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Keywords: Hereditary hemorrhagic telangiectasia
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Journal Articles
Journal: Development
Development (2016) 143 (14): 2593–2602.
Published: 15 July 2016
...Elizabeth R. Rochon; Prahlad G. Menon; Beth L. Roman Heterozygous loss of the arterial-specific TGFβ type I receptor, activin receptor-like kinase 1 ( ALK1 ; ACVRL1 ), causes hereditary hemorrhagic telangiectasia (HHT). HHT is characterized by development of fragile, direct connections between...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2013) 140 (16): 3403–3412.
Published: 15 August 2013
.../Acvrl1 Hereditary hemorrhagic telangiectasia Arteriovenous malformation Zebrafish Flow response Blood flow imparts mechanical forces and distributes endocrine factors that influence vascular development and remodeling and allow maintenance of arterial-venous identity...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2011) 138 (8): 1573–1582.
Published: 15 April 2011
... of blood flow in their development, we analyzed AVM development in zebrafish embryos harboring a mutation in activin receptor-like kinase I ( alk1 ), which encodes a TGFβ family type I receptor implicated in the human vascular disorder hereditary hemorrhagic telangiectasia type 2 (HHT2). Our analyses...
Includes: Multimedia, Supplementary data
Journal Articles
Journal: Development
Development (2002) 129 (12): 3009–3019.
Published: 15 June 2002
... dominant disorder, hereditary hemorrhagic telangiectasia type 2, in which disruption of ACVRL1 causes vessel malformations that may result in hemorrhage or stroke. Movies available on-line P19 cells maintained in DMEM with 10% fetal bovine serum and antibiotics were transiently transfected with Smad2/3...
Includes: Multimedia, Supplementary data