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    Research 241–270 of 1000+

    1. Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries) BMC Genomics · 2024 · 7 citations
    2. Advances in Hair Diseases Advances in Dermatology · 2008 · 5 citations
    3. The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients British Journal of Dermatology · 2013 · 4 citations
    4. Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus 2019 · 3 citations
    5. The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria 2022 · 2 citations
    6. Dicer- and BSC-dependent miRNAs during murine anagen development bioRxiv (Cold Spring Harbor Laboratory) · 2020 · 1 citations
    7. Expression and Distribution of the Guanine Nucleotide-binding Protein Subunit Alpha-s in Mice Skin Tissues and Its Association with White and Black Coat Colors Asian-Australasian journal of animal sciences · 2016 · 1 citations
    8. Stem Cells and their Niches Journal of Investigative Dermatology · 2013 · 1 citations
    9. Ischemic Stroke in a Young Adult Male During Finasteride Therapy Cureus · 2026
    10. Clinical analysis of 78 patients with non-classical 21-hydroxylase deficiency 2022
    11. Australasian Society for Dermatology Research Meeting, May 2006 Journal of Investigative Dermatology · 2007
    12. AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis bioRxiv (Cold Spring Harbor Laboratory) · 2023
    13. Editors' Picks Journal of Investigative Dermatology · 2007
    14. Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness Human Genetics · 2009 · 42 citations
    15. The Rotterdam Study: 2018 update on objectives, design and main results European Journal of Epidemiology · 2017 · 359 citations
    16. To grow or not to grow: Hair morphogenesis and human genetic hair disorders Seminars in Cell & Developmental Biology · 2013 · 43 citations
    17. CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism? The Journal of Sexual Medicine · 2013 · 29 citations
    18. Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters BMC Genomics · 2018 · 16 citations
    19. Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature BMC pediatrics · 2020 · 11 citations
    20. Autoimmune gastritis and parietal cell reactivity in two children with abnormal intestinal permeability European Journal of Pediatrics · 2008 · 8 citations
    21. Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases European Journal of Human Genetics · 2019 · 7 citations
    22. Cutaneous signals of immune system disease Current problems in dermatology · 1991
    23. Physiological Doses of Red Light Induce IL‐4 Release in Cocultures between Human Keratinocytes and Immune Cells Photochemistry and Photobiology · 2017 · 9 citations
    24. Cyproterone Acetate: A Genotoxic Carcinogen? Pharmacology & Toxicology · 2001 · 1 citations
    25. Inherited Epidermolysis Bullosa: A Clinical Case Medical journal of clinical trials & case studies · 2020
    26. A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features Nature Communications · 2016 · 196 citations
    27. Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities 2013 · 15 citations
    28. Maternal PPARγ protects nursing neonates by suppressing the production of inflammatory milk Genes & Development · 2007 · 102 citations
    29. Association between SQSTM1 dysregulation and risk in alopecia areata: a Mendelian randomization study Frontiers in Immunology · 2025
    30. Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss Cell Stem Cell · 2007 · 688 citations