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    Research 871–900 of 1000+

    1. ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy The Application of Clinical Genetics · 2022 · 15 citations
    2. Restoration of Spermatogenesis and Male Fertility Using an Androgen Receptor Transgene PloS one · 2015 · 15 citations
    3. Endogenous Skin Fluorescence is a Good Marker for Objective Evaluation of Comedolysis 2000 · 15 citations
    4. Comparative Gene Expression Profiling of Senescent and Androgenetic Alopecia Using Microarray Analysis Springer eBooks · 2010 · 6 citations
    5. Cell Surface B2m-Free Human Leukocyte Antigen (HLA) Monomers and Dimers: Are They Neo-HLA Class and Proto-HLA? Biomolecules · 2023 · 3 citations
    6. Direct cellular reprogramming enables development of viral T antigen–driven Merkel cell carcinoma in mice 2022 · 14 citations
    7. Evaluation of Personalized Skincare Through in-silico Gene Interactive Networks and Cellular Responses to UVR and Oxidative Stress Clinical Cosmetic and Investigational Dermatology · 2022 · 11 citations
    8. Cultivation of Human Hair Follicle Cells 1990 · 7 citations
    9. Clinical and preclinical approach in AGA treatment: a review of current and new therapies in the regenerative field Stem Cell Research & Therapy · 2024
    10. New frontiers in CRISPR/Cas9 delivery systems delivery for gene editing Authorea (Authorea) · 2022
    11. Human acellular amniotic membrane incorporating exosomes from adipose-derived mesenchymal stem cells promotes diabetic wound healing Stem Cell Research & Therapy · 2021 · 132 citations
    12. The enzyme and inhibitors of 4-ene-3-oxosteroid 5α-oxidoreductase Steroids · 1995 · 64 citations
    13. Treatment of Alopecia Areata With Topical Sensitizers Dermatitis · 2015 · 15 citations
    14. Male Androgenetic Alopecia Springer eBooks · 2008 · 13 citations
    15. Trichohyalin-Like Proteins Have Evolutionarily Conserved Roles in the Morphogenesis of Skin Appendages Journal of Investigative Dermatology · 2014 · 68 citations
    16. 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
    17. Krtap11-1, a hair keratin-associated protein, as a possible crucial element for the physical properties of hair shafts Journal of Dermatological Science · 2014 · 38 citations
    18. Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep PloS one · 2017 · 25 citations
    19. An epistatic effect of KRT25 on SP6 is involved in curly coat in horses Scientific Reports · 2018 · 13 citations
    20. Identification of the C-terminal tail domain of AHF/trichohyalin as the critical site for modulation of the keratin filamentous meshwork in the keratinocyte Journal of Dermatological Science · 2011 · 12 citations
    21. Expression analysis of KAP9.2 and Hoxc13 genes during different cashmere growth stages by qRT-PCR method Molecular biology reports · 2014 · 9 citations
    22. Prostaglandins: Key players in immunomodulation of the nervous system Neural Regeneration Research · 2025 · 3 citations
    23. FGF5 is a crucial regulator of hair length in humans Proceedings of the National Academy of Sciences of the United States of America · 2014 · 136 citations
    24. Regenerating the skin: a task for the heterogeneous stem cell pool and surrounding niche Nature Reviews Molecular Cell Biology · 2013 · 133 citations
    25. Stretching the limits: from homeostasis to stem cell plasticity in wound healing and cancer Nature Reviews Genetics · 2018 · 124 citations
    26. BAC-mediated gene-dosage analysis reveals a role for Zipro1 (Ru49/Zfp38) in progenitor cell proliferation in cerebellum and skin Nature Genetics · 1999 · 117 citations
    27. Pulmonary manifestations of Birt-Hogg-Dubé syndrome Familial cancer · 2013 · 99 citations
    28. Hox in hair growth and development Die Naturwissenschaften · 2003 · 98 citations
    29. Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases PLOS Genetics · 2012 · 87 citations
    30. A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers The American Journal of Human Genetics · 1998 · 83 citations