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...
Guardado en:
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 |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2016
|
Materias: | |
Acceso en línea: | https://doaj.org/article/7b411bab54424730b576b6b6c001bd4f |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Predictors of heart failure symptoms in hereditary hemorrhagic telangiectasia patients with hepatic arteriovenous malformations
por: Lucas R. Cusumano, et al.
Publicado: (2021) -
Genetic Variants and Clinical Phenotypes in Korean Patients With Hereditary Hemorrhagic Telangiectasia
por: Bo-Gyeong Kim, et al.
Publicado: (2021) -
Hemorrhage-adjusted iron requirements, hematinics and hepcidin define hereditary hemorrhagic telangiectasia as a model of hemorrhagic iron deficiency.
por: Helen Finnamore, et al.
Publicado: (2013) -
Endophilin-A2 dependent VEGFR2 endocytosis promotes sprouting angiogenesis
por: Gael Genet, et al.
Publicado: (2019) -
The Robo4 cytoplasmic domain is dispensable for vascular permeability and neovascularization
por: Feng Zhang, et al.
Publicado: (2016)