載入...
A Comment on “Muscle Xenografts Reproduce Key Molecular Features of Facioscapulohumeral Muscular Dystrophy”: What Is New and What Has Already been Done and Reported but Was Not Quoted?
A study was recently published that sought to develop an in vivo model of facioscapulohumeral muscular dystrophy by transplanting muscle precursor cells from a patient into immunodeficient mice. The study largely applied the methodology used by our team in a study published more than two decades ago...
Na minha lista:
| 發表在: | Cell Transplant |
|---|---|
| Main Authors: | , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
SAGE Publications
2020
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7563933/ https://ncbi.nlm.nih.gov/pubmed/32830546 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0963689720939120 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|