Eicosanoid profiling in patients with complete form of pachydermoperiostosis carrying SLCO2A1 mutations-Reference-Cited by-同舟云学术

Eicosanoid profiling in patients with complete form of pachydermoperiostosis carrying SLCO2A1 mutations

Published:2021-06-11 Issue:9 Volume:48 Page:1442-1446
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Oiwa Tomohiro¹,Ishibashi Mami¹²^ORCID,Okuno Toshiaki³^ORCID,Ohba Mai³,Endo Yuichiro¹^ORCID,Uozumi Ryuji⁴^ORCID,Ghazawi Feras M.⁵^ORCID,Yoshida Kazue⁶^ORCID,Niizeki Hironori⁶^ORCID,Yokomizo Takehiko³^ORCID,Nomura Takashi¹^ORCID,Kabashima Kenji¹⁷^ORCID

Affiliation:

1. Department of Dermatology Kyoto University Graduate School of Medicine Kyoto Japan

2. Department of Dermatology Kitano HospitalTazuke Kofukai Medical Research Institute Osaka Japan

3. Department of Biochemistry (I) Juntendo University Graduate School of Medicine Tokyo Japan

4. Institute for Advancement of Clinical and Translational Science (iACT) Koto University Hospital Kyoto Japan

5. Division of Dermatology University of Ottawa Ottawa Canada

6. Division of Dermatology Department of Surgical Subspecialties National Center for Child Health and Development Tokyo Japan

7. A*STAR Singapore Immunology Network (SIgN)/Skin Research Institute of Singapore (SRIS) Singapore Singapore

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.16012

Reference14 articles.

1. Pachydermoperiostosis: an update

2. Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy

3. Prostaglandin catabolizing enzymes

4. Exome Sequencing Identifies SLCO2A1 Mutations as a Cause of Primary Hypertrophic Osteoarthropathy

5. Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype–genotype correlation in Japanese patients with pachydermoperiostosis

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