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    Research 271–300 of 1000+

    1. Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5 Proceedings of the National Academy of Sciences of the United States of America · 2017 · 18 citations
    2. Novel de novo pathogenic variant in the <i>ODC1</i> gene in a girl with developmental delay, alopecia, and dysmorphic features American Journal of Medical Genetics Part A · 2018 · 39 citations
    3. Functional histopathology of keloid disease. PubMed · 2015 · 142 citations
    4. A rational approach to the diagnosis of polycystic ovarian syndrome during adolescence Arquivos Brasileiros De Endocrinologia E Metabologia · 2011 · 26 citations
    5. AAPS and PSRC 2016 Abstract Supplement Plastic and reconstructive surgery. Global open · 2016
    6. Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report Frontiers in Medicine · 2025
    7. Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis British Journal of Dermatology · 2024
    8. Myotonic Dystrophy—A Progeroid Disease? Frontiers in Neurology · 2018 · 41 citations
    9. Weathering the Storm: Harnessing the Resolution of Inflammation to Limit COVID-19 Pathogenesis Frontiers in Immunology · 2022 · 17 citations
    10. PolyQ length co-evolution in neural proteins NAR Genomics and Bioinformatics · 2021 · 6 citations
    11. GC-TOF/MS-Based Metabolomics for Comparison of Volar and Non-Volar Skin Types Metabolites · 2022
    12. 0750 Proteomics and transcriptomics profiling define molecular subtypes of advanced cutaneous T cell lymphoma and prognostic biomarkers Journal of Investigative Dermatology · 2025
    13. Immunosenescence and inflammaging in Parkinson’s disease: mechanisms and therapeutic prospects Frontiers in Immunology · 2026
    14. 090 Reactive lipids from the secretome of senescent fibroblasts modify the extracellular matrix with functional consequences for resident cells Journal of Investigative Dermatology · 2024
    15. 증례 : 모발의 황 농도 감소를 보인 모발유황이영양증 대한피부과학회지 · 2011
    16. Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility 2009 · 189 citations
    17. Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development Case Reports in Genetics · 2025
    18. STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity Orphanet Journal of Rare Diseases · 2014 · 65 citations
    19. Neuregulin3 alters cell fate in the epidermis and mammary gland BMC developmental biology · 2007 · 39 citations
    20. Fibroblasts in Diabetic Foot Ulcers International Journal of Molecular Sciences · 2024 · 33 citations
    21. A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue Journal of Investigative Dermatology · 2004 · 31 citations
    22. Cell Proteomic Footprinting: Advances in the Quality of Cellular and Cell-Derived Cancer Vaccines Pharmaceutics · 2023 · 1 citations
    23. A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene Clinical Case Reports · 2025
    24. Dynamic immunomodulatory nanoarchitectonics: Rewiring tissue regenerative microenvironment via intelligent regulation Nano Research · 2025
    25. Approach to the Patient: Diagnostic Challenges in the Work Up for Polycystic Ovary Syndrome The Journal of Clinical Endocrinology & Metabolism · 2025
    26. Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review Biomedicines · 2024
    27. A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report Pediatric rheumatology online journal · 2024
    28. Abstract 4385: Live-imaging the interface between homeostasis and cancer initiation Cancer research · 2016
    29. Inducible deletion of Dicer or Drosha reveals multiple functions for miRNAs in postnatal epidermis and hair follicles ScholarlyCommons (University of Pennsylvania) · 2012
    30. Defects in Androgen Biosynthesis Causing 46,XY Disorders of Sexual Development Seminars in reproductive medicine · 2012 · 46 citations