書誌事項
- タイトル別名
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- Myotonic Dystrophy: Advances in Translational Research
- 筋強直性ジストロフィー研究の進歩 : 治療の可能性
- キン ゴウチョクセイ ジストロフィー ケンキュウ ノ シンポ : チリョウ ノ カノウセイ
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説明
Myotonic dystrophy (DM) is the most common form of muscular dystrophy in adults, which is caused by unstable genomic expansions of CTG or CCTG repeats. Mutant RNA transcripts containing the expanded repeats cause toxic gain-of-function by perturbing splicing factors in the nucleus, resulting in misregulation of alternative pre-mRNA splicing. Recent advances in basic and translational research and pharmacological approaches have provided clues for therapeutic intervention in DM. Herein, we review the RNA-dominant mechanism of DM and therapeutic approaches for targeting the toxic RNA.
収録刊行物
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- BRAIN and NERVE
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BRAIN and NERVE 69 (1), 61-69, 2017-01-01
株式会社医学書院
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詳細情報 詳細情報について
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- CRID
- 1390846634924497920
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- NII論文ID
- 40021086879
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- NII書誌ID
- AN00144970
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- ISSN
- 13448129
- 18816096
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- NDL書誌ID
- 027959050
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- PubMed
- 28126979
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- 資料種別
- journal article
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- データソース種別
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- JaLC
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