytes is not sufficient to produce a pore-forming P2Z-like phenotype | Q48955005 | ||
The ATP4− Receptor-Operated Channel (P2Z Class) of Human Lymphocytes Allows Ba2+ and Ethidium+ Uptake: Inhibition of Fluxes by Suramin | Q50125006 | ||
Characteristics of P2X7 receptors from human B lymphocytes expressed in Xenopus oocytes. | Q50722562 | ||
Kinetics of cell lysis, dye uptake and permeability changes in cells expressing the rat P2X7 receptor. | Q52536118 | ||
Identification of Amino Acid Residues Contributing to the ATP-binding Site of a Purinergic P2X Receptor | Q56828299 | ||
The permeabilizing ATP receptor, P2X7. Cloning and expression of a human cDNA | Q24321060 | ||
Proteomic and functional evidence for a P2X7 receptor signalling complex | Q24535912 | ||
Evidence for non-independent gating of P2X2 receptors expressed in Xenopus oocytes | Q24799255 | ||
Molecular physiology of P2X receptors | Q28203477 | ||
Characterization of the maitotoxin-activated cationic current from human skin fibroblasts | Q28344401 | ||
The cytolytic P2Z receptor for extracellular ATP identified as a P2X receptor (P2X7) | Q28568856 | ||
ATP-induced pore formation in the plasma membrane of rat peritoneal mast cells | Q28678688 | ||
ATP induces nucleotide permeability in rat mast cells | Q28678698 | ||
Extracellular ATP: effects, sources and fate | Q39500098 | ||
Are second messengers crucial for opening the pore associated with P2X7 receptor? | Q40506943 | ||
Identification of ectodomain regions contributing to gating, deactivation, and resensitization of purinergic P2X receptors. | Q40528321 | ||
Pharmacological and biophysical properties of the human P2X5 receptor | Q40645853 | ||
ATP-induced [Ca(2+)](i) changes and depolarization in GH3 cells | Q40859898 | ||
Pore dilation of neuronal P2X receptor channels | Q40960421 | ||
Ionic effects on human recombinant P2X7 receptor function | Q40970589 | ||
Effects of divalent cations, protons and calmidazolium at the rat P2X7 receptor | Q41080074 | ||
Neuronal P2X transmitter-gated cation channels change their ion selectivity in seconds. | Q41646184 | ||
The ATP4- receptor-operated ion channel of human lymphocytes: inhibition of ion fluxes by amiloride analogs and by extracellular sodium ions | Q42453923 | ||
P2X(7) receptors in rat parotid acinar cells: formation of large pores | Q43959161 | ||
P2X purinergic receptor channel expression and function in bovine aortic endothelium | Q43988574 | ||
Characteristics of ATP-induced current through P2X7 receptor in NG108-15 cells: unique antagonist sensitivity and lack of pore formation | Q44015991 | ||
Chicken DT40 cells stably transfected with the rat P2X7 receptor ion channel: a system suitable for the study of purine receptor-mediated cell death | Q44542007 | ||
P433 | issue | 5 | |
P304 | page(s) | C1295-302 | |
P577 | publication date | 2005-08-10 | |
P1433 | published in | American Journal of Physiology - Cell Physiology | Q2227080 |
P1476 | title | N-methyl-D-glucamine and propidium dyes utilize different permeation pathways at rat P2X(7) receptors | |
P478 | volume | 289 |
Q59336312 | A central role for P2X7 receptors in human microglia |
Q39834758 | A functional P2X7 splice variant with an alternative transmembrane domain 1 escapes gene inactivation in P2X7 knock-out mice. |
Q40821990 | A novel role for P2X7 receptor signalling in the survival of mouse embryonic stem cells. |
Q41847565 | ATP-induced P2X Receptor-Dependent Large Pore Formation: How Much Do We Know? |
Q35122793 | Activation and regulation of purinergic P2X receptor channels |
Q39959451 | Activation kinetics of single P2X receptors |
Q35545223 | Activation of ERK1/2 by extracellular nucleotides in macrophages is mediated by multiple P2 receptors independently of P2X7-associated pore or channel formation. |
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Q40813474 | C-terminal calmodulin-binding motif differentially controls human and rat P2X7 receptor current facilitation |
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Q39099142 | Canine erythrocytes express the P2X7 receptor: greatly increased function compared with human erythrocytes |
Q33801926 | Clemastine potentiates the human P2X7 receptor by sensitizing it to lower ATP concentrations. |
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Q37084254 | Interaction of P2 purinergic receptors with cellular macromolecules. |
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Q39966619 | Na+ modulates anion permeation and block of P2X7 receptors from mouse parotid glands. |
Q33781729 | Neuromodulation by extracellular ATP and P2X receptors in the CNS. |
Q37708660 | New structure enlivens interest in P2X receptors. |
Q38820111 | On the permeation of large organic cations through the pore of ATP-gated P2X receptors. |
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Q48601198 | P2X2 and P2X5 subunits define a new heteromeric receptor with P2X7-like properties. |
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Q39868233 | Pharmacological properties of a pore induced by raising intracellular Ca2+. |
Q38650165 | Pharmacological properties of the rhesus macaque monkey P2X7 receptor |
Q28237411 | Pharmacology of P2X channels |
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Q28569169 | Regulation of the desensitization and ion selectivity of ATP-gated P2X2 channels by phosphoinositides |
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