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Generation of dyskeratosis congenita-like hematopoietic stem cells through the stable inhibition of DKC1
Dyskeratosis congenita (DC) is a rare telomere biology disorder, which results in different clinical manifestations, including severe bone marrow failure. To date, the only curative treatment for the bone marrow failure in DC patients is allogeneic hematopoietic stem cell transplantation. However, d...
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| Publicado no: | Stem Cell Res Ther |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7844988/ https://ncbi.nlm.nih.gov/pubmed/33514435 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13287-021-02145-8 |
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