Induced Pluripotent Stem Cell Reprogramming by Integration-Free Sendai Virus Vectors from Peripheral Blood of Patients with Craniometaphyseal Dysplasia

Studies of rare genetic bone disorders are often limited due to unavailability of tissue specimens and the lack of animal models fully replicating phenotypic features. Craniometaphyseal dysplasia (CMD) is a rare monogenic disorder characterized by hyperostosis of craniofacial bones concurrent with a...

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Bibliografske podrobnosti
Main Authors: Chen, I-Ping, Fukuda, Keiichi, Fusaki, Noemi, Iida, Akihiro, Hasegawa, Mamoru, Lichtler, Alexander, Reichenberger, Ernst J.
Format: Artigo
Jezik:Inglês
Izdano: Mary Ann Liebert, Inc. 2013
Teme:
Original Articles
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3848480/
https://ncbi.nlm.nih.gov/pubmed/24219578
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/cell.2013.0037
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