טוען...
The Providence Mutation (βK82D) in Human Hemoglobin Substantially Reduces βCysteine 93 Oxidation and Oxidative Stress in Endothelial Cells
The highly toxic oxidative transformation of hemoglobin (Hb) to the ferryl state (HbFe(4+)) is known to occur in both in vitro and in vivo settings. We recently constructed oxidatively stable human Hbs, based on the Hb Providence (βK82D) mutation in sickle cell Hb (βE6V/βK82D) and in a recombinant c...
שמור ב:
| הוצא לאור ב: | Int J Mol Sci |
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| Main Authors: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
MDPI
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7763657/ https://ncbi.nlm.nih.gov/pubmed/33322551 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21249453 |
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