Correction: Hao et al. Phosphorylation of Akt by SC79 Prevents Iron Accumulation and Ameliorates Early Brain Injury in a Model of Experimental Subarachnoid Hemorrhage. Molecules 2016, 21, 325
Shuangying Hao, Chuanhui Song, Longcheng Shang, Yu Jiang, Tong Qiao, Kuanyu Li

Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsIntracerebral and Subarachnoid Hemorrhage Research
Author Name Correction
In the published publication [1], there was an error regarding the author name. We changed Jiang Yu to Yu Jiang.
Error in Figure
In the original publication [1], there was a mistake in Figure 3D as published. There were overlapping panels in Figure 3D’s SAH and SAH+vehicle panels. The corrected Figure 3 appears below.
SC79 administration after SAH largely rescues the impairment of Fe-S cluster biogenesis and alleviates the damage of neurons. (A) Western blot analysis for frataxin and ISCU. Upper panel: representative protein levels of frataxin and ISCU. Lower panel: quantitative data of the protein levels; (B) in-gel assay of aconitase activity. Upper panel: representative result. Lower panel: quantitative data of enzymatic activities; (C) enzymatic activity (upper panel) and Western blot (bottom panel) assays of XOD and CS; (D) representative slides of Nissl staining (left panel) and quantitative data (right panel) visualizing the neuronal cell outline and structure; and (E) alterations in brain water content. Data are expressed as mean ± SD (n = 8 in each group). * p < 0.05, *** p < 0.001 vs. sham group, # p < 0.05, ### p < 0.001 vs. SAH group. ISCU, Fe-S cluster scaffold protein; XOD, xanthine oxidase; CS, citrate synthase.
The authors state that the scientific conclusions are unaffected. This correction was approved by the Academic Editor. The original publication has also been updated.
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