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    Research 571–600 of 1000+

    1. A missense mutation in Lama3 causes androgen alopecia Scientific Reports · 2023
    2. Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep Cell & bioscience · 2023
    3. Health-related quality of life in adult Mediterranean women with polycystic ovary syndrome attending to a tertiary hospital: a case-control study. Research Square (Research Square) · 2020
    4. A Multimodal Approach to Augmenting Wound Healing: Progress Toward Dermal Regeneration in Mammals PRISM (University of Calgary) · 2019
    5. Molecular genetics of androgen insensitivity Adolescent and pediatric gynecology · 1995
    6. Microenvironmental reprogramming of thymic epithelial cells to skin multipotent stem cells Nature · 2010 · 116 citations
    7. Microskin‐Inspired Injectable MSC‐Laden Hydrogels for Scarless Wound Healing with Hair Follicles Advanced Healthcare Materials · 2020 · 89 citations
    8. Role of cholesterol sulfate in epidermal structure and function: Lessons from X-linked ichthyosis Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · 2014 · 87 citations
    9. Obesity resistance of the stearoyl-CoA desaturase-deficient (<i>scd1</i> <sup>-/-</sup>) mouse results from disruption of the epidermal lipid barrier and adaptive thermoregulation Biological Chemistry · 2007 · 87 citations
    10. New clinico‐genetic classification of trichothiodystrophy American Journal of Medical Genetics Part A · 2009 · 68 citations
    11. Generalized trichoepitheliomas with alopecia and myasthenia gravis: Clinicopathologic and immunohistochemical study and comparison with classic and desmoplastic trichoepithelioma Journal of the American Academy of Dermatology · 1986 · 54 citations
    12. Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis Proceedings of the National Academy of Sciences of the United States of America · 2013 · 44 citations
    13. D’orenone blocks polarized tip growth of root hairs by interfering with the PIN2‐mediated auxin transport network in the root apex Plant journal · 2008 · 44 citations
    14. Disorders of Keratinization American journal of clinical dermatology · 2004 · 44 citations
    15. THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS 1946 · 40 citations
    16. MSC-derived sEV-loaded hyaluronan hydrogel promotes scarless skin healing by immunomodulation in a large skin wound model Biomedical Materials · 2022 · 39 citations
    17. What may be the markers of the male equivalent of polycystic ovary syndrome? Physiological Research · 2004 · 39 citations
    18. Effect of Hyaluronic Acid and Poly-L-Lactic Acid Dermal Fillers on Collagen Synthesis: An in vitro and in vivo Study Clinical, cosmetic and investigational dermatology · 2020 · 34 citations
    19. Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals Frontiers in Zoology · 2017 · 25 citations
    20. Autonomous, Moisture‐Driven Flexible Electrogenerative Dressing for Enhanced Wound Healing Advanced Materials · 2025 · 23 citations
    21. Eyelash Length in Children and Adolescents with Allergic Diseases Pediatric dermatology · 2004 · 16 citations
    22. iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice PLoS ONE · 2014 · 15 citations
    23. Boosting and Rescuing Epidermal Superior Population from Fresh Keratinocyte Cultures Stem Cells and Development · 2013 · 15 citations
    24. The physical and physiological effects of vacuum massage on the different skin layers: a current status of the literature Burns & Trauma · 2016 · 13 citations
    25. Assessment of replication rates of human keratinocytes in engineered skin substitutes grafted to athymic mice Wound Repair and Regeneration · 2012 · 12 citations
    26. Characterization of polycystic ovary syndrome among Flo app users around the world Reproductive Biology and Endocrinology · 2021 · 11 citations
    27. Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature BMC pediatrics · 2020 · 11 citations
    28. A mutation in MAP2 is associated with prenatal hair follicle density The FASEB Journal · 2019 · 11 citations
    29. Stanowisko Polskiego Towarzystwa Endokrynologicznego, Polskiego Towarzystwa Ginekologów i Położników oraz Polskiego Towarzystwa Endokrynologii Ginekologicznej w sprawie diagnostyki i leczenia zespołu policystycznych jajników Endokrynologia Polska · 2018 · 11 citations
    30. Inherited Disorders of Corneocyte Proteins Current problems in dermatology · 2010 · 11 citations