ロード中...
Correction of the genetic defect in hepatocytes from the Watanabe heritable hyperlipidemic rabbit.
Familial hypercholesterolemia is an inherited disease in humans that is caused by a defect in the receptor for low density lipoproteins (LDLR). The existence of an animal model for this disease, the Watanabe heritable hyperlipidemic (WHHL) rabbit, makes it an attractive candidate for developing new...
保存先:
| 出版年: | Proc Natl Acad Sci U S A |
|---|---|
| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
National Academy of Sciences
1988
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC280441/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2454468/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.85.12.4421 |
| 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!
|