Biologic Scaffolds

Exploring the full spectrum of macrophage activation

Mosser, D. M., & Edwards, J. P. (2008) · Nature Reviews Immunology · doi:10.1038/nri2448 · Cited by 9,144 · see citing works

The chemokine system in diverse forms of macrophage activation and polarization

MANTOVANI, A., SICA, A., SOZZANI, S., ALLAVENA, P., VECCHI, A., & LOCATI, M. (2004) · Trends in Immunology · doi:10.1016/j.it.2004.09.015 · Cited by 6,534 · see citing works

Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes

MANTOVANI, A., SOZZANI, S., LOCATI, M., ALLAVENA, P., & SICA, A. (2002) · Trends in Immunology · doi:10.1016/s1471-4906(02)02302-5 · Cited by 5,528 · see citing works

Monocyte and macrophage heterogeneity

Gordon, S., & Taylor, P. R. (2005) · Nature Reviews Immunology · doi:10.1038/nri1733 · Cited by 5,190 · see citing works

Foreign body reaction to biomaterials

Anderson, J. M., Rodriguez, A., & Chang, D. T. (2008) · Seminars in Immunology · doi:10.1016/j.smim.2007.11.004 · Cited by 5,138 · cited 6× · see citing works

A perivascular origin for mesenchymal stem cells in multiple human organs

Crisan, M., Yap, S., Casteilla, L., Chen, C.-W., Corselli, M., Park, T. S., Andriolo, G., Sun, B., Zheng, B., Zhang, L., et al. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2008.07.003 · Cited by 3,991 · see citing works

An overview of tissue and whole organ decellularization processes

Crapo, P. M., Gilbert, T. W., & Badylak, S. F. (2011) · Biomaterials · doi:10.1016/j.biomaterials.2011.01.057 · Cited by 3,591 · see citing works

The many faces of macrophage activation

Mosser, D. M. (2003) · Journal of Leukocyte Biology · doi:10.1189/jlb.0602325 · Cited by 1,902 · see citing works

Recruitment of Stem and Progenitor Cells from the Bone Marrow Niche Requires MMP-9 Mediated Release of Kit-Ligand

Heissig, B., Hattori, K., Dias, S., Friedrich, M., Ferris, B., Hackett, N. R., Crystal, R. G., Besmer, P., Lyden, D. C., Moore, M. A. S., et al. (2002) · Cell · doi:10.1016/s0092-8674(02)00754-7 · Cited by 1,744 · see citing works

Extracellular matrix as a biological scaffold material: Structure and function

BADYLAK, S., FREYTES, D., & GILBERT, T. (2009) · Acta Biomaterialia · doi:10.1016/j.actbio.2008.09.013 · Cited by 1,671 · see citing works

How does the extracellular matrix direct gene expression?

Bissell, M. J., Hall, H. G., & Parry, G. (1982) · Journal of Theoretical Biology · doi:10.1016/0022-5193(82)90388-5 · Cited by 1,522 · see citing works

MicroRNAs and other non-coding RNAs as targets for anticancer drug development

Ling, H. Y., Fabbri, M., & Călin, G. A. (2013) · Nature Reviews Drug Discovery · doi:10.1038/nrd4140 · Cited by 1,465 · 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

Immune responses to implants – a review of the implications for the design of immunomodulatory biomaterials

Franz, S., Rammelt, S., Scharnweber, D., & Simon, J. C. (2011) · Biomaterials · doi:10.1016/j.biomaterials.2011.05.078 · Cited by 1,391 · see citing works

Reprint of: Extracellular matrix as a biological scaffold material: Structure and function

Badylak, S. F., Freytes, D. O., & Gilbert, T. W. (2015) · Acta Biomaterialia · doi:10.1016/j.actbio.2015.07.016 · Cited by 1,361 · see citing works

Ligand Binding to Integrins

Plow, E. F., Haas, T. A., Zhang, L., Loftus, J. C., & Smith, J. W. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.r000003200 · Cited by 1,359 · see citing works

Regulatory interactions between muscle and the immune system during muscle regeneration

Tidball, J. G., & Villalta, S. A. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00735.2009 · Cited by 1,105 · see citing works

Hyaluronic acid based scaffolds for tissue engineering—A review

Collins, M. N., & Birkinshaw, C. (2012) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2012.10.028 · Cited by 1,094 · see citing works

Matricellular proteins: extracellular modulators of cell function

BORNSTEIN, P. K., & Sage, E. H. (2002) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(02)00361-7 · Cited by 966 · see citing works

Macrophage phenotype and remodeling outcomes in response to biologic scaffolds with and without a cellular component

Brown, B. N., Valentin, J. E., Stewart-Akers, A. M., McCabe, G. P., & Badylak, S. F. (2009) · Biomaterials · doi:10.1016/j.biomaterials.2008.11.040 · Cited by 896 · cited 8× · see citing works

Immune response to biologic scaffold materials

Badylak, S. F., & Gilbert, T. W. (2008) · Seminars in Immunology · doi:10.1016/j.smim.2007.11.003 · Cited by 857 · see citing works

Collagen scaffolds for tissue engineering

Glowacki, J., & Mizuno, S. (2007) · Biopolymers · doi:10.1002/bip.20871 · Cited by 798 · see citing works

Interaction of high molecular weight kininogen, factor XII, and fibrinogen in plasma at interfaces

Vroman, L., Adams, A., Fischer, G., & Munoz, P. (1980) · Blood · doi:10.1182/blood.v55.1.156.156 · Cited by 781 · see citing works

Xenogeneic extracellular matrix as a scaffold for tissue reconstruction

Badylak, S. F. (2004) · Transplant Immunology · doi:10.1016/j.trim.2003.12.016 · Cited by 747 · see citing works

Macrophage phenotype as a predictor of constructive remodeling following the implantation of biologically derived surgical mesh materials

Brown, B. N., Londono, R., Tottey, S., Zhang, L., Kukla, K. A., Wolf, M. T., Daly, K. A., Reing, J. E., & Badylak, S. F. (2012) · Acta Biomaterialia · doi:10.1016/j.actbio.2011.11.031 · Cited by 745 · see citing works

Macrophage Phenotype as a Determinant of Biologic Scaffold Remodeling

Badylak, S. F., Valentin, J. E., Ravindra, A. K., McCabe, G. P., & Stewart-Akers, A. M. (2008) · Tissue Engineering Part A · doi:10.1089/ten.tea.2007.0264 · Cited by 729 · see citing works

Methods of tissue decellularization used for preparation of biologic scaffolds and in vivo relevance

Keane, T. J., Swinehart, I. T., & Badylak, S. F. (2015) · Methods · doi:10.1016/j.ymeth.2015.03.005 · Cited by 670 · see citing works

Chitosan and Its Potential Use as a Scaffold for Tissue Engineering in Regenerative Medicine

Rodríguez-Vázquez, M., Vega-Ruiz, B., Ramos-Zúñiga, R., Saldaña-Koppel, D. A., & Quiñones-Olvera, L. F. (2015) · BioMed Research International · doi:10.1155/2015/821279 · Cited by 628 · see citing works

Consequences of ineffective decellularization of biologic scaffolds on the host response

Keane, T. J., Londono, R., Turner, N. J., & Badylak, S. F. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2011.10.054 · Cited by 613 · see citing works

Interaction between human natural anti-alpha-galactosyl immunoglobulin G and bacteria of the human flora

Galili, U., Mandrell, R. E., Hamadeh, R. M., Shohet, S., & Griffiss, J. M. (1988) · Infection and Immunity · doi:10.1128/iai.56.7.1730-1737.1988 · Cited by 549 · see citing works

Preparation and rheological characterization of a gel form of the porcine urinary bladder matrix

Freytes, D. O., Martin, J. D., Velankar, S., Lee, A. S., & Badylak, S. F. (2008) · Biomaterials · doi:10.1016/j.biomaterials.2007.12.014 · Cited by 531 · see citing works

The freezing step in lyophilization: Physico-chemical fundamentals, freezing methods and consequences on process performance and quality attributes of biopharmaceuticals

Kasper, J. C., & Frieß, W. (2011) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2011.03.010 · Cited by 527 · 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

PORCINE SMALL INTESTINE SUBMUCOSA AUGMENTATION OF SURGICAL REPAIR OF CHRONIC TWO-TENDON ROTATOR CUFF TEARS

Iannotti, J. P., Codsi, M. J., Kwon, Y. W., Derwin, K. A., Ciccone, J., & Brems, J. J. (2006) · Journal of Bone and Joint Surgery · doi:10.2106/jbjs.e.00524 · Cited by 479 · see citing works

An Acellular Biologic Scaffold Promotes Skeletal Muscle Formation in Mice and Humans with Volumetric Muscle Loss

Sicari, B. M., Rubin, J., Dearth, C. L., Wolf, M. T., Ambrosio, F., Boninger, M., Turner, N., Weber, D., Simpson, T. W., Wyse, A., et al. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3008085 · Cited by 476 · see citing works

The effects of processing methods upon mechanical and biologic properties of porcine dermal extracellular matrix scaffolds

Reing, J. E., Brown, B. N., Daly, K. A., Freund, J. M., Gilbert, T. W., Hsiong, S. X., Huber, A., Kullas, K. E., Tottey, S., Wolf, M. T., et al. (2010) · Biomaterials · doi:10.1016/j.biomaterials.2010.07.083 · Cited by 475 · see citing works

Decellularization protocols of porcine heart valves differ importantly in efficiency of cell removal and susceptibility of the matrix to recellularization with human vascular cells

Rieder, E., Kasimir, M.-T., Silberhumer, G., Seebacher, G., Wolner, E., Simon, P., & Weigel, G. (2004) · The Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/j.jtcvs.2003.06.017 · Cited by 430 · see citing works

EXTRACELLULAR MATRIX BIOSCAFFOLDS FOR ORTHOPAEDIC APPLICATIONS

Valentin, J. E., Badylak, J. S., McCabe, G. P., & Badylak, S. F. (2006) · Journal of Bone and Joint Surgery · doi:10.2106/jbjs.e.01008 · Cited by 410 · see citing works

Volumetric muscle loss

Grogan, B. F., & Hsu, J. R. (2011) · American Academy of Orthopaedic Surgeon · doi:10.5435/00124635-201102001-00007 · Cited by 402 · see citing works

Ethylene oxide sterilization of medical devices: A review

Mendes, G. C., Brandão, T. R. S., & Silva, C. L. M. (2007) · American Journal of Infection Control · doi:10.1016/j.ajic.2006.10.014 · Cited by 398 · see citing works

XENOGENEIC EXTRACELLULAR MATRIX GRAFTS ELICIT A TH2-RESTRICTED IMMUNE RESPONSE1

Allman, A. J., McPherson, T. B., Badylak, S. F., Merrill, L. C., Kallakury, B., Sheehan, C., Raeder, R. H., & Metzger, D. W. (2001) · Transplantation · doi:10.1097/00007890-200106150-00024 · Cited by 388 · see citing works

Effectiveness of an extracellular matrix graft (OASIS Wound Matrix) in the treatment of chronic leg ulcers: A randomized clinical trial

Mostow, E. N., Haraway, G. D., Dalsing, M. C., Hodde, J. P., & King, D. W. (2005) · Journal of Vascular Surgery · doi:10.1016/j.jvs.2005.01.042 · Cited by 387 · see citing works

Degradation Products of Extracellular Matrix Affect Cell Migration and Proliferation

Reing, J. E., Zhang, L., Myers-Irvin, J., Cordero, K. E., Freytes, D. O., Heber-Katz, E., Bedelbaeva, K., McIntosh, D., Dewilde, A., Braunhut, S. J., et al. (2009) · Tissue Engineering Part A · doi:10.1089/ten.tea.2007.0425 · Cited by 387 · see citing works

Matrix-bound nanovesicles within ECM bioscaffolds

Huleihel, L., Hussey, G. S., Naranjo, J. D., Zhang, L., Dziki, J. L., Turner, N. J., Stolz, D. B., & Badylak, S. F. (2016) · Science Advances · doi:10.1126/sciadv.1600502 · Cited by 387 · see citing works

Influence of Acellular Natural Lung Matrix on Murine Embryonic Stem Cell Differentiation and Tissue Formation

Cortiella, J., Niles, J. A., Cantu, A., Brettler, A. C., Pham, A. N., Vargas, G., Winston, S., Wang, J. P., Walls, S., & Nichols, J. E. (2010) · Tissue Engineering Part A · doi:10.1089/ten.tea.2009.0730 · Cited by 381 · see citing works

Embryonic Stem Cells Proliferate and Differentiate when Seeded into Kidney Scaffolds

Ross, E. A., Williams, M. J., Hamazaki, T., Terada, N., Clapp, W. L., Adin, C. A., Ellison, G. W., Jorgensen, M. J., & Batich, C. D. (2009) · Journal of the American Society of Nephrology · doi:10.1681/asn.2008111196 · Cited by 380 · see citing works

Extracellular matrix: A gatekeeper in the transition from dormancy to metastatic growth

Barkan, D., Green, J. E., & Chambers, A. F. (2010) · European Journal of Cancer · doi:10.1016/j.ejca.2010.02.027 · Cited by 378 · see citing works

Human Allograft Limbal Transplantation for Corneal Surface Reconstruction

Tsai, R. J.-F., & Tseng, S. C. G. (1994) · Cornea · doi:10.1097/00003226-199409000-00003 · Cited by 377 · see citing works

Catheter-Deliverable Hydrogel Derived From Decellularized Ventricular Extracellular Matrix Increases Endogenous Cardiomyocytes and Preserves Cardiac Function Post-Myocardial Infarction

Singelyn, J. M., Sundaramurthy, P., Johnson, T. D., Schup-Magoffin, P. J., Hu, D. P., Faulk, D. M., Wang, J. C. Y., Mayle, K. M., Bartels, K., Salvatore, M. A., et al. (2012) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2011.10.888 · Cited by 374 · see citing works

Macrophage Participation in the Degradation and Remodeling of Extracellular Matrix Scaffolds

Valentin, J. E., Stewart-Akers, A. M., Gilbert, T. W., & Badylak, S. F. (2009) · Tissue Engineering Part A · doi:10.1089/ten.tea.2008.0419 · Cited by 356 · see citing works

AngiogenesisPreprint

Senger, D. R., & Davis, G. E. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005090 · Cited by 351 · see citing works

Vascular Endothelial Growth Factor in Porcine-Derived Extracellular Matrix

Hodde, J. P., Record, R. D., Liang, H.-L., & Badylak, S. F. (2001) · Endothelium · doi:10.3109/10623320109063154 · Cited by 348 · see citing works

Cell mechanics: principles, practices, and prospects

Moeendarbary, E., & Harris, A. R. (2014) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1275 · Cited by 346 · see citing works

A simple, versatile, nondisruptive method for the isolation of morphologically and chemically pure basement membranes from several tissues

Meezan, E., Hjelle, J. T., Brendel, K., & Carlson, E. C. (1975) · Life Sciences · doi:10.1016/0024-3205(75)90119-8 · Cited by 334 · see citing works

A Whole-Organ Regenerative Medicine Approach for Liver Replacement

Soto-Gutierrez, A., Zhang, L., Medberry, C., Fukumitsu, K., Faulk, D., Jiang, H., Reing, J., Gramignoli, R., Komori, J., Ross, M., et al. (2011) · Tissue Engineering Part C: Methods · doi:10.1089/ten.tec.2010.0698 · Cited by 311 · see citing works

Decellularized Allogeneic and Xenogeneic Tissue as a Bioscaffold for Regenerative Medicine: Factors that Influence the Host Response

Badylak, S. F. (2014) · Annals of Biomedical Engineering · doi:10.1007/s10439-013-0963-7 · Cited by 307 · see citing works

The Many Alternative Faces of Macrophage Activation

Hume, D. A. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00370 · Cited by 303 · see citing works

Perivascular cells for regenerative medicine

Crisan, M., Corselli, M., Chen, W. C. W., & Péault, B. (2012) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2012.01617.x · Cited by 299 · see citing works

Esophageal Reconstruction with ECM and Muscle Tissue in a Dog Model

Badylak, S. F., Vorp, D. A., Spievack, A. R., Simmons-Byrd, A., Hanke, J., Freytes, D. O., Thapa, A., Gilbert, T. W., & Nieponice, A. (2005) · Journal of Surgical Research · doi:10.1016/j.jss.2005.03.002 · Cited by 291 · see citing works

Chondrogenic Differentiation of Adipose-Derived Adult Stem Cells by a Porous Scaffold Derived from Native Articular Cartilage Extracellular Matrix

Cheng, N., Estes, B. T., Awad, H. A., & Guilak, F. (2008) · Tissue Engineering Part A · doi:10.1089/ten.tea.2008.0253 · Cited by 290 · see citing works

Hydrogels derived from demineralized and decellularized bone extracellular matrix

Sawkins, M. J., Bowen, W., Dhadda, P., Markides, H., Sidney, L. E., Taylor, A. J., Rose, F. R. A. J., Badylak, S. F., Shakesheff, K. M., & White, L. J. (2013) · Acta Biomaterialia · doi:10.1016/j.actbio.2013.04.029 · Cited by 282 · see citing works

Maintenance of Human Hepatocyte Function In Vitro by Liver-Derived Extracellular Matrix Gels

Sellaro, T. L., Ranade, A. R., Faulk, D. M., McCabe, G. P., Dorko, K., Badylak, S. F., & Strom, S. C. (2009) · Tissue Engineering Part A · doi:10.1089/ten.tea.2008.0587 · Cited by 276 · see citing works

Degradation and Remodeling of Small Intestinal Submucosa in Canine Achilles Tendon Repair

Gilbert, T. W., Stewart‐Akers, A. M., Simmons-Byrd, A., & Badylak, S. F. (2007) · Journal of Bone and Joint Surgery · doi:10.2106/jbjs.e.00742 · Cited by 274 · see citing works

Biologic scaffolds composed of central nervous system extracellular matrix

Crapo, P. M., Medberry, C. J., Reing, J. E., Tottey, S., van der Merwe, Y., Jones, K. E., & Badylak, S. F. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2012.01.044 · Cited by 263 · see citing works

Biologic scaffold composed of skeletal muscle extracellular matrix

Wolf, M. T., Daly, K. A., Reing, J. E., & Badylak, S. F. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2011.12.055 · Cited by 259 · see citing works

HMG1 and 2: architectural DNA-binding proteins

Thomas, J. O. (2001) · Biochemical Society Transactions · doi:10.1042/bst0290395 · Cited by 254 · see citing works

Sterilization using high-pressure carbon dioxide

Zhang, J., Davis, T. A., Matthews, M., Drews, M. J., LaBerge, M., & An, Y. H. (2006) · The Journal of Supercritical Fluids · doi:10.1016/j.supflu.2005.05.005 · Cited by 243 · see citing works

Biaxial strength of multilaminated extracellular matrix scaffolds

Freytes, D. O., Badylak, S. F., Webster, T. J., Geddes, L. A., & Rundell, A. E. (2003) · Biomaterials · doi:10.1016/j.biomaterials.2003.09.015 · Cited by 235 · see citing works

Mesenchymal stem cell migration is regulated by fibronectin through α5β1-integrin-mediated activation of PDGFR-β and potentiation of growth factor signals

Veevers, J., Ball, S. G., Shuttleworth, A., & Kielty, C. M. (2011) · Journal of Cell Science · doi:10.1242/jcs.076935 · Cited by 234 · see citing works

Biologic Scaffolds for Regenerative Medicine: Mechanisms of In vivo Remodeling

Londoño, R., & Badylak, S. F. (2014) · Annals of Biomedical Engineering · doi:10.1007/s10439-014-1103-8 · Cited by 232 · see citing works

Strength over Time of a Resorbable Bioscaffold for Body Wall Repair in a Dog Model

Badylak, S. F., Kokini, K., Tullius, B., & Whitson, B. A. (2001) · Journal of Surgical Research · doi:10.1006/jsre.2001.6176 · Cited by 231 · see citing works

Extracellular matrix-derived products modulate endothelial and progenitor cell migration and proliferation in vitro and stimulate regenerative healing in vivo

Vorotnikova, E., McIntosh, D., Dewilde, A. H., Zhang, J., Reing, J. E., Zhang, L., Cordero, K. E., Bedelbaeva, K., Gourevitch, D. L., Heber‐Katz, E., et al. (2010) · Matrix Biology · doi:10.1016/j.matbio.2010.08.007 · Cited by 231 · see citing works

Dermal Matrices and Bioengineered Skin Substitutes: A Critical Review of Current Options

Debels, H., Hamdi, M., Abberton, K., & Morrison, W. (2015) · Plastic and Reconstructive Surgery Global Open · doi:10.1097/gox.0000000000000219 · Cited by 227 · see citing works

The effects of collagen concentration and crosslink density on the biological, structural and mechanical properties of collagen-GAG scaffolds for bone tissue engineering

Tierney, C. M., Haugh, M. G., Liedl, J., Mulcahy, F., Hayes, B., & O’Brien, F. J. (2008) · Journal of the mechanical behavior of biomedical materials/Journal of mechanical behavior of biomedical materials · doi:10.1016/j.jmbbm.2008.08.007 · Cited by 223 · see citing works

Esophageal Preservation in Five Male Patients After Endoscopic Inner-Layer Circumferential Resection in the Setting of Superficial Cancer: A Regenerative Medicine Approach with a Biologic Scaffold

Badylak, S. F., Hoppo, T., Nieponice, A., Gilbert, T. W., Davison, J. M., & Jobe, B. A. (2011) · Tissue Engineering Part A · doi:10.1089/ten.tea.2010.0739 · Cited by 222 · see citing works

The effect of detergents on the basement membrane complex of a biologic scaffold material

Faulk, D. M., Carruthers, C. A., Warner, H. J., Kramer, C. R., Reing, J. E., Zhang, L., D’Amore, A., & Badylak, S. F. (2013) · Acta Biomaterialia · doi:10.1016/j.actbio.2013.09.006 · Cited by 220 · see citing works

An acellular biologic scaffold treatment for volumetric muscle loss: Results of a 13-patient cohort study

Dziki, J., Badylak, S., Yabroudi, M., Sicari, B., Ambrosio, F., Stearns, K., Turner, N., Wyse, A., Boninger, M. L., Brown, E. H. P., et al. (2016) · npj Regenerative Medicine · doi:10.1038/npjregenmed.2016.8 · Cited by 219 · see citing works

Chemoattraction of Progenitor Cells by Remodeling Extracellular Matrix Scaffolds

Beattie, A. J., Gilbert, T. W., Guyot, J. P., Yates, A. J., & Badylak, S. F. (2008) · Tissue Engineering Part A · doi:10.1089/ten.tea.2008.0162 · Cited by 218 · see citing works

ECM Remodeling Regulates Angiogenesis: Endothelial Integrins Look for New Ligands

Stupack, D. G., & Cheresh, D. A. (2002) · Science Signaling · doi:10.1126/stke.2002.119.pe7 · Cited by 217 · see citing works

Integrins in cell adhesion and signaling.

Akiyama, S. K. (1996) · PubMed · Cited by 217 · see citing works

Inflammatory and alternatively activated human macrophages attract vessel-associated stem cells, relying on separate HMGB1- and MMP-9-dependent pathways

Lolmede, K., Campana, L., Vezzoli, M., Bosurgi, L., Tonlorenzi, R., Clementi, E., Bianchi, M. E., Cossu, G., Manfredi, A. A., Brunelli, S., et al. (2009) · Journal of Leukocyte Biology · doi:10.1189/jlb.0908579 · Cited by 216 · see citing works

Injectable hydrogel scaffold from decellularized human lipoaspirate

Young, D. A., Ibrahim, D. O., Hu, D. P., & Christman, K. L. (2010) · Acta Biomaterialia · doi:10.1016/j.actbio.2010.09.035 · Cited by 213 · see citing works

Macrophage activation and skeletal muscle healing following traumatic injury

Novak, M. L., Weinheimer-Haus, E. M., & Koh, T. J. (2013) · The Journal of Pathology · doi:10.1002/path.4301 · Cited by 208 · see citing works

Low-Molecular-Weight Peptides Derived from Extracellular Matrix as Chemoattractants for Primary Endothelial Cells

Li, F., Li, W., Johnson, S. A., Ingram, D. A., Yöder, M. C., & Badylak, S. F. (2004) · Endothelium · doi:10.1080/10623320490512390 · Cited by 197 · see citing works

Basement‐membrane heparan sulfate proteoglycan binds to laminin by its heparan sulfate chains and to nidogen by sites in the protein core

Battaglia, C., Mayer, U., Aumailley, M., & Timpl, R. (1992) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1992.tb17195.x · Cited by 192 · see citing works

Xenogeneic Extracellular Matrix as an Inductive Scaffold for Regeneration of a Functioning Musculotendinous Junction

Turner, N. J., Yates, A. J., Weber, D. J., Qureshi, I. R., Stolz, D. B., Gilbert, T. W., & Badylak, S. F. (2010) · Tissue Engineering Part A · doi:10.1089/ten.tea.2010.0169 · Cited by 188 · see citing works

Injectable extracellular matrix derived hydrogel provides a platform for enhanced retention and delivery of a heparin-binding growth factor

Seif-Naraghi, S. B., Horn, D., Schup-Magoffin, P. J., & Christman, K. L. (2012) · Acta Biomaterialia · doi:10.1016/j.actbio.2012.06.030 · Cited by 187 · see citing works

The influence of extracellular matrix derived from skeletal muscle tissue on the proliferation and differentiation of myogenic progenitor cells ex vivo

Stern, M. M., Myers, R. L., Hammam, N., Stern, K. A., Eberli, D., Kritchevsky, S. B., Söker, S., & Dyke, M. E. V. (2009) · Biomaterials · doi:10.1016/j.biomaterials.2008.12.069 · Cited by 185 · see citing works

Surface characterization of extracellular matrix scaffolds

Brown, B. N., Barnes, C. A., Kasick, R. T., Michel, R., Gilbert, T. W., Beer–Stolz, D., Castner, D. G., Ratner, B. D., & Badylak, S. F. (2009) · Biomaterials · doi:10.1016/j.biomaterials.2009.09.061 · Cited by 180 · see citing works

Recruitment of Progenitor Cells by an Extracellular Matrix Cryptic Peptide in a Mouse Model of Digit Amputation

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Acellular human heart matrix: A critical step toward whole heart grafts

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Evaluation of licofelone as an adjunct anti-inflammatory therapy to biologic scaffolds in the treatment of volumetric muscle loss

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Tissue Engineering the Pinna: Comparison and Characterization of Human Decellularized Auricular Biological Scaffolds

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Injectable Scaffolds for Adipose Tissue Reconstruction

Pruzzo, V., Bonomi, F., Limido, E., Weinzierl, A., Harder, Y., & Laschke, M. W. (2026) · Gels · doi:10.3390/gels12010081 · Cited by 5 · see citing works

Optimizing natural human-derived decellularized tissue materials for periodontal bone defect repair

Zhang, X., Wang, H., Cao, Y., Liu, L., Zhang, Z., Liu, J., Mu, S.-H., Yuan, Y., Cai, X., Sui, B., et al. (2025) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2025.151297 · Cited by 5 · see citing works

A collagen-based amniotic membrane scaffold combined with photobiomodulation accelerates wound repair in diabetic rats through modulation of inflammation and tissue regeneration

Hjazi, A. (2025) · Tissue and Cell · doi:10.1016/j.tice.2025.103063 · Cited by 5 · see citing works

Interdisciplinary Methods for Zoonotic Tissue Acellularization for Natural Heart Valve Substitute of Biomimetic Materials

Major, R., Kopernik, M., Ostrowski, R., Wilczek, P., Bartkowiak, A., Szawiraacz, K., LIS, G. J., Lekki, J., Gawlikowski, M., & Major, Ł. (2022) · Materials · doi:10.3390/ma15072594 · Cited by 5 · see citing works

Tissue Engineering Scaffolds: The Importance of Collagen

Correa-Araujo, L., Lara-Bertrand, A. L., & Silva-Cote, I. (2024) · Biochemistry · doi:10.5772/intechopen.1004077 · Cited by 5 · see citing works

Decellularization of Extracellular Matrix from Equine Skeletal Muscle

Miranda, C. M. F. D. C., Therrien, J., Leonel, L., Smith, O. E., Miglino, M. A., & Smith, L. C. (2020) · Journal of Equine Veterinary Science · doi:10.1016/j.jevs.2020.102962 · Cited by 5 · see citing works

AXTEX-4D: A Three-Dimensional Ex Vivo Platform for Preclinical Investigations of Immunotherapy Agents

Baru, A., Sharma, S., Purakayastha, B. P. D., Khan, S. M., Mazumder, S., Gupta, R., Kundu, P. K., & Arora, N. M. (2021) · Assay and Drug Development Technologies · doi:10.1089/adt.2021.031 · Cited by 5 · see citing works

Structural and biomechanical characterizations of acellular porcine mitral valve scaffolds: anterior leaflets, posterior leaflets, and chordae tendineae

Wang, B., Sierad, L. N., Mercuri, J. J., Simionescu, A., Simionescu, D. T., Williams, L. N., Vela, R. J., Bajona, P., Peltz, M., Ramaswamy, S. D., et al. (2022) · Engineered Regeneration · doi:10.1016/j.engreg.2022.08.003 · Cited by 5 · see citing works

Advancing Soft Tissue Reconstruction with a Ready-to-Use Human Adipose Allograft

Fanniel, V., Atawneh, I., Savoie, J., Izaguirre-Ramirez, M., Marquez, J., Khorsandi, C., & Hill, S. (2025) · Bioengineering · doi:10.3390/bioengineering12060612 · Cited by 4 · see citing works

Proposing Novel Biological Scaffolds for the Regeneration of the Dura Mater

monazah, M. M., Alimohammadi, E., Rostaminasab, G., Zarrintaj, P., & Rezakhani, L. (2024) · Polymers for Advanced Technologies · doi:10.1002/pat.6602 · Cited by 4 · see citing works

Advances in preparation of acellular human dermis for tissue banking and transplantation

Stern, I., Barrera, V., Randles, M. J., & Rooney, P. (2024) · Cell and Tissue Banking · doi:10.1007/s10561-024-10153-0 · Cited by 4 · see citing works

Comparative Analysis of Hydrogels From Porcine Extracellular Matrix for 3D Bioprinting of Adipose Tissue

Füge, L., Schüssler, F., Gerhardus, J. S., Schwab, R. M., Harms, G. S., Hasenburg, A., Blaeser, A., Brenner, W., & Peters, K. (2025) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.37832 · Cited by 4 · see citing works

Decellularizing Bone Tissue: Various Protocols

Emami, A., & Izadi, E. (2024) · Regenerative Engineering and Translational Medicine · doi:10.1007/s40883-024-00375-9 · Cited by 4 · see citing works

Effect of Hyaluronic Acid on the Acceleration of Bone Fracture Healing: A Systematic Review

Surroca, H. F., Pardo, E. C., Andrés, L. R., Nieto-González, E., Ferrer‐Torregrosa, J., & García, E. N. (2025) · Biomedicines · doi:10.3390/biomedicines13061353 · Cited by 4 · see citing works

Utility of Air Bladder-Derived Nanostructured ECM for Tissue Regeneration

Wang, J., Chen, J., Ran, Y., He, Q., Jiang, T., Li, W., & Yu, X. (2020) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2020.553529 · Cited by 4 · see citing works

Nanomaterial-Based Bio Scaffolds for Enhanced Biomedical Applications

Madathil, B. K., Kumar, P. R. A., Thomas, V., & Velayudhan, S. (2021) · Springer eBooks · doi:10.1007/978-3-030-67223-2_7 · Cited by 4 · see citing works

Perpendicular implantation of porcine trachea extracellular matrix for enhanced xenogeneic scaffold surface epithelialization in a canine model

Kato, A., Go, T., Otsuki, Y., Yokota, N., Soo, C. S., Misaki, N., Yajima, T., & Yokomise, H. (2023) · Frontiers in Surgery · doi:10.3389/fsurg.2022.1089403 · Cited by 3 · see citing works

Physicochemical Decellularization of Bovine Pericardium: Effects on DNA Elimination, Extracellular Matrix Preservation, and Biocompatibility

Filho, R. C. G., Martinez, A. M., Calmon, M. F., Tiera, M. J., Alvares, D. S., Agreli, G., & Nery, J. G. (2024) · Waste and Biomass Valorization · doi:10.1007/s12649-024-02465-9 · Cited by 3 · see citing works

Nanotechnologies, Biomaterials, and Scaffolds

Peng, T., Maity, A., & Grande, D. A. (2025) · Springer eBooks · doi:10.1007/978-3-031-84693-9_33 · Cited by 3 · see citing works

Bioactive materials for clinical applications of soft tissue regeneration

(2024) · Elsevier eBooks · doi:10.1016/b978-0-323-99998-4.00004-3 · Cited by 2 · see citing works

Sustainable Biomaterials: Turning Food Waste into Advanced Regenerative Technology

Dempsey, S. G., Young, D. A., Veale, R. W. F., & May, B. C. H. (2025) · Biomedical engineering · doi:10.5772/intechopen.1010994 · Cited by 2 · see citing works

Advances in Biomaterials for Tissue Regeneration: From Scaffold Design to CAP-Enabled Interfaces and AI-Driven Optimization

Gaudio, L. D., Lattanzio, S., Pietro, R. D., & Sancilio, S. (2026) · Biomimetics · doi:10.3390/biomimetics11050330 · Cited by 2 · see citing works

Extracellular Matrix-Based Biomaterials and Their Influence Upon Cell Behavior

Cramer, M. C., & Badylak, S. F. (2020) · Annals of Biomedical Engineering · doi:10.1007/s10439-019-02408-9 · Cited by 196 · see citing works

Decellularized Allogeneic and Xenogeneic Tissue as a Bioscaffold for Regenerative Medicine: Factors that Influence the Host Response

Badylak, S. F. (2014) · Annals of Biomedical Engineering · doi:10.1007/s10439-013-0963-7 · Cited by 307 · see citing works

Xenogeneic extracellular matrix as a scaffold for tissue reconstruction

Badylak, S. F. (2004) · Transplant Immunology · doi:10.1016/j.trim.2003.12.016 · Cited by 747 · see citing works

Extracellular matrix as a bioscaffold for tissue engineering

Sicari, B. M., Londoño, R., Dziki, J. L., & Badylak, S. F. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-824459-3.00005-6 · Cited by 10 · see citing works

Biologic Scaffolds for Regenerative Medicine: Mechanisms of In vivo Remodeling

Londoño, R., & Badylak, S. F. (2014) · Annals of Biomedical Engineering · doi:10.1007/s10439-014-1103-8 · Cited by 232 · see citing works