[HTML][HTML] Heterotopic ossification: a comprehensive review

C Meyers, J Lisiecki, S Miller, A Levin, L Fayad… - JBMR …, 2019 - Wiley Online Library
Heterotopic ossification (HO) is a diverse pathologic process, defined as the formation of
extraskeletal bone in muscle and soft tissues. HO can be conceptualized as a tissue repair …

Osteoblast Differentiation and Bone Matrix Formation In Vivo and In Vitro

HC Blair, QC Larrouture, Y Li, H Lin… - … Engineering Part B …, 2017 - liebertpub.com
We review the characteristics of osteoblast differentiation and bone matrix synthesis. Bone in
air breathing vertebrates is a specialized tissue that developmentally replaces simpler solid …

ACVR1R206H receptor mutation causes fibrodysplasia ossificans progressiva by imparting responsiveness to activin A

SJ Hatsell, V Idone, DMA Wolken, L Huang… - Science translational …, 2015 - science.org
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder characterized by
episodically exuberant heterotopic ossification (HO), whereby skeletal muscle is abnormally …

Neofunction of ACVR1 in fibrodysplasia ossificans progressiva

K Hino, M Ikeya, K Horigome… - Proceedings of the …, 2015 - National Acad Sciences
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease characterized by
extraskeletal bone formation through endochondral ossification. FOP patients harbor point …

[HTML][HTML] Activin-dependent signaling in fibro/adipogenic progenitors causes fibrodysplasia ossificans progressiva

JB Lees-Shepard, M Yamamoto, AA Biswas… - Nature …, 2018 - nature.com
Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal-dominant disorder
characterized by progressive and profoundly disabling heterotopic ossification (HO). Here …

Two tissue-resident progenitor lineages drive distinct phenotypes of heterotopic ossification

D Dey, J Bagarova, SJ Hatsell, KA Armstrong… - Science translational …, 2016 - science.org
Fibrodysplasia ossificans progressiva (FOP), a congenital heterotopic ossification (HO)
syndrome caused by gain-of-function mutations of bone morphogenetic protein (BMP) type I …

Palovarotene Inhibits Heterotopic Ossification and Maintains Limb Mobility and Growth in Mice With the Human ACVR1R206H Fibrodysplasia Ossificans …

SA Chakkalakal, K Uchibe, MR Convente… - Journal of Bone and …, 2016 - academic.oup.com
Fibrodysplasia ossificans progressiva (FOP), a rare and as yet untreatable genetic disorder
of progressive extraskeletal ossification, is the most disabling form of heterotopic ossification …

Depletion of Mast Cells and Macrophages Impairs Heterotopic Ossification in an Acvr1R206H Mouse Model of Fibrodysplasia Ossificans Progressiva

MR Convente, SA Chakkalakal, EJ Yang… - Journal of Bone and …, 2018 - academic.oup.com
Heterotopic ossification (HO) is a clinical condition that often reduces mobility and
diminishes quality of life for affected individuals. The most severe form of progressive HO …

Cellular hypoxia promotes heterotopic ossification by amplifying BMP signaling

H Wang, C Lindborg, V Lounev, JH Kim… - Journal of Bone and …, 2016 - academic.oup.com
Hypoxia and inflammation are implicated in the episodic induction of heterotopic
endochondral ossification (HEO); however, the molecular mechanisms are unknown. HIF …

[HTML][HTML] Signaling pathways in bone development and their related skeletal dysplasia

A Guasto, V Cormier-Daire - International journal of molecular sciences, 2021 - mdpi.com
Bone development is a tightly regulated process. Several integrated signaling pathways
including HH, PTHrP, WNT, NOTCH, TGF-β, BMP, FGF and the transcription factors SOX9 …