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    Research 451–480 of 1000+

    1. The Spectrum of Cutaneous Manifestations in Lupus Erythematosus: A Comprehensive Review Journal of clinical medicine · 2024
    2. Resident’s Bag 2023
    3. The anatomical distribution of lentiginous melanoma (lentigo maligna and lentigo maligna melanoma): Differences according to sex Australasian Journal of Dermatology · 2023
    4. Genital Dermatology Australasian Journal of Dermatology · 2022
    5. Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities Signal Transduction and Targeted Therapy · 2022 · 318 citations
    6. Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans American journal of human genetics · 2009 · 234 citations
    7. Fluorescence Microscopy—An Outline of Hardware, Biological Handling, and Fluorophore Considerations Cells · 2021 · 97 citations
    8. Hox genes in development and beyond Development · 2023 · 83 citations
    9. New clinico‐genetic classification of trichothiodystrophy American Journal of Medical Genetics Part A · 2009 · 68 citations
    10. Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex International Journal of Molecular Sciences · 2021 · 40 citations
    11. Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment Cells · 2019 · 39 citations
    12. Madarosis: A marker of many Maladies International Journal of Trichology · 2012 · 36 citations
    13. A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis Journal of Investigative Dermatology · 2017 · 33 citations
    14. Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles Proceedings of the National Academy of Sciences · 2020 · 25 citations
    15. Transcriptomic landscape of early hair follicle and epidermal development Cell Reports · 2023 · 23 citations
    16. Adaptive Triboelectric Nanogenerators for Long-Term Self-Treatment: A Review Biosensors · 2022 · 17 citations
    17. Human Adipose-Derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition Stem Cell Reviews and Reports · 2021 · 12 citations
    18. A rare case of woolly hair with unusual associations Indian dermatology online journal · 2013 · 12 citations
    19. Extracellular vesicles in age-related diseases: disease pathogenesis, intervention, and biomarker Stem Cell Research & Therapy · 2025 · 9 citations
    20. Hair follicles modulate skin barrier function Cell Reports · 2024 · 9 citations
    21. Congenital atrichia with papular lesions Indian Journal of Paediatric Dermatology · 2014 · 8 citations
    22. <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome Journal of Clinical Laboratory Analysis · 2024 · 6 citations
    23. Eyebrow and Eyelash Alopecia: A Clinical Review American journal of clinical dermatology · 2022 · 6 citations
    24. RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development Orphanet journal of rare diseases · 2022 · 5 citations
    25. Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease PloS one · 2019 · 5 citations
    26. GRowing an Epidermal Tumor Journal of Investigative Dermatology · 2013 · 5 citations
    27. Resident macrophages of the lung and liver: The guardians of our tissues Frontiers in Immunology · 2022 · 4 citations
    28. Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion Journal of Clinical Medicine · 2021 · 4 citations
    29. Hypotrichosis with juvenile macular dystrophy International Journal of Trichology · 2018 · 4 citations
    30. Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita Science Advances · 2025 · 3 citations