טוען...
Molecular Insights into the Irreversible Mechanical Behavior of Sickle Hemoglobin
Sickle cell disease is caused by the amino acid substitution of glutamic acid to valine, which leads to the polymerization of deoxygenated sickle hemoglobin (HbS) into long strands. These strands are responsible for the sickling of red blood cells (RBCs), making blood hyper-coagulable leading to an...
שמור ב:
| הוצא לאור ב: | J Biomol Struct Dyn |
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| Main Authors: | , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2018
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6918955/ https://ncbi.nlm.nih.gov/pubmed/29651930 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/07391102.2018.1456362 |
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