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- TRPV3 Ion Channel: From Gene to Pharmacology
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- The genetic evolution of skin squamous cell carcinoma: tumor suppressor identity matters
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Natural phenylethanoid glycoside forsythoside A alleviates androgenetic alopecia by selectively inhibiting TRPV3 channels in mice
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- Influence of TRPV3 mutation on hair growth cycle in mice
- Direct cellular reprogramming enables development of viral T antigen–driven Merkel cell carcinoma in mice
- Expanding the Phenotypic Spectrum of Olmsted Syndrome
- Two familial cases of Olmsted-like syndrome with a G573V mutation of the<i>TRPV3</i>gene
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