Article
Recapitulation of pro-inflammatory signature of monocytes with ACVR1 mutation using FOP patient-derived iPSCs.
2022-05-05
Abstract excerpt
<title>Abstract</title> <p><bold>Background</bold> Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease characterized by progressive heterotopic ossification (HO) in soft tissues due to a heterozygous mutation of the ACVR1A/ALK2 gene (FOP-ACVR1A), which erroneously transduces the BMP signal by Activin-A. Although inflammation is known to trigger HO in FOP, the role of FOP-ACVR1A on inflammatory c...
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Identifiers and source
- Literature Corpus work
- 722736b0-f8d0-532b-b8ec-a5272fa8713d
- DOI
- 10.21203/rs.3.rs-1544500/v1
