Takizawa H - Search Results

1

Six years' accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures.

Takahashi Y, Date H, Oi H, Adachi T, Imanishi N, Kimura E, Takizawa H, Kosugi S, Matsumoto N, Kosaki K, Matsubara Y; IRUD Consortium; Mizusawa H. Takahashi Y, et al. Among authors: takizawa h. J Hum Genet. 2022 Sep;67(9):505-513. doi: 10.1038/s10038-022-01025-0. Epub 2022 Mar 23. J Hum Genet. 2022. PMID: 35318459 Free PMC article.

2

Severe cardiac involvement with preserved truncated dystrophin expression in Becker muscular dystrophy by +1G>A DMD splice-site mutation: a case report.

Komaki R, Hashimoto Y, Mori-Yoshimura M, Oya Y, Takizawa H, Minami N, Nishino I, Aoki Y, Takahashi Y. Komaki R, et al. Among authors: takizawa h. J Hum Genet. 2020 Oct;65(10):903-909. doi: 10.1038/s10038-020-0788-9. Epub 2020 Jun 5. J Hum Genet. 2020. PMID: 32504006 Free PMC article.

3

Cricopharyngeal bar on videofluoroscopy: high specificity for inclusion body myositis.

Taira K, Yamamoto T, Mori-Yoshimura M, Sajima K, Takizawa H, Shinmi J, Oya Y, Nishino I, Takahashi Y. Taira K, et al. Among authors: takizawa h. J Neurol. 2021 Mar;268(3):1016-1024. doi: 10.1007/s00415-020-10241-7. Epub 2020 Sep 26. J Neurol. 2021. PMID: 32980980

4

More prominent fibrosis of the cricopharyngeal muscle in inclusion body myositis.

Taira K, Mori-Yoshimura M, Yamamoto T, Sajima K, Takizawa H, Shinmi J, Oya Y, Nito T, Nishino I, Takahashi Y. Taira K, et al. Among authors: takizawa h. J Neurol Sci. 2021 Mar 15;422:117327. doi: 10.1016/j.jns.2021.117327. Epub 2021 Jan 23. J Neurol Sci. 2021. PMID: 33529855 No abstract available.

5

Highly sensitive screening of antisense sequences for different types of DMD mutations in patients' urine-derived cells.

Takizawa H, Takeshita E, Sato M, Shimizu-Motohashi Y, Ishiyama A, Mori-Yoshimura M, Takahashi Y, Komaki H, Aoki Y. Takizawa H, et al. J Neurol Sci. 2021 Apr 15;423:117337. doi: 10.1016/j.jns.2021.117337. Epub 2021 Feb 15. J Neurol Sci. 2021. PMID: 33610829 Free article.

6

A symptomatic male carrier of Duchenne muscular dystrophy with Klinefelter's syndrome mimicking Becker muscular dystrophy.

Takizawa H, Mori-Yoshimura M, Minami N, Murakami N, Yatabe K, Taira K, Hashimoto Y, Aoki Y, Nishino I, Takahashi Y. Takizawa H, et al. Neuromuscul Disord. 2021 Jul;31(7):666-672. doi: 10.1016/j.nmd.2021.04.006. Epub 2021 Apr 27. Neuromuscul Disord. 2021. PMID: 34172357

7

Exon Skipping Therapy Using Phosphorodiamidate Morpholino Oligomers in the mdx52 Mouse Model of Duchenne Muscular Dystrophy.

Miyatake S, Mizobe Y, Takizawa H, Hara Y, Yokota T, Takeda S, Aoki Y. Miyatake S, et al. Among authors: takizawa h. Methods Mol Biol. 2018;1687:123-141. doi: 10.1007/978-1-4939-7374-3_9. Methods Mol Biol. 2018. PMID: 29067660

8

Exon Skipping in Directly Reprogrammed Myotubes Obtained from Human Urine-Derived Cells.

Takizawa H, Sato M, Aoki Y. Takizawa H, et al. J Vis Exp. 2020 May 7;(159). doi: 10.3791/60840. J Vis Exp. 2020. PMID: 32449741

9

In Vivo Evaluation of Single-Exon and Multiexon Skipping in mdx52 Mice.

Mizobe Y, Miyatake S, Takizawa H, Hara Y, Yokota T, Nakamura A, Takeda S, Aoki Y. Mizobe Y, et al. Among authors: takizawa h. Methods Mol Biol. 2018;1828:275-292. doi: 10.1007/978-1-4939-8651-4_17. Methods Mol Biol. 2018. PMID: 30171548

10

Exon Skipping Using Antisense Oligonucleotides for Laminin-Alpha2-Deficient Muscular Dystrophy.

Hara Y, Mizobe Y, Miyatake S, Takizawa H, Nagata T, Yokota T, Takeda S, Aoki Y. Hara Y, et al. Among authors: takizawa h. Methods Mol Biol. 2018;1828:553-564. doi: 10.1007/978-1-4939-8651-4_36. Methods Mol Biol. 2018. PMID: 30171567

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

942 results

Search Page

Filters