Molecular and cellular mechanisms of heterotopic ossification (Q35212915)

7 August 2017

title

Molecular and cellular mechanisms of heterotopic ossification (English)

1 reference

7 August 2017

Diana M Ramirez

1

1 reference

7 August 2017

Melissa R Ramirez

series ordinal

2

1 reference

7 August 2017

Anthony M Reginato

series ordinal

3

1 reference

7 August 2017

Damian Medici

series ordinal

4

1 reference

7 August 2017

publication date

5 May 2014

1 reference

Histology & Histopathology

7 August 2017

published in

1 reference

7 August 2017

volume

29

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7 August 2017

issue

10

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7 August 2017

page(s)

1281-1285

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BMP-9 expression in human traumatic heterotopic ossification: a case report

7 August 2017

cites work

1 reference

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A role for the endothelium in vascular calcification

28 July 2018

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RhoA mediates defective stem cell function and heterotopic ossification in dystrophic muscle of mice

28 July 2018

1 reference

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Constitutively active ALK2 receptor mutants require type II receptor cooperation

28 July 2018

1 reference

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Glast-expressing progenitor cells contribute to heterotopic ossification

28 July 2018

1 reference

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Fibrodysplasia ossificans progressiva: mechanisms and models of skeletal metamorphosis

28 July 2018

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An Acvr1 R206H knock-in mouse has fibrodysplasia ossificans progressiva

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

Multipotent progenitors resident in the skeletal muscle interstitium exhibit robust BMP-dependent osteogenic activity and mediate heterotopic ossification

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

Fibrodysplasia ossificans progressiva: clinical and genetic aspects

28 July 2018

1 reference

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Substance P signaling mediates BMP-dependent heterotopic ossification

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

Sensory nerve induced inflammation contributes to heterotopic ossification

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

Conversion of vascular endothelial cells into multipotent stem-like cells

28 July 2018

1 reference

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Inherited human diseases of heterotopic bone formation

28 July 2018

1 reference

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The fibrodysplasia ossificans progressiva R206H ACVR1 mutation activates BMP-independent chondrogenesis and zebrafish embryo ventralization

28 July 2018

1 reference

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Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

Identification of progenitor cells that contribute to heterotopic skeletogenesis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

BMP type I receptor inhibition reduces heterotopic [corrected] ossification

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

Dysregulation of local stem/progenitor cells as a common cellular mechanism for heterotopic ossification

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

ACVR1 (587T>C) mutation in a variant form of fibrodysplasia ossificans progressiva: second report.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

Fibrodysplasia ossificans progressiva: middle-age onset of heterotopic ossification from a unique missense mutation (c.974G>C, p.G325A) in ACVR1.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

BMP-9-induced muscle heterotopic ossification requires changes to the skeletal muscle microenvironment.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

Potent inhibition of heterotopic ossification by nuclear retinoic acid receptor-γ agonists

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

A novel ACVR1 mutation in the glycine/serine-rich domain found in the most benign case of a fibrodysplasia ossificans progressiva variant reported to date

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

Mutational analysis of the ACVR1 gene in Italian patients affected with fibrodysplasia ossificans progressiva: confirmations and advancements.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

Iatrogenic harm caused by diagnostic errors in fibrodysplasia ossificans progressiva

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

Bone morphogenetic protein 2/4 in early fibromatous lesions of fibrodysplasia ossificans progressiva

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4372050

A unique case of fibrodysplasia ossificans progressiva with an ACVR1 mutation, G356D, other than the common mutation (R206H)

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24796520

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Pulmonary and cardiac function in advanced fibrodysplasia ossificans progressiva

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24796520

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

4372050

1 reference

7 August 2017

1 reference