ロード中...
Regulation of the fetal hemoglobin silencing factor BCL11A
The clinical severity of sickle cell disease and β-thalassemia, the major disorders of β-globin, can be ameliorated by increased production of fetal hemoglobin (HbF). Here, we provide a brief overview of the fetal-to-adult hemoglobin switch that occurs in humans shortly after birth and review our cu...
保存先:
出版年: | Ann N Y Acad Sci |
---|---|
主要な著者: | , |
フォーマット: | Artigo |
言語: | Inglês |
出版事項: |
2016
|
主題: | |
オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4870126/ https://ncbi.nlm.nih.gov/pubmed/26963603 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/nyas.13024 |
タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|