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In line with these results, a low residual GPX4 activity in Gpx4 flox/cys;Rosa26_CreERT2 mice (exchange of the catalytic selenocysteine to cysteine on the residual allele) was sufficient to prevent spontaneous renal failure after tamoxifen application, whereas Gpx4 flox/ser;Rosa26_CreERT2 mice (lacking residual activity) failed to prevent spontaneous tubular necrosis [72]
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Early signs of DN are often subtle and nonspecific, which can lead to delayed diagnosis and progression to irreversible stages of nerve damage
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