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    Research 511–540 of 1000+

    1. Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis Cosmetics · 2025
    2. Insulin resistance as risk factor for the development of type 2 diabetes mellitus: a systematic approach Acta Marisiensis · 2021
    3. THE IMPACT OF HAIR LOSS IN CAMBODIA: CAUSES, PREVENTION METHODS, AND TREATMENT SOLUTIONS Journal Of Social Sciences And Humanites · 2024
    4. Genome-Wide Associations with Body and Fleece Weight in United States Sheep Genes · 2025
    5. Hutchinson-Gilford syndrome: History, causes, phenotype and research advances GSC Advanced Research and Reviews · 2023
    6. Polymorphism of keratin-associated protein (KAP) 7 gene and its association with wool traits in Rambouillet sheep The Indian Journal of Animal Sciences · 2018 · 3 citations
    7. The color of human hair 2011
    8. Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2) Journal of Investigative Dermatology · 2003 · 22 citations
    9. Salt-losing tubulopathy and chronic dermatitis Kidney international · 2018
    10. A case report of a novel homozygote mutation causing severe Leydig cell hypoplasia: insights in the coexistence of nonsense mutation and polymorphism in the same LHCGR gene locus Experimental and Clinical Endocrinology & Diabetes · 2012
    11. Single-Cell Omics Advances in Understanding Tissue Development and Complex Trait Formation in Sheep and Goats Animals · 2026
    12. Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata Frontiers in Immunology · 2026
    13. An immune regulatory CCT repeat containing oligodeoxynucleotide capable of causing hair loss in male mice Human & Experimental Toxicology · 2016
    14. Nonclassic adrenal hyperplasia Reviews in endocrine and metabolic disorders · 2008 · 55 citations
    15. Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency—x-linked recessive ichthyosis: a case report and review of literature European Journal of Pediatrics · 2012 · 7 citations
    16. CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy Cureus · 2026
    17. Activator Protein-1 Activity Regulates Epithelial Tumor Cell Identity Cancer Research · 2006 · 70 citations
    18. Functional mapping of the mouse <i>hairless</i> gene promoter region bioRxiv (Cold Spring Harbor Laboratory) · 2018
    19. Upadacitinib in dermatologic therapy: Emerging evidence and expanding indications Journal of Skin and Sexually Transmitted Diseases · 2026
    20. Genomic Surveillance Reveals the Rapid Expansion of the XBB Lineage among Circulating SARS-CoV-2 Omicron Lineages in Southeastern Wisconsin, USA Viruses · 2023 · 9 citations
    21. Hashimoto Thyroiditis - A Comprehensive Review Physician's journal of medicine · 2023
    22. Proteomic analysis identifies differentially expressed proteins participating in forming Type III brush hair in Yangtze River Delta white goat Genetics and molecular research · 2015 · 8 citations
    23. ASSESSMENT OF SOCIODEMOGRAPHIC CHARACTERISTICS AND COMPARATIVE ANALYSIS OF ADVERSE DRUG REACTIONS AMONG OROPHARYNGEAL CANCER PATIENTS RECEIVING DIFFERENT CHEMOTHERAPEUTIC REGIMENS IN KARACHI, SINDH, PAKISTAN Genetics and Molecular Research · 2026
    24. Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population Molecular genetics and metabolism reports · 2019 · 8 citations
    25. Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats Genetics Selection Evolution · 2025 · 1 citations
    26. Genetically modified laboratory mice with sebaceous glands abnormalities Cellular and Molecular Life Sciences · 2016 · 22 citations
    27. Decay of Skin-Specific Gene Modules in Pangolins Journal of molecular evolution · 2023 · 1 citations
    28. Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives International Journal of Molecular Sciences · 2024 · 9 citations
    29. FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures Frontiers in Genetics · 2025 · 1 citations
    30. Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin Genetics in medicine · 2018 · 10 citations