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Bone|July 19, 2017
Application of human induced pluripotent stem cells to model fibrodysplasia ossificans progressivaEmilie Barruet, Edward C HsiaoMethods in Molecular Biology (Clifton, N.J.)|January 1, 2015
Using Human Induced Pluripotent Stem Cells to Model Skeletal DiseasesEmilie Barruet, Edward C HsiaoCurrent Osteoporosis Reports|November 14, 2019
Inflammation in Fibrodysplasia Ossificans Progressiva and Other Forms of Heterotopic OssificationKoji Matsuo, Robert Dalton Chavez, Emilie Barruet, et al.Elife|November 10, 2021
Modeling the <i>ACVR1</i><sup></sup> mutation in human skeletal muscle stem cellsEmilie Barruet, Steven M Garcia, Jake Wu, et al.STAR Protocols|February 8, 2021
Purification and preservation of satellite cells from human skeletal muscleKatharine Striedinger, Emilie Barruet, Jason H PomerantzStem Cell Research & Therapy|August 18, 2016
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 signalingEmilie Barruet, Blanca M Morales, Wint Lwin, et al.Bone Reports|July 26, 2016
Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralizationCorey J Cain, Nathalie Gaborit, Wint Lwin, et al.Plos One|May 16, 2023
Loss of transcriptional heterogeneity in aged human muscle stem cellsEmilie Barruet, Katharine Striedinger, Pauline Marangoni, et al.Elife|December 30, 2022
Heterogeneous levels of delta-like 4 within a multinucleated niche cell maintains muscle stem cell diversitySusan Eliazer, Xuefeng Sun, Emilie Barruet, et al.Bone|July 26, 2021
ACVR1<sup>R206H</sup> extends inflammatory responses in human induced pluripotent stem cell-derived macrophagesKoji Matsuo, Abigail Lepinski, Robert D Chavez, et al.Pageof 11