Extracellular Matrix and Dermal Fibroblast Function in the Healing Wound

Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors

Takahashi, K., & Yamanaka, S. (2006) · Cell · doi:10.1016/j.cell.2006.07.024 · Cited by 26,673

Induction of Pluripotent Stem Cells from Adult Human Fibroblasts by Defined Factors

Takahashi, K., Tanabe, K., Ohnuki, M., Narita, M., Ichisaka, T., Tomoda, K., & Yamanaka, S. (2007) · Cell · doi:10.1016/j.cell.2007.11.019 · Cited by 20,221

Induced Pluripotent Stem Cell Lines Derived from Human Somatic Cells

Yu, J., Vodyanik, M. A., Smuga-Otto, K., Antosiewicz-Bourget, J., Frane, J. L., Tian, S., Nie, J., Jonsdottir, G. A., Ruotti, V., Stewart, R., et al. (2007) · Science · doi:10.1126/science.1151526 · Cited by 10,310

The extracellular matrix at a glance

Frantz, C., Stewart, K. M., & Weaver, V. M. (2010) · Journal of Cell Science · doi:10.1242/jcs.023820 · Cited by 4,334

PERSPECTIVE ARTICLE: Growth factors and cytokines in wound healing

Barrientos, S., Stojadinovic, O., Golinko, M. S., Brem, H., & Tomic‐Canic, M. (2008) · Wound Repair and Regeneration · doi:10.1111/j.1524-475x.2008.00410.x · Cited by 3,583

Interactions between extracellular matrix and growth factors in wound healing

Schultz, G. S., & Wysocki, A. (2009) · Wound Repair and Regeneration · doi:10.1111/j.1524-475x.2009.00466.x · Cited by 1,126

Effects of Aloe 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

Interaction of the small interstitial proteoglycans biglycan, decorin and fibromodulin with transforming growth factor β

Hildebrand, A., Romarı́s, M., Rasmussen, L. M., Heinegård, D. K., Twardzik, D. R., Border, W. A., & Ruoslahti, E. I. (1994) · Biochemical Journal · doi:10.1042/bj3020527 · Cited by 995

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 980

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

Effects and formulation of silver nanoscaffolds on cytotoxicity dependent ion release kinetics towards enhanced excision wound healing patterns in Wistar albino rats

Sethuram, L., Thomas, J., Mukherjee, A., & Chandrasekaran, N. (2019) · RSC Advances · doi:10.1039/c9ra06913e · Cited by 24

Chondroitin Sulfate Promotes the Proliferation of Keloid Fibroblasts Through Activation of the Integrin and Protein Kinase B Pathways

Katayama, Y., Naitoh, M., KUBOTA, H. Y., Yamawaki, S., Aya, R., Ishiko, T., & Morimoto, N. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21061955 · Cited by 24

Microphysiological systems for the modeling of wound healing and evaluation of pro-healing therapies

Deal, H. E., Brown, A. C., & Daniele, M. A.-A. (2020) · Journal of Materials Chemistry B · doi:10.1039/d0tb00544d · Cited by 25

Red-COLA1: a human fibroblast reporter cell line for type I collagen transcription

Wong, H. H., Seet, S. H., Bascom, C. C., Isfort, R. J., & Bard, F. (2020) · Scientific Reports · doi:10.1038/s41598-020-75683-5 · Cited by 22

Treatment of Burn and Surgical Wounds With Recombinant Human Tropoelastin Produces New Elastin Fibers in Scars

Xie, H., Lucchesi, L., Zheng, B., Ladich, E. R., Pineda, T. J., Merten, R., Gregory, C. R., Rutten, M. J., & Gregory, K. W. (2017) · Journal of Burn Care & Research · doi:10.1097/bcr.0000000000000507 · Cited by 24

Neutrophil Migration is a Crucial Factor in Wound Healing and the Pathogenesis of Diabetic Foot Ulcers: Insights into Pharmacological Interventions

Asunama, A. S. R., Nambi, N., Radhakrishnan, L., Prasad, M. K., & Ramkumar, K. M. (2024) · Current Vascular Pharmacology · doi:10.2174/0115701611308960241014155413 · Cited by 25

Extracellular matrix-based biomaterials in burn wound repair: A promising therapeutic strategy

Song, Y., Liu, P., Zhou, X., Chen, Y., Wu, W., Zhang, J.-Y., Li‐Ling, J., & Xie, H. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.137633 · Cited by 25

Mechanical Stimulation of Fibroblasts by Extracorporeal Shock Waves: Modulation of Cell Activation and Proliferation Through a Transient Proinflammatory Milieu

Basoli, V., Chaudary, S., Cruciani, S., Santaniello, S., Balzano, F., Ventura, C., Redl, H., Dungel, P., & Maioli, M. (2020) · Cell Transplantation · doi:10.1177/0963689720916175 · Cited by 25

Strategies Targeting the Innate Immune Response for the Treatment of Hepatitis C Virus-Associated Liver Fibrosis

Sepúlveda‐Crespo, D., Resino, S., & Martínez, I. (2021) · Drugs · doi:10.1007/s40265-020-01458-x · Cited by 23

Controlling morphology evolution of titanium oxide–gold nanourchin for photocatalytic degradation of dyes and photoinactivation of bacteria in the infected wound

Unnikrishnan, B., Gultom, I. S., Tseng, Y., Chang, H., & Huang, C. (2021) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2021.04.035 · Cited by 23

Autoimmunity, cancer and COVID-19 abnormally activate wound healing pathways: critical role of inflammation

Gál, P., Brábek, J., Holub, M., Jakubek, M., Šedo, A., Lacina, L., Strnadová, K., Dubový, P., Hornychová, H., Ryška, A., et al. (2022) · Histochemistry and Cell Biology · doi:10.1007/s00418-022-02140-x · Cited by 22

Synthetic Calcium Phosphate Ceramics as a Potential Treatment for Bisphosphonate-Related Osteonecrosis of the Jaw

Paulo, S., Laranjo, M., Abrantes, A. M., Casalta‐Lopes, J., Santos, K., Gonçalves, A. C., Paula, A. B., Marto, C. M., Sarmento‐Ribeiro, A. B., Carrilho, E., et al. (2019) · Materials · doi:10.3390/ma12111840 · Cited by 23

Biomimetic Hydrogel Scaffolds with Copper Peptide-Functionalized RADA16 Nanofiber Improve Wound Healing in Diabetes

Yang, X., Zhang, Y., Huang, C., Lu, L., Chen, J., & Weng, Y. (2022) · Macromolecular Bioscience · doi:10.1002/mabi.202200019 · Cited by 22

Efficient Generation of Skin Organoids from Pluripotent Cells via Defined Extracellular Matrix Cues and Morphogen Gradients in a Spindle‐Shaped Microfluidic Device

Quílez, C., Jeon, E. Y., Pappalardo, A., Pathak, P., & Abaci, H. E. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202400405 · Cited by 22

Dynamic duo: Cell–extracellular matrix interactions in hair follicle development and regeneration

Fujiwara, H. (2024) · Developmental Biology · doi:10.1016/j.ydbio.2024.07.012 · Cited by 22

One-step harvest and delivery of micropatterned cell sheets mimicking the multi-cellular microenvironment of vascularized tissue

Kim, S., Lee, S., Kim, C., & Shin, H. (2021) · Acta Biomaterialia · doi:10.1016/j.actbio.2021.02.009 · Cited by 22

Native Spider Silk-Based Antimicrobial Hydrogels for Biomedical Applications

Withanage, S., Savin, A. M., Nikolaeva, V. O., Kiseleva, A. P., Сергеевна, Д. М., Krivoshapkin, P. V., & Krivoshapkina, E. F. (2021) · Polymers · doi:10.3390/polym13111796 · Cited by 22

Notoginsenoside R1 Facilitated Wound Healing in High‐Fat Diet/Streptozotocin‐Induced Diabetic Rats

Cao, G., Xiang, C., Zhou, R., Zhang, Y., Xu, H., Yang, H., & Zhang, J. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/2476493 · Cited by 22

Gravitational effects on fibroblasts’ function in relation to wound healing

Radstake, W. E., Gautam, K., Miranda, S., Rompay, C. V., Vermeesen, R., Tabury, K., Verslegers, M., Dowson, A., Gorissen, J., van Loon, J. J. W. A., et al. (2023) · npj Microgravity · doi:10.1038/s41526-023-00286-z · Cited by 23

Embryo-derive TNF promotes decidualization via fibroblast activation

Chen, S., Shi, W., Lin, Y.-Q., Yang, Z., Wang, Y., Li, Y., Liu, A.-X., Liu, A.-X., Hu, Y., & Yang, Z. (2023) · eLife · doi:10.7554/elife.82970 · Cited by 22

Cerium oxide nanoparticles in diabetic foot ulcer management: Advances, limitations, and future directions

Xu, H., Li, S., Ma, X., Xue, T., Shen, F., Ru, Y., Jiang, J., Kuai, L., Li, B., Zhao, H., et al. (2023) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2023.113535 · Cited by 22

Antimicrobial peptide KSL-W promotes gingival fibroblast healing properties in vitro

Park, H.-J., Salem, M., Semlali, A., Leung, K. P., & Rouabhia, M. (2017) · Peptides · doi:10.1016/j.peptides.2017.05.003 · Cited by 22

Extracellular matrix constitution and function for tissue regeneration and repair

Caldeira, J., Sousa, A., Sousa, D. M., & Barros, D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-08-100803-4.00002-4 · Cited by 24

Wound healing-related properties detected in an experimental model with a collagen gel contraction assay are affected in the absence of tenascin-X

Hashimoto, K., Kajitani, N., Miyamoto, Y., & Matsumoto, K. (2017) · Experimental Cell Research · doi:10.1016/j.yexcr.2017.12.025 · Cited by 22

DDR1 and DDR2 in skin

Cario, M. (2018) · Cell Adhesion & Migration · doi:10.1080/19336918.2018.1485618 · Cited by 24

A mechanistic evaluation of the angiogenic properties of a dehydrated amnion chorion membrane in vitro and in vivo

McQuilling, J. P., Burnette, M. D., Kimmerling, K. A., Kammer, M., & Mowry, K. C. (2019) · Wound Repair and Regeneration · doi:10.1111/wrr.12757 · Cited by 22

Design and Biofabrication of Dermal Regeneration Scaffolds: Role of Oligomeric Collagen Fibril Density and Architecture

Sohutskay, D. O., Buno, K., Tholpady, S. S., Nier, S. J., & Voytik‐Harbin, S. L. (2020) · Regenerative Medicine · doi:10.2217/rme-2019-0084 · Cited by 22

Accelerated in vitro recellularization of decellularized porcine pericardium for cardiovascular grafts

Filová, E., Steinerová, M., Trávníčková, M., Knitlová, J., Musı́lková, J., Eckhardt, A., Hadraba, D., Matějka, R., Pražák, Š., Štěpanovská, J., et al. (2020) · Biomedical Materials · doi:10.1088/1748-605x/abbdbd · Cited by 22

The Regenerative Potential of Donkey and Human Milk on the Redox-Sensitive and Proliferative Signaling Pathways of Skin Fibroblasts

Kocić, H., Langerholc, T., Kostić, M. S., Stojanović, S., Najman, S. J., Krstic, M., Nesic, I., Godic, A., & Wollina, U. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/5618127 · Cited by 22

Structural extracellular matrix-mediated molecular signaling in wound repair and tissue regeneration

Cheong, S., Peng, Y., Lu, F., & He, Y. (2024) · Biochimie · doi:10.1016/j.biochi.2024.10.003 · Cited by 21

Current application of tissue-engineered dermal scaffolds mimicking the extracellular matrix microenvironment in wound healing

Ding, X.-R., Xie, S.-J., Zhang, W., Zhu, Y.-S., Xu, D., Xian, S.-Y., Sun, H.-L., Guo, X., Li, Y.-X., Lu, J.-Y., et al. (2025) · Regenerative Therapy · doi:10.1016/j.reth.2024.12.018 · Cited by 19

Targeting Dermal Fibroblast Senescence: From Cellular Plasticity to Anti-Aging Therapies

Jipu, R., Șerban, I. L., Goriuc, A., Jipu, A. G., Luchian, I. A., Amititeloaie, C., Tărniceriu, C. C., Hurjui, I., Butnaru, O., & Hurjui, L. L. (2025) · Biomedicines · doi:10.3390/biomedicines13081927 · Cited by 25

Cancer-Associated Fibroblasts in Solid Tumors and Sarcomas: Heterogeneity, Function, and Therapeutic Implications

Badran, O., Cohen, I., & Bar‐Sela, G. (2025) · Cells · doi:10.3390/cells14171398 · Cited by 25

Photobiomodulation in fibroblasts: from light to healing through molecular pathways, omics and artificial intelligence

Ucci, S., Caradonna, E., Aliberti, A., & Cusano, A. (2025) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2025.1675619 · Cited by 23

LincRNA TINCR facilitates excessive proliferation and inflammation in post-burn skin fibroblasts by directly binding with SND1 protein and inducing SND1-mediated TGF-β1 expression

Qin, G., Song, Y., Guo, Y., Sun, Y., & Zeng, W. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.01.013 · Cited by 21

Atorvastatin reduces zoledronic acid-induced osteonecrosis of the jaws of rats

Ferreira, V. C. D. S., de Sousa, F. R. N., de Vasconcelos, R. F., Martins, C. S., Lopes, A. P., Alves, N. M., Viana, D., Alves, K., Leitão, R. F. D. C., Brito, G. A. D. C., et al. (2022) · Bone · doi:10.1016/j.bone.2022.116523 · Cited by 21

SEMA7a primes integrin α5β1 engagement instructing fibroblast mechanotransduction, phenotype and transcriptional programming

Hu, P., Miller, A. E., Yeh, C., Bingham, G. C., Civelek, M., & Barker, T. H. (2023) · Matrix Biology · doi:10.1016/j.matbio.2023.06.006 · Cited by 21

Evaluation of antifungal effect and toxicity of xanthyletin and two bacterial metabolites against Thai isolates of Pythium insidiosum

Wittayapipath, K., Yenjai, C., Prariyachatigul, C., & Hamal, P. (2020) · Scientific Reports · doi:10.1038/s41598-020-61271-0 · Cited by 21

Lucilia sericata Larval Secretions Stimulating Wound Healing Effects on Rat Dermal Fibroblast Cells

Akbaş, F., Özaydın, A., Polat, E., & Onaran, İ. (2020) · Records of Natural Products · doi:10.25135/rnp.180.20.03.1582 · Cited by 21

Fibroblast exosomes promote wound healing and improve the quality of healed skin via miR-29a-3p-mediated KEAP1/Nrf2 pathway activation

Yan, L., Fan, D., Yang, J., Wang, J., Hu, X., Zhang, X., Huang, Y., Wang, H., Yin, W., Cai, X., et al. (2025) · Burns & Trauma · doi:10.1093/burnst/tkaf035 · Cited by 21

Tissue Mechanics in Haired Murine Skin: Potential Implications for Skin Aging

Harn, H. I., Chen, C., Wang, S., Lei, M., & Chuong, C. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.635340 · Cited by 18

Identification of potential hub genes associated with skin wound healing based on time course bioinformatic analyses

Zhu, H., Fan, M., & Gao, W. (2021) · BMC Surgery · doi:10.1186/s12893-021-01298-w · Cited by 22

In vivo-wound healing studies of sodium thiosulfate gel in rats

Grover, P., Khanna, K., Bhatnagar, A., & Purkayastha, J. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.111797 · Cited by 20

Local Administration of Ginkgolide B Using a Hyaluronan-Based Hydrogel Improves Wound Healing in Diabetic Mice

Wang, L., Xia, K., Han, L., Zhang, M., Fan, J., Song, L., Liao, A., Wang, W., & Guo, J. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.898231 · Cited by 20

Single-cell RNA-seq reveals cellular heterogeneity from deep fascia in patients with acute compartment syndrome

Wang, T., Long, Y., Ma, L., Dong, Q., Li, Y., Guo, J., Jin, L., Di, L., Zhang, Y., Wang, L., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1062479 · Cited by 20

Human Dermal Decellularized ECM Hydrogels as Scaffolds for 3D In Vitro Skin Aging Models

Fernández-Carro, E., Remacha, A. R., Orera, I., Lattanzio, G., Barrios, A. G., del Barrio, J., Alcaine, C., & Ciriza, J. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25074020 · Cited by 20

Multifunctional Molybdenum-Based Nanoclusters Engineered Gelatin Methacryloyl as In Situ Photo-Cross-Linkable Hybrid Hydrogel Dressings for Enhanced Wound Healing

Kurian, A. G., Mandakhbayar, N., Singh, R. K., Lee, J., & Kim, H. (2024) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.4c05636 · Cited by 20

Gelatin promotes cell aggregation and pro-inflammatory cytokine production in PMA-stimulated U937 cells by augmenting endocytosis-autophagy pathway

Zhao, Y., Lu, Z.-Y., Zhang, X., Liu, W.-W., Yao, G., Liu, X., Liu, W., Wu, Q.-J., Hayashi, T., Yamato, M., et al. (2018) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2018.01.002 · Cited by 20

Graphene-based 2D constructs for enhanced fibroblast support

Safina, I., Bourdo, S. E., Algazali, K. M., Kannarpady, G. K., Watanabe, F., Vang, K. B., & Biris, A. S. (2020) · PLoS ONE · doi:10.1371/journal.pone.0232670 · Cited by 20

Effect of a high-fat diet and alcohol on cutaneous repair: A systematic review of murine experimental models

Rosa, D. F., Sarandy, M. M., Novaes, R. D., da Matta, S. L. P., & Gonçalves, R. V. (2017) · PLOS ONE · doi:10.1371/journal.pone.0176240 · Cited by 19

Natural biopolymer-based hydrogels: an advanced material for diabetic wound healing

Arunim, Sarita, S., Mishra, R., & Bajpai, S. (2024) · Diabetology International · doi:10.1007/s13340-024-00737-2 · Cited by 19

Regulatory Mechanisms of Natural Active Ingredients and Compounds on Keratinocytes and Fibroblasts in Mitigating Skin Photoaging

Hu, X., Chen, M., Nawaz, J., & Duan, X. (2024) · Clinical Cosmetic and Investigational Dermatology · doi:10.2147/ccid.s478666 · Cited by 20

Self-assembled ROS-triggered Bletilla striata polysaccharide-releasing hydrogel dressing for inflammation-regulation and enhanced tissue-healing

Zhang, L., Wang, K., Zhou, L., Zhu, Y., Chen, X., Wang, Y., Zhao, Y., Huang, N., Luo, R., Li, X., et al. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.135194 · Cited by 19

Radiation therapy-induced normal tissue damage: involvement of EMT pathways and role of FLASH-RT in reducing toxicities

Srinivasan, D., Subbarayan, R., Krishnan, M., Balakrishna, R., Adtani, P., Shrestha, R., Chauhan, A., Babu, S., & Radhakrishnan, A. (2025) · Radiation and Environmental Biophysics · doi:10.1007/s00411-024-01102-2 · Cited by 19

Dysfunctional crosstalk between macrophages and fibroblasts under LPS-infected and hyperglycemic environment in diabetic wounds

Sharma, S. R. R., & Kishen, A. (2025) · Scientific Reports · doi:10.1038/s41598-025-00673-4 · Cited by 24

Human Adventitial Fibroblast Phenotype Depends on the Progression of Changes in Substrate Stiffness

Scott, R. A., Robinson, K. G., Kiick, K. L., & Akins, R. E. (2020) · Advanced Healthcare Materials · doi:10.1002/adhm.201901593 · Cited by 19

Expression of collagen type III in healing tympanic membrane

Makuszewska, M., Bonda, T. A., Cieślińska, M., Bialuk, I., Winnicka, M. M., & Niemczyk, K. (2020) · International Journal of Pediatric Otorhinolaryngology · doi:10.1016/j.ijporl.2020.110196 · Cited by 19

Therapeutic downregulation of neuronal PAS domain 2 (Npas2) promotes surgical skin wound healing

Shibuya, Y., Hokugo, A., Okawa, H., Kondo, T., Khalil, D., Wang, L., Roca, Y., Clements, A., Sasaki, H., Berry, E., et al. (2022) · eLife · doi:10.7554/elife.71074 · Cited by 20

Topical application of melatonin accelerates the maturation of skin wounds and increases collagen deposition in a rat model of diabetes

de Souza, T. R., Rocha, V. L., Rincon, G. D. C. N., de Oliveira, E. R., Celes, M. R. N., Lima, E. M., Amaral, A. C., Miguel, M. P., & de Menezes, L. B. (2022) · Journal of Tissue Viability · doi:10.1016/j.jtv.2022.07.015 · Cited by 19

Lipase-Responsive Amphotericin B Loaded PCL Nanoparticles for Antifungal Therapies

Uroro, E. O., Bright, R., Hayles, A., & Vasilev, K. A. (2022) · Nanomaterials · doi:10.3390/nano13010155 · Cited by 21

Gly-Pro-Val-Gly-Pro-Ser Peptide Fish Collagen Improves Skin Moisture and Wrinkles with Ameliorated the Oxidative Stress and Pro-inflammatory Factors in Skin Photoaging Mimic Models

Cho, W., Park, J., Lee, M., Park, S.-H., Jung, J., Kim, J., Eun, S., & Kim, J. (2023) · Preventive Nutrition and Food Science · doi:10.3746/pnf.2023.28.1.50 · Cited by 25

eEF2 improves dense connective tissue repair and healing outcome by regulating cellular death, autophagy, apoptosis, proliferation and migration

(2023) · doi:10.1007/s00018-023-04776-x · Cited by 19

Human Acellular Amniotic Membrane as Skin Substitute and Biological Scaffold: A Review of Its Preparation, Preclinical Research, and Clinical Application

Li, Y., An, S., Deng, C., & Xiao, S. (2023) · Pharmaceutics · doi:10.3390/pharmaceutics15092249 · Cited by 19

Ellagic acid containing collagen-chitosan scaffolds as potential antioxidative bio-materials for tissue engineering applications

Shaik, M. M., & Kowshik, M. (2018) · International Journal of Polymeric Materials · doi:10.1080/00914037.2018.1443927 · Cited by 18

Morphology of a fibrin nanocoating influences dermal fibroblast behavior

Pajorová, J., Bačáková, M., Musı́lková, J., Brož, A., Hadraba, D., Lopot, F., & Bačáková, L. (2018) · International Journal of Nanomedicine · doi:10.2147/ijn.s162644 · Cited by 19

Cellular retinoic acid binding protein-II expression and its potential role in skin aging

Bielli, A., Scioli, M. G., D’Amico, F., Tarquini, C., Agostinelli, S., Costanza, G., Doldo, E., Campione, E., Passeri, D., Coniglione, F., et al. (2019) · Aging · doi:10.18632/aging.101813 · Cited by 20

Uvaol Improves the Functioning of Fibroblasts and Endothelial Cells and Accelerates the Healing of Cutaneous Wounds in Mice

Carmo, J., Cavalcante-Araújo, P., Silva, J., Ferro, J., Correia, A. C., Lagente, V., & Barreto, E. (2020) · Molecules · doi:10.3390/molecules25214982 · Cited by 18

Resveratrol inhibits matrix metalloproteinase-1 and -3 expression by suppressing of p300/NFκB acetylation in TNF-α-treated human dermal fibroblasts

Lu, Y.-E., & Chen, Y. (2021) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2021.109395 · Cited by 18

Preparation and characterization of a novel polysialic acid/gelatin composite hydrogels cross-linked by tannic acid to improve wound healing after cesarean section dressing

Xu, J. M., Li, Y., Chen, Y., Wang, L., & Liao, M. (2021) · Journal of Biomaterials Science Polymer Edition · doi:10.1080/09205063.2021.1950961 · Cited by 17

Anti-biofilm and anti-inflammatory effects of Lycosin-II isolated from spiders against multi-drug resistant bacteria

Oh, J. H., Park, J., & Park, Y. (2021) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2021.183769 · Cited by 18

An Investigation for Skin Tissue Regeneration Enhancement/Augmentation by Curcumin-Loaded Self-Emulsifying Drug Delivery System (SEDDS)

Mahmood, S., Bhattarai, P., Khan, N. R., Subhan, Z., Razaque, G., Albarqi, H. A., Alqahtani, A. A., Alasiri, A., & Zhu, L. (2022) · Polymers · doi:10.3390/polym14142904 · Cited by 18

The hallmarks of ovarian cancer: Focus on angiogenesis and micro-environment and new models for their characterisation

Heredia-Soto, V., López‐Guerrero, J. A., Redondo, A., & Mendiola, M. (2020) · European Journal of Cancer Supplements · doi:10.1016/j.ejcsup.2019.11.003 · Cited by 21

Impact of stress, immunity, and signals from endocrine and nervous system on fascia

Barsotti, N., Chiera, M., Lanaro, D., & Fioranelli, M. (2020) · Frontiers in Bioscience-Elite · doi:10.2741/870 · Cited by 18

The Paracrine Effect of Adipose-Derived Stem Cells Orchestrates Competition between Different Damaged Dermal Fibroblasts to Repair UVB-Induced Skin Aging

Qin, F., Huang, J., Zhang, W., Zhang, M., Li, Z., Si, L., Long, X., & Wang, X. (2020) · Stem Cells International · doi:10.1155/2020/8878370 · Cited by 18

Preoperative vitamin C supplementation improves colorectal anastomotic healing and biochemical parameters in malnourished rats

Danielski, L. G., Walczewski, E. A. B., de Jesus, C. R., Florentino, D., Giustina, A. D., Goldim, M. P. D. S., Κanis, L. A., Pereira, G. W., Pereira, V. D., Felisberto, F., et al. (2016) · International Journal of Colorectal Disease · doi:10.1007/s00384-016-2647-x · Cited by 17

trans-Cinnamic acid, but not p-coumaric acid or methyl cinnamate, induces fibroblast migration through PKA- and p38-MAPK signalling pathways

de Aquino, F. L. T., da Silva, J. P., Ferro, J. N. D. S., Lagente, V., & Barreto, E. (2021) · Journal of Tissue Viability · doi:10.1016/j.jtv.2021.05.003 · Cited by 17

Collagen synthesis in the skin, its functional and structural features

Borzykh, O. B., Schneider, N. A., Карпова, Е. И., Petrova, M. M., Demina, O. M., & Nasyrova, R. F. (2021) · Medical news of the North Caucasus · doi:10.14300/mnnc.2021.16108 · Cited by 20

In vitro and in vivo wound healing-promoting activities of phosvitin-derived peptide Pt5-1c

Wu, F., Gong, Y., Song, L., Li, H., Zhang, X., Li, H., & Zhang, S. (2022) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2022.174833 · Cited by 17

A Straightforward Approach towards Antibacterial and Anti‐Inflammatory Multifunctional Nanofiber Membranes with Sustained Drug Release Profiles

Wang, W., Wang, Y., Zhao, W., & Zhao, C. (2022) · Macromolecular Bioscience · doi:10.1002/mabi.202200150 · Cited by 16

Potential of Nanoencapsulated Quercetin Topical Formulations in the Management of Diabetic Foot Ulcer

Chaturvedi, S., Agrawal, S., Garg, A., & Rastogi, V. (2022) · Revista Brasileira de Farmacognosia · doi:10.1007/s43450-022-00345-8 · Cited by 17

Past and Current Prospectives of Herbal Product for Skin Care

Prajapati, A. K., Sagar, S., & Kumar, R. (2022) · Journal for Research in Applied Sciences and Biotechnology · doi:10.55544/jrasb.1.5.16 · Cited by 18

Bioactive wound powders as wound healing dressings and drug delivery systems

Emami, S., & Ebrahimi, M. (2023) · Powder Technology · doi:10.1016/j.powtec.2023.118501 · Cited by 20

Enhanced skin neocollagenesis through the transdermal delivery of poly-L-lactic acid microparticles by using a needle-free supersonic atomizer

Chuang, F.-J., Wang, Y., Chang, L.-R., Chang, C., Cheng, H.-Y., & Kuo, S. (2023) · Biomaterials Advances · doi:10.1016/j.bioadv.2023.213619 · Cited by 17

Layer-by-Layer Analysis of In Vitro Skin Models

Footner, E., Firipis, K., Liu, E. I., Baker, C., Foley, P. A., Kapsa, R. M. I., Pirogova, E., O’Connell, C. D., & Quigley, A. F. (2023) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.3c00283 · Cited by 19

Fibroblasts alter the physical properties of dermal ECM-derived hydrogels to create a pro-angiogenic microenvironment

Zhang, M., Zhao, F., Zhang, X., Brouwer, L. A., Burgess, J. K., & Harmsen, M. C. (2023) · Materials Today Bio · doi:10.1016/j.mtbio.2023.100842 · Cited by 17

Therapeutic Potential of Adipose-Derived Stem Cell-Conditioned Medium and Extracellular Vesicles in an In Vitro Radiation-Induced Skin Injury Model

Lin, Z., Shibuya, Y., Imai, Y., Oshima, J., Sasaki, M., Sasaki, K., Aihara, Y., Khánh, V. C., & Sekido, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242417214 · Cited by 19

Thrombospondin‐4 critically controls transforming growth factor β1 induced hypertrophic scar formation

Qian, W., Li, N., Cao, Q., & Fan, J. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.26877 · Cited by 17

Spirulina protein promotes skin wound repair in a mouse model of full-thickness dermal excisional wound

Liu, P., Choi, J., Lee, M., Choi, Y., & Nam, T. (2020) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2020.4571 · Cited by 17

Synergistic effect of copper and amino acid mixtures on the production of extracellular matrix proteins in skin fibroblasts

Chung, K. W., Song, S. H., & Kim, M.-S. (2021) · Molecular Biology Reports · doi:10.1007/s11033-021-06403-z · Cited by 19

The utility of dermal fibroblasts in treatment of skin disorders: A paradigm of recessive dystrophic epidermolysis bullosa

Shams, F., Rahimpour, A., Vahidnezhad, H., Hosseinzadeh, S., Moravvej, H., Kazemi, B., Rajabibazl, M., Abdollahimajd, F., & Uitto, J. (2021) · Dermatologic Therapy · doi:10.1111/dth.15028 · Cited by 17

Synergistic effect of photobiomodulation and phthalocyanine photosensitizer on fibroblast signaling responses in an in vitro three-dimensional microenvironment

Souza, C., Jayme, C. C., Rezende, N., & Tedesco, A. C. (2021) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2021.112256 · Cited by 17

A review of regenerative medicine and tissue engineering with a focus on wound healing and anti-aging

Ganesan, O., Kiwanuka, H., Hamaguchi, R., & Orgill, D. P. (2025) · Frontiers in Surgery · doi:10.3389/fsurg.2025.1504563 · Cited by 20

Laricitrin 3-Rutinoside from Ginkgo biloba Fruits Prevents Damage in TNF-α-Stimulated Normal Human Dermal Fibroblasts

Lee, S., Choi, Y. J., Huo, C., Alishir, A., Kang, K. S., Park, I.-H., Jang, T., & Kim, K. H. (2023) · Antioxidants · doi:10.3390/antiox12071432 · Cited by 16

Integrative Approaches for Advancing Organoid Engineering: From Mechanobiology to Personalized Therapeutics

Akhtar, Z. B., & Gupta, A. D. (2024) · Journal of Applied Artificial Intelligence · doi:10.48185/jaai.v5i1.974 · Cited by 16

Increase of collagen in diabetes-related traumatic ulcers after the application of liquid smoke coconut shell

Surboyo, M. D. C., Arundina, I., & Rahayu, R. P. (2017) · Dental Journal (Majalah Kedokteran Gigi) · doi:10.20473/j.djmkg.v50.i2.p71-75 · Cited by 16

Zooming in across the Skin: A Macro-to-Molecular Panorama

Deniz, A. A. H., Abdik, E. A., Abdik, H., Aydın, S., Şahin, F., & Taşlı, P. N. (2019) · Advances in experimental medicine and biology · doi:10.1007/5584_2019_442 · Cited by 19

Ozonated Aloe vera Oil Effective Increased the Number of Fibroblasts and Collagen Thickening in the Healing Response of Full-Thickness Skin Defects

Hidayat, A. T., Arifin, M. T., Nur, M., Muniroh, M., & Susilaningsih, N. (2021) · International Journal of Inflammation · doi:10.1155/2021/6654343 · Cited by 16

PAX5 activates telomerase activity and proliferation in keloid fibroblasts by transcriptional regulation of SND1, thus promoting keloid growth in burn-injured skin

Qin, G., Sun, Y., Guo, Y., & Song, Y. (2021) · Inflammation Research · doi:10.1007/s00011-021-01444-3 · Cited by 16

Conditioned media derived from human fetal progenitor cells improves skin regeneration in burn wound healing

Tran, N.-T., Park, I., Truong, M., Park, D. Y., Park, S., & Min, B. (2022) · Cell and Tissue Research · doi:10.1007/s00441-022-03638-5 · Cited by 15

Nanocrystalline cerium dioxide efficacy for prophylaxis of erosive and ulcerative lesions in the gastric mucosa of rats induced by stress

Golyshkin, D., Kobyliak, N. M., Virchenko, O., Falalyeyeva, T. M., Beregova, T. V., Остапченко, Л. І., Čaprnda, M., Skladaný, Ľ., Opatřilová, R., Rodrigo, L., et al. (2016) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2016.10.060 · Cited by 15

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

Extracellular matrix and wound healing

Maquart, F., & Monboisse, J. C. (2014) · Pathologie Biologie · doi:10.1016/j.patbio.2014.02.007 · Cited by 143

Cutaneous wound healing—insights from the matricellular perspective

Klaas, M., Mäemets‐Allas, K., Cárdenas‐León, C. G., & Jaks, V. (2025) · FEBS Letters · doi:10.1002/1873-3468.70220 · Cited by 2

Extra cellular matrix molecules (ECM) and wound healing

Westerhof, W. (1995) · Journal of the European Academy of Dermatology and Venereology · doi:10.1016/0926-9959(95)95982-7

Role of the Extracellular Matrix Components in Cutaneous Wound Healing

Sreenivasulu, M., Reshma, S., & Theerdhala, S. (2022) · Zenodo (CERN European Organization for Nuclear Research) · doi:10.5281/zenodo.7559734