Chargement en cours...
Knockdown of Fanconi anemia genes in human embryonic stem cells reveals early developmental defects in the hematopoietic lineage
Fanconi anemia (FA) is a genetically heterogeneous, autosomal recessive disorder characterized by pediatric bone marrow failure and congenital anomalies. The effect of FA gene deficiency on hematopoietic development in utero remains poorly described as mouse models of FA do not develop hematopoietic...
Enregistré dans:
| Auteurs principaux: | , , , , , , , |
|---|---|
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
American Society of Hematology
2010
|
| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2867260/ https://ncbi.nlm.nih.gov/pubmed/20089964 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2009-10-246694 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|