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    Research 91–120 of 1000+

    1. Uncombable hair improved by biotin JEADV Clinical Practice · 2023
    2. Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1 American journal of medical genetics. Part A · 2022
    3. Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix Chinese Medical Journal · 2013 · 4 citations
    4. Toe-tourniquet syndrome: a diagnostic dilemma! Annals of The Royal College of Surgeons of England · 2006 · 22 citations
    5. Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome American journal of human genetics · 2016 · 119 citations
    6. Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families Molecular genetics & genomic medicine · 2022 · 5 citations
    7. Identification of Hair Growth Promoting Components in the Kernels of Prunus mira Koehne and Their Mechanism of Action Molecules · 2022 · 1 citations
    8. Porokeratotic eccrine ostial and dermal duct nevus: A noteworthy presentation Indian Dermatology Online Journal · 2015 · 6 citations
    9. Alopecia Areata and Habit Tic Deformities Skin Appendage Disorders · 2018 · 3 citations
    10. A counter gradient of Activin A and follistatin instructs the timing of hair cell differentiation in the murine cochlea eLife · 2019 · 15 citations
    11. Decision letter: A counter gradient of Activin A and follistatin instructs the timing of hair cell differentiation in the murine cochlea 2019
    12. Biologics and Small Molecules for Inflammatory Nail Disorders: A Narrative Review Indian Dermatology Online Journal · 2024 · 1 citations
    13. Approach to Nail Pitting in Pediatric and Adolescent Patients: A Dermatology Perspective JEADV Clinical Practice · 2026
    14. Risk of meningioma among users of high doses of cyproterone acetate as compared with the general population: evidence from a population-based cohort study British Journal of Clinical Pharmacology · 2011 · 88 citations
    15. SOX9 in organogenesis: shared and unique transcriptional functions Cellular and Molecular Life Sciences · 2022 · 10 citations
    16. In vivo expression of VCAM1 precedes nephron loss following kidney tubular necrosis Science Advances · 2025 · 4 citations
    17. Alopecia Areata of the Nails: Diagnosis and Management Journal of Clinical Medicine · 2024 · 2 citations
    18. Is the Loose Anagen Hair Syndrome a Keratin Disorder? Archives of Dermatology · 2002 · 84 citations
    19. A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis Journal of Investigative Dermatology · 2012 · 78 citations
    20. A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis Journal of Investigative Dermatology · 2017 · 33 citations
    21. Genetic Hair Disorders: A Review Dermatology and Therapy · 2019 · 26 citations
    22. Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer Cells · 2020 · 22 citations
    23. Hair shaft disorders in children – An update Indian Dermatology Online Journal · 2023 · 12 citations
    24. Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease PloS one · 2019 · 5 citations
    25. Progress on mitochondria and hair follicle development in androgenetic alopecia: relationships and therapeutic perspectives Stem Cell Research & Therapy · 2025
    26. Peculiarities of clinical course and diagnostic of alopecia areata with comorbidity. Clinical observations Rossijskij žurnal kožnyh i veneričeskih boleznej · 2022
    27. [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II 2022
    28. Trichoscopy in genetic hair shaft abnormalities Journal of Dermatological Case Reports · 2008 · 74 citations
    29. Gene detection in a family with monilethrix and treatment with 5% topical minoxidil Skin research and technology · 2022 · 2 citations
    30. Stimulation of ectodermal organ development by Ectodysplasin-A1 Developmental Biology · 2003 · 249 citations