Associated Papers
Rare Germline Variants in CDKN2A-Negative Children and Adolescents With Cutaneous Melanoma.
Johansson PA et al.
Pigment Cell & Melanoma Research, 2026
41673532 (PubMed )
Supplement: PCMR-39-0-s001.xlsx › TableS3
Structure and transport mechanism of the human prostaglandin transporter SLCO2A1.
Xia Z et al.
Nature Communications, 2025
Primary hypertrophic osteoarthropathy: phenotypic variability and penetrance rate in heterozygotes for SLCO2A1 variants.
Arcanjo AM et al.
Jbmr Plus, 2025
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
A novel mutation in the SLCO2A1 gene in a Chinese family with pachydermoperiostosis.
Xiao J et al.
The Australasian Journal of Dermatology, 2019
Identification of two novel mutations in the SLCO2A1 prostaglandin transporter gene in a Chinese patient with primary hypertrophic osteoarthropathy.
Guo T et al.
Molecular Medicine Reports, 2017
Chronic Enteropathy Associated with SLCO2A1 Gene.
Umeno J et al.
Inflammatory Intestinal Diseases, 0
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