Estrogen Effects on Wound Healing

Hypertrophic Scarring and Keloids: Pathomechanisms and Current and Emerging Treatment Strategies

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Distinct fibroblast lineages determine dermal architecture in skin development and repair

Driskell, R. R., Lichtenberger, B. M., Hoste, E., Kretzschmar, K., Simons, B. D., Charalambous, M., Ferron, S. R., Herault, Y., Pavlovic, G., Ferguson-Smith, A. C., et al. (2013) · Nature · doi:10.1038/nature12783 · Cited by 1,291 · see citing works

Diabetes and Wound Angiogenesis

Okonkwo, U. A., & DiPietro, L. A. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18071419 · Cited by 1,037 · see citing works

Estrogen receptors regulate innate immune cells and signaling pathways

Kovats, S. (2015) · Cellular Immunology · doi:10.1016/j.cellimm.2015.01.018 · Cited by 987 · see citing works

Keloid and Hypertrophic Scars Are the Result of Chronic Inflammation in the Reticular Dermis

Ogawa, R. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18030606 · Cited by 985 · see citing works

Macrophage Phenotypes Regulate Scar Formation and Chronic Wound Healing

Hesketh, M., Sahin, K. B., West, Z. E., & Murray, R. Z. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18071545 · Cited by 852 · see citing works

Keloids and Hypertrophic Scars: Pathophysiology, Classification, and Treatment

Berman, B., Maderal, A. D., & Raphael, B. A. (2016) · Dermatologic Surgery · doi:10.1097/dss.0000000000000819 · Cited by 692 · see citing works

Regeneration of fat cells from myofibroblasts during wound healing

Plikus, M. V., Guerrero-Juarez, C. F., Ito, M., Li, Y. R., Dedhia, P. H., Zheng, Y., Shao, M., Gay, D. L., Ramos, R., Hsi, T.-C., et al. (2017) · Science · doi:10.1126/science.aai8792 · Cited by 584 · see citing works

The Immune System Is a Natural Target for Estrogen Action: Opposing Effects of Estrogen in Two Prototypical Autoimmune Diseases

Khan, D., & Ahmed, S. A. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00635 · Cited by 458 · see citing works

Topical Estrogen Accelerates Cutaneous Wound Healing in Aged Humans Associated with an Altered Inflammatory Response

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Secretory leukocyte protease inhibitor mediates non-redundant functions necessary for normal wound healing

Ashcroft, G. S., Lei, K.-J., Jin, W., Longenecker, G., Kulkarni, A. B., Greenwell‐Wild, T., Hale‐Donze, H., McGrady, G., Song, X.-Y., & Wahl, S. M. (2000) · Nature Medicine · doi:10.1038/80489 · Cited by 417 · see citing works

Understanding fibroblast heterogeneity in the skin

Driskell, R. R., & Watt, F. M. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.10.001 · Cited by 406 · see citing works

Effects of Hormone-Replacement Therapy on Fibrinolysis in Postmenopausal Women

Koh, K. K., Mincemoyer, R., Bui, M. N., Csákó, G., Pucino, F., Guetta, V., Waclawiw, M. A., & Cannon, R. O. (1997) · New England Journal of Medicine · doi:10.1056/nejm199703063361002 · Cited by 372 · see citing works

The role of matrix metalloproteinases in aging: Tissue remodeling and beyond

Freitas‐Rodríguez, S., Folgueras, A. R., & López-Otı́n, C. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2017.05.007 · Cited by 367 · see citing works

Biology and Biomarkers for Wound Healing

Lindley, L. E., Stojadinović, O., Pastar, I., & Tomic‐Canic, M. (2016) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000002682 · Cited by 365 · see citing works

Sex, the aging immune system, and chronic disease

Bupp, M. G. (2015) · Cellular Immunology · doi:10.1016/j.cellimm.2015.02.002 · Cited by 333 · see citing works

Defining dermal adipose tissue

Driskell, R. R., Jahoda, C. A. B., Chuong, C., Watt, F. M., & Horsley, V. (2014) · Experimental Dermatology · doi:10.1111/exd.12450 · Cited by 316 · see citing works

Stem Cells in Skin Regeneration, Wound Healing, and Their Clinical Applications

Ojeh, N. O., Pastar, I., Tomic‐Canic, M., & Stojadinović, O. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms161025476 · Cited by 305 · see citing works

Estrogens and aging skin

Thornton, M. J. (2013) · Dermato-Endocrinology · doi:10.4161/derm.23872 · Cited by 279 · see citing works

Matrix metalloproteinases as regulators of inflammatory processes

Fingleton, B. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2017.05.010 · Cited by 263 · see citing works

Estradiol suppresses NF-κB activation through coordinated regulation of let-7a and miR-125b in primary human macrophages

Murphy, A., Guyre, P., & Pioli, P. (2010) · Journal of Immunology · doi:10.4049/jimmunol.0903463 · Cited by 255 · see citing works

Cutaneous scarring: Pathophysiology, molecular mechanisms, and scar reduction therapeutics

Profyris, C., Tziotzios, C., & Do Vale, I. (2012) · Journal of the American Academy of Dermatology · doi:10.1016/j.jaad.2011.05.055 · Cited by 250 · see citing works

Matrix metalloproteinase collagenolysis in health and disease

Amar, S., Smith, L., & Fields, G. B. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2017.04.015 · Cited by 236 · see citing works

Macrophage Differentiation in Normal and Accelerated Wound Healing

Kotwal, G. J., & Chien, S. (2017) · Results and problems in cell differentiation · doi:10.1007/978-3-319-54090-0_14 · Cited by 205 · see citing works

Wound Healing: Part I. Basic Science

Janis, J. E., & Harrison, B. L. (2016) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000002773 · Cited by 204 · see citing works

Effect of estrogens on skin aging and the potential role of SERMs

Thornton, J. (2007) · Clinical Interventions in Aging · doi:10.2147/cia.s798 · Cited by 193 · see citing works

Next generation matrix metalloproteinase inhibitors — Novel strategies bring new prospects

Levin, M., Udi, Y., Solomonov, I., & Sagi, I. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2017.06.009 · Cited by 185 · see citing works

New intracellular activities of matrix metalloproteinases shine in the moonlight

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

Matrix metalloproteinases: The sculptors of chronic cutaneous wounds

Krishnaswamy, V. R., Mintz, D., & Sagi, I. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2017.08.003 · Cited by 184 · see citing works

Skin collagen changes in postmenopausal women receiving different regimens of estrogen therapy.

Brincat, M., Versi, E., Cf, M., Magos, A. L., de Trafford, J., & Jw, S. (1987) · PubMed · Cited by 178 · see citing works

Effects of postmenopausal hypoestrogenism on skin collagen

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Estrogen Receptor-Dependent Regulation of Dendritic Cell Development and Function

Laffont, S., Seillet, C., & Guéry, J. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00108 · Cited by 164 · see citing works

The role of estrogen in cutaneous ageing and repair

Wilkinson, H. N., & Hardman, M. J. (2017) · Maturitas · doi:10.1016/j.maturitas.2017.06.026 · Cited by 162 · see citing works

Estrogen, not intrinsic aging, is the major regulator of delayed human wound healing in the elderly

Hardman, M. J., & Ashcroft, G. S. (2008) · Genome Biology · doi:10.1186/gb-2008-9-5-r80 · Cited by 157 · see citing works

Currently known risk factors for hypertrophic skin scarring: A review

Butzelaar, L., Ulrich, M. M. W., van der Molen, A. B. M., Niessen, F. B., & Beelen, R. H. J. (2015) · Journal of Plastic Reconstructive & Aesthetic Surgery · doi:10.1016/j.bjps.2015.11.015 · Cited by 156 · see citing works

Are keloid and hypertrophic scar different forms of the same disorder? A fibroproliferative skin disorder hypothesis based on keloid findings

Huang, C., Akaishi, S., Hyakusoku, H., & Ogawa, R. (2012) · International Wound Journal · doi:10.1111/j.1742-481x.2012.01118.x · Cited by 155 · see citing works

Scarless Wound Healing

Walmsley, G. G., Maan, Z. N., Wong, V., Duscher, D., Hu, M. S.-M., Zielins, E. R., Wearda, T. L., Muhonen, E. G., McArdle, A., Tevlin, R., et al. (2015) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000000972 · Cited by 152 · see citing works

Regulation of TH17 Cells and Associated Cytokines in Wound Healing, Tissue Regeneration, and Carcinogenesis

Brockmann, L., Giannou, A. D., Gagliani, N., & Huber, S. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18051033 · Cited by 143 · see citing works

Estradiol Regulates Expression of Estrogen Receptor ERα46 in Human Macrophages

Murphy, A. J., Guyre, P. M., Wira, C. R., & Pioli, P. A. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005539 · Cited by 138 · see citing works

Tamoxifen Resistance: Emerging Molecular Targets

Rondón‐Lagos, M., Villegas, V. E., Rangel, N., Sánchez, M. C., & Zaphiropoulos, P. G. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17081357 · Cited by 138 · see citing works

The effect of estrogen on tendon and ligament metabolism and function

LeBlanc, D., Schneider, M., Angele, P., Vollmer, G., & Docheva, D. (2017) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2017.06.008 · Cited by 134 · see citing works

The effect of topical oestradiol on skin collagen of postmenopausal women

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Nonsteroidal Anti-Inflammatory Drugs for Wounds: Pain Relief or Excessive Scar Formation?

Su, W., Cheng, M., Lee, W.-L., Tsou, T., Chang, W.-H., Chen, C., & Wang, P. (2010) · Mediators of Inflammation · doi:10.1155/2010/413238 · Cited by 128 · see citing works

Regeneration of injured skin and peripheral nerves requires control of wound contraction, not scar formation

Yannas, I. V., Tzeranis, D. S., & So, P. T. C. (2017) · Wound Repair and Regeneration · doi:10.1111/wrr.12516 · Cited by 119 · see citing works

The effects of systemic hormonal replacement therapy on the skin of postmenopausal women

Sauerbronn, A. V. D., da Fonseca, Â. M., Bagnoli, V. R., Saldiva, P. H. N., & Pinotti, J. A. (1999) · International Journal of Gynecology & Obstetrics · doi:10.1016/s0020-7292(99)00166-6 · Cited by 117 · see citing works

Hormone replacement therapy and prevention of pressure ulcers and venous leg ulcers

Margolis, D. J., KNAUSS, J. S., & Bilker, W. B. (2002) · The Lancet · doi:10.1016/s0140-6736(02)07806-6 · Cited by 102 · see citing works

Macrophage Migration Inhibitory Factor

Hardman, M. J., Waite, A., Zeef, L. A. H., Burow, M. E., Nakayama, T., & Ashcroft, G. S. (2005) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)61241-2 · Cited by 101 · see citing works

Scar Prevention and Enhanced Wound Healing Induced by Polydeoxyribonucleotide in a Rat Incisional Wound-Healing Model

Jeong, W., Yang, C. E., Roh, T. S., Kim, J. H., Lee, J. H., & Lee, W. J. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18081698 · Cited by 97 · see citing works

Skin collagen changes in postmenopausal women receiving different regimens of estrogen therapy

Brincat, M., Versi, E., & Cf, M. (1988) · Maturitas · doi:10.1016/0378-5122(88)90119-3 · Cited by 95 · see citing works

Site-Specific Keloid Fibroblasts Alter the Behaviour of Normal Skin and Normal Scar Fibroblasts through Paracrine Signalling

Ashcroft, K. J., Syed, F., & Bayat, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075600 · Cited by 92 · see citing works

Cellular Reparative Mechanisms of Mesenchymal Stem Cells for Retinal Diseases

Ding, S. L. S., Kumar, S. S., & Mok, P. L. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18081406 · Cited by 90 · see citing works

Self-renewal and phenotypic conversion are the main physiological responses of macrophages to the endogenous estrogen surge

Pepe, G., Braga, D., Renzi, T. A., Villa, A., Bolego, C., D’Avila, F., Barlassina, C., Maggi, A., Locati, M., & Vegeto, E. (2017) · Scientific Reports · doi:10.1038/srep44270 · Cited by 80 · see citing works

Gypenoside XVII Prevents Atherosclerosis by Attenuating Endothelial Apoptosis and Oxidative Stress: Insight into the ERα-Mediated PI3K/Akt Pathway

Yang, K., Zhang, H., Luo, Y., Zhang, J., Wang, M., Liao, P., Cao, L. H., Guo, P., Sun, G., & Sun, X. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18020077 · Cited by 77 · see citing works

Dietary Management of Skin Health: The Role of Genistein

Irrera, N., Pizzino, G., D’Anna, R., Vaccaro, M., Arcoraci, V., Squadrito, F., Altavilla, D., & Bitto, A. (2017) · Nutrients · doi:10.3390/nu9060622 · Cited by 75 · see citing works

The Sex Steroid Precursor DHEA Accelerates Cutaneous Wound Healing Via the Estrogen Receptors

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Estrogen Modulates Specific Life and Death Signals Induced by LH and hCG in Human Primary Granulosa Cells In Vitro

Casarini, L., Riccetti, L., Pascali, F. D., Gilioli, L., Marino, M., Vecchi, E., Morini, D., Nicoli, A., Sala, G. B. L., & Simoni, M. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18050926 · Cited by 73 · see citing works

siRNA-Targeting Transforming Growth Factor-β Type I Receptor Reduces Wound Scarring and Extracellular Matrix Deposition of Scar Tissue

Wang, Y.-W., Liou, N.-H., Cherng, J., Chang, S., Ma, K., Fu, E., Liu, J.-C., & Dai, N. (2014) · Journal of Investigative Dermatology · doi:10.1038/jid.2014.84 · Cited by 72 · see citing works

Postmenopausal skin and estrogen

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Myofibroblast repair mechanisms post-inflammatory response: a fibrotic perspective

Gerarduzzi, C., & Battista, J. A. D. (2016) · Inflammation Research · doi:10.1007/s00011-016-1019-x · Cited by 70 · see citing works

Fibroblast fate regulation by time dependent TGF-β1 and IL-10 stimulation in biomimetic 3D matrices

Sapudom, J., Wu, X., Chkolnikov, M., Ansorge, M., Anderegg, U., & Pompe, W. (2017) · Biomaterials Science · doi:10.1039/c7bm00286f · Cited by 69 · see citing works

Prostaglandin Transporter Modulates Wound Healing in Diabetes by Regulating Prostaglandin-Induced Angiogenesis

Syeda, M. M., Jing, X., Mirza, R. H., Yu, H., Sellers, R. S., & Chi, Y. (2012) · American Journal Of Pathology · doi:10.1016/j.ajpath.2012.03.012 · Cited by 63 · see citing works

Identification of Collagen 1 as a Post-transcriptional Target of miR-29b in Skin Fibroblasts: Therapeutic Implication for Scar Reduction

Cheng, J., Wang, Y., Wang, D., & Wu, Y. (2012) · The American Journal of the Medical Sciences · doi:10.1097/maj.0b013e318267680d · Cited by 61 · see citing works

MicroRNAs: New Insight in Modulating Follicular Atresia: A Review

Worku, T., Rehman, Z. U., Talpur, H. S., Bhattarai, D., Ullah, F., Malobi, N., Kebede, T., & Yang, L. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18020333 · Cited by 57 · see citing works

DHEA protects mitochondria against dual modes of apoptosis and necroptosis in human granulosa HO23 cells

Tsui, K., Wang, P., Lin, L., & Li, C. (2017) · Reproduction · doi:10.1530/rep-17-0016 · Cited by 57 · see citing works

Effects of Vitex agnus-castus fruit on sex hormones and antioxidant indices in a d-galactose-induced aging female mouse model

Ahangarpour, A., Najimi, S. A., & Farbood, Y. (2016) · Journal of the Chinese Medical Association · doi:10.1016/j.jcma.2016.05.006 · Cited by 56 · see citing works

Estrogen Accelerates Cutaneous Wound Healing by Promoting Proliferation of Epidermal Keratinocytes via Erk/Akt Signaling Pathway

Zhou, T., Yang, Z., Chen, Y., Chen, Y. Z., Huang, Z., You, B. R., Peng, Y., & Chen, J. (2016) · Cellular Physiology and Biochemistry · doi:10.1159/000443048 · Cited by 53 · see citing works

Functional differences between neonatal and adult fibroblasts and keratinocytes: Donor age affects epithelial-mesenchymal crosstalk in vitro

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Hormone therapy and hemostasis among postmenopausal women

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Preventive Effects of Rhodiola rosea L. on Bleomycin-Induced Pulmonary Fibrosis in Rats

Zhang, K., Si, X.-P., Huang, J., Han, J., Xu, L., Xu, X., Wang, Y.-T., Li, G., Wang, H., & Wang, J. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17060879 · Cited by 47 · see citing works

The Role of Elastic Fibers in Scar Formation and Treatment

Cohen, B. E., Geronemus, R. G., McDaniel, D. H., & Brauer, J. A. (2016) · Dermatologic Surgery · doi:10.1097/dss.0000000000000840 · Cited by 46 · see citing works

Knockdown of XBP1 by RNAi in Mouse Granulosa Cells Promotes Apoptosis, Inhibits Cell Cycle, and Decreases Estradiol Synthesis

Wang, N., Zhao, F., Lin, P., Zhang, G., Tang, K., Wang, A., & Jin, Y. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18061152 · Cited by 46 · see citing works

Mesenchymal stem cell in wound healing and regeneration

Tsai, H., Wang, P., & Tsui, K. (2017) · Journal of the Chinese Medical Association · doi:10.1016/j.jcma.2017.06.011 · Cited by 46 · see citing works

17β-estradiol ameliorates age-associated loss of fibroblast function by attenuating IFN-γ/STAT1-dependent miR-7 upregulation

Midgley, A. C., Morris, G., Phillips, A. O., & Steadman, R. (2016) · Aging Cell · doi:10.1111/acel.12462 · Cited by 44 · see citing works

Pharmacological Modulation of Radiation Damage. Does It Exist a Chance for Other Substances than Hematopoietic Growth Factors and Cytokines?

Hofer, M., Hoferová, Z., & Falk, M. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18071385 · Cited by 39 · see citing works

Estrogens Induce Rapid Cytoskeleton Re-Organization in Human Dermal Fibroblasts via the Non-Classical Receptor GPR30

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Evaluation of Effects of Topical Estradiol Benzoate Application on Cutaneous Wound Healing in Ovariectomized Female Mice

Mukai, K., Urai, T., Asano, K., Nakajima, Y., & Nakatani, T. (2016) · PLoS ONE · doi:10.1371/journal.pone.0163560 · Cited by 37 · see citing works

Aspirin treatment for chronic wounds: Potential beneficial and inhibitory effects

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Impact of adjuvant anti-estrogen therapies (tamoxifen and aromatase inhibitors) on perioperative outcomes of breast reconstruction

Billon, R., Bosc, R., Belkacémi, Y., Assaf, E., SidAhmed‐Mezi, M., Hersant, B., & Meningaud, J. (2017) · Journal of Plastic Reconstructive & Aesthetic Surgery · doi:10.1016/j.bjps.2017.05.046 · Cited by 36 · see citing works

Calcineurin and CRTC2 mediate FSH and TGF 1 upregulation of Cyp19a1 and Nr5a in ovary granulosa cells

Lai, W.-A., Yeh, Y., Fang, W., Wu, L., Harada, N., Wang, P.-Y., Ke, F.-C., Lee, W.-L., & Hwang, J.-J. (2014) · Journal of Molecular Endocrinology · doi:10.1530/jme-14-0048 · Cited by 31 · see citing works

The benefits of estrogen or selective estrogen receptor modulator on kidney and its related disease—chronic kidney disease—mineral and bone disorder: Osteoporosis

Lee, W.-L., Cheng, M., Tarng, D., Yang, W.-C., Lee, F.-K., & Wang, P. (2013) · Journal of the Chinese Medical Association · doi:10.1016/j.jcma.2013.03.010 · Cited by 30 · see citing works

Oestrogen-induced angiogenesis and implantation contribute to the development of parasitic myomas after laparoscopic morcellation

Huang, B., Yang, M., Wang, P., Li, H.-Y., Chou, T., & Chen, Y. (2016) · Reproductive Biology and Endocrinology · doi:10.1186/s12958-016-0200-y · Cited by 30 · see citing works

Repeal and Replace: Adipocyte Regeneration in Wound Repair

Horsley, V., & Watt, F. M. (2017) · Cell stem cell · doi:10.1016/j.stem.2017.03.015 · Cited by 30 · see citing works

Pharmacological activation of estrogen receptors-α and -β differentially modulates keratinocyte differentiation with functional impact on wound healing

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Tamoxifen Treatment of Breast Cancer Cells: Impact on Hedgehog/GLI1 Signaling

Villegas, V. E., Rondón‐Lagos, M., Annaratone, L., Castellano, I., Grismaldo, A., Sapino, A., & Zaphiropoulos, P. G. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17030308 · Cited by 28 · see citing works

Alteration of Mammary Gland Development and Gene Expression by In Utero Exposure to Cadmium

Parodi, D. A., Greenfield, M., Evans, C., Chichura, A. M., Alpaugh, A., Williams, J. K., Cyrus, K., & Martin, M. C. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18091939 · Cited by 27 · see citing works

Modeling the effects of systemic mediators on the inflammatory phase of wound healing

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Non-classical estrogen receptors action on human dermal fibroblasts

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Peripheral membrane associations of matrix metalloproteinases

Doren, S. R. V., Marcink, T. C., Koppisetti, R. K., Jurkevich, A., & Fulcher, Y. G. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2017.04.013 · Cited by 24 · see citing works

A Comparison of Gene Expression of Decorin and MMP13 in Hypertrophic Scars Treated With Calcium Channel Blocker, Steroid, and Interferon: A Human-Scar-Carrying Animal Model Study

Yang, S., Yang, J., Hsiao, Y., & Chuang, S. (2016) · Dermatologic Surgery · doi:10.1097/dss.0000000000000990 · Cited by 22 · see citing works

Testosterone Prevents Cutaneous Ischemia and Necrosis in Males Through Complementary Estrogenic and Androgenic Actions

Chenu, C., Adlanmérini, M., Boudou, F., Chantalat, É., Guihot, A., Toutain, C. E., Raymond‐Letron, I., Vicendo, P., Gadeau, A., Henrion, D., et al. (2017) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.117.309219 · Cited by 22 · see citing works

Low-dose add-back therapy during postoperative GnRH agonist treatment

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The rates of second lung cancers and the survival of surgically-resected second primary lung cancers in patients undergoing resection of an initial primary lung cancer

Varlotto, J. M., Voland, R. P., DeCamp, M. M., Rava, P., FitzGerald, T. J., Maxfield, M. W., Lou, F., Oliveira, P., Sood, R., Baima, J. A., et al. (2020) · Lung Cancer · doi:10.1016/j.lungcan.2020.07.015 · Cited by 11 · see citing works

Establishment and translational evaluation of animal models for skin wound healing: a systematic review

Zhang, Y., Leng, K., Dong, M., Wu, J., Wang, Z., Zhu, Q., Gao, X., & Sun, Y. (2026) · Frontiers in Physiology · doi:10.3389/fphys.2026.1800001 · Cited by 11 · see citing works

Estrogen via GPER downregulated HIF-1a and MIF expression, attenuated cardiac arrhythmias, and myocardial inflammation during hypobaric hypoxia

Wowui, P. I., Mprah, R., Noah, M. L. N., Adu‐Amankwaah, J., Kanoseh, A. W. L., Li, T., Chulu, D., Yalley, S. K., Shaheen, S., & Sun, H. (2025) · Molecular Medicine · doi:10.1186/s10020-025-01144-2 · Cited by 10 · see citing works

The Therapeutic Effects of Oral Intake of Hydrogen Rich Water on Cutaneous Wound Healing in Dogs

Qi, D.-D., Ding, M., Wang, T., Hayat, M. A., Liu, T., & Zhang, J. (2021) · Veterinary Sciences · doi:10.3390/vetsci8110264 · Cited by 10 · see citing works

Literature Review on the Effectiveness of Medicinal Leech Therapy in the Wound Healing

Ünal, K., Erol, M. E., & Ayhan, H. (2023) · Ankara Medical Journal · doi:10.5505/amj.2023.20280 · Cited by 10 · see citing works

Post-refractive Surgery Dry Eye: A Systematic Review Exploring Pathophysiology, Risk Factors, and Novel Management Strategies

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Efficacy of MSC-derived small extracellular vesicles in treating type II diabetic cutaneous wounds: a systematic review and meta-analysis of animal models

Yue, G., Li, Y., Liu, Z., Yu, S., Cao, Y., & Wang, X. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1375632 · Cited by 9 · see citing works

Predictors of hospital-acquired pressure injuries in patients with complete spinal cord injury: a retrospective case–control study

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Profiling of Metabolites in a Fermented Soy Dietary Supplement Reinforces its Role in the Management of Intestinal Inflammation

Ethier, R., Krishnamurthy, A., Jeffrey, M. P., & Tompkins, T. A. (2024) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202300770 · Cited by 9 · see citing works

Androgenic steroids induce pathologic scarring in a preclinical porcine model via dysfunctional extracellular matrix deposition

Reiche, E., Keller, P. R., Soares, V. V., Schuster, C. R., Rahmayanti, S., Mroueh, J., Mroueh, V., Billaud, M., Hu, S., Hoover‐Watson, H., et al. (2024) · The FASEB Journal · doi:10.1096/fj.202302144rrr · Cited by 9 · see citing works

Trends in the Treatment of Chronic Wounds

Sharma, R., Hruška, J., Peter, L., Randlová, K., & Kuča, K. (2024) · Current Medicinal Chemistry · doi:10.2174/0109298673312649240829103906 · Cited by 8 · see citing works

Tamoxifen Alters TGF ‐β1/Smad Signaling in Vocal Fold Injury

Matsushita, H., Mukudai, S., Ozawa, S., Kinoshita, S., Hashimoto, K., Kaneko, M., Sugiyama, Y., Branski, R. C., & Hirano, S. (2022) · The Laryngoscope · doi:10.1002/lary.30448 · Cited by 8 · see citing works

A review of pediatric macromastia etiology and indications for reduction mammaplasty

Kikuchi, D. S., Mustin, D. E., Ghanouni, A., & Walsh, M. D. (2022) · Journal of Plastic Reconstructive & Aesthetic Surgery · doi:10.1016/j.bjps.2022.12.003 · Cited by 8 · see citing works

Androgen therapy worsens scar formation in masculinizing mastectomy

Mroueh, V., Reiche, E., Mroueh, J., Keller, P. R., Marano, A. A., Suresh, V., Schuster, C. R., Soares, V. V., & Coon, D. (2023) · British journal of surgery · doi:10.1093/bjs/znad148 · Cited by 8 · see citing works

Natural product-loaded nanoparticles for wound healing

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Comparison of digital and traditional skin wound closure assessment methods in mice

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Postoperative incision scars and cosmetic satisfaction of living liver donors

Hsu, Y., Hsieh, C., Lin, P., Lin, S.-L., Lin, K., Weng, L., & Chen, Y. (2021) · Medicine · doi:10.1097/md.0000000000026187 · Cited by 8 · see citing works

Functional Gene Clusters in Global Pathogenesis of Clear Cell Carcinoma of the Ovary Discovered by Integrated Analysis of Transcriptomes

Hsu, Y.-H., Wang, P., & Chang, C.-M. (2020) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph17113951 · Cited by 8 · see citing works

Mid-urethral sling in the management of women with stress urinary incontinence after pelvic organ prolapse treatment

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Toward Sex-Specific Biomaterials Innovation: A Perspective

Koons, G. L. (2025) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.5c00342 · Cited by 7 · see citing works

Behavioral alterations, brain oxidative stress, and elevated levels of corticosterone associated with a pressure injury model in male mice

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Vaginal Cuff Dehiscence After Endometriosis Surgery

Boersen, Z., Aalders, C. I. M., Klinkert, E. R., Maas, J. W. M., & Nap, A. W. (2019) · JSLS Journal of the Society of Laparoscopic & Robotic Surgeons · doi:10.4293/jsls.2019.00018 · Cited by 7 · see citing works

Mesenchymal stem cells-derived magic bullets for burns

Li, Y., Lee, F., & Wang, P. (2019) · Journal of the Chinese Medical Association · doi:10.1097/jcma.0000000000000240 · Cited by 7 · see citing works

Mesenchymal stem cells and cerebral palsy

Lee, F., Lin, Y., & Wang, P. (2020) · Journal of the Chinese Medical Association · doi:10.1097/jcma.0000000000000263 · Cited by 7 · see citing works

Arsenic Impairs Wound Healing Processes in Dermal Fibroblasts and Mice

Dresler, S. R., Pinto, B. I., Salanga, M. C., Propper, C. R., Berry, S. R., & Kellar, R. S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25042161 · Cited by 6 · see citing works

Current and advanced therapies for chronic wound infection

Hoang, T. P. N., Ghori, M. U., Ousey, K. J., & Conway, B. R. (2022) · Pharmaceutical journal/The pharmaceutical journal · doi:10.1211/pj.2022.1.148212 · Cited by 6 · see citing works

A closer look at wound infections and healing

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The role of estrogenic substances in regulation of biological processes involved into wound healing

Filocamo, L., Migneco, L. M., Ceccacci, F., & Leonelli, F. (2020) · IRIS Research product catalog (Sapienza University of Rome)

Role of Estrogen in Wound Healing

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Estrogen deficiency and wound healing

Oki, A. S., Ming, C. H., Nabiilah, C. C., & Hutapea, J. A. (2025) · World Journal of Advanced Research and Reviews · doi:10.5281/zenodo.17007833

Potential Role of Estrogens in Wound Healing

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