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    Research 121–150 of 1000+

    1. CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation American journal of ophthalmology. Case reports · 2017 · 9 citations
    2. The medusa head: Dermoscopic diagnosis of woolly hair syndrome International Journal of Trichology · 2012 · 7 citations
    3. Expression of mineralized tissue associated proteins: Dentin sialoprotein and phosphophoryn in rodent hair follicles Journal of Dermatological Science · 2011 · 5 citations
    4. CONGENITAL ATRICHIA.* Australasian journal of dermatology · 1964 · 5 citations
    5. NEW YORK ACADEMY OF MEDICINE, SECTION ON DERMATOLOGY AND SYPHILIS Archives of dermatology · 1925 · 5 citations
    6. Monilethrix 2020 · 4 citations
    7. Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b The Journal of Dermatology · 2013 · 4 citations
    8. Tooth tissue and organ regeneration using stem cells Inflammation and Regeneration · 2013 · 4 citations
    9. Keratin 75 Is a Component of the LINC Complex and Has an Essential Role in Mediating the SOX2 Rapid Healing Response during Wound Repair 2022 · 3 citations
    10. Ptch2 is a Potential Regulator of Mesenchymal Stem Cells Frontiers in Physiology · 2022 · 3 citations
    11. Post-natal development of rats` offspring treated with the ethanol extract of Neem leaves (<i>Azadirachta indica</i> A. Juss) during pregnancy and lactation Acta Scientiarum Biological Sciences · 2015 · 3 citations
    12. Erythrokeratodermia Variabilis 2004 · 3 citations
    13. [An infant with short stature and red cheeks (Rothmund-Thomson syndrome)]. PubMed · 1991 · 3 citations
    14. Fully functional salivary gland regeneration as a next-generation regenerative therapy Nihon Rinshō Men'eki Gakkai kaishi · 2015 · 2 citations
    15. Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn Cureus · 2023 · 1 citations
    16. Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature? Diagnostics · 2022 · 1 citations
    17. Papillon-Lefévre Syndrome: A Rare Case Report and a Brief Review of Literature Curēus · 2022 · 1 citations
    18. ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India Indian dermatology online journal · 2018 · 1 citations
    19. Co-option of Hair Follicle Keratins into Amelogenesis Is Associated with the Evolution of Prismatic Enamel: A Hypothesis Frontiers in Physiology · 2017 · 1 citations
    20. Global Landscapes of Human Phenotypic Variation in Inherited Traits Evolutionary studies · 2017 · 1 citations
    21. Alopecia triangularis congenita in combination with androgenetic alopecia Journal of The European Academy of Dermatology and Venereology · 2004 · 1 citations
    22. Your good health : how to stay well, and what to do when you're not Harvard University Press eBooks · 1987 · 1 citations
    23. Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report Journal of Chittagong Medical College Teachers Association · 2026
    24. Phytochemical Investigation of Tamarix aphylla (L.) Karst: A Plant of Medicinal Value from Gujarat, India CyberLeninK (CyberLeninka) · 2025
    25. Structural and Pigmentary Characteristics of the Skin in Hairless Dog Breeds International Journal of Advanced Multidisciplinary Research and Studies · 2025
    26. Stable isotope analyses of carbon and nitrogen in hair keratin of suspected man-eating wolves from 1880s Scientific Reports · 2024
    27. 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
    28. Feed Management and Nutritional Status of Gibbons (Symphalangus Syndactylus Raffles, 1821) at Tegal Alur Animal Rescue Center, Jakarta Al-Kauniyah · 2023
    29. PA05 A rare case of cardiocutaneous syndrome in a young child 2023
    30. Case Report: 7 Year-Old Saudi Female with Monilethrix Journal of Pakistan Association of Dermatologists · 2022