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    Research 511–540 of 1000+

    1. Frontotemporal dementia with parkinsonism presenting as posterior cortical atrophy Movement Disorders · 2011 · 4 citations
    2. SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection Frontiers in Bioscience-Scholar · 2024 · 3 citations
    3. Therapeutic inhibition of keratinocyte TRPV3 sensory channel by local anesthetic dyclonine 2020 · 3 citations
    4. Abstracts Experimental Dermatology · 2018 · 3 citations
    5. Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy European Journal of Dermatology · 2018 · 3 citations
    6. Spontaneous fertility in a male patient with testotoxicosis despite suppression of FSH levels Human Reproduction · 2018 · 3 citations
    7. Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation Dermatologica Sinica · 2010 · 3 citations
    8. Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene Clinical Pediatric Endocrinology · 1992 · 3 citations
    9. Nanofibers: An Effective Biomedical Tool for Burn Management International Journal for Research in Applied Science and Engineering Technology · 2023 · 2 citations
    10. Progeroide Syndrome Die Dermatologie · 2023 · 2 citations
    11. The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria 2022 · 2 citations
    12. The urine as a diagnostic key for a homozygous EGFR mutation Portuguese Journal of Nephrology & Hypertension · 2022 · 2 citations
    13. Premature Greying of Hair (Premature Canities): A Concern for Parent and Child Journal of Pigmentary Disorders · 2017 · 2 citations
    14. Inherited Disorders of the Hair Elsevier eBooks · 2013 · 2 citations
    15. Acne Harper's Textbook of Pediatric Dermatology · 2011 · 2 citations
    16. Skin Elsevier eBooks · 2011 · 2 citations
    17. Corneodesmosin: Structure, Function and Involvement in Pathophysiology The Open Dermatology Journal · 2010 · 2 citations
    18. HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype Frontiers in Immunology · 2025 · 1 citations
    19. Causality of Aging Hallmarks Aging and Disease · 2025 · 1 citations
    20. MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters Nature communications · 2023 · 1 citations
    21. Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta Frontiers in endocrinology · 2023 · 1 citations
    22. Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case Вопросы современной педиатрии · 2022 · 1 citations
    23. Papillon-Lefévre Syndrome: A Rare Case Report and a Brief Review of Literature Curēus · 2022 · 1 citations
    24. Metabolomic analysis of SMP30/GNL knockout mice treated with fermented vegetable and fruit extract (OM-X®) 2020 · 1 citations
    25. 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells Journal of Investigative Dermatology · 2019 · 1 citations
    26. Rac-dependent signaling from keratinocytes promotes differentiation of intradermal white adipocytes bioRxiv (Cold Spring Harbor Laboratory) · 2018 · 1 citations
    27. Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities Revista da Sociedade Portuguesa de Dermatologia e Venereologia · 2018 · 1 citations
    28. Global Landscapes of Human Phenotypic Variation in Inherited Traits Evolutionary studies · 2017 · 1 citations
    29. Mister XX Medicinski glasnik Specijalne bolnice za bolesti štitaste žlezde i bolesti metabolizma · 2016 · 1 citations
    30. SOX2 in the Skin Elsevier eBooks · 2015 · 1 citations