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- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Insertional mutation of the hairless locus on mouse Chromosome 14
- The Near-Naked Hairless (Hr) Mutation Disrupts Hair Formation but Is Not Due to a Mutation in the Hairless Coding Region
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
Community 10 of 228
- Hairloss Progress (August 2024-September 2026)
- hairloss still losing after a little over 10.5 months on treatment
- Hairloss still progressing on 1mg fin and 5 percent topical min
- Hairloss Guidance - Female ( FPHL + TE)
- Hairloss Treatments discussion on upcoming treatments by Bloomberg
- Hairloss progress over the last 3 years
- Hairloss progress (since october 2025)
- Hairloss has made me unrecognisable
- Hairloss Treatment Tier List (efficacy, convenience and safety)
- What I learnt after 5 years of styling diffuse thinned and receded hair - after meds stabilised
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