An atypical mutation in the activin a receptor, type 1 gene (ACVR1) in a severely affected Fibrodysplasia Ossificans Progressiva patient

An atypical mutation in the activin a receptor, type 1 gene (ACVR1) in a severely affected Fibrodysplasia Ossificans Progressiva patient

Bibliografski detalji
Glavni autori:	Petrie, K, Pointon, J, Smith, R, Russell, R, Wordsworth, P, Triffitt, J
Format:	Conference item
Izdano:	2007

Slični predmeti

Identification of a novel mutation in activin receptor type 1 (ACVR1) in a fibrodysplasia ossificans progressiva (FOP) patient
od: Petrie, K, i dr.
Izdano: (2007)

Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
od: Petrie, K, i dr.
Izdano: (2009)

Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
od: Petrie, K, i dr.
Izdano: (2009)

Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.
od: Kirsten A Petrie, i dr.
Izdano: (2009-01-01)

ACVR1 mutation and Fibrodysplasia Ossificans Progressiva in Chinese children
od: Ng Bobby KW, i dr.
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Mutation Detection in Activin A Receptor, Type I (ACVR1) Gene in Fibrodysplasia Ossificans Progressiva in An Iranian Family
od: Ziba Morovvati, i dr.
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Genomic Context and Mechanisms of the <i>ACVR1</i> Mutation in Fibrodysplasia Ossificans Progressiva
od: Roberto Ravazzolo, i dr.
Izdano: (2021-02-01)

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.
od: Shore, E, i dr.
Izdano: (2006)

AAV-Mediated Targeting of the Activin A-ACVR1<sup>R206H</sup> Signaling in Fibrodysplasia Ossificans Progressiva
od: Yeon-Suk Yang, i dr.
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Characterization of Fibrodysplasia Ossificans Progessiva relevant Acvr1/Acvr2 Activin receptors in medaka (Oryzias latipes).
od: Michael Trumpp, i dr.
Izdano: (2023-01-01)

Characterization of Fibrodysplasia Ossificans Progessiva relevant Acvr1/Acvr2 Activin receptors in medaka (Oryzias latipes)
od: Michael Trumpp, i dr.
Izdano: (2023-01-01)

Fibrodysplasia ossificans progressiva mutant ACVR1 signals by multiple modalities in the developing zebrafish
od: Robyn S Allen, i dr.
Izdano: (2020-09-01)

Anti-ACVR1 antibodies exacerbate heterotopic ossification in fibrodysplasia ossificans progressiva (FOP) by activating FOP-mutant ACVR1
od: Senem Aykul, i dr.
Izdano: (2022-06-01)

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
od: Gregson, C, i dr.
Izdano: (2011)

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.
od: Gregson, C, i dr.
Izdano: (2011)

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.
od: Gregson, C, i dr.
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ABNORMAL BONE FORMATION IN ANKYLOSING SPONDYLITIS: WHAT CAN WE LEARN FROM ACVR1 AND FIBRODYSPLASIA OSSIFICANS PROGRESSIVA?
od: Cain, P, i dr.
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A case of Fibrodysplasia Ossificans Progressiva associated with a novel variant of the ACVR1 gene
od: Serena Cappato, i dr.
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An Activin Receptor IA/Activin-Like Kinase-2 (R206H) Mutation in Fibrodysplasia Ossificans Progressiva
od: Rafael Herrera-Esparza, i dr.
Izdano: (2013-01-01)

FIBRODYSPLASIA OSSIFICANS PROGRESSIVA
od: Mehul M Gosai, i dr.
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Fibrodysplasia ossificans progressiva
od: Chané Smit, i dr.
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Phenotypic and molecular heterogeneity in fibrodysplasia ossificans progressiva.
od: Virdi, A, i dr.
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How Activin A Became a Therapeutic Target in Fibrodysplasia Ossificans Progressiva
od: Dushyanth Srinivasan, i dr.
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Activin-dependent signaling in fibro/adipogenic progenitors causes fibrodysplasia ossificans progressiva
od: John B. Lees-Shepard, i dr.
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Fibrodysplasia ossificans progressiva: Lumps, bumps and biologics
od: Atukorala, I, i dr.
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An anti-ACVR1 antibody exacerbates heterotopic ossification by fibro-adipogenic progenitors in fibrodysplasia ossificans progressiva mice
od: John B. Lees-Shepard, i dr.
Izdano: (2022-06-01)

Response to "Mutations of the NOGGIN and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)" by Lucotte et al.
od: Kaplan, F, i dr.
Izdano: (2008)

Correction: High-throughput screening for modulators of ACVR1 transcription: discovery of potential therapeutics for fibrodysplasia ossificans progressiva
od: Serena Cappato, i dr.
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Lymphoblastoid cells in fibrodysplasia ossificans progressiva - Do they play a role?
od: Cohen, T, i dr.
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Erratum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527))
od: Shore, E, i dr.
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Fibrodysplasia Ossificans Progressiva: Case Report
od: Enver Şimşek, i dr.
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od: Anastasia Diolintzi, i dr.
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od: ANAMARLI NUCCI, i dr.
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Late-onset fibrodysplasia ossificans progressiva with atypical presentation: A case report
od: Conor M. Cunningham, i dr.
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Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in ACVR1 Gene: A Case Report and Review of Literature
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