PI3 kinase inhibition improves vascular malformations in mouse models of hereditary haemorrhagic telangiectasia

Arteriovenous malformations (AVM) is a hallmark of hereditary haemorrhagic telangiectasia type 2, a disease caused by mutations in BMP receptor ALK1. Ola et al. show that AVM can be caused by blocking BMP9 and BMP10 in mice, leading to increased VEGF and PI3K activity, and that pharmacologic inhibit...

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Autores principales: Roxana Ola, Alexandre Dubrac, Jinah Han, Feng Zhang, Jennifer S. Fang, Bruno Larrivée, Monica Lee, Ana A. Urarte, Jan R. Kraehling, Gael Genet, Karen K. Hirschi, William C. Sessa, Francesc V. Canals, Mariona Graupera, Minhong Yan, Lawrence H. Young, Paul S. Oh, Anne Eichmann
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Lenguaje:EN
Publicado: Nature Portfolio 2016
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Acceso en línea:https://doaj.org/article/7b411bab54424730b576b6b6c001bd4f
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spelling oai:doaj.org-article:7b411bab54424730b576b6b6c001bd4f2021-12-02T14:40:11ZPI3 kinase inhibition improves vascular malformations in mouse models of hereditary haemorrhagic telangiectasia10.1038/ncomms136502041-1723https://doaj.org/article/7b411bab54424730b576b6b6c001bd4f2016-11-01T00:00:00Zhttps://doi.org/10.1038/ncomms13650https://doaj.org/toc/2041-1723Arteriovenous malformations (AVM) is a hallmark of hereditary haemorrhagic telangiectasia type 2, a disease caused by mutations in BMP receptor ALK1. Ola et al. show that AVM can be caused by blocking BMP9 and BMP10 in mice, leading to increased VEGF and PI3K activity, and that pharmacologic inhibition of PI3K prevents AVM development.Roxana OlaAlexandre DubracJinah HanFeng ZhangJennifer S. FangBruno LarrivéeMonica LeeAna A. UrarteJan R. KraehlingGael GenetKaren K. HirschiWilliam C. SessaFrancesc V. CanalsMariona GrauperaMinhong YanLawrence H. YoungPaul S. OhAnne EichmannNature PortfolioarticleScienceQENNature Communications, Vol 7, Iss 1, Pp 1-12 (2016)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Roxana Ola
Alexandre Dubrac
Jinah Han
Feng Zhang
Jennifer S. Fang
Bruno Larrivée
Monica Lee
Ana A. Urarte
Jan R. Kraehling
Gael Genet
Karen K. Hirschi
William C. Sessa
Francesc V. Canals
Mariona Graupera
Minhong Yan
Lawrence H. Young
Paul S. Oh
Anne Eichmann
PI3 kinase inhibition improves vascular malformations in mouse models of hereditary haemorrhagic telangiectasia
description Arteriovenous malformations (AVM) is a hallmark of hereditary haemorrhagic telangiectasia type 2, a disease caused by mutations in BMP receptor ALK1. Ola et al. show that AVM can be caused by blocking BMP9 and BMP10 in mice, leading to increased VEGF and PI3K activity, and that pharmacologic inhibition of PI3K prevents AVM development.
format article
author Roxana Ola
Alexandre Dubrac
Jinah Han
Feng Zhang
Jennifer S. Fang
Bruno Larrivée
Monica Lee
Ana A. Urarte
Jan R. Kraehling
Gael Genet
Karen K. Hirschi
William C. Sessa
Francesc V. Canals
Mariona Graupera
Minhong Yan
Lawrence H. Young
Paul S. Oh
Anne Eichmann
author_facet Roxana Ola
Alexandre Dubrac
Jinah Han
Feng Zhang
Jennifer S. Fang
Bruno Larrivée
Monica Lee
Ana A. Urarte
Jan R. Kraehling
Gael Genet
Karen K. Hirschi
William C. Sessa
Francesc V. Canals
Mariona Graupera
Minhong Yan
Lawrence H. Young
Paul S. Oh
Anne Eichmann
author_sort Roxana Ola
title PI3 kinase inhibition improves vascular malformations in mouse models of hereditary haemorrhagic telangiectasia
title_short PI3 kinase inhibition improves vascular malformations in mouse models of hereditary haemorrhagic telangiectasia
title_full PI3 kinase inhibition improves vascular malformations in mouse models of hereditary haemorrhagic telangiectasia
title_fullStr PI3 kinase inhibition improves vascular malformations in mouse models of hereditary haemorrhagic telangiectasia
title_full_unstemmed PI3 kinase inhibition improves vascular malformations in mouse models of hereditary haemorrhagic telangiectasia
title_sort pi3 kinase inhibition improves vascular malformations in mouse models of hereditary haemorrhagic telangiectasia
publisher Nature Portfolio
publishDate 2016
url https://doaj.org/article/7b411bab54424730b576b6b6c001bd4f
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