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Small Molecule Antagonists of NAADP-Induced Ca(2+) Release in T-Lymphocytes Suggest Potential Therapeutic Agents for Autoimmune Disease
Nicotinic acid adenine dinucleotide phosphate (NAADP) is the most potent Ca(2+)-releasing second messenger known to date, but the precise NAADP/Ca(2+) signalling mechanisms are still controversial. We report the synthesis of small-molecule inhibitors of NAADP-induced Ca(2+) release based upon the ni...
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| Vydáno v: | Sci Rep |
|---|---|
| Hlavní autoři: | , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Nature Publishing Group UK
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6233153/ https://ncbi.nlm.nih.gov/pubmed/30425261 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-34917-3 |
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