Vascular deficiency of Smad4 causes arteriovenous malformations: a mouse model of Hereditary Hemorrhagic Telangiectasia
出版年份 2018 全文链接
标题
Vascular deficiency of Smad4 causes arteriovenous malformations: a mouse model of Hereditary Hemorrhagic Telangiectasia
作者
关键词
Smad4, Arteriovenous malformations (AVM), Hereditary hemorrhagic telangiectasia (HHT), Vegfr2, TGFβ
出版物
ANGIOGENESIS
Volume 21, Issue 2, Pages 363-380
出版商
Springer Nature
发表日期
2018-02-19
DOI
10.1007/s10456-018-9602-0
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Characterization of arteriovenous identity in the developing neonate mouse retina
- (2017) Angela M. Crist et al. GENE EXPRESSION PATTERNS
- 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
- Interaction Between ALK1 Signaling and Connexin40 in the Development of Arteriovenous MalformationsSignificance
- (2016) Konstantinos Gkatzis et al. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
- Alk1 controls arterial endothelial cell migration in lumenized vessels
- (2016) Elizabeth R. Rochon et al. DEVELOPMENT
- 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
- Executive summary of the 11th HHT international scientific conference
- (2015) Helen Arthur et al. ANGIOGENESIS
- Context-specific interactions between Notch and ALK1 cannot explain ALK1-associated arteriovenous malformations
- (2015) Elizabeth R. Rochon et al. CARDIOVASCULAR RESEARCH
- VEGFR3 does not sustain retinal angiogenesis without VEGFR2
- (2015) Georgia Zarkada et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Research on potential biomarkers in hereditary hemorrhagic telangiectasia
- (2015) Luisa-MarÃa Botella et al. Frontiers in Genetics
- Hereditary hemorrhagic telangiectasia: genetics and molecular diagnostics in a new era
- (2015) Jamie McDonald et al. Frontiers in Genetics
- VEGF neutralization can prevent and normalize arteriovenous malformations in an animal model for hereditary hemorrhagic telangiectasia 2
- (2014) Chul Han et al. ANGIOGENESIS
- Deletion of Rbpj from postnatal endothelium leads to abnormal arteriovenous shunting in mice
- (2014) C. M. Nielsen et al. DEVELOPMENT
- Imatinib inhibits VEGF-independent angiogenesis by targeting neuropilin 1–dependent ABL1 activation in endothelial cells
- (2014) Claudio Raimondi et al. JOURNAL OF EXPERIMENTAL MEDICINE
- A comparative encyclopedia of DNA elements in the mouse genome
- (2014) Feng Yue et al. NATURE
- 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
- Constitutively active Notch4 receptor elicits brain arteriovenous malformations through enlargement of capillary-like vessels
- (2014) Patrick A. Murphy et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Neuropilin-1 functions as a VEGFR2 co-receptor to guide developmental angiogenesis independent of ligand binding
- (2014) Maria V Gelfand et al. eLife
- Endothelial signaling and the molecular basis of arteriovenous malformation
- (2013) Deepak Atri et al. CELLULAR AND MOLECULAR LIFE SCIENCES
- Bevacizumab in the treatment of hereditary hemorrhagic telangiectasia
- (2013) Theoni Kanellopoulou et al. EXPERT OPINION ON BIOLOGICAL THERAPY
- The use of US health insurance data for surveillance of rare disorders: hereditary hemorrhagic telangiectasia
- (2013) Scott D. Grosse et al. GENETICS IN MEDICINE
- ALK1 Signaling Inhibits Angiogenesis by Cooperating with the Notch Pathway
- (2012) Bruno Larrivée et al. DEVELOPMENTAL CELL
- TGF-β signaling in development and disease
- (2012) Joan Massagué FEBS LETTERS
- Bevacizumab in hereditary hemorrhagic telangiectasia-associated epistaxis: Effectiveness of an injection protocol based on the vascular anatomy of the nose
- (2012) Sinan Dheyauldeen et al. LARYNGOSCOPE
- Bevacizumab Attenuates VEGF-Induced Angiogenesis and Vascular Malformations in the Adult Mouse Brain
- (2012) Espen J. Walker et al. STROKE
- Interaction between alk1 and blood flow in the development of arteriovenous malformations
- (2011) P. Corti et al. DEVELOPMENT
- Endothelial Smad4 Maintains Cerebrovascular Integrity by Activating N-Cadherin through Cooperation with Notch
- (2011) Fangfei Li et al. DEVELOPMENTAL CELL
- Pericytes: Developmental, Physiological, and Pathological Perspectives, Problems, and Promises
- (2011) Annika Armulik et al. DEVELOPMENTAL CELL
- Overlapping spectra ofSMAD4mutations in juvenile polyposis (JP) and JP-HHT syndrome
- (2010) Carol Gallione et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- 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
- Notch1activation in mice causes arteriovenous malformations phenocopied by ephrinB2 and EphB4 mutants
- (2010) Luke T. Krebs et al. GENESIS
- Ephrin-B2 controls VEGF-induced angiogenesis and lymphangiogenesis
- (2010) Yingdi Wang et al. NATURE
- Isolation and Culture of Pulmonary Endothelial Cells from Neonatal Mice
- (2010) Magdalena Sobczak et al. Jove-Journal of Visualized Experiments
- Hereditary haemorrhagic telangiectasia: a clinical and scientific review
- (2009) Fatima S Govani et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- 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
- Alternatively spliced vascular endothelial growth factor receptor-2 is an essential endogenous inhibitor of lymphatic vessel growth
- (2009) Romulo J C Albuquerque et al. NATURE MEDICINE
- Bevacizumab in Hereditary Hemorrhagic Telangiectasia
- (2009) Prithviraj Bose et al. NEW ENGLAND JOURNAL OF MEDICINE
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started