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    Research 601–630 of 1000+

    1. The vitamin D receptor functions as a transcription regulator in the absence of 1,25-dihydroxyvitamin D3 The Journal of Steroid Biochemistry and Molecular Biology · 2015 · 37 citations
    2. Study of Postpartum Alopecia Archives of Dermatology · 1963 · 24 citations
    3. Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia Movement Disorders · 2011 · 7 citations
    4. Autosomal Dominant Obstructive Sleep Apnea Syndrome Due to the New Variant c.980_984dup in COL1A2: A Case Report Cureus · 2026
    5. Serum markers thrombophilia in pregnant women with Systemic Lupus Erythematosus Revista Brasileira de Saúde Materno Infantil · 2017
    6. Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome The American Journal of Human Genetics · 2012 · 71 citations
    7. Familial Cortisol Resistance: Differential Diagnostic and Therapeutic Aspects The Journal of Clinical Endocrinology & Metabolism · 1986 · 65 citations
    8. A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13 Human Molecular Genetics · 1995 · 54 citations
    9. Tryptophan Missense Mutation in the Ligand‐Binding Domain of the Vitamin D Receptor Causes Severe Resistance to 1,25‐Dihydroxyvitamin D Journal of Bone and Mineral Research · 2002 · 47 citations
    10. Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia Scientific Reports · 2017 · 20 citations
    11. Serine palmitoyltransferase and peripheral neuropathy: studies on neuropathy-causing mutations and their biochemical hallmarks Zurich Open Repository and Archive (University of Zurich) · 2016
    12. Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene Open Archive (Karolinska Institutet) · 1997
    13. Female Androgenetic (?) Alopecia Hair transplant forum international · 2015
    14. Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene Journal of the European Academy of Dermatology and Venereology · 2017 · 6 citations
    15. Alopecia X em cães: revisão PubVet · 2020 · 4 citations
    16. P‐35 
Nonlethal junctional epidermolysis bullosa in a dog Veterinary Dermatology · 2004 · 2 citations
    17. Mutation analysis of type II hair keratin gene in a pedigree with monilethrix Chinese Journal of Dermatology · 2010
    18. Rates of polycystic ovary syndrome (PCOS) symptoms in relatives of patients with PCOS Fertility and sterility · 2002
    19. Factors affecting the development of alopecia areata in children Health care of Tajikistan · 2022
    20. Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans British Journal of Dermatology · 2001 · 38 citations
    21. Gene-knockout mice with abnormal epidermal and hair follicular development Journal of dermatological science · 1998 · 11 citations
    22. Monilethrix 2020 · 4 citations
    23. Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1 Case Reports · 2019 · 3 citations
    24. Hypothyroidism in Dogs 2013 · 3 citations
    25. [Netherton's syndrome in two sisters]. PubMed · 2002 · 3 citations
    26. This Week in JAMA JAMA · 2012 · 2 citations
    27. P‐41 Psychogenic alopecia by fur‐plucking in a family of seal‐point Siamese cats: three cases Veterinary Dermatology · 2004 · 1 citations
    28. ABC of Dermatology: Diseases of the hair and scalp The BMJ · 1988 · 1 citations
    29. BIOCHEMICAL FACTORS INFLUENCING FAMILIAL HIRSUTISM IN THE SOUTHERN REGION OF KPK Journal of medical & health sciences review. · 2025
    30. Research Snippets Journal of Investigative Dermatology · 2010