Steven D. Funk

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2006-2013 Washington University, Saint Louis, St. Louis, MO 
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"Steven Funk"
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Funk SD, Bayer RH, McKee KK, et al. (2020) A deletion in the N-terminal polymerizing domain of laminin β2 is a new mouse model of chronic nephrotic syndrome. Kidney International
Funk SD, Bayer RH, Miner JH. (2019) Endothelial Cell-Specific Collagen IV α3 Expression Does not Rescue Alport Syndrome in Col4a3-/- Mice. American Journal of Physiology. Renal Physiology
Funk SD, Finney AC, Yurdagul A, et al. (2018) EphA2 stimulates VCAM-1 expression through calcium-dependent NFAT1 activity. Cellular Signalling. 49: 30-38
Funk SD, Lin MH, Miner JH. (2018) Alport syndrome and Pierson syndrome: Diseases of the glomerular basement membrane. Matrix Biology : Journal of the International Society For Matrix Biology
Funk SD, Bayer RH, Malone AF, et al. (2017) Pathogenicity of a Human Laminin β2 Mutation Revealed in Models of Alport Syndrome. Journal of the American Society of Nephrology : Jasn
Finney AC, Funk SD, Green J, et al. (2017) EphA2 Expression Regulates Inflammation and Fibroproliferative Remodeling in Atherosclerosis. Circulation
Funk SD, Miner JH. (2017) Muscular dystrophy meets protein biochemistry, the mother of invention. The Journal of Clinical Investigation
Malone AF, Funk SD, Alhamad T, et al. (2016) Functional assessment of a novel COL4A5 splice region variant and immunostaining of plucked hair follicles as an alternative method of diagnosis in X-linked Alport syndrome. Pediatric Nephrology (Berlin, Germany)
Yurdagul A, Chen J, Funk SD, et al. (2013) Altered nitric oxide production mediates matrix-specific PAK2 and NF-κB activation by flow. Molecular Biology of the Cell. 24: 398-408
Funk SD, Orr AW. (2013) Ephs and ephrins resurface in inflammation, immunity, and atherosclerosis. Pharmacological Research : the Official Journal of the Italian Pharmacological Society. 67: 42-52
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