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    Research 481–510 of 1000+

    1. Clinical use of 5α-reductase inhibitors Cambridge University Press eBooks · 2001 · 3 citations
    2. The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation American Journal Of Pathology · 1999 · 166 citations
    3. Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis American journal of human genetics · 2019 · 53 citations
    4. Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency Journal of Investigative Dermatology · 2003 · 42 citations
    5. Activated Kras Alters Epidermal Homeostasis of Mouse Skin, Resulting in Redundant Skin and Defective Hair Cycling Journal of Investigative Dermatology · 2010 · 29 citations
    6. A kindred with mutant IKAROS and autoimmunity Journal of Allergy and Clinical Immunology · 2018 · 37 citations
    7. Birt–Hogg–Dubé syndrome Familial cancer · 2013 · 7 citations
    8. Survival of patchwork melanoblasts is dependent upon their number in the hair follicle at the end of embryogenesis Developmental Biology · 1998 · 29 citations
    9. H3K9me3 controls epidermis morphogenesis by regulating RNA Pol II dynamics at developmental promoters and enhancers Nature Communications · 2026
    10. RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS 2017 · 2 citations
    11. Hair follicles and their role in skin health Expert Review of Dermatology · 2006 · 16 citations
    12. 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review Hormones · 2018 · 39 citations
    13. Murine Epidermal Ceramide Synthase 4 Is a Key Regulator of Skin Barrier Homeostasis Journal of Investigative Dermatology · 2020 · 15 citations
    14. Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family Frontiers in genetics · 2021 · 1 citations
    15. FLCN regulates transferrin receptor 1 transport and iron homeostasis 2021 · 1 citations
    16. Author response: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome 2016
    17. Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency Journal of Investigative Dermatology · 2014 · 24 citations
    18. Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases Journal of Cellular Biochemistry · 2019 · 16 citations
    19. Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance Open Archive (Karolinska Institutet) · 2011
    20. Hair Follicle Stem Cells Provide a Functional Niche for Melanocyte Stem Cells Cell stem cell · 2011 · 283 citations
    21. The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice Proceedings of the National Academy of Sciences · 2009 · 73 citations
    22. Impaired osteoblastic differentiation, reduced bone formation, and severe osteoporosis in noggin-overexpressing mice Journal of Clinical Investigation · 2003 · 21 citations
    23. Role of EZH2 in Uterine Gland Development International Journal of Molecular Sciences · 2022 · 6 citations
    24. E-Poster Indian Journal of Endocrinology and Metabolism · 2023
    25. Genetically separable determinants of hair keratin gene expression Developmental Dynamics · 2000 · 27 citations
    26. Successful plasmapheresis and immunoglobulin treatment for severe lipid storage myopathy: Doing the right thing for the wrong reason 2021 · 2 citations
    27. Intraretinal variation in disease severity in the Oat mouse model of gyrate atrophy Experimental Eye Research · 2025
    28. Carcinogenesis of the Human Scalp. An Immunometabolic Centered View Preprints.org · 2024
    29. Carcinogenesis of the Human Scalp. An Immunometabolic Centered View Preprints.org · 2024
    30. Functional mapping of the mouse <i>hairless</i> gene promoter region bioRxiv (Cold Spring Harbor Laboratory) · 2018