INT25119
From wiki-pain
|
|
|
|
|
Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
PGD2 exerts its effects principally by binding and activating two plasma membrane receptors, the D prostanoid receptor (DP) 1 [15] and chemoattractant-receptor-like molecule expressed on Th2 cells (CRTH2), also known as DP2 [16]. | |||||||||||||||
| |||||||||||||||
|
It can be assumed that inhibition of this receptor does not reduce the production of prostaglandins, but inhibits the vasodilatation following the formation of PGD2. | |||||||||||||||
| |||||||||||||||
|
Interestingly, the promoter region of the human L-PGDS contains binding sites for NF-? | |||||||||||||||
| |||||||||||||||
|
On the mechanism of interaction of potent surmountable and insurmountable antagonists with the prostaglandin D2 receptor CRTH2. | |||||||||||||||
| |||||||||||||||
|
In washed platelet suspensions labeled with 3H-arachidonate, both APAP and aspirin inhibited the formation of labeled PGD2 and PGE2, as well as TxB2. | |||||||||||||||
| |||||||||||||||
|
It can bind to both PGH2 and PGD2 [15]. | |||||||||||||||
| |||||||||||||||
|
Taken altogether, our data suggest that COX-2-derived PGD2 and/or its metabolite 15-deoxy-? | |||||||||||||||
| |||||||||||||||
|
The aim of the present study was to determine the mechanism by which aspirin acutely increases the activity of NO synthase type 3 (NOS-3), the predominant NOS isoform expressed by platelets, and specifically whether this occurs through an increase in its acetylation. | |||||||||||||||
| |||||||||||||||
|
We also found significant inverse association between the same genotype with PDS among H. pylori positive subjects (ins/ins vs del carrier; OR = 0.22, 95% CI = 0.070.70, p = 0.01). | |||||||||||||||
| |||||||||||||||
|
General Comments
This test has worked.