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    Research 451–480 of 1000+

    1. FLCN regulates transferrin receptor 1 transport and iron homeostasis 2021 · 1 citations
    2. Skin as a Window to Endocrine Dysfunction: Dermatological and Metabolic Interactions in Polycystic Ovary Syndrome JOJ Dermatology & Cosmetics · 2026
    3. Specific In Vivo Ablation of Lrig1-Positive Follicular Progenitor Cells Results in Sebaceous Gland Loss in Mice International Journal of Molecular Sciences · 2026
    4. <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis Animal Genetics · 2026
    5. Skin-inspired phototherapeutic cryogel ameliorates infected wound healing by orchestrating mechanotransduction and immunomodulation Bioactive Materials · 2025
    6. Polycystic Ovary Syndrome-Associated Acne: The Interplay of Hyperandrogenism, Insulin Resistance, and Therapeutic Strategies Cureus · 2025
    7. Molecular Predictors of Ritlecitinib Efficacy in Alopecia Areata: Role of JAK3-Dependent Inflammation and Follicular Integrity 2025
    8. LB1081 Three-dimensional imaging of tight junction-network across multiple layers of human epidermis by array tomography using backscattered electron-mode scanning electron microscopy Journal of Investigative Dermatology · 2019
    9. 308 Epidermal keratinocytes regulate bacterial immune responses and host defense through EGFR 2017
    10. Serum-Free Expanded Hair Follicle Mesenchymal Stem Cells Promote Cartilage Repair in a Murine Full-Thickness Defect Model Transplantation and Cellular Therapy · 2026
    11. Anti-Müllerian Hormone and Ovarian Morphology in Polycystic Ovary Syndrome (PCOS)/Polyendocrine Metabolic Ovarian Syndrome (PMOS): Toward More Precise Diagnosis and Phenotype Stratification Biomedical and Therapeutics Letters · 2026
    12. PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation British Journal of Dermatology · 2026
    13. BH28 Breaking the pattern: frontal fibrosing alopecia in men, a case series British Journal of Dermatology · 2025
    14. The IVIG treatment response in autoimmune polyendocrine syndromes type 2 with anti-GAD65 antibody-associated stiff person syndrome: a case report and literature review Frontiers in Immunology · 2025
    15. Hutchinson-Gilford syndrome: History, causes, phenotype and research advances Zenodo (CERN European Organization for Nuclear Research) · 2023
    16. 361 p120-catenin regulates epidermal inflammation in a cadherin-dependent manner 2023
    17. Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient International journal of dermatology and venereology · 2022
    18. 478 Mutation-specific siRNA Knockdown of GJB2 − Potential gene therapy for Keratitis-ichthyosis-deafness Syndrome Journal of Investigative Dermatology · 2017
    19. Abstract 5020: Characterization of epidermal stem cells in SKH1 hairless mice, a widely used mouse model to investigate ultraviolet radiation carcinogenesis. Cancer Research · 2013
    20. Paradoxical Effect After IPL Photoepilation Dermatologic Surgery · 2002 · 11 citations
    21. Update on Melasma—Part I: Pathogenesis Dermatology and Therapy · 2022 · 10 citations
    22. Heat Enhanced Follicular Delivery of Isotretinoin to the Skin Pharmaceutical research · 2019 · 8 citations
    23. Skin phenotype diversity across populations: from skin morphology to molecular phenotype Frontiers in Medicine · 2026
    24. Inferring Spatially Resolved Transcriptomics Data from Whole Slide Images for the Assessment of Colorectal Tumor Metastasis: A Feasibility Study bioRxiv (Cold Spring Harbor Laboratory) · 2022
    25. Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1 Proceedings of the National Academy of Sciences · 2000 · 333 citations
    26. Clonal Growth of Dermal Papilla Cells in Hydrogels Reveals Intrinsic Differences between Sox2-Positive and -Negative Cells In Vitro and In Vivo Journal of Investigative Dermatology · 2011 · 68 citations
    27. Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes ˜The œAmerican journal of pathology · 2010 · 35 citations
    28. Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements Journal of Human Genetics · 2016 · 30 citations
    29. Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro American Journal Of Pathology · 2003 · 20 citations
    30. Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix Experimental Dermatology · 2015 · 18 citations