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    Research 241–270 of 1000+

    1. Androgenetic Alopecia in Men: An Update On Genetics Indian Journal of Dermatology · 2024
    2. Rare and Underappreciated Causes of Polycystic Ovarian Syndrome IntechOpen eBooks · 2022
    3. Hypotrichosis with juvenile macular dystrophy: a case report with molecular study 2018
    4. Hair Anomalies in a 6-Year-Old Girl Case reports in clinical medicine · 2016
    5. Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep Cell & bioscience · 2023
    6. Latanoprost-Loaded Nanotransfersomes Designed for Scalp Administration Enhance Keratinocytes Proliferation Molecular Pharmaceutics · 2022
    7. Biological Function of Long Non-coding RNA (LncRNA) Xist Frontiers in Cell and Developmental Biology · 2021 · 247 citations
    8. Cantú Syndrome Is Caused by Mutations in ABCC9 The American Journal of Human Genetics · 2012 · 148 citations
    9. Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02 Nature Communications · 2019 · 115 citations
    10. The enzyme and inhibitors of 4-ene-3-oxosteroid 5α-oxidoreductase Steroids · 1995 · 64 citations
    11. Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us? Experimental Dermatology · 2016 · 46 citations
    12. Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6 Journal of Investigative Dermatology · 1999 · 29 citations
    13. Fertility counseling and preservation: considerations for the pediatric endocrinologist Translational pediatrics · 2017 · 9 citations
    14. Updates to Male Infertility: AUA/ASRM Guideline (2024) The Journal of Urology · 2024
    15. Adipocyte Lineage Cells Contribute to the Skin Stem Cell Niche to Drive Hair Cycling Cell · 2011 · 499 citations
    16. Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature Jaypee's international journal of clinical pediatric dentistry · 2018 · 11 citations
    17. Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan Genes · 2016 · 9 citations
    18. A review of genotrichoses and hair pathology associated with inherited skin diseases British Journal of Dermatology · 2023 · 8 citations
    19. Monilethrix in three generations Indian Journal of Dermatology · 2008 · 6 citations
    20. Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine Archives de Pédiatrie · 2011 · 5 citations
    21. Functional and long-lived melanocytes from human pluripotent stem cells with transient ectopic expression of JMJD3 Stem Cell Research & Therapy · 2023 · 3 citations
    22. Claves diagnósticas en displasias pilosas II 2021 · 2 citations
    23. <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks FEBS open bio · 2021 · 2 citations
    24. It’s X-Related: Biological Bases of Increased COVID-19 Morbidity and Mortality in Men Journal of the Endocrine Society · 2020 · 1 citations
    25. Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata Frontiers in Immunology · 2026
    26. Cell death as an architect of adult skin stem cell niches Cell death and differentiation · 2024
    27. Cellular senescence in skin‐related research: Targeted signaling pathways and naturally occurring therapeutic agents Aging Cell · 2023 · 48 citations
    28. Epidermal stem cells: skin surveillance and clinical perspective Journal of Translational Medicine · 2024 · 19 citations
    29. Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes European journal of medical genetics · 2012 · 13 citations
    30. A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia Genesis · 2012 · 4 citations