In Vitro Modeling of Atherosclerosis Using iPSC‐Derived Blood Vessel Organoids

Improved Synthesis of Graphene Oxide

Marcano, D. C., Kosynkin, D. V., Berlin, J. M., Sinitskii, A. S., Sun, Z., Slesarev, A. S., Alemany, L. B., Lu, W. D., & Tour, J. M. (2010) · ACS Nano · doi:10.1021/nn1006368 · Cited by 12,090 · see citing works

Inflammation and Atherosclerosis

Libby, P., Ridker, P. M., & Maseri, A. (2002) · Circulation · doi:10.1161/hc0902.104353 · Cited by 7,724 · see citing works

Ezetimibe Added to Statin Therapy after Acute Coronary Syndromes

Cannon, C. P., Blazing, M. A., Giugliano, R. P., McCagg, A., White, J. A., Theroux, P., Darius, H., Lewis, B. S., Ophuis, T. O., Jukema, J. W., et al. (2015) · New England Journal of Medicine · doi:10.1056/nejmoa1410489 · Cited by 4,487 · see citing works

Atherosclerosis

Libby, P., Buring, J. E., Badimon, L., Hansson, G. K., Deanfield, J., Bittencourt, M. S., Tokgözoğlu, L., & Lewis, E. F. (2019) · Nature Reviews Disease Primers · doi:10.1038/s41572-019-0106-z · Cited by 3,211 · see citing works

Mechanisms of plaque formation and rupture

Bentzon, J. F., Otsuka, F., Virmani, R., & Falk, E. (2014) · Circulation Research · doi:10.1161/circresaha.114.302721 · Cited by 2,391 · see citing works

Epidemiology of Atherosclerosis and the Potential to Reduce the Global Burden of Atherothrombotic Disease

Herrington, W. G., Lacey, B., Sherliker, P., Armitage, J., & Lewington, S. (2016) · Circulation Research · doi:10.1161/circresaha.115.307611 · Cited by 1,483 · see citing works

Inflammatory cytokines in vascular dysfunction and vascular disease

Sprague, A. H., & Khalil, R. A. (2009) · Biochemical Pharmacology · doi:10.1016/j.bcp.2009.04.029 · Cited by 1,347 · see citing works

Current Perspectives on Statins

Maron, D. J., Fazio, S., & Linton, M. F. (2000) · Circulation · doi:10.1161/01.cir.101.2.207 · Cited by 1,217 · see citing works

Inflammation and atherosclerosis: signaling pathways and therapeutic intervention

Kong, P., Cui, Z.-Y., Huang, X.-F., Zhang, D.-D., Guo, R.-J., & Han, M. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-00955-7 · Cited by 1,183 · see citing works

The role of shear stress in the pathogenesis of atherosclerosis

Cunningham, K. S., & Gotlieb, A. I. (2004) · Laboratory Investigation · doi:10.1038/labinvest.3700215 · Cited by 1,155 · see citing works

Vascular smooth muscle cells in atherosclerosis

Basatemur, G. L., Jørgensen, H. F., Clarke, M. C. H., Bennett, M. R., & Mallat, Z. (2019) · Nature Reviews Cardiology · doi:10.1038/s41569-019-0227-9 · Cited by 1,099 · see citing works

Pathophysiology of Atherosclerosis

Jebari‐Benslaiman, S., Galicia-García, U., Larrea, A., Olaetxea, J. R., Alloza, I., Vandenbroeck, K., Benito‐Vicente, A., & Martı́n, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23063346 · Cited by 1,078 · see citing works

Engineering of human brain organoids with a functional vascular-like system

Çakır, B., Xiang, Y., Tanaka, Y., Kural, M. H., Parent, M. J., Kang, Y., Chapeton, K., Patterson, B., Yuan, Y., He, C., et al. (2019) · Nature Methods · doi:10.1038/s41592-019-0586-5 · Cited by 959 · see citing works

Imaging of neutral lipids by oil red O for analyzing the metabolic status in health and disease

Mehlem, A., Hagberg, C. E., Muhl, L., Eriksson, U., & Falkevall, A. (2013) · Nature Protocols · doi:10.1038/nprot.2013.055 · Cited by 897 · see citing works

Effect of lovastatin on early carotid atherosclerosis and cardiovascular events. Asymptomatic Carotid Artery Progression Study (ACAPS) Research Group.

Furberg, C. D., Adams, H. P., Applegate, W. B., Byington, R. P., Espeland, M. A., Hartwell, T., Hunninghake, D. B., Lefkowitz, D. S., Probstfield, J. L., & Riley, W. A. (1994) · Circulation · doi:10.1161/01.cir.90.4.1679 · Cited by 865 · see citing works

Human blood vessel organoids as a model of diabetic vasculopathy

Wimmer, R. A., Leopoldi, A., Aichinger, M., Wick, N., Hantusch, B., Novatchkova, M., Taubenschmid, J., Hämmerle, M., Esk, C., Bagley, J. A., et al. (2019) · Nature · doi:10.1038/s41586-018-0858-8 · Cited by 803 · see citing works

Graphene, hexagonal boron nitride, and their heterostructures: properties and applications

Wang, J., Ma, F., & Sun, M. (2017) · RSC Advances · doi:10.1039/c7ra00260b · Cited by 738 · see citing works

The reactive oxygen species in macrophage polarization: reflecting its dual role in progression and treatment of human diseases

Tan, H.-Y., Wang, N., Li, S., Hong, M., Wang, X., & Feng, Y. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/2795090 · Cited by 657 · see citing works

Animal Models of Atherosclerosis

Getz, G. S., & Reardon, C. A. (2012) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.237693 · Cited by 643 · see citing works

Oxidative Stress Induces Vascular Calcification through Modulation of the Osteogenic Transcription Factor Runx2 by AKT Signaling

Byon, C. H., Javed, A., Dai, Q., Kappes, J. C., Clemens, T. L., Darley-Usmar, V. M., McDonald, J. M., & Chen, Y. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m800021200 · Cited by 639 · see citing works

Macrophages in Atherosclerosis Regression

Barrett, T. J. (2019) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.119.312802 · Cited by 633 · see citing works

How the immune system shapes atherosclerosis: roles of innate and adaptive immunity

Roy, P., Orecchioni, M., & Ley, K. F. (2021) · Nature reviews. Immunology · doi:10.1038/s41577-021-00584-1 · Cited by 584 · see citing works

Inflammatory Mechanisms Contributing to Endothelial Dysfunction

Theofilis, P., Sagris, Μ., Oikonomou, E. K., Antonopoulos, A. S., Siasos, G., Tsioufis, C. P., & Tousoulis, D. (2021) · Biomedicines · doi:10.3390/biomedicines9070781 · Cited by 574 · see citing works

From endothelial dysfunction to atherosclerosis

Sitia, S., TOMASONI, L., Atzeni, F., Ambrosio, G., Cordiano, C., Catapano, A. L., Tramontana, S., Perticone, F., Naccarato, P., Camici, P. G., et al. (2010) · Autoimmunity Reviews · doi:10.1016/j.autrev.2010.07.016 · Cited by 573 · see citing works

Lovastatin and phenylacetate inhibit the induction of nitric oxide synthase and cytokines in rat primary astrocytes, microglia, and macrophages.

Pahan, K., Sheikh, F. G., Namboodiri, A. M., & Singh, I. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119812 · Cited by 565 · see citing works

Inducible Nitric Oxide Synthase and Inflammatory Diseases

Zamora, R., Yoram Vodovotz, B., & Billiar, T. R. (2000) · Molecular Medicine · doi:10.1007/bf03401781 · Cited by 560 · see citing works

Regulation of the expression of inducible nitric oxide synthase

Pautz, A., Art, J., Hahn, S., Nowag, S., Voss, C., & Kleinert, H. (2010) · Nitric Oxide · doi:10.1016/j.niox.2010.04.007 · Cited by 549 · see citing works

Animal models of atherosclerosis

Emini Veseli, B., Perrotta, P., De Meyer, G. R. A., Roth, L., Van der Donckt, C., Martinet, W., & De Meyer, G. R. Y. (2017) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2017.05.010 · Cited by 548 · see citing works

Mouse Models for Atherosclerosis and Pharmaceutical Modifiers

Zadelaar, S., Kleemann, R., Verschuren, L., der Weij, J. D. V.-V., van der Hoorn, J., Princen, H. M. G., & Kooistra, T. (2007) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.107.142570 · Cited by 526 · see citing works

A CD36-dependent signaling cascade is necessary for macrophage foam cell formation

Rahaman, S. O., Lennon, D. J., Febbraio, M., Podrez, E. A., Hazen, S. L., & Silverstein, R. L. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.06.007 · Cited by 506 · see citing works

Inhibition of Tumor Necrosis Factor-α Reduces Atherosclerosis in Apolipoprotein E Knockout Mice

Brånén, L., Hovgaard, L., Nitulescu, M., Bengtsson, E., Nilsson, J. Å., & Jovinge, S. V. (2004) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000143933.20616.1b · Cited by 495 · see citing works

Dysfunction of Endothelial Nitric Oxide Synthase and Atherosclerosis

Kawashima, S., & Yokoyama, M. (2004) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000125114.88079.96 · Cited by 455 · see citing works

How vascular smooth muscle cell phenotype switching contributes to vascular disease

Cao, G., Xuan, X., Hu, J. H., Zhang, R., Jin, H., & Dong, H. (2022) · Cell Communication and Signaling · doi:10.1186/s12964-022-00993-2 · Cited by 440 · see citing works

Vascular smooth muscle cell in atherosclerosis

Chistiakov, D. A., Orekhov, A. N., & Bobryshev, Y. V. (2015) · Acta Physiologica · doi:10.1111/apha.12466 · Cited by 384 · see citing works

Differential effects of orbital and laminar shear stress on endothelial cells

Dardik, A., Chen, L., Frattini, J. C., Asada, H., Aziz, F., Kudo, F. A., & Sumpio, B. E. (2005) · Journal of Vascular Surgery · doi:10.1016/j.jvs.2005.01.020 · Cited by 319 · see citing works

Generation of blood vessel organoids from human pluripotent stem cells

Wimmer, R. A., Leopoldi, A., Aichinger, M., Kerjaschki, D., & Penninger, J. M. (2019) · Nature Protocols · doi:10.1038/s41596-019-0213-z · Cited by 317 · see citing works

Inflammation in Peripheral Artery Disease

Brevetti, G., Giugliano, G., Brevetti, L., & Hiatt, W. R. (2010) · Circulation · doi:10.1161/circulationaha.109.918417 · Cited by 317 · see citing works

Role for TNF in atherosclerosis? Lessons from autoimmune disease

McKellar, G., McCarey, D. W., Sattar, N. A., & McInnes, I. B. (2009) · Nature Reviews Cardiology · doi:10.1038/nrcardio.2009.57 · Cited by 295 · see citing works

The role of efferocytosis in atherosclerosis

Kojima, Y., Weissman, I. L., & Leeper, N. J. (2017) · Circulation · doi:10.1161/circulationaha.116.025684 · Cited by 289 · see citing works

Dual Roles of Graphene Oxide To Attenuate Inflammation and Elicit Timely Polarization of Macrophage Phenotypes for Cardiac Repair

Han, J., Kim, Y. S., Lim, M.-Y., Kim, H. Y., Kong, S., Kang, M., Choo, Y. W., Jun, J. H., Ryu, S., Jeong, H.-Y., et al. (2018) · ACS Nano · doi:10.1021/acsnano.7b09107 · Cited by 261 · see citing works

Intracellular and Intercellular Aspects of Macrophage Immunometabolism in Atherosclerosis

Tabas, I. A., & Bornfeldt, K. (2020) · Circulation Research · doi:10.1161/circresaha.119.315939 · Cited by 249 · see citing works

Graphene Oxides Show Angiogenic Properties

Mukherjee, S., Sriram, P., Barui, A. K., Nethi, S. K., Veeriah, V., Chatterjee, S., Suresh, K. I., & Patra, C. R. (2015) · Advanced Healthcare Materials · doi:10.1002/adhm.201500155 · Cited by 223 · see citing works

Phenotypic Switching of Vascular Smooth Muscle Cells in Atherosclerosis

Chen, R., McVey, D. G., Shen, D., Huang, X., & Ye, S. (2023) · Journal of the American Heart Association · doi:10.1161/jaha.123.031121 · Cited by 210 · see citing works

Effect of MMP-2 Deficiency on Atherosclerotic Lesion Formation in ApoE-Deficient Mice

Kuzuya, M., Nakamura, K., Sasaki, T., et al. (2006) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000218496.60097.e0 · Cited by 202 · see citing works

TNF-α promotes early atherosclerosis by increasing transcytosis of LDL across endothelial cells: Crosstalk between NF-κB and PPAR-γ

Zhang, Y., Yang, X., Bian, F., Wu, P., Xing, S., Xu, G., Li, W., Chi, J., Ouyang, C., Zheng, T., et al. (2014) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2014.02.012 · Cited by 193 · see citing works

Defective Mer Receptor Tyrosine Kinase Signaling in Bone Marrow Cells Promotes Apoptotic Cell Accumulation and Accelerates Atherosclerosis

Ait-Oufella, H., Pouresmail, V., Simon, T., Blanc-Brude, O., Kinugawa, K., Merval, R., Offenstadt, G., Lesèche, G., Cohen, P. L., Tedgui, A., et al. (2008) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/atvbaha.108.169078 · Cited by 187 · see citing works

Capillary diameter and geometry in cardiac and skeletal muscle studied by means of corrosion casts

Potter, R. F., & Groom, A. C. (1983) · Microvascular Research · doi:10.1016/0026-2862(83)90044-4 · Cited by 180 · see citing works

Tissue-Engineered Vascular Grafts with Advanced Mechanical Strength from Human iPSCs

Luo, J., Qin, L., Zhao, L., Gui, L., Ellis, M. W., Huang, Y., Kural, M. H., Clark, J. A., Ono, S., Wang, J., et al. (2020) · Cell stem cell · doi:10.1016/j.stem.2019.12.012 · Cited by 150 · see citing works

Graphene quantum dots as anti-inflammatory therapy for colitis

Lee, B., Lee, J. Y., Kim, J., Yoo, J. M., Kang, I., Kim, J.-J., Shin, N., Kim, D. J., Choi, S. W., Kim, D., et al. (2020) · Science Advances · doi:10.1126/sciadv.aaz2630 · Cited by 144 · see citing works

Dual role of lipoproteins in endothelial cell dysfunction in atherosclerosis

Stancu, C. S., Toma, L., & Sima, A. V. (2012) · Cell and Tissue Research · doi:10.1007/s00441-012-1437-1 · Cited by 104 · see citing works

The Use of Stem Cell-Derived Organoids in Disease Modeling: An Update

Azar, J. H., Bahmad, H. F., Daher, D., Moubarak, M. M., Hadadeh, O., Monzer, A., Bitar, S. A., Jamal, M., Al‐Sayegh, M., & Abou-Kheir, W. G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147667 · Cited by 101 · see citing works

Modeling early stage atherosclerosis in a primary human vascular microphysiological system

Zhang, X., Bishawi, M. M., Zhang, G., Prasad, V., Salmon, E., Breithaupt, J. J., Zhang, Q., & Truskey, G. A. (2020) · Nature Communications · doi:10.1038/s41467-020-19197-8 · Cited by 100 · see citing works

An early-stage atherosclerosis research model based on microfluidics

Zheng, W., Huang, R., Jiang, B., Zhao, Y., Zhang, W., & Jiang, X. (2016) · Small · doi:10.1002/smll.201503241 · Cited by 97 · see citing works

Human assembloids.

Kanton, S., & Pașca, S. (2022) · Development · doi:10.1242/dev.201120 · Cited by 95 · see citing works

TNF-alpha blockade induces a reversible but transient effect on endothelial dysfunction in patients with long-standing severe rheumatoid arthritis

Bosello, S. L., Santoliquido, A., Zoli, A., Campli, C. D., Flore, R. A., Tondi, P., & Ferraccioli, G. (2007) · Clinical Rheumatology · doi:10.1007/s10067-007-0803-y · Cited by 93 · see citing works

Expression of inducible nitric oxide synthase in human coronary atherosclerotic plaque

Depre, C. (1999) · Cardiovascular Research · doi:10.1016/s0008-6363(98)00304-6 · Cited by 79 · see citing works

Enzymatically Modified Low-Density Lipoprotein Promotes Foam Cell Formation in Smooth Muscle Cells via Macropinocytosis and Enhances Receptor-Mediated Uptake of Oxidized Low-Density Lipoprotein

Chellan, B., Reardon, C. A., Getz, G. S., & Bowman, M. A. H. (2016) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.116.307306 · Cited by 76 · see citing works

Identification of HMOX1 as a Critical Ferroptosis-Related Gene in Atherosclerosis

Wu, D., Hu, Q., Wang, Y., Jin, M., Tao, Z., & Wan, J. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.833642 · Cited by 75 · see citing works

Fate and state transitions during human blood vessel organoid development

Nikolova, M. T., He, Z., Seimiya, M., Jonsson, G., Cao, W., Okuda, R., Wimmer, R., Okamoto, R., Nikoloff, J. M., Dittrich, P. S., et al. (2025) · Cell · doi:10.1016/j.cell.2025.03.037 · Cited by 74 · see citing works

A role for collagen type IV in cardiovascular disease?

Steffensen, L. B., & Rasmussen, L. M. (2018) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00070.2018 · Cited by 73 · see citing works

Recent progress of national banking project on homozygous HLA ‐typed induced pluripotent stem cells in S outh K orea

Rim, Y. A., Park, N., Nam, Y., Ham, D., Kim, J., Ha, H., Jung, J., Jung, S. M., Baek, I., Kim, S., et al. (2017) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.2578 · Cited by 71 · see citing works

Core–shell hydrogel microcapsules enable formation of human pluripotent stem cell spheroids and their cultivation in a stirred bioreactor

Fattahi, P., Rahimian, A., Slama, M. Q., Gwon, K., Gonzalez‐Suarez, A. M., Wolf, J., Baskaran, H., Duffy, C. D., Stybayeva, G., Peterson, Q. P., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-85786-2 · Cited by 69 · see citing works

Nox4 NADPH oxidase contributes to smooth muscle cell phenotypes associated with unstable atherosclerotic plaques

Xu, S., Chamseddine, A. H., Carrell, S., & Miller, F. J. (2014) · Redox Biology · doi:10.1016/j.redox.2014.04.004 · Cited by 66 · see citing works

Thin-Cap Fibroatheroma Rupture Is Associated With a Fine Interplay of Shear and Wall Stress

Pedrigi, R. M., de Silva, R., Bovens, S. M., Mehta, V. V., Petretto, E. G., & Krams, R. (2014) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.114.303426 · Cited by 63 · see citing works

Graphene oxide induces apoptotic cell death in endothelial cells by activating autophagy via calcium-dependent phosphorylation of c-Jun N-terminal kinases

Lim, M., Jeung, I. C., Jeong, J., Yoon, S., Lee, S., Park, J., Kang, Y.-S., Lee, H., Park, Y., Lee, H. G., et al. (2016) · Acta Biomaterialia · doi:10.1016/j.actbio.2016.09.018 · Cited by 63 · see citing works

Bioengineered liver crosslinked with nano-graphene oxide enables efficient liver regeneration via MMP suppression and immunomodulation

Kim, D.-H., Kim, M.-J., Kwak, S.-Y., Jeong, J., Choi, D., Choi, S. W., Ryu, J., & Kang, K.-S. (2023) · Nature Communications · doi:10.1038/s41467-023-35941-2 · Cited by 53 · see citing works

Cortical-blood vessel assembloids exhibit Alzheimer’s disease phenotypes by activating glia after SARS-CoV-2 infection

Kong, D., Park, K. H., Kim, D., Kim, N. G., Lee, S., Shin, N., Kook, M. G., Kim, Y. B., & Kang, K. (2023) · Cell Death Discovery · doi:10.1038/s41420-022-01288-8 · Cited by 47 · see citing works

Generation of human tonsil epithelial organoids as an ex vivo model for SARS-CoV-2 infection

Kim, H. K., Kim, H., Lee, M. K., Choi, W. H., Jang, Y., Shin, J. S., Park, J.-Y., Bae, D. H., Hyun, S., Kim, K. H., et al. (2022) · Biomaterials · doi:10.1016/j.biomaterials.2022.121460 · Cited by 44 · see citing works

Absence of Interferon Regulatory Factor 1 Protects Against Atherosclerosis in Apolipoprotein E-Deficient Mice

Du, M., Wang, X., Mao, X., Yang, L., Huang, K., Zhang, F., Wang, Y., Luo, X., Wang, C., Peng, J., et al. (2019) · Theranostics · doi:10.7150/thno.36862 · Cited by 43 · see citing works

Graphene Quantum Dots Alleviate Impaired Functions in Niemann-Pick Disease Type C in Vivo

Kang, I., Yoo, J. M., Kim, D., Kim, J., Cho, M. K., Lee, S. E., Kim, D. J., Lee, B.-C., Lee, J. Y., Kim, J.-J., et al. (2021) · Nano Letters · doi:10.1021/acs.nanolett.0c03741 · Cited by 38 · see citing works

Antiangiogenic Effect of Graphene Oxide in Primary Human Endothelial Cells

Cibecchini, G., Veronesi, M., Catelani, T., Bandiera, T., Guarnieri, D., & Pompa, P. P. (2020) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.0c03404 · Cited by 37 · see citing works

Design and utilization of macrophage and vascular smooth muscle cell co-culture systems in atherosclerotic cardiovascular disease investigation

Zuniga, M. C., White, S. L. P., & Zhou, W. (2014) · Vascular Medicine · doi:10.1177/1358863x14550542 · Cited by 33 · see citing works

Different Approaches in Therapy Aiming to Stabilize an Unstable Atherosclerotic Plaque

Kowara, M., & Cudnoch‐Jędrzejewska, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094354 · Cited by 33 · see citing works

Emulating Early Atherosclerosis in a Vascular Microphysiological System Using Branched Tissue‐Engineered Blood Vessels

Lee, J. H., Chen, Z., He, S., et al. (2021) · Advanced Biology · doi:10.1002/adbi.202000428 · Cited by 32 · see citing works

Co-culture models of endothelial cells, macrophages, and vascular smooth muscle cells for the study of the natural history of atherosclerosis

Liu, M. J., Samant, S., Vasa, C. H., Pedrigi, R. M., Oguz, U. M., Ryu, S., Wei, T., Anderson, D. R., Agrawal, D. K., & Chatzizisis, Y. S. (2023) · PLoS ONE · doi:10.1371/journal.pone.0280385 · Cited by 32 · see citing works

Updated perspectives on vascular cell specification and pluripotent stem cell-derived vascular organoids for studying vasculopathies

Liu, C., Niu, K., & Xiao, Q. (2020) · Cardiovascular Research · doi:10.1093/cvr/cvaa313 · Cited by 31 · see citing works

Autoxidation-Resistant, ROS-Scavenging, and Anti-Inflammatory Micellar Nanoparticles Self-Assembled from Poly(acrylic acid)–Green Tea Catechin Conjugates

Bae, K. H., Chan, K. H., & Kurisawa, M. (2022) · ACS Macro Letters · doi:10.1021/acsmacrolett.2c00239 · Cited by 29 · see citing works

Fate and state transitions during human blood vessel organoid developmentPreprint

Nikolova, M., He, Z., Wimmer, R., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.23.485329 · Cited by 22 · see citing works

Preventive effects of nano-graphene oxide against Parkinson’s disease via reactive oxygen species scavenging and anti-inflammation

Kim, H., Yoon, H. H., Seong, H. Y., et al. (2023) · BMB Reports · doi:10.5483/bmbrep.2022-0137 · Cited by 21 · see citing works

Prescribing and administration of opioid analgesics in residents of aged care facilities

Hussein, A., & Emmerton, L. (2019) · Journal of Research in Pharmacy Practice · doi:10.4103/jrpp.jrpp_18_56 · Cited by 19 · see citing works

Statins inhibit iNOS‐mediated microbicidal potential of activated monocyte‐derived dendritic cells by an IFN‐β‐dependent mechanism

Domínguez, P. M., López‐Bravo, M., Kalinke, U., & Ardavı́n, C. (2011) · European Journal of Immunology · doi:10.1002/eji.201141674 · Cited by 15 · see citing works

Graphene oxide links alterations of anti-viral signaling pathways with lipid metabolism via suppressing TLR3 in vascular smooth muscle cells

Luo, Y., Li, J., Huang, C., Wang, X., Long, D., & Cao, Y. (2022) · Molecular Omics · doi:10.1039/d2mo00086e · Cited by 14 · see citing works

Effect of Lovastatin on lipid peroxidation and total antioxidant concentrations in hemodialysis patients.

Argani, H., Ghorbani, A., ., N. R., & Rahbani-Nobar, M. (2004) · Lipids in Health and Disease · doi:10.1186/1476-511x-3-6 · Cited by 11 · see citing works

Capillary dynamics, interstitial fluid and the lymphatic system

Haggerty, A., & Nirmalan, M. (2022) · Anaesthesia & intensive care medicine · doi:10.1016/j.mpaic.2021.10.016 · Cited by 6 · see citing works

Organoid Vascularization: Strategies and Applications

Gao, Q., Wang, J., Zhang, H., Wang, J., Jing, Y., & Su, J. (2025) · Advanced Healthcare Materials · doi:10.1002/adhm.202500301 · Cited by 53 · see citing works

From organoids to organoids-on-a-chip: Current applications and challenges in biomedical research

Liu, K., Chen, X., Fan, Z., Ren, F., Liu, J., & Hu, B. (2025) · Chinese Medical Journal · doi:10.1097/cm9.0000000000003535 · Cited by 56 · see citing works

Organoids in respiratory virus research: advances and perspectives

Li, X., Xiao, H., Zhou, M., Yang, C., Yang, X., Cheng, T., Yuan, L., & Xia, N. (2025) · Molecular Biomedicine · doi:10.1186/s43556-025-00343-x · Cited by 11 · see citing works

Harnessing iPSCs, 3D organoids, and multiomics to model rare vascular diseases: Emerging new approach methodologies

Liu, L., Wu, D., Tsao, P. S., Leeper, N. J., & Sayed, N. (2026) · Vascular Medicine · doi:10.1177/1358863x251394285 · Cited by 5 · see citing works

Modeling the metastatic tumor microenvironment: a co-culture platform of lung cancer and blood vessel organoids for drug evaluation

Lee, M., Yoon, Y.-J., Lee, J. Y., Hwang, M., Park, S., Lee, M. H., Um, S., Cho, B. C., Rheey, J., Sato, T., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-29214-9 · Cited by 4 · see citing works

Nanotechnology for the treatment of atherosclerosis: Strategies, practical applications and future perspectives

Zhang, Y., Chai, Z., Chen, M., Li, S., Zhuang, W., Hu, W. W., & Chen, M. (2025) · Precision medicine and engineering. · doi:10.1016/j.preme.2025.100046 · Cited by 5 · see citing works

Modelling Cardiovascular Diseases Using Human Microphysiological Systems

Ribeiro, Q., Lopes, E., Ferreira, I. S., Simões, C. G., Vital, C. M., Inácio, J. M., Belo, J. A., Rybak‐Wolf, A., Marques, A. R. A., & Vieira, O. V. (2026) · BioChip Journal · doi:10.1007/s13206-025-00247-6 · Cited by 3 · see citing works

Engineering a cancer organoid-based platform for the early preclinical evaluation of the antitumor efficacy and safety of hydrophilic 2D metallic MoS2 nanosheets

Jin, C., Gao, X., Chen, C., et al. (2025) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2025.139206 · Cited by 2 · see citing works

Animal-origin-free method for generating blood vessel organoids

Hoffmann, A., Schorn, D., Thönig, J., Teng, Y.-H., Bisson, J.-F., & Yordanov, T. E. (2026) · Scientific Reports · doi:10.1038/s41598-026-42977-z · Cited by 2 · see citing works

A 3D Composite Model Using Electrospinning Technology to Study Endothelial Damage

Ciavarella, C., Lisa, L. D., Pasquinelli, G., et al. (2025) · Biomolecules · doi:10.3390/biom15060865 · Cited by 1 · see citing works

Advanced strategies in organoids for metabolic monitoring and metabolic disease modeling

Ma, W., Xu, Y., Gu, Z., & Li, D. (2025) · Nano Research · doi:10.26599/nr.2025.94907988 · Cited by 1 · see citing works

Unravelling hepatic metabolism patterns of Gegen Qinlian decoction through a comparative in vivo and in vitro study

Wang, M., Fan, Y., Zhang, Y., et al. (2026) · Journal of Chromatography B · doi:10.1016/j.jchromb.2026.124941 · Cited by 1 · see citing works

Enabling Technologies in Vascular Biology: Microphysiological Systems, Organoids, and Beyond

Gholizadeh, H., & Benam, K. H. (2026) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.126.323054 · Cited by 1 · see citing works

Beyond lipid lowering: targeting lncRNAs as a novel therapeutic strategy for vascular wall defense in atherosclerosis

Chen, T., Shang, Y., Liu, S., Pan, Y., Wu, C., Meng, C., Zheng, T., Mao, W., & Chen, T. (2026) · Pharmacological Research · doi:10.1016/j.phrs.2026.108342 · Cited by 1 · see citing works

The mechanism of traditional chinese medicine against atherosclerotic cardiovascular disease: Molecular targets in non-immune and immune cells

Liu, X., Wei, H., Yang, J., Sun, P., Zhan, Z., & Wang, J. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103267 · Cited by 1 · see citing works

Human iPSC-derived vascularized organoids: strategy-based insights from 2D endothelial cells to 3D blood vessel organoids

Kong, S.-Y., & Kim, D. (2026) · Biofabrication · doi:10.1088/1758-5090/ae94b5 · Cited by 1 · see citing works

Leveraging IGF signaling to improve the spatial organization and regenerative potential of iPSC-derived vascularized liver organoids

Kim, D., Lee, Y., Kim, M.-J., Lee, A. C., Kwon, S., & Kang, K. (2026) · Science Advances · doi:10.1126/sciadv.aea3814 · Cited by 1 · see citing works

Vascularized human skin assembloids model compartmental skin organization and immune responsiveness in vitro

Kim, M.-J., Lee, S., & Kang, K.-S. (2026) · Experimental & Molecular Medicine · doi:10.1038/s12276-026-01840-x

Exploring the effect of dynamic deformation on the tight junctions of endothelial cellsPreprint

Jahagirdar, D., Kumar, R., & Majumder, A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.23.677978

A Cross-scale Causal Mapping Framework Pinpoints Macrophage Orchestrators of Balanced Arterial DevelopmentPreprint

Han, J., Kong, D., Schwarz, E. L., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.08.681286

Fine particulate matter promoted vascular calcification through the miR-27b-5p/HES1 signaling pathway

Ding, R., Yan, K., Huang, L., Ding, M., Duan, J., & Sun, Z. (2025) · Journal of Environmental Sciences · doi:10.1016/j.jes.2025.12.074

Stem cells and vascular organoids

Wang, K., Wang, X., Hong, Y., & Wang, W. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-40423-8.00011-7

Advances in microfluidic devices and materials for atherosclerosis research

Zhu, M., Bai, N., Yang, Z., & Wang, Y. (2026) · Smart Materials in Medicine · doi:10.1016/j.smaim.2026.03.003

Engineering and Integrating Blood Vessel Organoids: a Comprehensive Blueprint for Physiological and Disease Modeling

Xu, Y., Wubuli, N., & Zhang, J. (2026) · Stem Cell Reviews and Reports · doi:10.1007/s12015-026-11145-1

Stem cells and pyroptosis in atherosclerosis

Rasmi, Y., Mahheidari, N., Madan, A., Dehghani, L., & Ghoshal, K. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-40471-9.00011-2

Bridging discovery and clinical science: A framework for advancing atherosclerosis research using innovative models

Takov, K., Depuydt, M. A. C., Stevens, C. A. T., Fogacci, F., Vico, T. A., Dalt, L. D., Mußbacher, M., Oleksiak, A., Hendrikx, T., Cutruzzolà, A., et al. (2026) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2026.120787

Research progress on coronary heart disease and cytokines: mechanisms, clinical implications, and future directions

Zhang, L., Xu, J., & Sun, G. (2026) · Journal of Cardiothoracic Surgery · doi:10.1186/s13019-026-04332-1

Endothelium—The regulator of atherosclerosis

Ning, K., Shao, C., Xue, W., Shen, Y., & Guo, H.-D. (2026) · Genes & Diseases · doi:10.1016/j.gendis.2026.102286

Coronary atherosclerosis: From plaque evolution and stent–biomaterial interface to rehabilitation-induced vascular remodeling

Yang, P., He, M., Liu, L., & Wang, J. (2026) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2026.106986

Inflammation in atherosclerosis: Drivers, mechanisms and therapies

Su, Z., & Xu, S. (2026) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2026.06.047

Compression benchmarking of holotomography data using OME-Zarr format

Lee, D., Park, J., Lee, J., et al. (2026) · PLoS ONE · doi:10.1371/journal.pone.0351560

Next-generation vascular organoids: multi-lineage and immune integration for disease modeling and regenerative medicine

Chen, Q., Jin, J., Kantawong, F., Li, G., & Li, J. (2026) · Vessel Plus · doi:10.20517/2574-1209.2026.69

Modeling inflammation and inflammatory diseases in organoids

Moor, A. D., Vankelecom, H. E. J., & Arnauts, K. (2026) · British Medical Bulletin · doi:10.1093/bmb/ldag028

Muscle Organoids and Organs-on-Chips: A 15-Year Global Bibliometric Perspective

Lv, Z., Yang, Y., Zhou, Z., et al. (2026) · Tissue Engineering Part B Reviews · doi:10.1177/19373368261486378

Label-free 4D holotomography with depth-adaptive segmentation for quantitative analysis of lipid droplet dynamics in hepatic organoids

Cho, J., Lee, H., Oh, C., Park, J., Park, Y., Koo, B., & Park, Y. (2026) · Biophotonics discovery. · doi:10.1117/1.bios.3.3.035005

Vascularized Organoids for Modeling Cardiovascular Diseases: Advances and Challenges

Xiang, H., Yang, Y., & Li, P. (2026) · Organoids · doi:10.3390/organoids5040037

CD98 promotes vascular smooth muscle cell accumulation in atherosclerosis to confer plaque stability

Zernecke, A. (2016) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2016.11.028 · Cited by 4 · see citing works

Sphingosine-1-Phosphate-Receptor 1 as a Marker for Endothelial Cells in Mouse Xenograft Models of Human Cancer

Lüders, N., & Schumacher, U. (2017) · Anticancer Research · doi:10.21873/anticanres.11731 · Cited by 2 · see citing works

CD98 regulates vascular smooth muscle cell proliferation in atherosclerosis

Baumer, Y., McCurdy, S., Alcalá, M., et al. (2016) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2016.11.017 · Cited by 51 · see citing works

Endothelial Function and Calcium Metabolism

Vliegen, H. W., Jukema, J. W., van der Laarse, A., et al. (1997) · Developments in cardiovascular medicine · doi:10.1007/978-94-009-0037-0_5

Detection of endothelium in cerebral blood vessels

Abrol, R. P., Hughes, V. M., Krueger, C. A., et al. (1984) · Journal of Pharmacological Methods · doi:10.1016/0160-5402(84)90062-7 · Cited by 49 · see citing works