Kagawa Reiko

カガワレイコ | Kagawa Reiko

Research theme for competitive and other funds (2)：

2021 - 2023 CARD9遺伝子変異の機能解析法の確立
2019 - 2022 Study of molecular pathology in which STAT1 gain-of-function mutations cause autoimmune endocrine disorders

Papers (22)：

Go Tajima, Junko Aisaki, Keiichi Hara, Miyuki Tsumura, Reiko Kagawa, Fumiaki Sakura, Hideo Sasai, Miori Yuasa, Yosuke Shigematsu, Satoshi Okada. Using the C14:1/Medium-Chain Acylcarnitine Ratio Instead of C14:1 to Reduce False-Positive Results for Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency in Newborn Screening in Japan. International Journal of Neonatal Screening. 2024
Go Tajima, Keiichi Hara, Miyuki Tsumura, Reiko Kagawa, Fumiaki Sakura, Hideo Sasai, Miori Yuasa, Yosuke Shigematsu, Satoshi Okada. Newborn Screening with (C16 + C18:1)/C2 and C14/C3 for Carnitine Palmitoyltransferase II Deficiency throughout Japan Has Revealed C12/C0 as an Index of Higher Sensitivity and Specificity. International Journal of Neonatal Screening. 2023
Takaki Asano, Takanori Utsumi, Reiko Kagawa, Shuhei Karakawa, Satoshi Okada. Inborn errors of immunity with loss- and gain-of-function germline mutations in STAT1. Clinical and Experimental Immunology. 2023. 212. 2. 96-106
Keiichi Sugihara, Miori Yuasa, Yuko Isozaki, Ikue Hata, Yusei Ohshima, Takashi Hamazaki, Toshihiko Kakiuchi, Masato Arao, Noboru Igarashi, Yumiko Kotani, et al. Severity estimation of very-long-chain acyl-CoA dehydrogenase deficiency via 13C-fatty acid loading test. Pediatric research. 2022
Miyuki Tsumura, Mizuka Miki, Yoko Mizoguchi, Osamu Hirata, Shiho Nishimura, Moe Tamaura, Reiko Kagawa, Seiichi Hayakawa, Masao Kobayashi, Satoshi Okada. Enhanced osteoclastogenesis in patients with MSMD due to impaired response to IFN-γ. The Journal of allergy and clinical immunology. 2022. 149. 1. 252-261

ｍore...

MISC (3)：

宇都宮朱里, 香川礼子, 坂田園子, 宮河真一郎, 岡田賢, 神野和彦, 原圭一. 成人身長に到達した21水酸化酵素欠損症患者における遺伝子型と臨床経過の検討. 日本マス・スクリーニング学会誌. 2019. 29. 2. 230-230
香川礼子, 岡田賢, 藤木亮次, 津村弥来, 坂田園子, 西村志帆, 加藤善一郎, 大西秀典, 小原收, 小林正夫. 網羅的アラニンスキャニングを用いたSTAT1変異データベースの確立. 日本小児科学会雑誌. 2017. 121. 2. 497-497
Shiho Nishimura, Miyuki Tsumura, Osamu Hirata, Reiko Kagawa, Yoko Mizoguchi, Satoshi Okada, Masao Kobayashi. MSMD Patients with IFN-g-STAT1 Signaling Defect Present Enhanced Osteoclastogenesis and Bone Resorption. BLOOD. 2015. 126. 23

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