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Stem cell-based therapy for α(1)-antitrypsin deficiency
Human induced pluripotent stem cells offer the possibility of generating unlimited quantities of cells for autologous transplantation. By correcting the genetic defect underlying Z-allele α(1)-antitrypsin deficiency, we recently provided the first proof of principle for application of human induced...
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| Autori principali: | , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2012
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3340548/ https://ncbi.nlm.nih.gov/pubmed/22340671 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/scrt95 |
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