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    Research 331–360 of 1000+

    1. Hypotrichosis and Hair Loss on the Occipital Scalp Cutis · 2023
    2. Painful thickened skin on the soles of the feet JAAD case reports · 2022
    3. Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes ˜The œAmerican journal of pathology · 2010 · 35 citations
    4. TRACHYONYCHIA ASSOCIATED WITH ALOPECIA AREATA AND SECONDARY ONYCHOMYCOSIS Jurnal Biomedik : JBM · 2014
    5. Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis American journal of human genetics · 2019 · 53 citations
    6. Generalized atrophic benign epidermolysis bullosa. PubMed · 1997 · 51 citations
    7. Structural Stability of Wild Type and Mutated α-Keratin Fragments:  Molecular Dynamics and Free Energy Calculations Biomacromolecules · 2004 · 40 citations
    8. Comprehensive treatment of Cronkhite-Canada syndrome: A case report and literature review Medicine · 2023 · 9 citations
    9. Primary hypothyroidism with exuberant dermatological manifestations Anais Brasileiros de Dermatologia · 2020 · 6 citations
    10. Prevention of chemotherapy drug-mediated human hair follicle damage: combined use of cooling with antioxidant suppresses oxidative stress and prevents matrix keratinocyte cytotoxicity Frontiers in Pharmacology · 2025 · 4 citations
    11. Alopecia Areata and Habit Tic Deformities Skin Appendage Disorders · 2018 · 3 citations
    12. Koilonychia in a Patient with Alopecia Areata. PubMed · 2021 · 2 citations
    13. Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome Dermatopathology · 2025
    14. FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program Frontiers in Immunology · 2013 · 69 citations
    15. Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing ACS Nano · 2020 · 60 citations
    16. FOXN1 deficient nude severe combined immunodeficiency Orphanet journal of rare diseases · 2017 · 32 citations
    17. Chronic graft versus host disease and skin Journal of the European Academy of Dermatology and Venereology · 2003 · 32 citations
    18. Poster Presentations Australasian Journal of Dermatology · 2021 · 25 citations
    19. Clinical Case Notes. Tamoxifen optic neuropathy Clinical and Experimental Ophthalmology · 2004 · 23 citations
    20. Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia Australasian Journal of Dermatology · 2004 · 21 citations
    21. Clinical Case Notes. Intraorbital ophthalmic artery aneurysms Clinical and Experimental Ophthalmology · 2004 · 20 citations
    22. Primary and Secondary Disturbances in Trace Element Metabolism Connected with Genetic Metabolic Disorders Annals of Nutrition and Metabolism · 1977 · 18 citations
    23. Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases Journal of Cellular Biochemistry · 2019 · 16 citations
    24. Clinical Case Notes. Lipoid proteinosis: a rare disorder with pathognomonic lid lesions Clinical and Experimental Ophthalmology · 2004 · 13 citations
    25. The hair shaft: normality, abnormality, and genetics Clinics in Dermatology · 2001 · 11 citations
    26. From structural resilience to cell specification — Intermediate filaments as regulators of cell fate ˜The œFASEB journal · 2020 · 9 citations
    27. Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings Indian Journal of Dermatology Venereology and Leprology · 2012 · 9 citations
    28. Skin problems in the long‐distance runner 2500 years after the Battle of Marathon International Journal of Dermatology · 2012 · 8 citations
    29. “Nail loss after teriflunomide treatment: A new potential adverse event” Multiple Sclerosis and Related Disorders · 2017 · 6 citations
    30. Disease Prevention and Alleviation by Human Myoblast Transplantation Open Journal of Regenerative Medicine · 2016 · 5 citations