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    Research 121–150 of 1000+

    1. Folliculin: A surprising molecular brake in the human hair follicle Journal of Investigative Dermatology · 2026
    2. Genome-Wide Association Studies of Hair Whorl in Pigs Genes · 2024
    3. Genetic association of wool quality characteristics in United States Rambouillet sheep Frontiers in genetics · 2023 · 1 citations
    4. Treatment of cutaneous leiomyomas with botulinum toxin. Case report and review of literature Dermatologic Therapy · 2021 · 1 citations
    5. Differential Expression and Analysis of TBX3 Gene in Skin Tissues of Dun Mongolian Horses with and Without Bider Markings Animals · 2026
    6. Identification and characterization of Birt–Hogg–Dubé associated renal carcinoma The Journal of Pathology · 2007 · 50 citations
    7. Pathogenesis and management of TRPV3-related Olmsted syndrome Frontiers in Genetics · 2024
    8. A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer PLOS Genetics · 2020 · 43 citations
    9. Treatment of lipomas and diffuse lipomatosis with NDYAG 1064 NM laser and their impact on the quality of life Journal of Mind and Medical Sciences · 2020 · 5 citations
    10. Focused Review on Metal Nanoparticles in Hair Regeneration and Alopecia: Insights into Mechanisms, Assessment Techniques, Toxicity, Regulatory and Intellectual Property Perspectives Journal of Cluster Science · 2025
    11. Alternative androgen pathways WikiJournal of Medicine · 2023
    12. Desmoplastic Trichoepithelioma: Histopathologic and Immunohistochemical Criteria for Differentiation of a Rare Benign Hair Follicle Tumor From Other Cutaneous Adnexal Tumors Curēus · 2020 · 5 citations
    13. Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters European Journal of Human Genetics · 2023 · 1 citations
    14. Comparative histomorphometric and transcriptomic analysis reveals potential genetic determinants of pelage variation between hairy and coarse-woolly sheep BMC Genomics · 2025
    15. Anti-Müllerian Hormone and Polycystic Ovary Syndrome in Women and Its Male Equivalent Biomedicines · 2022 · 18 citations
    16. Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications Journal of Genome Biotechnology and Genetics · 2026
    17. Strategies for High-Efficiency Mutation Using the CRISPR/Cas System Frontiers in Cell and Developmental Biology · 2022 · 29 citations
    18. Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome European Journal of Medical Genetics · 2025
    19. Premature graying of hairs: Ayurveda perspective Journal of Indian System of Medicine · 2023
    20. CLINICAL UPDATES IN HAIR Dermatologic Clinics · 1997 · 19 citations
    21. Monilethrix: A case report imaged by trichoscopy, reflectance confocal microscopy and histopathology Australasian journal of dermatology · 2018 · 1 citations
    22. Loose Anagen Hair Syndrome in Black‐Haired Indian Children Pediatric Dermatology · 2013 · 8 citations
    23. Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia 2009 · 42 citations
    24. Creatine phosphokinase levels and isotretinoin therapy Journal of The American Academy of Dermatology · 1987 · 1 citations
    25. What may be the markers of the male equivalent of polycystic ovary syndrome? Physiological Research · 2004 · 39 citations
    26. A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family Journal of Cutaneous Pathology · 2010 · 7 citations
    27. Premature graying of hair Indian Journal of Dermatology, Venereology and Leprology · 2013 · 47 citations
    28. Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report Skin appendage disorders · 2020 · 1 citations
    29. Comparison of comedolytic effect of benzoyl peroxide and adapalene in rhino mice Journal of Dermatological Science · 2017
    30. WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes American journal of human genetics · 2009 · 197 citations