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Cloning of cDNA encoding a regeneration-associated muscle protease whose expression is attenuated in cell lines derived from Duchenne muscular dystrophy patients.
Nakayama Y, Nara N, Kawakita Y, Takeshima Y, Arakawa M, Katoh M, Morita S, Iwatsuki K, Tanaka K, Okamoto S, Kitamura T, Seki N, Matsuda R, Matsuo M, Saito K, Hara T. Nakayama Y, et al. Among authors: saito k. Am J Pathol. 2004 May;164(5):1773-82. doi: 10.1016/S0002-9440(10)63735-2. Am J Pathol. 2004. PMID: 15111323 Free PMC article.
[Muscular dystrophy].
Kondo E, Saito K, Osawa M. Kondo E, et al. Among authors: saito k. Nihon Rinsho. 2005 Mar;63(3):420-8. Nihon Rinsho. 2005. PMID: 15773340 Review. Japanese.
Human first-trimester chorionic villi have a myogenic potential.
Arakawa R, Aoki R, Arakawa M, Saito K. Arakawa R, et al. Among authors: saito k. Cell Tissue Res. 2012 Apr;348(1):189-97. doi: 10.1007/s00441-012-1340-9. Epub 2012 Feb 28. Cell Tissue Res. 2012. PMID: 22370594 Free PMC article.
Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patients.
Yamamoto T, Sato H, Lai PS, Nurputra DK, Harahap NI, Morikawa S, Nishimura N, Kurashige T, Ohshita T, Nakajima H, Yamada H, Nishida Y, Toda S, Takanashi J, Takeuchi A, Tohyama Y, Kubo Y, Saito K, Takeshima Y, Matsuo M, Nishio H. Yamamoto T, et al. Among authors: saito k. Brain Dev. 2014 Nov;36(10):914-20. doi: 10.1016/j.braindev.2013.11.009. Epub 2013 Dec 17. Brain Dev. 2014. PMID: 24359787
Intron-retained transcripts of the spinal muscular atrophy genes, SMN1 and SMN2.
Harahap NIF, Niba ETE, Ar Rochmah M, Wijaya YOS, Saito T, Saito K, Awano H, Morioka I, Iijima K, Lai PS, Matsuo M, Nishio H, Shinohara M. Harahap NIF, et al. Among authors: saito k, saito t. Brain Dev. 2018 Sep;40(8):670-677. doi: 10.1016/j.braindev.2018.03.001. Epub 2018 Mar 23. Brain Dev. 2018. PMID: 29580671
9,159 results