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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2014 | 1 |
2015 | 3 |
2024 | 0 |
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Page 1
Structural basis and biological consequences for JNK2/3 isoform selective aminopyrazoles.
Sci Rep. 2015 Jan 27;5:8047. doi: 10.1038/srep08047.
Sci Rep. 2015.
PMID: 25623238
Free PMC article.
Pyridopyrimidinone Derivatives as Potent and Selective c-Jun N-Terminal Kinase (JNK) Inhibitors.
Zheng K, Park CM, Iqbal S, Hernandez P, Park H, LoGrasso PV, Feng Y.
Zheng K, et al.
ACS Med Chem Lett. 2015 Mar 2;6(4):413-8. doi: 10.1021/ml500474d. eCollection 2015 Apr 9.
ACS Med Chem Lett. 2015.
PMID: 25893042
Free PMC article.
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Design and synthesis of highly potent and isoform selective JNK3 inhibitors: SAR studies on aminopyrazole derivatives.
Zheng K, Iqbal S, Hernandez P, Park H, LoGrasso PV, Feng Y.
Zheng K, et al.
J Med Chem. 2014 Dec 11;57(23):10013-30. doi: 10.1021/jm501256y. Epub 2014 Nov 21.
J Med Chem. 2014.
PMID: 25393557
Free PMC article.
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Serum- and Glucocorticoid-Inducible Kinase 1 Confers Protection in Cell-Based and in In Vivo Neurotoxin Models via the c-Jun N-Terminal Kinase Signaling Pathway.
Iqbal S, Howard S, LoGrasso PV.
Iqbal S, et al.
Mol Cell Biol. 2015 Jun 1;35(11):1992-2006. doi: 10.1128/MCB.01510-14. Epub 2015 Mar 30.
Mol Cell Biol. 2015.
PMID: 25825522
Free PMC article.
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