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Human COL7A1-corrected induced pluripotent stem cells for the treatment of recessive dystrophic epidermolysis bullosa

Patients with recessive dystrophic epidermolysis bullosa (RDEB) lack functional type VII collagen owing to mutations in the gene COL7A1 and suffer severe blistering and chronic wounds that ultimately lead to infection and development of lethal squamous cell carcinoma. The discovery of induced plurip...

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Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:	Sci Transl Med
Κύριοι συγγραφείς:	Sebastiano, Vittorio, Zhen, Hanson Hui, Haddad, Bahareh, Bashkirova, Elizaveta, Melo, Sandra P., Wang, Pei, Leung, Thomas L., Siprashvili, Zurab, Tichy, Andrea, Li, Jiang, Ameen, Mohammed, Hawkins, John, Lee, Susie, Li, Lingjie, Schwertschkow, Aaron, Bauer, Gerhard, Lisowski, Leszek, Kay, Mark A., Kim, Seung K., Lane, Alfred T., Wernig, Marius, Oro, Anthony E.
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	2014
Θέματα:	Article
Διαθέσιμο Online:	https://ncbi.nlm.nih.gov/pmc/articles/PMC4428910/ https://ncbi.nlm.nih.gov/pubmed/25429056 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/scitranslmed.3009540
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Human COL7A1-corrected induced pluripotent stem cells for the treatment of recessive dystrophic epidermolysis bullosa

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