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    Research 751–780 of 1000+

    1. 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
    2. Connexin mutations in human disease Experimental Dermatology · 2004 · 4 citations
    3. 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
    4. Analogs of human genetic skin disease in domesticated animals International journal of women’s dermatology · 2017 · 3 citations
    5. Alopecia in Cronkhite-Canada syndrome British Journal of Dermatology · 2017 · 2 citations
    6. Dysfunction of keratinocyte adhesion Experimental Dermatology · 2004 · 2 citations
    7. ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India Indian dermatology online journal · 2018 · 1 citations
    8. MICRO-MORPHOMETRIC STUDY OF SKIN IN DEVELOPING HUMAN FETUSES AND ITS CLINICAL RELEVANCE International journal of anatomy and research · 2017 · 1 citations
    9. The amazing miniorgan: Hair follicle TURKDERM · 2014 · 1 citations
    10. The Roles of EDA2R in Ageing and Disease Aging Cell · 2025 · 1 citations
    11. Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases 2026
    12. Structural and Pigmentary Characteristics of the Skin in Hairless Dog Breeds International Journal of Advanced Multidisciplinary Research and Studies · 2025
    13. Approach to Alopecia in Dogs in Clinical Practice 2025
    14. Atrichia congenita with papular lesions: A rare cause of pediatric alopecia TURKDERM · 2025
    15. Polarized microscopy in genetic hair disorders: case series 2025
    16. DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS Kırıkkale Üniversitesi Tıp Fakültesi Dergisi · 2024
    17. Clinical features of taste disorders in Cronkhite-Canada syndrome: A report of 10 cases Chemical Senses · 2024
    18. Short anagen hair syndrome is caused by mutations in the <i>WNT10A</i> gene and has a genetic overlap with male pattern hair loss British Journal of Dermatology · 2023
    19. Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation Case reports in dermatological medicine · 2023
    20. Congenital Atrichia: A Case Report International journal of science and healthcare research · 2023
    21. Omenn syndrome in a 10-month-old male with athymia and VACTERL association Journal of allergy and clinical Immunology. Global · 2023
    22. Dermatological diseases from a genetic perspective Medizinische Genetik · 2023
    23. Mediator 1 ablation induces enamel-to-hair lineage conversion through enhancer dynamics bioRxiv (Cold Spring Harbor Laboratory) · 2022
    24. BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations British Journal of Dermatology · 2021
    25. Clouston’s syndrome: a rare case report International Journal of Research in Dermatology · 2020
    26. The Naked (N) Mutation, Chromosome 15 2020
    27. Index Harper's Textbook of Pediatric Dermatology · 2019
    28. Strange cutaneous abnormalities and polyposis in an Asiatic man European journal of internal medicine · 2019
    29. Hair Loss in Children, Etiologies, and Treatment InTech eBooks · 2017
    30. El teorema del 0,7 o el otro teorema de Pitágoras Epsilon: Revista de la Sociedad Andaluza de Educación Matemática "Thales" · 2009