Fibroblast biology in three-dimensional collagen matrices

Myofibroblasts and mechano-regulation of connective tissue remodelling

Tomasek, J. J., Gabbiani, G., Hinz, B., Chaponnier, C., & Brown, R. A. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm809 · Cited by 4,290 · see citing works

Compensation mechanism in tumor cell migration

Wolf, K., Mazo, I. B., Leung, H. C. H., Engelke, K., von Andrian, U. H., Deryugina, E. I., Strongin, A. Y., Bröcker, E., & Friedl, P. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200209006 · Cited by 1,392 · see citing works

Alpha-Smooth Muscle Actin Expression Upregulates Fibroblast Contractile Activity

Hinz, B., Celetta, G., Tomasek, J. J., Gabbiani, G., & Chaponnier, C. (2001) · Molecular Biology of the Cell · doi:10.1091/mbc.12.9.2730 · Cited by 1,288 · see citing works

Fibroblasts, myofibroblasts, and wound contraction

Grinnell, F. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.124.4.401 · Cited by 1,141 · see citing works

Living Tissue Formed in Vitro and Accepted as Skin-Equivalent Tissue of Full Thickness

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Plasma Membrane Repair Is Mediated by Ca2+-Regulated Exocytosis of Lysosomes

Reddy, A. J., Caler, E. V., & Andrews, N. W. (2001) · Cell · doi:10.1016/s0092-8674(01)00421-4 · Cited by 1,043 · see citing works

RHO GTPASES in neuronal morphogenesis

Luo, L. (2000) · Nature reviews. Neuroscience · doi:10.1038/35044547 · Cited by 985 · see citing works

Mechanotransduction in bone—role of the lacunocanalicular network

Burger, E. H., & Klein‐Nulend, J. (1999) · The FASEB Journal · doi:10.1096/fasebj.13.9001.s101 · Cited by 897 · see citing works

Cell interactions with three-dimensional matrices

Cukierman, E., Pankov, R. G., & Yamada, K. M. (2002) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(02)00364-2 · Cited by 889 · see citing works

The Role of Apoptosis in Creating and Maintaining Luminal Space within Normal and Oncogene-Expressing Mammary Acini

Debnath, J., Mills, K. R., Collins, N. L., Reginato, M. J., Muthuswamy, S. K., & Brugge, J. S. (2002) · Cell · doi:10.1016/s0092-8674(02)01001-2 · Cited by 763 · see citing works

The biology of cell locomotion within three-dimensional extracellular matrix

Friedl, P., & Br�cker, E.-B. (2000) · Cellular and Molecular Life Sciences · doi:10.1007/s000180050498 · Cited by 651 · see citing works

Mechanical Tension Controls Granulation Tissue Contractile Activity and Myofibroblast Differentiation

Hinz, B., Mastrangelo, D., Iselin, C. E., Chaponnier, C., & Gabbiani, G. (2001) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)61776-2 · Cited by 638 · see citing works

Tensile Mechanical Properties of Three-Dimensional Type I Collagen Extracellular Matrices With Varied Microstructure

Roeder, B. A., Kokini, K., Sturgis, J. E., Robinson, J. P., & Voytik-Harbin, S. L. (2002) · Journal of Biomechanical Engineering · doi:10.1115/1.1449904 · Cited by 620 · see citing works

Life's Irreducible Structure

Polanyi, M. F. D. (1968) · Science · doi:10.1126/science.160.3834.1308 · Cited by 617 · see citing works

Mechanotransduction: All Signals Point to Cytoskeleton, Matrix, and Integrins

Alenghat, F. J., & Ingber, D. E. (2002) · Science s STKE · doi:10.1126/stke.2002.119.pe6 · Cited by 498 · see citing works

Transforming Growth Factor-β1 Promotes the Morphological and Functional Differentiation of the Myofibroblast

Vaughan, M. B., Howard, E. W., & Tomasek, J. J. (2000) · Experimental Cell Research · doi:10.1006/excr.2000.4869 · Cited by 468 · see citing works

The Compliance of Collagen Gels Regulates Transforming Growth Factor-β Induction of α-Smooth Muscle Actin in Fibroblasts

Arora, P. D., Narani, N., & McCulloch, C. A. (1999) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)65334-5 · Cited by 465 · see citing works

Fibroblast–collagen-matrix contraction: growth-factor signalling and mechanical loading

Grinnell, F. (2000) · Trends in Cell Biology · doi:10.1016/s0962-8924(00)01802-x · Cited by 405 · see citing works

Collagen-based biomaterials as 3D scaffold for cell cultures: applications for tissue engineering and gene therapy

Chevallay, B., & Herbage, D. (2000) · Medical & Biological Engineering & Computing · doi:10.1007/bf02344779 · Cited by 403 · see citing works

Exploring the Neighborhood

Geiger, B., & Bershadsky, A. D. (2002) · Cell · doi:10.1016/s0092-8674(02)00831-0 · Cited by 402 · see citing works

The interplay of matrix metalloproteinases, morphogens and growth factors is necessary for branching of mammary epithelial cells

Simian, M., Hirai, Y., Navre, M., Werb, Z., Lochter, A., & Bissell, M. J. (2001) · Development · doi:10.1242/dev.128.16.3117 · Cited by 392 · see citing works

Mechanobiology of force transduction in dermal tissue

Silver, F. H., Siperko, L. M., & Seehra, G. P. (2003) · Skin Research and Technology · doi:10.1034/j.1600-0846.2003.00358.x · Cited by 380 · see citing works

Fibroblasts in Mechanically Stressed Collagen Lattices Assume a “Synthetic” Phenotype

Kessler, D., Dethlefsen, S., Haase, I., Plomann, M., Hirche, F., Krieg, T., & Eckes, B. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m101602200 · Cited by 369 · see citing works

Rho GTPases in growth cone guidance

Dickson, B. J. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00180-x · Cited by 362 · see citing works

Loss, Restoration, and Maintenance of Plasma Membrane Integrity

McNeil, P. L., & Steinhardt, R. A. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.137.1.1 · Cited by 339 · see citing works

β1 Integrin-mediated collagen gel contraction is stimulated by PDGF

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In vivo co-distribution of fibronectin and actin fibers in granulation tissue: immunofluorescence and electron microscope studies of the fibronexus at the myofibroblast surface.

Singer, I. I., Kawka, D. W., Kazazis, D. M., & Clark, R. A. F. (1984) · The Journal of Cell Biology · doi:10.1083/jcb.98.6.2091 · Cited by 260 · see citing works

Flexible substrata for the detection of cellular traction forces

Beningo, K. A., & Wang, Y.-L. (2002) · Trends in Cell Biology · doi:10.1016/s0962-8924(01)02205-x · Cited by 258 · see citing works

Modulation of Fibroblast Morphology and Adhesion during Collagen Matrix Remodeling

Tamaríz, E., & Grinnell, F. (2002) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-05-0291 · Cited by 253 · see citing works

Cell Mechanics Studied by a Reconstituted Model Tissue

Wakatsuki, T., Kolodney, M. S., Zahalak, G. I., & Elson, E. L. (2000) · Biophysical Journal · doi:10.1016/s0006-3495(00)76481-2 · Cited by 236 · see citing works

The NH2-terminal peptide of α–smooth muscle actin inhibits force generation by the myofibroblast in vitro and in vivo

Hinz, B., Gabbiani, G., & Chaponnier, C. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200201049 · Cited by 226 · see citing works

Osteocyte function, osteocyte death and bone fracture resistance

Noble, B., & REEVE, J. (2000) · Molecular and Cellular Endocrinology · doi:10.1016/s0303-7207(99)00174-4 · Cited by 211 · see citing works

Dendritic Fibroblasts in Three-dimensional Collagen Matrices

Grinnell, F., Ho, C.-H., Tamaríz, E., Lee, D. J., & Skuta, G. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-08-0493 · Cited by 204 · see citing works

Regulation of LPA-Promoted Myofibroblast Contraction: Role of Rho, Myosin Light Chain Kinase, and Myosin Light Chain Phosphatase

Parizi, M., Howard, E. W., & Tomasek, J. J. (2000) · Experimental Cell Research · doi:10.1006/excr.1999.4754 · Cited by 188 · see citing works

β1 Integrin Regulates Fibroblast Viability during Collagen Matrix Contraction through a Phosphatidylinositol 3-Kinase/Akt/Protein Kinase B Signaling Pathway

Tian, B., Lessan, K., Kahm, J., Kleidon, J., & Henke, C. A. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m203565200 · Cited by 166 · see citing works

Quantification of the fiber architecture and biaxial mechanical behavior of porcine intestinal submucosa

Sacks, M. S., & Gloeckner, D. C. (1999) · Journal of Biomedical Materials Research · doi:10.1002/(sici)1097-4636(199907)46:1 · Cited by 161 · see citing works

Rac Regulates Endothelial Morphogenesis and Capillary Assembly

Connolly, J. O., Simpson, N., Hewlett, L. J., & Hall, A. (2002) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-01-0006 · Cited by 157 · see citing works

Establishment and transformation diminish the ability of fibroblasts to contract a native collagen gel.

Steinberg, B. M., Smith, K., Colozzo, M. T., & Pollack, R. (1980) · The Journal of Cell Biology · doi:10.1083/jcb.87.1.304 · Cited by 156 · see citing works

Tenascin-C Modulates Matrix Contraction via Focal Adhesion Kinase– and Rho-mediated Signaling Pathways

Midwood, K. S., & Schwarzbauer, J. E. (2002) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-05-0292 · Cited by 143 · see citing works

Stimulation of Integrin-mediated Cell Contractility by Fibronectin Polymerization

Hocking, D. C., Sottile, J., & Langenbach, K. J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.14.10673 · Cited by 140 · see citing works

Actin stress fibres and cell–cell adhesion molecules in tendons: organisation in vivo and response to mechanical loading of tendon cells in vitro

Ralphs, J. R., Waggett, A. D., & Benjamin, M. (2002) · Matrix Biology · doi:10.1016/s0945-053x(01)00179-2 · Cited by 128 · see citing works

Fibroblast responses to mechanical forces

Eastwood, M., McGrouther, D. A., & Brown, R. A. (1998) · Proceedings of the Institution of Mechanical Engineers Part H Journal of Engineering in Medicine · doi:10.1243/0954411981533854 · Cited by 127 · see citing works

Invited Review: Plasma membrane stress failure in alveolar epithelial cells

Vlahakis, N. E., & Hubmayr, R. D. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.89.6.2490 · Cited by 118 · see citing works

Organization and Function of Stress Fibers in Cells in Vitro and in Situ

Byers, H. R., White, G. E., & Fujiwara, K. (1984) · Springer eBooks · doi:10.1007/978-1-4684-4592-3_2 · Cited by 115 · see citing works

Molecular Signaling in Bioengineered Tissue Microenvironments

Bottaro, D. P., Liebmann-Vinson, A., & Heidaran, M. A. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb03068.x · Cited by 101 · see citing works

Cell-to-cell communication within intact human skin.

Salomón, O. D., Saurat, J. ‐., & Mêda, P. (1988) · Journal of Clinical Investigation · doi:10.1172/jci113578 · Cited by 99 · see citing works

Studying actin-dependent processes in tissue culture

Walpita, D., & Hay, E. D. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm727 · Cited by 98 · see citing works

Contraction of collagen matrices mediated by α2β1A and αvβ3 integrins

Cooke, M. E., Sakai, T., & Mosher, D. F. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.13.2375 · Cited by 95 · see citing works

Evidence for sequential utilization of fibronectin, vitronectin, and collagen during fibroblast‐mediated collagen contraction

Sethi, K. K., Yannas, I. V., Mudera, V., Eastwood, M., McFarland, C., & Brown, R. A. (2002) · Wound Repair and Regeneration · doi:10.1046/j.1524-475x.2002.10609.x · Cited by 87 · see citing works

Fibroblast Quiescence and the Disruption of ERK Signaling in Mechanically Unloaded Collagen Matrices

Rosenfeldt, H. M., & Grinnell, F. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.5.3088 · Cited by 87 · see citing works

Cellular Dynamics

Weiss, P. A. (1959) · Reviews of Modern Physics · doi:10.1103/revmodphys.31.11 · Cited by 85 · see citing works

Lysophosphatidic Acid Enhances Collagen Gel Contraction by Hepatic Stellate Cells: Association with Rho-Kinase

Yanase, M., Ikeda, H., Matsui, A., et al. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.3634 · Cited by 80 · see citing works

The Werner syndrome protein: an update

Oshima, J. (2000) · BioEssays · doi:10.1002/1521-1878(200010)22:10 · Cited by 80 · see citing works

Effects of PDGF-BB on Rat Dermal Fibroblast Behavior in Mechanically Stressed and Unstressed Collagen and Fibrin Gels

Shreiber, D. I., Enever, P. A. J., & Tranquillo, R. T. (2001) · Experimental Cell Research · doi:10.1006/excr.2001.5208 · Cited by 68 · see citing works

Development and Differentiation of Dermal Cells in Man

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Control of interstitial fluid pressure: Role of [beta ]-integrins

Reed, R. K., Berg, A., Gjerde, E.-A. B., & Rubin, K. (2001) · Seminars in Nephrology · doi:10.1053/snep.2001.21646 · Cited by 61 · see citing works

Interactions of fibroblasts with the extracellular matrix: implications for the understanding of fibrosis

Eckes, B., Kessler, D., Aumailley, M., & Krieg, T. (2000) · Springer Seminars in Immunopathology · doi:10.1007/s002810000034 · Cited by 60 · see citing works

Skin flap‐induced regression of granulation tissue correlates with reduced growth factor and increased metalloproteinase expression

Darby, I. A., Bisucci, T., Pittet, B., Garbin, S., Gabbiani, G., & Desmoulière, A. (2002) · The Journal of Pathology · doi:10.1002/path.1074 · Cited by 56 · see citing works

Mechanosensitive induction of apoptosis in fibroblasts is regulated by thrombospondin-1 and integrin associated protein (CD47)

Graf, R., Freyberg, M. A., Kaiser, D., et al. (2002) · APOPTOSIS · doi:10.1023/a:1020634924760 · Cited by 51 · see citing works

Interactions of fibroblasts with the extracellular matrix: implications for the understanding of fibrosis

Eckes, B., Kessler, D., Aumailley, M., & Krieg, T. (1999) · Springer Seminars in Immunopathology · doi:10.1007/bf00870303 · Cited by 40 · see citing works

Fibroblasts contracting collagen matrices form transient plasma membrane passages through which the cells take up fluorescein isothiocyanate-dextran and Ca2+.

Lin, Y., Ho, C. H., & Grinnell, F. (1997) · Molecular Biology of the Cell · doi:10.1091/mbc.8.1.59 · Cited by 38 · see citing works

Signal Transduction Pathways Activated During Fibroblast Contraction of Collagen Matrices

Grinnell, F. (1999) · Current topics in pathology · doi:10.1007/978-3-642-58456-5_7 · Cited by 34 · see citing works

Fibroblast‐mediated collagen gel contraction does not require fibronectin‐α5β1 integrin interaction

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Cytochalasin D induces edema formation and lowering of interstitial fluid pressure in rat dermis

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The differentiation of the dermis in the laboratory mouse

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Granulation tissue regression induced by musculocutaneous advancement flap coverage

Carlson, M. A., Longaker, M. T., & Thompson, J. S. (2002) · Surgery · doi:10.1067/msy.2002.120673 · Cited by 16 · see citing works

The Interaction of Cellular Fibronectin with Collagen During Fibroblast-Mediated Contraction of Collagen Gels

Yoshizato, K., Tsukahara, M., Oki, T., et al. (1999) · Journal of Investigative Dermatology Symposium Proceedings · doi:10.1038/sj.jidsp.5640207 · Cited by 8 · see citing works

Synthetic biomaterials as instructive extracellular microenvironments for morphogenesis in tissue engineering

Lutolf, M. P., & Hubbell, J. A. (2005) · Nature Biotechnology · doi:10.1038/nbt1055 · Cited by 4,551 · see citing works

Senescent cells, tumor suppression, and organismal aging: good citizens, bad neighbors

Campisi, J. (2005) · Cell · doi:10.1016/j.cell.2005.02.003 · Cited by 2,359 · see citing works

Modeling physiological events in 2D vs. 3D cell culture

Duval, K., Grover, H., Han, L.-H., Mou, Y., Pegoraro, A. F., Fredberg, J., & Chen, Z. (2017) · Physiology · doi:10.1152/physiol.00036.2016 · Cited by 1,849 · see citing works

Deconstructing the third dimension – how 3D culture microenvironments alter cellular cues

Baker, B. M., & Chen, C. S. (2012) · Journal of Cell Science · doi:10.1242/jcs.079509 · Cited by 1,760 · see citing works

Formation and function of the myofibroblast during tissue repair

Hinz, B. (2007) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5700613 · Cited by 1,658 · see citing works

The Basic Science of Wound Healing

Broughton, G., Janis, J. E., & Attinger, C. E. (2006) · Plastic and Reconstructive Surgery · doi:10.1097/01.prs.0000225430.42531.c2 · Cited by 1,519 · see citing works

Effects of <b><i>Aloe</i></b> Sterol Supplementation on Skin Elasticity, Hydration, and Collagen Score: A 12-Week Double-Blind, Randomized, Controlled Trial

Tanaka, M., Yamamoto, Y., Misawa, E., Nabeshima, K., Saito, M., Yamauchi, K., Abe, F., & Furukawa, F. (2016) · Skin Pharmacology and Physiology · doi:10.1159/000454718 · Cited by 1,092 · see citing works

Decreased Collagen Production in Chronologically Aged Skin

Varani, J., Dame, M. K., Rittie, L., Fligiel, S. E. G., Kang, S., Fisher, G. J., & Voorhees, J. J. (2006) · The American Journal of Pathology · doi:10.2353/ajpath.2006.051302 · Cited by 910 · see citing works

Perspective Article: Tissue repair, contraction, and the myofibroblast

Desmoulière, A., Chaponnier, C., & Gabbiani, G. (2005) · Wound Repair and Regeneration · doi:10.1111/j.1067-1927.2005.130102.x · Cited by 892 · see citing works

Looking Older: Fibroblast Collapse and Therapeutic Implications

Fisher, G. J., Varani, J., & Voorhees, J. J. (2008) · Archives of Dermatology · doi:10.1001/archderm.144.5.666 · Cited by 540 · see citing works

Dynamic reciprocity in the wound microenvironment

Schultz, G. S., Davidson, J. M., Kirsner, R. S., Bornstein, P., & Herman, I. M. (2011) · Wound Repair and Regeneration · doi:10.1111/j.1524-475x.2011.00673.x · Cited by 490 · see citing works

Collagen fragmentation promotes oxidative stress and elevates matrix metalloproteinase-1 in fibroblasts in aged human skin

Fisher, G. J., Quan, T., Purohit, T., Shao, Y., Cho, M. K., He, T., Varani, J., Kang, S., & Voorhees, J. J. (2009) · The American Journal of Pathology · doi:10.2353/ajpath.2009.080599 · Cited by 487 · see citing works

Defining Physiological Normoxia for Improved Translation of Cell Physiology to Animal Models and Humans

Keeley, T. P., & Mann, G. E. (2019) · Physiological Reviews · doi:10.1152/physrev.00041.2017 · Cited by 329 · see citing works

Skeletal muscle tissue engineering: methods to form skeletal myotubes and their applications

Ostrovidov, S., Hosseini, V., Ahadian, S., Fujie, T., Parthiban, S. P., Ramalingam, M., Bae, H., Kaji, H., & Khademhosseini, A. (2014) · Tissue Engineering Part B: Reviews · doi:10.1089/ten.teb.2013.0534 · Cited by 302 · see citing works

From mechanical resilience to active material properties in biopolymer networks

Burla, F., Mulla, Y., Vos, B. E., Aufderhorst-Roberts, A., & Koenderink, G. H. (2019) · Nature Reviews Physics · doi:10.1038/s42254-019-0036-4 · Cited by 224 · see citing works

Cell-matrix interactions in dermal repair and scarring

Eckes, B., Nischt, R., & Krieg, T. (2010) · Fibrogenesis & Tissue Repair · doi:10.1186/1755-1536-3-4 · Cited by 205 · see citing works

Microfluidic 3D models of cancer

Sung, K. E., & Beebe, D. J. (2014) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2014.07.002 · Cited by 190 · see citing works

Hydrogels for Musculoskeletal Tissue Engineering

Varghese, S., & Elisseeff, J. H. (2006) · Advances in Polymer Science · doi:10.1007/12_072 · Cited by 173 · see citing works

p38 Inhibitors Prevent TGF-β–Induced Myofibroblast Transdifferentiation in Human Tenon Fibroblasts

Meyer-ter-Vehn, T., Gebhardt, S., Sebald, W., Buttmann, M., Grehn, F., Schlunck, G., & Knaus, P. (2006) · Investigative Opthalmology & Visual Science · doi:10.1167/iovs.05-0361 · Cited by 125 · see citing works

Treatment of volumetric muscle loss in mice using nanofibrillar scaffolds enhances vascular organization and integration

Nakayama, K. H., Quarta, M., Paine, P., Alcazar, C., Karakikes, I., Garcia, V., Abilez, O. J., Calvo, N. S., Simmons, C. S., Rando, T. A., et al. (2019) · Communications Biology · doi:10.1038/s42003-019-0416-4 · Cited by 113 · see citing works

Regulation of fibroblast functions by lysophospholipid mediators: Potential roles in wound healing

Watterson, K. R., Lanning, D. A., Diegelmann, R. F., & Spiegel, S. (2007) · Wound Repair and Regeneration · doi:10.1111/j.1524-475x.2007.00292.x · Cited by 113 · see citing works

Targeting tumour microenvironment by tyrosine kinase inhibitor

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Scarless wound healing: From development to senescence

Pratsinis, H., Mavrogonatou, E., & Kletsas, D. (2019) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2018.04.011 · Cited by 103 · see citing works

Alteration of Cellular Behavior and Response to PI3K Pathway Inhibition by Culture in 3D Collagen Gels

Fallica, B., Maffei, J. S., Villa, S., Makin, G., & Zaman, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048024 · Cited by 84 · see citing works

Differentiation Patterns of Embryonic Stem Cells in Two- versus Three-Dimensional Culture

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A clinical trial shows improvement in skin collagen, hydration, elasticity, wrinkles, scalp, and hair condition following 12-week oral intake of a supplement containing hydrolysed collagen

Reilly, D. M., Kynaston, L., Naseem, S., Proudman, E., & Laceby, D. (2024) · Dermatology Research and Practice · doi:10.1155/2024/8752787 · Cited by 18 · see citing works

Effects of Repeated <scp>UVA</scp> Irradiation on Human Skin Fibroblasts Embedded in 3D Tense Collagen Matrix

Nakyai, W., Tissot, M., Humbert, P., Grandmottet, F., Viyoch, J., & Viennet, C. (2018) · Photochemistry and Photobiology · doi:10.1111/php.12895 · Cited by 15 · see citing works

Living tissues are more than cell clusters: The extracellular matrix as a driving force in morphogenesis

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The Role of Extracellular Matrix in Wound Healing

Lin, P., Zhang, G., & Li, H. (2023) · Dermatologic Surgery · doi:10.1097/dss.0000000000003779 · Cited by 40 · see citing works

The Role of Extracellular Matrix in the Morphogenesis and Differentiation of Salivary Glands

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Substances Secreted by Starved Human Dermal Fibroblasts Enhancing the Wound Healing Process in Rat without Scar: A Potential Acellular System for Wound Healing

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Effects of elevated glucose levels on interactions of cardiac fibroblasts with the extracellular matrix

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