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    Research 211–240 of 1000+

    1. Skin-type-dependent development of murine mechanosensory neurons Developmental Cell · 2023 · 13 citations
    2. Transcription factor-based transdifferentiation of human embryonic to trophoblast stem cells Development · 2024 · 4 citations
    3. Modelling androgen synthesis and action during human sexual differentiation ePrints Soton (University of Southampton) · 2010
    4. Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex American journal of human genetics · 2018 · 55 citations
    5. The ITGB6 gene: its role in experimental and clinical biology Gene · 2019 · 28 citations
    6. Absorption of Excess Selenium and Sulfur by Plants and Animals Journal American Society of Mining and Reclamation · 1995 · 7 citations
    7. An Exploratory In Vivo Study on the Effect of Annurca Apple Extract on Hair Growth in Mice Current Issues in Molecular Biology · 2022 · 1 citations
    8. Growth Differentiation Factor 11 (GDF11)/Transforming Growth Factor - β (TGF - β)/Mesenchymal Stem Cells (MSCs) Balance: A Complicated Partnership in Skin Rejuvenation Journal of Embryology & Stem Cell Research · 2019 · 1 citations
    9. Application and Prospect of Mesenchymal Stem Cells in the Field of Skin Academic Journal of Science and Technology · 2025
    10. Comparative Proteomics Indicates That Biosynthesis of Pectic Precursors Is Important for Cotton Fiber and Arabidopsis Root Hair Elongation Molecular & cellular proteomics · 2010 · 169 citations
    11. The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis PLoS Genetics · 2012 · 99 citations
    12. The antiviral activity of a small molecule drug targeting the NSP1-ribosome complex against Omicron, especially in elderly patients Frontiers in Cellular and Infection Microbiology · 2023 · 6 citations
    13. Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation Dermatologica Sinica · 2010 · 3 citations
    14. Trichotillomania: Bizzare Patern of Hair Loss at 11-Year-old Girl. PubMed · 2016 · 2 citations
    15. Roles for Msx and Dlx homeoproteins in vertebrate development Gene · 2000 · 234 citations
    16. ATP-dependent chromatin remodeling during mammalian development Development · 2016 · 182 citations
    17. Melatonin promotes secondary hair follicle development of early postnatal cashmere goat and improves cashmere quantity and quality by enhancing antioxidant capacity and suppressing apoptosis Journal of Pineal Research · 2019 · 46 citations
    18. Ameliorative effects of rutin against metabolic, biochemical and hormonal disturbances in polycystic ovary syndrome in rats Journal of Ovarian Research · 2016 · 40 citations
    19. Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle Scientific Reports · 2011 · 9 citations
    20. ラット精巣におけるビタミンD 代謝関連遺伝子の発現解析 Institutional Repositories DataBase (IRDB) · 2025
    21. Follikelhormone Springer Reference Medizin · 2019
    22. Exosomes and Hair Regeneration: A Systematic Review of Clinical Evidence Across Alopecia Types and Exosome Sources Clinical Cosmetic and Investigational Dermatology · 2025
    23. Novel Anti-Melanogenesis Properties of Polydeoxyribonucleotide, a Popular Wound Healing Booster International Journal of Molecular Sciences · 2016 · 18 citations
    24. Avaliação do perfil fenotípico, proliferativo e secretório de células-tronco mesenquimais do tecido adiposo captadas por lipoaspiração assistida por laser 2023
    25. <i>Hoxc13</i> mutant mice lack external hair Genes & Development · 1998 · 245 citations
    26. Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis Nature Genetics · 2009 · 181 citations
    27. Androgenic alopecia: A counterproductive outcome of the anabolic effect of androgens Medical Hypotheses · 2009 · 11 citations
    28. Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair Journal of Investigative Dermatology · 2017 · 10 citations
    29. A Case Report of Werner’s Syndrome With a Novel Mutation From India Cureus · 2020 · 4 citations
    30. Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings International journal of contemporary pediatrics · 2020