Overview of the Matrisome--An Inventory of Extracellular Matrix Constituents and Functions

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Hynes (2002) · doi:10.1016/s0092-8674(02)00971-6 · Cited by 8,606

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Kessenbrock, K., Plaks, V., & Werb, Z. (2010) · Cell · doi:10.1016/j.cell.2010.03.015 · Cited by 5,151

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Hynes, R. O. (2009) · Science · doi:10.1126/science.1176009 · Cited by 3,527

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Page-McCaw, A., Ewald, A. J., & Werb, Z. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2125 · Cited by 2,630

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Uhlen, M., Oksvold, P., Fagerberg, L., Lundberg, E., Jonasson, K., Forsberg, M., Zwahlen, M., Kampf, C., Wester, K., Hober, S., et al. (2010) · Nature Biotechnology · doi:10.1038/nbt1210-1248 · Cited by 2,440

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Ricard-Blum, S. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a004978 · Cited by 2,305

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Lu, P., Takai, K., Weaver, V. M., & Werb, Z. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005058 · Cited by 2,265

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Humphries, J. D., Byron, A., & Humphries, M. J. (2006) · Journal of Cell Science · doi:10.1242/jcs.03098 · Cited by 1,711

Heparan sulphate proteoglycans fine-tune mammalian physiology

Bishop, J. R., Schuksz, M., & Esko, J. D. (2007) · Nature · doi:10.1038/nature05817 · Cited by 1,631

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Sarrazin, S., Lamanna, W. C., & Esko, J. D. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a004952 · Cited by 1,605

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Mule, S. N., Manchola, N. C., de Oliveira, G. S., Pereira, M. C. A., Magalhães, R. D. M., Teixeira, A. A., Colli, W., Alves, M. J. M., & Palmisano, G. (2020) · Journal of Proteomics · doi:10.1016/j.jprot.2020.104020 · Cited by 9

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Mierke, C. T. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.720494 · Cited by 9

Tailored Polyelectrolyte Multilayer Systems by Variation of Polyelectrolyte Composition and EDC/NHS Cross-Linking: Physicochemical Characterization and In Vitro Evaluation

Schirmer, U., Ludolph, J., Rothe, H., Hauptmann, N., Behrens, C., Bittrich, E., Schliephake, H., & Liefeith, K. (2022) · Nanomaterials · doi:10.3390/nano12122054 · Cited by 9

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Büyükdoğan, K., Doral, M. N., Bilge, O., Turhan, E., Huri, G., & Sargon, M. F. (2016) · Acta Orthopaedica et Traumatologica Turcica · doi:10.1016/j.aott.2016.08.003 · Cited by 9

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Corradetti, B., Taraballi, F., Giretti, I., Bauza, G., Pistillo, R. S., Niclot, F. B., Pandolfi, L., Demarchi, D., & Tasciotti, E. (2017) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2017.00054 · Cited by 9

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Dubbin, K., Robertson, C., Hinckley, A., Alvarado, J. A., Gilmore, S. F., Hynes, W. F., Wheeler, E. K., & Moya, M. L. (2020) · Biomaterials · doi:10.1016/j.biomaterials.2020.120035 · Cited by 9

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Knoflacher, M. (2024) · Springer eBooks · doi:10.1007/978-3-662-69423-7_6 · Cited by 9

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Linden, T. A., & King, N. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.08.463732 · Cited by 9

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Teo, Y. X., Lee, K. Y., Goh, C. J. H., Wang, L. C., Sobota, R. M., Chiam, K., Du, C., & Wan, A. C. A. (2023) · npj Science of Food · doi:10.1038/s41538-023-00209-y · Cited by 8

Wnt pathway inhibition with the porcupine inhibitor LGK974 decreases trabecular bone but not fibrosis in a murine model with fibrotic bone

Lung, H., Wentworth, K. L., Moody, T. A., Zamarioli, A., Ram, A., Ganesh, G., Kang, M., Ho, S. P., & Hsiao, E. C. (2024) · JBMR Plus · doi:10.1093/jbmrpl/ziae011 · Cited by 9

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Wu, C., Zhai, Y., Ji, J., Yang, X., Ye, L., Lu, G., Shi, X., & Zhai, G. (2024) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2024.124580 · Cited by 9

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Nissa, M. U., Pinto, N., Ghosh, B., Banerjee, A., Singh, U., Goswami, M., & Srivastava, S. (2024) · mSystems · doi:10.1128/msystems.00247-24 · Cited by 8

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Dzyubenko, E., & Hermann, D. M. (2025) · Handbook of clinical neurology · doi:10.1016/b978-0-443-19104-6.00010-3 · Cited by 8

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Sun, Y., Zhang, Z., Wang, Y., Wu, X., Sun, Y., Lou, H., Xu, J., Yao, J., & Cong, D. (2025) · Frontiers in Endocrinology · doi:10.3389/fendo.2025.1560396 · Cited by 9

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Wang, Q., Pan, L., Chen, S., Zhang, Y., Liu, G., Wu, Y., Qin, X., Zhang, P., Zhang, W., Zhang, J., et al. (2025) · Fluids and Barriers of the CNS · doi:10.1186/s12987-025-00660-x · Cited by 8

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Naserkhaki, R., Shokouhian, B., Tahamtani, Y., Khosravi, A., Iravani, S., Zarrabi, A., & Vosough, M. (2025) · BME Frontiers · doi:10.34133/bmef.0144 · Cited by 10

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Yang, H., Zeng, T., Jiang, T., Wei, Q., Taherzade, S. D., Peng, X., Zhu, J., & Zhou, Z. (2025) · Results in Chemistry · doi:10.1016/j.rechem.2025.102464 · Cited by 8

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Child, F., Lunj, S., Gough, J. E., Humphries, M. J., Biolatti, L. V., Hoskin, P., Choudhury, A., & Quiles, C. G. (2025) · Nature Reviews Urology · doi:10.1038/s41585-025-01092-w · Cited by 8

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Jou, V., Semelsberger, S. D., Smerczynski, J., & Lehoczky, J. A. (2026) · Science Advances · doi:10.1126/sciadv.adz0229 · Cited by 8

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Streuli, C. H. (2012) · Development · doi:10.1242/dev.084541

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Engel, J., & Chiquet, M. (2010) · Springer eBooks · doi:10.1007/978-3-642-16555-9_1 · Cited by 28

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