BMP10 functions independently from BMP9 for the development of a proper arteriovenous network
出版年份 2022 全文链接
标题
BMP10 functions independently from BMP9 for the development of a proper arteriovenous network
作者
关键词
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出版物
ANGIOGENESIS
Volume -, Issue -, Pages -
出版商
Springer Science and Business Media LLC
发表日期
2022-11-09
DOI
10.1007/s10456-022-09859-0
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Hereditary Haemorrhagic Telangiectasia, an Inherited Vascular Disorder in Need of Improved Evidence-Based Pharmaceutical Interventions
- (2021) Ryan O. Snodgrass et al. Genes
- Different cardiovascular and pulmonary phenotypes for single- and double-knock-out mice deficient in BMP9 and BMP10
- (2021) Claire Bouvard et al. CARDIOVASCULAR RESEARCH
- Identification and validation of a novel pathogenic variant in GDF2 ( BMP9 ) responsible for hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations
- (2021) Srimmitha Balachandar et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- BMP-SMAD1/5 Signaling Regulates Retinal Vascular Development
- (2020) Andreas Benn et al. Biomolecules
- Overexpression of Activin Receptor-Like Kinase 1 in Endothelial Cells Suppresses Development of Arteriovenous Malformations in Mouse Models Of Hereditary Hemorrhagic Telangiectasia
- (2020) Yong Hwan Kim et al. CIRCULATION RESEARCH
- BMP9 and BMP10 Act Directly on Vascular Smooth Muscle Cells for Generation and Maintenance of the Contractile State
- (2020) Lei Wang et al. CIRCULATION
- BMP10-mediated ALK1 signaling is continuously required for vascular development and maintenance
- (2019) Teresa L. Capasso et al. ANGIOGENESIS
- Correcting Smad1/5/8, mTOR, and VEGFR2 treats pathology in hereditary hemorrhagic telangiectasia models
- (2019) Santiago Ruiz et al. JOURNAL OF CLINICAL INVESTIGATION
- Vascular deficiency of Smad4 causes arteriovenous malformations: a mouse model of Hereditary Hemorrhagic Telangiectasia
- (2018) Angela M. Crist et al. ANGIOGENESIS
- SMAD4 Prevents Flow Induced Arterial-Venous Malformations by Inhibiting Casein Kinase 2
- (2018) Roxana Ola et al. CIRCULATION
- A heterodimer formed by bone morphogenetic protein 9 (BMP9) and BMP10 provides most BMP biological activity in plasma
- (2018) Emmanuelle Tillet et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- BMP9, but not BMP10, acts as a quiescence factor on tumor growth, vessel normalization and metastasis in a mouse model of breast cancer
- (2018) Marie Ouarné et al. JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH
- SMAD4 Deficiency Leads to Development of Arteriovenous Malformations in Neonatal and Adult Mice
- (2018) Yong Hwan Kim et al. Journal of the American Heart Association
- Endoglin prevents vascular malformation by regulating flow-induced cell migration and specification through VEGFR2 signalling
- (2017) Yi Jin et al. NATURE CELL BIOLOGY
- Endoglin controls blood vessel diameter through endothelial cell shape changes in response to haemodynamic cues
- (2017) Wade W. Sugden et al. NATURE CELL BIOLOGY
- Structural Basis of the Human Endoglin-BMP9 Interaction: Insights into BMP Signaling and HHT1
- (2017) Takako Saito et al. Cell Reports
- Defective fluid shear stress mechanotransduction mediates hereditary hemorrhagic telangiectasia
- (2016) Nicolas Baeyens et al. JOURNAL OF CELL BIOLOGY
- PI3 kinase inhibition improves vascular malformations in mouse models of hereditary haemorrhagic telangiectasia
- (2016) Roxana Ola et al. Nature Communications
- A mouse model of hereditary hemorrhagic telangiectasia generated by transmammary-delivered immunoblocking of BMP9 and BMP10
- (2016) Santiago Ruiz et al. Scientific Reports
- Mouse Models of Cerebral Arteriovenous Malformation
- (2015) Corinne M. Nielsen et al. STROKE
- Common and Distinctive Pathogenetic Features of Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia 1 and Hereditary Hemorrhagic Telangiectasia 2 Animal Models—Brief Report
- (2014) Eva M. Garrido-Martin et al. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
- Functional analysis of endoglin mutations from hereditary hemorrhagic telangiectasia type 1 patients reveals different mechanisms for endoglin loss of function
- (2014) C. Mallet et al. HUMAN MOLECULAR GENETICS
- Novel Brain Arteriovenous Malformation Mouse Models for Type 1 Hereditary Hemorrhagic Telangiectasia
- (2014) Eun-Jung Choi et al. PLoS One
- Endothelial Depletion of Acvrl1 in Mice Leads to Arteriovenous Malformations Associated with Reduced Endoglin Expression
- (2014) Simon Tual-Chalot et al. PLoS One
- De Novo Cerebrovascular Malformation in the Adult Mouse After Endothelial Alk1 Deletion and Angiogenic Stimulation
- (2014) Wanqiu Chen et al. STROKE
- Hemorrhage Rates and Risk Factors in the Natural History Course of Brain Arteriovenous Malformations
- (2014) W. Caleb Rutledge et al. Translational Stroke Research
- BMP9 Mutations Cause a Vascular-Anomaly Syndrome with Phenotypic Overlap with Hereditary Hemorrhagic Telangiectasia
- (2013) Whitney L. Wooderchak-Donahue et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Bone morphogenetic protein 9 (BMP9) controls lymphatic vessel maturation and valve formation
- (2013) S. Levet et al. BLOOD
- Circulating Bmp10 acts through endothelial Alk1 to mediate flow-dependent arterial quiescence
- (2013) D. W. Laux et al. DEVELOPMENT
- Bone morphogenetic protein-9 inhibits lymphatic vessel formation via activin receptor-like kinase 1 during development and cancer progression
- (2013) Y. Yoshimatsu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Context-dependent signaling defines roles of BMP9 and BMP10 in embryonic and postnatal development
- (2013) H. Chen et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- BMP9 and BMP10 are critical for postnatal retinal vascular remodeling
- (2012) N. Ricard et al. BLOOD
- Hereditary haemorrhagic telangiectasia: Pathophysiology, diagnosis and treatment
- (2010) Claire L. Shovlin BLOOD REVIEWS
- Pathogenesis of Arteriovenous Malformations in the Absence of Endoglin
- (2010) Marwa Mahmoud et al. CIRCULATION RESEARCH
- Real-time imaging of de novo arteriovenous malformation in a mouse model of hereditary hemorrhagic telangiectasia
- (2009) Sung Ok Park et al. JOURNAL OF CLINICAL INVESTIGATION
- Direct Hematological Toxicity and Illegitimate Chromosomal Recombination Caused by the Systemic Activation of CreERT2
- (2009) A. Y. Higashi et al. JOURNAL OF IMMUNOLOGY
- Bone Morphogenetic Protein-9 Is a Circulating Vascular Quiescence Factor
- (2008) Laurent David et al. CIRCULATION RESEARCH
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