Associated Papers
Pachydermoperiostosis Associated With a Rare SLCO2A1 Mutation: A Case Report and Literature Review.
Mohammad M et al.
Cureus, 2025
Structure and post-translational modification of the prostaglandin transporter.
Yu P et al.
Communications Biology, 2025
40681657 (PubMed )
Supplement: 42003_2025_8510_MOESM5_ESM.pdf
Recent advances in studies of SLCO2A1 as a key regulator of the delivery of prostaglandins to their sites of action.
Nakanishi T et al.
Pharmacology & Therapeutics, 2021
Novel SLCO2A1 mutations cause gender-differentiated pachydermoperiostosis.
Yuan L et al.
Endocrine Connections, 2018
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