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Transgenic knockout mice exclusively expressing human hemoglobin S after transfer of a 240-kb β(s)-globin yeast artificial chromosome: A mouse model of sickle cell anemia
Sickle cell anemia (SCA) and thalassemia are among the most common genetic diseases worldwide. Current approaches to the development of murine models of SCA involve the elimination of functional murine α- and β-globin genes and substitution with human α and β(s) transgenes. Recently, two groups have...
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| Main Authors: | , , , , , , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
The National Academy of Sciences
1998
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC24545/ https://ncbi.nlm.nih.gov/pubmed/9843985 |
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