Molecular mechanism of lysophosphatidic acid-induced hypertensive response
Author:
Funder
Japan Agency for Medical Research and Development
MEXT | Japan Society for the Promotion of Science
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-019-39041-4.pdf
Reference29 articles.
1. Aikawa, S., Hashimoto, T., Kano, K. & Aoki, J. Lysophosphatidic acid as a lipid mediator with multiple biological actions. J. Biochem. 157, 81–89 (2015).
2. Kihara, Y., Mizuno, H. & Chun, J. Lysophospholipid receptors in drug discovery. Exp. Cell Res. 333, 171–177 (2015).
3. Aoki, J., Inoue, A. & Okudaira, S. Two pathways for lysophosphatidic acid production. Biochimica Et Biophysica Acta-Molecular and Cell Biology of Lipids 1781, 513–518 (2007).
4. Saga, H. et al. A Novel Highly Potent Autotaxin/ENPP2 Inhibitor Produces Prolonged Decreases in Plasma Lysophosphatidic Acid Formation In Vivo and Regulates Urethral Tension. PLoS ONE 9, e93230–e93230 (2013).
5. Tokumura, A. et al. Identification of vasopressor phospholipid in crude soybean lecithin. 13, 468–72 (1978).
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