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    Research 481–510 of 1000+

    1. Research Progress on the Molecular Mechanism of Poultry Feather Follicle Development Current Issues in Molecular Biology · 2025
    2. Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report Frontiers in Medicine · 2025
    3. A bibliometric analysis of strabismus (from 2004 to 2023) Frontiers in Medicine · 2025
    4. Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant Genes · 2025
    5. Diagnosis of polycystic ovaries syndrome: establishment of reference values of nine hormones on Maglumi X- 8 Middle East Fertility Society Journal · 2025
    6. Intraretinal variation in disease severity in the Oat mouse model of gyrate atrophy Experimental Eye Research · 2025
    7. Decoding the ZmNF-YC1–ZmAPRG pathway for phosphorus efficiency Frontiers in Plant Science · 2025
    8. Drug History and SLE Laboratory Findings Among Iraqi Patients: A Hospital‐Based Study Health Science Reports · 2025
    9. Screened of long non-coding RNA related to wool development and fineness in Gansu alpine fine-wool sheep BMC Genomics · 2025
    10. Alopecia universalis following human papillomavirus vaccine administration: a case report Clinical and Experimental Vaccine Research · 2025
    11. Carotid Intima Media Thickness Measurement in Alopecia Areata Patients Dermatologic Therapy · 2025
    12. POLYCYSTIC OVARY SYNDROME (PCOS): DIAGNOSIS, PATHOPHYSIOLOGY AND CONTEMPORARY THERAPEUTIC APPROACHES Archiv Euromedica · 2024
    13. Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma Frontiers in Oncology · 2024
    14. Chemotherapy-Induced Alopecia by Docetaxel: Prevalence, Treatment and Prevention Current Oncology · 2024
    15. Current Protocols: Alopecia Areata Mouse Models for Drug Efficacy and Mechanism Studies Current Protocols · 2024
    16. The Trotter collection: A review of Mildred Trotter's hair research and an update for studies of human variation American Journal of Biological Anthropology · 2024
    17. PCSK9: From Nature’s Loss to Patient’s Gain Circulation · 2024
    18. Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review Biomedicines · 2024
    19. Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing Psychiatry research. Case reports · 2023
    20. Proteome Analysis of Alpine Merino Sheep Skin Reveals New Insights into the Mechanisms Involved in Regulating Wool Fiber Diameter International journal of molecular sciences · 2023
    21. Developmental Mapping of Hair Follicles in the Embryonic Stages of Cashmere Goats Using Proteomic and Metabolomic Construction Animals · 2023
    22. Alopecias: Practical Tips for the Management of Biopsies and Main Diagnostic Clues for General Pathologists and Dermatopathologists Journal of Clinical Medicine · 2023
    23. Effects of different concentrations of androgens on KAP24.1 gene expression in Hetian sheep and Karakul sheep Gene · 2023
    24. Decision letter: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma 2016
    25. Volatile organic compounds: A proinflammatory activator in autoimmune diseases Frontiers in Immunology · 2022 · 18 citations
    26. Comprehensive analysis of the expression profiles of mRNA, lncRNA, circRNA, and miRNA in primary hair follicles of coarse sheep fetal skin BMC Genomics · 2024 · 13 citations
    27. Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage Reproductive biomedicine online · 2017 · 3 citations
    28. Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives Computational and Structural Biotechnology Journal · 2024
    29. Single-Cell RNA Profiling of Human Skin Reveals Age-Related Loss of Dermal Sheath Cells and Their Contribution to a Juvenile Phenotype Frontiers in Genetics · 2022 · 37 citations
    30. KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype PLoS Genetics · 2017 · 87 citations