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Integrin-dependent and -independent functions of astrocytic fibronectin in retinal angiogenesis

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cne.20179openalex-snapshot
Nestin promoter/enhancer directs transgene expression to precursors of adult generated periglomerular neurons
inferredcites →https://doi.org/10.1002/dvg.20367openalex-snapshot
Efficient, inducible Cre‐recombinase activation in vascular endothelium
inferredcites →https://doi.org/10.1002/jcp.1121openalex-snapshot
Expression of vascular endothelial growth factor receptors in smooth muscle cells
inferredcites →https://doi.org/10.1002/jcp.20525openalex-snapshot
Implication of the hypoxia response element of the vegf promoter in mouse models of retinal and choroidal neovascularization, but not retinal vascular development
inferredcites →https://doi.org/10.1006/dbio.1999.9451openalex-snapshot
Overlapping and Independent Functions of Fibronectin Receptor Integrins in Early Mesodermal Development
inferredcites →https://doi.org/10.1006/dbio.2000.0106openalex-snapshot
Tie2-Cre Transgenic Mice: A New Model for Endothelial Cell-Lineage Analysis in Vivo
inferredcites →https://doi.org/10.1016/0012-1606(88)90225-4openalex-snapshot
Changes in the vascular extracellular matrix during embryonic vasculogenesis and angiogenesis
inferredcites →https://doi.org/10.1016/0014-4827(86)90570-7openalex-snapshot
Fibronectin is expressed by astrocytes cultured from embryonic and early postnatal rat brain
inferredcites →https://doi.org/10.1016/j.ceb.2008.06.001openalex-snapshot
The role of integrin binding sites in fibronectin matrix assembly in vivo
inferredcites →https://doi.org/10.1016/j.cell.2005.10.034openalex-snapshot
Ephrin-B2 Controls Cell Motility and Adhesion during Blood-Vessel-Wall Assembly
inferredcites →https://doi.org/10.1016/j.devcel.2006.03.009openalex-snapshot
Heparan Sulfate in trans Potentiates VEGFR-Mediated Angiogenesis
inferredcites →https://doi.org/10.1016/j.ejca.2008.06.031openalex-snapshot
VEGF release by MMP-9 mediated heparan sulphate cleavage induces colorectal cancer angiogenesis
inferredcites →https://doi.org/10.1016/j.yexcr.2006.04.005openalex-snapshot
Directed cell migration on fibronectin gradients: Effect of gradient slope
inferredcites →https://doi.org/10.1016/j.yexcr.2007.06.005openalex-snapshot
Analysis of directional cell migration on defined FN gradients: Role of intracellular signaling molecules
inferredcites →https://doi.org/10.1021/la701435xopenalex-snapshot
Endothelial Cell Migration on Surface-Density Gradients of Fibronectin, VEGF, or Both Proteins
inferredcites →https://doi.org/10.1038/85471openalex-snapshot
Plasma fibronectin supports neuronal survival and reduces brain injury following transient focal cerebral ischemia but is not essential for skin-wound healing and hemostasis.
inferredcites →https://doi.org/10.1038/nature01124openalex-snapshot
Progenitor cell maintenance requires numb and numblike during mouse neurogenesis
inferredcites →https://doi.org/10.1038/nature06892openalex-snapshot
Angiogenesis selectively requires the p110α isoform of PI3K to control endothelial cell migration
inferredcites →https://doi.org/10.1038/sj.onc.1208602openalex-snapshot
A functional heparan sulfate mimetic implicates both heparanase and heparan sulfate in tumor angiogenesis and invasion in a mouse model of multistage cancer
inferredcites →https://doi.org/10.1073/pnas.0902510106openalex-snapshot
PDGF-A interactions with fibronectin reveal a critical role for heparan sulfate in directed cell migration during Xenopus gastrulation
inferredcites →https://doi.org/10.1074/jbc.m002016200openalex-snapshot
Analysis of Biological Effects and Signaling Properties of Flt-1 (VEGFR-1) and KDR (VEGFR-2)
inferredcites →https://doi.org/10.1074/jbc.m109.009712openalex-snapshot
Heparan Sulfate Phage Display Antibodies Identify Distinct Epitopes with Complex Binding Characteristics
inferredcites →https://doi.org/10.1074/jbc.m110.177006openalex-snapshot
Heparan Sulfate Regulates VEGF165- and VEGF121-mediated Vascular Hyperpermeability
inferredcites →https://doi.org/10.1074/jbc.m704917200openalex-snapshot
Endothelial Cell Migration in Stable Gradients of Vascular Endothelial Growth Factor A and Fibroblast Growth Factor 2
inferredcites →https://doi.org/10.1083/jcb.200302047openalex-snapshot
VEGF guides angiogenic sprouting utilizing endothelial tip cell filopodia
inferredcites →https://doi.org/10.1083/jcb.200703021openalex-snapshot
The RGD motif in fibronectin is essential for development but dispensable for fibril assembly
inferredcites →https://doi.org/10.1083/jcb.200906044openalex-snapshot
Anchorage of VEGF to the extracellular matrix conveys differential signaling responses to endothelial cells
inferredcites →https://doi.org/10.1096/fj.00-0868fjeopenalex-snapshot
Differentiation and migration of astrocyte precursor cells (APCs) and astrocytes in human fetal retina: relevance to optic nerve coloboma
inferredcites →https://doi.org/10.1096/fj.05-4134comopenalex-snapshot
Fibronectin is required for integrin o:vβ6‐mediated activation of latent TGF‐β complexes containing LTBP‐1
inferredcites →https://doi.org/10.1101/gad.242002openalex-snapshot
Spatially restricted patterning cues provided by heparin-binding VEGF-A control blood vessel branching morphogenesis
inferredcites →https://doi.org/10.1111/j.1460-9568.1989.tb00797.xopenalex-snapshot
Immunocytochemical Localization of Glia‐Derived Nexin, Laminin and Fibronectin on the Surface or Extracellular Matrix of C6 Rat Glioma Cells, Astrocytes and Fibroblasts
inferredcites →https://doi.org/10.1126/science.1090497openalex-snapshot
Mammalian Brain Morphogenesis and Midline Axon Guidance Require Heparan Sulfate
inferredcites →https://doi.org/10.1126/science.1176009openalex-snapshot
The Extracellular Matrix: Not Just Pretty Fibrils
inferredcites →https://doi.org/10.1128/mcb.22.14.5100-5113.2002openalex-snapshot
Astrocyte-Specific Inactivation of the Neurofibromatosis 1 Gene (NF1) Is Insufficient for Astrocytoma Formation
inferredcites →https://doi.org/10.1161/01.res.0000026420.22406.79openalex-snapshot
Novel Vascular Endothelial Growth Factor Binding Domains of Fibronectin Enhance Vascular Endothelial Growth Factor Biological Activity
inferredcites →https://doi.org/10.1161/01.res.0000246849.17887.66openalex-snapshot
Heparin-II Domain of Fibronectin Is a Vascular Endothelial Growth Factor-Binding Domain
inferredcites →https://doi.org/10.1161/circresaha.107.167908openalex-snapshot
Integrin β1 Subunit Controls Mural Cell Adhesion, Spreading, and Blood Vessel Wall Stability
inferredcites →https://doi.org/10.1172/jci25964openalex-snapshot
Tlx acts as a proangiogenic switch by regulating extracellular assembly of fibronectin matrices in retinal astrocytes
inferredcites →https://doi.org/10.1182/blood.v90.8.3073openalex-snapshot
Fibronectins Are Essential for Heart and Blood Vessel Morphogenesis But Are Dispensable for Initial Specification of Precursor Cells
inferredcites →https://doi.org/10.1242/dev.01732openalex-snapshot
Stabilization of the retinal vascular network by reciprocal feedback between blood vessels and astrocytes
inferredcites →https://doi.org/10.1242/dev.049551openalex-snapshot
Endothelial α5 and αv integrins cooperate in remodeling of the vasculature during development
inferredcites →https://doi.org/10.1242/dev.119.4.1079openalex-snapshot
Defects in mesoderm, neural tube and vascular development in mouse embryos lacking fibronectin
inferredcites →https://doi.org/10.1242/dev.119.4.1093openalex-snapshot
Embryonic mesodermal defects in α5 integrin-deficient mice
inferredcites →https://doi.org/10.1242/jcs.107.9.2499openalex-snapshot
Astrocytes modulate retinal vasculogenesis: effects on fibronectin expression
inferredcites →https://doi.org/10.1371/journal.pone.0011863openalex-snapshot
Astrocyte-Derived Vascular Endothelial Growth Factor Stabilizes Vessels in the Developing Retinal Vasculature
inferredcites →https://doi.org/10.1523/jneurosci.15-07-04738.1995openalex-snapshot
Development of retinal vasculature is mediated by hypoxia-induced vascular endothelial growth factor (VEGF) expression by neuroglia

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Understanding Post-Angiogenic Tumor Growth: Insights from Vascular Network Properties in Cellular Automata Modeling
inferred← citeshttps://doi.org/10.1002/ar.22998openalex-snapshot
Ephrin‐A3 and Ephrin‐A4 Contribute to Microglia‐Induced Angiogenesis in Brain Endothelial Cells
inferred← citeshttps://doi.org/10.1002/ar.23922openalex-snapshot
Cranial Pair II: The Optic Nerves
inferred← citeshttps://doi.org/10.1002/bdrc.21010openalex-snapshot
Pattern formation during vasculogenesis
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Interactions between neural cells and blood vessels in central nervous system development
inferred← citeshttps://doi.org/10.1002/dvdy.24190openalex-snapshot
Development of astrocytes in the vertebrate eye
inferred← citeshttps://doi.org/10.1002/dvdy.24389openalex-snapshot
Syndactyly in a novel Fras1rdf mutant results from interruption of signals for interdigital apoptosis
inferred← citeshttps://doi.org/10.1002/dvdy.263openalex-snapshot
Pharmacological depletion of retinal neurons prevents vertical angiogenic sprouting without affecting the superficial vascular plexus
inferred← citeshttps://doi.org/10.1002/dvdy.389openalex-snapshot
Reduced mTORC1 ‐signaling in retinal ganglion cells leads to vascular retinopathy
inferred← citeshttps://doi.org/10.1002/glia.22748openalex-snapshot
The EIIIA domain from astrocyte‐derived fibronectin mediates proliferation of oligodendrocyte progenitor cells following CNS demyelination
inferred← citeshttps://doi.org/10.1002/glia.22839openalex-snapshot
The extracellular matrix compartment of neural stem and glial progenitor cells
inferred← citeshttps://doi.org/10.1002/glia.22939openalex-snapshot
Astrocytes spatially restrict VEGF signaling by polarized secretion and incorporation of VEGF into the actively assembling extracellular matrix
inferred← citeshttps://doi.org/10.1002/glia.22956openalex-snapshot
Altered astrocyte morphology and vascular development in dystrophin‐ D p71‐null mice
inferred← citeshttps://doi.org/10.1002/glia.23189openalex-snapshot
Astrocytes follow ganglion cell axons to establish an angiogenic template during retinal development
inferred← citeshttps://doi.org/10.1002/glia.24571openalex-snapshot
Transcriptional profiling of retinal astrocytes identifies a specific marker and points to functional specialization
inferred← citeshttps://doi.org/10.1002/path.4805openalex-snapshot
ANGPTL4 –αvβ3 interaction counteracts hypoxia‐induced vascular permeability by modulating Src signalling downstream of vascular endothelial growth factor receptor 2
inferred← citeshttps://doi.org/10.1002/wsbm.1233openalex-snapshot
Endothelial cell motility, coordination and pattern formation during vasculogenesis
inferred← citeshttps://doi.org/10.1007/978-1-4939-1086-1_13openalex-snapshot
III.A. Congenital Vascular Vitreoretinopathies
inferred← citeshttps://doi.org/10.1007/978-3-031-19616-4_1openalex-snapshot
Fibronectin Fibrillogenesis During Angiogenesis
inferred← citeshttps://doi.org/10.1007/978-3-031-19616-4_11openalex-snapshot
Lymphatic Mechanoregulation in Development and Disease
inferred← citeshttps://doi.org/10.1007/978-3-031-19616-4_2openalex-snapshot
Functional Interplay Between Fibronectin and Matricellular Proteins in the Control of Endothelial Tubulogenesis
inferred← citeshttps://doi.org/10.1007/978-3-642-35935-4_2openalex-snapshot
Extracellular Matrix Dynamics in Early Development
inferred← citeshttps://doi.org/10.1007/978-3-642-35935-4_5openalex-snapshot
Interactions Between Neural Crest-Derived Cells and Extracellular Microenvironment During Cardiovascular Development
inferred← citeshttps://doi.org/10.1007/s00018-013-1277-5openalex-snapshot
Neurovascular development and links to disease
inferred← citeshttps://doi.org/10.1007/s00395-014-0404-2openalex-snapshot
Brag2 differentially regulates β1- and β3-integrin-dependent adhesion in endothelial cells and is involved in developmental and pathological angiogenesis
inferred← citeshttps://doi.org/10.1007/s10456-017-9563-8openalex-snapshot
Endothelium-derived fibronectin regulates neonatal vascular morphogenesis in an autocrine fashion
inferred← citeshttps://doi.org/10.1007/s10456-019-09681-1openalex-snapshot
Stabilization of myeloid-derived HIFs promotes vascular regeneration in retinal ischemia
inferred← citeshttps://doi.org/10.1007/s10741-020-10032-2openalex-snapshot
Heal the heart through gut (hormone) ghrelin: a potential player to combat heart failure
inferred← citeshttps://doi.org/10.1007/s11011-021-00709-4openalex-snapshot
RhoA/ROCK signaling pathway and astrocytes in ischemic stroke
inferred← citeshttps://doi.org/10.1007/s11033-014-3320-5openalex-snapshot
Long non-coding RNAs: new players in ocular neovascularization
inferred← citeshttps://doi.org/10.1007/s11064-017-2272-2openalex-snapshot
The Unwanted Cell Migration in the Brain: Glioma Metastasis
inferred← citeshttps://doi.org/10.1007/s11064-025-04500-0openalex-snapshot
Extracellular Matrix Proteins Differentiate Postnatal Mouse Retina Neurospheres into Neurons or Glia Profiles
inferred← citeshttps://doi.org/10.1007/s12035-013-8396-8openalex-snapshot
Astrocyte-Derived Sonic Hedgehog Contributes to Angiogenesis in Brain Microvascular Endothelial Cells via RhoA/ROCK Pathway After Oxygen–Glucose Deprivation
inferred← citeshttps://doi.org/10.1007/s13577-019-00272-2openalex-snapshot
Bit1-a novel regulator of astrocyte function during retinal development: proliferation, migration, and paracrine effects on vascular endothelial cell
inferred← citeshttps://doi.org/10.1016/b978-0-12-386503-8.00002-8openalex-snapshot
Essential Roles of EphB Receptors and EphrinB Ligands in Endothelial Cell Function and Angiogenesis
inferred← citeshttps://doi.org/10.1016/b978-0-323-90599-2.00009-xopenalex-snapshot
Lumen formation and perfusion
inferred← citeshttps://doi.org/10.1016/j.ajo.2025.07.023openalex-snapshot
Placental Transcriptomic Analysis in Retinopathy of Prematurity Reactivation After Anti-VEGF Treatment
inferred← citeshttps://doi.org/10.1016/j.biopha.2025.118516openalex-snapshot
Interactions between astrocytes and cerebral endothelial cells in central nervous system diseases
inferred← citeshttps://doi.org/10.1016/j.brainres.2013.01.043openalex-snapshot
Potential role of fibronectin in microglia/macrophage activation following cryoinjury in the rat brain: An immunohistochemical study
inferred← citeshttps://doi.org/10.1016/j.ccell.2017.08.001openalex-snapshot
Increased Vascular Permeability in the Bone Marrow Microenvironment Contributes to Disease Progression and Drug Response in Acute Myeloid Leukemia
inferred← citeshttps://doi.org/10.1016/j.ceb.2011.10.002openalex-snapshot
Endothelial development taking shape
inferred← citeshttps://doi.org/10.1016/j.ceb.2013.10.005openalex-snapshot
Role of G protein-coupled receptor kinases in cell migration
inferred← citeshttps://doi.org/10.1016/j.cell.2014.09.025openalex-snapshot
Neurons Limit Angiogenesis by Titrating VEGF in Retina
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.05.018openalex-snapshot
NRP1 Regulates CDC42 Activation to Promote Filopodia Formation in Endothelial Tip Cells
inferred← citeshttps://doi.org/10.1016/j.celrep.2016.10.035openalex-snapshot
Retinal Proteoglycans Act as Cellular Receptors for Basement Membrane Assembly to Control Astrocyte Migration and Angiogenesis
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109616openalex-snapshot
The Amot/integrin protein complex transmits mechanical forces required for vascular expansion
inferred← citeshttps://doi.org/10.1016/j.chaos.2024.115199openalex-snapshot
Understanding post-angiogenic tumor growth: Insights from vascular network properties in cellular automata modeling
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2013.11.002openalex-snapshot
Extracellular regulation of VEGF: Isoforms, proteolysis, and vascular patterning
inferred← citeshttps://doi.org/10.1016/j.exer.2014.08.011openalex-snapshot
Extracellular matrix, gap junctions, and retinal vascular homeostasis in diabetic retinopathy
inferred← citeshttps://doi.org/10.1016/j.exer.2014.10.021openalex-snapshot
The role of extracellular matrix in retinal vascular development and preretinal neovascularization
inferred← citeshttps://doi.org/10.1016/j.exer.2026.111075openalex-snapshot
Comprehensive proteomic meta-analysis identifies novel proteomics alterations in proliferative diabetic retinopathy
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110273openalex-snapshot
ADAMTS18-fibronectin interaction regulates the morphology of liver sinusoidal endothelial cells
inferred← citeshttps://doi.org/10.1016/j.jbc.2021.100584openalex-snapshot
VEGF and VEGFR2 bind to similar pH-sensitive sites on fibronectin, exposed by heparin-mediated conformational changes
inferred← citeshttps://doi.org/10.1016/j.jtbi.2018.08.005openalex-snapshot
Soluble VEGFR1 signaling guides vascular patterns into dense branching morphologies
inferred← citeshttps://doi.org/10.1016/j.matbio.2020.02.004openalex-snapshot
Fibronectin has multifunctional roles in posterior capsular opacification (PCO)
inferred← citeshttps://doi.org/10.1016/j.mod.2015.07.001openalex-snapshot
Vascularisation of the central nervous system
inferred← citeshttps://doi.org/10.1016/j.mtcomm.2025.112761openalex-snapshot
A recombinant fibronectin3-chitosan nanoparticle dressing with neovascularization functions for full-thickness wound treatment
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2018.02.002openalex-snapshot
Cell adhesion and matricellular support by astrocytes of the tripartite synapse
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2016.02.003openalex-snapshot
NRP1 function and targeting in neurovascular development and eye disease
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2017.11.001openalex-snapshot
Retinal vasculature development in health and disease
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2021.100966openalex-snapshot
Targeting RGD-binding integrins as an integrative therapy for diabetic retinopathy and neovascular age-related macular degeneration
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.08.007openalex-snapshot
Extracellular matrix scaffolding in angiogenesis and capillary homeostasis
inferred← citeshttps://doi.org/10.1016/j.trsl.2015.06.008openalex-snapshot
MicroRNA expression profiles differentiate chronic pain condition subtypes
inferred← citeshttps://doi.org/10.1016/j.ydbio.2011.12.027openalex-snapshot
The formation of an angiogenic astrocyte template is regulated by the neuroretina in a HIF-1-dependent manner
inferred← citeshttps://doi.org/10.1016/j.ydbio.2011.12.036openalex-snapshot
Convective tissue movements play a major role in avian endocardial morphogenesis
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.09.018openalex-snapshot
“Sprouting angiogenesis”, a reappraisal
inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.08.015openalex-snapshot
Filopodia and focal adhesions: An integrated system driving branching morphogenesis in neuronal pathfinding and angiogenesis
inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.07.017openalex-snapshot
Fibulin-1 is required for microvascular integrity in the developing brain and retina
inferred← citeshttps://doi.org/10.1016/j.ymthe.2022.01.008openalex-snapshot
Engineered clustered myoblast cell injection augments angiogenesis and muscle regeneration in peripheral artery disease
inferred← citeshttps://doi.org/10.1038/ncomms7429openalex-snapshot
Integrin β1 controls VE-cadherin localization and blood vessel stability
inferred← citeshttps://doi.org/10.1038/nn.3930openalex-snapshot
Astrocytic adenosine receptor A2A and Gs-coupled signaling regulate memory
inferred← citeshttps://doi.org/10.1038/s41467-018-07172-3openalex-snapshot
Endothelial cell rearrangements during vascular patterning require PI3-kinase-mediated inhibition of actomyosin contractility
inferred← citeshttps://doi.org/10.1038/s41598-017-17962-2openalex-snapshot
Retinal Angiogenesis Regulates Astrocytic Differentiation in Neonatal Mouse Retinas by Oxygen Dependent Mechanisms
inferred← citeshttps://doi.org/10.1038/s41598-020-66278-1openalex-snapshot
Periostin and tenascin-C interaction promotes angiogenesis in ischemic proliferative retinopathy
inferred← citeshttps://doi.org/10.1038/s42003-024-06320-4openalex-snapshot
A proteomics approach to isolating neuropilin-dependent α5 integrin trafficking pathways: neuropilin 1 and 2 co-traffic α5 integrin through endosomal p120RasGAP to promote polarised fibronectin fibrillogenesis in endothelial cells
inferred← citeshttps://doi.org/10.1038/srep43470openalex-snapshot
Ischemic injury leads to extracellular matrix alterations in retina and optic nerve
inferred← citeshttps://doi.org/10.1042/bst20140141openalex-snapshot
Neuropilin-1 enforces extracellular matrix signalling via ABL1 to promote angiogenesis
inferred← citeshttps://doi.org/10.1056/nejmc1301021openalex-snapshot
Mechanisms and Management of Retinopathy of Prematurity
inferred← citeshttps://doi.org/10.1073/pnas.1614970113openalex-snapshot
Epithelial cell integrin β1 is required for developmental angiogenesis in the pituitary gland
inferred← citeshttps://doi.org/10.1073/pnas.1722317115openalex-snapshot
Targeting β1-integrin inhibits vascular leakage in endotoxemia
inferred← citeshttps://doi.org/10.1080/02713683.2020.1748659openalex-snapshot
Analysis of Long Noncoding RNAs in Choroid Neovascularization
inferred← citeshttps://doi.org/10.1083/jcb.201508047openalex-snapshot
Collective cell migration in development
inferred← citeshttps://doi.org/10.1083/jcb.202103098openalex-snapshot
Endothelial depletion of Atg7 triggers astrocyte–microvascular disassociation at blood–brain barrier
inferred← citeshttps://doi.org/10.1084/jem.20132330openalex-snapshot
Imatinib inhibits VEGF-independent angiogenesis by targeting neuropilin 1–dependent ABL1 activation in endothelial cells
inferred← citeshttps://doi.org/10.1088/1478-3975/10/6/066007openalex-snapshot
Dynamics of VEGF matrix-retention in vascular network patterning
inferred← citeshttps://doi.org/10.1093/med/9780199794591.003.0033openalex-snapshot
The Role of Glia in the Formation and Function of the Blood-Brain Barrier
inferred← citeshttps://doi.org/10.1097/md.0000000000014074openalex-snapshot
Identification of key regulators of pancreatic ductal adenocarcinoma using bioinformatics analysis of microarray data
inferred← citeshttps://doi.org/10.1097/moh.0b013e3283523ebcopenalex-snapshot
Vascular lumen formation
inferred← citeshttps://doi.org/10.1101/2022.01.12.476001openalex-snapshot
Complement facilitates developmental microglial pruning of astrocyte and vascular networks
inferred← citeshttps://doi.org/10.1101/2023.11.28.568967openalex-snapshot
Together, Neuropilin 1 and Neuropilin 2 direct α5 integrin trafficking through GTPase-activating-protein p120RasGAP in endothelial cells to promote fibronectin fibrillogenesis
inferred← citeshttps://doi.org/10.1101/2024.02.22.24303109openalex-snapshot
Defective CAPSL function causes impaired retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
inferred← citeshttps://doi.org/10.1101/2025.08.15.670628openalex-snapshot
LDL Signals Through Scarf1 to Drive a Pro-Fibrotic Secretory Response in Endothelial Cells
inferred← citeshttps://doi.org/10.1111/micc.12492openalex-snapshot
Insulin resistance disrupts cell integrity, mitochondrial function, and inflammatory signaling in lymphatic endothelium
inferred← citeshttps://doi.org/10.1126/scitranslmed.3006666openalex-snapshot
Angiopoietin-1 Guides Directional Angiogenesis Through Integrin α v β 5 Signaling for Recovery of Ischemic Retinopathy
inferred← citeshttps://doi.org/10.1146/annurev-vision-121423-013153openalex-snapshot
Development of Retinal Astroglia
inferred← citeshttps://doi.org/10.1161/atvbaha.112.300142openalex-snapshot
MicroRNA Control of Vascular Endothelial Growth Factor Signaling Output During Vascular Development
inferred← citeshttps://doi.org/10.1161/atvbaha.112.300782openalex-snapshot
Analysis of Stromal Cell Secretomes Reveals a Critical Role for Stromal Cell–Derived Hepatocyte Growth Factor and Fibronectin in Angiogenesis
inferred← citeshttps://doi.org/10.1167/iovs.63.6.21openalex-snapshot
Irisin Attenuates Pathological Neovascularization in Oxygen-Induced Retinopathy Mice
inferred← citeshttps://doi.org/10.1167/iovs.66.3.10openalex-snapshot
Fibronectin Mediates Endothelial-to-Mesenchymal Transition in Retina Angiogenesis
inferred← citeshttps://doi.org/10.1167/tvst.15.3.1openalex-snapshot
Mathematical Modeling of Human Retinal Vascular Pattern Around the Foveal Avascular Zone
inferred← citeshttps://doi.org/10.1172/jci.insight.177819openalex-snapshot
Endothelial TDP-43 controls sprouting angiogenesis and vascular barrier integrity, and its deletion triggers neuroinflammation
inferred← citeshttps://doi.org/10.1172/jci58832openalex-snapshot
Angiopoietin-2 differentially regulates angiogenesis through TIE2 and integrin signaling
inferred← citeshttps://doi.org/10.1172/jci67333openalex-snapshot
Developmental and tumoral vascularization is regulated by G protein–coupled receptor kinase 2
inferred← citeshttps://doi.org/10.1186/s12920-019-0596-2openalex-snapshot
Transcriptome analysis identified a novel 3-LncRNA regulatory network of transthyretin attenuating glucose induced hRECs dysfunction in diabetic retinopathy
inferred← citeshttps://doi.org/10.1210/en.2015-1799openalex-snapshot
Ghrelin Promotes Functional Angiogenesis in a Mouse Model of Critical Limb Ischemia Through Activation of Proangiogenic MicroRNAs
inferred← citeshttps://doi.org/10.1242/bio.059684openalex-snapshot
Tailless and hypoxia inducible factor-2α cooperate to sustain proangiogenic states of retinal astrocytes in neonatal mice
inferred← citeshttps://doi.org/10.1242/dev.069153openalex-snapshot
The astrocyte-expressed integrin αvβ8 governs blood vessel sprouting in the developing retina
inferred← citeshttps://doi.org/10.1242/dev.097949openalex-snapshot
Crim1 maintains retinal vascular stability during development by regulating endothelial cell Vegfa autocrine signaling
inferred← citeshttps://doi.org/10.1242/dev.125286openalex-snapshot
Neural crest cell-autonomous roles of fibronectin in cardiovascular development
inferred← citeshttps://doi.org/10.1242/dev.157511openalex-snapshot
Late neuroprogenitors contribute to normal retinal vascular development in a Hif2a-dependent manner
inferred← citeshttps://doi.org/10.1242/dev.200569openalex-snapshot
Chondroitin sulfate enhances the barrier function of basement membrane assembled by heparan sulfate
inferred← citeshttps://doi.org/10.1242/dev.201047openalex-snapshot
Microglia refine developing retinal astrocytic and vascular networks through the complement C3/C3aR axis
inferred← citeshttps://doi.org/10.1371/journal.pone.0046115openalex-snapshot
Overexpression of HTRA1 Leads to Down-Regulation of Fibronectin and Functional Changes in RF/6A Cells and HUVECs
inferred← citeshttps://doi.org/10.1371/journal.pone.0048001openalex-snapshot
A Functional Requirement for Astroglia in Promoting Blood Vessel Development in the Early Postnatal Brain
inferred← citeshttps://doi.org/10.1371/journal.pone.0084736openalex-snapshot
Hypoxia Inducible Factor-2α Regulates the Development of Retinal Astrocytic Network by Maintaining Adequate Supply of Astrocyte Progenitors
inferred← citeshttps://doi.org/10.1371/journal.pone.0116119openalex-snapshot
Angiogenesis in the Developing Spinal Cord: Blood Vessel Exclusion from Neural Progenitor Region Is Mediated by VEGF and Its Antagonists
inferred← citeshttps://doi.org/10.1371/journal.pone.0145210openalex-snapshot
Walking the Line: A Fibronectin Fiber-Guided Assay to Probe Early Steps of (Lymph)angiogenesis
inferred← citeshttps://doi.org/10.14800/rd.371openalex-snapshot
MiR-92a – a key player in cardiovascular remodeling
inferred← citeshttps://doi.org/10.15476/elte.2018.069openalex-snapshot
Collective features in the control of cell behavior
inferred← citeshttps://doi.org/10.1681/asn.2021020140openalex-snapshot
Integrin α5 Is Regulated by miR-218-5p in Endothelial Progenitor Cells
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4310491/v1openalex-snapshot
Modeling human retinal vascular pattern around foveal avascular zone.
inferred← citeshttps://doi.org/10.2174/1874357901307010041openalex-snapshot
Role of Filopodia in HSV-1 Entry into Zebrafish 3-O-Sulfotransferase-3-Expressing Cells
inferred← citeshttps://doi.org/10.22215/etd/2022-15194openalex-snapshot
Amphiregulin and Growth Differentiation Factor 11 Promote Retinal Ganglion Cell Survival In Vivo through Activation of Smad3
inferred← citeshttps://doi.org/10.3389/fcell.2018.00083openalex-snapshot
Using Zebrafish to Study Collective Cell Migration in Development and Disease
inferred← citeshttps://doi.org/10.3389/fcell.2023.1169962openalex-snapshot
Loss of TDP-43 causes ectopic endothelial sprouting and migration defects through increased fibronectin, vcam 1 and integrin α4/β1
inferred← citeshttps://doi.org/10.3389/fendo.2017.00350openalex-snapshot
Ghrelin, MicroRNAs, and Critical Limb Ischemia: Hungering for a Novel Treatment Option
inferred← citeshttps://doi.org/10.3389/fmed.2024.1393057openalex-snapshot
The mechanics of the retina: Müller glia role on retinal extracellular matrix and modelling
inferred← citeshttps://doi.org/10.3389/fnana.2022.995369openalex-snapshot
The heterogeneity of astrocytes in glaucoma
inferred← citeshttps://doi.org/10.3389/fonc.2020.00641openalex-snapshot
Shaping Up the Tumor Microenvironment With Cellular Fibronectin
inferred← citeshttps://doi.org/10.3390/cells9092055openalex-snapshot
Signalling, Metabolic Pathways and Iron Homeostasis in Endothelial Cells in Health, Atherosclerosis and Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/ijms20194759openalex-snapshot
Cellular Mechanisms of Angiogenesis in Neonatal Rat Models of Retinal Neurodegeneration
inferred← citeshttps://doi.org/10.3390/ijms23052646openalex-snapshot
Key Role of Astrocytes in Postnatal Brain and Retinal Angiogenesis
inferred← citeshttps://doi.org/10.3390/life12111761openalex-snapshot
Crosstalk between Blood Vessels and Glia during the Central Nervous System Development
inferred← citeshttps://doi.org/10.4161/cam.22862openalex-snapshot
The role of extracellular matrix in vascular branching morphogenesis
inferred← citeshttps://doi.org/10.4199/c00122ed1v01y201412ngl003openalex-snapshot
Retinal Glia
inferred← citeshttps://doi.org/10.70675/15295310zf24bz4fe3zb7d8z90acc0afe2a7openalex-snapshot
Control by CCM complex of the dialog between integrins and cadherins for the vascular stability
inferred← citeshttps://doi.org/10.70675/39dada9azb659z4d43z88d9z13c1fa14c3c7openalex-snapshot
Rôle du récepteur LRP-1 dans la croissance tumorale et l’angiogenèse associée dans un modèle de cancer mammaire triple négatif
inferred← citeshttps://doi.org/10.70675/52bcdc87z9aedz40abz9459z9019f91b56feopenalex-snapshot
Régulation dépendante du contexte de la morphogenèse et de l’intégrité capillaire par angiopoietin-like 4
inferred← citeshttps://doi.org/10.70675/8d2ee1a0z35c9z46e5z9d09z1453ed8a738dopenalex-snapshot
Développement d’un substitut cutané vascularisé au derme compartimenté : impact des microenvironnements papillaires et réticulaires
inferred← citeshttps://doi.org/10.7314/apjcp.2015.16.6.2561openalex-snapshot
Analysis of Molecular Pathways in Pancreatic Ductal Adenocarcinomas with a Bioinformatics Approach
inferred← citeshttps://doi.org/10.7507/1002-1892.202203028openalex-snapshot
[Effect of fibroblasts on promoting the sprout and migration of endothelial cells in three-dimensional pre-vascularized microstructures].
inferred← citeshttps://doi.org/10.7554/elife.96907openalex-snapshot
Dysfunction of Calcyphosine-Like gene impairs retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
inferred← citeshttps://doi.org/10.7554/elife.96907.1openalex-snapshot
Defective CAPSL function causes impaired retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
inferred← citeshttps://doi.org/10.7554/elife.96907.2openalex-snapshot
Defective CAPSL function causes impaired retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
inferred← citeshttps://doi.org/10.7554/elife.96907.2.sa0openalex-snapshot
Author response: Defective CAPSL function causes impaired retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
inferred← citeshttps://doi.org/10.7554/elife.96907.2.sa1openalex-snapshot
Reviewer #3 (Public Review): Defective CAPSL function causes impaired retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
inferred← citeshttps://doi.org/10.7554/elife.96907.2.sa2openalex-snapshot
Reviewer #2 (Public Review): Defective CAPSL function causes impaired retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
inferred← citeshttps://doi.org/10.7554/elife.96907.2.sa3openalex-snapshot
Reviewer #1 (Public Review): Defective CAPSL function causes impaired retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
inferred← citeshttps://doi.org/10.7554/elife.96907.2.sa4openalex-snapshot
eLife Assessment: Defective CAPSL function causes impaired retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
inferred← citeshttps://doi.org/10.7554/elife.96907.3openalex-snapshot
Dysfunction of Calcyphosine-Like gene impairs retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.