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    Glossary U2HR gene

    regulates hair growth and can cause hair loss when mutated

    The U2HR gene is not a standard term in genetics. However, it is often associated with a specific region within the U2HR (U2 Hairless Region) of the human genome that is involved in hair growth regulation. Mutations or alterations in this region can lead to conditions like alopecia, where individuals experience hair loss.

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    Research 10 of 22

    1. Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report Journal of the American Academy of Dermatology · 2011 · 14 citations
    2. Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation American Journal of Medical Genetics - Part A · 2010 · 11 citations
    3. Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis The Journal of Dermatology · 2013 · 6 citations
    4. Marie-unna hereditary hypotrichosis International Journal of Trichology · 2014 · 4 citations
    5. Two females with hair loss Journal der Deutschen Dermatologischen Gesellschaft · 2019
    6. Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report European Journal of Dermatology · 2018
    7. Odd-Looking Hair and Progressive Alopecia in Mother and Son JAMA Dermatology · 2014
    8. Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis Nature Genetics · 2009 · 181 citations
    9. Biology and Genetics of Hair Annual Review of Genomics and Human Genetics · 2010 · 89 citations
    10. Molecular Genetics of Alopecias Current problems in dermatology · 2015 · 9 citations
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