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    Research 181–210 of 1000+

    1. The molecular basis of human keratin disorders Human Genetics · 2009 · 79 citations
    2. Trichohyalin-Like Proteins Have Evolutionarily Conserved Roles in the Morphogenesis of Skin Appendages Journal of Investigative Dermatology · 2014 · 68 citations
    3. Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix Journal of Investigative Dermatology · 1999 · 20 citations
    4. Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks Genes · 2022 · 9 citations
    5. The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat ) Molecular Genetics and Metabolism Reports · 2014 · 9 citations
    6. Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75 Journal of Investigative Dermatology · 2015 · 6 citations
    7. Off-label uses of retinoids in dermatology Our Dermatology Online · 2012 · 6 citations
    8. 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
    9. “Structural imprinting” of the cutaneous immune effector function Tissue Barriers · 2020 · 4 citations
    10. A guide to diagnosis and management of hypertrichosis JAAD reviews. · 2025 · 1 citations
    11. Proteomic Analysis of Two Stem Cell Secretomes Used in Combination in a Topical Skin Care Product That Has Demonstrated Efficacy in a Double-Blinded, Vehicle-Controlled Clinical Trial Preprints.org · 2026
    12. Role of the ABCA4 Gene Expression in the Clearance of Toxic Vitamin A Derivatives in Human Hair Follicle Stem Cells and Keratinocytes International journal of molecular sciences · 2023
    13. Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility 2009 · 189 citations
    14. An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves BMC Veterinary Research · 2026
    15. Distinct Developmental Functions of Prostasin (CAP1/PRSS8) Zymogen and Activated Prostasin 2015 · 28 citations
    16. Positive Impact of Fish Oil on Diabetic and Hypercholestrolemic Skin Disorders Journal of nutrition & health · 2015 · 1 citations
    17. Suppression of Vitamin D Receptor and Induction of Retinoid X Receptor α Expression During Squamous Differentiation of Cultured Keratinocytes 2000 · 15 citations
    18. Hydrobiome of Thermal Waters: Potential Use in Dermocosmetics Cosmetics · 2023
    19. Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System 2019 · 142 citations
    20. Genetic architecture of mouse skin inflammation and tumour susceptibility Nature · 2009 · 133 citations
    21. Intracrine androgen biosynthesis, metabolism and action revisited Molecular and Cellular Endocrinology · 2017 · 131 citations
    22. Type XVII collagen coordinates proliferation in the interfollicular epidermis eLife · 2017 · 124 citations
    23. A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity The Journal of Cell Biology · 2015 · 98 citations
    24. Natural killer cells in atopic and autoimmune diseases of the skin Journal of Allergy and Clinical Immunology · 2010 · 91 citations
    25. Trichoscopy in genetic hair shaft abnormalities Journal of Dermatological Case Reports · 2008 · 74 citations
    26. Dupilumab in Inflammatory Skin Diseases: A Systematic Review Biomolecules · 2023 · 72 citations
    27. Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype Journal of Investigative Dermatology · 1999 · 62 citations
    28. Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation American Journal Of Pathology · 2002 · 57 citations
    29. Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex American journal of human genetics · 2018 · 55 citations
    30. A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1 Journal of Investigative Dermatology · 1998 · 47 citations