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    Research 601–630 of 1000+

    1. Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs PLoS ONE · 2012 · 28 citations
    2. Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes Biochemical and Biophysical Research Communications · 2000 · 12 citations
    3. Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report Clinical Cosmetic and Investigational Dermatology · 2023
    4. EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia Genes · 2024
    5. Advances in regenerative medicine-based approaches for skin regeneration and rejuvenation Frontiers in Bioengineering and Biotechnology · 2025 · 25 citations
    6. Male androgenetic alopecia Human health handbooks · 2012 · 1 citations
    7. A Comprehensive Review on Alopecia: Mechanisms, Classification, and Therapeutic Strategies Zenodo (CERN European Organization for Nuclear Research) · 2026
    8. Alopecia and cardiovascular events The Lancet · 2000 · 1 citations
    9. Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation Frontiers in pediatrics · 2022
    10. Senescence-accelerated Mouse (SAM): With Special Reference to Development and Pathobiological Phenotypes ILAR Journal · 1997 · 30 citations
    11. Chapter 23. Therapeutic Control of Androgen Action Annual Reports in Medicinal Chemistry · 1994 · 7 citations
    12. 176 Myeloid cell-specific deletion of mTOR suppresses psoriasis-like skin inflammation in C57BL/6 mice Journal of Investigative Dermatology · 2023
    13. Autosomal Dominant Obstructive Sleep Apnea Syndrome Due to the New Variant c.980_984dup in COL1A2: A Case Report Cureus · 2026
    14. [Androgenetic alopecia]. PubMed · 2002
    15. Topical minoxidil treatment for congenital alopecia in hypohidrotic ectodermal dysplasia 2013 · 12 citations
    16. GLOMERULAR MEMBRANOUS NEPHROPATHY AND WERNER SYNDROME: A CASE REPORT Journal of the American Geriatrics Society · 2011 · 1 citations
    17. Nonclassic Congenital Adrenal Hyperplasia: An Overview Journal of Pediatric Nursing · 2009
    18. A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome Orphanet Journal of Rare Diseases · 2017 · 11 citations
    19. Loose Anagen Syndrome: A Retrospective Chart Review of 37 Cases Pediatric Dermatology · 2016 · 13 citations
    20. Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families The Journal of Dermatology · 2011 · 11 citations
    21. Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice International journal of genomics · 2018 · 5 citations
    22. Hair Follicle Melanogenesis Reflected in Hair Pigmentation as a Developmental Factor in Alopecia Areata Skin appendage disorders · 2021 · 3 citations
    23. Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease Skin appendage disorders · 2018 · 2 citations
    24. Premature Greying of Hair (Premature Canities): A Concern for Parent and Child Journal of Pigmentary Disorders · 2017 · 2 citations
    25. Why Do Not All Chemotherapy Patients Lose Their Hair? Answering an Intriguing Question Skin appendage disorders · 2021 · 1 citations
    26. Research on Mental Stress Recognition of Depressive Disorders in Patients With Androgenic Alopecia Based on Machine Learning and Fuzzy K-Means Clustering Frontiers in Genetics · 2021
    27. Lipedematous Scalp Occurring in Two Female Siblings: Further Evidence for a Genetic Role Skin Appendage Disorders · 2023 · 2 citations
    28. Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review Pediatric Dermatology · 2025
    29. Kératose pilaire Pan African Medical Journal · 2019 · 1 citations
    30. A Comprehensive Review on Alopecia: Mechanisms, Classification, and Therapeutic Strategies Zenodo (CERN European Organization for Nuclear Research) · 2026