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Did you mean megumi ogawa (9 results)?
Branchpoints as potential targets of exon-skipping therapies for genetic disorders.
Ohara H, Hosokawa M, Awaya T, Hagiwara A, Kurosawa R, Sako Y, Ogawa M, Ogasawara M, Noguchi S, Goto Y, Takahashi R, Nishino I, Hagiwara M. Ohara H, et al. Among authors: ogawa m. Mol Ther Nucleic Acids. 2023 Jul 17;33:404-412. doi: 10.1016/j.omtn.2023.07.011. eCollection 2023 Sep 12. Mol Ther Nucleic Acids. 2023. PMID: 37547287 Free PMC article.
Causative variant profile of collagen VI-related dystrophy in Japan.
Inoue M, Saito Y, Yonekawa T, Ogawa M, Iida A, Nishino I, Noguchi S. Inoue M, et al. Among authors: ogawa m. Orphanet J Rare Dis. 2021 Jun 24;16(1):284. doi: 10.1186/s13023-021-01921-2. Orphanet J Rare Dis. 2021. PMID: 34167565 Free PMC article.
A recurrent homozygous ACTN2 variant associated with core myopathy.
Inoue M, Noguchi S, Sonehara K, Nakamura-Shindo K, Taniguchi A, Kajikawa H, Nakamura H, Ishikawa K, Ogawa M, Hayashi S, Okada Y, Kuru S, Iida A, Nishino I. Inoue M, et al. Among authors: ogawa m. Acta Neuropathol. 2021 Oct;142(4):785-788. doi: 10.1007/s00401-021-02363-7. Epub 2021 Sep 1. Acta Neuropathol. 2021. PMID: 34471957 Free PMC article. No abstract available.
Distinctive chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB4.
Inoue M, Noguchi S, Inoue YU, Iida A, Ogawa M, Bengoechea R, Pittman SK, Hayashi S, Watanabe K, Hosoi Y, Sano T, Takao M, Oya Y, Takahashi Y, Miyajima H, Weihl CC, Inoue T, Nishino I. Inoue M, et al. Among authors: ogawa m. Acta Neuropathol. 2023 Feb;145(2):235-255. doi: 10.1007/s00401-022-02530-4. Epub 2022 Dec 13. Acta Neuropathol. 2023. PMID: 36512060
Simultaneous measurement of the size and methylation of chromosome 4qA-D4Z4 repeats in facioscapulohumeral muscular dystrophy by long-read sequencing.
Hiramuki Y, Kure Y, Saito Y, Ogawa M, Ishikawa K, Mori-Yoshimura M, Oya Y, Takahashi Y, Kim DS, Arai N, Mori C, Matsumura T, Hamano T, Nakamura K, Ikezoe K, Hayashi S, Goto Y, Noguchi S, Nishino I. Hiramuki Y, et al. Among authors: ogawa m. J Transl Med. 2022 Nov 8;20(1):517. doi: 10.1186/s12967-022-03743-7. J Transl Med. 2022. PMID: 36348371 Free PMC article.
Multidimensional analyses of the pathomechanism caused by the non-catalytic GNE variant, c.620A>T, in patients with GNE myopathy.
Yoshioka W, Iida A, Sonehara K, Yamamoto K, Oya Y, Mori-Yoshimura M, Kurashige T, Okubo M, Ogawa M, Matsuda F, Higasa K, Hayashi S, Nakamura H, Sekijima M, Okada Y, Noguchi S, Nishino I. Yoshioka W, et al. Among authors: ogawa m. Sci Rep. 2022 Dec 16;12(1):21806. doi: 10.1038/s41598-022-26419-0. Sci Rep. 2022. PMID: 36526893 Free PMC article.
Homozygous nonsense variant in LRIF1 associated with facioscapulohumeral muscular dystrophy.
Hamanaka K, Šikrová D, Mitsuhashi S, Masuda H, Sekiguchi Y, Sugiyama A, Shibuya K, Lemmers RJLF, Goossens R, Ogawa M, Nagao K, Obuse C, Noguchi S, Hayashi YK, Kuwabara S, Balog J, Nishino I, van der Maarel SM. Hamanaka K, et al. Among authors: ogawa m. Neurology. 2020 Jun 9;94(23):e2441-e2447. doi: 10.1212/WNL.0000000000009617. Epub 2020 May 28. Neurology. 2020. PMID: 32467133 Free PMC article.
A Nationwide Survey on Danon Disease in Japan.
Sugie K, Komaki H, Eura N, Shiota T, Onoue K, Tsukaguchi H, Minami N, Ogawa M, Kiriyama T, Kataoka H, Saito Y, Nonaka I, Nishino I. Sugie K, et al. Among authors: ogawa m. Int J Mol Sci. 2018 Nov 8;19(11):3507. doi: 10.3390/ijms19113507. Int J Mol Sci. 2018. PMID: 30413001 Free PMC article.
Limb-girdle muscular dystrophy type 2I is not rare in Taiwan.
Liang WC, Hayashi YK, Ogawa M, Wang CH, Huang WT, Nishino I, Jong YJ. Liang WC, et al. Among authors: ogawa m. Neuromuscul Disord. 2013 Aug;23(8):675-81. doi: 10.1016/j.nmd.2013.05.010. Epub 2013 Jun 22. Neuromuscul Disord. 2013. PMID: 23800702
29 results