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P2RX7 gene

Known as: P2X7, P2RX7, PURINERGIC RECEPTOR P2X, LIGAND-GATED ION CHANNEL, 7 
National Institutes of Health

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P2RX6 genepurinoceptor P2Z

Papers overview

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2019
2019
Effects of chronic lead exposure on the sympathoexcitatory response associated with the P2X7 receptor in rat superior cervical ganglia
2018
2018
P2RX7-MAPK1/2-SP1 axis inhibits MTOR independent HSPB1-mediated astroglial autophagy
Recently, we have reported that heat shock protein B1 (HSPB1) and purinergic receptor P2X7 (P2RX7) are involved in astroglial… 
2017
2017
P2X7 Participates in Intracerebral Hemorrhage-Induced Secondary Brain Injury in Rats via MAPKs Signaling Pathways
This study aimed to study the role of P2X7 in intracerebral hemorrhage (ICH)-induced secondary brain injury (SBI) and the… 
2016
2016
High Level P2X7-Mediated Signaling Impairs Function of Hematopoietic Stem/Progenitor Cells
Nucleotides, which bind to P2 receptors, have emerged as a family of mediators in intercellular communication. P2X7 is a member… 
2016
2016
Genetically dissecting P2rx7 expression within the central nervous system using conditional humanized mice
The purinergic P2X7 receptor (P2X7R) has attracted considerable interest as a potential target for various central nervous system… 
2015
2015
Neuropharmacology and analgesia A novel radioligand for the ATP-gated ion channel P 2 X 7 : [ 3 H ] JNJ-54232334
The ATP-gated ion channel P2X7 has emerged as a potential central nervous system (CNS) drug target based on the hypotheses that… 
2015
2015
Interdependence of ATP signalling and pannexin channels; the servant was really the master all along?
Pannexin channels are recognized as important conduits for the release of ATP, which contributes to purinergic signalling… 
2015
2015
P2X7/PANX1 as a new target for melanoma?
Alon Mantel and Valerie Harvey Hampton University Skin of Color Research Institute, Hampton University, Hampton, VA, USA… 
2015
2015
Evaluation of p2x7 and IFN-γ gene polymorphisms in patients with pulmonary tuberculosis using PCR-RFLP method
2010
2010
A Microdeletion at 12q24.31 Can Mimic Beckwith-Wiedemann Syndrome Neonatally
We report on a patient who was initially suspected to have Beckwith-Wiedemann syndrome because of recurrent neonatal… 
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