Common and distinctive pathogenetic features of arteriovenous malformations in hereditary hemorrhagic telangiectasia 1 and hereditary hemorrhagic telangiectasia 2 animal models--brief report.
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The pathobiology of vascular malformations: insights from human and model organism genetics.Genetic variation in the functional ENG allele inherited from the non-affected parent associates with presence of pulmonary arteriovenous malformation in hereditary hemorrhagic telangiectasia 1 (HHT1) and may influence expression of PTPN14Matrix Gla protein limits pulmonary arteriovenous malformations in ALK1 deficiency.The Role of Macrophage in the Pathogenesis of Brain Arteriovenous Malformation.Alk1 controls arterial endothelial cell migration in lumenized vesselsDefective fluid shear stress mechanotransduction mediates hereditary hemorrhagic telangiectasia.Mouse Models of Cerebral Arteriovenous Malformation.Anti-angiogenic therapeutic strategies in hereditary hemorrhagic telangiectasia.Mouse models of hereditary hemorrhagic telangiectasia: recent advances and future challenges.Pericytes as targets in hereditary hemorrhagic telangiectasia.Is the Hepatic Factor a miRNA that Maintains the Integrity of Pulmonary Microvasculature by Inhibiting the Vascular Endothelial Growth Factor?Pathogenesis of Brain Arteriovenous Malformations.PI3 kinase inhibition improves vascular malformations in mouse models of hereditary haemorrhagic telangiectasia.A mouse model of hereditary hemorrhagic telangiectasia generated by transmammary-delivered immunoblocking of BMP9 and BMP10.Conflicting forces of warfarin and matrix gla protein in the artery wall.Executive summary of the 11th HHT international scientific conference.Endoglin prevents vascular malformation by regulating flow-induced cell migration and specification through VEGFR2 signalling.The roles of endoglin gene in cerebrovascular diseases.Inhibiting DPP4 in a mouse model of HHT1 results in a shift towards regenerative macrophages and reduces fibrosis after myocardial infarction.Tacrolimus rescues the signaling and gene expression signature of endothelial ALK1 loss-of-function and improves HHT vascular pathology.ALK1 signaling in development and disease: new paradigms.Selective effects of oral antiangiogenic tyrosine kinase inhibitors on an animal model of hereditary hemorrhagic telangiectasia.
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P2860
Common and distinctive pathogenetic features of arteriovenous malformations in hereditary hemorrhagic telangiectasia 1 and hereditary hemorrhagic telangiectasia 2 animal models--brief report.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh-hant
name
Common and distinctive pathoge ...... 2 animal models--brief report.
@en
Common and distinctive pathoge ...... 2 animal models--brief report.
@nl
type
label
Common and distinctive pathoge ...... 2 animal models--brief report.
@en
Common and distinctive pathoge ...... 2 animal models--brief report.
@nl
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Common and distinctive pathoge ...... 2 animal models--brief report.
@en
Common and distinctive pathoge ...... 2 animal models--brief report.
@nl
P2093
P1476
Common and distinctive pathoge ...... 2 animal models--brief report
@en
P2093
Ha-Long Nguyen
Se-Woon Choe
Tyler A Cunningham
Young-Jae Lee
Zhihua Jiang
P304
P356
10.1161/ATVBAHA.114.303984
P407
P577
2014-07-31T00:00:00Z