Antimicrobials from human skin commensal bacteria protect against Staphylococcus aureus and are deficient in atopic dermatitis

QIIME allows analysis of high-throughput community sequencing data

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Greengenes, a Chimera-Checked 16S rRNA Gene Database and Workbench Compatible with ARB

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Ribosomal Database Project: data and tools for high throughput rRNA analysis

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Atopic Dermatitis: Global Epidemiology and Risk Factors

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Topographical and Temporal Diversity of the Human Skin Microbiome

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Differential abundance analysis for microbial marker-gene surveys

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antiSMASH: rapid identification, annotation and analysis of secondary metabolite biosynthesis gene clusters in bacterial and fungal genome sequences

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Topical Probiotics Reduce Atopic Dermatitis Severity: A Systematic Review and Meta-Analysis of Double-Blind, Randomized, Placebo-Controlled Trials

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Complete genome sequencing and antibiofilm activity of an endophytic bacterium associated with marine sponge Hyrtios erectus collected from the Red Sea

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Repopulate, not just decolonise—a microbial ecological strategy against multidrug resistance in intensive care units

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DISORDERS OF SKIN MICROBIOTA AND FORMATION OF ATOPIC DERMATITIS IN CHILDREN

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Staphylococcus aureus wall teichoic acid is a pathogen-associated molecular pattern that is recognized by langerin (CD207) on skin Langerhans cellsPreprint

van Dalen, R., Diaz, J. S. D. L. C., Rumpret, M., Fuchsberger, F. F., van Teijlingen, N. H., Hanske, J., Rademacher, C., Geijtenbeek, T. B. H., van Strijp, J. A. G., Weidenmaier, C., et al. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/238469 · Cited by 3

Commensal skin bacteria exacerbate inflammation and delay skin healingPreprint

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The new era of immune skin diseases: Exploring advances in basic research and clinical translations

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Skin microbiome and modern treatment options for complicated forms of atopic dermatitis

Chernushevich, D. D., Elisyutina, O. G., & Fedenko, E. S. (2023) · Russian Journal of Allergy · doi:10.36691/rja6221 · Cited by 4

Antimicrobial Peptides From the Gut Microbiome of the Centenarians: Diversification of Biosynthesis and Youthful Development of Resistance Genes

Lu, C., Wang, X., Ye, P., Lu, Z., Ma, J., Luo, W., Wang, S., & Chen, X. (2024) · The Journals of Gerontology Series A · doi:10.1093/gerona/glae218 · Cited by 2

The Acari Hypothesis, VII: accounting for the comorbidity of allergy with other contemporary medical conditions, especially metabolic syndrome

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Protective roles of genistein and icaritin in skin barrier integrity and hydration in an atopic dermatitis model

Mohammad, S., Valappil, A. K., Karim, M. R., Iqbal, S., Yang, D., Chen, C., Ling, L., & Yang, D. U. (2025) · European Journal of Integrative Medicine · doi:10.1016/j.eujim.2025.102483 · Cited by 2

Antimicrobial Resistance in Petting Zoo Animals in the United Kingdom

Nishigaki, A., Arden, K., & Frosini, S. (2025) · Applied Microbiology · doi:10.3390/applmicrobiol5040115 · Cited by 2

Bioactive Plasmid- and Phage-Encoded Antimicrobial Peptides (AMPs) in the Human Gut: A Metatranscriptome–Virome Profiling Reveals Exploratory Links to Metabolic Human Diseases

Gallardo-Becerra, L., Cornejo‐Granados, F., Bikel, S., Arenas, I., López-Leal, G., Alvarado-González, C., Sánchez-López, F., Manzo, R., Corzo, G. A., Espino-Solís, G. P., et al. (2025) · Microbial Ecology · doi:10.1007/s00248-025-02620-2 · Cited by 2

An antimicrobial daptide from human skin commensal Staphylococcus hominis protects against skin pathogens

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Immunomodulatory Activity of Lantibiotics Isolated from Growth Media of Coagulase-Negative Staphylococci In Vitro

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Smartphone-based multispectral autofluorescence analysis of bacteria mixtures of staphylococci using convolutional neural network

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A skin isolate of Micrococcus luteus negates the Staphylococcus aureus-induced release of type 2 cytokines from keratinocytes

Elias, A., Pennock, J. L., McBain, A. J., Keevill, E.-J., & O’Neill, C. A. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1711723 · Cited by 2

Interaction between tick and host microbiotas: a four-step waltz

Baquer, F., & Grillon, A. (2026) · Parasites & Vectors · doi:10.1186/s13071-026-07308-1 · Cited by 3

Probiotics for skin aging and skin conditions in the elderly

Kömürcügil, İ., Türsen, Ü., Türsen, B., Solak, B., Bakay, Ö. S. K., & Kroumpouzos, G. (2026) · Clinics in Dermatology · doi:10.1016/j.clindermatol.2026.02.016 · Cited by 4

Exploring the role of cathelicidin LL-37 and ceragenins in wound healing processes

Łuckiewicz, M., Wnorowska, U., Zakrzewska, M., Błażejczyk, I., Daniluk, T., Kondziołka, W., Savage, P. B., Bucki, R., & Piktel, E. (2026) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2026.178727 · Cited by 2

The Expanding Landscape of Microbiota Medicine: Indications, Therapeutic Modalities, and the Path Towards Integrative Microbiome‐Targeting Healthcare

Dai, M., Lin, Y., Gan, R., Shen, X., Park, S. Y., Lee, S., & Su, Q. (2026) · Microbiota Medicine Research · doi:10.1002/mmr3.70004 · Cited by 1

Atopic Dermatitis Beyond Cutaneous Inflammation: The Interplay Between Progesterone, Testosterone, Gut Microbiota, and Immune Dysregulation

Guevara‐Ramírez, P., Paz‐Cruz, E., Ruiz‐Pozo, V. A., Cadena-Ullauri, S., Tamayo‐Trujillo, R., Paredes, A. S. C., Jaramillo, N. H., Melo, L. H., & Zambrano, A. K. (2026) · Microorganisms · doi:10.3390/microorganisms14071565 · Cited by 2

Role of Tight Junctions and Their Protein Expression in Atopic Dermatitis

Namrata, K., & Bai, B. (2020) · International Journal of Dermatology and Venereology · doi:10.1097/jd9.0000000000000114 · Cited by 2

Hautmikrobiom – Wertvoll für Diagnostik und Therapie?

Hülpüsch, C., & Reiger, M. (2021) · Der Hautarzt · doi:10.1007/s00105-021-04830-4 · Cited by 2

The skin microbiome and atopic dermatitis: a review

Olisova, O. Y., Свитич, О. А., & Potapova, M. B. (2022) · Russian Journal of Skin and Venereal Diseases · doi:10.17816/dv80125 · Cited by 2

Stability Versus Meta-stability in a Skin Microbiome Model

Greugny, E. T., Stamatas, G. N., & Fages, F. (2022) · Lecture notes in computer science · doi:10.1007/978-3-031-15034-0_9 · Cited by 2

Autoantigens in atopic dermatitis: The characterization of autoantigens and their diagnostic value

Múnera, M., Sánchez, A., Buendía, E., & Sánchez, J. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-85389-7.00019-3 · Cited by 2

A simplified bacterial community found within the epidermis than at the epidermal surface of atopic dermatitis patients and healthy controls

Barnes, C. J., Asplund, M., Clausen, M., Rasmussen, L., Olesen, C. M., Yüksel, Y. T., Andersen, P. S., Litman, T., Holmstrøm, K., Bay, L., et al. (2023) · BMC Microbiology · doi:10.1186/s12866-023-03012-7 · Cited by 2

Coagulase negative staphylococci

Foster, T. J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-818619-0.00016-2 · Cited by 2

The Microbiome and Atopic Dermatitis

Khosrojerdi, M., Azad, F. J., Khoshkhui, M., Yadegari, Y., Ahanchian, H., & Azimian, A. (2024) · Journal of Microbiota · doi:10.5812/jmb-151599 · Cited by 2

Metagenomics-guided reengineering of the gut microbiome

Dhotre, D. P., & Karmarkar, B. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-91631-8.00011-1 · Cited by 1

Bacteriocins and Antimicrobial Peptides

Singh, B., Mal, G., Kalra, R. S., & Marotta, F. (2024) · Springer eBooks · doi:10.1007/978-3-031-65459-6_27 · Cited by 2

Bacillus xiamenensis Inhibits the Growth of Moraxella osloensis by Producing Indole‐3‐Carboxaldehyde

Watanabe, M., Sekino, Y., Kuramochi, K., & Furuyama, Y. (2024) · MicrobiologyOpen · doi:10.1002/mbo3.70009 · Cited by 2

Multi-Omic Data Integration Suggests Putative Microbial Drivers of Aetiopathogenesis in Mycosis Fungoides

Licht, P., & Mailänder, V. (2024) · Cancers · doi:10.3390/cancers16233947 · Cited by 5

Antimicrobial activity of Lactobacillus casei on Staphylococcus pseudintermedius isolates

Diniz, D. C. D. C., Ribeiro, M. G., Dias, G. S., Viana, G. D. B., Okamoto, A. S., & Machado, L. H. D. A. (2025) · Veterinary Dermatology · doi:10.1111/vde.13325 · Cited by 2

Multi-perspective analysis of skin microbiota in elderly eczema patients

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Staphylococcus hominis as a source of antimicrobial peptides: identification of a new peptide with potential antimicrobial properties using in silico approach

Chemao-Elfihri, M. W., Hakmi, M., Abbou, H., Kartti, S., Fahime, E. E., Belyamani, L., & Boutayeb, S. (2025) · Archives of Microbiology · doi:10.1007/s00203-025-04323-1 · Cited by 2

Staphylococcus Strains in Atopic Dermatitis in Children: Toxins Production and Resistance Properties

Kudryavtseva, А. V., Fs, F., Khachatryan, L., Makarova, S. G., Osipenko, O., Ryzhii, E., Titarev, S., Zaslavsky, D. V., & Gelezhe, K. A. (2025) · Life · doi:10.3390/life15071120 · Cited by 2

Different bacterial growth of major mastitis pathogens after coculturing with Staphylococcus chromogenes and Staphylococcus hominis in milk in vitro

Chuasakhonwilai, A., Keeklangdon, P., Chaisri, W., Saipinta, D., Photiboon, K., Kaewmuangma, D., Anuphom, W., Intanon, M., & Suriyasathaporn, W. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1707938 · Cited by 2

Atopic Dermatitis, The Skin‐Disease

Wallach, D. (2017) · Journal of the European Academy of Dermatology and Venereology · doi:10.1111/jdv.14487 · Cited by 2

Externe Therapie des atopischen Ekzems

Knop, M., Gürtler, A.-L., Heratizadeh, A., ASZODI, N., Werfel, T., & Wollenberg, A. (2018) · Der Hautarzt · doi:10.1007/s00105-018-4135-4 · Cited by 2

Microbiome and Diseases: Allergy

Wölbing, F., Köberle, M., Volz, T., & Biedermann, T. (2018) · Springer eBooks · doi:10.1007/978-3-319-90545-7_12 · Cited by 2

Recurrent Bacterial Infections in Cutaneous T-cell Lymphoma

Sateesh, B. A., Bhagat, Y. V., Thomas, S., Sood, A., & Michael, M. B. (2022) · Cureus · doi:10.7759/cureus.20912 · Cited by 2

Basic skin therapy effects on skin inflammation and microbiome composition in patients with atopic dermatitis after challenges with grass pollen

Heratizadeh, A., Roesner, L. M., Traidl, S., Moitinho‐Silva, L., Ellinghusen, B., Rodríguez, E., Harder, I., Sapák, M., Weidinger, S., Badorrek, P., et al. (2022) · Journal of the European Academy of Dermatology and Venereology · doi:10.1111/jdv.17966 · Cited by 2

Identification of skin microbiota in Saudi female community and their effects on keratinocytes viability (in vitro)

Mohammedsaeed, W. M. (2022) · Journal of Taibah University for Science · doi:10.1080/16583655.2021.2015899 · Cited by 2

Skin Commensal Bacteria Modulates the Immune Balance of Mice to Alleviate Atopic Dermatitis-Induced Damage

Yu, X., Chen, T., Huang, N., Jin, Y., & Yang, L. (2022) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2022/4731675 · Cited by 2

Interactions Between Microbial Therapeutics and the Endogenous Microbiome

Hallowell, H. A., Gao, A. L., Kelly, K. E., & Suez, J. (2023) · Springer eBooks · doi:10.1007/978-981-99-1463-0_21 · Cited by 2

Natural Topical Treatment Contributes to a Reduction of Dry Scalp Symptoms in Children

Fithian, E., Thivalapill, N., Kosner, J., Necheles, J., & Bilaver, L. (2023) · Clinical Cosmetic and Investigational Dermatology · doi:10.2147/ccid.s424077 · Cited by 2

Targeting the cutaneous microbiota in atopic dermatitis: ‘A new hope’ or ‘attack of the CoNS’?

Chu, C. (2022) · Clinical and Translational Medicine · doi:10.1002/ctm2.865 · Cited by 2

Editorial: faecal microbiota transplantation for ulcerative colitis—not quite there yet?

Lim, M. H., & Radford‐Smith, G. L. (2017) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.14228 · Cited by 2

Advanced methodology for bacterial colonization of 3D organotypic epidermal models: a gateway to long-term host-microbe interaction and intervention studiesPreprint

Rikken, G., Meesters, L. D., Jansen, P. A. M., Rodijk‐Olthuis, D., van Vlijmen‐Willems, I. M. J. J., Niehues, H., Oláh, P., Homey, B., Schalkwijk, J., Zeeuwen, P. L. J. M., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.06.21.545853 · Cited by 2

Androgens at the skin surface regulate S. aureus pathogenesis through the activation of agr quorum sensingPreprint

John, M. S., Chinnappan, M., Artami, M., Bhattacharya, M., Keogh, R. A., Kavanaugh, J. S., Sharma, T., Horswill, A. R., & Harris-Tryon, T. A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.10.579753 · Cited by 2

Large-scale investigation for antimicrobial activity reveals novel defensive species across the healthy skin microbiomePreprint

Nguyen, U. T., Salamzade, R., Sandstrom, S., Swaney, M. H., Townsend, E. C., Wu, S. Y., Cheong, J. Z. A., Sardina, J. A., Ludwikoski, I., Rybolt, M. L., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.04.621544 · Cited by 2

Skin-resident T cells play an important role in controlling skin colonization of Candidozyma (Candida) auris

Xie, J., Yan, L., Kadosh, D., & Xiong, N. (2026) · iScience · doi:10.1016/j.isci.2026.115862 · Cited by 1

THE PROBLEM OF DECOLONIZATION OF STAPHYLOCOCCUS AUREUS NASAL CARRIERS FROM THE MICROBIOLOGIST’S POINT OF VIEW (REVIEW OF LITERATURE)

Melnikov, V. G., Villena, J., & Kombarova, S. Y. (2019) · Russian Clinical Laboratory Diagnostics · doi:10.18821/0869-2084-2019-64-11-693-699 · Cited by 1

Microbial Chemical Ecology in the Human Microbiome

Balaich, J. N., & Donia, M. S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-409547-2.14847-4 · Cited by 2

Electrogenic Staphylococcus epidermidis colonizes nasal cavities and alleviates IL-6 progression induced by the SARS2-CoV nucleocapsid protein

Zayabaatar, E., Tang, N. M. T., & Pham, M. T. (2023) · Journal of Applied Microbiology · doi:10.1093/jambio/lxad179 · Cited by 1

Skin Microbiome Composition and Key Factors of its Barrier Function

Murashkin, N. N., Pavlova, E. S., Epishev, R. V., Materikin, A. I., Ivanov, R. A., Savelova, A. A., Fedorov, D. V., & Leonova, M. A. (2023) · Вопросы современной педиатрии · doi:10.15690/vsp.v22i5.2624 · Cited by 1

Features of Staphylococcus Aureus Antibiotic Sensitivity in Children with Atopic Dermatitis

Murashkin, N. N., Materikin, A. I., Epishev, R. V., Leonova, M. A., Opryatin, L. A., Ivanov, R. A., & Savelova, A. A. (2023) · Вопросы современной педиатрии · doi:10.15690/vsp.v22i5.2640 · Cited by 1

SENILE ATOPIC DERMATITIS — CURRENT VISION AND UNRESOLVED ISSUES

Smirnova, I. O., Ptashnikova, P. D., Ten, M., Головченко, В. В., & Khazhomiya, K. D. (2023) · Успехи геронтологии · doi:10.34922/ae.2023.36.5.007 · Cited by 1

Redox state of aging skin: A double-edged sword in wound healing

Chen, Q., Sophabmixay, A., Albertson, T., Ghasb, G., Terzian, A., Yan, L., Young, L. H., & Barsotti, R. (2024) · Advances in biogerontology · doi:10.1016/bs.abger.2024.05.008 · Cited by 1

Investigating the causal relationship between skin microbiota and hypertrophic scar using bidirectional mendelian randomization

Hou, K., Tan, Y., & Zhang, Q. (2025) · Burns · doi:10.1016/j.burns.2025.107376 · Cited by 1

Research hotspots and trends of skin barrier in atopic dermatitis in the past 24-year: a bibliometric analysis

Huang, F., Zhu, X., & Liang, X. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1539386 · Cited by 1

The Role of Vulture (Accipitriformes) Cutaneous Microbiota in Infectious Disease Protection

Lobello, M., Bava, R., Castagna, F., Sotgiu, F. D., Berlinguer, F., & Tilocca, B. (2025) · Microorganisms · doi:10.3390/microorganisms13040898 · Cited by 2

Hydrocarbon Stapling Enables Improvement of Antimicrobial Activity and Proteolytic Stability of Host‐Defense Peptide Ocellatin‐3N

Yang, H., Yuan, F., Xie, G., Fu, Y., Mi, J., Yu, L. J., Liu, W., & Li, Y. (2025) · ChemBioChem · doi:10.1002/cbic.202500204 · Cited by 1

Modern tendencies of influence on skin microbiome by means of dermatocosmetics: practical aspects of probiotic bacteria application in the composition of biotic complexes

Адаскевич, В. П., Gorodovich, A. N., Zaslavsky, D. V., Okhlopkov, V. A., Smirnova, I. O., Таганов, А. В., Тамразова, О. Б., Леонидовна, Ш. И., & Khazhomiya, K. D. (2025) · Russian Journal of Skin and Venereal Diseases · doi:10.17816/dv642248 · Cited by 1

Infectious complications of atopic dermatitis

Wang, V. Y., van Rensburg, P. J. J., Boguniewicz, J., & Ong, P. Y. (2025) · Annals of Allergy Asthma & Immunology · doi:10.1016/j.anai.2025.05.021 · Cited by 3

Changes in the Skin Microbiome of a Patient with Head and Neck Cancer with Severe Radiodermatitis: A Case Report

Miyamae, N., Ogai, K., Kunimitsu, M., Okamoto, S., Fujiwara, M., Nagai, M., Okuwa, M., & Oe, M. (2025) · Case Reports in Oncology · doi:10.1159/000546634 · Cited by 1

Substantial co-trimoxazole resistant S. aureus nasal carriage despite low colonization among people living with HIV in Ethiopia

Ali, S., Terefe, B., Ambachew, R., Fantahun, B., Tessema, S., Tufa, T. B., Luedde, T., & Feldt, T. (2025) · Scientific Reports · doi:10.1038/s41598-025-07748-2 · Cited by 1

Microbiome as a Potential Target for Treatment and Prevention of Atopic Dermatitis

Gao, J. L., & Hata, T. R. (2025) · Immunology and Allergy Clinics of North America · doi:10.1016/j.iac.2025.06.003 · Cited by 1

МИКРОБИОТА КОЖНЫХ ПОКРОВОВ ЧЕЛОВЕКА И ЕЕ ВЛИЯНИЕ НА ТЕЧЕНИЕ АТОПИЧЕСКОГО ДЕРМАТИТА

Пырх, А. Ю., Гладин, Д. П., Андреева, А. Н., & Косова, А. Н. (2025) · Russian Biomedical Research · doi:10.56871/rbr.2025.70.84.009 · Cited by 1

Topical Administration of a Mixed Microbial Culture of Lactobacillus paracasei, Pichia membranifaciens and Saccharomyces cerevisiae Significantly Inhibits the Development of Atopic Dermatitis in a Mouse Model Through IL-10 Overexpression by Dendritic Cells

Kaneki, M., Ohira, C., Magami, T., Hamauzu, A., Inaba, Y., Togase, H., & Fukuyama, T. (2025) · Biomedicines · doi:10.3390/biomedicines13102536 · Cited by 1

Atopic dermatitis, primary atopic disorders, and the cutaneous microbiome: current understanding of an expanding field

Abidov, A., & Bayer, D. K. (2025) · Frontiers in Pediatrics · doi:10.3389/fped.2025.1670623 · Cited by 1

Redefining acne treatment: emerging role of probiotics in dermatology

Umekar, M., Chaudhary, A. A., Koche, S., Dhule, D., Shidhaye, S. S., Khobragade, R., Bonde, S., Rudayni, H. A., Ali, M. A. M., & Trivedi, R. (2025) · Archives of Microbiology · doi:10.1007/s00203-025-04582-y · Cited by 1

Cotton gauze wound-dressing patches loaded with dapsone derivative and silver nanoparticles for promoting wound healing via antibacterial acceleration function

Rashdan, H. R. M., Tolba, E., & Abdelraof, M. (2025) · RSC Advances · doi:10.1039/d5ra04951b · Cited by 1

Skin Microbiota: A Novel Target for Promoting Burn Wound Healing

Yang, H., Chen, Y. Z., Lan, Y., Gong, Y., Zhang, L., Zuo, F., Li, J., Zhang, C., Chen, Y., Yang, J., et al. (2025) · Wound Repair and Regeneration · doi:10.1111/wrr.70118 · Cited by 1

AHR: The Overlooked Mediator in Skincare─Bridging Environmental Sensing and Skin Physiology

Hu, X., Zhu, R., Zhen, Y., Li, Q., Liu, Y., Xu, T., Yang, G., Chen, Y., Xie, H. Q., Xu, S. L., et al. (2026) · Environment & Health · doi:10.1021/envhealth.5c00424 · Cited by 1

Fungal–Bacterial Crosstalk Modulates Glucocorticoid-Primed TLR2 Signaling in the Human Skin

Cho, O., Watanabe, K., & Sugita, T. (2026) · Microorganisms · doi:10.3390/microorganisms14020450 · Cited by 1

Microbiota–fibroblast crosstalk represents the missing link in skin barrier dysfunction and fibrosis

Lin, Z. N., Yang, L., Han, Y., Qi, C., Chen, L., Luo, Y., Lin, Y.-F., Sweren, E., Chen, P., Alphonse, M. P., et al. (2026) · British Journal of Dermatology · doi:10.1093/bjd/ljag068 · Cited by 1

Changes in nasal and throat microbiota composition during and after mupirocin and chlorhexidine decolonization treatment in asymptomatic methicillin-resistant Staphylococcus aureus carriers: a longitudinal observational study

Edslev, S. M., Liu, C. M., Lo, B. Z. S., Meiniche, H. K., Lilje, B., Park, D. K., Rendboe, A. K., Pham, T., Salazar, J. E., Toudahl, T., et al. (2026) · Clinical Microbiology and Infection · doi:10.1016/j.cmi.2026.02.020 · Cited by 2

The light side of the microbiome in trauma: Mechanism and applications

Luo, H.-Y., Cao, L., Zhou, K., Yu, Y.-F., Xiao, Y., Wang, G.-R., Liu, B., Qiu-ji, W., Wang, X.-L., Song, Z., et al. (2026) · Chemical Engineering Journal · doi:10.1016/j.cej.2026.175578 · Cited by 1

Lactobacillus-derived extracellular vesicles provide multi-target acne treatment by enriched proteins and skin microbiota protection

Liu, K., Zhang, Z., Su, Y., Ma, X., Wang, J., Yang, Q., Nie, Q., Mo, Z., Zhou, H., Zouboulis, C. C., et al. (2026) · Journal of Nanobiotechnology · doi:10.1186/s12951-026-04291-8 · Cited by 2

The ecological dynamics of skin microbiota in skin health and diseases

Pu, P., Wang, Y., Liu, X., Pang, Y., Qiang, L., & Wang, W. (2026) · Clinical Microbiology Reviews · doi:10.1128/cmr.00305-25 · Cited by 1

The human skin virome: Ecological dynamics, aberrant profiles, and therapeutic opportunities

Che, Y., & Kong, H. H. (2026) · Cell Host & Microbe · doi:10.1016/j.chom.2026.04.008 · Cited by 2

Microbial Dysbiosis in Photodermatoses: Formation, Pathogenesis and Intervention Strategies

Zhong, L., Wang, T., Tang, L., Han, J., Zhao, Q., & Lin, N. (2026) · Current Issues in Molecular Biology · doi:10.3390/cimb48050493 · Cited by 1

The Acari Hypothesis, VIII: the human apocrine–mammary–microbiota axis and Staphylococcus epidermidis mutualism

Retzinger, A. C. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1714798 · Cited by 1

S. aureus colonization and clinical symptoms remain stable upon topical XZ.700 treatment: Results of a double‐blind randomized clinical trial in patients with mild to moderate atopic dermatitis

van der Meulen, L. W. J., Bergmans, M., Assil, S., Klarenbeek, N., de Kam, M. L., Tibboel, A. J., Brach, T., Herpers, B. L., Frieling, J. T. M., de Jong, V., et al. (2026) · British Journal of Clinical Pharmacology · doi:10.1002/bcp.70630 · Cited by 1

The skin microbiome: from historical ecology to therapeutic frontiers

Sanabani, S. S. (2026) · Anais Brasileiros de Dermatologia · doi:10.1016/j.abd.2026.501393 · Cited by 2

Scalp microbiome in male androgenetic alopecia: 16S rRNA sequencing-based clinical characterization, mouse model validation, and effects on hair follicle cells

Zhang, L., Qin, M., Li, D., Wang, K. J., Wang, T., Zhou, Y., Yao, X., Tian, Y., & Pang, M. (2026) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2026.1878609 · Cited by 1

Shotgun Metagenomics Reveals Skin Microbiome Composition and Function in Infant Atopic Disease

Shen, Z., Eckert, J., Saffery, R., Allen, K. J., Walsh, A., VITALITY team, Deming, C., Chen, Q., Laky, K., Li, J. M., et al. (2026) · Allergy · doi:10.1111/all.70449 · Cited by 1

Current research landscape and future prospects of in silico modeling approaches for atopic dermatitis

Wu, H. L. A., Floch, P. L., Duverdier, A., Irvine, A. D., Dubrac, S., & Tanaka, R. J. (2026) · JID Innovations · doi:10.1016/j.xjidi.2026.100513 · Cited by 1

From sequence space to ecological function: microbiome-derived antimicrobial peptides as community effectors and therapeutic leads

Oyama, L. B. (2026) · Essays in Biochemistry · doi:10.1042/ebc20250036 · Cited by 1

Gram-Positive and Gram-Negative Probiotic Extracellular Vesicles: Mechanisms of Immune Modulation and Therapeutic Opportunities in Atopic Dermatitis

Wayal, V., Lee, M.-F., Wang, J., & Chen, Y. (2026) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-026-09201-2 · Cited by 1

Assessing "Start-up Readiness" for Research Topics and Researchers: Case Studies of Research-Based Start-Ups in the Biopharmaceutical Domain

Goji, T., Hayashi, Y., Yamano, H., Matsuda, T., & Sakata, I. (2018) · Portland International Conference on Management of Engineering and Technology (PICMET) · doi:10.23919/picmet.2018.8481821 · Cited by 1

Positive and Negative Effects of the Commensal Bacteria on Carcinogenesis

Lafta, I. J., & Alkaabawi, N. A. M. (2019) · Sudan Journal of Medical Sciences · doi:10.18502/sjms.v14i2.4688 · Cited by 1

Microbiome Modulation

Blackcloud, P., & Hsiao, J. L. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-84744-5.00024-3 · Cited by 1

Microbioma cutâneo e dermatite atópica

Abreu, D. B., Silva, D., Moreira, A. M., Lopes, C., & Unidade de Imunoalergologia, U. L. D. S. (2022) · Revista Portuguesa de Imunoalergologia · doi:10.32932/rpia.2022.09.086 · Cited by 3

Antimicrobial peptides and the skin and gut microbiomes

Joseph, A. K., Nuriel‐Ohayon, M., Bel, S., & Harris-Tryon, T. A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-820141-1.00016-9 · Cited by 1

Case studies: application of lantibiotics as novel drugs

Dutta, B., Lahiri, D., Sarkar, T., Nag, M., Bhattacharya, D., & Ray, R. R. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-99141-4.00011-4 · Cited by 1

Selection of the isolate of Staphylococcus hominis for bacteriotherapy in patients with atopic dermatitis

Mozyrska, O. V., Boianovskiy, S., & Rudnieva, K. L. (2023) · Polish Annals of Medicine · doi:10.29089/paom/157118 · Cited by 1

Skin’s Natural Bacteria May Protect Against Pathogens

Hampton, T. (2017) · JAMA · doi:10.1001/jama.2017.3111

Le microbiote cutané: le poids lourd sort de l'ombre [The skin microbiota: a colossus steps into the spotlight]

Di Domizio, J., Pagnoni, A., Huber, M., Hohl, D., & Gilliet, M. (2016) · SERVAL (Université de Lausanne)

Bacterial battles on your skin

Pujanandez, L. (2017) · Science · doi:10.1126/science.355.6327.808-b

Skin cream kills pathogen

(2017) · Nature · doi:10.1038/543008d

The role of skin dysbiosis in atopic dermatitis

Braun, C., Patra, V., Lina, G., Nicolas, J., Vocanson, M., & Nosbaum, A. (2022) · European Journal of Dermatology · doi:10.1684/ejd.2022.4289 · Cited by 12