Angiogenesis

Papers
(The TQCC of Angiogenesis is 14. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-05-01 to 2025-05-01.)
ArticleCitations
Granzyme B degrades extracellular matrix and promotes inflammation and choroidal neovascularization200
Blood flow regulates acvrl1 transcription via ligand-dependent Alk1 activity138
Senescent endothelial cells: a potential target for diabetic retinopathy114
Inhibition of the prolyl isomerase Pin1 improves endothelial function and attenuates vascular remodelling in pulmonary hypertension by inhibiting TGF-β signalling75
Role of TGFβ1 and WNT6 in FGF2 and BMP4-driven endothelial differentiation of murine embryonic stem cells70
Copper stress impairs angiogenesis and lymphangiogenesis during zebrafish embryogenesis by down-regulating pERK1/2-foxm1-MMP2/9 axis and epigenetically regulating ccbe1 expression69
People with a connective tissue disorder may be especially vulnerable to the endothelial damage that characterizes long COVID due to the fragility of their vasculature and slow wound healing65
The endosomal RIN2/Rab5C machinery prevents VEGFR2 degradation to control gene expression and tip cell identity during angiogenesis56
The role of vasculature and angiogenesis in respiratory diseases54
The vascular gene Apold1 is dispensable for normal development but controls angiogenesis under pathological conditions51
Proinflammatory activity of VEGF-targeted treatment through reversal of tumor endothelial cell anergy43
Soluble FLT-1 in angiogenesis: pathophysiological roles and therapeutic implications38
Somatic BrafV600E mutation in the cerebral endothelium induces brain arteriovenous malformations37
PDGFD switches on stem cell endothelial commitment35
Letter in response to: circulating von Willebrand factor and high molecular weight multimers as markers of endothelial injury predict COVID-19 in-hospital mortality35
Alk1/Endoglin signaling restricts vein cell size increases in response to hemodynamic cues33
Successful management of lung adenocarcinoma with ALK/EGFR co-alterations and PD-L1 over-expression by bevacizumab combined with chemotherapy33
BMP10 functions independently from BMP9 for the development of a proper arteriovenous network32
Coalescent angiogenesis—evidence for a novel concept of vascular network maturation32
Notch regulates vascular collagen IV basement membrane through modulation of lysyl hydroxylase 3 trafficking30
In vivo dissection of Rhoa function in vascular development using zebrafish28
Nectins and Nectin-like molecules drive vascular development and barrier function26
Impact of heterozygous ALK1 mutations on the transcriptomic response to BMP9 and BMP10 in endothelial cells from hereditary hemorrhagic telangiectasia and pulmonary arterial hypertension donors26
FGF21 via mitochondrial lipid oxidation promotes physiological vascularization in a mouse model of Phase I ROP25
Persistent endothelial dysfunction in post-COVID-19 syndrome and its associations with symptom severity and chronic inflammation24
Multimodality imaging reveals angiogenic evolution in vivo during calvarial bone defect healing24
Endothelial cells require functional FLVCR1a during developmental and adult angiogenesis24
Endothelial cell plasticity at the single-cell level22
Correction: Celecoxib and octreotide synergistically ameliorate portal hypertension via inhibition of angiogenesis in cirrhotic rats21
Correction to: Phosphorylation of pericyte FAK‑Y861 affects tumour cell apoptosis and tumour blood vessel regression21
Pazopanib for severe bleeding and transfusion-dependent anemia in hereditary hemorrhagic telangiectasia20
Diminished vasculogenesis under inflammatory conditions is mediated by Activin A19
Persistent capillary rarefication in long COVID syndrome19
On coalescent angiogenesis and the remarkable flexibility of blood vessels18
KIT is dispensable for physiological organ vascularisation in the embryo18
Vascular mimicry in zebrafish fin regeneration: how macrophages build new blood vessels18
Correction to: Notch regulates vascular collagen IV basement membrane through modulation of lysyl hydroxylase 3 trafficking17
Blood vessels sense dermal stiffness via a novel mechanotransducer, APJ17
CCL4 contributes to aging related angiogenic insufficiency through activating oxidative stress and endothelial inflammation16
The rising impact of angiogenesis research16
Inhibition of Angiopoietin-2 rescues sporadic brain arteriovenous malformations by reducing pericyte loss16
Localized conditional induction of brain arteriovenous malformations in a mouse model of hereditary hemorrhagic telangiectasia16
Extracellular matrix stiffness controls VEGF165 secretion and neuroblastoma angiogenesis via the YAP/RUNX2/SRSF1 axis15
MicroRNA-375 repression of Kruppel-like factor 5 improves angiogenesis in diabetic critical limb ischemia14
Correction to: Depletion of Arg/Abl2 improves endothelial cell adhesion and prevents vascular leak during inflammation14
Capillary morphogenesis gene 2 (CMG2) mediates growth factor-induced angiogenesis by regulating endothelial cell chemotaxis14
Similarities and differences between brain and skin GNAQ p.R183Q driven capillary malformations14
Effect of oral nintedanib vs placebo on epistaxis in hereditary hemorrhagic telangiectasia: the EPICURE multicenter randomized double-blind trial14
Role of endothelial PDGFB in arterio-venous malformations pathogenesis14
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