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    Research 631–660 of 1000+

    1. The Role of 5αR Inhibitors in the Early Growth of Pca Cells Urologia Journal · 2005
    2. New drugs: Iobenguane sulfate Australian Prescriber · 2004
    3. ATP-dependent chromatin remodeling during mammalian development Development · 2016 · 182 citations
    4. Cantú Syndrome Is Caused by Mutations in ABCC9 The American Journal of Human Genetics · 2012 · 148 citations
    5. The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling ˜The œAmerican journal of pathology · 2002 · 146 citations
    6. British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology British Journal of Dermatology · 2010 · 136 citations
    7. Type XVII collagen coordinates proliferation in the interfollicular epidermis eLife · 2017 · 124 citations
    8. Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease Journal of Cell Science · 2008 · 85 citations
    9. Edar Signaling in the Control of Hair Follicle Development 2005 · 71 citations
    10. New clinico‐genetic classification of trichothiodystrophy American Journal of Medical Genetics Part A · 2009 · 68 citations
    11. Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia Journal of Investigative Dermatology · 1999 · 66 citations
    12. Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles Journal of Investigative Dermatology · 2002 · 53 citations
    13. Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis 2013 · 51 citations
    14. Specific morphogenetic events in mouse external genitalia sex differentiation are responsive/dependent upon androgens and/or estrogens Differentiation · 2012 · 51 citations
    15. Primary cicatricial alopecia: diagnosis and treatment Canadian Medical Association Journal · 2013 · 48 citations
    16. An unexpected role for keratin 10 end domains in susceptibility to skin cancer Journal of Cell Science · 2006 · 43 citations
    17. The regulation of skin homeostasis, repair and the pathogenesis of skin diseases by spatiotemporal activation of epidermal mTOR signaling Frontiers in Cell and Developmental Biology · 2022 · 35 citations
    18. FOXN1 deficient nude severe combined immunodeficiency Orphanet journal of rare diseases · 2017 · 32 citations
    19. Plastic surgery : indications, operations, and outcomes Mosby eBooks · 2000 · 30 citations
    20. Pleiotropic Role of Notch Signaling in Human Skin Diseases International Journal of Molecular Sciences · 2020 · 29 citations
    21. Premature aging syndromes: From patients to mechanism Journal of dermatological science · 2019 · 29 citations
    22. Developing stratified epithelia: lessons from the epidermis and thymus Wiley interdisciplinary reviews. Developmental biology · 2014 · 27 citations
    23. The Genetics of Human Skin Disease Cold Spring Harbor Perspectives in Medicine · 2014 · 24 citations
    24. Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice PLOS genetics · 2020 · 23 citations
    25. Sebaceous immunobiology - skin homeostasis, pathophysiology, coordination of innate immunity and inflammatory response and disease associations Frontiers in immunology · 2022 · 21 citations
    26. Systematic analyses of murine masculinization processes based on genital sex differentiation parameters Development Growth & Differentiation · 2015 · 21 citations
    27. Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells 2019 · 17 citations
    28. Best Practices for FACE-Q Aesthetics Research: A Systematic Review of Study Methodology Aesthetic Surgery Journal · 2023 · 15 citations
    29. YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate International Journal of Molecular Sciences · 2024 · 14 citations
    30. Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome ˜The œAmerican journal of case reports · 2018 · 14 citations