The ACVR1 R206H mutation found in fibrodysplasia ossificans progressiva increases human induced pluripotent stem cell-derived endothelial cell formation and collagen production through BMP-mediated SMAD1/5/8 signaling (Q37182424)

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scientific article published on 17 August 2016

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English	The ACVR1 R206H mutation found in fibrodysplasia ossificans progressiva increases human induced pluripotent stem cell-derived endothelial cell formation and collagen production through BMP-mediated SMAD1/5/8 signaling	scientific article published on 17 August 2016

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scholarly article

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21 March 2020

The ACVR1 R206H mutation found in fibrodysplasia ossificans progressiva increases human induced pluripotent stem cell-derived endothelial cell formation and collagen production through BMP-mediated SMAD1/5/8 signaling (English)

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21 March 2020

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fibrodysplasia ossificans progressiva

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Human Induced Pluripotent Stem Cells

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Sarah Anne Wong

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Emilie Barruet

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Blanca M Morales

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Wint Lwin

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Mark P White

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Christina V Theodoris

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Hannah Kim

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Ashley Urrutia

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Deepak Srivastava

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Edward C Hsiao

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17 August 2016

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Stem Cell Research & Therapy

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1

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ImageQuant

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CZ Software Mentions: A large dataset of software mentions in the biomedical literature

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Transforming Growth Factor-β Family Ligands Can Function as Antagonists by Competing for Type II Receptor Binding.

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Neofunction of ACVR1 in fibrodysplasia ossificans progressiva

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Induced pluripotent stem cells from patients with human fibrodysplasia ossificans progressiva show increased mineralization and cartilage formation

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Extracellular-matrix tethering regulates stem-cell fate

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Fibrodysplasia ossificans progressiva: clinical and genetic aspects

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Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1

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A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

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Fibrodysplasia ossificans progressiva (FOP), a disorder of ectopic osteogenesis, misregulates cell surface expression and trafficking of BMPRIA.

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Fibrodysplasia ossificans progressiva. The clinical features and natural history of 34 patients.

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12 December 2020

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10.1186/S13287-016-0372-6

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