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| 16647138 | FAAH | FAAH | 2.2 | the metabolism of AEA is fatty acid amide hydrolase (FAAH) FAAH | |  |
| 16647138 | FAAH | FAAH | 2.2 | which is not a substrate for fatty acid amidohydrolase (FAAH), FAAH produced a similar increase in PGE 2 production as AEA | |  |
| 17350694 | FAAH | FAAH | 2.2 | opening of intracellular Ca 2 stores inhibition of AMT and FAAH antioxidative effects | |  |
| 17350694 | FAAH | FAAH | 2.2 | obtained through genetic ablation of fatty acid amide hydrolase (FAAH) FAAH 38 exert robust anti-inflammatory and neuroprotective effects in hSOD1G93A mice | |  |
| 17350694 | FAAH | FAAH | 2.2 | Several studies have provided strong evidence that FAAH owing to its broad distribution might represent an attractive therapeutic | |  |
| 17350694 | FAAH | FAAH | 2.2 | For example inhibition of FAAH by URB597 can augment endogenous brain levels of AEA and | |  |
| 17350694 | FAAH | FAAH | 2.2 | Similarly AM374 another FAAH inhibitor has been shown to exert potent neuroprotective effects in | |  |
| 17350694 | FAAH | FAAH | 2.2 | Furthermore another selective and powerful FAAH inhibitor that has been used for the treatment of pathological | |  |
| 17350694 | FAAH | FAAH | 2.2 | on the endocannabinoid tone and thus favors the use of FAAH inhibitors to treat the inflammatory and neurodegenerative damage associated with | |  |
| 17350694 | FAAH | FAAH | 2.2 | -acylphosphatidylethanolamine (NAPE)-specific NAPE -specific phospholipase D (NAPE-PLD) NAPE-PLD 59 and FAAH 60 and 61 with respect to AEA | |  |
| 17350694 | FAAH | FAAH | 2.2 | AEA seems to be largely dependent on its hydrolysis by FAAH rather than on its synthesis by Ca 2 -dependent N | |  |
| 17350694 | FAAH | FAAH | 2.2 | If not therapeutic agents per se inhibitors of NAPE-PLD FAAH AMT DAGL or MAGL could be used together with AEA | |  |
| 17350694 | FAAH | FAAH | 2.2 | The mechanism of action of cannabidiol relies on AMT and FAAH inhibition and on antioxidative properties as a result this natural | |  |
| 17350694 | FAAH | FAAH | 2.2 | up by cells AEA is a substrate for the hydrolase FAAH which breaks the amide bond and releases arachidonic acid and | |  |
| 17350694 | FAAH | FAAH | 2.2 | Once accumulated in the cell 2-AG can be degraded by FAAH or more efficiently by a specific MAGL | |  |
| 17350694 | FAAH | FAAH | 2.2 | the ECS are located in the plasma membrane apart from FAAH which is bound to intracellular membranes and MAGL which is | |  |
| 17350694 | FAAH | FAAH | 2.2 | are able to modulate the AEA metabolic enzymes NAPE-PLD and FAAH might be exploited to curb neuroinflammation | |  |
| 16647138 | fatty acid amide hydrolase | fatty acid amide hydrolase | 1.0 | the principal enzyme for the metabolism of aea is fatty acid amide hydrolase faah . | |  |
| 17350694 | fatty acid amide hydrolase | fatty acid amide hydrolase | 1.0 | pharmacological agonists of cb receptors and increased levels of endocannabinoids obtained through genetic ablation of fatty acid amide hydrolase faah [38] exert robust anti inflammatory and neuroprotective effects in hsod1g93a mice delaying disease progression 39 and 40 . | |  |