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    Research 331–360 of 1000+

    1. IL-15 in alopecia areata: the immune tolerance mechanistic insights and translational perspectives Frontiers in Medicine · 2026
    2. A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia Endocrinology · 2014 · 25 citations
    3. Volatile organic compounds: A proinflammatory activator in autoimmune diseases Frontiers in Immunology · 2022 · 18 citations
    4. Generalised Glucocorticoid Resistance US endocrinology · 2008
    5. Disruption of microtubules with low intensity ultrasound rescues hair follicle damage by paclitaxel in mouse models Nature Communications · 2026
    6. Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency Journal of Investigative Dermatology · 2003 · 42 citations
    7. Hair Keratins and Hair Follicle–Specific Epithelial Keratins Methods in cell biology · 2004 · 31 citations
    8. Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2 Clinical Therapeutics · 2021 · 22 citations
    9. Current Protocols: Alopecia Areata Mouse Models for Drug Efficacy and Mechanism Studies Current Protocols · 2024
    10. SnapshotDx Quiz: August 2019 Journal of Investigative Dermatology · 2019
    11. The role of mutations on gene AR, in androgenetic alopecia syndrome International journal of molecular biology · 2020
    12. Hair Diseases (Alopecia Areata and Androgenetic Alopecia) 2010
    13. Expression Profiles of Tyrosine Kinases in Cultured Follicular Papilla Cells Versus Dermal Fibroblasts Journal of Investigative Dermatology · 2004 · 11 citations
    14. Biochemistry of Vitamin B: Metabolic Regulations, Deficiency Disorders and Emerging Therapeutic Strategies IntechOpen eBooks · 2026
    15. The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation American Journal Of Pathology · 1999 · 166 citations
    16. The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene Genomics · 2004 · 50 citations
    17. APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex Nature · 2010 · 199 citations
    18. Distinct Phenotypic and Genomic Signatures Underlie Contrasting Pathogenic Potential of Staphylococcus epidermidis Clonal Lineages Frontiers in Microbiology · 2019 · 37 citations
    19. Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants Frontiers in Genetics · 2024 · 13 citations
    20. Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation Veterinary sciences · 2023 · 3 citations
    21. Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek Genes · 2022 · 2 citations
    22. FLCN regulates transferrin receptor 1 transport and iron homeostasis 2021 · 1 citations
    23. Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development Biology Direct · 2016 · 19 citations
    24. Evolution and genetic architecture of sex-limited polymorphism in cuckoos Science Advances · 2024 · 1 citations
    25. Laser therapies in androgenetic alopecia: Review and clinical experiences Journal of Cutaneous and Aesthetic Surgery · 2025
    26. Pathology of Mouse Models of Accelerated Aging Veterinary pathology · 2016 · 81 citations
    27. Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions Journal of Investigative Dermatology · 2006 · 81 citations
    28. Liver and Kidney Dysfunction in Wistar Rats Exposed to Municipal Landfill Leachate Resources and Environment · 2012 · 55 citations
    29. Recent advances on skin‐resident stem/progenitor cell functions in skin regeneration, aging and cancers and novel anti‐aging and cancer therapies Journal of Cellular and Molecular Medicine · 2009 · 36 citations
    30. The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i> G3 Genes Genomes Genetics · 2021 · 29 citations