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Application of Human Induced Pluripotent Stem Cells to Model Fibrodysplasia Ossificans Progressiva

Fibrodysplasia ossificans progressiva (FOP) is a genetic condition characterized by massive heterotopic ossification. FOP patients with mutations in the Activin A type I receptor (ACVR1), a bone morphogenetic protein (BMP) receptor. FOP is a progressive and debilitating disease characterized by bone...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Bone
Päätekijät: Barruet, Emilie, Hsiao, Edward C.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2017
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5767535/
https://ncbi.nlm.nih.gov/pubmed/28716551
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2017.07.003
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