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    Research 211–240 of 1000+

    1. Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages Cells · 2024 · 7 citations
    2. A study on efficacy of oral zinc therapy for treatment of acrodermatitis enteropathica Nasza Dermatologia Online · 2013 · 5 citations
    3. Clinical Presentations and Comorbidities of Pediatric Alopecia Areata Pediatric Dermatology · 2025 · 4 citations
    4. Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family Journal of clinical laboratory analysis · 2021 · 4 citations
    5. Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy JAAD Case Reports · 2019 · 4 citations
    6. Hypotrichosis with juvenile macular dystrophy International Journal of Trichology · 2018 · 4 citations
    7. [Evaluation of the role of dietary intake in the occurrence of alopecia]. PubMed · 2010 · 3 citations
    8. SKIN MANIFESTATIONS OF RHEUMATOLOGICAL DISEASES Rheumatology quarterly · 2024
    9. Dermatologic manifestations of thyroid disease: a literature review Frontiers in Endocrinology · 2023
    10. Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity Pediatrics in review · 2021
    11. Moniletherix ˜The œPan African medical journal · 2013
    12. 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
    13. Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament Genomics · 2007 · 27 citations
    14. Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice Cell death and disease · 2014 · 16 citations
    15. Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2 2022 · 8 citations
    16. Pigmentary mosaicism: An update Indian Journal of Dermatology · 2008 · 7 citations
    17. A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease Movement disorders clinical practice · 2022 · 1 citations
    18. 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR Journal of Investigative Dermatology · 2016
    19. Zone 1 Hepatocellular Necrosis: A Manifestation of Selenium Toxicity? The American Journal of Gastroenterology · 2009
    20. Keratins and disease at a glance Journal of Cell Science · 2012 · 87 citations
    21. Inherited ichthyoses/generalized Mendelian disorders of cornification European journal of human genetics · 2012 · 81 citations
    22. FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program Frontiers in Immunology · 2013 · 69 citations
    23. FOXN1 deficient nude severe combined immunodeficiency Orphanet journal of rare diseases · 2017 · 32 citations
    24. Chronic graft versus host disease and skin Journal of the European Academy of Dermatology and Venereology · 2003 · 32 citations
    25. The scope of the dermoscope Indian Dermatology Online Journal · 2016 · 27 citations
    26. Poster Presentations Australasian Journal of Dermatology · 2021 · 25 citations
    27. Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice Journal of Biological Chemistry · 2002 · 15 citations
    28. Zinc and Zinc Transporters in Dermatology International Journal of Molecular Sciences · 2022 · 4 citations
    29. A folliculocentric perspective of dandruff pathogenesis: Could a troublesome condition be caused by changes to a natural secretory mechanism? BioEssays · 2021 · 3 citations
    30. Epstein-Barr virus associated with high-grade B-cell lymphoma in nude severe combined immunodeficiency BMJ case reports · 2019 · 3 citations