Literature DB >> 25810087

Complete form of pachydermoperiostosis with SLCO2A1 gene mutation in a Korean family.

Hee Joo Kim1, Kyo Yeon Koo2, Dong Youn Shin1, Do Young Kim1, Jin-Sung Lee3, Min Geol Lee1.   

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Year:  2015        PMID： 25810087     DOI： 10.1111/1346-8138.12856

Source DB:  PubMed          Journal:  J Dermatol        ISSN： 0385-2407            Impact factor:   4.005


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  3 in total

Review 1.  Roles of Organic Anion Transporting Polypeptide 2A1 (OATP2A1/SLCO2A1) in Regulating the Pathophysiological Actions of Prostaglandins.

Authors:  Takeo Nakanishi; Ikumi Tamai
Journal:  AAPS J       Date:  2017-12-04       Impact factor: 4.009

2.  Compound Heterozygous Pathogenic Variants of the 15-Hydroxyprostaglandin Dehydrogenase Gene in a Patient With Hypertrophic Osteoarthropathy: First Case in Korea.

Authors:  Mi Ra Ryu; Ji Hyun Yang; Sang Youl Rhee; Ahra Cho; Seong Yoon Kim; Chang Seok Ki
Journal:  Ann Lab Med       Date:  2019-01       Impact factor: 3.464

3.  Identification of the Mutations in the Prostaglandin Transporter Gene, SLCO2A1 and Clinical Characterization in Korean Patients with Pachydermoperiostosis.

Authors:  Sihoon Lee; So Young Park; Hyun Jin Kwon; Chul-Ho Lee; Ok-Hwa Kim; Yumie Rhee
Journal:  J Korean Med Sci       Date:  2016-03-22       Impact factor: 2.153
  3 in total

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