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research Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family
research 19th Annual Dermatology Update and All That Jazz
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research Cyberspace Chat: Scalp biopsies: to refer or not to refer?
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research Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
Researchers found a gene mutation responsible for a rare hair loss condition.
research A Word from Helen
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research Date.zip
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research My Clinical Experience with Needle and Laser SMP Devices
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research Devices and genomic therapies
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research Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.
research Plastic Needle Shield: A Two-in-One Solution
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research ABHRS Profile
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research Co-editor’s note
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research Meeting Announcement
research Co-Editors' Messages
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research Calendar
research Notes from the Editor Emeritus, 2002–04
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research Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
Certain mutations in a hair growth-related gene cause a type of genetic hair loss.
research Aesthetic Practice in Nepal
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research Finasteride
research Index
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research Index
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research Notes from the Editor Emeritus
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research P22-023-23 Pilot Study Protocol on Application of Non-Invasive Vitamin D Hair Test and Screening E-Tool for Indigenous Populations in the Great Northern Plains
research Megatransplants in Transition: A Pictorial Review
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research NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.
research A review of HAIRCON 2011
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research The Notable Articles Project
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research Reversible Activation of c-Myc in Skin
Activating c-Myc in skin causes rapid cell growth and changes, but these effects are reversible.