Results 1 to 6 of 6
Page 1 of 1
TypeTitleAuthor(s)YearViews
Citrin/mitochondrial glycerol-3-phosphate dehydrogenase double knock-out mice recapitulate features of human citrin deficiencySaheki, 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, T2007219
 
Pyruvate ameliorates the defect in ureogenesis from ammonia in citrin-deficient miceMoriyama, M; Li, MX; Kobayashi, K; Sinasac, DS; Kannan, Y; Iijima, M; Horiuchi, M; Tsui, LC; Tanaka, M; Nakamura, Y; Saheki, T2006138
 
Slc25a13-Knockout Mice Harbor Metabolic Deficits but Fail to Display Hallmarks of Adult-Onset Type II CitrullinemiaSinasac, DS; Moriyama, M; Jalil, MA; Begum, L; Li, MX; Iijima, M; Horiuchi, M; Robinson, BH; Kobayashi, K; Saheki, T; Tsui, LC20041,329
 
Genomic structure of the adult-onset type II citrullinemia gene, SLC25A13, and cloning and expression of its mouse homologueSinasac, DS; Crackower, MA; Lee, JR; Kobayashi, K; Saheki, T; Scherer, SW; Tsui, LC1999287
 
Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24Crackower, MA; Sinasac, DS; Lee, JR; Herbrick, JA; Tsui, LC; Scherer, SW1999121
 
The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier proteinKobayashi, 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, T1999298
 
Page 1 of 1
Export Records
Step 1: Select content and export format
  • Citation only
Step 2: Select export method
  • Download