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    Research 691–720 of 830

    1. Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature BMC pediatrics · 2020 · 11 citations
    2. Skin, a mirror reflecting diabetes mellitus: A longitudinal study in a tertiary care hospital in Gujarat Indian Journal of Endocrinology and Metabolism · 2013 · 11 citations
    3. Gene-knockout mice with abnormal epidermal and hair follicular development Journal of dermatological science · 1998 · 11 citations
    4. Ultrastructure of the contrasting types of keratinization seen in the tail epidermis of the laboratory mouseMus musculus Archives of dermatological research · 1977 · 11 citations
    5. Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin Genetics in medicine · 2018 · 10 citations
    6. Micronutrients in hair loss Our Dermatology Online · 2018 · 10 citations
    7. Advancements in Dermatological Imaging Modalities Indian Dermatology Online Journal · 2024 · 9 citations
    8. The PI3K-Akt-mTOR and Associated Signaling Pathways as Molecular Drivers of Immune-Mediated Inflammatory Skin Diseases: Update on Therapeutic Strategy Using Natural and Synthetic Compounds Cells · 2023 · 9 citations
    9. Solubility of Foreign Molecules in Stratum Corneum Brick and Mortar Structure Langmuir · 2023 · 9 citations
    10. Medical aesthetics – Current trends and a review of its applications Indian Dermatology Online Journal · 2023 · 9 citations
    11. Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks Genes · 2022 · 9 citations
    12. Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82 Nature communications · 2022 · 9 citations
    13. The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat ) Molecular Genetics and Metabolism Reports · 2014 · 9 citations
    14. Systematic characterization of the barrier function of diverse ex vivo models of damaged human skin Frontiers in Medicine · 2024 · 8 citations
    15. Microscopic polyangiitis secondary to Mycobacterium abscessus in a patient with bronchiectasis: a case report BMC Pulmonary Medicine · 2018 · 8 citations
    16. Metabolism and skin diseases Reviews in Endocrine and Metabolic Disorders · 2016 · 8 citations
    17. Putting the Human Hair Follicle Cycle on the Map Journal of Investigative Dermatology · 2016 · 8 citations
    18. Frontal fibrosing alopecia: a review of eleven patients European Journal of Dermatology · 2011 · 8 citations
    19. Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages Cells · 2024 · 7 citations
    20. Hair Keratin 1990 · 7 citations
    21. Site of beige (<i>bg</i>) and leaden (<i>ln</i>) pigment gene expression determined by recombinant embryonic skin grafts and aggregation mouse chimaeras employing sash (<i>W</i><sup><i>sh</i></sup>) homozygotes Genetics Research · 1985 · 7 citations
    22. Mechanisms of autophagy and their implications in dermatological disorders Frontiers in Immunology · 2024 · 6 citations
    23. Eyes open on stem cells Stem Cell Reports · 2023 · 6 citations
    24. Eyebrow and Eyelash Alopecia: A Clinical Review American journal of clinical dermatology · 2022 · 6 citations
    25. Essential Role of STAT3 Signaling in Hair Follicle Homeostasis Frontiers in immunology · 2021 · 6 citations
    26. A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan Indian Journal of Dermatology · 2019 · 6 citations
    27. The Scientific Legacy of Stephen Rothman 2014 · 6 citations
    28. Androgenetische Alopezie Der Hautarzt · 2004 · 6 citations
    29. Tolerability, acceptability, and reproducibility of topical STAR particles in human subjects Bioengineering & Translational Medicine · 2023 · 5 citations
    30. RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development Orphanet journal of rare diseases · 2022 · 5 citations