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    Research 811–840 of 1000+

    1. Diagnostic and therapeutic management of notoederic mange in persian cats: A report of three cases International Journal of Advanced Biochemistry Research · 2025
    2. Investigation of the comprehensive treatment’s clinical efficacy of various types of alopecia using proteoglycan replacement therapy Russian Journal of Clinical Dermatology and Venereology · 2023
    3. [Keratin dielectric parameters in the millimeter wavelength range]. PubMed · 2001
    4. Platelet-Rich Plasma: New Performance Understandings and Therapeutic Considerations in 2020 International Journal of Molecular Sciences · 2020 · 848 citations
    5. Advances in skin grafting and treatment of cutaneous wounds Science · 2014 · 518 citations
    6. Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria PLOS Genetics · 2018 · 308 citations
    7. Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness Journal of Investigative Dermatology · 2001 · 299 citations
    8. Apoptosis in human skin development: Morphogenesis, periderm, and stem cells Developmental dynamics · 1994 · 253 citations
    9. Bald scalp in men with androgenetic alopecia retains hair follicle stem cells but lacks CD200-rich and CD34-positive hair follicle progenitor cells Journal of Clinical Investigation · 2011 · 235 citations
    10. Food Bioactive Compounds and Emerging Techniques for Their Extraction: Polyphenols as a Case Study Foods · 2020 · 188 citations
    11. BRAF Inhibitor Dabrafenib in Patients with Metastatic <i>BRAF</i>-Mutant Thyroid Cancer Thyroid · 2014 · 188 citations
    12. p63 regulates <i>Satb1</i> to control tissue-specific chromatin remodeling during development of the epidermis The Journal of Cell Biology · 2011 · 166 citations
    13. BMP signaling in the control of skin development and hair follicle growth Differentiation · 2004 · 165 citations
    14. Hierarchical patterning modes orchestrate hair follicle morphogenesis PLoS Biology · 2017 · 149 citations
    15. Cantú Syndrome Is Caused by Mutations in ABCC9 The American Journal of Human Genetics · 2012 · 148 citations
    16. Historical and Current Adenosine Receptor Agonists in Preclinical and Clinical Development Frontiers in Cellular Neuroscience · 2019 · 142 citations
    17. Somatic stem cell heterogeneity: diversity in the blood, skin and intestinal stem cell compartments Nature Reviews Molecular Cell Biology · 2015 · 137 citations
    18. HOXC13 Is Involved in the Regulation of Human Hair Keratin Gene Expression Journal of Biological Chemistry · 2002 · 132 citations
    19. Human hair follicle organ culture: theory, application and perspectives Experimental Dermatology · 2015 · 130 citations
    20. K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1 Journal of Investigative Dermatology · 2003 · 130 citations
    21. RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome The American Journal of Human Genetics · 2012 · 112 citations
    22. Male-pattern baldness susceptibility locus at 20p11 Nature Genetics · 2008 · 111 citations
    23. Skin Adipocyte Stem Cell Self-Renewal Is Regulated by a PDGFA/AKT-Signaling Axis Cell Stem Cell · 2016 · 106 citations
    24. Fidelity of the Human Mitochondrial DNA Polymerase Journal of Biological Chemistry · 2006 · 101 citations
    25. Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis American Journal Of Pathology · 2006 · 100 citations
    26. Immunohistochemical localization of types 1 and 2 5α-reductase in human scalp British Journal of Dermatology · 1999 · 100 citations
    27. Pemphigus Vulgaris IgG and Methylprednisolone Exhibit Reciprocal Effects on Keratinocytes Journal of Biological Chemistry · 2004 · 99 citations
    28. Fluorescence Microscopy—An Outline of Hardware, Biological Handling, and Fluorophore Considerations Cells · 2021 · 97 citations
    29. WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation Nature Communications · 2017 · 96 citations
    30. KGF and EGF signalling block hair follicle induction and promote interfollicular epidermal fate in developing mouse skin Development · 2009 · 82 citations