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- 1391 Immune cells may have a role in hair loss process caused by TRPV3 gain-of-function mutation
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- QuantAnts machines discover biomarkers for RAS signaling activation and design sgRNAs for CRISPR to target complex CD9, CD34, and CD74.
- Myeloproliferative disorder associated with alopecia universalis
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- Overlapping features of atopic dermatitis and alopecia areata: from pathogenesis to treatment
- Keratins: Dynamic, flexible structural proteins of epithelial cells
- Mitochondrial dysfunction as a cause of ageing
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