Inflammation and thrombosis

CD40 ligand on activated platelets triggers an inflammatory reaction of endothelial cells

Henn, V., Slupsky, J. R., Gräfe, M., Anagnostopoulos, I., Förster, R., MÜLLER‐BERGHAUS, G., & Kroczek, R. A. (1998) · Nature · doi:10.1038/35393 · Cited by 2,082

Selective cellular expression of tissue factor in human tissues. Implications for disorders of hemostasis and thrombosis.

Drake, T. A., Morrissey, J. H., & Edgington, T. S. (1989) · Europe PMC (PubMed Central) · Cited by 1,192

Blood-borne tissue factor: Another view of thrombosis

Giesen, P. L. A., Rauch, U., Bohrmann, B., Kling, D., Roqué, M., Fallon, J. T., Badimón, J. J., Himber, J., Riederer, M. A., & Nemerson, Y. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.5.2311 · Cited by 990

Activation of Endothelial Cell Protease Activated Receptor 1 by the Protein C Pathway

Riewald, M., Petrovan, R. J., Donner, A. J., Mueller, B. M., & Ruf, W. (2002) · Science · doi:10.1126/science.1071699 · Cited by 832

Protein C prevents the coagulopathic and lethal effects of Escherichia coli infusion in the baboon.

Taylor, F. B., Chang, A. C. K., Esmon, C. T., D’Angelo, A., Vigano’D’Angelo, S., & Blick, K. E. (1987) · Journal of Clinical Investigation · doi:10.1172/jci112902 · Cited by 820

Leukocyte accumulation promoting fibrin deposition is mediated in vivo by P-selectin on adherent platelets

Palabrica, T. M., Lobb, R. R., Furie, B. C., Aronovitz, M. J., Benjamin, C. D., Hsu, Y., Sajer, S. A., & Furie, B. (1992) · Nature · doi:10.1038/359848a0 · Cited by 811

CD40L stabilizes arterial thrombi by a β3 integrin–dependent mechanism

André, P., Prasad, K. S. S., Denis, C. V., He, M.-S., Papalia, J. M., Hynes, R. O., Phillips, D. R., & Wagner, D. D. (2002) · Nature Medicine · doi:10.1038/nm0302-247 · Cited by 725

Dysfunction of Endothelial Protein C Activation in Severe Meningococcal Sepsis

Faust, S. N., Levin, M., Harrison, O. B., Goldin, R. D., Lockhart, M. S., Kondaveeti, S., Laszik, Z. G., Esmon, C. T., & Heyderman, R. S. (2001) · New England Journal of Medicine · doi:10.1056/nejm200108093450603 · Cited by 694

Complement proteins C5b-9 cause release of membrane vesicles from the platelet surface that are enriched in the membrane receptor for coagulation factor Va and express prothrombinase activity.

Sims, P. J., Faioni, E. M., Wiedmer, T., & Shattil, S. J. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)81346-7 · Cited by 673

Particulate Matter Air Pollution and Cardiovascular Disease: An Update to the Scientific Statement From the American Heart Association

Brook, R. D., Rajagopalan, S., Pope, C. A., Brook, J. R., Bhatnagar, A., Diez-Roux, A. V., Holguin, F., Hong, Y., Luepker, R. V., Mittleman, M. A., et al. (2010) · Circulation · doi:10.1161/cir.0b013e3181dbece1 · Cited by 6,548

Burnout and risk of cardiovascular disease: Evidence, possible causal paths, and promising research directions.

Melamed, S., Shirom, A., Toker, S., Berliner, S., & Shapira, I. (2006) · Psychological Bulletin · doi:10.1037/0033-2909.132.3.327 · Cited by 943

Anti-Inflammatory Effects of Statins: Clinical Evidence and Basic Mechanisms

Jain, M. K., & Ridker, P. M. (2005) · Nature Reviews Drug Discovery · doi:10.1038/nrd1901 · Cited by 930

The hypercoagulable state in COVID-19: Incidence, pathophysiology, and management

Abou-Ismail, M. Y., Diamond, A., Kapoor, S., Arafah, Y., & Nayak, L. (2020) · Thrombosis Research · doi:10.1016/j.thromres.2020.06.029 · Cited by 694

A multicenter, prospective validation of disseminated intravascular coagulation diagnostic criteria for critically ill patients: Comparing current criteria*

Gando, S., Iba, T., Eguchi, Y., Ohtomo, Y., Okamoto, K., Koseki, K., Mayumi, T., Murata, A., Ikeda, T., Ishikura, H., et al. (2006) · Critical Care Medicine · doi:10.1097/01.ccm.0000202209.42491.38 · Cited by 647

Loss of Endothelial Glycocalyx During Acute Hyperglycemia Coincides With Endothelial Dysfunction and Coagulation Activation In Vivo

Nieuwdorp, M., van Haeften, T. W., Gouverneur, M., Mooij, H. L., van Lieshout, M. H. P., Levi, M. M., Meijers, J. C. M., Holleman, F., Hoekstra, J. B. L., Vink, H., et al. (2006) · Diabetes · doi:10.2337/diabetes.55.02.06.db05-1103 · Cited by 628

Disseminated intravascular coagulation

Gando, S., Levi, M. M., & Toh, C. (2016) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2016.37 · Cited by 605

The multifaceted role of fibrinogen in tissue injury and inflammation

Luyendyk, J. P., Schoenecker, J. G., & Flick, M. J. (2018) · Blood · doi:10.1182/blood-2018-07-818211 · Cited by 560

The Hepatic Microcirculation: Mechanistic Contributions and Therapeutic Targets in Liver Injury and Repair

Vollmar, B., & Menger, M. D. (2009) · Physiological Reviews · doi:10.1152/physrev.00027.2008 · Cited by 518

Obesity: A Chronic Low-Grade Inflammation and Its Markers

Khanna, D., Khanna, S., Khanna, P., Kahar, P., & Patel, B. M. (2022) · Cureus · doi:10.7759/cureus.22711 · Cited by 567

Interplay between platelets and coagulation

Sang, Y., Roest, M., de Laat, B., de Groot, P. G., & Huskens, D. (2020) · Blood Reviews · doi:10.1016/j.blre.2020.100733 · Cited by 406

Mechanisms of Venous Thrombosis and Resolution

Wakefield, T. W., Myers, D. D., & Henke, P. K. (2008) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.108.162289 · Cited by 387

Kruppel-Like Factor 2 (KLF2) Regulates Endothelial Thrombotic Function

Lin, Z., Kumar, A., SenBanerjee, S., Staniszewski, K. E., Parmar, K. M., Vaughan, D. E., Gimbrone, M. A., Balasubramanian, V., García‐Cardeña, G., & Jain, M. K. (2005) · Circulation Research · doi:10.1161/01.res.0000159707.05637.a1 · Cited by 385

Thrombomodulin-Protein C-EPCR System

de Wouwer, M. V., Collen, D., & Conway, E. M. (2004) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000134298.25489.92 · Cited by 375

Kruppel-Like Factor 2 as a Novel Mediator of Statin Effects in Endothelial Cells

SenBanerjee, S., Mir, S. S., Lin, Z., Hamik, A., Atkins, G. B., Das, H., Banerjee, P., Kumar, A., & Jain, M. K. (2005) · Circulation · doi:10.1161/circulationaha.104.525774 · Cited by 348

Serpins in thrombosis, hemostasis and fibrinolysis

Rau, J. C., Beaulieu, L. M., Huntington, J. A., & Church, F. (2007) · Journal of Thrombosis and Haemostasis · doi:10.1111/j.1538-7836.2007.02516.x · Cited by 349

Blood Coagulation: Hemostasis and Thrombin Regulation

Tanaka, K. A., Key, N. S., & Levy, J. H. (2009) · Anesthesia & Analgesia · doi:10.1213/ane.0b013e31819bcc9c · Cited by 357

Thrombin

Di, E. (2008) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2008.01.001 · Cited by 335

Sepsis, thrombosis and organ dysfunction

Semeraro, N., Ammollo, C. T., Semeraro, F., & Colucci, M. (2011) · Thrombosis Research · doi:10.1016/j.thromres.2011.10.013 · Cited by 331

Air particulate matter and cardiovascular disease: A narrative review

Martinelli, N., Olivieri, O., & Girelli, D. (2013) · European Journal of Internal Medicine · doi:10.1016/j.ejim.2013.04.001 · Cited by 327

The endothelial glycocalyx: a potential barrier between health and vascular disease

Nieuwdorp, M., Meuwese, M. C., Vink, H., Hoekstra, J. B. L., Kastelein, J. J. P., & Stroes, E. S. G. (2005) · Current Opinion in Lipidology · doi:10.1097/01.mol.0000181325.08926.9c · Cited by 311

Microvascular thrombosis and multiple organ dysfunction syndrome

Gando, S. (2010) · Critical Care Medicine · doi:10.1097/ccm.0b013e3181c9e31d · Cited by 315

Efficacy and Safety of Anticoagulant Treatment in Acute Cardioembolic Stroke: A Meta-Analysis of Randomized Controlled Trials

Paciaroni, M., Agnelli, G., Micheli, S., & Caso, V. (2007) · Stroke · doi:10.1161/01.str.0000254600.92975.1f · Cited by 307

Estrogen and thrombosis: a bench to bedside review

Abou-Ismail, M. Y., Citla Sridhar, D., & Nayak, L. (2020) · Thrombosis Research · doi:10.1016/j.thromres.2020.05.008 · Cited by 261

Incidence, risk factors, and outcomes of venous and arterial thromboembolism in immune checkpoint inhibitor therapy

Moik, F., Chan, W.-S. E., Wiedemann, S., Höeller, C., Tuchmann, F., Aretin, M., Fuereder, T., Zöchbauer‐Müller, S., Preusser, M., Pabinger, I., et al. (2020) · Blood · doi:10.1182/blood.2020007878 · Cited by 235

Inflammation and Stroke Risk: A New Target for Prevention

Kelly, P. J., Lemmens, R., & Tsivgoulis, G. K. (2021) · Stroke · doi:10.1161/strokeaha.121.034388 · Cited by 218

Risk of Arterial Thrombotic Events in Inflammatory Bowel Disease

Ha, C. Y., Magowan, S. H., Accortt, N. A., Chen, J., & Stone, C. D. (2009) · The American Journal of Gastroenterology · doi:10.1038/ajg.2009.81 · Cited by 207

Challenges and emerging technologies in the immunoisolation of cells and tissues.

Wilson, J. T., & Chaikof, E. (2008) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2007.08.034 · Cited by 197

Platelet activation and prothrombotic mediators at the nexus of inflammation and atherosclerosis: Potential role of antiplatelet agents

Lordan, R., Τσούπρας, Α., & Zabetakis, I. (2020) · Blood Reviews · doi:10.1016/j.blre.2020.100694 · Cited by 186

Inflammation and hemostasis

Margetić, S. (2012) · Biochemia Medica · doi:10.11613/bm.2012.006 · Cited by 179

Among inflammation and coagulation markers, PAI-1 is a true component of the metabolic syndrome

Mertens, I. L., Verrijken, A., Michiels, J. J., van der Planken, M., Ruige, J. B., & Gaal, L. F. V. (2006) · International Journal of Obesity · doi:10.1038/sj.ijo.0803189 · Cited by 176

Trauma, Shock, and Disseminated Intravascular Coagulation

Gando, S., Sawamura, A., & Hayakawa, M. (2011) · Annals of Surgery · doi:10.1097/sla.0b013e31821221b1 · Cited by 169

Reactive Oxygen Species Scavenging Nanomedicine for the Treatment of Ischemic Heart Disease

Zhang, Z., Dalan, R., Hu, Z., Wang, J., Chew, N., Poh, K. K., Tan, R., Soong, T. W., Dai, Y., Ye, L., et al. (2022) · Advanced Materials · doi:10.1002/adma.202202169 · Cited by 174

Coagulopathy of Acute Sepsis

Ammollo, C. T., Semeraro, F., Colucci, M., & Semeraro, N. (2015) · Seminars in Thrombosis and Hemostasis · doi:10.1055/s-0035-1556730 · Cited by 166

SEPSIS-ASSOCIATED DISSEMINATED INTRAVASCULAR COAGULATION AND THROMBOEMBOLIC DISEASE

Semeraro, N., Ammollo, C. T., Semeraro, F., & Colucci, M. (2010) · Mediterranean Journal of Hematology and Infectious Diseases · doi:10.4084/mjhid.2010.024 · Cited by 166

Tumor necrosis factor-α-induced TRPC1 expression amplifies store-operated Ca2+influx and endothelial permeability

Paria, B. C., Vogel, S. M., Ahmmed, G. U., Alamgir, S., Shroff, J., Malik, A. B., & Tiruppathì, C. (2004) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00240.2004 · Cited by 157

Inflammation and haemostasis.

Margetić, S. (2012) · PubMed Central · Cited by 155

Hyperglycemia is an important predictor of impaired coronary flow before reperfusion therapy in ST-segment elevation myocardial infarction

Timmer, J. R., Ottervanger, J. P., de Boer, M., Dambrink, J. E., Hoorntje, J. C. A., Gosselink, A. T. M., Suryapranata, H., Zijlstra, F., & Hof, A. W. J. V. ’. (2005) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2004.12.050 · Cited by 150

Risk of Arterial Thrombotic Events in Inflammatory Bowel Disease

Picco, M. F. (2009) · Yearbook of Gastroenterology · doi:10.1016/s0739-5930(09)79360-2 · Cited by 146

Local hemostasis, immunothrombosis, and systemic disseminated intravascular coagulation in trauma and traumatic shock

Gando, S., & Otomo, Y. (2015) · Critical Care · doi:10.1186/s13054-015-0735-x · Cited by 144

Platelets as Mediators of Neuroinflammation and Thrombosis

Rawish, E., Nording, H., Münte, T., & Langer, H. F. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.548631 · Cited by 149

Inflammatory bowel disease

Yoshida, H., & Granger, N. D. (2009) · Inflammatory Bowel Diseases · doi:10.1002/ibd.20896 · Cited by 143

Polyphosphate elicits pro‐inflammatory responses that are counteracted by activated protein C in both cellular and animal models

Bae, J.-E., Lee, W., & Rezaie, A. R. (2012) · Journal of Thrombosis and Haemostasis · doi:10.1111/j.1538-7836.2012.04671.x · Cited by 138

Anticoagulants in heart disease: current status and perspectives

Caterina, R. D., Husted, S., Wallentin, L. C., Agnelli, G., Bachmann, F., Baigent, C., Jespersen, J., Kristensen, S., Montalescot, G., Siegbahn, A. G., et al. (2007) · European Heart Journal · doi:10.1093/eurheartj/ehl492 · Cited by 136

Shear stress sustains atheroprotective endothelial KLF2 expression more potently than statins through mRNA stabilization

Vanthienen, J., Fledderus, J. O., Dekker, R. J., Rohlena, J., VANIJZENDOORN, G., Kootstra, N. A., Pannekoek, H., & Horrevoets, A. J. G. (2006) · Cardiovascular Research · doi:10.1016/j.cardiores.2006.07.008 · Cited by 135

Activated protein C preserves functional islet mass after intraportal transplantation: a novel link between endothelial cell activation, thrombosis, inflammation, and islet cell death.

Contreras, J., Eckstein, C., Smyth, C. A., Bilbao, G., Vilatoba, M., Ringland, S., Young, C., Thompson, J., Fernández, J. A., Griffin, J., et al. (2004) · Diabetes · doi:10.2337/diabetes.53.11.2804 · Cited by 138

Targeting drug delivery in the vascular system: Focus on endothelium

Glassman, P. M., Myerson, J. W., Ferguson, L. T., Kiseleva, R. Y., Shuvaev, V. V., Brenner, J. S., & Muzykantov, V. R. (2020) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2020.06.013 · Cited by 134

Blood coagulation-dependent inflammation. Coagulation-dependent inflammation and inflammation-dependent thrombosis

Strukova, S. M. (2006) · Frontiers in bioscience · doi:10.2741/1780 · Cited by 133

Ovarian cancer, the coagulation pathway, and inflammation

Wang, X., Wang, E., Kavanagh, J. J., & Freedman, R. S. (2005) · Journal of Translational Medicine · doi:10.1186/1479-5876-3-25 · Cited by 135

The coagulopathy and thrombotic risk associated with L-Asparaginase treatment in adults with acute lymphoblastic leukaemia

Truelove, E., Fielding, A. K., & Hunt, B. J. (2012) · Leukemia · doi:10.1038/leu.2012.290 · Cited by 133

Elevated Levels of High-Sensitivity C-Reactive Protein and Serum Amyloid-A Late After Kawasaki Disease

Mitani, Y., Sawada, H., Hayakawa, H., Aoki, K., Ohashi, H., Matsumura, M., Kuroe, K., Shimpo, H., Nakano, M., & Komada, Y. (2004) · Circulation · doi:10.1161/01.cir.0000151311.38708.29 · Cited by 128

NLRP3 regulates platelet integrin αIIbβ3 outside-in signaling, hemostasis and arterial thrombosis

Qiao, J., Wu, X., Luo, Q., Wei, G., Xu, M., Wu, Y., Liu, Y., Li, X., Zi, J., Ju, W., et al. (2018) · Haematologica · doi:10.3324/haematol.2018.191700 · Cited by 127

Crucial role of the protein C pathway in governing microvascular inflammation in inflammatory bowel disease

Scaldaferri, F., Sans, M., Vetrano, S., Graziani, C., CRISTOFARO, R. D., Gerlitz, B., Repici, A., Arena, V., Malesci, A., Panés, J., et al. (2007) · Journal of Clinical Investigation · doi:10.1172/jci31027 · Cited by 127

Platelet-derived microvesicles transfer tissue factor to monocytes but not to neutrophils

Lösche, W., Scholz, T., Temmler, U., Oberle, V., & Claus, R. A. (2004) · Platelets · doi:10.1080/09537100310001649885 · Cited by 116

The antithrombotic profile of aspirin. Aspirin resistance, or simply failure?

Altman, R., Luciardi, H. L., Muntaner, J. A., & Herrera, R. N. (2004) · Thrombosis Journal · doi:10.1186/1477-9560-2-1 · Cited by 115

Blood coagulation and the risk of atherothrombosis: a complex relationship.

Spronk, H. M. H., van der Voort, D., & Cate, H. T. (2004) · Thrombosis Journal · doi:10.1186/1477-9560-2-12 · Cited by 116

Regulation of endothelial thrombomodulin expression by inflammatory cytokines is mediated by activation of nuclear factor-kappa B

Sohn, R. H., Deming, C., Johns, D. C., Champion, H. C., Bian, C., Gardner, K. L., & Rade, J. J. (2005) · Blood · doi:10.1182/blood-2004-03-0928 · Cited by 110

Cerebral Microvascular Responses to Hypercholesterolemia

Ishikawa, M., Stokes, K. Y., Zhang, J. H., Nanda, A., & Granger, D. N. (2003) · Circulation Research · doi:10.1161/01.res.0000111524.05779.60 · Cited by 109

Fibrin(ogen)-α M β 2 Interactions Regulate Leukocyte Function and Innate Immunity In Vivo

Flick, M. J., Du, X., & Degen, J. L. (2004) · Experimental Biology and Medicine · doi:10.1177/153537020422901104 · Cited by 107

Structure and functions of the endothelial cell protein C receptor

Esmon, C. T. (2004) · Critical Care Medicine · doi:10.1097/01.ccm.0000126128.64614.81 · Cited by 107

Genetic and Plasma Markers of Venous Thromboembolism in Patients with High Grade Glioma

Sciacca, F. L., Ciusani, E., Silvani, A., Corsini, E., Frigerio, S., Pogliani, S., Parati, E. A., Croci, D., Boiardi, A., & Salmaggi, A. (2004) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-03-0198 · Cited by 102

Advanced drug delivery systems for antithrombotic agents

Greineder, C. F., Howard, M. D., Carnemolla, R., Cines, D. B., & Muzykantov, V. R. (2013) · Blood · doi:10.1182/blood-2013-03-453498 · Cited by 97

The influence of clinical characteristics, laboratory and inflammatory markers on ‘high on-treatment platelet reactivity’ as measured with different platelet function tests

Elsenberg, E. H. A. M., van de Wal, R. M. A., Zomer, C. A., Bouman, H. J., Verheugt, F. W. A., ten Berg, J. M., Hackeng, C. M., & van Werkum, J. W. (2009) · Thrombosis and Haemostasis · doi:10.1160/th09-05-0285 · Cited by 97

Neutrophil extracellular traps mediate deep vein thrombosis: from mechanism to therapy

Yao, M., Ma, J., Wu, D., Fang, C., Wang, Z., Guo, T., & Mo, J. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1198952 · Cited by 104

Therapy Insight: vascular complications in patients with inflammatory bowel disease

Κoutroubakis, I. E. (2005) · Nature Clinical Practice Gastroenterology & Hepatology · doi:10.1038/ncpgasthep0190 · Cited by 97

microRNAs Distinctively Regulate Vascular Smooth Muscle and Endothelial Cells: Functional Implications in Angiogenesis, Atherosclerosis, and In-Stent Restenosis

Santulli, G. (2015) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-22380-3_4 · Cited by 96

Heart failure and anti tumor necrosis factor-alpha in systemic chronic inflammatory diseases

Sinagra, E., Perricone, G., Romano, C., & Cottone, M. (2013) · European Journal of Internal Medicine · doi:10.1016/j.ejim.2012.12.015 · Cited by 95

Protease-activated Receptor-1 Activation of Endothelial Cells Induces Protein Kinase Cα-dependent Phosphorylation of Syntaxin 4 and Munc18c

Fu, J., Naren, A. P., Gao, X., Ahmmed, G. U., & Malik, A. B. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m410044200 · Cited by 95

Inflammation markers and their trajectories after deep vein thrombosis in relation to risk of post‐thrombotic syndrome

Rabinovich, A., Cohen, J. M., Cushman, M., Wells, P. S., Rodger, M. A., Kovacs, M. J., Anderson, D. R., Tagalakis, V., Lazo‐Langner, A., Solymoss, S., et al. (2014) · Journal of Thrombosis and Haemostasis · doi:10.1111/jth.12814 · Cited by 93

Coagulation, Inflammation, and the Risk of Neonatal White Matter Damage

Leviton, A., & Dammann, O. (2004) · Pediatric Research · doi:10.1203/01.pdr.0000121197.24154.82 · Cited by 93

C-Reactive Protein, Interleukin-6, and Vascular Recurrence After Stroke: An Individual Participant Data Meta-Analysis

McCabe, J. J., Walsh, C., Gorey, S., Harris, K., Hervella, P., Iglesias‐Rey, R., Jern, C., Li, L., Miyamoto, N., Montaner, J., et al. (2023) · Stroke · doi:10.1161/strokeaha.122.040529 · Cited by 92

Expression of complement components and inhibitors on platelet microparticles

Yin, W., Ghebrehiwet, B., & Peerschke, E. I. B. (2008) · Platelets · doi:10.1080/09537100701777311 · Cited by 92

Thrombophilia and Arteriovenous Fistula Survival in ESRD

Salmela, B., Hartman, J., Peltonen, S., Albäck, A., & Lassila, R. (2013) · Clinical Journal of the American Society of Nephrology · doi:10.2215/cjn.03860412 · Cited by 88

Activated protein C: Potential therapy for severe sepsis, thrombosis, and stroke

Griffin, J. H., Zloković, B. V., & Fernández, J. A. (2002) · Seminars in Hematology · doi:10.1053/shem.2002.34093 · Cited by 84

The roles of cellular and molecular components of a hematoma at early stage of bone healing

Shiu, H. T., Leung, P., & Ko, C. (2017) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.2622 · Cited by 87

Unexpected role of anticoagulant protein C in controlling epithelial barrier integrity and intestinal inflammation

Vetrano, S., Ploplis, V. A., Sala, E., Sandoval-Cooper, M. J., Donahue, D. L., Correale, C., Arena, V., Spinelli, A., Repici, A., Malesci, A., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1107140108 · Cited by 83

Colorectal cancer is associated with increased circulating lipopolysaccharide, inflammation and hypercoagulability

de Waal, G. M., de Villiers, W. J. S., Forgan, T., Roberts, T. J., & Pretorius, E. (2020) · Scientific Reports · doi:10.1038/s41598-020-65324-2 · Cited by 82

Age-dependent vulnerability to endotoxemia is associated with reduction of anticoagulant factors activated protein C and thrombomodulin

Starr, M. E., Ueda, J., Takahashi, H., Weiler-Guettler, H., Esmon, C. T., Evers, B. M., & Saitō, H. (2010) · Blood · doi:10.1182/blood-2009-10-246678 · Cited by 82

Leukocyte- and platelet-derived microparticles correlate with thrombus weight and tissue factor activity in an experimental mouse model of venous thrombosis.

Ramacciotti, E., Hawley, A. E., Farris, D. M., Ballard, N., Wrobleski, S. K., Myers, D. D., Henke, P. K., & Wakefield, T. W. (2009) · PubMed · Cited by 81

SIRS-ASSOCIATED COAGULOPATHY AND ORGAN DYSFUNCTION IN CRITICALLY ILL PATIENTS WITH THROMBOCYTOPENIA

Ogura, H., Gando, S., Iba, T., Eguchi, Y., Ohtomo, Y., Okamoto, K., Koseki, K., Mayumi, T., Murata, A., Ikeda, T., et al. (2007) · Shock · doi:10.1097/shk.0b013e31804f7844 · Cited by 79

Meta‐Analysis for Correlating Structure of Bioactive Peptides in Foods of Animal Origin with Regard to Effect and Stability

Maestri, E., Pavlićević, M., Montorsi, M., & Marmiroli, N. (2018) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/1541-4337.12402 · Cited by 80

Leukocyte- and platelet-derived microparticles correlate with thrombus weight and tissue factor activity in an experimental mouse model of venous thrombosis

Hawley, A. E., Farris, D. M., Ballard, N., Wrobleski, S. K., Myers, D. D., Henke, P. K., Wakefield, T. W., & Ramacciotti, E. (2009) · Thrombosis and Haemostasis · doi:10.1160/th08-09-0620 · Cited by 78

C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S–independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies

Buil, A., Trégouët, D., Souto, J. C., Saut, N., Germain, M., Rotival, M., Tiret, L., Cambien, F., Lathrop, M. G., Zeller, T., et al. (2010) · Blood · doi:10.1182/blood-2010-01-263038 · Cited by 76

Biomaterials Regulating Bone Hematoma for Osteogenesis

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Hematologic concerns in extracorporeal membrane oxygenation

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