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ACS Chemical Biology|October 1, 2015
MAP4K4 Is a Threonine Kinase That Phosphorylates FARP1Adam G Schwaid, Chunyan Su, Paula Loos, et al.
Bioorganic & Medicinal Chemistry Letters|April 3, 2007
The discovery of highly selective erbB2 (Her2) inhibitors for the treatment of cancerBlaise Lippa, Goss S Kauffman, Joel Arcari, et al.
Plos One|March 20, 2019
Myeloperoxidase inhibition in mice alters atherosclerotic lesion compositionRachel J Roth Flach, Chunyan Su, Eliza Bollinger, et al.
Pest Management Science|January 6, 2026
Interspecific comparison reveals disparities in insecticide adaptive evolutionary capacity in insect pestsChengyue Li, Sai Chai, Qinghong Zeng, et al.
The Journal of Pharmacology and Experimental Therapeutics|February 21, 2015
PF-1355, a mechanism-based myeloperoxidase inhibitor, prevents immune complex vasculitis and anti-glomerular basement membrane glomerulonephritisWei Zheng, Roscoe Warner, Roger Ruggeri, et al.
Molecular Therapy. Methods & Clinical Development|March 7, 2022
<i>In vivo</i> overexpression of frataxin causes toxicity mediated by iron-sulfur cluster deficiencyClaudia Huichalaf, Tyler L Perfitt, Anna Kuperman, et al.
Molecular Cancer Therapeutics|April 1, 2010
PF-03814735, an orally bioavailable small molecule aurora kinase inhibitor for cancer therapyJitesh P Jani, Joel Arcari, Vincent Bernardo, et al.
Science (New York, N.Y.)|November 1, 2003
Prevention of organ allograft rejection by a specific Janus kinase 3 inhibitorPaul S Changelian, Mark E Flanagan, Douglas J Ball, et al.
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