Receptors, Purinergic P2X3
"Receptors, Purinergic P2X3" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A purinergic P2X neurotransmitter receptor involved in sensory signaling of TASTE PERCEPTION, chemoreception, visceral distension, and NEUROPATHIC PAIN. The receptor comprises three P2X3 subunits. The P2X3 subunits are also associated with P2X2 RECEPTOR subunits in a heterotrimeric receptor variant.
| Descriptor ID |
D058477
|
| MeSH Number(s) |
D12.776.157.530.400.400.750.300 D12.776.543.550.450.500.600.300 D12.776.543.585.400.500.600.300 D12.776.543.750.695.700.720.250.300 D12.776.543.750.720.700.720.500.300
|
| Concept/Terms |
Receptors, Purinergic P2X3- Receptors, Purinergic P2X3
- P2X3 Receptors, Purinergic
- Purinergic P2X3 Receptors
- P2X3 Receptor
- Receptor, P2X3
- Purinergic Receptor P2X, Ligand-Gated Ion Channel, 3
- P2X3 Purinoceptor
- Purinoceptor, P2X3
|
Below are MeSH descriptors whose meaning is more general than "Receptors, Purinergic P2X3".
- Chemicals and Drugs [D]
- Amino Acids, Peptides, and Proteins [D12]
- Proteins [D12.776]
- Carrier Proteins [D12.776.157]
- Membrane Transport Proteins [D12.776.157.530]
- Ion Channels [D12.776.157.530.400]
- Ligand-Gated Ion Channels [D12.776.157.530.400.400]
- Receptors, Purinergic P2X [D12.776.157.530.400.400.750]
- Receptors, Purinergic P2X3 [D12.776.157.530.400.400.750.300]
- Membrane Proteins [D12.776.543]
- Membrane Glycoproteins [D12.776.543.550]
- Ion Channels [D12.776.543.550.450]
- Ligand-Gated Ion Channels [D12.776.543.550.450.500]
- Receptors, Purinergic P2X [D12.776.543.550.450.500.600]
- Receptors, Purinergic P2X3 [D12.776.543.550.450.500.600.300]
- Membrane Transport Proteins [D12.776.543.585]
- Ion Channels [D12.776.543.585.400]
- Ligand-Gated Ion Channels [D12.776.543.585.400.500]
- Receptors, Purinergic P2X [D12.776.543.585.400.500.600]
- Receptors, Purinergic P2X3 [D12.776.543.585.400.500.600.300]
- Receptors, Cell Surface [D12.776.543.750]
- Receptors, G-Protein-Coupled [D12.776.543.750.695]
- Receptors, Purinergic [D12.776.543.750.695.700]
- Receptors, Purinergic P2 [D12.776.543.750.695.700.720]
- Receptors, Purinergic P2X [D12.776.543.750.695.700.720.250]
- Receptors, Purinergic P2X3 [D12.776.543.750.695.700.720.250.300]
- Receptors, Neurotransmitter [D12.776.543.750.720]
- Receptors, Purinergic [D12.776.543.750.720.700]
- Receptors, Purinergic P2 [D12.776.543.750.720.700.720]
- Receptors, Purinergic P2X [D12.776.543.750.720.700.720.500]
- Receptors, Purinergic P2X3 [D12.776.543.750.720.700.720.500.300]
Below are MeSH descriptors whose meaning is more specific than "Receptors, Purinergic P2X3".
This graph shows the total number of publications written about "Receptors, Purinergic P2X3" by people in this website by year, and whether "Receptors, Purinergic P2X3" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 0 | 1 | 1 |
| 2015 | 1 | 0 | 1 |
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Below are the most recent publications written about "Receptors, Purinergic P2X3" by people in Profiles.
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Localized inhibition of P2X7R at the spinal cord injury site improves neurogenic bladder dysfunction by decreasing urothelial P2X3R expression in rats. Life Sci. 2017 Feb 15; 171:60-67.
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P2X3 purinergic receptor overexpression is associated with poor recurrence-free survival in hepatocellular carcinoma patients. Oncotarget. 2015 Dec 01; 6(38):41162-79.
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Inhibition of urothelial P2X3 receptors prevents desensitization of purinergic detrusor contractions in the rat bladder. BJU Int. 2015 Aug; 116(2):293-301.
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Distribution of TRPVs, P2X3, and parvalbumin in the human nodose ganglion. Cell Mol Neurobiol. 2014 Aug; 34(6):851-8.
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Modulation of bladder afferent signals in normal and spinal cord-injured rats by purinergic P2X3 and P2X2/3 receptors. BJU Int. 2012 Oct; 110(8 Pt B):E409-14.
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Eccentric muscle contraction and stretching evoke mechanical hyperalgesia and modulate CGRP and P2X(3) expression in a functionally relevant manner. Pain. 2010 May; 149(2):284-295.