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    Research 451–480 of 1000+

    1. EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia Genes · 2024
    2. E-Poster Indian Journal of Endocrinology and Metabolism · 2023
    3. Hair regeneration using microneedle-assisted human basic fibroblast growth factor Journal of analytical & pharmaceutical research · 2023
    4. Current understanding and treatment of sex hormone-related hair diseases Dermatologica Sinica · 2023
    5. Association of Acne Tarda with Endocrinological Disorders Dermato · 2022
    6. Compliance to Topical Minoxidil and Reasons for Discontinuation among Patients with Androgenetic Alopecia Dermatology and therapy · 2023
    7. Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China Scientific reports · 2022 · 4 citations
    8. Identification of lncRNAs involved in the hair follicle cycle transition of cashmere goats in response to photoperiod change BMC Genomics · 2025 · 1 citations
    9. Androgenetic Alopecia: a Review and Emerging Treatments Clinical research in dermatology · 2017 · 1 citations
    10. Androgenetic alopecia Nature Reviews Disease Primers · 2025
    11. The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia International Journal of Molecular Sciences · 2024
    12. Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets BoneKEy Reports · 2014 · 107 citations
    13. Hereditary 1,25-Dihydroxyvitamin D Resistant Rickets due to a Mutation Causing Multiple Defects in Vitamin D Receptor Function Endocrinology · 2004 · 67 citations
    14. Topical minoxidil therapy in hereditary androgenetic alopecia Archives of Dermatology · 1985 · 55 citations
    15. Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor Molecular Genetics and Metabolism · 2009 · 50 citations
    16. Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor Journal of bone and mineral research · 1998 · 47 citations
    17. Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor Journal of Bone and Mineral Research · 2011 · 37 citations
    18. Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene Journal of Pediatric Endocrinology and Metabolism · 2010 · 36 citations
    19. Zinc‐responsive dermatosis in goats suggestive of hereditary malabsorption: two field cases Veterinary Dermatology · 2005 · 34 citations
    20. Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene Journal of Veterinary Internal Medicine · 2009 · 30 citations
    21. Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets KARGER eBooks · 2003 · 29 citations
    22. A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia Endocrinology · 2014 · 25 citations
    23. A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation 2019 · 21 citations
    24. A Comparative Study of a New Food Supplement, ViviScal®, with Fish Extract for the Treatment of Hereditary Androgenic Alopecia in Young Males Journal of International Medical Research · 1992 · 16 citations
    25. Topical minoxidil therapy for hereditary male pattern alopecia. PubMed · 1987 · 14 citations
    26. Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets JDR Clinical & Translational Research · 2017 · 12 citations
    27. Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene Journal of Pediatric Endocrinology and Metabolism · 2014 · 10 citations
    28. Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria. PubMed · 2002 · 9 citations
    29. Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets Bone Research · 2016 · 7 citations
    30. Hereditary mucoepithelial dysplasia: unique histopathological findings in skin lesions Journal of cutaneous pathology · 2012 · 7 citations