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    Research 481–510 of 1000+

    1. Fibroproliferative genes are preferentially expressed in central centrifugal cicatricial alopecia Journal of The American Academy of Dermatology · 2018 · 25 citations
    2. INVESTIGATIONS INTO THE ROLE OF THE X-LINKED EPIGENETIC REGULATOR UTX (KDM6A) IN SELF-RENEWING STRATIFYING EPITHELIA Scholarly Commons (University of Pennsylvania) · 2025
    3. Are STK11 polymorphisms a predictor of the response to metformin in polycystic ovarian syndrome? Biomedical reports · 2022
    4. Physical and mechanical cues affecting biomaterial-mediated plasmid DNA delivery: insights into non-viral delivery systems Journal of Genetic Engineering and Biotechnology · 2021 · 15 citations
    5. Expression of Signaling Components in Embryonic Eyelid Epithelium PloS one · 2014 · 5 citations
    6. Transcriptome Sequencing Reveals Differences between Primary and Secondary Hair Follicle-derived Dermal Papilla Cells of the Cashmere Goat (Capra hircus) PLoS ONE · 2013 · 81 citations
    7. Tissue-Specific Multi-Omics Integration Demonstrates Molecular Signatures Connecting Obesity to Immune Vulnerability Metabolites · 2026
    8. Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency Journal of Investigative Dermatology · 2003 · 42 citations
    9. [Expressions and effects of autophagy-related genes in bleomycin-induced skin fibrosis of mice]. PubMed · 2020 · 1 citations
    10. Transcriptome sequencing reveals the key genes associated with hair follicle development in Qianhua Mutton Merino Frontiers in Veterinary Science · 2025
    11. Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study Journal of Thoracic Disease · 2023
    12. Expressão gênica da aromatase em folículos pilosos do vértice do escalpo de mulheres com ciclos ovulatórios e pacientes com síndrome dos ovários policísticos (PCOS) : análise de associação com parâmetros hormonais e metabolicos LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · 2008
    13. FGF5 is a crucial regulator of hair length in humans Proceedings of the National Academy of Sciences of the United States of America · 2014 · 136 citations
    14. Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria Journal of Investigative Dermatology · 2013 · 99 citations
    15. Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture The American Journal of Human Genetics · 2010 · 97 citations
    16. The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice Proceedings of the National Academy of Sciences · 2009 · 73 citations
    17. STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity Orphanet Journal of Rare Diseases · 2014 · 65 citations
    18. Transcriptomic analyses of regenerating adult feathers in chicken BMC Genomics · 2015 · 45 citations
    19. Unravelling the molecular basis for symbiotic signal transduction in legumes Molecular Plant Pathology · 2006 · 27 citations
    20. Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82 Nature communications · 2022 · 9 citations
    21. Epigenetic regulation of 5α reductase-1 underlies adaptive plasticity of reproductive function and pubertal timing BMC Biology · 2022 · 8 citations
    22. Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous Diagnostics · 2022 · 5 citations
    23. Treatment with Light-Emitting Diodes of Wavelength 863 nm Delays DMBA/TPA-Induced Skin Tumor Formation and Decreases Proinflammatory Cytokine Levels in ICR Mice BioMed Research International · 2022 · 2 citations
    24. Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair Nature genetics · 2008 · 210 citations
    25. Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix Journal of Investigative Dermatology · 2001 · 130 citations
    26. Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome American journal of human genetics · 2020 · 34 citations
    27. Gsdma3 is required for hair follicle differentiation in mice Biochemical and biophysical research communications · 2010 · 30 citations
    28. Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats Journal of Investigative Dermatology Symposium Proceedings · 2005 · 13 citations
    29. The Peach RGF/GLV Signaling Peptide pCTG134 Is Involved in a Regulatory Circuit That Sustains Auxin and Ethylene Actions Frontiers in plant science · 2017 · 9 citations
    30. Single-Cell Sequencing Reveals Differential Cell Types in Skin Tissues of Liaoning Cashmere Goats and Key Genes Related Potentially to the Fineness of Cashmere Fiber Frontiers in Genetics · 2021 · 3 citations