Evolving functions of endothelial cells in inflammation

The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine

Furchgott, R. F., & Zawadzki, J. V. (1980) · Nature · doi:10.1038/288373a0 · Cited by 12,064

Induction of TNF receptor I-mediated apoptosis via two sequential signaling complexes

Micheau, O., & Tschopp, J. (2003) · Cell · doi:10.1016/s0092-8674(03)00521-x · Cited by 2,738

The immune response in atherosclerosis: a double-edged sword

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Phenotypic Heterogeneity of the Endothelium

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Nitric oxide decreases cytokine-induced endothelial activation. Nitric oxide selectively reduces endothelial expression of adhesion molecules and proinflammatory cytokines.

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Vascular Permeability Factor/Vascular Endothelial Growth Factor: A Critical Cytokine in Tumor Angiogenesis and a Potential Target for Diagnosis and Therapy

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Endothelial Cell-to-Cell Junctions: Molecular Organization and Role in Vascular Homeostasis

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Angiopoietin-1 protects the adult vasculature against plasma leakage

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Phenotypic Heterogeneity of the Endothelium

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Signal transduction by VEGF receptors in regulation of angiogenesis and lymphangiogenesis

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Endothelial type I interferon response and brain diseases: identifying STING as a therapeutic target

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Innovations in studying in vivo cell behavior and pharmacology in complex tissues – microvascular endothelial cells in the spotlight

Langenkamp, E., Kamps, J. A. A. M., Mrug, M. M., Verpoorte, E. M. J., Niyaz, Y., Horvatovich, P. L., Bischoff, R., Struijker-Boudier, H. A. J., & Molema, G. (2013) · Cell and Tissue Research · doi:10.1007/s00441-013-1714-7 · Cited by 19

Epigenetic profiling of gallbladder cancer and gall stone diseases: Evaluation of role of tumour associated genes

Singh, T. D., Gupta, S., Shrivastav, B. R., & Tiwari, P. K. (2015) · Gene · doi:10.1016/j.gene.2015.10.004 · Cited by 20

Increased expression of NTPDases 2 and 3 in mesenteric endothelial cells during schistosomiasis favors leukocyte adhesion through P2Y1 receptors

Oliveira, S. D., Oliveira, N. F., Meyer‐Fernandes, J. R., Savio, L. E. B., Ornelas, F. G. I., Ferreira, Z. S., Coutinho‐Silva, R., & Silva, C. L. M. (2016) · Vascular Pharmacology · doi:10.1016/j.vph.2016.02.005 · Cited by 20

Autotaxin and lysophosphatidic acid signalling in lung pathophysiology

Magkrioti, C. (2013) · World Journal of Respirology · doi:10.5320/wjr.v3.i3.77 · Cited by 20

Polystyrene-Divinylbenzene-Based Adsorbents Reduce Endothelial Activation and Monocyte Adhesion Under Septic Conditions in a Pore Size-Dependent Manner

Eichhorn, T., Rauscher, S., Hammer, C., Gröger, M., Fischer, M. B., & Weber, V. (2016) · Inflammation · doi:10.1007/s10753-016-0408-1 · Cited by 20

Upregulation of P2Y2R, Active uPA, and PAI-1 Are Essential Components of Hantavirus Cardiopulmonary Syndrome

Bondu, V., Bitting, C. P., Poland, V. L., Hanson, J. A., Harkins, M. S., Lathrop, S. L., Nolte, K. B., Lawrence, D. A., & Buranda, T. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00169 · Cited by 20

Endothelium-dependent remote signaling in ischemia and reperfusion: Alterations in the cardiometabolic continuum

Erkens, R., Totzeck, M., Brum, A., Duse, D. A., Bøtker, H. E., Rassaf, T., & Kelm, M. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.01.040 · Cited by 19

Inflammatory Environment Promotes the Adhesion of Tumor Cells to Brain Microvascular Endothelial Cells

Wang, K., Dong, S., Higazy, D., Jin, L., Zou, Q., Chen, H., Inayat, A., Hu, S., & Cui, M. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.691771 · Cited by 20

Identification of Endothelial Proteins in Plasma Associated With Cardiovascular Risk Factors

Iglesias, M., Kruse, L., Sanchez-Rivera, L., Enge, L., Dusart, P., Hong, M., Uhlén, M., Renné, T., Schwenk, J. M., Bergstrom, G., et al. (2021) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.121.316779 · Cited by 22

Synthesis, toxicity study and anti-inflammatory effect of MHTP, a new tetrahydroisoquinoline alkaloid

de Oliveira, M. T. P., Ramalho, T. R. D. O., Ferreira, L. K. L. P., Lima, A. L. A., Cordeiro, M. B., Costa, H. F., Rodrigues, L. C., & Piuvezam, M. R. (2015) · Immunopharmacology and Immunotoxicology · doi:10.3109/08923973.2015.1070173 · Cited by 20

NADPH oxidase and nitric oxide synthase-dependent superoxide production is increased in proliferative lupus nephritis

Oates, J. C., Mashmoushi, A., Shaftman, S., & Gilkeson, G. (2013) · Lupus · doi:10.1177/0961203313507988 · Cited by 20

Endothelial Dysfunction in Patients Undergoing Cardiac Surgery: A Narrative Review and Clinical Implications

Knežević, D., Ćurko‐Cofek, B., Batinac, T., Laškarin, G., Rakić, M., Šoštarič, M., Zdravković, M., Šustić, A., Tokmadžić, V. S., & Batičić, L. (2023) · Journal of Cardiovascular Development and Disease · doi:10.3390/jcdd10050213 · Cited by 19

Aerobic glycolysis of vascular endothelial cells: a novel perspective in cancer therapy

Xu, S., Liao, J., Liu, B., Zhang, C., & Xu, X. (2024) · Molecular Biology Reports · doi:10.1007/s11033-024-09588-1 · Cited by 20

Synthesis and biological activities of a nitro-shiff base compound as a potential anti-inflammatory agent

Roriz, B. C., Buccini, D. F., dos Santos, B. F., Silva, S. R. D. S., Domingues, N. L. D. C., & Moreno, S. E. (2020) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2020.105300 · Cited by 19

Degradation of the Endothelial Glycocalyx Contributes to Metabolic Acidosis in Children Following Cardiopulmonary Bypass Surgery

Bangalore, H., Carter, M. J., Parmar, K., Austin, C. B., Shankar‐Hari, M., Hunt, B. J., & Tibby, S. M. (2021) · Pediatric Critical Care Medicine · doi:10.1097/pcc.0000000000002746 · Cited by 19

Infection risk with the use of interleukin inhibitors in hospitalized patients with COVID-19: A narrative review

Koritala, T., Pattan, V., Tirupathi, R., Rabaan, A. A., Mutair, A. S. A., Alhumaid, S., Adhikari, R., Deepika, K., Jain, N. K., Bansal, V., et al. (2021) · Infezioni in Medicina · doi:10.53854/liim-2904-1 · Cited by 20

Amyloid β aggregation induces human brain microvascular endothelial cell death with abnormal actin organization

Take, Y., Chikai, Y., Shimamori, K., Kuragano, M., Kurita, H., & Tokuraku, K. (2021) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2021.101189 · Cited by 20

IFI16-STING-NF-κB signaling controls exogenous mitochondrion-induced endothelial activation

Li, S., Xu, H., Song, M., Shaw, B. I., Li, Q.-J., & Kirk, A. D. (2022) · American Journal of Transplantation · doi:10.1111/ajt.17034 · Cited by 19

Mediators of Capillary-to-Venule Conversion in the Chronic Inflammatory Skin Disease Psoriasis

He, Y., Kim, J., Tacconi, C., Moody, J., Dieterich, L. C., Anzengruber, F., Maul, J., Gousopoulos, E., Restivo, G., Levesque, M. P., et al. (2022) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2022.05.1089 · Cited by 20

Neutrophils as drivers of vascular injury in sickle cell disease

Torres, L. S., & Hidalgo, A. (2022) · Immunological Reviews · doi:10.1111/imr.13146 · Cited by 22

MiR-146a encapsulated liposomes reduce vascular inflammatory responses through decrease of ICAM-1 expression, macrophage activation, and foam cell formation

Ho, D., Lynd, T. O., Jun, C., Shin, J., Millican, R. C., Estep, B. K., Chen, J., Zhang, X., Brott, B. C., Kim, D. W., et al. (2023) · Nanoscale · doi:10.1039/d2nr03280e · Cited by 19

Inhibition of VCAM-1 expression in endothelial cells by CORM-3: The role of the ubiquitin–proteasome system, p38, and mitochondrial respiration

Bergstraesser, C., Hoeger, S., Song, H., Ermantraut, L., Hottenrot, M., Czymai, T., Schmidt, M., Goebeler, M., Ponelies, N., Stich, C., et al. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.11.035 · Cited by 19

MicroRNAs and Cardiovascular Disease

Fernandez-Hernando, C. F., & Baldán, Á. (2013) · Current Genetic Medicine Reports · doi:10.1007/s40142-013-0008-4 · Cited by 19

Alterations to vascular endothelium in the optic nerve head in patients with vascular comorbidities

Kang, M. H., Balaratnasingam, C., Yu, P. K., Morgan, W. H., McAllister, I. L., Cringle, S. J., & Yu, D. (2013) · Experimental Eye Research · doi:10.1016/j.exer.2013.03.005 · Cited by 19

Endothelial Cell Focal Adhesion Regulates Transendothelial Migration and Subendothelial Crawling of T Cells

Lee, J., Song, K. H., Kim, T., & Doh, J. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00048 · Cited by 19

Cholesterol crystals increase vascular permeability by inactivating SHP2 and disrupting adherens junctions

Mani, A. M., Chattopadhyay, R., Singh, N. K., & Rao, G. N. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.05.068 · Cited by 19

In vitro evaluation of vascular endothelial cell behaviors on biomimetic vascular basement membranes

Yu, C., Xing, M., Sun, S., Guan, G., & Wang, L. (2019) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2019.110381 · Cited by 20

NF-κB Activity in Endothelial Cells is Modulated by Cell Substratum Interactions and Influences Chemokine-Mediated Adhesion of Natural Killer Cells

Hess, S., Methe, H., Kim, J., & Edelman, E. R. (2009) · Cell Transplantation · doi:10.3727/096368909788534979 · Cited by 19

Catastrophic antiphospholipid syndrome in a community-acquired methicillin-resistant Staphylococcus aureus infection: A review of pathogenesis with a case for molecular mimicry

Martin, E., Winn, R. E., & NUGENT, K. M. (2010) · Autoimmunity Reviews · doi:10.1016/j.autrev.2010.09.023 · Cited by 19

Reprogramming towards endothelial cells for vascular regeneration

Hong, X., Bras, A. L., Margariti, A., & Xu, Q. (2016) · Genes & Diseases · doi:10.1016/j.gendis.2016.02.003 · Cited by 19

Tailoring of TiO2 films by H2SO4 treatment and UV irradiation to improve anticoagulant ability and endothelial cell compatibility

Liao, Y., Li, L., Jiang, C., Yang, P., Zhao, A., Sun, H., & Huang, N. (2017) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2017.04.021 · Cited by 19

AMPK/NF-κB signaling pathway regulated by ghrelin participates in the regulation of HUVEC and THP1 Inflammation

Zhang, M., Wang, S., Pan, Z., Ou, T., Ma, J., Liu, H., Li, R., Yang, P., Han, W., Guan, S., et al. (2017) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-017-3094-x · Cited by 19

Decreased CCN3 in Systemic Sclerosis Endothelial Cells Contributes to Impaired Angiogenesis

Henrot, P., Moisan, F., Laurent, P., Manicki, P., Kaulanjan‐Checkmodine, P., Jolivel, V., Rezvani, H. R., Leroy, V., Picard, F., Boulon, C., et al. (2020) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2019.11.026 · Cited by 19

Endothelial Injury in COVID-19 and Acute Infections

Levy, J. H., Iba, T., & Gardiner, E. E. (2021) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.121.316101 · Cited by 19

Understanding the effects of mature adipocytes and endothelial cells on fatty acid metabolism and vascular tone in physiological fatty tissue for vascularized adipose tissue engineering

Huber, B., Volz, A., & Kluger, P. J. (2015) · Cell and Tissue Research · doi:10.1007/s00441-015-2274-9 · Cited by 18

Relationship between serum vascular cell adhesion molecule-1 and endothelin-1 levels with organ involvement and disease activity in systemic lupus erythematosus patients

Hajialilo, M., Tayari, P., Ghorbanihaghjo, A., Khabbazi, A., Mahdavi, A. M., & Rashtchizadeh, N. (2018) · Lupus · doi:10.1177/0961203318796285 · Cited by 18

Inhibitory Effect of Punicalagin on Inflammatory and Angiogenic Activation of Human Umbilical Vein Endothelial Cells

Liu, W. Y., Yang-hui, O., Yang, Y., Zhang, X., Huang, L., Wang, X., Wu, B., & Huang, M. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.727920 · Cited by 18

Cardiovascular Dysfunction in COVID-19: Association Between Endothelial Cell Injury and Lactate

Yang, K., Holt, M., Fan, M., Lam, V. L., Yang, Y., Ha, T., Williams, D. L., Li, C., & Wang, X. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.868679 · Cited by 19

Baicalin inhibited both the Furin/TGFβ1/Smad3/TSP-1 pathway in endothelial cells and the AKT/Ca2+/ROS pathway in platelets to ameliorate inflammatory coagulopathy

Wang, P., Wu, J., Wang, Q., Zhuang, S., Zhao, J., Yu, Y., Zhang, W., Zheng, Y., & Liu, X. (2023) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2023.175674 · Cited by 18

Designer high-density lipoprotein particles enhance endothelial barrier function and suppress inflammation

Lin, Y., Swendeman, S. L., Moreira, I. S., Ghosh, A., Kuo, A., Rosário‐Ferreira, N., Guo, S., Culbertson, A., Levesque, M. V., Cartier, A., et al. (2024) · Science Signaling · doi:10.1126/scisignal.adg9256 · Cited by 18

Viruses and thrombocytopenia

Rasizadeh, R., Ebrahimi, F., Kermanshahi, A. Z., Sorkhabi, A. D., Sarkesh, A., Nahand, J. S., & Baghi, H. B. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e27844 · Cited by 18

Mesenchymal Stem Cell Membrane‐Camouflaged Liposomes for Biomimetic Delivery of Cyclosporine A for Hepatic Ischemia‐Reperfusion Injury Prevention

Chen, H., Yin, W., Yao, K., Liang, J., Cai, J., Sui, X. Y., Zhao, X., Zhang, J., Xiao, J., Li, R., et al. (2024) · Advanced Science · doi:10.1002/advs.202404171 · Cited by 17

Endothelial cell damage in idiopathic pneumonia syndrome

Altmann, T., Slack, J., Slatter, M. A., O’Brien, C., Cant, A. J., Thomas, M. F., Brodlie, M., Annavarapu, S., & Gennery, A. R. (2018) · Bone Marrow Transplantation · doi:10.1038/s41409-017-0042-z · Cited by 18

Immunoresolvents in asthma and allergic diseases: Review and update

Lotfi, R., Rezaiemanesh, A., Mortazavi, S. H., Karaji, A. G., & Salari, F. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27836 · Cited by 18

Effects of CXCL4/CXCR3 on the lipopolysaccharide‐induced injury in human umbilical vein endothelial cells

Wang, X., Zhao, Z., Kaimin, Z., Bao, R., Meng, Y., Bian, J., Wan, X., & Yang, T. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28803 · Cited by 18

Salidroside prevents tumor necrosis factor‑α‑induced vascular inflammation by blocking mitogen‑activated protein kinase and NF‑κB signaling activation

Li, R., Dong, Z., Zhuang, X., Liu, R., Yan, F., Chen, Y., Gao, X., & Shi, H. (2019) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2019.8064 · Cited by 18

The Secretive Liaison of Particulate Matter and SARS-CoV-2. A Hypothesis and Theory Investigation

Mescoli, A., Maffei, G., Pillo, G., Bortone, G., Marchesi, S., Morandi, E., Ranzi, A., Rotondo, F., Serra, S., Vaccari, M., et al. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.579964 · Cited by 18

Altered Vascular Endothelium-Dependent Responsiveness in Frail Elderly Patients Recovering from COVID-19 Pneumonia: Preliminary Evidence

Paneroni, M., Pasini, E., Vitacca, M., Scalvini, S., Comini, L., Pedrinolla, A., & Venturelli, M. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10122558 · Cited by 18

Exploiting polypharmacology to dissect host kinases and kinase inhibitors that modulate endothelial barrier integrity

Dankwa, S., Dols, M.-M., Wei, L., Glennon, E. K. K., Kain, H. S., Kaushansky, A., & Smith, J. D. (2021) · Cell chemical biology · doi:10.1016/j.chembiol.2021.06.004 · Cited by 18

Vascular Regulation of Hematopoietic Stem Cell Homeostasis, Regeneration, and Aging

Ramalingam, P., Butler, J. M., & Poulos, M. G. (2021) · Current Stem Cell Reports · doi:10.1007/s40778-021-00198-2 · Cited by 18

Label-Free Imaging of Histamine Mediated G Protein-Coupled Receptors Activation in Live Cells

Lü, J., Yang, Y., Wang, W., Li, J., Tao, N. J., & Wang, S. (2016) · Analytical Chemistry · doi:10.1021/acs.analchem.6b02677 · Cited by 18

Polymer Scaffolds for peripheral nerve injury repair

Yang, S., Chen, L., Bai, C., Zhao, S., Wu, H., Dong, X., Wang, Y., Qian, Y., Du, B., & Chen, S. (2025) · Progress in Materials Science · doi:10.1016/j.pmatsci.2025.101497 · Cited by 18

Small-Nucleic-Acid-Based Therapeutic Strategy Targeting the Transcription Factors Regulating the Vascular Inflammation, Remodeling and Fibrosis in Atherosclerosis

Youn, S. W., & Park, K.-K. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms160511804 · Cited by 17

TNF-α promotes human antibody-mediated complement-dependent cytotoxicity of porcine endothelial cells through downregulating P38-mediated Occludin expression

Gao, H., Cao, M., Chen, P., Cooper, D. K. C., Zhao, Y., Wei, L., Xu, J., Cai, Z., Zeng, C., Luan, S., et al. (2019) · Cell Communication and Signaling · doi:10.1186/s12964-019-0386-7 · Cited by 17

Effect of HIV‐1 Infection on Angiopoietin 1 and 2 Levels and Measures of Microvascular and Macrovascular Endothelial Dysfunction

Thakkar, A., Ma, Y., Cruz, M. D., Wu, Y., Arechiga, V. M., Swaminathan, S., Ganz, P., Wu, A. H. B., Scherzer, R., Deeks, S. G., et al. (2021) · Journal of the American Heart Association · doi:10.1161/jaha.121.021397 · Cited by 17

Early shedding of membrane-bounded ACE2 could be an indicator for disease severity in SARS-CoV-2

Mariappan, V., Ranganadin, P., Lokesh, S., Rao, S. R., & Pillai, A. B. (2022) · Biochimie · doi:10.1016/j.biochi.2022.06.005 · Cited by 17

The impact of platelets on pulmonary microcirculation throughout COVID-19 and its persistent activating factors

Xiang, M., Wu, X., Jing, H., Liu, L., Wang, C., Wang, Y., Novakovic, V. A., & Shi, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.955654 · Cited by 21

The role of class IIa histone deacetylases in regulating endothelial function

Shen, Z., Bei, Y., Lin, H., Wei, T.-F., Dai, Y., Hu, Y., Zhang, C., & Dai, H. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1091794 · Cited by 17

Probing cerebral malaria inflammation in 3D human brain microvessels

Howard, C. C., Joof, F., Hu, R., Smith, J. D., & Zheng, Y. Y. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113253 · Cited by 19

Immunomodulation of periodontitis with SPMs

Sahni, V., & Dyke, T. E. V. (2023) · Frontiers in Oral Health · doi:10.3389/froh.2023.1288722 · Cited by 20

ω3-PUFA alleviates neuroinflammation by upregulating miR-107 targeting PIEZO1/NFκB p65

Liu, H., Zhou, L., Yi, P., Zhan, F., Zhou, L., Dong, Y., Xiong, Y., Hua, F., & Guohai, X. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.111996 · Cited by 18

Exploring Zika Virus Impact on Endothelial Permeability: Insights into Transcytosis Mechanisms and Vascular Leakage

Marcellin, D. F. H., & Huang, J. (2024) · Viruses · doi:10.3390/v16040629 · Cited by 16

Endothelial Cell Dysfunction Due to Molecules Secreted by Macrophages in Sepsis

He, H., Zhang, W., Jiang, L., Tong, X., Zheng, Y., & Xia, Z. (2024) · Biomolecules · doi:10.3390/biom14080980 · Cited by 19

Endothelialized Bronchioalveolar Lung Organoids Model Endothelial Cell Responses to Injury

Ament, A.-L., Heiner, M., Hessler, M. C., Alexopoulos, I., Steeg, K., Gärtner, U., Vazquez-Armendariz, A. I., & Herold, S. (2025) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2023-0373ma · Cited by 17

RelB activation in anti-inflammatory decidual endothelial cells: a master plan to avoid pregnancy failure?

Masat, E., Gasparini, C., Agostinis, C., Bossi, F., Radillo, O., Seta, F. D., Tamassia, N., Cassatella, M. A., & Bulla, R. (2015) · Scientific Reports · doi:10.1038/srep14847 · Cited by 17

Therapeutic blockade of CD54 attenuates pulmonary barrier damage in T cell-induced acute lung injury

Svedova, J., Ménoret, A., Mittal, P., Ryan, J. M., Buturla, J. A., & Vella, A. T. (2017) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00050.2017 · Cited by 17

Cellular and Vascular Components of Tertiary Lymphoid Structures

Mueller, C. G., Nayar, S., Gardner, D. H., & Barone, F. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8709-2_2 · Cited by 17

CD226 deficiency promotes glutaminolysis and alleviates mitochondria damage in vascular endothelial cells under hemorrhagic shock

Zhou, S., Xie, J., Yu, C., Feng, Z., Cheng, K., Ma, J., Wang, Y., Duan, C., Zhang, Y., Jin, B., et al. (2021) · The FASEB Journal · doi:10.1096/fj.202101134r · Cited by 17

Endothelial dysfunction as the typical pathological state

Vlasova, T. I., Петрищев, Н. Н., & Vlasov, T. D. (2022) · Regional blood circulation and microcirculation · doi:10.24884/1682-6655-2022-21-2-4-15 · Cited by 21

CD4+CD25+Foxp3+Regulatory T Cells Protect Endothelial Function Impaired by Oxidized Low Density Lipoprotein via the KLF-2 Transcription Factor

Li, M., Wang, X., Fu, W., He, S., Li, D., & Ke, Q. (2011) · Cellular Physiology and Biochemistry · doi:10.1159/000335759 · Cited by 17

Tight control – decision-making during T cell–vascular endothelial cell interaction

Firner, S., Onder, L., Nindl, V., & Ludewig, B. (2012) · Frontiers in Immunology · doi:10.3389/fimmu.2012.00279 · Cited by 17

Toll-like receptor 3 regulates cord blood-derived endothelial cell function in vitro and in vivo

Grelier, A., Cras, A., Balitrand, N., Delmau, C., Lecourt, S., Lepelletier, Y., Riesterer, H., Freida, D., Lataillade, J., Bousse‐Kerdilès, M. L., et al. (2013) · Angiogenesis · doi:10.1007/s10456-013-9358-5 · Cited by 17

Propofol-enhanced autophagy increases motility and angiogenic capacity of cultured human umbilical vascular endothelial cells

Chang, C.-Y., Chen, P., Lu, S.-C., Hsieh, M.-C., Lin, C.-W., Lee, H.-M., Jawan, B., & Kao, Y.-H. (2015) · Life Sciences · doi:10.1016/j.lfs.2015.10.014 · Cited by 17

Protein Phosphatase 2A Promotes Endothelial Survival via Stabilization of Translational Inhibitor 4E-BP1 Following Exposure to Tumor Necrosis Factor-α

Janzen, C., Sen, S., Cuevas, J., Reddy, S. T., & Chaudhuri, G. (2011) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.230946 · Cited by 17

Gene delivery of hypoxia-inducible VEGF targeting collagen effectively improves cardiac function after myocardial infarction

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Endothelial cell-surface tissue transglutaminase inhibits neutrophil adhesion by binding and releasing nitric oxide

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