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

Generation of complex human organoid models including vascular networks by incorporation of mesodermal progenitor cells

Wörsdörfer, P., Dalda, N., Kern, A., Krüger, S., Wagner, N., Kwok, C. K., Henke, E., & Ergün, S. (2019) · Scientific Reports · doi:10.1038/s41598-019-52204-7 · Cited by 280

Heparan Sulfate in trans Potentiates VEGFR-Mediated Angiogenesis

Jakobsson, L., Kreuger, J., Holmborn, K., Lundin, L., Eriksson, I., Kjellén, L., & Claesson, L. (2006) · Developmental Cell · doi:10.1016/j.devcel.2006.03.009 · Cited by 282

Cellular and molecular pathways of renal repair after acute kidney injury

Kumar, S. (2018) · Kidney International · doi:10.1016/j.kint.2017.07.030 · Cited by 271

Fibronectins in vascular morphogenesis

Astrof, S., & Hynes, R. O. (2009) · Angiogenesis · doi:10.1007/s10456-009-9136-6 · Cited by 280

Antagomir‐mediated silencing of endothelial cell specific microRNA‐126 impairs ischemia‐induced angiogenesis

Solingen, C. V., Seghers, L., Bijkerk, R., Duijs, J. M. G. J., Roeten, M. K., van Oeveren‐Rietdijk, A. M., Baelde, H. J., Monge, M., Vos, J. B., de Boer, H. C., et al. (2008) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2008.00613.x · Cited by 267

The Adventitia

Majesky, M. W., Dong, X. R., Hoglund, V. J., Mahoney, W. M., & Daum, G. (2011) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.110.221549 · Cited by 279

Targeting Endothelium-Pericyte Cross Talk by Inhibiting VEGF Receptor Signaling Attenuates Kidney Microvascular Rarefaction and Fibrosis

Lin, S., Chang, F., Schrimpf, C., Chen, Y., Wu, C.-F., Wu, V., Chiang, W., Kuhnert, F., Kuo, C. J., Chen, Y., et al. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2010.10.012 · Cited by 266

Spatial and temporal role of the apelin/APJ system in the caliber size regulation of blood vessels during angiogenesis

Kidoya, H., Ueno, M., Yamada, Y., Mochizuki, N., Nakata, M., Yano, T., Fujii, R., & Takakura, N. (2008) · The EMBO Journal · doi:10.1038/sj.emboj.7601982 · Cited by 270

The Effect of Matrix Density on the Regulation of 3-D Capillary Morphogenesis

Ghajar, C. M., Chen, X., Harris, J. W., Suresh, V., Hughes, C. C. W., Jeon, N. L., Putnam, A. J., & George, S. C. (2007) · Biophysical Journal · doi:10.1529/biophysj.107.120774 · Cited by 263

Vascular Cell Senescence Contributes to Blood–Brain Barrier Breakdown

Yamazaki, Y., Baker, D. J., Tachibana, M., Liu, C.-C., van Deursen, J. M., Brott, T. G., Bu, G., & Kanekiyo, T. (2016) · Stroke · doi:10.1161/strokeaha.115.010835 · Cited by 263

Platelets, Petechiae, and Preservation of the Vascular Wall

Nachman, R. L., & Rafii, S. (2008) · New England Journal of Medicine · doi:10.1056/nejmra0800887 · Cited by 278

Biology of Vascular Malformations of the Brain

Leblanc, G. G., Golanov, E. V., Awad, I. A., Young, W. L., & Collaborators, B. O. V. M. O. T. B. N. W. (2009) · Stroke · doi:10.1161/strokeaha.109.563692 · Cited by 263

Antiangiogenic treatment with Sunitinib ameliorates inflammatory infiltrate, fibrosis, and portal pressure in cirrhotic rats

Tugues, S., Fernández‐Varo, G., Muñoz, J., Ros, J., Arroyo, V., Rodés, J., Friedman, S. L., Carmeliet, P., Jiménez, W., & Morales‐Ruiz, M. (2007) · Hepatology · doi:10.1002/hep.21921 · Cited by 263

Neuronal and vascular interactions

Andreone, B. J., Lacoste, B., & Gu, C. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-033835 · Cited by 256

Endothelial Smad4 Maintains Cerebrovascular Integrity by Activating N-Cadherin through Cooperation with Notch

Li, F., Lan, Y., Wang, Y., Wang, J., Yang, G., Meng, F., Han, H., Meng, A., Wang, Y., & Yang, X. Y. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.01.011 · Cited by 268

Regulation of Angiogenesis by Eph–Ephrin Interactions

Kuijper, S. J. M., Turner, C. J., & Adams, R. H. (2007) · Trends in Cardiovascular Medicine · doi:10.1016/j.tcm.2007.03.003 · Cited by 258

Targeting pericyte–endothelial cell crosstalk by circular RNA-cPWWP2A inhibition aggravates diabetes-induced microvascular dysfunction

Liu, C., Ge, H., Liu, B.-H., Dong, R., Shan, K. Y., Chen, X., Yao, M.-D., Li, X., Yao, J., Zhou, R., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1814874116 · Cited by 260

Laminin isoforms in endothelial and perivascular basement membranes

Yousif, L. F., Russo, J. D., & Sorokin, L. M. (2013) · Cell Adhesion & Migration · doi:10.4161/cam.22680 · Cited by 262

Bone and the hematopoietic niche: a tale of two stem cells

Bianco, P. (2011) · Blood · doi:10.1182/blood-2011-01-315069 · Cited by 259

Pericyte-endothelial crosstalk: implications and opportunities for advanced cellular therapies

Geevarghese, A., & Herman, I. M. (2014) · Translational research · doi:10.1016/j.trsl.2014.01.011 · Cited by 258

Interleukin-6 Stimulates Defective Angiogenesis

Gopinathan, G., Milagre, C., Pearce, O. M. T., Reynolds, L. E., Hodivala-Dilke, K., Leinster, D. A., Zhong, H., Hollingsworth, R. E., Thompson, R., Whiteford, J. R., et al. (2015) · Cancer Research · doi:10.1158/0008-5472.can-15-1227 · Cited by 249

CNS pericytes: Concepts, misconceptions, and a way out

Krueger, M. W., & Bechmann, I. (2009) · Glia · doi:10.1002/glia.20898 · Cited by 257

Transforming Growth Factor β-1 Stimulates Profibrotic Epithelial Signaling to Activate Pericyte-Myofibroblast Transition in Obstructive Kidney Fibrosis

Wu, C.-F., Chiang, W., Lai, C., Chang, F., Chen, Y., Chou, Y., Wu, T.-H., Linn, G. R., Ling, H., Wu, K., et al. (2012) · American Journal Of Pathology · doi:10.1016/j.ajpath.2012.09.009 · Cited by 247

Pericyte Migration

Pfister, F., Feng, Y., Hagen, F. V., Hoffmann, S., Molema, G., Hillebrands, J., Shani, M., Deutsch, U., & Hammes, H. (2008) · Diabetes · doi:10.2337/db08-0325 · Cited by 245

Brain and Retinal Pericytes: Origin, Function and Role

Trost, A., Lange, S., Schroedl, F., Bruckner, D., Motloch, K. A., Bogner, B., Kaser-Eichberger, A., Strohmaier, C., Runge, C., Aigner, L., et al. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00020 · Cited by 244

Control of Perfusable Microvascular Network Morphology Using a Multiculture Microfluidic System

Whisler, J. A., Chen, M. B., & Kamm, R. D. (2012) · Tissue Engineering Part C Methods · doi:10.1089/ten.tec.2013.0370 · Cited by 240

Regulation of Placental Angiogenesis

Chen, D., & Zheng, J. J. (2013) · Microcirculation · doi:10.1111/micc.12093 · Cited by 256

Endothelial–mesenchymal transition and its contribution to the emergence of stem cell phenotype

Medici, D., & Kalluri, R. (2012) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2012.04.004 · Cited by 250

Dynamic Remodeling of Pericytes In Vivo Maintains Capillary Coverage in the Adult Mouse Brain

Berthiaume, A.-A., Grant, R. I., McDowell, K. P., Underly, R. G., Hartmann, D. A., Levy, M., Bhat, N. R., & Shih, A. Y. (2018) · Cell Reports · doi:10.1016/j.celrep.2017.12.016 · Cited by 223

Brain Microvascular Pericytes in Vascular Cognitive Impairment and Dementia

Uemura, M. T., Maki, T., Ihara, M., Lee, V. M. ‐., & Trojanowski, J. Q. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.00080 · Cited by 246

Sinusoidal remodeling and angiogenesis: A new function for the liver-specific pericyte?

Lee, J. S., Semela, D., Iredale, J. P., & Shah, V. H. (2007) · Hepatology · doi:10.1002/hep.21564 · Cited by 236

Chapter 4 An Optimized Three‐Dimensional In Vitro Model for the Analysis of Angiogenesis

Nakatsu, M. N., & Hughes, C. C. W. (2008) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(08)02004-1 · Cited by 242

Endothelial influences on cerebrovascular tone

Andresen, J., Shafi, N. I., & Bryan, R. M. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00937.2005 · Cited by 235

Bone marrow-derived mesenchymal stem cells promote growth and angiogenesis of breast and prostate tumors

Zhang, T., Lee, W., Rui, Y., Cheng, T.-Y., Jiang, X., & Li, G. (2013) · Stem Cell Research & Therapy · doi:10.1186/scrt221 · Cited by 244

Human Pericytes for Ischemic Heart Repair

Chen, C.-W., Okada, M., Proto, J. D., Gao, X., Sekiya, N., Beckman, S., Corselli, M., Crisan, M., Saparov, A., Tobita, K., et al. (2012) · Stem Cells · doi:10.1002/stem.1285 · Cited by 241

Generation of 3D functional microvascular networks with human mesenchymal stem cells in microfluidic systems

Jeon, J. S., Bersini, S., Whisler, J. A., Chen, M. B., Dubini, G., Charest, J. L., Moretti, M., & Kamm, R. D. (2014) · Integrative Biology · doi:10.1039/c3ib40267c · Cited by 229

Pericytes, an overlooked player in vascular pathobiology

Ferland-McCollough, D., Slater, S. C., Richard, J. S., Reni, C., & Mangialardi, G. (2016) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2016.11.008 · Cited by 238

Pericyte-Endothelial Interactions in the Retinal Microvasculature

Hu, H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21197413 · Cited by 230

Impairment of pericyte-endothelium crosstalk leads to blood-brain barrier dysfunction following traumatic brain injury

Bhowmick, S., D’Mello, V., Caruso, D., Wallerstein, A., & Muneer, P. M. A. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.03.014 · Cited by 231

Diabetic kidney diseases revisited: A new perspective for a new era

Fu, H., Liu, S., Bastacky, S., Wang, X., Tian, X., & Zhou, D. F. (2019) · Molecular Metabolism · doi:10.1016/j.molmet.2019.10.005 · Cited by 236

Self-organized vascular networks from human pluripotent stem cells in a synthetic matrix

Kusuma, S., Shen, Y., Hanjaya‐Putra, D., Mali, P., Cheng, L., & Gerecht, S. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1306562110 · Cited by 226

Resolved

Zeisberg, M., & Duffield, J. S. (2010) · Journal of the American Society of Nephrology · doi:10.1681/asn.2010060616 · Cited by 224

Specification and Diversification of Pericytes and Smooth Muscle Cells from Mesenchymoangioblasts

Kumar, A., D'Souza, S. S., Moskvin, O. V., Toh, H., Wang, B., Zhang, J., Swanson, S. A., Guo, L., Thomson, J. A., & Slukvin, I. I. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.05.019 · Cited by 220

The promotion of bone regeneration through positive regulation of angiogenic–osteogenic coupling using microRNA-26a

Li, Y., Fan, L., Liu, S., Liu, W., Zhang, H., Zhou, T., Wu, D., Yang, P., Shen, L., Chen, J., et al. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.03.052 · Cited by 220

Semaphorin 3A is an endogenous angiogenesis inhibitor that blocks tumor growth and normalizes tumor vasculature in transgenic mouse models

Maione, F., Molla, F., Meda, C., Latini, R., Zentilin, L., Giacca, M., Seano, G., Serini, G., Bussolino, F., & Giraudo, E. (2009) · Journal of Clinical Investigation · doi:10.1172/jci36308 · Cited by 227

Vascular morphogenesis in the zebrafish embryo

Ellertsdóttir, E., Lenard, A., Blum, Y., Krudewig, A., Herwig, L., Affolter, M., & Belting, H. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.10.035 · Cited by 222

Endothelial-derived FGF2 contributes to the progression of pulmonary hypertension in humans and rodents

Izikki, M., Guignabert, C., Fadel, É., Humbert, M. J. C., Tu, L., Zadigue, P., Dartevelle, P., Simonneau, G., Adnot, S., Maître, B., et al. (2009) · Journal of Clinical Investigation · doi:10.1172/jci35070 · Cited by 217

A role for pericytes as microenvironmental regulators of human skin tissue regeneration

Paquet‐Fifield, S., Schlüter, H., Li, A., Aitken, T., Gangatirkar, P., Blashki, D., Koelmeyer, R., Pouliot, N., Palatsides, M., Ellis, S. L., et al. (2009) · Journal of Clinical Investigation · doi:10.1172/jci38535 · Cited by 215

MCP-1 mediates TGF-β–induced angiogenesis by stimulating vascular smooth muscle cell migration

Ma, J., Wang, Q., Fei, T., Han, J. J., & Chen, Y. (2006) · Blood · doi:10.1182/blood-2006-07-036400 · Cited by 219

PFKFB3-mediated endothelial glycolysis promotes pulmonary hypertension

Cao, Y., Zhang, X., Wang, L., Yang, Q., Ma, Q., Xu, J., Wang, J., Kovács, L., Ayon, R. J., Liu, Z., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1821401116 · Cited by 213

Compromised angiogenesis and vascular Integrity in impaired diabetic wound healing

Okonkwo, U. A., Chen, L., Ma, D., Haywood, V. A., Barakat, M., Urao, N., & DiPietro, L. A. (2020) · PLoS ONE · doi:10.1371/journal.pone.0231962 · Cited by 227

Proteolytic Degradation of VE-Cadherin Alters the Blood-Retinal Barrier in Diabetes

Navaratna, D., McGuire, P. G., Menicucci, G., & Das, A. (2007) · Diabetes · doi:10.2337/db06-1694 · Cited by 211

Increased Pericyte Coverage Mediated by Endothelial-Derived Fibroblast Growth Factor-2 and Interleukin-6 Is a Source of Smooth Muscle–Like Cells in Pulmonary Hypertension

Ricard, N., Tu, L., Le Hiress, M., Huertas, A., Phan, C., Thuillet, R., Sattler, C., Fadel, E., Seferian, A., Montani, D., et al. (2014) · Circulation · doi:10.1161/circulationaha.113.007469 · Cited by 208

Identification and Characterization of Aortic Valve Mesenchymal Progenitor Cells with Robust Osteogenic Calcification Potential

Chen, J., Yip, C. Y. Y., Sone, E. D., & Simmons, C. A. (2009) · American Journal Of Pathology · doi:10.2353/ajpath.2009.080750 · Cited by 209

Integrin-specific hydrogels modulate transplanted human bone marrow-derived mesenchymal stem cell survival, engraftment, and reparative activities

Clark, A. Y., Martin, K. E., García, J. R., Johnson, C. T., Theriault, H. S., Han, W. M., Zhou, D. W., Botchwey, E. A., & García, A. J. (2020) · Nature Communications · doi:10.1038/s41467-019-14000-9 · Cited by 222

The CNS microvascular pericyte: pericyte-astrocyte crosstalk in the regulation of tissue survival

Bonkowski, D., Katyshev, V., Balabanov, R. D., Borisov, A., & Dore-Duffy, P. (2011) · Fluids and Barriers of the CNS · doi:10.1186/2045-8118-8-8 · Cited by 207

Glycosaminoglycan-based hydrogels to modulate heterocellular communication in in vitro angiogenesis models

Chwalek, K., Tsurkan, M. V., Freudenberg, U., & Werner, C. (2014) · Scientific Reports · doi:10.1038/srep04414 · Cited by 212

Pericyte TIMP3 and ADAMTS1 Modulate Vascular Stability after Kidney Injury

Schrimpf, C., Xin, C., Campanholle, G., Gill, S. E., Stallcup, W. B., Lin, S., Davis, G. E., Gharib, S. A., Humphreys, B. D., & Duffield, J. S. (2012) · Journal of the American Society of Nephrology · doi:10.1681/asn.2011080851 · Cited by 204

IDO Expression in Cancer: Different Compartment, Different Functionality?

Meireson, A., Devos, M., & Brochez, L. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.531491 · Cited by 215

Perivascular Multipotent Progenitor Cells in Human Organs

Crisan, M., Chen, C., Corselli, M., Andriolo, G., Lazzari, L., & Péault, B. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04967.x · Cited by 204

Arteriolar Involvement in the Microvascular Lesions of Diabetic Retinopathy: Implications for Pathogenesis

Gardiner, T. A., ARCHER, D. B., Curtis, T. M., & Stitt, A. W. (2007) · Microcirculation · doi:10.1080/10739680601072123 · Cited by 204

Involvement of Advanced Glycation End Products in the Pathogenesis of Diabetic Retinopathy

Xu, J., Chen, L.-J., Yu, J., Wang, H.-J., Zhang, F., Liu, Q., & Wu, J. (2018) · Cellular Physiology and Biochemistry · doi:10.1159/000491897 · Cited by 204

TGFβ Triggers miR-143/145 Transfer From Smooth Muscle Cells to Endothelial Cells, Thereby Modulating Vessel Stabilization

Climent, M., Quintavalle, M., Miragoli, M., Chen, J., Condorelli, G., & Elia, L. (2015) · Circulation Research · doi:10.1161/circresaha.116.305178 · Cited by 206

The Adult Human Brain Harbors Multipotent Perivascular Mesenchymal Stem Cells

Paul, G., Özen, Í., Christophersen, N. S., Reinbothe, T. M., Bengzon, J., Visse, E., Jansson, K., Dannaeus, K., Henriques-Oliveira, C., Roybon, L., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035577 · Cited by 206

CCL18 from tumor-associated macrophages promotes angiogenesis in breast cancer

Lin, L., Chen, Y.-S., Yao, Y., Chen, J., Chen, J.-N., Huang, S., Zeng, Y., Yao, H., Zeng, S.-H., Fu, Y., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.5325 · Cited by 209

Diabetes and retinal vascular dysfunction.

Shin, E. S., Sorenson, C. M., & Sheibani, N. (2014) · Europe PMC (PubMed Central) · doi:10.4103/2008-322x.143378 · Cited by 204

Microarray analysis of blood microvessels from PDGF‐B and PDGF‐Rβ mutant mice identifies novel markers for brain pericytes

Bondjers, C., He, L., Takemoto, M., Norlin, J., Asker, N., Hellström, M., Lindahl, P., Betsholtz, C., Bondjers, C., He, L., et al. (2006) · The FASEB Journal · doi:10.1096/fj.05-4944fje · Cited by 193

The Pericyte of the Pancreatic Islet Regulates Capillary Diameter and Local Blood Flow

Almaça, J., Weitz, J., Rodriguez‐Diaz, R., Pereira, E., & Caicedo, A. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.02.016 · Cited by 200

Cellular Elements of the Blood-Brain Barrier

Correale, J. D., & Villa, A. M. (2009) · Neurochemical Research · doi:10.1007/s11064-009-0081-y · Cited by 210

PDGF signaling is required for epicardial function and blood vessel formation in regenerating zebrafish hearts

Kim, J., Wu, Q., Zhang, Y., Wiens, K. M., Huang, Y., Rubin, N., Shimada, H., Handin, R. I., Chao, M. Y., Tuan, T., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0915016107 · Cited by 196

Human pluripotent stem cell–derived brain pericyte–like cells induce blood-brain barrier properties

Stebbins, M. J., Gastfriend, B. D., Canfield, S. G., Lee, M.-S., Richards, D., Faubion, M. G., Li, W.-J., Daneman, R., Palecek, S. P., & Shusta, E. V. (2019) · Science Advances · doi:10.1126/sciadv.aau7375 · Cited by 195

Angiogenic factors as potential drug target: Efficacy and limitations of anti-angiogenic therapy

Gacche, R. N., & Meshram, R. J. (2014) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2014.05.002 · Cited by 203

Tumor microenvironment: The culprit for ovarian cancer metastasis?

Luo, Z., Wang, Q., Lau, W. B., Lau, B., Xu, L., Zhao, L., Yang, H., Feng, M., Yu, X., Yang, Y., et al. (2016) · Cancer Letters · doi:10.1016/j.canlet.2016.04.038 · Cited by 194

PDGFRβ Signaling Regulates Mural Cell Plasticity and Inhibits Fat Development

Olson, L. E., & Soriano, P. M. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.04.019 · Cited by 199

Molecular and Cellular Aspects of Calcific Aortic Valve Disease

Towler, D. A. (2013) · Circulation Research · doi:10.1161/circresaha.113.300155 · Cited by 199

A Validated Tumorgraft Model Reveals Activity of Dovitinib Against Renal Cell Carcinoma

Sivanand, S., Peña‐Llopis, S., Zhao, H., Kucejová, B., Spence, P., Pavía-Jiménez, A., Yamasaki, T., McBride, D. J., Gillen, J. M., Wolff, N. C., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003643 · Cited by 197

Vascular remodeling in cancer

Farnsworth, R. H., Lackmann, M., Achen, M. G., & Stacker, S. A. (2013) · Oncogene · doi:10.1038/onc.2013.304 · Cited by 197

Two-Wave Nanotherapy To Target the Stroma and Optimize Gemcitabine Delivery To a Human Pancreatic Cancer Model in Mice

Meng, H., Zhao, Y., Dong, J. I., Xue, M., Lin, Y., Ji, Z., Mai, W. X., Zhang, H., Chang, C. H., Brinker, C. J., et al. (2013) · ACS Nano · doi:10.1021/nn404083m · Cited by 192

Peptide Hormone Regulation of Angiogenesis

Clapp, C., Thébault, S. C., Jeziorski, M. C., & de la Escalera, G. M. (2009) · Physiological Reviews · doi:10.1152/physrev.00024.2009 · Cited by 198

Vascular Smooth Muscle Progenitor Cells

Majesky, M. W., Dong, X. R., Regan, J. N., & Hoglund, V. J. (2011) · Circulation Research · doi:10.1161/circresaha.110.223800 · Cited by 196

Angiogenic morphogenesis driven by dynamic and heterogeneous collective endothelial cell movement

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