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

Targeting neural precursors in the adult brain rescues injured dopamine neurons

Androutsellis‐Theotokis, A., Rueger, M. A., Park, D. M., Mkhikian, H., Korb, E., Poser, S., Walbridge, S., Munasinghe, J., Koretsky, A. P., Lonser, R. R., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905125106 · Cited by 94

Characterization of the tumor microenvironment and tumor–stroma interaction by non-invasive preclinical imaging

Ramamonjisoa, N., & Ackerstaff, E. (2017) · Frontiers in Oncology · doi:10.3389/fonc.2017.00003 · Cited by 93

PDGFRβ Regulates Adipose Tissue Expansion and Glucose Metabolism via Vascular Remodeling in Diet-Induced Obesity

Onogi, Y., Wada, T., Kamiya, C., Inata, K., Matsuzawa, T., Inaba, Y., Kimura, K., Inoue, H., Yamamoto, S., Ishii, Y., et al. (2017) · Diabetes · doi:10.2337/db16-0881 · Cited by 93

Molecular and functional characterization of circulating extracellular vesicles from diabetic patients with and without retinopathy and healthy subjects

Mazzeo, A., Beltramo, E., Lopatina, T., Gai, C., Trento, M., & Porta, M. (2018) · Experimental Eye Research · doi:10.1016/j.exer.2018.07.003 · Cited by 95

Diabetic retinopathy and endothelin system: microangiopathy versus endothelial dysfunction

Sorrentino, F. S., Matteini, S., Bonifazzi, C., Sebastiani, A., & Parmeggiani, F. (2018) · Eye · doi:10.1038/s41433-018-0032-4 · Cited by 93

Human in vitro 3D co-culture model to engineer vascularized bone-mimicking tissues combining computational tools and statistical experimental approach

Bersini, S., Gilardi, M., Arrigoni, C., Talò, G., Zamai, M., Zagra, L., Caiolfa, V. R., & Moretti, M. (2015) · Biomaterials · doi:10.1016/j.biomaterials.2015.10.057 · Cited by 93

Developmental Angiogenesis of the Central Nervous System

Mancuso, M. R., Kuhnert, F., & Kuo, C. J. (2008) · Lymphatic Research and Biology · doi:10.1089/lrb.2008.1014 · Cited by 97

Pericyte-Derived MFG-E8 Regulates Pathologic Angiogenesis

Motegi, S., Leitner, W. W., Lu, M., Tada, Y., Sárdy, M., Wu, C.-J., Chavakis, T., & Udey, M. C. (2011) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.232587 · Cited by 92

Brain Pericytes: Emerging Concepts and Functional Roles in Brain Homeostasis

Kamouchi, M., Ago, T., & Kitazono, T. (2010) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-010-9605-x · Cited by 96

Coadministration of Endothelial and Smooth Muscle Progenitor Cells Enhances the Efficiency of Proangiogenic Cell-Based Therapy

Foubert, P., Matrone, G., Souttou, B., Déan, C., Barateau, V., Plouët, J., Ricousse-Roussanne, S. L., Levy, B. I., Silvestre, J., & Tobelem, G. (2008) · Circulation Research · doi:10.1161/circresaha.108.175083 · Cited by 91

Cerebral Small Vessel Disease (CSVD) – Lessons From the Animal Models

Mustapha, M., Nassir, C. M. N. C. M., Aminuddin, N., Safri, A. A., & Ghazali, M. M. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.01317 · Cited by 94

Skeletal muscle differentiation of human iPSCs meets bioengineering strategies: perspectives and challenges

Iberite, F., Gruppioni, E., & Ricotti, L. (2022) · npj Regenerative Medicine · doi:10.1038/s41536-022-00216-9 · Cited by 99

Molecular Mechanisms Controlling Vascular Lumen Formation in Three-Dimensional Extracellular Matrices

Sacharidou, A., Stratman, A. N., & Davis, G. E. (2012) · Cells Tissues Organs · doi:10.1159/000331410 · Cited by 90

Multifaceted roles of pericytes in central nervous system homeostasis and disease

Zheng, Z., Chopp, M., & Chen, J. (2020) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x20911331 · Cited by 93

Perivascular cells in blood vessel regeneration

Wanjare, M., Kusuma, S., & Gerecht, S. (2013) · Biotechnology Journal · doi:10.1002/biot.201200199 · Cited by 94

A Glycosaminoglycan Based, Modular Tissue Scaffold System for Rapid Assembly of Perfusable, High Cell Density, Engineered Tissues

Annamalai, R. T., Armant, D. R., & Matthew, H. W. T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084287 · Cited by 90

Effect of Prenatal Glucocorticoids on Cerebral Vasculature of the Developing Brain

Vinukonda, G., Dummula, K., Malik, S., Hu, F.-R., Thompson, C. I., Csiszar, A., Ungvari, Z., & Ballabh, P. (2010) · Stroke · doi:10.1161/strokeaha.110.588400 · Cited by 85

Pericytes: brain-immune interface modulators

Hurtado‐Alvarado, G., Cabañas-Morales, A. M., & Gómez‐González, B. (2014) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2013.00080 · Cited by 92

Increased cortical capillary transit time heterogeneity in Alzheimer's disease: a DSC-MRI perfusion study

Eskildsen, S. F., Gyldensted, L., Nagenthiraja, K., Nielsen, R. B., Hansen, M. B., Dalby, R. B., Frandsen, J. R., Rodell, A. B., Gyldensted, C., Jespersen, S. N., et al. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.11.004 · Cited by 90

Emerging vascular endothelial growth factor antagonists to treat neovascular age-related macular degeneration

Hussain, R. M., & Ciulla, T. A. (2017) · Expert Opinion on Emerging Drugs · doi:10.1080/14728214.2017.1362390 · Cited by 91

Neuropilins in the Context of Tumor Vasculature

Niland, S., & Eble, J. A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20030639 · Cited by 91

Dual Targeting of Endothelial Cells and Pericytes in Antivascular Therapy for Ovarian Carcinoma

Lü, C., Kamat, A. A., Lin, Y. G., Merritt, W. M., Landen, C. N., Kim, T. J., Spannuth, W. A., Arumugam, T., Han, L. Y., Jennings, N. B., et al. (2007) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-07-0197 · Cited by 89

Characterization of vasculogenic potential of human adipose-derived endothelial cells in a three-dimensional vascularized skin substitute

Klar, A. S., Güven, S., Zimoch, J., Zapiorkowska, N. A., Biedermann, T., Sophie Böttcher-haberzeth, A., Meuli‐Simmen, C., Martín, I., Scherberich, A., Ernst Reichmann, A., et al. (2015) · Pediatric Surgery International · doi:10.1007/s00383-015-3808-7 · Cited by 91

Isolation, bulk cultivation, and characterization of coronary microvascular pericytes: the second most frequent myocardial cell type in vitro

Nees, S., Weiss, D., Senftl, A., Knott, M., Förch, S., Schnurr, M., Weyrich, P., & Juchem, G. (2011) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00359.2011 · Cited by 92

Platelet-derived growth factor signaling in mesenchymal cells

Donovan, J. (2012) · Frontiers in bioscience · doi:10.2741/4090 · Cited by 88

Capillary rarefaction from the kidney point of view

Afşar, B., Afşar, R. E., Dağel, T., Kaya, E., Erus, S., Ortíz, A., Covic, A. C., & Kanbay, M. (2017) · Clinical Kidney Journal · doi:10.1093/ckj/sfx133 · Cited by 88

Pericyte-Mediated Tissue Repair through PDGFRβ Promotes Peri-Infarct Astrogliosis, Oligodendrogenesis, and Functional Recovery after Acute Ischemic Stroke

Shibahara, T., Ago, T., Nakamura, K., Tachibana, M., Yoshikawa, Y., Komori, M., Yamanaka, K., Wakisaka, Y., & Kitazono, T. (2020) · eNeuro · doi:10.1523/eneuro.0474-19.2020 · Cited by 89

Strategies for re-vascularization and promotion of angiogenesis in trauma and disease

Gonçalves, R. C., Banfi, A., Oliveira, M. B., & Mano, J. F. (2020) · Biomaterials · doi:10.1016/j.biomaterials.2020.120628 · Cited by 90

Sex differences in the blood–brain barrier: Implications for mental health

Dion‐Albert, L., Binder, L. B., Daigle, B., Hong-Minh, A., Lebel, M., & Ménard, C. (2022) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2022.100989 · Cited by 93

LncRNAs associated with oxidative stress in diabetic wound healing: Regulatory mechanisms and application prospects

Yang, Q., Fang, D., Chen, J., Hu, S., Ni, C., Jiang, J., Zeng, M., & Luo, M. (2023) · Theranostics · doi:10.7150/thno.85823 · Cited by 89

Regulation of the blood–brain barrier integrity by pericytes via matrix metalloproteinases mediated activation of vascular endothelial growth factor in vitro

Thanabalasundaram, G., Pieper, C., Lischper, M., & Galla, H. (2010) · Brain Research · doi:10.1016/j.brainres.2010.05.096 · Cited by 92

Pericyte Rho GTPase Mediates Both Pericyte Contractile Phenotype and Capillary Endothelial Growth State

Kutcher, M., Kolyada, A. Y., Surks, H. K., & Herman, I. M. (2007) · American Journal Of Pathology · doi:10.2353/ajpath.2007.070102 · Cited by 92

Strategies to Stimulate Mobilization and Homing of Endogenous Stem and Progenitor Cells for Bone Tissue Repair

Herrmann, M., Verrier, S., & Alini, M. (2015) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2015.00079 · Cited by 92

Biomechanical strain induces elastin and collagen production in human pluripotent stem cell-derived vascular smooth muscle cells

Wanjare, M., Agarwal, N., & Gerecht, S. (2015) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00366.2014 · Cited by 89

Brain injury-induced dysfunction of the blood brain barrier as a risk for dementia

Abrahamson, E. E., & Ikonomović, M. D. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113257 · Cited by 91

Peritubular Capillary Rarefaction: An Underappreciated Regulator of CKD Progression

Kida, Y. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21218255 · Cited by 93

The Emerging Roles of Pericytes in Modulating Tumor Microenvironment

Sun, R., Kong, X., Qiu, X., Huang, C., & Wong, P. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.676342 · Cited by 92

Brain capillary pericytes are metabolic sentinels that control blood flow through a KATP channel-dependent energy switch

Hariharan, A., Robertson, C. D., Garcia, D. C. G., & Longden, T. A. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111872 · Cited by 97

Neurovascular dysfunction in glaucoma

Alarcón-Martínez, L., Shiga, Y., Villafranca‐Baughman, D., Vargas, J. L. C., Vidal-Paredes, I. A., Quintero, H., Fortune, B. A., Danesh-Meyer, H. V., & Polo, A. D. (2023) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2023.101217 · Cited by 89

Angiogenesis in inflammatory bowel disease

Pousa, I. D., Maté, J., & Gisbert, J. P. (2008) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2007.01914.x · Cited by 86

Pericyte Requirement for Anti-Leak Action of Angiopoietin-1 and Vascular Remodeling in Sustained Inflammation

Fuxe, J., Tabruyn, S. P., Colton, K., Zaid, H. B., Adams, A., Bałuk, P., Lashnits, E. W., Morisada, T., Le, T., O’Brien, S., et al. (2011) · American Journal Of Pathology · doi:10.1016/j.ajpath.2011.02.008 · Cited by 84

Vascular stem cells and ischaemic retinopathies

Stitt, A. W., O’Neill, C. L., O’Doherty, M., ARCHER, D. B., Gardiner, T. A., & Medina, R. J. (2011) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2011.02.001 · Cited by 86

Platelet-derived growth factor receptor-β promotes early endothelial cell differentiation

Rolny, C., Nilsson, I., Magnusson, P. U., Armulik, A., Jakobsson, L., Wentzel, P., Lindblom, P., Norlin, J., Betsholtz, C., Heuchel, R. L., et al. (2006) · Blood · doi:10.1182/blood-2006-04-014894 · Cited by 87

Combination of Injectable Multiple Growth Factor–Releasing Scaffolds and Cell Therapy as an Advanced Modality to Enhance Tissue Neovascularization

Saif, J., Schwarz, T., Chau, D. Y. S., Henstock, J. R., Sami, P., Leicht, S. F., Hermann, P. C., Alcalá, S., Mulero, F., Shakesheff, K. M., et al. (2010) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.110.207928 · Cited by 88

Tunneling nanotubes evoke pericyte/endothelial communication during normal and tumoral angiogenesis

Errede, M., Mangieri, D., Longo, G., Girolamo, F., de Trizio, I., Vimercati, A., Serio, G., Frei, K., Perris, R., & Virgintino, D. (2018) · Fluids and Barriers of the CNS · doi:10.1186/s12987-018-0114-5 · Cited by 88

Perivascular Unit: This Must Be the Place. The Anatomical Crossroad Between the Immune, Vascular and Nervous System

Troili, F., Cipollini, V., Moci, M., Morena, E., Palotai, M., Rinaldi, V., Romano, C., Ristori, G., Giubilei, F., Salvetti, M., et al. (2020) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2020.00017 · Cited by 91

A new angle on blood–CNS interfaces: A role for connexins?

Bock, M. D., Vandenbroucke, R. E., Decrock, E., Culot, M., Cecchelli, R., & Leybaert, L. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.02.060 · Cited by 87

Intratumoral LIGHT Restores Pericyte Contractile Properties and Vessel Integrity

Johansson, A., Li, Z., Lakhiani, D. D., He, B., Wang, X., Hamzah, J., & Ganß, R. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.12.004 · Cited by 87

Neural Crest Origin of Retinal and Choroidal Pericytes

Trost, A., Schroedl, F., Lange, S., Rivera, F. J., Tempfer, H., Korntner, S. H., Stolt, C. C., Wegner, M., Bogner, B., Kaser-Eichberger, A., et al. (2013) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.13-12946 · Cited by 85

Lineage Tracing Reveals the Dynamic Contribution of Pericytes to the Blood Vessel Remodeling in Pulmonary Hypertension

Bordenave, J., Tu, L., Berrebeh, N., Thuillet, R., Cumont, A., Vely, B. L., Fadel, É., Nadaud, S., Savale, L., Humbert, M. J. C., et al. (2020) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.119.313715 · Cited by 89

CircRNA Is a Rising Star in Researches of Ocular Diseases

Zhang, C., Hu, J., & Yu, Y. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00850 · Cited by 84

Regulation of endometrial vascular remodelling: role of the vascular endothelial growth factor family and the angiopoietin–TIE signalling system

Girling, J. E., & Rogers, P. A. W. (2009) · Reproduction · doi:10.1530/rep-09-0147 · Cited by 85

Seizure progression and inflammatory mediators promote pericytosis and pericyte-microglia clustering at the cerebrovasculature

Klément, W., Garbelli, R., Zub, E., Rossini, L., Tassi, L., Girard, B. J. T., Blaquière, M., Bertaso, F., Perroy, J., de Bock, F., et al. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.02.002 · Cited by 85

The cells involved in the pathological process of diabetic retinopathy

Yang, S., Zhang, J., & Chen, L. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110818 · Cited by 88

In vivo methods for imaging blood–brain barrier function and dysfunction

Harris, W. J., Asselin, M., Hinz, R., Parkes, L. M., Allan, S. M., Schießl, I., Boutin, H., & Dickie, B. (2022) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/s00259-022-05997-1 · Cited by 91

Pericytes as a new target for pathological processes in CADASIL

Dziewulska, D., & Lewandowska, E. (2012) · Neuropathology · doi:10.1111/j.1440-1789.2011.01290.x · Cited by 86

Recruitment and retention: factors that affect pericyte migration

Aguilera, K. Y., & Brekken, R. A. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1432-z · Cited by 83

Matrix metalloproteinase-13 mediated degradation of hyaluronic acid-based matrices orchestrates stem cell engraftment through vascular integration

Jha, A. K., Tharp, K. M., Browne, S., Ye, J., Stahl, A., Yeghiazarians, Y., & Healy, K. E. (2016) · Biomaterials · doi:10.1016/j.biomaterials.2016.02.023 · Cited by 89

Enrichment of CD146+ Adipose-Derived Stem Cells in Combination with Articular Cartilage Extracellular Matrix Scaffold Promotes Cartilage Regeneration

Li, X., Guo, W., Zha, K., Jing, X., Wang, M., Zhang, Y., Hao, C., Gao, S., Chen, M., Yuan, Z., et al. (2019) · Theranostics · doi:10.7150/thno.33904 · Cited by 83

Smad2/Smad3 in endothelium is indispensable for vascular stability via S1PR1 and N-cadherin expressions

Itoh, F., Itoh, S., Adachi, T., Ichikawa, K., Matsumura, Y., Takagi, T., Festing, M. H., Watanabe, T., Weinstein, M. B., Karlsson, S., et al. (2012) · Blood · doi:10.1182/blood-2011-12-395772 · Cited by 83

Assembly of complex cell microenvironments using geometrically docked hydrogel shapes

Eng, G. M., Lee, B. W., Parsa, H., Chin, C. D., Schneider, J., Linkov, G., Sia, S. K., & Vunjak‐Novakovic, G. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1300569110 · Cited by 84

A novel role of cellular interactions in vascular calcification

Bardeesi, A. S. A., Gao, J., Zhang, K., Yu, S., Wei, M., Liu, P., & Huang, H. (2017) · Journal of Translational Medicine · doi:10.1186/s12967-017-1190-z · Cited by 82

Endothelial Heparan Sulfate in Angiogenesis

Fuster, M. M., & Wang, L. (2010) · Progress in molecular biology and translational science · doi:10.1016/s1877-1173(10)93009-3 · Cited by 84

Activation of the Wnt/Planar Cell Polarity Pathway Is Required for Pericyte Recruitment during Pulmonary Angiogenesis

Yuan, K., Orcholski, M. E., Panaroni, C., Shuffle, E. M., Huang, N. F., Jiang, X., Tian, W., Vladar, E. K., Wang, L., Nicolls, M. R., et al. (2014) · American Journal Of Pathology · doi:10.1016/j.ajpath.2014.09.013 · Cited by 86

Exploring the Potential of Nanotherapeutics in Targeting Tumor Microenvironment for Cancer Therapy

Muntimadugu, E., Kommineni, N., & Khan, W. (2017) · Pharmacological Research · doi:10.1016/j.phrs.2017.05.010 · Cited by 82

Isletopathy in Type 2 Diabetes Mellitus: Implications of Islet RAS, Islet Fibrosis, Islet Amyloid, Remodeling, and Oxidative Stress

Hayden, M. R., & Sowers, J. R. (2007) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.1610 · Cited by 79

Interstitial cells of Cajal are innervated by nitrergic nerves and express nitric oxide–sensitive guanylate cyclase in the guinea-pig gastrointestinal tract

Iino, S., Horiguchi, K., & Nojyo, Y. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2007.12.044 · Cited by 81

Pericytes: Properties, Functions and Applications in Tissue Engineering

Yağcı, B. G., Uçkan, D., & Çelebi‐Saltik, B. (2015) · Stem Cell Reviews and Reports · doi:10.1007/s12015-015-9590-z · Cited by 82

Excess vascular endothelial growth factor-A disrupts pericyte recruitment during blood vessel formation

Darden, J. A., Payne, L. B., Zhao, H., & Chappell, J. C. (2018) · Angiogenesis · doi:10.1007/s10456-018-9648-z · Cited by 82

Recent Advances on Cell-Based Co-Culture Strategies for Prevascularization in Tissue Engineering

Shafiee, S., Shariatzadeh, S., Zafari, A., Majd, A., & Niknejad, H. (2021) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2021.745314 · Cited by 84

VEGF Receptor Inhibitor-Induced Hypertension: Emerging Mechanisms and Clinical Implications

Camarda, N. D., Travers, R. J., Yang, V. K., London, C. A., & Jaffe, I. Z. (2022) · Current Oncology Reports · doi:10.1007/s11912-022-01224-0 · Cited by 87

Pericyte Loss in Diseases

Li, P., & Fan, H. (2023) · Cells · doi:10.3390/cells12151931 · Cited by 81

Platelet‐derived growth factor receptor‐β‐positive telocytes in skeletal muscle interstitium

Ceafalan, L. C., Popescu, B. O., Sawa Kostin, D., & Popescu, L. M. (2011) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2011.01505.x · Cited by 80

Periodontal Ligament Stem Cells Possess the Characteristics of Pericytes

Iwasaki, K., Komaki, M., Yokoyama, N., Tanaka, Y., Taki, A., Kimura, Y., Takeda, M., Oda, S., Izumi, Y., & Morita, I. (2012) · Journal of Periodontology · doi:10.1902/jop.2012.120547 · Cited by 80

Tumor cell-derived PDGF-B potentiates mouse mesenchymal stem cells-pericytes transition and recruitment through an interaction with NRP-1

Dhar, K., Dhar, G., Majumder, M., Haque, I., Mehta, S., Veldhuizen, P. J. V., Banerjee, S. K., & Banerjee, S. (2010) · Molecular Cancer · doi:10.1186/1476-4598-9-209 · Cited by 87

Identification of a clonally expanding haematopoietic compartment in bone marrow

Wang, L., Benedito, R., Bixel, M. G., Zeuschner, D., Stehling, M., Savendahl, L. S., Haigh, J. J., Snippert, H. J. G., Clevers, H. C., Breier, G., et al. (2012) · The EMBO Journal · doi:10.1038/emboj.2012.308 · Cited by 81

N-cadherin signaling via Trio assembles adherens junctions to restrict endothelial permeability

Kruse, K. J., Lee, Q. S., Sun, Y., Klomp, J. A., Yang, X., Huang, F., Sun, M., Zhao, S., Hong, Z., Vogel, S. M., et al. (2018) · The Journal of Cell Biology · doi:10.1083/jcb.201802076 · Cited by 80

The Blood-Brain Barrier

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Nadeau, V., & Charron, J. (2014) · Development · doi:10.1242/dev.107409 · Cited by 79

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Fujio, M., Yamamoto, A., Ando, Y., Shohara, R., Kinoshita, K., Kaneko, T., Hibi, H., & Ueda, M. (2011) · Bone · doi:10.1016/j.bone.2011.06.024 · Cited by 79

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Warthi, G., Faulkner, J., Doja, J., Ghanam, A. R., Gao, P., Yang, A. C., Slivano, O. J., Barris, C. T., Kress, T. C., Zawieja, S. D., et al. (2022) · Nature Cardiovascular Research · doi:10.1038/s44161-022-00162-1 · Cited by 78

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Oh, E. J., Choi, J.-S., Kim, H., Joo, C.-K., & Hahn, S. K. (2011) · Biomaterials · doi:10.1016/j.biomaterials.2011.01.003 · Cited by 77

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Quesada, A. R., Medina, M. Á., & Alba, E. (2007) · BioEssays · doi:10.1002/bies.20655 · Cited by 77

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Abramovich, D., Irusta, G., Bas, D., Cataldi, N. I., Parborell, F., & Tesone, M. (2012) · Endocrinology · doi:10.1210/en.2012-1105 · Cited by 77

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Siao, C.-J., Lorentz, C. U., Kermani, P., Marinic, T. E., Carter, J., McGrath, K., Padow, V. A., Mark, W. H., Falcone, D. J., Cohen‐Gould, L., et al. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20111749 · Cited by 76

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Kim, J., Mirando, A. C., Popel, A. S., & Green, J. J. (2016) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2016.11.003 · Cited by 78

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Escudero, C., Herlitz, K., Troncoso, F., Guevara, K., Acurio, J., Aguayo, C. R., Godoy, A., & González, M. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00204 · Cited by 77

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Løvschall, H., Mitsiadis, T. A., Poulsen, K., Jensen, K. H., & Kjeldsen, A. L. (2007) · The International Journal of Developmental Biology · doi:10.1387/ijdb.072393hl · Cited by 76

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Blaschuk, O. W., & Devemy, E. (2009) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2009.05.033 · Cited by 76

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Carter, R. N., Casillo, S. M., Mazzocchi, A. R., DesOrmeaux, J. S., Roussie, J. A., & Gaborski, T. R. (2017) · Biofabrication · doi:10.1088/1758-5090/aa5ba7 · Cited by 78

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Li, Y., Zhang, X., Cui, L., Chen, R., Zhang, Y., Zhang, C., Zhu, X., He, T., Shen, Z., Dong, L., et al. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14140 · Cited by 76

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Hongu, T., Funakoshi, Y., Fukuhara, S., Suzuki, T., Sakimoto, S., Takakura, N., Ema, M., Takahashi, S., Itoh, S., Kato, M., et al. (2015) · Nature Communications · doi:10.1038/ncomms8925 · Cited by 76

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Bergers, G. (2008) · Springer eBooks · doi:10.1007/978-0-387-71518-6_4 · Cited by 3

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