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Modelling urea-cycle disorder citrullinemia type 1 with disease-specific iPSCs.
Yoshitoshi-Uebayashi EY, Toyoda T, Yasuda K, Kotaka M, Nomoto K, Okita K, Yasuchika K, Okamoto S, Takubo N, Nishikubo T, Soga T, Uemoto S, Osafune K. Yoshitoshi-Uebayashi EY, et al. Among authors: nishikubo t. Biochem Biophys Res Commun. 2017 May 6;486(3):613-619. doi: 10.1016/j.bbrc.2017.03.037. Epub 2017 Mar 14. Biochem Biophys Res Commun. 2017. PMID: 28302489
Corrigendum to "Modelling urea-cycle disorder citrullinemia type 1 with disease-specific iPSCs" [Biochem. Biophys. Res. Commun. 486(3) (2017) 613-619].
Yoshitoshi-Uebayashi EY, Toyoda T, Yasuda K, Kotaka M, Nomoto K, Okita K, Yasuchika K, Okamoto S, Takubo N, Nishikubo T, Soga T, Uemoto S, Osafune K. Yoshitoshi-Uebayashi EY, et al. Among authors: nishikubo t. Biochem Biophys Res Commun. 2017 Jul 1;488(3):570-571. doi: 10.1016/j.bbrc.2017.05.055. Epub 2017 May 18. Biochem Biophys Res Commun. 2017. PMID: 28528898 No abstract available.
Investigation of type IIC von Willebrand disease.
Uno H, Nishida N, Ishizaki J, Suzuki M, Nishikubo T, Miyata S, Takahashi Y, Yoshioka A, Tsuda K. Uno H, et al. Among authors: nishikubo t. Int J Hematol. 1994 Apr;59(3):219-25. Int J Hematol. 1994. PMID: 8011991
Neonatal erythema infectiosum.
Minowa H, Nishikubo T, Uchida Y, Nogami K, Yamashita C, Kamitsuji H, Takahashi Y, Yoshioka A. Minowa H, et al. Among authors: nishikubo t. Acta Paediatr Jpn. 1998 Feb;40(1):88-90. doi: 10.1111/j.1442-200x.1998.tb01411.x. Acta Paediatr Jpn. 1998. PMID: 9583210
Mutation spectrum of the PCCA and PCCB genes in Japanese patients with propionic acidemia.
Yang X, Sakamoto O, Matsubara Y, Kure S, Suzuki Y, Aoki Y, Yamaguchi S, Takahashi Y, Nishikubo T, Kawaguchi C, Yoshioka A, Kimura T, Hayasaka K, Kohno Y, Iinuma K, Ohura T. Yang X, et al. Among authors: nishikubo t. Mol Genet Metab. 2004 Apr;81(4):335-42. doi: 10.1016/j.ymgme.2004.01.003. Mol Genet Metab. 2004. PMID: 15059621
73 results