Pharmacological inhibition of CaMKK2 with the selective antagonist STO-609 regresses NAFLD-Reference-Cited by-同舟云学术

Pharmacological inhibition of CaMKK2 with the selective antagonist STO-609 regresses NAFLD

Published:2017-09-18 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

York Brian,Li Feng,Lin Fumin,Marcelo Kathrina L.,Mao Jianqiang,Dean Adam,Gonzales Naomi,Gooden David,Maity Suman,Coarfa Cristian,Putluri Nagireddy,Means Anthony R.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-12139-3.pdf

Reference48 articles.

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3. Heitman, J., Movva, N. R., Hiestand, P. C. & Hall, M. N. FK 506-binding protein proline rotamase is a target for the immunosuppressive agent FK 506 in Saccharomyces cerevisiae. Proc Natl Acad Sci USA 88, 1948–1952 (1991).

4. Aramburu, J., Rao, A. & Klee, C. B. Calcineurin: from structure to function. Current topics in cellular regulation 36, 237–295 (2000).

5. Marcelo, K. L., Means, A. R. & York, B. The Ca(2+)/Calmodulin/CaMKK2 Axis: Nature’s Metabolic CaMshaft. Trends in endocrinology and metabolism: TEM 27, 706–718, https://doi.org/10.1016/j.tem.2016.06.001 (2016).

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