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

Untitled work

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

Matrix Metalloproteinases: Regulators of the Tumor Microenvironment

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

The Extracellular Matrix: Not Just Pretty Fibrils

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

Matrix metalloproteinases and the regulation of tissue remodelling

Page, A. W., Ewald, A. J., & Werb, Z. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2125 · Cited by 3,011 · see citing works

Towards a knowledge-based Human Protein Atlas

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 · see citing works

The Collagen Family

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

Extracellular Matrix Degradation and Remodeling in Development and Disease

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 · see citing works

Integrin ligands at a glance

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

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 · see citing works

Sea Anemone Genome Reveals Ancestral Eumetazoan Gene Repertoire and Genomic Organization

Putnam, N. H., Srivastava, M., Hellsten, U., Dirks, B., Chapman, J., Salamov, A., Terry, A., Shapiro, H., Lindquist, E., Kapitonov, V. V., et al. (2007) · Science · doi:10.1126/science.1139158 · Cited by 1,555 · see citing works

Heparan Sulfate ProteoglycansPreprint

Sarrazin, S., Lamanna, W. C., & Esko, J. D. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a004952 · Cited by 1,524 · see citing works

Cell Biology of Extracellular Matrix

Hay, E. D. (1988) · Springer eBooks · doi:10.1007/978-1-4613-0881-2 · Cited by 1,475 · see citing works

The extracellular matrix in development and morphogenesis: A dynamic view

Rozario, T., & DeSimone, D. W. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.10.026 · Cited by 1,449 · see citing works

Transglutaminases: crosslinking enzymes with pleiotropic functions

Lorand, L., & Graham, R. M. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1014 · Cited by 1,439 · see citing works

The Matrisome: In Silico Definition and In Vivo Characterization by Proteomics of Normal and Tumor Extracellular Matrices

Naba, A., Clauser, K. R., Hoersch, S., Liu, H., Carr, S. A., & Hynes, R. O. (2012) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m111.014647 · Cited by 1,354 · see citing works

Integrin Structure, Activation, and InteractionsPreprint

Campbell, I. D., & Humphries, M. J. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a004994 · Cited by 1,192 · see citing works

The Human Protein Atlas—a tool for pathology

Pontén, F., Jirström, K., & Uhlén, M. (2008) · The Journal of Pathology · doi:10.1002/path.2440 · Cited by 1,126 · see citing works

Of Extracellular Matrix, Scaffolds, and Signaling: Tissue Architecture Regulates Development, Homeostasis, and Cancer

Nelson, C. M., & Bissell, M. J. (2006) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.22.010305.104315 · Cited by 1,121 · see citing works

Regulation of matrix biology by matrix metalloproteinases

Mott, J. D., & Werb, Z. (2004) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2004.07.010 · Cited by 1,104 · see citing works

The Amphimedon queenslandica genome and the evolution of animal complexity

Srivastava, M., Simakov, O., Chapman, J., Fahey, B., Gauthier, M. E. A., Mitros, T., Richards, G. S., Conaco, C., Dacre, M., Hellsten, U., et al. (2010) · Nature · doi:10.1038/nature09201 · Cited by 1,049 · see citing works

Extracellular matrix dynamics in development and regenerative medicine

Daley, W. P., Peters, S. B., & Larsen, M. (2008) · Journal of Cell Science · doi:10.1242/jcs.006064 · Cited by 972 · see citing works

Basement Membranes: Cell Scaffoldings and Signaling PlatformsPreprint

Yurchenco, P. D. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a004911 · Cited by 960 · see citing works

A simplified laminin nomenclature

Aumailley, M., Bruckner‐Tuderman, L., Carter, W. G., Deutzmann, R., EDGAR, D., Ekblom, P., Engel, J., Engvall, E., Hohenester, E., & Jones, J. (2005) · Matrix Biology · doi:10.1016/j.matbio.2005.05.006 · Cited by 928 · see citing works

The dynamic genome of Hydra

Chapman, J. A., Kirkness, E. F., Simakov, O., Hampson, S. E., Mitros, T., Weinmaier, T., Rattei, T., Balasubramanian, P. G., Borman, J., Busam, D., et al. (2010) · Nature · doi:10.1038/nature08830 · Cited by 810 · see citing works

The ADAMTS metalloproteinases

PORTER, S., CLARK, I. M., KEVORKIAN, L., & EDWARDS, D. R. (2005) · Biochemical Journal · doi:10.1042/bj20040424 · Cited by 779 · see citing works

Integrins in Cell MigrationPreprint

Anna Huttenlocher, A., & Horwitz, A. R. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005074 · Cited by 762 · see citing works

Integrins and Extracellular Matrix in Mechanotransduction

Schwartz, M. A. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005066 · Cited by 662 · see citing works

Proteoglycans of the extracellular environment: clues from the gene and protein side offer novel perspectives in molecular diversity and function

Iozzo, R. V., & Murdoch, A. D. (1996) · The FASEB Journal · doi:10.1096/fasebj.10.5.8621059 · Cited by 647 · see citing works

Dystroglycan: from biosynthesis to pathogenesis of human disease

Barresi, R., & Campbell, K. P. (2006) · Journal of Cell Science · doi:10.1242/jcs.02814 · Cited by 598 · see citing works

Endogenous Inhibitors of Angiogenesis

Nyberg, P., Xie, L., & Kalluri, R. (2005) · Cancer Research · doi:10.1158/0008-5472.can-04-2427 · Cited by 557 · see citing works

Proteoglycans: from structural compounds to signaling molecules

Schaefer, L., & Schaefer, R. M. (2009) · Cell and Tissue Research · doi:10.1007/s00441-009-0821-y · Cited by 550 · see citing works

Functions and mechanisms of action of CCN matricellular proteins

Chen, C.-C., & Lau, L. F. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2008.07.025 · Cited by 549 · see citing works

Molecular Architecture and Function of Matrix AdhesionsPreprint

Geiger, B., & Yamada, K. M. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005033 · Cited by 548 · see citing works

The ADAMs: signalling scissors in the tumour microenvironment

Murphy, G. (2008) · Nature reviews. Cancer · doi:10.1038/nrc2459 · Cited by 528 · see citing works

A Disintegrin-like and Metalloprotease (Reprolysin-type) with Thrombospondin Type 1 Motif (ADAMTS) Superfamily: Functions and Mechanisms

Apte, S. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.r109.052340 · Cited by 506 · see citing works

Extracellular Matrix: Functions in the Nervous System

Barros, C. S., Franco, S. J., & Muller, U. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005108 · Cited by 506 · see citing works

The Evolution of Cell Adhesion

Hynes, R. O., & Zhao, Q. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.150.2.f89 · Cited by 487 · see citing works

The ThrombospondinsPreprint

Adams, J. C., & Lawler, J. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a009712 · Cited by 468 · see citing works

Fibronectins, Their Fibrillogenesis, and In Vivo FunctionsPreprint

Schwarzbauer, J. E., & DeSimone, D. W. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005041 · Cited by 445 · see citing works

Mammalian collagen receptors

Leitinger, B., & Hohenester, E. (2006) · Matrix Biology · doi:10.1016/j.matbio.2006.10.007 · Cited by 427 · see citing works

Genome evolution and the evolution of exon-shuffling — a review

Patthy, L. (1999) · Gene · doi:10.1016/s0378-1119(99)00228-0 · Cited by 423 · see citing works

Transmembrane Signaling Proteoglycans

Couchman, J. (2010) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100109-104126 · Cited by 403 · see citing works

Cell-Extracellular Matrix Interactions in Normal and Diseased Skin

Watt, F. M., & Fujiwara, H. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005124 · Cited by 384 · see citing works

Cross Talk among TGF- Signaling Pathways, Integrins, and the Extracellular Matrix

Munger, J. S., & Sheppard, D. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005017 · Cited by 372 · see citing works

Shaping morphogen gradients by proteoglycans.Preprint

Yan, D., & Lin, X. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a002493 · Cited by 353 · see citing works

The Evolution of Extracellular Matrix

Özbek, S., Balasubramanian, P. G., Chiquet-Ehrismann, R., Tucker, R. P., & Adams, J. C. (2010) · Molecular Biology of the Cell · doi:10.1091/mbc.e10-03-0251 · Cited by 347 · see citing works

The Cell Biology of the Extracellular Matrix

Knaggs, H. (1992) · Biochemical Education · doi:10.1016/0307-4412(92)90083-x · Cited by 345 · see citing works

Genetic diseases of connective tissues: cellular and extracellular effects of ECM mutations

Bateman, J. F., Boot-Handford, R. P., & Lamandé, S. R. (2009) · Nature Reviews Genetics · doi:10.1038/nrg2520 · Cited by 338 · see citing works

Type IV collagens regulate BMP signalling in Drosophila

Wang, X., Harris, R. E., Bayston, L. J., & Ashe, H. L. (2008) · Nature · doi:10.1038/nature07214 · Cited by 336 · see citing works

Transglutaminases and Disease: Lessons From Genetically Engineered Mouse Models and Inherited Disorders

Iismaa, S. E., Mearns, B. M., Lorand, L., & Graham, R. M. (2009) · Physiological Reviews · doi:10.1152/physrev.00044.2008 · Cited by 331 · see citing works

Heparin-II Domain of Fibronectin Is a Vascular Endothelial Growth Factor-Binding Domain: Enhancement of VEGF Biological Activity by a Singular Growth Factor/Matrix Protein Synergism

Wijelath, E., Rahman, S., Namekata, M., Murray, J., Nishimura, T., Mostafavi-Pour, Z., Patel, Y. M., Suda, Y., Humphries, M., & Sobel, M. (2006) · Circulation Research · doi:10.1161/01.res.0000246849.17887.66 · Cited by 288 · see citing works

Tenascins and the Importance of Adhesion ModulationPreprint

Chiquet‐Ehrismann, R., & Tucker, R. P. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a004960 · Cited by 272 · see citing works

Fibulins: Multiple roles in matrix structures and tissue functions

de Vega, S., Iwamoto, T., & Yamada, Y. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-8632-6 · Cited by 270 · see citing works

Conservation and Novelty in the Evolution of Cell Adhesion and Extracellular Matrix Genes

Hutter, H., Vogel, B. E., Plenefisch, J. D., Norris, C. R., Proenca, R. B., Spieth, J., Guo, C. B., Mastwal, S. S., Zhu, X., Scheel, J., et al. (2000) · Science · doi:10.1126/science.287.5455.989 · Cited by 265 · see citing works

Syndecans as receptors and organizers of the extracellular matrix

Xian, X., Gopal, S., & Couchman, J. (2009) · Cell and Tissue Research · doi:10.1007/s00441-009-0829-3 · Cited by 264 · see citing works

Cell–matrix adhesion in vascular development

Hynes, R. O. (2007) · Journal of Thrombosis and Haemostasis · doi:10.1111/j.1538-7836.2007.02569.x · Cited by 262 · see citing works

The Extracellular Matrix: an Overview

Mecham, R. P. (2011) · Springer eBooks · doi:10.1007/978-3-642-16555-9 · Cited by 235 · see citing works

Domain structure and organisation in extracellular matrix proteins

Hohenester, E., & Engel, J. (2002) · Matrix Biology · doi:10.1016/s0945-053x(01)00191-3 · Cited by 219 · see citing works

Extracellular microfibrils: contextual platforms for TGFβ and BMP signaling

Ramirez, F., & Rifkin, D. B. (2009) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2009.05.005 · Cited by 207 · see citing works

The matricellular functions of small leucine-rich proteoglycans (SLRPs)

Merline, R., Schaefer, R. M., & Schaefer, L. (2009) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-009-0066-2 · Cited by 201 · see citing works

Biochemistry and functional significance of collagen cross-linking

Sp, R. (2007) · Biochemical Society Transactions · doi:10.1042/bst0350849 · Cited by 199 · see citing works

Collagen Cross-Links

Eyre, D. R., & Wu, J.-J. (2005) · Topics in current chemistry · doi:10.1007/b103828 · Cited by 194 · see citing works

What Mouse Mutants Teach Us About Extracellular Matrix Function

Aszódi, A., Legate, K. R., Nakchbandi, I. A., & Fässler, R. (2006) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.22.010305.104258 · Cited by 184 · see citing works

The echinoderm adhesome

Whittaker, C. A., Bergeron, K.-F., Whittle, J., Brandhorst, B. P., Burke, R. D., & Hynes, R. O. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.07.044 · Cited by 183 · see citing works

Extracellular Matrix Proteins in Hemostasis and ThrombosisPreprint

Bergmeier, W., & Hynes, R. O. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005132 · Cited by 182 · see citing works

Proteinases involved in matrix turnover during cartilage and bone breakdown

Cawston, T. E., & Young, D. A. (2009) · Cell and Tissue Research · doi:10.1007/s00441-009-0887-6 · Cited by 173 · see citing works

Novel hepatocyte growth factor (HGF) binding domains on fibronectin and vitronectin coordinate a distinct and amplified Met-integrin induced signalling pathway in endothelial cells

Rahman, S., Patel, Y. M., Murray, J., Patel, K., Sumathipala, R. N., Sobel, M., & Wijelath, E. (2005) · BMC Cell Biology · doi:10.1186/1471-2121-6-8 · Cited by 162 · see citing works

MatrixDB, the extracellular matrix interaction database

Chautard, É., Fatoux-Ardore, M., Ballut, L., Thierry‐Mieg, N., & Ricard‐Blum, S. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq830 · Cited by 134 · see citing works

Matrix revolutions: ‘tails’ of basement-membrane components with angiostatic functions

Bix, G. J., & Iozzo, R. V. (2004) · Trends in Cell Biology · doi:10.1016/j.tcb.2004.11.008 · Cited by 133 · see citing works

Biosynthesis and processing of fibronectin in NIL.8 hamster cells.

Choi, M. G., & Hynes, R. O. (1979) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)86426-8 · Cited by 124 · see citing works

On the origins of the extracellular matrix in vertebrates

Huxley‐Jones, J., Robertson, D. L., & Boot-Handford, R. (2006) · Matrix Biology · doi:10.1016/j.matbio.2006.09.008 · Cited by 123 · see citing works

Nidogens—Extracellular matrix linker molecules

Ho, M. S. P., Böse, K., Mokkapati, S., Nischt, R., & Smyth, N. R. (2008) · Microscopy Research and Technique · doi:10.1002/jemt.20567 · Cited by 116 · see citing works

MatrixDB, a database focused on extracellular protein–protein and protein–carbohydrate interactions

Chautard, É., Ballut, L., Thierry‐Mieg, N., & Ricard‐Blum, S. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp025 · Cited by 97 · see citing works

Genetic Analyses of Integrin SignalingPreprint

Wickstrom, S. A., Radovanac, K., & Fassler, R. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005116 · Cited by 95 · see citing works

The Evolution of Thrombospondins and Their Ligand-Binding Activities

Bentley, A. A., & Adams, J. C. (2010) · Molecular Biology and Evolution · doi:10.1093/molbev/msq107 · Cited by 82 · see citing works

Glycoprotein Ibα and von Willebrand factor in primary platelet adhesion and thrombus formation: Lessons from mutant mice

Chauhan, A. K., Wagner, D. D., & Bergmeier, W. (2008) · Thrombosis and Haemostasis · doi:10.1160/th07-10-0638 · Cited by 80 · see citing works

Fibronectin Growth Factor-Binding Domains Are Required for Fibroblast Survival

Lin, F., Ren, X.-D., Pan, Z., Macri, L. K., Zong, W., Tonnesen, M. G., Rafailovich, M. H., Bar‐Sagi, D., & Clark, R. A. F. (2010) · Journal of Investigative Dermatology · doi:10.1038/jid.2010.253 · Cited by 77 · see citing works

Evidence for the evolution of tenascin and fibronectin early in the chordate lineage

Tucker, R. P., & Chiquet‐Ehrismann, R. (2008) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2008.08.003 · Cited by 60 · see citing works

Extracellular Microfibrils in Vertebrate Development and Disease Processes

Ramirez, F., & Dietz, H. C. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.r900004200 · Cited by 52 · see citing works

Heparan Sulfate Proteoglycans

Schwab, M. (2011) · Springer eBooks · doi:10.1007/978-3-642-16483-5_2638 · Cited by 41 · see citing works

Domain organizations of modular extracellular matrix proteins and their evolution

ENGEL, J. (1996) · Matrix Biology · doi:10.1016/s0945-053x(96)90130-4 · Cited by 37 · see citing works

Agrin Binds BMP2, BMP4 and TGFβ1

Bányai, L., Sonderegger, P., & Patthy, L. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010758 · Cited by 27 · see citing works

Bioinformatic Analysis of Adhesion Proteins

Adams, J. C., & Engel, J. (2007) · Methods in molecular biology · doi:10.1007/978-1-59745-353-0_12 · Cited by 15 · see citing works

CELL-MATRIX ADHESION IN VASCULAR DEVELOPMENT

HYNES, R. O. (2007) · Journal of Thrombosis and Haemostasis · doi:10.1111/j.1538-7836.2007.tb00826.x · Cited by 15 · see citing works

Bioinformatic Analysis of Adhesion Proteins

Adams, J. C., & Engel, J. (2007) · Humana Press eBooks · doi:10.1385/1-59745-353-6:147 · Cited by 1 · see citing works

3D bioprinting of tissues and organs

Murphy, S. V., & Atala, A. (2014) · Nature Biotechnology · doi:10.1038/nbt.2958 · Cited by 7,034 · see citing works

Remodelling the extracellular matrix in development and disease

Bonnans, C., Chou, J., & Werb, Z. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3904 · Cited by 4,367 · see citing works

Mechanotransduction and extracellular matrix homeostasis

Humphrey, J. D., Dufresne, E. R., & Schwartz, M. A. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3896 · Cited by 2,187 · see citing works

Molecular and cellular mechanisms of liver fibrosis and its regression

Kisseleva, T., & Brenner, D. (2021) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-020-00372-7 · Cited by 2,024 · see citing works

Targeting cancer stem cell pathways for cancer therapy

Yang, L., Shi, P., Zhao, G., Xu, J., Peng, W., Zhang, J., Zhang, G., Wang, X., Dong, Z., Chen, F., et al. (2020) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-020-0110-5 · Cited by 1,920 · see citing works

Three-dimensional in vitro cell culture models in drug discovery and drug repositioning

Langhans, S. A. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00006 · Cited by 1,522 · see citing works

Altered regulation of IL-6 production with normal aging. Possible linkage to the age-associated decline in dehydroepiandrosterone and its sulfated derivative

Daynes, R. A., Araneo, B. A., Ershler, W. B., Maloney, C., Li, G. Z., & Ryu, S. Y. (1993) · The Journal of Immunology · doi:10.4049/jimmunol.150.12.5219 · Cited by 1,264 · see citing works

Fibroblasts: Origins, definitions, and functions in health and disease

Plikus, M. V., Wang, X., Sinha, S., Forte, E., Thompson, S. M., Herzog, E. L., Driskell, R. R., Rosenthal, N. A., Biernaskie, J. A., & Horsley, V. (2021) · Cell · doi:10.1016/j.cell.2021.06.024 · Cited by 1,162 · see citing works

A guide to the composition and functions of the extracellular matrix

Karamanos, N. K., Theocharis, A. D., Piperigkou, Z., Manou, D., Passi, A. G., Skandalis, S. S., Vynios, D. H., Orian‐Rousseau, V., Ricard‐Blum, S., Schmelzer, C. E. H., et al. (2021) · FEBS Journal · doi:10.1111/febs.15776 · Cited by 1,100 · see citing works

Targeting the tumour stroma to improve cancer therapy

Valkenburg, K. C., de Groot, A. E., & Pienta, K. J. (2018) · Nature Reviews Clinical Oncology · doi:10.1038/s41571-018-0007-1 · Cited by 1,084 · see citing works

The extracellular matrix: tools and insights for the "omics" era

Naba, A., Clauser, K. R., Ding, H., Whittaker, C. A., Carr, S. A., & Hynes, R. O. (2016) · Matrix Biology · doi:10.1016/j.matbio.2015.06.003 · Cited by 1,037 · see citing works

Extracellular matrix-based materials for regenerative medicine

Hussey, G. S., Dziki, J. L., & Badylak, S. F. (2018) · Nature Reviews Materials · doi:10.1038/s41578-018-0023-x · Cited by 844 · see citing works

Biology of the Extracellular Matrix: An Overview

Yue, B. (2014) · Journal of Glaucoma · doi:10.1097/ijg.0000000000000108 · Cited by 805 · see citing works

A Comprehensive Evaluation of the Activity and Selectivity Profile of Ligands for RGD-binding Integrins

Kapp, T. G., Rechenmacher, F., Neubauer, S., Maltsev, O. V., Cavalcanti‐Adam, E. A., Zarka, R., Reuning, U., Notni, J., Wester, H., Mas‐Moruno, C., et al. (2017) · Scientific Reports · doi:10.1038/srep39805 · Cited by 623 · see citing works

Spatial organization of the extracellular matrix regulates cell–cell junction positioning

Tseng, Q., Duchemin-Pelletier, E., Deshière, A., Balland, M., Guillou, H., Filhol, O., & Théry, M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1106377109 · Cited by 596 · see citing works

Large-scale deep multi-layer analysis of Alzheimer’s disease brain reveals strong proteomic disease-related changes not observed at the RNA level

Johnson, E. C. B., Carter, E. K., Dammer, E. B., Duong, D. M., Gerasimov, E. S., Liu, Y., Liu, J., Betarbet, R., Ping, L., Yin, L., et al. (2022) · Nature Neuroscience · doi:10.1038/s41593-021-00999-y · Cited by 561 · see citing works

3D Cell Culture Systems: Tumor Application, Advantages, and Disadvantages

Habanjar, O., Diab‐Assaf, M., Caldefie‐Chezet, F., & Delort, L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222212200 · Cited by 556 · see citing works

Molecular Architecture and Function of Matrix AdhesionsPreprint

Geiger, B., & Yamada, K. M. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005033 · Cited by 548 · see citing works

Matrix Metalloproteinases: From Molecular Mechanisms to Physiology, Pathophysiology, and Pharmacology

de Almeida, L. G. N., Thode, H., Eslambolchi, Y., Chopra, S., Young, D. W., Gill, S. E., Devel, L., & Dufour, A. (2022) · Pharmacological Reviews · doi:10.1124/pharmrev.121.000349 · Cited by 555 · see citing works

Extracellular matrix as an inductive scaffold for functional tissue reconstruction

Brown, B. N., & Badylak, S. F. (2013) · Translational research · doi:10.1016/j.trsl.2013.11.003 · Cited by 518 · see citing works

Extracellular matrix hydrogel derived from decellularized tissues enables endodermal organoid culture

Giobbe, G. G., Crowley, C., Luni, C., Campinoti, S., Khedr, M., Kretzschmar, K., De Santis, M. M., Zambaiti, E., Michielin, F., Meran, L., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-13605-4 · Cited by 500 · see citing works

3D extracellular matrix mimics: fundamental concepts and role of materials chemistry to influence stem cell fate

Nicolas, J., Magli, S., Rabbachin, L., Sampaolesi, S., Nicotra, F., & Russo, L. (2020) · Biomacromolecules · doi:10.1021/acs.biomac.0c00045 · Cited by 504 · see citing works

The instructive extracellular matrix of the lung: basic composition and alterations in chronic lung disease

Burgstaller, G., Oehrle, B., Gerckens, M., White, E. S., Schiller, H. B., & Eickelberg, O. (2017) · European Respiratory Journal · doi:10.1183/13993003.01805-2016 · Cited by 483 · see citing works

Decellularized Extracellular Matrix-based Bioinks for Engineering Tissue- and Organ-specific Microenvironments

Kim, B. S., Das, S., Jang, J., & Cho, D.-W. (2020) · Chemical Reviews · doi:10.1021/acs.chemrev.9b00808 · Cited by 465 · see citing works

Role of Age-Associated Alterations of the Dermal Extracellular Matrix Microenvironment in Human Skin Aging: A Mini-Review

Quan, T., & Fisher, G. J. (2015) · Gerontology · doi:10.1159/000371708 · Cited by 464 · see citing works

Targeting stromal remodeling and cancer stem cell plasticity overcomes chemoresistance in triple negative breast cancer

Cazet, A. S., Hui, M. N., Elsworth, B. L., Wu, S. Z., Roden, D., Chan, C.-L., Skhinas, J. N., Collot, R., Yang, J., Harvey, K., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05220-6 · Cited by 437 · see citing works

Emergence of a High-Plasticity Cell State during Lung Cancer Evolution

Marjanovic, N. D., Hofree, M., Chan, J. E., Canner, D. A., Wu, K., Trakala, M., Hartmann, G. G., Smith, O. C. G., Kim, J. Y., Evans, K. V., et al. (2020) · Cancer Cell · doi:10.1016/j.ccell.2020.06.012 · Cited by 388 · see citing works

Towards organoid culture without Matrigel

Kozlowski, M. T., Crook, C. J., & Ku, H. T. (2021) · Communications Biology · doi:10.1038/s42003-021-02910-8 · Cited by 409 · see citing works

Ovarian Cancer Cell Line Panel (OCCP): Clinical Importance of In Vitro Morphological Subtypes

Beaufort, C. M., Helmijr, J. C. A., Piskorz, A. M., Hoogstraat, M., Ruigrok-Ritstier, K., Besselink, N., Murtaza, M., van IJcken, W. F. J., Heine, A. A. J., Smid, M., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0103988 · Cited by 403 · see citing works

Single-Cell Genomic Characterization Reveals the Cellular Reprogramming of the Gastric Tumor Microenvironment

Sathe, A., Grimes, S. M., Lau, B. T., Chen, J., Suarez, C. J., Huang, R. J., Poultsides, G. A., & Ji, H. P. (2020) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-19-3231 · Cited by 381 · see citing works

The Interplay between Extracellular Matrix Remodeling and Cancer Therapeutics

Prakash, J., & Shaked, Y. (2024) · Cancer Discovery · doi:10.1158/2159-8290.cd-24-0002 · Cited by 391 · see citing works

Extracellular matrix signatures of human mammary carcinoma identify novel metastasis promoters

Naba, A., Clauser, K. R., Lamar, J. M., Carr, S. A., & Hynes, R. O. (2014) · eLife · doi:10.7554/elife.01308 · Cited by 377 · see citing works

Extracellular matrix regulation of fibroblast function: redefining our perspective on skin aging

Cole, M. A., Quan, T., Voorhees, J. J., & Fisher, G. J. (2018) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-018-0459-1 · Cited by 365 · see citing works

Multicomponent peptide assemblies

Raymond, D. M., & Nilsson, B. L. (2018) · Chemical Society Reviews · doi:10.1039/c8cs00115d · Cited by 348 · see citing works

Emerging roles of ECM remodeling processes in cancer

Mohan, V., Das, A., & Sagi, I. (2019) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2019.09.004 · Cited by 339 · see citing works

Mechanisms of Assembly and Remodeling of the Extracellular Matrix

Naba, A. (2024) · Nature reviews. Molecular cell biology · doi:10.1038/s41580-024-00767-3 · Cited by 311 · see citing works

Fibronectin: Molecular Structure, Fibrillar Structure and Mechanochemical Signaling

Dalton, C. J., & Lemmon, C. A. (2021) · Cells · doi:10.3390/cells10092443 · Cited by 325 · see citing works

Role of matrix metalloproteinases in the pathogenesis of idiopathic pulmonary fibrosis

Pardo, A., Cabrera, S., Maldonado, M., & Selman, M. (2016) · Respiratory Research · doi:10.1186/s12931-016-0343-6 · Cited by 307 · see citing works

Chimeric antigen receptor macrophage therapy for breast tumours mediated by targeting the tumour extracellular matrix

Zhang, W., Liu, L., Su, H., Liu, Q., Shen, J., Dai, H., Zheng, W., Lu, Y., Zhang, W., Bei, Y., et al. (2019) · British Journal of Cancer · doi:10.1038/s41416-019-0578-3 · Cited by 296 · see citing works

Extracellular matrix in lung development, homeostasis and disease

Zhou, Y., Horowitz, J. C., Naba, A., Ambalavanan, N., Atabai, K., Balestrini, J. L., Bitterman, P. B., CORLEY, R. A., Ding, B., Engler, A. J., et al. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.03.005 · Cited by 285 · see citing works

The Functional Role of Extracellular Matrix Proteins in Cancer

Popova, N. V., & Jücker, M. (2022) · Cancers · doi:10.3390/cancers14010238 · Cited by 277 · see citing works

The evolution of metazoan extracellular matrix

Hynes, R. O. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201109041 · Cited by 267 · see citing works

Therapeutic targets in lung tissue remodelling and fibrosis

Liu, G., Philp, A. M., Corte, T. J., Travis, M. A., Schilter, H. C., Hansbro, N. G., Burns, C. J., Eapen, M. S., Sohal, S. S., Burgess, J. K., et al. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.107839 · Cited by 251 · see citing works

Basement Membranes in Development and Disease

Sekiguchi, R., & Yamada, K. M. (2018) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2018.02.005 · Cited by 243 · see citing works

Identification, discrimination and heterogeneity of fibroblasts

Lendahl, U., Muhl, L., & Betsholtz, C. (2022) · Nature Communications · doi:10.1038/s41467-022-30633-9 · Cited by 242 · see citing works

Complexities of the glomerular basement membrane

Naylor, R. W., Morais, M., & Lennon, R. (2020) · Nature Reviews Nephrology · doi:10.1038/s41581-020-0329-y · Cited by 241 · see citing works

Extracellular matrix signatures of human primary metastatic colon cancers and their metastases to liver

Naba, A., Clauser, K. R., Whittaker, C. A., Carr, S. A., Tanabe, K. K., & Hynes, R. O. (2014) · BMC Cancer · doi:10.1186/1471-2407-14-518 · Cited by 238 · see citing works

Dermal extracellular matrix molecules in skin development, homeostasis, wound regeneration and diseases

Huang, J., Heng, S., Zhang, W., Liu, Y., Xia, T., Ji, C., & Zhang, L.-J. (2022) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2022.02.027 · Cited by 238 · see citing works

Future Directions in Idiopathic Pulmonary Fibrosis Research. An NHLBI Workshop Report

Blackwell, T. S., Tager, A. M., Borok, Z., Moore, B. B., Schwartz, D. A., Anstrom, K. J., Bar‐Joseph, Z., Bitterman, P. B., Blackburn, M. R., Bradford, W. S., et al. (2013) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201306-1141ws · Cited by 236 · see citing works

Integrins in Wound Healing

Koivisto, L., Heino, J., Häkkinen, L., & Larjava, H. (2013) · Advances in Wound Care · doi:10.1089/wound.2013.0436 · Cited by 234 · see citing works

New insights into fibrosis from the ECM degradation perspective: the macrophage-MMP-ECM interaction

Zhao, X., Chen, J., Sun, H., Zhang, Y., & Zou, D. (2022) · Cell & Bioscience · doi:10.1186/s13578-022-00856-w · Cited by 237 · see citing works

Lung Extracellular Matrix and Fibroblast Function

White, E. S. (2015) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201406-240mg · Cited by 231 · see citing works

Cancer drug resistance induced by EMT: novel therapeutic strategies

Rivas, J. D. L., Brozović, A., Izraely, S., Casas-Pais, A., Witz, I. P., & Figueroa, A. (2021) · Archives of Toxicology · doi:10.1007/s00204-021-03063-7 · Cited by 232 · see citing works

Extracellular matrix regulation of inflammation in the healthy and injured spinal cord

Gaudet, A. D., & Popovich, P. G. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2013.11.020 · Cited by 223 · see citing works

Active site specificity profiling of the matrix metalloproteinase family: Proteomic identification of 4300 cleavage sites by nine MMPs explored with structural and synthetic peptide cleavage analyses

Eckhard, U., Huesgen, P. F., Schilling, O., Bellac, C. L., Butler, G. S., Cox, J. H., Dufour, A., Goebeler, V., Kappelhoff, R., Keller, U. A. D., et al. (2015) · Matrix Biology · doi:10.1016/j.matbio.2015.09.003 · Cited by 208 · see citing works

Exuberant fibroblast activity compromises lung function via ADAMTS4

Boyd, D. F., Allen, E. K., Randolph, A. G., Guo, X.-Z. J., Weng, Y., Sanders, C. J., Bajracharya, R., Lee, N. K., Guy, C. S., Vogel, P., et al. (2020) · Nature · doi:10.1038/s41586-020-2877-5 · Cited by 212 · see citing works

The Gene Ontology knowledgebase in 2026

G, S. A. J. P. S. J. M. D. M. P. N. A. B. C. C. E. F., Aleksander, S. A., Balhoff, J., Carbon, S., Cherry, J., Ebert, D., Feuermann, M., Gaudet, P., Harris, N., Hill, D. P., et al. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf1292 · Cited by 261 · see citing works

Extracellular matrix scaffolding in angiogenesis and capillary homeostasis

Marchand, M., Monnot, C., Muller, L., & Germain, S. (2019) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2018.08.007 · Cited by 205 · see citing works

A basement membrane discovery pipeline uncovers network complexity, regulators, and human disease associations

Jayadev, R., Morais, M., Ellingford, J. M., Srinivasan, S., Naylor, R. W., Lawless, C., Li, A. S., Ingham, J., Hastie, E. L., Chi, Q., et al. (2022) · Science Advances · doi:10.1126/sciadv.abn2265 · Cited by 202 · see citing works

A complex interplay between the extracellular matrix and the innate immune response to microbial pathogens

Tomlin, H., & Piccinini, A. M. (2018) · Immunology · doi:10.1111/imm.12972 · Cited by 198 · see citing works

Extracellular Matrices and Cancer-Associated Fibroblasts: Targets for Cancer Diagnosis and Therapy?

Belhabib, I., Zaghdoudi, S., Lac, C., Bousquet, C., & Jean, C. (2021) · Cancers · doi:10.3390/cancers13143466 · Cited by 196 · see citing works

ECM-modulated cellular dynamics as a driving force for tissue morphogenesis

Daley, W. P., & Yamada, K. M. (2013) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2013.05.005 · Cited by 193 · see citing works

Endocrine Disruptors Leading to Obesity and Related Diseases

Petrakis, D., Vassilopoulou, L., Mamoulakis, C., Psycharakis, C., Anifantaki, A., Sifakis, S., Docea, A. O., Tsiaoussis, J., Makrigiannakis, A., & Tsatsakis, A. M. (2017) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph14101282 · Cited by 194 · see citing works

Complex mechanics of the heterogeneous extracellular matrix in cancer

Malandrino, A., Mak, M., Kamm, R. D., & Moeendarbary, E. (2018) · Extreme Mechanics Letters · doi:10.1016/j.eml.2018.02.003 · Cited by 192 · see citing works

Fibronectin and stem cell differentiation – lessons from chondrogenesis

Singh, P., & Schwarzbauer, J. E. (2012) · Journal of Cell Science · doi:10.1242/jcs.095786 · Cited by 191 · see citing works

Circulating tumor cells: from new biological insights to clinical practice

Gu, X., Wei, S., & Lv, X. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01938-6 · Cited by 196 · see citing works

From Structure to Phenotype: Impact of Collagen Alterations on Human Health

Arseni, L., Lombardi, A., & Orioli, D. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19051407 · Cited by 186 · see citing works

New intracellular activities of matrix metalloproteinases shine in the moonlight

Jobin, P. G., Butler, G. S., & Overall, C. M. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2017.05.013 · Cited by 184 · see citing works

Understanding the role of tissue-specific decellularized spinal cord matrix hydrogel for neural stem/progenitor cell microenvironment reconstruction and spinal cord injury

Xu, Y., Zhou, J., Liu, C., Zhang, S., Gao, F., Guo, W., Sun, X., Zhang, C., Li, H., Rao, Z., et al. (2020) · Biomaterials · doi:10.1016/j.biomaterials.2020.120596 · Cited by 183 · see citing works

Bi-allelic alterations in AEBP1 lead to defective collagen assembly and connective tissue structure resulting in a variant of Ehlers-Danlos syndrome

Blackburn, P. R., Xu, Z., Tumelty, K. E., Zhao, R. W., Monis, W. J., Harris, K. G., Gass, J. M., Cousin, M. A., Boczek, N. J., Mitkov, M. V., et al. (2018) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2018.02.018 · Cited by 176 · see citing works

Danger-Associated Molecular Patterns Derived From the Extracellular Matrix Provide Temporal Control of Innate Immunity

Frevert, C. W., Felgenhauer, J. L., Wygrecka, M., Nastase, M. V., & Schaefer, L. (2018) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155417740880 · Cited by 183 · see citing works

Comprehensive proteomic characterization of stem cell-derived extracellular matrices

Ragelle, H., Naba, A., Larson, B. L., Zhou, F., Miralem, P., Whittaker, C. A., Rosario, A. M. D., Langer, R., Hynes, R. O., & Anderson, D. G. (2017) · Biomaterials · doi:10.1016/j.biomaterials.2017.03.008 · Cited by 173 · see citing works

Pathological features of COVID-19-associated lung injury: a preliminary proteomics report based on clinical samples

Leng, L., Cao, R., Ma, J., Mou, D., Zhu, Y., Li, W., Lv, L., Gao, D., Zhang, S., Gong, F., et al. (2020) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-020-00355-9 · Cited by 168 · see citing works

The Extracellular Matrix: Its Composition, Function, Remodeling, and Role in Tumorigenesis

Dzobo, K., & Dandara, C. (2023) · Biomimetics · doi:10.3390/biomimetics8020146 · Cited by 209 · see citing works

The role of extracelluar matrix in osteosarcoma progression and metastasis

Cui, J., Dean, D. C., Hornicek, F. J., Chen, Z., & Duan, Z. (2020) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-020-01685-w · Cited by 170 · see citing works

Cerebrospinal fluid proteomics define the natural history of autosomal dominant Alzheimer’s disease

Johnson, E. C. B., Bian, S., Haque, R. U., Carter, E. K., Watson, C. M., Gordon, B. A., Ping, L., Duong, D. M., Epstein, M. P., McDade, E., et al. (2023) · Nature Medicine · doi:10.1038/s41591-023-02476-4 · Cited by 170 · see citing works

Biomimicry of microbial polysaccharide hydrogels for tissue engineering and regenerative medicine – A review

Ng, J. Y., Obuobi, S. A. O., Chua, M. L., Zhang, C., Hong, S., Kumar, Y., Gokhale, R. D., & Ee, P. L. R. (2020) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2020.116345 · Cited by 170 · see citing works

Carbon nanotubes leading the way forward in new generation 3D tissue engineering

Hopley, E. L., Salmasi, S., Kalaskar, D. M., & Seifalian, A. M. (2014) · Biotechnology Advances · doi:10.1016/j.biotechadv.2014.05.003 · Cited by 167 · see citing works

Tumor matrix remodeling and novel immunotherapies: the promise of matrix-derived immune biomarkers

Mushtaq, M. U., Papadas, A., Pagenkopf, A. C., Flietner, E., Morrow, Z. T., Chaudhary, S. G., & Asimakopoulos, F. A. (2018) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-018-0376-0 · Cited by 164 · see citing works

Overview of Extracellular Matrix

Mecham, R. P. (2012) · Current Protocols in Cell Biology · doi:10.1002/0471143030.cb1001s57 · Cited by 166 · see citing works

CRISPR-Cas-amplified urinary biomarkers for multiplexed and portable cancer diagnostics

Hao, L., Zhao, R. T., Welch, N. L., Tan, E. K. W., Zhong, Q., Harzallah, N. S., Ngambenjawong, C., Ko, H., Fleming, H. E., Sabeti, P. C., et al. (2023) · Nature Nanotechnology · doi:10.1038/s41565-023-01372-9 · Cited by 174 · see citing works

The cancer matrisome: From comprehensive characterization to biomarker discovery

Socovich, A. M., & Naba, A. (2018) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2018.06.005 · Cited by 158 · see citing works

From Low to High Saturation Magnetization in Magnetite Nanoparticles: The Crucial Role of the Molar Ratios Between the Chemicals

Hadadian, Y., Masoomi, H., Dinari, A., Ryu, C., Hwang, S.-J., Kim, S., Cho, B. K., Lee, J. Y., & Yoon, J. (2022) · ACS Omega · doi:10.1021/acsomega.2c01136 · Cited by 162 · see citing works

ECM formation and degradation during fibrosis, repair, and regeneration

Mayorca‐Guiliani, A. E., Leeming, D. J., Henriksen, K., Mortensen, J. H., Nielsen, S. H., Anstee, Q. M., Sanyal, A. J., Karsdal, M. A., & Schuppan, D. (2025) · npj Metabolic Health and Disease · doi:10.1038/s44324-025-00063-4 · Cited by 172 · see citing works

Recent advances and challenges in materials for 3D bioprinting

Mao, H., Yang, L., Zhu, H., Wu, L., Ji, P., Yang, J., & Gu, Z. (2020) · Progress in Natural Science Materials International · doi:10.1016/j.pnsc.2020.09.015 · Cited by 159 · see citing works

The bright side of fibroblasts: molecular signature and regenerative cues in major organs

Gomes, R. N., Manuel, F., & Nascimento, D. S. (2021) · npj Regenerative Medicine · doi:10.1038/s41536-021-00153-z · Cited by 180 · see citing works

Extracellular Matrix Cross-Linking Enhances Fibroblast Growth and Protects against Matrix Proteolysis in Lung Fibrosis

Philp, C. J., Siebeke, I., Clements, D., Miller, S., Habgood, A., John, A. E., Navaratnam, V. V., Hubbard, R., Jenkins, G. R., & Johnson, S. R. (2017) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2016-0379oc · Cited by 155 · see citing works

Gum Tragacanth (GT): A Versatile Biocompatible Material beyond Borders

Yazdi, M. E. T., Nazarnezhad, S., Mousavi, S., Amiri, M. S., Darroudi, M., Baino, F., & Kargozar, S. (2021) · Molecules · doi:10.3390/molecules26061510 · Cited by 154 · see citing works

Linking Oxidative Stress and DNA Damage to Changes in the Expression of Extracellular Matrix Components

Martins, S. G., Zilhão, R., Þorsteinsdóttir, S., & Carlos, A. R. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.673002 · Cited by 160 · see citing works

Decellularization for the retention of tissue niches

Moffat, D., Ye, K., & Jin, S. (2022) · Journal of Tissue Engineering · doi:10.1177/20417314221101151 · Cited by 152 · see citing works

The Proteolysis of ECM in Intervertebral Disc Degeneration

Liang, H., Luo, R., Li, G., Zhang, W., Song, Y., & Cao, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031715 · Cited by 151 · see citing works

An active role for basement membrane assembly and modification in tissue sculpting

Morrissey, M. A., & Sherwood, D. R. (2015) · Journal of Cell Science · doi:10.1242/jcs.168021 · Cited by 147 · see citing works

Dynamic matrisome: ECM remodeling factors licensing cancer progression and metastasis

Yuzhalin, A. E., Lim, S. Y., Kutikhin, A. G., & Gordon-Weeks, A. N. (2018) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2018.09.002 · Cited by 144 · see citing works

Polarity in Mammalian Epithelial MorphogenesisPreprint

Roignot, J., Xu, P., & Mostov, K. E. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a013789 · Cited by 146 · see citing works

Preparation and Use of Decellularized Extracellular Matrix for Tissue Engineering

McInnes, A. D., Moser, M., & Chen, D. (2022) · Journal of Functional Biomaterials · doi:10.3390/jfb13040240 · Cited by 141 · see citing works

Small intestinal submucosa extracellular matrix (CorMatrix®) in cardiovascular surgery: a systematic review

Nezhad, Z. M., Poncelet, A. J., de Kerchove, L., Gianello, P., Fervaille, C., & Khoury, G. A. E. (2016) · Interactive Cardiovascular and Thoracic Surgery · doi:10.1093/icvts/ivw020 · Cited by 143 · see citing works

Remodeling extracellular matrix based on functional covalent organic framework to enhance tumor photodynamic therapy

Wang, S., Chen, Z., Gao, F., Zhang, C., Zou, M., Ye, J., Zeng, X., & Zhang, X. (2020) · Biomaterials · doi:10.1016/j.biomaterials.2020.119772 · Cited by 143 · see citing works

Dynamic cell–matrix interactions modulate microbial biofilm and tissue 3D microenvironments

Koo, H., & Yamada, K. M. (2016) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2016.05.005 · Cited by 141 · see citing works

Cancer-specific PERK signaling drives invasion and metastasis through CREB3L1

Feng, Y., Jin, D. X., Sokol, E. S., Reinhardt, F., Miller, D. H., & Gupta, P. B. (2017) · Nature Communications · doi:10.1038/s41467-017-01052-y · Cited by 142 · see citing works

Polysaccharides for tissue engineering: Current landscape and future prospects

Tchobanian, A., Oosterwyck, H. V., & Fardim, P. (2018) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2018.10.039 · Cited by 139 · see citing works

Life and the matrix

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

An Overview of Extracellular Matrix Structure and Function

Engel, J., & Chiquet, M. (2010) · Springer eBooks · doi:10.1007/978-3-642-16555-9_1 · Cited by 26 · see citing works

The evolution of metazoan extracellular matrix

Hynes, R. O. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201109041 · Cited by 267 · see citing works

Evolution of the Metazoan Extracellular Matrix

Adams, J. C. (2013) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0024606 · Cited by 10 · see citing works

Extracellular Matrix Evolution: An Overview

Adams, J. C. (2013) · Biology of Extracellular Matrix · doi:10.1007/978-3-642-36002-2_1 · Cited by 16 · see citing works