Human γ-globin gene promoter element regulates human β-globin gene developmental specificity
The persistence of fetal hemoglobin in many patients with deletion type β thalassemias and the expression patterns of human globin genes in transgenic mice suggest that γ- to β-globin gene switching results primarily from competition of γ- and β-globin genes for interaction with the β-globin locus c...
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| Publicado en: | Nucleic Acids Res |
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| Autores principales: | , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Oxford University Press
2000
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC102642/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10908330/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/28.14.2736 |
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