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A Proposal for Practical Diagnosis of Renal Hypouricemia: Evidenced from Genetic Studies of Nonfunctional Variants of URAT1/SLC22A12 among 30,685 Japanese Individuals.
Biomedicines. 2021 Aug 13;9(8):1012. doi: 10.3390/biomedicines9081012.
Biomedicines. 2021.
PMID: 34440216
Free PMC article.
Porphyrin accumulation in humans with common dysfunctional variants of ABCG2, a porphyrin transporter: potential association with acquired photosensitivity.
Sakiyama M, Matsuo H, Toyoda Y, Yonekura Y, Ishikawa T, Nakayama A, Higashino T, Kawamura Y, Fujimoto N, Shinomiya N, Satoh T.
Sakiyama M, et al.
Hum Cell. 2021 Jul;34(4):1082-1086. doi: 10.1007/s13577-021-00534-y. Epub 2021 May 19.
Hum Cell. 2021.
PMID: 34009629
Free PMC article.
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Increase of serum uric acid levels associated with APOE ε2 haplotype: a clinico-genetic investigation and in vivo approach.
Ogura M, Toyoda Y, Sakiyama M, Kawamura Y, Nakayama A, Yamanashi Y, Takada T, Shimizu S, Higashino T, Nakajima M, Naito M, Hishida A, Kawai S, Okada R, Sasaki M, Ayaori M, Suzuki H, Takata K, Ikewaki K, Harada-Shiba M, Shinomiya N, Matsuo H.
Ogura M, et al.
Hum Cell. 2021 Nov;34(6):1727-1733. doi: 10.1007/s13577-021-00609-w. Epub 2021 Sep 16.
Hum Cell. 2021.
PMID: 34532841
Free PMC article.
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