| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1045720229 |
| P356 | DOI | 10.1038/NATURE05577 |
| P698 | PubMed publication ID | 17259972 |
| P5875 | ResearchGate publication ID | 6544116 |
| P2093 | author name string | Nathan D Lawson | |
| Arndt F Siekmann | |||
| P2860 | cites work | Direct recruitment of CRK and GRB2 to VEGFR-3 induces proliferation, migration, and survival of endothelial cells through the activation of ERK, AKT, and JNK pathways | Q24312658 |
| Notch signaling: cell fate control and signal integration in development | Q27861061 | ||
| Notch activation during endothelial cell network formation in vitro targets the basic HLH transcription factor HESR-1 and downregulates VEGFR-2/KDR expression | Q28216123 | ||
| Haploinsufficient lethality and formation of arteriovenous malformations in Notch pathway mutants | Q28505269 | ||
| VEGF guides angiogenic sprouting utilizing endothelial tip cell filopodia | Q29617501 | ||
| In vivo imaging of embryonic vascular development using transgenic zebrafish | Q29619921 | ||
| Up-regulation of the Notch ligand Delta-like 4 inhibits VEGF-induced endothelial cell function | Q34458950 | ||
| Distinct genetic interactions between multiple Vegf receptors are required for development of different blood vessel types in zebrafish | Q34597815 | ||
| phospholipase C gamma-1 is required downstream of vascular endothelial growth factor during arterial development | Q35965422 | ||
| Distinct requirements for zebrafish angiogenesis revealed by a VEGF-A morphant | Q36750445 | ||
| The cloche and spadetail genes differentially affect hematopoiesis and vasculogenesis | Q38336476 | ||
| The role of Suppressor of Hairless in Notch mediated signalling during zebrafish somitogenesis | Q44612454 | ||
| The neurogenic suppressor of hairless DNA-binding protein mediates the transcriptional activation of the enhancer of split complex genes triggered by Notch signaling. | Q47072129 | ||
| gridlock, a localized heritable vascular patterning defect in the zebrafish | Q47073977 | ||
| sonic hedgehog and vascular endothelial growth factor act upstream of the Notch pathway during arterial endothelial differentiation | Q47074043 | ||
| Vascular expression of Notch pathway receptors and ligands is restricted to arterial vessels. | Q52129044 | ||
| Sequence and embryonic expression of deltaC in the zebrafish. | Q52172693 | ||
| Use of the Gal4-UAS technique for targeted gene expression in the zebrafish. | Q52178821 | ||
| P433 | issue | 7129 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Danio rerio | Q169444 |
| Recombination signal binding protein for immunoglobulin kappa J region a | Q29821634 | ||
| Recombination signal binding protein for immunoglobulin kappa J region b | Q56252189 | ||
| P304 | page(s) | 781-784 | |
| P577 | publication date | 2007-01-28 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | Notch signalling limits angiogenic cell behaviour in developing zebrafish arteries | |
| P478 | volume | 445 |
| Q38049000 | "Sprouting angiogenesis", a reappraisal |
| Q30581917 | 'In parallel' interconnectivity of the dorsal longitudinal anastomotic vessels requires both VEGF signaling and circulatory flow |
| Q48736453 | 3D quantitative analyses of angiogenic sprout growth dynamics. |
| Q64263430 | A PKA/cdc42 Signaling Axis Restricts Angiogenic Sprouting by Regulating Podosome Rosette Biogenesis and Matrix Remodeling |
| Q37094321 | A core human primary tumor angiogenesis signature identifies the endothelial orphan receptor ELTD1 as a key regulator of angiogenesis |
| Q37468040 | A genetic screen for vascular mutants in zebrafish reveals dynamic roles for Vegf/Plcg1 signaling during artery development |
| Q37237445 | A genetic screen in zebrafish defines a hierarchical network of pathways required for hematopoietic stem cell emergence |
| Q30489730 | A key role for the integrin alpha2beta1 in experimental and developmental angiogenesis. |
| Q26864897 | A role for partial endothelial-mesenchymal transitions in angiogenesis? |
| Q42010099 | A small molecule targeting ALK1 prevents Notch cooperativity and inhibits functional angiogenesis |
| Q30537569 | A truncation allele in vascular endothelial growth factor c reveals distinct modes of signaling during lymphatic and vascular development. |
| Q33802916 | A two-way communication between microglial cells and angiogenic sprouts regulates angiogenesis in aortic ring cultures |
| Q96577101 | ADP receptor P2y12 prevents excessive primitive hematopoiesis in zebrafish by inhibiting Gata1 |
| Q38888721 | AIBP Limits Angiogenesis Through γ-Secretase-Mediated Upregulation of Notch Signaling. |
| Q47856805 | ALK1 signaling in development and disease: new paradigms. |
| Q34876665 | Accelerated coronary angiogenesis by vegfr1-knockout endocardial cells |
| Q34628594 | Acetylation-dependent regulation of endothelial Notch signalling by the SIRT1 deacetylase |
| Q43106806 | Achieving tissue specific levels of angiogenesis: Not(ch) a big deal! |
| Q38929428 | Acute Blockage of Notch Signaling by DAPT Induces Neuroprotection and Neurogenesis in the Neonatal Rat Brain After Stroke |
| Q35375871 | Age-related Notch-4 quiescence is associated with altered wall remodeling during vein graft adaptation |
| Q36018663 | Alk1 and Alk5 inhibition by Nrp1 controls vascular sprouting downstream of Notch. |
| Q35953933 | Aminoacyl-tRNA synthetase dependent angiogenesis revealed by a bioengineered macrolide inhibitor |
| Q27342049 | An Intronic Flk1 Enhancer Directs Arterial-Specific Expression via RBPJ-Mediated Venous Repression |
| Q46569014 | An optimized three-dimensional in vitro model for the analysis of angiogenesis |
| Q37031888 | Analysis of Dll4 regulation reveals a combinatorial role for Sox and Notch in arterial development |
| Q33598375 | Angiocrine factors deployed by tumor vascular niche induce B cell lymphoma invasiveness and chemoresistance |
| Q51866048 | Angiogenesis and vascular remodelling in normal and cancerous tissues. |
| Q35562536 | Angiomotin-like2 gene (amotl2) is required for migration and proliferation of endothelial cells during angiogenesis. |
| Q34624256 | Angiopoietin-1/Tie2 signal augments basal Notch signal controlling vascular quiescence by inducing delta-like 4 expression through AKT-mediated activation of beta-catenin |
| Q47073226 | Antagonistic interactions among Plexins regulate the timing of intersegmental vessel formation. |
| Q47095675 | Anti-angiogenic effect of Livistona chinensis seed extract in vitro and in vivo |
| Q99587938 | Apelin signaling drives vascular endothelial cells towards a pro-angiogenic state |
| Q43730075 | Arap3 is dysregulated in a mouse model of hypotrichosis-lymphedema-telangiectasia and regulates lymphatic vascular development. |
| Q28741227 | Arterial-venous network formation during brain vascularization involves hemodynamic regulation of chemokine signaling |
| Q30494377 | Arterial-venous segregation by selective cell sprouting: an alternative mode of blood vessel formation. |
| Q30611116 | Arteries are formed by vein-derived endothelial tip cells |
| Q28506090 | Artery and vein size is balanced by Notch and ephrin B2/EphB4 during angiogenesis |
| Q30499438 | Assembly and patterning of the vascular network of the vertebrate hindbrain |
| Q34947480 | Association of Dll4/notch and HIF-1a -VEGF signaling in the angiogenesis of missed abortion |
| Q41301518 | Asymmetric division coordinates collective cell migration in angiogenesis |
| Q37746510 | Axon guidance molecules in vascular patterning |
| Q50146924 | Biology of Bone: The Vasculature of the Skeletal System |
| Q28285842 | Blocking VEGFR-3 suppresses angiogenic sprouting and vascular network formation |
| Q38366760 | Blood and lymphatic vessel formation |
| Q30831553 | Blood flow controls bone vascular function and osteogenesis. |
| Q42678883 | Blood flow suppresses vascular Notch signalling via dll4 and is required for angiogenesis in response to hypoxic signalling. |
| Q92509243 | Blood stem cell-forming haemogenic endothelium in zebrafish derives from arterial endothelium |
| Q37328390 | Blood-based biomarkers for the optimization of anti-angiogenic therapies |
| Q37502702 | Branching morphogenesis and antiangiogenesis candidates: tip cells lead the way. |
| Q42860051 | Branching morphogenesis. |
| Q36329454 | Branching morphogenesis: from cells to organs and back |
| Q27002903 | Broad targeting of angiogenesis for cancer prevention and therapy |
| Q37307320 | Brothers and sisters: molecular insights into arterial-venous heterogeneity |
| Q33365792 | C-reactive protein exerts angiogenic effects on vascular endothelial cells and modulates associated signalling pathways and gene expression |
| Q33649600 | Calycosin promotes angiogenesis involving estrogen receptor and mitogen-activated protein kinase (MAPK) signaling pathway in zebrafish and HUVEC |
| Q26744412 | Cell behaviors and dynamics during angiogenesis |
| Q92616609 | Cells as strain-cued automata |
| Q37325018 | Chapter 4. Using the zebrafish to study vessel formation |
| Q37379597 | Chemokine signaling guides regional patterning of the first embryonic artery |
| Q41851597 | Cilia Control Vascular Mural Cell Recruitment in Vertebrates. |
| Q41641853 | Clock controls angiogenesis. |
| Q93053225 | Cohesive and anisotropic vascular endothelial cell motility driving angiogenic morphogenesis |
| Q26771268 | Collective cell migration in development |
| Q29616634 | Collective cell migration in morphogenesis, regeneration and cancer |
| Q30525842 | Collective mesendoderm migration relies on an intrinsic directionality signal transmitted through cell contacts. |
| Q36517537 | Common cues regulate neural and vascular patterning |
| Q53492057 | Complex cell rearrangements during intersegmental vessel sprouting and vessel fusion in the zebrafish embryo. |
| Q36187221 | Computational Screening of Tip and Stalk Cell Behavior Proposes a Role for Apelin Signaling in Sprout Progression. |
| Q34521141 | Computer simulations reveal complex distribution of haemodynamic forces in a mouse retina model of angiogenesis |
| Q27302123 | Context-specific interactions between Notch and ALK1 cannot explain ALK1-associated arteriovenous malformations |
| Q42581913 | Control of angiogenesis by AIBP-mediated cholesterol efflux. |
| Q42909820 | Control of endothelial sprouting by a Tel–CtBP complex |
| Q42199745 | Coordinating cardiomyocyte interactions to direct ventricular chamber morphogenesis |
| Q38368549 | Coral-Derived Natural Marine Compound GB9 Impairs Vascular Development in Zebrafish |
| Q27331693 | DLL4 promotes continuous adult intestinal lacteal regeneration and dietary fat transport |
| Q35665027 | Deconstructing host-pathogen interactions in Drosophila |
| Q35538051 | Delta-like 4 mRNA is regulated by adjacent natural antisense transcripts |
| Q35175775 | Delta-like ligand 4 regulates central nervous system T cell accumulation during experimental autoimmune encephalomyelitis |
| Q36316559 | Determination of endothelial stalk versus tip cell potential during angiogenesis by H2.0-like homeobox-1. |
| Q47073276 | Different combinations of Notch ligands and receptors regulate V2 interneuron progenitor proliferation and V2a/V2b cell fate determination |
| Q35549652 | Different patterns of NF-κB and Notch1 signaling contribute to tumor-induced lymphangiogenesis of esophageal squamous cell carcinoma |
| Q36267269 | Differential gene expression of primary cultured lymphatic and blood vascular endothelial cells. |
| Q30581940 | Distinct Notch signaling outputs pattern the developing arterial system. |
| Q42506571 | Distinct and redundant functions of Esama and VE-cadherin during vascular morphogenesis |
| Q41993273 | Distinct signalling pathways regulate sprouting angiogenesis from the dorsal aorta and the axial vein |
| Q24309476 | Distinctive localization and opposed roles of vasohibin-1 and vasohibin-2 in the regulation of angiogenesis |
| Q38233800 | Diversity is in my veins: role of bone morphogenetic protein signaling during venous morphogenesis in zebrafish illustrates the heterogeneity within endothelial cells |
| Q46340126 | Dll4 and Notch signalling couples sprouting angiogenesis and artery formation |
| Q37933528 | Dll4-Notch signaling as a therapeutic target in tumor angiogenesis |
| Q38151514 | Dll4-Notch signaling in regulation of tumor angiogenesis |
| Q47099394 | Dual Roles of Fer Kinase Are Required for Proper Hematopoiesis and Vascular Endothelium Organization during Zebrafish Development |
| Q24296966 | E2F7 and E2F8 promote angiogenesis through transcriptional activation of VEGFA in cooperation with HIF1 |
| Q39328290 | ERK activation in endothelial cells is a novel marker during neovasculogenesis |
| Q47093719 | Effects of quercetin on the expression of MCP-1, MMP-9 and VEGF in rats with diabetic retinopathy |
| Q37042648 | Embryological Origin of Human Smooth Muscle Cells Influences Their Ability to Support Endothelial Network Formation |
| Q38771567 | Endoglin controls blood vessel diameter through endothelial cell shape changes in response to haemodynamic cues. |
| Q44839040 | Endoglin prevents vascular malformation by regulating flow-induced cell migration and specification through VEGFR2 signalling |
| Q90003059 | Endothelial CDS2 deficiency causes VEGFA-mediated vascular regression and tumor inhibition |
| Q36483799 | Endothelial Ca 2+ oscillations reflect VEGFR signaling-regulated angiogenic capacity in vivo. |
| Q98464985 | Endothelial Cell Dynamics in Vascular Development: Insights From Live-Imaging in Zebrafish |
| Q37091548 | Endothelial Notch activity promotes angiogenesis and osteogenesis in bone |
| Q48116044 | Endothelial Notch signalling limits angiogenesis via control of artery formation. |
| Q36833572 | Endothelial RAF1/ERK activation regulates arterial morphogenesis. |
| Q36193529 | Endothelial Wnt/β-catenin signaling inhibits glioma angiogenesis and normalizes tumor blood vessels by inducing PDGF-B expression |
| Q38922570 | Endothelial basement membrane limits tip cell formation by inducing Dll4/Notch signalling in vivo |
| Q30669143 | Endothelial cell division in angiogenic sprouts of differing cellular architecture |
| Q42876374 | Endothelial cells dynamically compete for the tip cell position during angiogenic sprouting |
| Q28267098 | Endothelial expression of the Notch ligand Jagged1 is required for vascular smooth muscle development |
| Q26865091 | Endothelial tip cells in ocular angiogenesis: potential target for anti-angiogenesis therapy |
| Q48145755 | Enhancement of vascular endothelial growth factor's angiogenic capacity by the therapeutic modulation of notch signalling improves tram flap survival in rats submitted to nicotine |
| Q92482647 | Epac1 inhibition ameliorates pathological angiogenesis through coordinated activation of Notch and suppression of VEGF signaling |
| Q39160262 | Epithelial-mesenchymal transition in morphogenesis, cancer progression and angiogenesis |
| Q91623219 | Exome sequencing revealed Notch ligand JAG1 as a novel candidate gene for familial exudative vitreoretinopathy |
| Q35923796 | Expression of FLT4 in hypoxia-induced neovascular models in vitro and in vivo |
| Q33745294 | Expression of vascular notch ligand delta-like 4 and inflammatory markers in breast cancer |
| Q34407315 | FIH-1, a novel interactor of mindbomb, functions as an essential anti-angiogenic factor during zebrafish vascular development |
| Q27332457 | Fbxw7 controls angiogenesis by regulating endothelial Notch activity |
| Q36382073 | Fellow travellers: emergent properties of collective cell migration |
| Q33687095 | Fine-tune regulation of carboxypeptidase N1 controls vascular patterning during zebrafish development. |
| Q27314354 | Fli+ etsrp+ hemato-vascular progenitor cells proliferate at the lateral plate mesoderm during vasculogenesis in zebrafish |
| Q30499862 | Flt1 acts as a negative regulator of tip cell formation and branching morphogenesis in the zebrafish embryo |
| Q35269444 | Focal adhesion kinase regulation of neovascularization |
| Q37631615 | Ftr82 Is Critical for Vascular Patterning during Zebrafish Development |
| Q28477769 | Gamma-secretase inhibitor treatment promotes VEGF-A-driven blood vessel growth and vascular leakage but disrupts neovascular perfusion |
| Q46428475 | Gene expression profile in colon cancer cells with respect to XIAP expression status. |
| Q37175244 | Genetic risk factors for portopulmonary hypertension in patients with advanced liver disease |
| Q30235241 | Genetics and Genomics of Congenital Heart Disease |
| Q47073319 | Glycogen synthase kinase 3 beta in somites plays a role during the angiogenesis of zebrafish embryos |
| Q28513845 | HOXA13 Is essential for placental vascular patterning and labyrinth endothelial specification |
| Q27318761 | Haemodynamics-driven developmental pruning of brain vasculature in zebrafish |
| Q94562195 | Heritable modifiers of the tumor microenvironment influence nanoparticle uptake, distribution and response to photothermal therapy |
| Q64076263 | High mitogenic stimulation arrests angiogenesis |
| Q38752236 | Host genetic modifiers of nonproductive angiogenesis inhibit breast cancer. |
| Q37945438 | How blood vessel networks are made and measured |
| Q55042335 | How to make less webby webs. |
| Q52762289 | Hyperactive FOXO1 results in lack of tip stalk identity and deficient microvascular regeneration during kidney injury. |
| Q33354053 | Hypoxia-induced retinal angiogenesis in zebrafish as a model to study retinopathy |
| Q30495907 | Inhibition of delta-like-4-mediated signaling impairs reparative angiogenesis after ischemia |
| Q50216641 | Inhibitory Effects of Red Wine on Lipid Oxidation in Fish Oil Emulsion and Angiogenesis in Zebrafish Embryo |
| Q30411281 | Integration of experimental and computational approaches to sprouting angiogenesis. |
| Q38088193 | Interactions between VEGFR and Notch signaling pathways in endothelial and neural cells |
| Q24297342 | Isolation of a small vasohibin-binding protein (SVBP) and its role in vasohibin secretion |
| Q33509506 | KSHV manipulates Notch signaling by DLL4 and JAG1 to alter cell cycle genes in lymphatic endothelia |
| Q38806486 | LITTLE FISH, BIG DATA: ZEBRAFISH AS A MODEL FOR CARDIOVASCULAR AND METABOLIC DISEASE. |
| Q34556483 | Leukotriene B4 antagonism ameliorates experimental lymphedema |
| Q38455525 | Linifanib: current status and future potential in cancer therapy |
| Q37422025 | Local cortical tension by myosin II guides 3D endothelial cell branching |
| Q89818890 | Low doses of ionizing radiation enhance angiogenesis and consequently accelerate post-embryonic development but not regeneration in zebrafish |
| Q38190359 | Lymphangiogenesis and lymphatic vessel remodelling in cancer |
| Q47744569 | Lymphangiogenesis guidance by paracrine and pericellular factors |
| Q37363751 | Malignant cell-derived PlGF promotes normalization and remodeling of the tumor vasculature |
| Q30505376 | Mechanoinduction of lymph vessel expansion |
| Q37643632 | Membrane-mediated regulation of vascular identity. |
| Q39983817 | Metabolic control of the cell cycle. |
| Q36799157 | MicroRNA 139-5p coordinates APLNR-CXCR4 crosstalk during vascular maturation |
| Q36554547 | MicroRNA control of vascular endothelial growth factor signaling output during vascular development |
| Q38294075 | MicroRNA-10a/10b represses a novel target gene mib1 to regulate angiogenesis |
| Q30495845 | MicroRNA-mediated integration of haemodynamics and Vegf signalling during angiogenesis |
| Q37006651 | Models of biological pattern formation: from elementary steps to the organization of embryonic axes |
| Q30496231 | Moesin1 and Ve-cadherin are required in endothelial cells during in vivo tubulogenesis |
| Q50423780 | Molecular Regulation of Sprouting Angiogenesis. |
| Q37863911 | Molecular basis for endothelial lumen formation and tubulogenesis during vasculogenesis and angiogenic sprouting |
| Q27007664 | Molecular control of endothelial cell behaviour during blood vessel morphogenesis |
| Q37889219 | Molecular control of vascular development in the zebrafish. |
| Q33639474 | Molecular mediators of angiogenesis |
| Q29616150 | Molecular regulation of angiogenesis and lymphangiogenesis |
| Q58799244 | Monitoring antiangiogenesis of bevacizumab in zebrafish |
| Q37148339 | Motor neuron-derived Thsd7a is essential for zebrafish vascular development via the Notch-dll4 signaling pathway. |
| Q91993914 | Multi-Faceted Notch in Allergic Airway Inflammation |
| Q64119426 | Multifactorial Contribution of Notch Signaling in Head and Neck Squamous Cell Carcinoma |
| Q34999181 | Multiple endothelial cells constitute the tip of developing blood vessels and polarize to promote lumen formation |
| Q30521486 | Multiscale mechanisms of cell migration during development: theory and experiment |
| Q27319553 | Mutation in utp15 disrupts vascular patterning in a p53-dependent manner in zebrafish embryos |
| Q37950901 | Neovascularization and hematopoietic stem cells |
| Q37584778 | Neuronal sFlt1 and Vegfaa determine venous sprouting and spinal cord vascularization. |
| Q41669132 | Neurovascular patterning cues and implications for central and peripheral neurological disease |
| Q36861805 | Notch Signaling in the Vasculature |
| Q47073573 | Notch activity levels control the balance between quiescence and recruitment of adult neural stem cells. |
| Q38074776 | Notch as a hub for signaling in angiogenesis. |
| Q38268444 | Notch functions in developmental and tumour angiogenesis by diverse mechanisms |
| Q37421707 | Notch regulates BMP responsiveness and lateral branching in vessel networks via SMAD6. |
| Q42542271 | Notch regulation of hematopoiesis, endothelial precursor cells, and blood vessel formation: orchestrating the vasculature |
| Q37861206 | Notch regulation of tumor angiogenesis |
| Q42583682 | Notch signaling functions as a cell-fate switch between the endothelial and hematopoietic lineages |
| Q38238021 | Notch signaling in blood vessels: from morphogenesis to homeostasis |
| Q34541286 | Notch signaling in descending thoracic aortic aneurysm and dissection |
| Q35719022 | Notch signaling in ocular vasculature development and diseases |
| Q38805816 | Notch signaling in regulating angiogenesis in a 3D biomimetic environment |
| Q37256455 | Notch signaling regulates tumor angiogenesis by diverse mechanisms |
| Q83229830 | Notch signaling restricts FGF pathway activation in parapineal cells to promote their collective migration |
| Q34970926 | Notch signalling and the regulation of angiogenesis |
| Q33649282 | Notch signalling in ischaemia-induced angiogenesis. |
| Q28587298 | Notch-dependent VEGFR3 upregulation allows angiogenesis without VEGF-VEGFR2 signalling |
| Q37429344 | Notch3 establishes brain vascular integrity by regulating pericyte number. |
| Q37657105 | Novel insights into the differential functions of Notch ligands in vascular formation |
| Q36286179 | Nr2f1b control venous specification and angiogenic patterning during zebrafish vascular development |
| Q24318627 | Nrarp coordinates endothelial Notch and Wnt signaling to control vessel density in angiogenesis |
| Q39857255 | Nuclear and membrane expression of the angiogenesis regulator delta-like ligand 4 (DLL4) in normal and malignant human tissues |
| Q34090024 | Nuclear receptor subfamily 2 group F member 1a (nr2f1a) is required for vascular development in zebrafish |
| Q33554587 | O-GlcNAc on NOTCH1 EGF repeats regulates ligand-induced Notch signaling and vascular development in mammals |
| Q28506962 | Overexpression of delta-like 4 induces arterialization and attenuates vessel formation in developing mouse embryos |
| Q33663049 | PTEN mediates Notch-dependent stalk cell arrest in angiogenesis |
| Q30855952 | Patterning mechanisms of the sub-intestinal venous plexus in zebrafish |
| Q24653433 | Perlecan regulates developmental angiogenesis by modulating the VEGF-VEGFR2 axis. |
| Q40000387 | Perturbation of invadolysin disrupts cell migration in zebrafish (Danio rerio). |
| Q38871489 | Polo-like kinase 2 regulates angiogenic sprouting and blood vessel development |
| Q34167150 | Polysaccharides from astragali radix restore chemical-induced blood vessel loss in zebrafish |
| Q64964532 | Positive Feedback Defines the Timing, Magnitude, and Robustness of Angiogenesis. |
| Q50454265 | Prdx1-encoded peroxiredoxin is important for vascular development in zebrafish. |
| Q38820186 | Prostaglandins and Other Lipid Mediators (POLM), Special Issue of the 6th European workshop on lipid mediators: Role of Müller cell cytochrome P450 2c44 in murine retinal angiogenesis. |
| Q44040143 | Protein kinase D2 and heat shock protein 90 beta are required for BCL6-associated zinc finger protein mRNA stabilization induced by vascular endothelial growth factor-A. |
| Q54959791 | Pseudopodium-enriched atypical kinase 1 mediates angiogenesis by modulating GATA2-dependent VEGFR2 transcription. |
| Q38060665 | Quantitative mass spectrometry-based proteomics in angiogenesis. |
| Q48352254 | R-spondin 1 is required for specification of hematopoietic stem cells through Wnt16 and Vegfa signaling pathways |
| Q33605773 | Radiotherapy suppresses angiogenesis in mice through TGF-betaRI/ALK5-dependent inhibition of endothelial cell sprouting |
| Q37259285 | Ras pathway inhibition prevents neovascularization by repressing endothelial cell sprouting |
| Q39456719 | Regulation of Vegf signaling by natural and synthetic ligands |
| Q27006807 | Regulation of blood vessel sprouting |
| Q38101895 | Regulation of endothelial cell differentiation and specification |
| Q38284407 | Regulation of signaling interactions and receptor endocytosis in growing blood vessels |
| Q27335807 | Reiterative use of the notch signal during zebrafish intrahepatic biliary development |
| Q36257821 | Release of endothelial cell associated VEGFR2 during TGF-β modulated angiogenesis in vitro |
| Q40962222 | Role of delta-like-4/Notch in the formation and wiring of the lymphatic network in zebrafish. |
| Q36072089 | Role of the DLL4-NOTCH system in PGF2alpha-induced luteolysis in the pregnant rat |
| Q34829230 | Role of the cytoskeleton in formation and maintenance of angiogenic sprouts |
| Q35445281 | Rspo1/Wnt signaling promotes angiogenesis via Vegfc/Vegfr3 |
| Q24617241 | Semaphorin-PlexinD1 signaling limits angiogenic potential via the VEGF decoy receptor sFlt1 |
| Q37705914 | Signaling circuitry in vascular morphogenesis |
| Q34213551 | Signalling pathways that control vertebrate haematopoietic stem cell specification |
| Q39569424 | Silencing of hHS6ST2 inhibits progression of pancreatic cancer through inhibition of Notch signalling |
| Q27342874 | Single-cell analysis of endothelial morphogenesis in vivo |
| Q33923897 | SoxF factors and Notch regulate nr2f2 gene expression during venous differentiation in zebrafish |
| Q38723349 | SoxF factors induce Notch1 expression via direct transcriptional regulation during early arterial development |
| Q93038138 | Sprouting and anastomosis in the Drosophila trachea and the vertebrate vasculature: Similarities and differences in cell behaviour |
| Q27348907 | Stable vascular connections and remodeling require full expression of VE-cadherin in zebrafish embryos |
| Q42098324 | Stalk cell phenotype depends on integration of Notch and Smad1/5 signaling cascades |
| Q36845727 | Statistical platform to discern spatial and temporal coordination of endothelial sprouting. |
| Q36249525 | Suppression of renal cell carcinoma growth by inhibition of Notch signaling in vitro and in vivo |
| Q43185593 | Syk and Zap-70 function redundantly to promote angioblast migration. |
| Q42198449 | TNF induction of jagged-1 in endothelial cells is NFkappaB-dependent |
| Q33323527 | TNF primes endothelial cells for angiogenic sprouting by inducing a tip cell phenotype |
| Q37696748 | Targeting notch signaling pathway in cancer: clinical development advances and challenges |
| Q44740531 | Targeting oncogene expression to endothelial cells induces proliferation of the myelo-erythroid lineage by repressing the Notch pathway |
| Q37234630 | Targeting the Notch1 and mTOR pathways in a mouse T-ALL model |
| Q53083368 | Thalidomide-induced angiopoietin 2, Notch1 and Dll4 downregulation under hypoxic condition in tissues with gastrointestinal vascular malformation and human umbilical vein endothelial cells. |
| Q80212331 | The Delta paradox: DLL4 blockade leads to more tumour vessels but less tumour growth |
| Q50320053 | The LIM-homeodomain transcription factor Islet2a promotes angioblast migration. |
| Q57566289 | The Notch Signaling System Is Involved in the Regulation of Reparative Angiogenesis in the Zone of Stasis |
| Q64244246 | The PERK Branch of the Unfolded Protein Response Promotes DLL4 Expression by Activating an Alternative Translation Mechanism |
| Q36092050 | The Retinoid Agonist Tazarotene Promotes Angiogenesis and Wound Healing |
| Q64958395 | The Role of Dll4/Notch Signaling in Normal and Pathological Ocular Angiogenesis: Dll4 Controls Blood Vessel Sprouting and Vessel Remodeling in Normal and Pathological Conditions. |
| Q41848212 | The STAT3-Ser/Hes3 signaling axis: an emerging regulator of endogenous regeneration and cancer growth |
| Q38281725 | The cardiovascular triad of dysfunctional angiogenesis. |
| Q26863506 | The critical roles of COUP-TFII in tumor progression and metastasis |
| Q38161389 | The dynamics of developmental and tumor angiogenesis-a comparison. |
| Q38685677 | The front and rear of collective cell migration. |
| Q30503349 | The maintenance and regeneration of the planarian excretory system are regulated by EGFR signaling |
| Q35852994 | The new era of the lymphatic system: no longer secondary to the blood vascular system |
| Q60308057 | The precise molecular signals that control endothelial cell-cell adhesion within the vessel wall |
| Q92226320 | The promise of zebrafish as a model of metabolic syndrome |
| Q54365519 | The role of differential VE-cadherin dynamics in cell rearrangement during angiogenesis. |
| Q36542074 | The role of extracellular matrix in vascular branching morphogenesis |
| Q37718432 | The somite-secreted factor Maeg promotes zebrafish embryonic angiogenesis |
| Q38082559 | The tip cell concept 10 years after: new players tune in for a common theme |
| Q40076736 | Therapeutic potential of novel modulators of neovascularization |
| Q38367121 | Therapeutic promise and challenges of targeting DLL4/NOTCH1. |
| Q35685757 | Tip cell-specific requirement for an atypical Gpr124- and Reck-dependent Wnt/β-catenin pathway during brain angiogenesis |
| Q26991847 | Tip cells: master regulators of tubulogenesis? |
| Q37627165 | Tissue remodelling through branching morphogenesis |
| Q37958944 | To sprout or to split? VEGF, Notch and vascular morphogenesis |
| Q48966518 | Transgenesis of the Wolffian duct visualizes dynamic behavior of cells undergoing tubulogenesis in vivo |
| Q27339985 | Tumor angiogenesis and vascular patterning: a mathematical model |
| Q39393740 | Tumor angiogenesis revisited: Regulators and clinical implications. |
| Q28533945 | Tumor endothelial cell-specific drug delivery system using apelin-conjugated liposomes |
| Q30538613 | UBIAD1-mediated vitamin K2 synthesis is required for vascular endothelial cell survival and development |
| Q35075783 | UXT potentiates angiogenesis by attenuating Notch signaling |
| Q41701270 | Uncontrolled angiogenic precursor expansion causes coronary artery anomalies in mice lacking Pofut1. |
| Q38219834 | Understanding the role of Notch in osteosarcoma |
| Q38833891 | Utilizing Zebrafish to Identify Anti-(Lymph)Angiogenic Compounds for Cancer Treatment: Promise and Future Challenges |
| Q37283444 | VEGF and Delta-Notch: interacting signalling pathways in tumour angiogenesis |
| Q42099822 | VEGF and Notch in tip and stalk cell selection |
| Q37406699 | VEGF and Notch signaling: the yin and yang of angiogenic sprouting |
| Q42078015 | VEGF and endothelial guidance in angiogenic sprouting |
| Q35682284 | VEGFR-3 controls tip to stalk conversion at vessel fusion sites by reinforcing Notch signalling. |
| Q51097984 | VEGFR3 Modulates Vascular Permeability by Controlling VEGF/VEGFR2 Signaling. |
| Q35031502 | VEGFR3 does not sustain retinal angiogenesis without VEGFR2 |
| Q38973271 | VEGFR3: a new target for antiangiogenesis therapy? |
| Q28259468 | Vascular actions of 20-HETE |
| Q38007161 | Vascular development in the zebrafish |
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