Endothelial/Pericyte Interactions

Angiopoietin-2, a Natural Antagonist for Tie2 That Disrupts in vivo Angiogenesis

Maisonpierre, P. C., Suri, C., Jones, P. F., Bartunkova, S., Wiegand, S. J., Radziejewski, C., Compton, D., McClain, J., Aldrich, T. H., Papadopoulos, N., et al. (1997) · Science · doi:10.1126/science.277.5322.55 · Cited by 3,570

Requisite Role of Angiopoietin-1, a Ligand for the TIE2 Receptor, during Embryonic Angiogenesis

Suri, C., Jones, P. F., Patan, S., Bartunkova, S., Maisonpierre, P. C., Davis, S. H., Sato, T. N., & Yancopoulos, G. D. (1996) · Cell · doi:10.1016/s0092-8674(00)81813-9 · Cited by 2,872

Pericyte Loss and Microaneurysm Formation in PDGF-B-Deficient Mice

Lindahl, P., Johansson, B. R., Levéen, P., & Betsholtz, C. (1997) · Science · doi:10.1126/science.277.5323.242 · Cited by 2,226

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

Joutel, A., Corpechot, C., Ducros, A., Vahedi, K., Chabriat, H., Mouton, P., Alamowitch, S., Domenga, V., Cécillion, M., Maréchal, E., et al. (1996) · Nature · doi:10.1038/383707a0 · Cited by 2,068

Isolation of Angiopoietin-1, a Ligand for the TIE2 Receptor, by Secretion-Trap Expression Cloning

Davis, S., Aldrich, T. H., Jones, P. F., Acheson, A., Compton, D. L., Jain, V., Ryan, T. E., Bruno, J., Radziejewski, C., Maisonpierre, P. C., et al. (1996) · Cell · doi:10.1016/s0092-8674(00)81812-7 · Cited by 1,989

Distinct roles of the receptor tyrosine kinases Tie-1 and Tie-2 in blood vessel formation

Sato, T. N., Tozawa, Y., Deutsch, U., Wolburg‐Buchholz, K., Fujiwara, Y., Gendron‐Maguire, M., Gridley, T., Wolburg, H., Risau, W., & Qin, Y. (1995) · Nature · doi:10.1038/376070a0 · Cited by 1,821

Role of PDGF-B and PDGFR-β in recruitment of vascular smooth muscle cells and pericytes during embryonic blood vessel formation in the mouse

Hellström, M., Kalén, M., Lindahl, P., Abramsson, A., & Betsholtz, C. (1999) · Development · doi:10.1242/dev.126.14.3047 · Cited by 1,734

Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

McAllister, K. A., Grogg, K. M., Johnson, D. W., Gallione, C. J., Baldwin, M. A., Jackson, C. E., Helmbold, E. A., Markel, D. S., McKinnon, W. C., Murrel, J., et al. (1994) · Nature Genetics · doi:10.1038/ng1294-345 · Cited by 1,475

Benefits of targeting both pericytes and endothelial cells in the tumor vasculature with kinase inhibitors

Bergers, G., Song, S., Meyer-Morse, N., Bergsland, E. K., & Hanahan, D. (2003) · Journal of Clinical Investigation · doi:10.1172/jci17929 · Cited by 1,361

Leakage-Resistant Blood Vessels in Mice Transgenically Overexpressing Angiopoietin-1

Thurston, G., Suri, C., Smith, K., McClain, J., Sato, T. T., Yancopoulos, G. D., & McDonald, D. M. (1999) · Science · doi:10.1126/science.286.5449.2511 · Cited by 1,350

Molecular Mechanisms of Resistance to Tumour Anti-Angiogenic Strategies

Grépin, R., & Pagès, G. (2010) · Journal of Oncology · doi:10.1155/2010/835680 · Cited by 76

The impact of Fli1 deficiency on the pathogenesis of systemic sclerosis

Asano, Y., Bujor, A. M., & Trojanowska, M. (2010) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2010.06.008 · Cited by 78

Cerebral Cavernous Malformation-1 Protein Controls DLL4-Notch3 Signaling Between the Endothelium and Pericytes

Schulz, G. B., Wieland, E., Wüstehube‐Lausch, J., Boulday, G., Moll, I., Tournier‐Lasserve, E., & Fischer, A. (2015) · Stroke · doi:10.1161/strokeaha.114.007512 · Cited by 74

Correlating Global Gene Regulation to Angiogenesis in the Developing Chick Extra-Embryonic Vascular System

Javerzat, S., Franco, M., Herbert, J. M. J., Platonova, N., Peille, A.-L., Pantesco, V., Vos, J. D., Assou, S., Bicknell, R., Bikfalvi, A., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007856 · Cited by 80

Hypoxia-Inducible Factor-1 Target Genes as Indicators of Tumor Vessel Response to Vascular Endothelial Growth Factor Inhibition

Dang, D. T., Chun, S. Y., Burkitt, K., Abe, M., Chen, S., Havre, P. A., Mabjeesh, N. J., Heath, E. I., Vogelzang, N. J., Cruz-Correa, M. R., et al. (2008) · Cancer Research · doi:10.1158/0008-5472.can-07-1589 · Cited by 75

Reduced pericyte and tight junction coverage in old diabetic rats are associated with hyperglycemia-induced cerebrovascular pericyte dysfunction

Liu, Y., Zhang, H., Wang, S., Guo, Y., Fang, X., Zheng, B., Gao, W., Yu, H., Chen, Z., Roman, R. J., et al. (2020) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00726.2020 · Cited by 73

Single-cell dual-omics reveals the transcriptomic and epigenomic diversity of cardiac non-myocytes

Wang, L., Yang, Y., Ma, H., Xie, Y., Xu, J., Near, D., Wang, H., Garbutt, T. A., Li, Y., Liu, J., et al. (2021) · Cardiovascular Research · doi:10.1093/cvr/cvab134 · Cited by 73

Disease-Related Growth Factor and Embryonic Signaling Pathways Modulate an Enhancer of TCF21 Expression at the 6q23.2 Coronary Heart Disease Locus

Miller, C. L., Anderson, D. R., Kundu, R. K., Raiesdana, A., Nürnberg, S., Caceres, R. D., Cheng, K. W., Leeper, N. J., Chen, C., Chang, I., et al. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003652 · Cited by 71

Sonic Hedgehog-activated engineered blood vessels enhance bone tissue formation

Rivron, N. C., Raiss, C. C., Liu, J., Nandakumar, A., Sticht, C., Gretz, N., Truckenmüller, R. K., Rouwkema, J., & van Blitterswijk, C. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1117627109 · Cited by 74

Tissue Engineering the Vascular Tree

Traoré, M. A., & George, S. C. (2017) · Tissue Engineering Part B Reviews · doi:10.1089/ten.teb.2017.0010 · Cited by 80

Gene Therapy Intervention in Neovascular Eye Disease: A Recent Update

Lin, F.-L., Wang, P.-Y., Chuang, Y.-F., Wang, J.-H., Wong, V. H. Y., Bui, B. V., & Liu, G.-S. (2020) · Molecular Therapy · doi:10.1016/j.ymthe.2020.06.029 · Cited by 74

Retinal ischemia induces α-SMA-mediated capillary pericyte contraction coincident with perivascular glycogen depletion

Alarcón-Martínez, L., Yilmaz-Ozcan, S., Yemişçi, M., Schallek, J. B., Kılıç, K., Villafranca‐Baughman, D., Can, A., Polo, A. D., & Dalkara, T. (2019) · Acta Neuropathologica Communications · doi:10.1186/s40478-019-0761-z · Cited by 75

Dynamic Interplay between Pericytes and Endothelial Cells during Sprouting Angiogenesis

Chiaverina, G., di Blasio, L., Monica, V., Accardo, M., Palmiero, M., Peracino, B., Vara-Messler, M., Puliafito, A., & Primo, L. (2019) · Cells · doi:10.3390/cells8091109 · Cited by 71

Oxidative Stress and Microvessel Barrier Dysfunction

He, P., Talukder, M. A. H., & Gao, F. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00472 · Cited by 79

ERK1/2 inhibition reduces vascular calcification by activating miR-126-3p-DKK1/LRP6 pathway

Zeng, P., Yang, J. A., Liu, L., Yang, X., Yao, Z., Ma, C., Zhu, H., Su, J., Zhao, Q., Feng, K., et al. (2020) · Theranostics · doi:10.7150/thno.49771 · Cited by 76

Emerging Role of Pericytes and Their Secretome in the Heart

Su, H., Cantrell, A. C., Zeng, H., Zhu, S., & Chen, J. (2021) · Cells · doi:10.3390/cells10030548 · Cited by 77

Nox4 Is a Major Source of Superoxide Production in Human Brain Pericytes

Kuroda, J., Ago, T., Nishimura, A., Nakamura, K., Matsuo, R., Wakisaka, Y., Kamouchi, M., & Kitazono, T. (2014) · Journal of Vascular Research · doi:10.1159/000369930 · Cited by 73

Hypertension and Dementia: Epidemiological and Experimental Evidence Revealing a Detrimental Relationship

Perrotta, M., Lembo, G., & Carnevale, D. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17030347 · Cited by 79

Genetic Analysis of Rare Human Variants of Regulators of G Protein Signaling Proteins and Their Role in Human Physiology and Disease

Squires, K. E., Montañez‐Miranda, C., Pandya, R. R., Torres, M. P., & Hepler, J. R. (2018) · Pharmacological Reviews · doi:10.1124/pr.117.015354 · Cited by 72

Contribution of Blood Vessel Activation, Remodeling and Barrier Function to Inflammatory Bowel Diseases

Britzen‐Laurent, N., Weidinger, C., & Stürzl, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065517 · Cited by 77

Mesenchymal stem cells regulate melanoma cancer cells extravasation to bone and liver at their perivascular niche

Correa, D., Somoza, R. A., Lin, P. Y., Schiemann, W. P., & Caplan, A. I. (2015) · International Journal of Cancer · doi:10.1002/ijc.29709 · Cited by 72

Human Blood-Vessel-Derived Stem Cells for Tissue Repair and Regeneration

Chen, C.-W., Corselli, M., Péault, B., & Huard, J. (2012) · BioMed Research International · doi:10.1155/2012/597439 · Cited by 72

Novel insights into pericyte–myofibroblast transition and therapeutic targets in renal fibrosis

Chang, F., Chou, Y., Chen, Y., & Lin, S. (2012) · Journal of the Formosan Medical Association · doi:10.1016/j.jfma.2012.09.008 · Cited by 72

Therapeutic angiogenesis in patients with severe limb ischemia by transplantation of a combination stem cell product

Lasala, G. P., Silva, J. A., & Minguell, J. J. (2011) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/j.jtcvs.2011.08.053 · Cited by 72

The immunosuppressant FTY720 inhibits tumor angiogenesis via the sphingosine 1‐phosphate receptor 1

Schmid, G., Guba, M. O., Ischenko, I., Papyan, A., Joka, M., Schrepfer, S., Bruns, C. J., Jauch, K., Heeschen, C., & Graeb, C. (2007) · Journal of Cellular Biochemistry · doi:10.1002/jcb.21181 · Cited by 74

Exosomal circEhmt1 Released from Hypoxia‐Pretreated Pericytes Regulates High Glucose‐Induced Microvascular Dysfunction via the NFIA/NLRP3 Pathway

Ye, L., Guo, H., Wang, Y., Peng, Y., Zhang, Y., Li, S., Yang, M., & Wang, L. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/8833098 · Cited by 71

Heterogeneous fibroblasts contribute to fibrotic scar formation after spinal cord injury in mice and monkeys

Xue, X., Wu, X., Fan, Y., Han, S., Zhang, H., Sun, Y., Yin, Y., Yin, M., Chen, B., Sun, Z., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-50564-x · Cited by 78

Anthrax toxin receptor 2 is expressed in murine and tumor vasculature and functions in endothelial proliferation and morphogenesis

Reeves, C., Dufraine, J., Young, J. A. T., & Kitajewski, J. (2009) · Oncogene · doi:10.1038/onc.2009.383 · Cited by 71

Bone regulatory factors NFATc1 and Osterix in human calcific aortic valves

Alexopoulos, A., Bravou, V., Peroukides, S., Kaklamanis, L., Varakis, J. N., Alexopoulos, D., & Papadaki, H. H. (2008) · International Journal of Cardiology · doi:10.1016/j.ijcard.2008.10.014 · Cited by 75

In vitro discrimination of the role of LRP1 at the BBB cellular level: Focus on brain capillary endothelial cells and brain pericytes

Candela, P., Saint‐Pol, J., Kuntz, M., Boucau, M., Lamartinière, Y., Gosselet, F., & Fénart, L. (2014) · Brain Research · doi:10.1016/j.brainres.2014.10.047 · Cited by 78

Regulation of Mesenchymal Stem Cell Activity by Endothelial Cells

Saleh, F., Whyte, M., Ashton, P. D., & Genever, P. G. (2010) · Stem Cells and Development · doi:10.1089/scd.2010.0168 · Cited by 71

Age-related changes in brain support cells: Implications for stroke severity

Sohrabji, F., Bake, S., & Lewis, D. K. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.06.013 · Cited by 74

The Cochlear Pericytes

Shi, X., HAN, W., Yamamoto, H., Tang, W., Lin, X., Xiu, R., Trune, D. R., & Nuttall, A. L. (2008) · Microcirculation · doi:10.1080/10739680802047445 · Cited by 71

The restorative role of annexin A1 at the blood–brain barrier

McArthur, S., Loiola, R. A., Maggioli, E., Errede, M., Virgintino, D., & Solito, E. (2016) · Fluids and Barriers of the CNS · doi:10.1186/s12987-016-0043-0 · Cited by 73

Identification of a common mesenchymal stromal progenitor for the adult haematopoietic niche

Hu, X., García, M., Weng, L., Jung, X., Murakami, J. L., Kumar, B., Warden, C., Todorov, I., & Chen, C. (2016) · Nature Communications · doi:10.1038/ncomms13095 · Cited by 71

Temporal and Spatial Effects of Blast Overpressure on Blood-Brain Barrier Permeability in Traumatic Brain Injury

Kuriakose, M., Rao, K. V. R., Younger, D., & Chandra, N. (2018) · Scientific Reports · doi:10.1038/s41598-018-26813-7 · Cited by 73

Retinoic Acid: A Key Regulator of Lung Development

Fernandes-Silva, H., Araújo-Silva, H., Correia‐Pinto, J., & Moura, R. S. (2020) · Biomolecules · doi:10.3390/biom10010152 · Cited by 71

Molecular Regulation of Sprouting Angiogenesis

Duran, C. L., Howell, D. W., Dave, J. M., Smith, R. L., Torrie, M. E., Essner, J. J., & Bayless, K. J. (2017) · Comprehensive physiology · doi:10.1002/cphy.c160048 · Cited by 80

Platelet-derived growth factor-BB has neurorestorative effects and modulates the pericyte response in a partial 6-hydroxydopamine lesion mouse model of Parkinson's disease

Padel, T., Özen, I., Boix, J., Barbariga, M., Gaceb, A., Roth, M., & Paul, G. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.06.002 · Cited by 70

Transendothelial Migration Enables Subsequent Transmigration of Neutrophils through Underlying Pericytes

Ayres-Sander, C. E., Lauridsen, H. M., Maier, C. L., Sava, P., Pober, J. S., & Gonzalez, A. L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060025 · Cited by 72

Endosialin-Expressing Pericytes Promote Metastatic Dissemination

Viski, C., König, C., Kijewska, M., Mogler, C., Isacke, C. M., & Augustin, H. G. (2016) · Cancer Research · doi:10.1158/0008-5472.can-16-0932 · Cited by 72

Angiogenic biomaterials to promote therapeutic regeneration and investigate disease progression

Ngo, M. T., & Harley, B. A. C. (2020) · Biomaterials · doi:10.1016/j.biomaterials.2020.120207 · Cited by 72

Identification of a subset of pericytes that respond to combination therapy targeting PDGF and VEGF signaling

Hasumi, Y., Kłosowska‐Wardęga, A., Furuhashi, M., Östman, A., Heldin, C., & Hellberg, C. B. (2007) · International Journal of Cancer · doi:10.1002/ijc.22999 · Cited by 71

Pericyte actomyosin-mediated contraction at the cell–material interface can modulate the microvascular niche

Lee, S., Zeiger, A. S., Maloney, J. M., Kotecki, M., Vliet, K. J. V., & Herman, I. M. (2010) · Journal of Physics Condensed Matter · doi:10.1088/0953-8984/22/19/194115 · Cited by 71

Topical administration of a multi‐targeted kinase inhibitor suppresses choroidal neovascularization and retinal edema

Doukas, J., Mahesh, S. P., Umeda, N., Kachi, S., Akiyama, H., Yokoi, K., Cao, J., Chen, Z., Dellamary, L. A., Tam, B. Y. Y., et al. (2008) · Journal of Cellular Physiology · doi:10.1002/jcp.21426 · Cited by 70

Functions of lipid raft membrane microdomains at the blood–brain barrier

Dodelet-Devillers, A., Cayrol, R., van Horssen, J., Haqqani, A. S., de Vries, H. E., Engelhardt, B., Greenwood, J., & Prat, A. (2009) · Journal of Molecular Medicine · doi:10.1007/s00109-009-0488-6 · Cited by 71

Emerging therapeutic targets in metastatic progression: A focus on breast cancer

Li, Z., & Kang, Y. (2016) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2016.03.003 · Cited by 71

Pericyte Regulation of Vascular Remodeling Through the CXC Receptor 3

Bodnar, R. J., Rodgers, M. E., Chen, W. C. W., & Wells, A. H. (2013) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.113.302012 · Cited by 69

Hepatic stellate cells display a functional vascular smooth muscle cell phenotype in a three-dimensional co-culture model with endothelial cells

Wirz, W., Antoine, M., Tag, C. G., Gressner, A. M., Korff, T., Hellerbrand, C., & Kiefer, P. (2008) · Differentiation · doi:10.1111/j.1432-0436.2007.00260.x · Cited by 73

Critical Role of Tissue Kallikrein in Vessel Formation and Maturation

Stone, O. A., Richer, C., Emanueli, C., van Weel, V., Quax, P. H. A., Katare, R., Kränkel, N., Campagnolo, P., Barcelos, L. S., Siragusa, M., et al. (2009) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.108.182139 · Cited by 69

Mesenchymal stem cells induce endothelial cell quiescence and promote capillary formation

Pedersen, T. Ø., Blois, A. L., Xue, Y., Xing, Z., Sun, Y., Finne‐Wistrand, A., Lorens, J. B., Fristad, I., Leknes, K. N., & Mustafa, K. (2014) · Stem Cell Research & Therapy · doi:10.1186/scrt412 · Cited by 69

Adipose-derived stem cells increase angiogenesis through matrix metalloproteinase-dependent collagen remodeling

Song, Y. H., Shon, S. H., Shan, M., Stroock, A. D., & Fischbach, C. (2016) · Integrative Biology · doi:10.1039/c5ib00277j · Cited by 69

Rapid generation of functional vascular organoids via simultaneous transcription factor activation of endothelial and mural lineages

Gong, L., Zhang, Y., Zhu, Y., Lee, U., Luo, A. C., Li, X., Wang, X., Chen, D., Pu, W. T., Lin, R., et al. (2025) · Cell stem cell · doi:10.1016/j.stem.2025.05.014 · Cited by 73

Microvascular endowment in the developing chicken embryo lung

Makanya, A. N., Hlushchuk, R., Baum, O., Velinov, N., Ochs, M., & Djonov, V. (2007) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00371.2006 · Cited by 67

Células-tronco mesenquimais

Monteiro, B. S., Neto, N. M. A., & Carlo, R. J. D. (2010) · Ciência Rural · doi:10.1590/s0103-84782010000100040 · Cited by 68

Endoglin plays distinct roles in vascular smooth muscle cell recruitment and regulation of arteriovenous identity during angiogenesis

Mancini, M., Terzic, A., Conley, B. A., Oxburgh, L. H., Nicola, T., & Vary, C. (2009) · Developmental Dynamics · doi:10.1002/dvdy.22066 · Cited by 69

Angiocrine endothelium: from physiology to cancer

Pasquier, J., Ghiabi, P., Chouchane, L., Razzouk, K., Rafii, S., & Rafii, A. (2020) · Journal of Translational Medicine · doi:10.1186/s12967-020-02244-9 · Cited by 68

The Role of Vascular Cells in Pancreatic Beta-Cell Function

Burganova, G., Bridges, C. A., Thorn, P., & Landsman, L. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.667170 · Cited by 70

Pulmonary vascular development goes awry in congenital lung abnormalities

Kool, H. M., Mous, D. S., Tibboel, D., de Klein, A., & Rottier, R. J. (2014) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.21085 · Cited by 69

Vascular development and hemodynamic force in the mouse yolk sac

Garcia, M. D., & Larina, I. V. (2014) · Frontiers in Physiology · doi:10.3389/fphys.2014.00308 · Cited by 68

Redistribution of PDGFRβ cells and NG2DsRed pericytes at the cerebrovasculature after status epilepticus

Milesi, S., Boussadia, B., Plaud, C., Catteau, M., Rousset, M.-C., de Bock, F., Schaeffer, M., Lerner‐Natoli, M., Rigau, V., & Marchi, N. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.07.010 · Cited by 67

Scleroderma Mesenchymal Stem Cells display a different phenotype from healthy controls; implications for regenerative medicine

Cipriani, P., Marrelli, A., Benedetto, P. D., Liakouli, V., Carubbi, F., Ruscitti, P., Alvaro, S., Pantano, I., Campese, A. F., Grazioli, P., et al. (2013) · Angiogenesis · doi:10.1007/s10456-013-9338-9 · Cited by 67

Cerebral ischemia/repefusion injury: From bench space to bedside

Nagy, Z., & Nardai, S. (2017) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.06.011 · Cited by 64

The pericyte microenvironment during vascular development

Payne, L. B., Zhao, H., James, C. C., Darden, J. A., McGuire, D. R., Taylor, S., Smyth, J. W., & Chappell, J. C. (2019) · Microcirculation · doi:10.1111/micc.12554 · Cited by 69

Role of Notch in endothelial biology

Fernández-Chacón, M., García-Gónzalez, I., Mühleder, S., & Benedito, R. (2021) · Angiogenesis · doi:10.1007/s10456-021-09793-7 · Cited by 67

Immunohistochemical analysis of TGF-β1 and VEGF in gingival and periodontal tissues: A role of these biomarkers in the pathogenesis of scleroderma and periodontal disease

Matarese, G., Isola, G., Anastasi, G., Favaloro, A., Milardi, D., Vermiglio, G., Vita, G., Cordasco, G., & Cutroneo, G. (2012) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2012.1024 · Cited by 66

Bone marrow Derived Pluripotent Cells are Pericytes which Contribute to Vascularization

Cai, X., Lin, Y., Friedrich, C. C., Neville, C. M., Pomerantseva, I., Sundback, C. A., Sharma, P., Zhang, Z., Vacanti, J. P., Hauschka, P. V., et al. (2009) · Stem Cell Reviews and Reports · doi:10.1007/s12015-009-9097-6 · Cited by 66

Recent developments on immunotherapy for brain cancer

Wainwright, D. A., Nigam, P., Thaçi, B., Dey, M., & Lesniak, M. S. (2012) · Expert Opinion on Emerging Drugs · doi:10.1517/14728214.2012.679929 · Cited by 66

Cellular Kinetics of Perivascular MSC Precursors

Chen, W. C. W., Park, T. S., Murray, I. R., Zimmerlin, L., Lazzari, L., Huard, J., & Péault, B. (2013) · Stem Cells International · doi:10.1155/2013/983059 · Cited by 68

Sodium glucose cotransporter 2 in mesangial cells and retinal pericytes and its implications for diabetic nephropathy and retinopathy

Wakisaka, M., & Nagao, T. (2017) · Glycobiology · doi:10.1093/glycob/cwx047 · Cited by 66

Engineering stem cell cardiac patch with microvascular features representative of native myocardium

Qian, Z., Sharma, D., Jia, W., Radke, D., Kamp, T. J., & Zhao, F. (2019) · Theranostics · doi:10.7150/thno.29552 · Cited by 64

High glucose‐induced changes in hyaloid‐retinal vessels during early ocular development of zebrafish: a short‐term animal model of diabetic retinopathy

Jung, S., Kim, Y. S., Lee, Y., & Kim, J. S. (2015) · British Journal of Pharmacology · doi:10.1111/bph.13279 · Cited by 67

M2 microglia-derived exosomes promote vascular remodeling in diabetic retinopathy

Wang, X., Xu, C., Bian, C., Ge, P., Lei, J., Wang, J., Xiao, T., Fan, Y., Gu, Q., Li, H., et al. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02330-w · Cited by 68

Vascular Development

Chappell, J. C., & Bautch, V. L. (2010) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(10)90002-1 · Cited by 65

Hypoxia upregulates expression of human endosialin gene via hypoxia-inducible factor 2

Ohradanova‐Repic, A., Gradin, K., Baráthová, M., Zaťovičová, M., Holotnakova, T., Kopáček, J., Parkkila, S., Poellinger, L., Pastoreková, S., & Pastorek, J. (2008) · British Journal of Cancer · doi:10.1038/sj.bjc.6604685 · Cited by 65

Impaired tumor angiogenesis and VEGF-induced pathway in endothelial CD146 knockout mice

Zeng, Q., Wu, Z., Duan, H., Jiang, X., Tu, T., Lü, D., Luo, Y., Wang, P., Song, L., Feng, J., et al. (2014) · Protein & Cell · doi:10.1007/s13238-014-0047-y · Cited by 65

Microfabricated Porous Silk Scaffolds for Vascularizing Engineered Tissues

Wray, L. S., Tsioris, K., Gil, E. S., Omenetto, F. G., & Kaplan, D. L. (2013) · Advanced Functional Materials · doi:10.1002/adfm.201202926 · Cited by 65

Non-reconstructable peripheral vascular disease of the lower extremity in ten patients treated with adipose-derived stromal vascular fraction cells

Carstens, M. H., Gómez, A., Cortés, R., Turner, E., Pérez, C., Ocon, M., & Correa, D. (2016) · Stem Cell Research · doi:10.1016/j.scr.2016.12.001 · Cited by 65

NAD-Biosynthetic and Consuming Enzymes as Central Players of Metabolic Regulation of Innate and Adaptive Immune Responses in Cancer

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