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    Research 751–780 of 1000+

    1. Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder Indian dermatology online journal · 2013 · 12 citations
    2. Dermatopathology and molecular genetics Journal of The American Academy of Dermatology · 2008 · 12 citations
    3. A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations Clinical and experimental dermatology · 2013 · 11 citations
    4. Clinical Case Notes. Propecia-associated bilateral cataract Clinical and Experimental Ophthalmology · 2004 · 11 citations
    5. Hair loss among a group of Egyptian children Journal of the Egyptian Women's Dermatologic Society (Print) · 2017 · 9 citations
    6. Canestick Lesion of Vellus Hair in Netherton's Syndrome Archives of Dermatology · 1985 · 9 citations
    7. Transcriptional activation of a subset of hair keratin genes by the NF-κB effector p65/RelA Differentiation · 2007 · 7 citations
    8. Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11 Mammalian Genome · 2000 · 7 citations
    9. The fundamentals of WNT10A Differentiation · 2025 · 6 citations
    10. Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família Anais Brasileiros de Dermatologia · 2004 · 6 citations
    11. Disorders of the Hair and Scalp in Children Pediatric Clinics of North America · 1991 · 6 citations
    12. Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i> The Journal of Dermatology · 2017 · 5 citations
    13. What Syndrome Is This? Pediatric dermatology · 1993 · 5 citations
    14. Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy JAAD Case Reports · 2019 · 4 citations
    15. Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b The Journal of Dermatology · 2013 · 4 citations
    16. Using High-Throughput Immunoblotting to Identify Proteins Involved in the Differentiation of ES Cells along the Hair Follicle Lineage in Vitro Stem Cell Reviews and Reports · 2011 · 4 citations
    17. Connexin mutations in human disease Experimental Dermatology · 2004 · 4 citations
    18. Recombinant Thrombomodulin Used to Successfully Treat Cronkhite-Canada Syndrome with Disseminated Intravascular Coagulation due to Sepsis in a Compromised Patient Internal Medicine · 2018 · 3 citations
    19. Analogs of human genetic skin disease in domesticated animals International journal of women’s dermatology · 2017 · 3 citations
    20. Alopecia in Cronkhite-Canada syndrome British Journal of Dermatology · 2017 · 2 citations
    21. Dysfunction of keratinocyte adhesion Experimental Dermatology · 2004 · 2 citations
    22. ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India Indian dermatology online journal · 2018 · 1 citations
    23. MICRO-MORPHOMETRIC STUDY OF SKIN IN DEVELOPING HUMAN FETUSES AND ITS CLINICAL RELEVANCE International journal of anatomy and research · 2017 · 1 citations
    24. The amazing miniorgan: Hair follicle TURKDERM · 2014 · 1 citations
    25. The Roles of EDA2R in Ageing and Disease Aging Cell · 2025 · 1 citations
    26. Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases 2026
    27. Structural and Pigmentary Characteristics of the Skin in Hairless Dog Breeds International Journal of Advanced Multidisciplinary Research and Studies · 2025
    28. Approach to Alopecia in Dogs in Clinical Practice 2025
    29. Atrichia congenita with papular lesions: A rare cause of pediatric alopecia TURKDERM · 2025
    30. Polarized microscopy in genetic hair disorders: case series 2025