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    Research 541–570 of 1000+

    1. Werner′s syndrome Indian Journal of Dermatology Venereology and Leprology · 2012 · 5 citations
    2. Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa Journal of the American Academy of Dermatology · 2005 · 5 citations
    3. Rare clinical features of the Ellis van Creveld syndrome: A case report and literature review Dermatologic Therapy · 2020 · 4 citations
    4. <i>egfl6</i> expression in the pharyngeal pouch is dispensable for craniofacial development Animal Cells and Systems · 2021 · 2 citations
    5. Case Report: Rare aplastic anemia in pediatric systemic lupus erythematosus: a case series and systematic literature review Frontiers in Pediatrics · 2025 · 1 citations
    6. [Association of a pediatric bullous eruption, cutaneous and muscular atrophy, hyperpigmentation and dysmorphism. A new entity?]. PubMed · 1986 · 1 citations
    7. Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report American Journal of Case Reports · 2025
    8. Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata) Journal of Cutaneous Pathology · 2025
    9. Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis British Journal of Dermatology · 2024
    10. Omenn syndrome in a 10-month-old male with athymia and VACTERL association Journal of allergy and clinical Immunology. Global · 2023
    11. Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin Journal of Biological Chemistry · 2011 · 35 citations
    12. Molecular basis of androgen insensitivity Molecular and Cellular Endocrinology · 2001 · 309 citations
    13. Skin abnormalities generated by temporally controlled RXRα mutations in mouse epidermis Nature · 2000 · 303 citations
    14. Abnormal differentiation of epidermis in transgenic mice constitutively expressing cyclooxygenase-2 in skin Proceedings of the National Academy of Sciences · 2001 · 201 citations
    15. The Rationale for Inhibiting 5α-Reductase Isoenzymes in the Prevention and Treatment of Prostate Cancer 2008 · 108 citations
    16. Genetically null mice reveal a central role for epidermal growth factor receptor in the differentiation of the hair follicle and normal hair development. PubMed · 1997 · 107 citations
    17. Retinol Esterification by DGAT1 Is Essential for Retinoid Homeostasis in Murine Skin 2008 · 91 citations
    18. Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency Molecular and Cellular Biology · 2004 · 75 citations
    19. Sebaceous Gland Atrophy in Psoriasis: An Explanation for Psoriatic Alopecia? Journal of Investigative Dermatology · 2016 · 69 citations
    20. Role of the vitamin D receptor in hair follicle biology The Journal of Steroid Biochemistry and Molecular Biology · 2007 · 54 citations
    21. Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice Genes Brain & Behavior · 2016 · 49 citations
    22. Clinical application of 5α-reductase inhibitors Journal of endocrinological investigation · 2001 · 46 citations
    23. Dutasteride Drugs · 2008 · 45 citations
    24. Pubic Hair Removal—Pearls and Pitfalls Journal of Pediatric and Adolescent Gynecology · 2006 · 41 citations
    25. Neuregulin3 alters cell fate in the epidermis and mammary gland BMC developmental biology · 2007 · 39 citations
    26. Cidea Control of Lipid Storage and Secretion in Mouse and Human Sebaceous Glands Molecular and Cellular Biology · 2014 · 36 citations
    27. Physiological Insights from the Vitamin D Receptor Knockout Mouse Calcified Tissue International · 2012 · 34 citations
    28. Ornithine decarboxylase expression in cutaneous papillomas in SENCAR mice is associated with altered expression of keratins 1 and 10. PubMed · 1994 · 33 citations
    29. Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis. PubMed · 1997 · 27 citations
    30. Human ClinicalPhenotype Associated with FOXN1 Mutations Advances in experimental medicine and biology · 2009 · 22 citations