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TDP-43 regulates cholesterol biosynthesis by inhibiting sterol regulatory element-binding protein 2.
Egawa N, Izumi Y, Suzuki H, Tsuge I, Fujita K, Shimano H, Izumikawa K, Takahashi N, Tsukita K, Enami T, Nakamura M, Watanabe A, Naitoh M, Suzuki S, Seki T, Kobayashi K, Toda T, Kaji R, Takahashi R, Inoue H. Egawa N, et al. Among authors: kobayashi k. Sci Rep. 2022 May 14;12(1):7988. doi: 10.1038/s41598-022-12133-4. Sci Rep. 2022. PMID: 35568729 Free PMC article.
Absence of post-phosphoryl modification in dystroglycanopathy mouse models and wild-type tissues expressing non-laminin binding form of α-dystroglycan.
Kuga A, Kanagawa M, Sudo A, Chan YM, Tajiri M, Manya H, Kikkawa Y, Nomizu M, Kobayashi K, Endo T, Lu QL, Wada Y, Toda T. Kuga A, et al. Among authors: kobayashi k. J Biol Chem. 2012 Mar 16;287(12):9560-7. doi: 10.1074/jbc.M111.271767. Epub 2012 Jan 23. J Biol Chem. 2012. PMID: 22270369 Free PMC article.
[Molecular targeting therapy for Fukuyama muscular dystrophy].
Toda T, Taniguchi-Ikeda M, Kobayashi K. Toda T, et al. Among authors: kobayashi k. Rinsho Shinkeigaku. 2012;52(11):1158. doi: 10.5692/clinicalneurol.52.1158. Rinsho Shinkeigaku. 2012. PMID: 23196548 Japanese. No abstract available.
Modeling Alzheimer's disease with iPSCs reveals stress phenotypes associated with intracellular Aβ and differential drug responsiveness.
Kondo T, Asai M, Tsukita K, Kutoku Y, Ohsawa Y, Sunada Y, Imamura K, Egawa N, Yahata N, Okita K, Takahashi K, Asaka I, Aoi T, Watanabe A, Watanabe K, Kadoya C, Nakano R, Watanabe D, Maruyama K, Hori O, Hibino S, Choshi T, Nakahata T, Hioki H, Kaneko T, Naitoh M, Yoshikawa K, Yamawaki S, Suzuki S, Hata R, Ueno S, Seki T, Kobayashi K, Toda T, Murakami K, Irie K, Klein WL, Mori H, Asada T, Takahashi R, Iwata N, Yamanaka S, Inoue H. Kondo T, et al. Among authors: kobayashi k. Cell Stem Cell. 2013 Apr 4;12(4):487-96. doi: 10.1016/j.stem.2013.01.009. Epub 2013 Feb 21. Cell Stem Cell. 2013. PMID: 23434393 Free article.
Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration of its severe phenotype by limited gene expression.
Kanagawa M, Yu CC, Ito C, Fukada S, Hozoji-Inada M, Chiyo T, Kuga A, Matsuo M, Sato K, Yamaguchi M, Ito T, Ohtsuka Y, Katanosaka Y, Miyagoe-Suzuki Y, Naruse K, Kobayashi K, Okada T, Takeda S, Toda T. Kanagawa M, et al. Among authors: kobayashi k. Hum Mol Genet. 2013 Aug 1;22(15):3003-15. doi: 10.1093/hmg/ddt157. Epub 2013 Apr 4. Hum Mol Genet. 2013. PMID: 23562821
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