Alleviation of accelerated diabetic atherogenesis in STZ-treated apoE/NOX1 DKO mice, apoE-/-/tg-EC-DHFR mice, and by folic acid

By sjmartinez • April 6, 2025

Zhang Y, Youn JY, Huang K, Zhang Y, Cai H. Alleviation of accelerated diabetic atherogenesis in STZ-treated apoE/NOX1 DKO mice, apoE^-/-/tg-EC-DHFR mice, and by folic acid. Redox Biol. 2025 Feb 27;82:103570. doi: 10.1016/j.redox.2025.103570. Epub ahead of print. PMID: 40184644.

Atherosclerosis, Diabetes, Diabetic atherogenesis, Dihydrofolate reductase, DHFR, Endothelial nitric oxide synthase, eNOS, uncoupling, Endothelial-specific DHFR transgenic mice, tg-EC-DHFR, NADPH oxidase isoform 1, NOX1, NOX1 knockout mice, apoE(-/-)/NOX1(-/y), apoE null mice, apoE(−/−), apoE/NOX1 double knockout mice, apoE(-/-)/NOX1(-/y),

Tags: apoE null mice, apoE(-/-)/NOX1(-/y), apoE(−/−), apoE/NOX1 double knockout mice, Atherosclerosis, Cardiology/Epi, DHFR, diabetes, Diabetic atherogenesis, Dihydrofolate reductase, Endothelial nitric oxide synthase, Endothelial-specific DHFR transgenic mice, eNOS, NADPH oxidase isoform 1, NOX1, NOX1 knockout mice, Post Doc, Publications, tg-EC-DHFR, Uncoupling

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