| Title | Author(s) | Year | View Count |  | Citrin/mitochondrial glycerol-3-phosphate dehydrogenase double knock-out mice recapitulate features of human citrin deficiency | Saheki, T; Iijima, M; Meng, XL; Kobayashi, K; Horiuchi, M; Ushikai, M; Okumura, F; Xiao, JM; Inoue, I; Tajima, A; Moriyama, M; Eto, K; Kadowaki, T; Sinasac, DS; Tsui, LC; Tsuji, M; Okano, A; Kobayashi, T | 2007 | 210 |
| Pyruvate ameliorates the defect in ureogenesis from ammonia in citrin-deficient mice | Moriyama, M; Li, MX; Kobayashi, K; Sinasac, DS; Kannan, Y; Iijima, M; Horiuchi, M; Tsui, LC; Tanaka, M; Nakamura, Y; Saheki, T | 2006 | 109 |
 | Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency | Lu, YB; Kobayashi, K; Ushikai, M; Tabata, A; Iijima, M; Li, MX; Lei, L; Kawabe, K; Taura, S; Yang, Y; Liu, TT; Chiang, SH; Hsiao, KJ; Lau, YL; Tsui, LC; Lee, DH; Saheki, T | 2005 | 798 |
| Slc25a13-Knockout Mice Harbor Metabolic Deficits but Fail to Display Hallmarks of Adult-Onset Type II Citrullinemia | Sinasac, DS; Moriyama, M; Jalil, MA; Begum, L; Li, MX; Iijima, M; Horiuchi, M; Robinson, BH; Kobayashi, K; Saheki, T; Tsui, LC | 2004 | 1,350 |
| The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein | Kobayashi, K; Sinasac, DS; Iijima, M; Boright, AP; Begum, L; Lee, JR; Yasuda, T; Ikeda, S; Hirano, R; Terazono, H; Crackower, MA; Kondo, I; Tsui, LC; Scherer, SW; Saheki, T | 1999 | 304 |
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