Pharmacological properties of the rhesus macaque monkey P2X7 receptor.
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Insights into the Molecular Mechanisms Underlying Mammalian P2X7 Receptor Functions and Contributions in Diseases, Revealed by Structural Modeling and Single Nucleotide PolymorphismsNon-synonymous single nucleotide polymorphisms in the P2X receptor genes: association with diseases, impact on receptor functions and potential use as diagnosis biomarkersStructure-based identification and characterisation of structurally novel human P2X7 receptor antagonistsParoxetine suppresses recombinant human P2X7 responsesThe microglial ATP-gated ion channel P2X7 as a CNS drug target.R270C polymorphism leads to loss of function of the canine P2X7 receptor.Docking of competitive inhibitors to the P2X7 receptor family reveals key differences responsible for changes in response between rat and human.The P2X7 Receptor.
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P2860
Pharmacological properties of the rhesus macaque monkey P2X7 receptor.
description
2011 nî lūn-bûn
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2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
@zh-my
2011年学术文章
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2011年學術文章
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2011年學術文章
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2011年學術文章
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name
Pharmacological properties of the rhesus macaque monkey P2X7 receptor.
@en
Pharmacological properties of the rhesus macaque monkey P2X7 receptor.
@en-gb
type
label
Pharmacological properties of the rhesus macaque monkey P2X7 receptor.
@en
Pharmacological properties of the rhesus macaque monkey P2X7 receptor.
@en-gb
prefLabel
Pharmacological properties of the rhesus macaque monkey P2X7 receptor.
@en
Pharmacological properties of the rhesus macaque monkey P2X7 receptor.
@en-gb
P2093
P2860
P1476
Pharmacological properties of the rhesus macaque monkey P2X7 receptor.
@en
P2093
Helen J Bradley
Liam E Browne
P2860
P304
P356
10.1111/J.1476-5381.2011.01399.X
P407
P577
2011-09-01T00:00:00Z