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    Research 301–330 of 1000+

    1. DMBA/TPA Treatment Is Necessary for BCC Formation from Patched Deficient Epidermal Cells in Ptch flox/flox CD4Cre +/− Mice Journal of Investigative Dermatology · 2014 · 11 citations
    2. Minoxidil oral en alopecia androgénica: estudio retrospectivo acerca de su seguridad en práctica clínica real e_Buah · 2021
    3. Transforming growth factor-β in stem cells and tissue homeostasis Bone Research · 2018 · 245 citations
    4. ATP-dependent chromatin remodeling during mammalian development Development · 2016 · 182 citations
    5. Epigenetic control of adult stem cell function Nature Reviews Molecular Cell Biology · 2016 · 179 citations
    6. Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing ACS Nano · 2020 · 60 citations
    7. Stem Cell-Based Hair Cell Regeneration and Therapy in the Inner Ear Neuroscience Bulletin · 2023 · 26 citations
    8. Epimorphic regeneration in mice is p53-independent Cell Cycle · 2010 · 20 citations
    9. Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia Gene · 2020 · 9 citations
    10. Integrated single-cell chromatin and transcriptomic analyses of peripheral immune cells in patients with alopecia areata Frontiers in Immunology · 2025 · 4 citations
    11. In vitro Differentiation of Melanocyte Stem Cells Derived from Vitiligo Patients into Functional Melanocytes The Indonesian Biomedical Journal · 2024
    12. Characterization and expression analysis of KAP7.1, KAP8.2 gene in Liaoning new-breeding cashmere goat hair follicle Molecular biology reports · 2010 · 48 citations
    13. Androgens/Androgen Receptor in the Management of Skin Diseases Journal of Biosciences and Medicines · 2022 · 1 citations
    14. Expression analysis of KAP9.2 and Hoxc13 genes during different cashmere growth stages by qRT-PCR method Molecular biology reports · 2014 · 9 citations
    15. Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene Journal of Molecular Neuroscience · 2022 · 9 citations
    16. Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria Journal of Investigative Dermatology · 2013 · 99 citations
    17. Resident Memory T Cells in Autoimmune Skin Diseases Frontiers in immunology · 2021 · 50 citations
    18. The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource iScience · 2023 · 4 citations
    19. Assessing Causality Between Androgenetic Alopecia with Depression: A Bidirectional Mendelian Randomization Study Clinical Cosmetic and Investigational Dermatology · 2025
    20. Laser therapies in androgenetic alopecia: Review and clinical experiences Journal of Cutaneous and Aesthetic Surgery · 2025
    21. Pathophysiology of Androgenetic Alopecia and Implications for Treatment: An Overview of Current Literature Journal of Biosciences and Medicines · 2026
    22. Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study Clinical Cosmetic and Investigational Dermatology · 2024
    23. Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study Human genomics · 2024
    24. Divergent progression pathways in male androgenetic alopecia and female pattern hair loss: Trichoscopic perspectives Journal of Cosmetic Dermatology · 2024
    25. Male pattern hair loss: Can developmental origins explain the pattern? Experimental Dermatology · 2023
    26. Female Androgenetic (?) Alopecia Hair transplant forum international · 2015
    27. Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats Journal of Heredity · 2007 · 75 citations
    28. Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata Journal of Investigative Dermatology · 2005 · 44 citations
    29. Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women Bioscience Reports · 2019 · 11 citations
    30. A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype ˜The œAmerican journal of pathology · 2014 · 11 citations