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January 2017 in “Orphanet journal of rare diseases” FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.
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November 2003 in “Journal of Investigative Dermatology” The K15 promoter effectively targets stem cells in the hair follicle bulge.
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January 2026 in “Mendeley Data” Hair follicle stem cell exosomes help nerve regeneration.
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September 2013 in “International Journal of Molecular Sciences” Keratin 15 is not a reliable sole marker for identifying epidermal stem cells because it's found in various cell types.
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November 2004 in “The journal of investigative dermatology/Journal of investigative dermatology” The Foxn1 gene is essential for normal nail and hair development.
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March 2012 in “British journal of dermatology/British journal of dermatology, Supplement” Using specific cleansers and moisturizers with niacinamide improves men's skin hydration and health.
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January 2020 in “Dermatology online journal” An adult with a rare skin condition improved with tazarotene treatment.
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November 2005 in “Forensic Science International” BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.
February 2026 in “Pediatric Dermatology” October 2022 in “Zenodo (CERN European Organization for Nuclear Research)” July 2025 in “Journal of Investigative Dermatology” Nelfb is essential for dermal fat development and survival.
SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.
June 2020 in “Zenodo (CERN European Organization for Nuclear Research)” The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.
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October 2005 in “Experimental Dermatology” The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.
January 2026 in “Mendeley Data” Hair follicle stem cell exosomes help nerve regeneration.