Tumor Necrosis Factor and Wound Healing

An endotoxin-induced serum factor that causes necrosis of tumors

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Shock and Tissue Injury Induced by Recombinant Human Cachectin

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Passive Immunization Against Cachectin/Tumor Necrosis Factor Protects Mice from Lethal Effect of Endotoxin

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The biology of platelet-derived growth factor

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Human tumour necrosis factor: precursor structure, expression and homology to lymphotoxin

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Tumor necrosis factor (cachectin) is an endogenous pyrogen and induces production of interleukin 1.

Dinarello, C. A., Cannon, J. G., Wolff, S. M., Bernheim, H. A., Beutler, B., Cerami, A., Figari, I. S., Palladino, M. A., & O'Connor, J. V. (1986) · The Journal of experimental medicine · doi:10.1084/jem.163.6.1433 · Cited by 1,472 · see citing works

The role of the macrophage in wound repair. A study with hydrocortisone and antimacrophage serum.

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Macrophage-induced angiogenesis is mediated by tumour necrosis factor-α

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Accelerated Healing of Incisional Wounds in Rats Induced by Transforming Growth Factor-β

Mustoe, T. A., Pierce, G. F., Thomason, A., Gramates, P. H., Sporn, M. B., & Deuel, T. F. (1987) · Science · doi:10.1126/science.2442813 · Cited by 930 · see citing works

Fibroblast growth enhancing activity of tumor necrosis factor and its relationship to other polypeptide growth factors.

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Regulation of wound-healing angiogenesis-effect of oxygen gradients and inspired oxygen concentration.

Knighton, D. R., Silver, I. A., & Hunt, T. K. (1981) · PubMed · Cited by 633 · see citing works

A Macrophage Factor Inhibits Adipocyte Gene Expression: An in Vitro Model of Cachexia

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Molecular cloning and expression of human tumor necrosis factor and comparison with mouse tumor necrosis factor

Marmenout, A., Fransen, L., Tavernier, J. H., der Heyden, J. V., Tizard, R., Kawashima, E. H., SHAW, A. R., JOHNSON, M., Semon, D., Müller, R., et al. (1985) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1985.tb09226.x · Cited by 239 · see citing works

Effects of growth factors in vivo. I. Cell ingrowth into porous subcutaneous chambers.

Sprugel, K. H., McPherson, J. M., Clowes, A. W., & Ross, R. (1987) · PubMed Central · Cited by 235 · see citing works

Tumor necrosis factor (TNF)-alpha but not TNF-beta induces secretion of colony stimulating factor for macrophages (CSF-1) by human monocytes

Oster, W., Lindemann, A., Horn, S., Mertelsmann, R., & Herrmann, F. (1987) · Blood · doi:10.1182/blood.v70.5.1700.1700 · Cited by 190 · see citing works

Induction of colony stimulating factor in vivo by recombinant interleukin 1 alpha and recombinant tumor necrosis factor alpha 1.

Vogel, S. N., Douches, S. D., Kaufman, E. N., & Neta, R. (1987) · The Journal of Immunology · doi:10.4049/jimmunol.138.7.2143 · Cited by 144 · see citing works

Tumor necrosis factor-alpha and hematopoietic progenitors: effects of tumor necrosis factor on the growth of erythroid progenitors CFU-E and BFU-E and the hematopoietic cell lines K562, HL60, and HEL cells.

Roodman, G. D., Bird, A., Hutzler, D. H., & Montgomery, W. (1987) · PubMed · Cited by 144 · see citing works

Effects of recombinant tumor necrosis factor, lymphotoxin, and immune interferon on proliferation and differentiation of enriched hematopoietic precursor cells.

Murphy, M. E., PERUSSIA, B., & Trinchieri, G. (1988) · PubMed · Cited by 122 · see citing works

Effect of enhanced macrophage function on early wound healing.

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Potentiation of lymphokine-induced macrophage activation by tumor necrosis factor- alpha .

Heidenreich, S., Weyers, M., Gong, J.-H., Sprenger, H., Nain, M., & Gemsa, D. (1988) · The Journal of Immunology · doi:10.4049/jimmunol.140.5.1511 · Cited by 68 · see citing works

Apoptosis mediates the decrease in cellularity during the transition between granulation tissue and scar.

Desmoulière, A., Redard, M., Darby, I. A., & Gabbiani, G. (1995) · Europe PMC (PubMed Central) · Cited by 1,173 · see citing works

Angiogenesis in wound healing

Arnold, F., & West, D. C. (1991) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(91)90034-j · Cited by 354 · see citing works

Growth factors in wound healing

Lawrence, W., & Diegelmann, R. F. (1994) · Clinics in Dermatology · doi:10.1016/0738-081x(94)90266-6 · Cited by 322 · see citing works

The Innate Immune System in Acute and Chronic Wounds

MacLeod, A. S., & Mansbridge, J. N. (2016) · Advances in Wound Care · doi:10.1089/wound.2014.0608 · Cited by 289 · see citing works

Intraarticular inflammatory cytokines in acute anterior cruciate ligament injured knee

入江, 一., Uchiyama, E., & Iwaso, H. (2003) · The Knee · doi:10.1016/s0968-0160(02)00083-2 · Cited by 270 · see citing works

Accelerated wound healing in tumor necrosis factor receptor p55‐deficient mice with reduced leukocyte infiltration

MORI, R., KONDO, T., OHSHIMA, T., ISHIDA, Y., & MUKAIDA, N. (2002) · The FASEB Journal · doi:10.1096/fj.01-0776com · Cited by 250 · see citing works

Stress-induced enhancement of leukocyte trafficking into sites of surgery or immune activation

Viswanathan, K., & Dhabhar, F. S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501650102 · Cited by 246 · see citing works

Acute and late changes in intraarticular cytokine levels following anterior cruciate ligament injury

Bigoni, M., Sacerdote, P., Turati, M., Franchi, S., Gandolla, M., Gaddi, D., Moretti, S., Munegato, D., Augusti, C. A., Bresciani, E., et al. (2012) · Journal of Orthopaedic Research® · doi:10.1002/jor.22208 · Cited by 175 · see citing works

Anti-tumor necrosis factor and postoperative complications in Crohnʼs disease: systematic review and meta-analysis

Kopylov, U., Ben‐Horin, S., Zmora, O., Eliakim, R., & Katz, L. H. (2012) · Inflammatory Bowel Diseases · doi:10.1002/ibd.22954 · Cited by 167 · see citing works

Meta‐analysis: peri‐operative anti‐ TNF α treatment and post‐operative complications in patients with inflammatory bowel disease

Narula, N., Charleton, D., & Marshall, J. K. (2013) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.12313 · Cited by 159 · see citing works

High glucose environment induces M1 macrophage polarization that impairs keratinocyte migration via TNF-α: An important mechanism to delay the diabetic wound healing

Huang, S., Wu, C., Chiu, M., Wu, C., Chang, Y., Chen, G., & Lan, C.-C. E. (2019) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2019.11.004 · Cited by 158 · see citing works

Therapeutic antibodies that target inflammatory cytokines in autoimmune diseases

Lai, Y., & Dong, C. (2015) · International Immunology · doi:10.1093/intimm/dxv063 · Cited by 153 · see citing works

The Cellular Derivation and the Life Span of the Myofibroblast

Gabbiani, G. (1996) · Pathology - Research and Practice · doi:10.1016/s0344-0338(96)80092-6 · Cited by 147 · see citing works

Cytokines and Wound Healing: The Role of Cytokine and Anticytokine Therapy in the Repair Response

Efron, P. A., & Moldawer, L. L. (2004) · Journal of Burn Care & Rehabilitation · doi:10.1097/01.bcr.0000111766.97335.34 · Cited by 141 · see citing works

Cytokines, growth factors, and plastic surgery.

Rumalla, V., & Borah, G. (2001) · Plastic and Reconstructive Surgery · doi:10.1097/00006534-200109010-00019 · Cited by 132 · see citing works

Complication rates of 127 surgical procedures performed in rheumatic patients receiving tumor necrosis factor alpha blockers.

Ruyssen‐Witrand, A., Gossec, L., Salliot, C., Luc, M., Duclos, M., Guignard, S., & Dougados, M. (2007) · PubMed · Cited by 125 · see citing works

Patients with Rheumatoid Arthritis Undergoing Surgery: How Should We Deal with Antirheumatic Treatment?

Pieringer, H., Stuby, U., & Biesenbach, G. (2007) · Seminars in Arthritis and Rheumatism · doi:10.1016/j.semarthrit.2006.10.003 · Cited by 118 · see citing works

Topical application of the tumour necrosis factor‐α antibody infliximab improves healing of chronic wounds

Streit, M., Beleznay, Z., & Braathen, L. R. (2006) · International Wound Journal · doi:10.1111/j.1742-481x.2006.00233.x · Cited by 117 · see citing works

Regulation of keratinocyte growth factor gene expression in human skin fibroblasts

Tang, A., & Gilchrest, B. A. (1996) · Journal of Dermatological Science · doi:10.1016/0923-1811(95)00418-1 · Cited by 107 · see citing works

Therapeutic Potential of Adipose-Derived SSEA-3-Positive Muse Cells for Treating Diabetic Skin Ulcers

Kinoshita, K., Kuno, S., Ishimine, H., D, N. A. M., Mineda, K., D, H. K. M., Doi, K., Kanayama, K., Feng, J., Mashiko, T., et al. (2015) · Stem Cells Translational Medicine · doi:10.5966/sctm.2014-0181 · Cited by 106 · see citing works

Production of monoclonal antibodies to study corrosion products of CO-CR biomaterials

Yang, J. M., & Merritt, K. (1996) · Journal of Biomedical Materials Research · doi:10.1002/(sici)1097-4636(199605)31:1 · Cited by 46 · see citing works

Hypertrophic scar formation is associated with an increased number of epidermal Langerhans cells

Niessen, F. B., Schalkwijk, J., Vos, H., & Timens, W. (2003) · The Journal of Pathology · doi:10.1002/path.1502 · Cited by 99 · see citing works

Surgery in the age of biologics

Wong, D. J., Roth, E. M., Feuerstein, J. D., & Poylin, V. Y. (2019) · Gastroenterology report · doi:10.1093/gastro/goz004 · Cited by 90 · see citing works

Pentoxifylline Accelerates Gastric Ulcer Healing in Rats: Roles of Tumor Necrosis Factor Alpha and Neutrophils during the Early Phase of Ulcer Healing

Shimizu, N., Watanabe, T., Arakawa, T., Fujiwara, Y., Higuchi, K., & Kuroki, T. (2000) · Digestion · doi:10.1159/000007752 · Cited by 87 · see citing works

Tumour necrosis factor α antagonists and early postoperative complications in patients with inflammatory joint disease undergoing elective orthopaedic surgery

Talwalkar, S. C., Grennan, D. M., Gray, J., Johnson, P., & Hayton, M. J. (2005) · Annals of the Rheumatic Diseases · doi:10.1136/ard.2004.028365 · Cited by 82 · see citing works

In vivo effect of hyperbaric oxygen on wound angiogenesis and epithelialization

Sander, A. L., Henrich, D. M., Muth, C. M., Marzi, İ., Barker, J. H., & Frank, J. M. (2009) · Wound Repair and Regeneration · doi:10.1111/j.1524-475x.2009.00455.x · Cited by 82 · see citing works

Carbohydrate-Coated Gold–Silver Nanoparticles for Efficient Elimination of Multidrug Resistant Bacteria and in Vivo Wound Healing

Kumar, S., Majhi, R. K., Singh, A., Mishra, M., Tiwari, A. K., Chawla, S., Guha, P., Satpati, B., Mohapatra, H., Goswami, L., et al. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b17086 · Cited by 81 · see citing works

Tumor necrosis factor-alpha is expressed by monocytes/macrophages following cardiac microembolization and is antagonized by cyclosporine

Arras, M., Sträßer, R., Mohri, M., Doll, R., Eckert, P., Schaper, W. K. A., & Schaper, J. (1998) · Basic Research in Cardiology · doi:10.1007/s003950050069 · Cited by 80 · see citing works

Blockade of the Complement C5a Receptor Reduces Incisional Allodynia, Edema, and Cytokine Expression

Clark, J. D., Qiao, Y., Li, X., Shi, X., Angst, M. S., & Yeomans, D. C. (2006) · Anesthesiology · doi:10.1097/00000542-200606000-00024 · Cited by 78 · see citing works

Topical application of Acalypha indica accelerates rat cutaneous wound healing by up-regulating the expression of Type I and III collagen

Ganeshkumar, M., Ponrasu, T., Krithika, R., Kuttalam, I., Gayathri, V. S., & Suguna, L. (2012) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2012.04.005 · Cited by 76 · see citing works

Arabinogalactan proteins contribute to the immunostimulatory properties of New Zealand honeys

Gannabathula, S., Skinner, M. A., Rosendale, D., Greenwood, J. M., Mutukumira, A. N., Steinhorn, G., Stephens, J., Krissansen, G. W., & Schlothauer, R. C. (2012) · Immunopharmacology and Immunotoxicology · doi:10.3109/08923973.2011.641974 · Cited by 74 · see citing works

Neutrophils Express Tumor Necrosis Factor-α During Mouse Skin Wound Healing

Feiken, E., Rømer, J., Eriksen, J., & Lund, L. R. (1995) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12313429 · Cited by 75 · see citing works

Perioperative management of patients with rheumatoid arthritis in the era of biologic response modifiers

Rosandich, P. A., Kelley, J. T., & Conn, D. L. (2004) · Current Opinion in Rheumatology · doi:10.1097/00002281-200405000-00005 · Cited by 72 · see citing works

Phenotypic Differences in Cytokine Responsiveness of Hypertrophic Scar Versus Normal Dermal Fibroblasts

Garner, W. L., Karmiol, S., Rodriguez, J. L., Smith, D. J., & Phan, S. H. (1993) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12371710 · Cited by 72 · see citing works

Tumor necrosis factor production by murine resident peritoneal macrophages is enhanced by dietary n−3 polyunsaturated fatty acids

Harðardóttir, I., & Kinsella, J. (1991) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/0167-4889(91)90098-i · Cited by 71 · see citing works

The effect of topical tripeptide-copper complex on healing of ischemic open wounds

Canapp, S. O., Farese, J. P., Schultz, G. S., Gowda, S., Ishak, A. M., Swaim, S. F., Vangilder, J., Lee‐Ambrose, L., & Martin, F. G. (2003) · Veterinary Surgery · doi:10.1111/j.1532-950x.2003.00515.x · Cited by 68 · see citing works

Influences of anti-tumour necrosis factor agents on postoperative recovery in patients with rheumatoid arthritis

Hirano, Y., Kojima, T., Kanayama, Y., Shioura, T., Hayashi, M., Kida, D., Kaneko, A., Eto, Y., & Ishiguro, N. (2010) · Clinical Rheumatology · doi:10.1007/s10067-009-1346-1 · Cited by 66 · see citing works

Contributions of different intraarticular tissues to the acute phase elevation of synovial fluid MMP‐2 following rat ACL rupture

Tang, Z., Yang, L., Wang, Y., Xue, R., Zhang, J., Huang, W., Chen, P. C., & Sung, K. ‐. P. (2008) · Journal of Orthopaedic Research® · doi:10.1002/jor.20763 · Cited by 68 · see citing works

Increasing the Dietary (n-3) to (n-6) Polyunsaturated Fatty Acid Ratio Increases Tumor Necrosis Factor Production by Murine Resident Peritoneal Macrophages without an Effect on Elicited Peritoneal Macrophages

Harðardóttir, I., & Kinsella, J. (1992) · Journal of Nutrition · doi:10.1093/jn/122.10.1942 · Cited by 66 · see citing works

Risk factors for total joint arthroplasty infection in patients receiving tumor necrosis factor α-blockers: a case-control study

Gilson, M., Gossec, L., Xavier Mariette, A., Gherissi, D. C., Guyot, M.-H., Berthelot, J., Wendling, D., Michelet, C., Dellamonica, P., Tubach, F., et al. (2010) · Arthritis Research & Therapy · doi:10.1186/ar3087 · Cited by 65 · see citing works

Inhibition of tumor necrosis factor‐α attenuates wound breaking strength in rats

Lee, R. H., Efron, D. T., Tantry, U., Stuelten, C., Moldawer, L. L., Abouhamze, A., & Barbul, A. (2000) · Wound Repair and Regeneration · doi:10.1046/j.1524-475x.2000.00547.x · Cited by 63 · see citing works

In Vivo Effect of Tumor Necrosis Factor Alpha on Wound Angiogenesis and Epithelialization

Frank, J. M., Born, K., Barker, J. H., & Marzi, İ. (2003) · European Journal of Trauma · doi:10.1007/s00068-003-1284-6 · Cited by 60 · see citing works

Suppression of Syndecan-1 Expression in Endothelial Cells by Tumor Necrosis Factor-α

Kainulainen, V., Nelimarkka, L. O., Järveläinen, H., Laato, M. K., Jalkanen, M., & Elenius, K. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.31.18759 · Cited by 58 · see citing works

Arnebin-1 Accelerates Normal and Hydrocortisone-Induced Impaired Wound Healing1

Sidhu, G. S., Singh, A., Banaudha, K. K., Gaddipati, J. P., Patnaik, G. K., & Maheshwari, R. K. (1999) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.1999.00761.x · Cited by 54 · see citing works

UK guidelines for management of acute pancreatitis: is it time to change?

Gurusamy, K. S. (2005) · Gut · doi:10.1136/gut.2005.071076 · Cited by 54 · see citing works

Tumor Necrosis Factor Mediates Impaired Wound Healing in Chronic Abdominal Sepsis

Cooney, R. N., Iocono, J. A., Maish, G. O., Smith, J. S., & Ehrlich, P. (1997) · doi:10.1097/00005373-199703000-00008 · Cited by 54 · see citing works

A durable, stretchable, and disposable electrochemical biosensor on three-dimensional micro-patterned stretchable substrate

Kim, B., Lee, H., & Lee, N. (2018) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2018.12.045 · Cited by 52 · see citing works

Growth factors and wound healing

Rothe, M. J., & Falanga, V. (1991) · Clinics in Dermatology · doi:10.1016/0738-081x(91)90084-x · Cited by 52 · see citing works

A comparison of the inflammatory response to a polydimethylsiloxane implant in male and female Balb/c mice

Dalu, A., Blaydes, B. S., Lomax, L. G., & Delclos, K. B. (2000) · Biomaterials · doi:10.1016/s0142-9612(00)00078-8 · Cited by 51 · see citing works

Effect of transforming growth factor beta and basic fibroblast growth factor on steroid-impaired healing intestinal wounds

Slavin, J. P., Nash, J. R. G., & Kingsnorth, A. N. (1992) · British journal of surgery · doi:10.1002/bjs.1800790124 · Cited by 51 · see citing works

Release of TNF‐α from macrophages is mediated by small GTPase Rab37

Mori, R., Ikematsu, K., Kitaguchi, T., Kim, S. E., Okamoto, M., Chiba, T., Miyawaki, A., Shimokawa, I., & Tsuboi, T. (2011) · European Journal of Immunology · doi:10.1002/eji.201141640 · Cited by 50 · see citing works

Role of tumor necrosis factor–α in wound repair in human vocal fold fibroblasts

Chen, X., & Thibeault, S. L. (2010) · The Laryngoscope · doi:10.1002/lary.21037 · Cited by 49 · see citing works

Increased release of tumour necrosis factor-alpha in human tear fluid after excimer laser induced corneal wound

Vesaluoma, M. H., Teppo, A.-M., Grönhagen‐Riska, C., & Tervo, T. T. (1997) · British Journal of Ophthalmology · doi:10.1136/bjo.81.2.145 · Cited by 48 · see citing works

Peptide growth factors and wound healing

Kingsnorth, A. N., & Slavin, J. P. (1991) · British journal of surgery · doi:10.1002/bjs.1800781104 · Cited by 47 · see citing works

Continuous versus intermittent therapy for moderate-to-severe psoriasis.

Ramirez‐Fort, M. K., Levin, A. A., Au, S.-C., & Gottlieb, A. B. (2013) · PubMed · Cited by 46 · see citing works

The utility of collagen-based vehicles in delivery of growth factors for hard and soft tissue wound repair

McPherson, J. M. (1992) · Clinical Materials · doi:10.1016/0267-6605(92)90103-z · Cited by 46 · see citing works

Wound Healing Associated with Severe Surgical Illness

Clark, M. A., Plank, L. D., & Hill, G. L. (2000) · World Journal of Surgery · doi:10.1007/s002689910106 · Cited by 46 · see citing works

Growth factors as wound healing agents

Robson, M. C. (1991) · Current Opinion in Biotechnology · doi:10.1016/s0958-1669(05)80122-3 · Cited by 45 · see citing works

Should anti-TNF therapy be discontinued in rheumatoid arthritis patients undergoing elective orthopaedic surgery? A systematic review of the evidence

Goh, L., Jewell, T., Laversuch, C. J., & Samanta, A. (2011) · Rheumatology International · doi:10.1007/s00296-011-2040-6 · Cited by 44 · see citing works

Influence of Hypoxia and Glucose Deprivation on Tumour Necrosis Factor-Alpha and Granulocyte- Macrophage Colony-Stimulating Factor Expression in Human Cultured Monocytes

Guida, E., & Stewart, A. G. (1998) · Cellular Physiology and Biochemistry · doi:10.1159/000016272 · Cited by 44 · see citing works

Combined effects of TNF‐α, IL‐1β, and HIF‐1α on MMP‐2 production in ACL fibroblasts under mechanical stretch: An in vitro study

Wang, Y., Tang, Z., Xue, R., Singh, G. K., Shi, K., Lv, Y., & Yang, L. (2011) · Journal of Orthopaedic Research® · doi:10.1002/jor.21349 · Cited by 41 · see citing works

Characterization of immunomodulatory responses induced by manuka honey

Masad, R. J., Nasser, R. A., Bashir, G. H., Mohamed, Y. A., Al-Sbiei, A., Al-Saafeen, B. H., Fernández-Cabezudo, M. J., & al-Ramadi, B. K. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1020574 · Cited by 41 · see citing works

Interleukin-1 beta influences on lysyl oxidases and matrix metalloproteinases profile of injured anterior cruciate ligament and medial collateral ligament fibroblasts

Xie, J., Wang, C., Yin, L. L., Xu, C., Zhang, Y., & Sung, K.-L. P. (2012) · International Orthopaedics · doi:10.1007/s00264-012-1549-y · Cited by 39 · see citing works

Randomised controlled trial of topical kanuka honey for the treatment of rosacea

Braithwaite, I. E., Hunt, A., Riley, J., Fingleton, J., Kocks, J. W. H., Corin, A., Helm, C., Sheahan, D., Tofield, C., Montgomery, B., et al. (2015) · BMJ Open · doi:10.1136/bmjopen-2015-007651 · Cited by 39 · see citing works

Tumor Necrosis Factor Binding Protein Improves Incisional Wound Healing in Sepsis

Maish, G. O., Shumate, M. L., Ehrlich, H. P., & Cooney, R. N. (1998) · Journal of Surgical Research · doi:10.1006/jsre.1998.5315 · Cited by 36 · see citing works

Particulate β‐glucan induces TNF‐α production in wound macrophages via a redox‐sensitive NF‐κβ‐dependent pathway

Roy, S., Dickerson, R. M., Khanna, S., Collard, E., Gnyawali, U. S., Gordillo, G. M., & Sen, C. K. (2011) · Wound Repair and Regeneration · doi:10.1111/j.1524-475x.2011.00688.x · Cited by 34 · see citing works

Refractory ulcers: The role of tumor necrosis factor–α

Weinstein, D. A., & Kirsner, R. S. (2010) · Journal of the American Academy of Dermatology · doi:10.1016/j.jaad.2009.08.004 · Cited by 33 · see citing works

Chronic intestinal pseudo-obstruction due to lymphocytic leiomyositis: is there a place for immunomodulatory therapy?

Oton, E., Moreira, V., Redondo, C., Lopez-San-Roman, A., Foruny, J. R., Plaza, G., de Vicente, E., & Quijano, Y. (2005) · Gut · doi:10.1136/gut.2005.071811 · Cited by 33 · see citing works

Risk of Delayed Healing of Tooth Extraction Wounds and Osteonecrosis of the Jaw among Patients Treated with Potential Immunosuppressive Drugs: A Retrospective Cohort Study

Hayashi, M., Morimoto, Y., Iida, T., Tanaka, Y., & Sugiyama, S. (2018) · The Tohoku Journal of Experimental Medicine · doi:10.1620/tjem.246.257 · Cited by 32 · see citing works

Scar remodeling after strabismus surgery.

Ludwig, I. (1999) · Europe PMC (PubMed Central) · Cited by 32 · see citing works

Do antitumor necrosis factor agents increase the risk of postoperative orthopedic infections?

Pappas, D. A., & Giles, J. T. (2008) · Current Opinion in Rheumatology · doi:10.1097/bor.0b013e3282fcc345 · Cited by 32 · see citing works

Peptide‐Based Functional Amyloid Hydrogel Enhances Wound Healing in Normal and Diabetic Rat Models

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