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    Research 91–120 of 1000+

    1. Understanding human aging and the fundamental cell signaling link in age-related diseases: the middle-aging hypovascularity hypoxia hypothesis Frontiers in Aging · 2023 · 4 citations
    2. SAT-080 An Atypical Adenoma Presenting with Hyperandrogenism: A Rare Case Presentation on a Pituitary Germ Cell Tumor Journal of the Endocrine Society · 2025
    3. Characteristics and Differences in the Antler Velvet Microbiota During Regeneration Microorganisms · 2024
    4. Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation Case reports in dermatological medicine · 2023
    5. Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor Springer eBooks · 2016
    6. Detection of Type IIHair Keratin Gene in a Family with Monilethrix Chinese Journal of Dermatovenereology of Integrated Traditional and Western Medicine · 2010
    7. [Studies on monilethrix]. PubMed · 1979 · 2 citations
    8. Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease Genes & Development · 2008 · 667 citations
    9. Chrousos syndrome: from molecular pathogenesis to therapeutic management European Journal of Clinical Investigation · 2015 · 47 citations
    10. Design of a RADA16-based self-assembling peptide nanofiber scaffold for biomedical applications Journal of Biomaterials Science, Polymer Edition · 2019 · 39 citations
    11. Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain 2018 · 14 citations
    12. The role of vasoactive peptides in skin homeostasis—focus on adiponectin and the kallikrein-kinin system American Journal of Physiology-Cell Physiology · 2023 · 8 citations
    13. Wear characteristics of epoxy based hybrid composites reinforced with short hair fibers and glass micro spheres Materials Today: Proceedings · 2018 · 7 citations
    14. Central Centrifugal Cicatricial Alopecia Cutis · 2022 · 3 citations
    15. Purified Vitexin Compound 1 Inhibits UVA-Induced Cellular Senescence in Human Dermal Fibroblasts by Binding Mitogen-Activated Protein Kinase 1 Frontiers in Cell and Developmental Biology · 2020 · 3 citations
    16. Central Diabetes Insipidus and Hypothalamic Type of Hypopituitarism Associated with Atypical Location of Rathke's Cleft Cyst Internal Medicine · 2012 · 3 citations
    17. Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene Clinical Pediatric Endocrinology · 1992 · 3 citations
    18. Short communication: Clinical evaluation of pea sprout extract in the treatment of hair loss Phytotherapy Research · 2019 · 2 citations
    19. Androgen Receptor Ligands: Agonists and Antagonists Elsevier eBooks · 2017 · 2 citations
    20. Central centrifugal cicatricial alopecia The Journal of Family Practice · 2022 · 1 citations
    21. The Role of Histone Demethylases in Disease Springer eBooks · 2011 · 1 citations
    22. Wellness claims and men’s health: Bridging the counseling gap in urology Canadian Urological Association Journal · 2026
    23. Precision-Based Management of Chronic Hair Fall: A Genomic-Guided Trichology Approach - A Case Analysis from Qatar Saudi Journal of Pathology and Microbiology · 2026
    24. Polarized microscopy in genetic hair disorders: case series 2025
    25. In vivo Study of the Effect of 5 and 10% Nebivolol Cream on Hair Growth in Mice Models International journal of drug delivery technology · 2022
    26. Viviscal: An answer for hair loss in women? Pharmacy Today · 2013
    27. Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses Archives of Dermatology · 2001 · 23 citations
    28. Proteomic analysis of balding and non-balding mesenchyme-derived dermal papilla cells from androgenetic alopecia patients using on-line two-dimensional reversed phase-reversed phase LC–MS/MS Journal of Proteomics · 2013 · 11 citations
    29. Hair loss Postgraduate Medicine · 1986 · 9 citations
    30. Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i> The Journal of Dermatology · 2017 · 5 citations