Search details
1.
Multifocal heterotopic ossification in a man with germline variants of LIM Mineralization Protein-1 (LMP-1).
Am J Med Genet A
; 191(8): 2164-2174, 2023 08.
Article
in English
| MEDLINE | ID: mdl-37218523
2.
Study methodology and insights from the palovarotene clinical development program in fibrodysplasia ossificans progressiva.
BMC Med Res Methodol
; 23(1): 269, 2023 11 13.
Article
in English
| MEDLINE | ID: mdl-37957586
3.
Most Fractures Treated Nonoperatively in Individuals With Fibrodysplasia Ossificans Progressiva Heal With a Paucity of Flareups, Heterotopic Ossification, and Loss of Mobility.
Clin Orthop Relat Res
; 481(12): 2447-2458, 2023 12 01.
Article
in English
| MEDLINE | ID: mdl-37156007
4.
Dysregulated BMP signaling through ACVR1 impairs digit joint development in fibrodysplasia ossificans progressiva (FOP).
Dev Biol
; 470: 136-146, 2021 02.
Article
in English
| MEDLINE | ID: mdl-33217406
5.
The natural history of fibrodysplasia ossificans progressiva: A prospective, global 36-month study.
Genet Med
; 24(12): 2422-2433, 2022 12.
Article
in English
| MEDLINE | ID: mdl-36152026
6.
An ACVR1R375P pathogenic variant in two families with mild fibrodysplasia ossificans progressiva.
Am J Med Genet A
; 188(3): 806-817, 2022 03.
Article
in English
| MEDLINE | ID: mdl-34854557
7.
Whole-body Computed Tomography Versus Dual Energy Xray Absorptiometry for Assessing Heterotopic Ossification in Fibrodysplasia Ossificans Progressiva.
Calcif Tissue Int
; 109(6): 615-625, 2021 12.
Article
in English
| MEDLINE | ID: mdl-34331548
8.
Nonclassic fibrodysplasia ossificans progressiva: A child from Angola with an ACVR1G328E variant.
Am J Med Genet A
; 185(8): 2572-2575, 2021 08.
Article
in English
| MEDLINE | ID: mdl-33973349
9.
Severe digital malformations in a rare variant of fibrodysplasia ossificans progressiva.
Am J Med Genet A
; 179(7): 1310-1314, 2019 07.
Article
in English
| MEDLINE | ID: mdl-31012264
10.
Granting immunity to FOP and catching heterotopic ossification in the Act.
Semin Cell Dev Biol
; 49: 30-6, 2016 Jan.
Article
in English
| MEDLINE | ID: mdl-26706149
11.
ACVR1 p.Q207E causes classic fibrodysplasia ossificans progressiva and is functionally distinct from the engineered constitutively active ACVR1 p.Q207D variant.
Hum Mol Genet
; 23(20): 5364-77, 2014 Oct 15.
Article
in English
| MEDLINE | ID: mdl-24852373
12.
Alk2 regulates early chondrogenic fate in fibrodysplasia ossificans progressiva heterotopic endochondral ossification.
Stem Cells
; 32(5): 1289-300, 2014 May.
Article
in English
| MEDLINE | ID: mdl-24449086
13.
Multi-system involvement in a severe variant of fibrodysplasia ossificans progressiva (ACVR1 c.772G>A; R258G): A report of two patients.
Am J Med Genet A
; 167A(10): 2265-71, 2015 Oct.
Article
in English
| MEDLINE | ID: mdl-26097044
14.
The immunological contribution to heterotopic ossification disorders.
Curr Osteoporos Rep
; 13(2): 116-24, 2015 Apr.
Article
in English
| MEDLINE | ID: mdl-25687936
15.
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.
Nat Genet
; 38(5): 525-7, 2006 May.
Article
in English
| MEDLINE | ID: mdl-16642017
16.
General anesthesia for dental procedures in patients with fibrodysplasia ossificans progressiva: a review of 42 cases in 30 patients.
Anesth Analg
; 118(2): 298-301, 2014 Feb.
Article
in English
| MEDLINE | ID: mdl-24361843
17.
The HIF-1α and mTOR Pathways Amplify Heterotopic Ossification.
Biomolecules
; 14(2)2024 Jan 24.
Article
in English
| MEDLINE | ID: mdl-38397384
18.
Cell Senescence in Heterotopic Ossification.
Biomolecules
; 14(4)2024 Apr 16.
Article
in English
| MEDLINE | ID: mdl-38672501
19.
Matrix metalloproteinase-9 deficiency confers resilience in fibrodysplasia ossificans progressiva in a man and mice.
J Bone Miner Res
; 39(4): 382-398, 2024 May 02.
Article
in English
| MEDLINE | ID: mdl-38477818
20.
Paternally inherited gsα mutation impairs adipogenesis and potentiates a lean phenotype in vivo.
Stem Cells
; 30(7): 1477-85, 2012 Jul.
Article
in English
| MEDLINE | ID: mdl-22511293