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Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45–55 of the Duchenne muscular dystrophy (DMD) gene

机译：患有Dystophinophaty患者缺失的缺失的缺失断裂点缺失（DMD）基因的外显子病45-55缺失

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Daigo Miyazaki; Kunihiro Yoshida; Kazuhiro Fukushima; Akinori Nakamura; Kayo Suzuki; Toshiyuki Sato; Shinichi Takeda; Shu-ichi Ikeda;
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1. Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45-55 of the Duchenne muscular dystrophy (DMD) gene. [J] . Miyazaki D, Yoshida K, Fukushima K, Journal of human genetics . 2009,第2期

机译：患有肌营养不良症患者携带杜兴氏肌营养不良症（DMD）基因外显子45-55缺失的缺失断点的特征。
2. Follow-up of three patients with a large in-frame deletion of exons 45-55 in the Duchenne muscular dystrophy (DMD) gene. [J] . Nakamura A, Yoshida K, Fukushima K, Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia . 2008,第7期

机译：对三例杜兴氏肌营养不良症（DMD）基因中外显子45-55大框内缺失的患者的随访。
3. Dystrophin-deficient cardiomyocyte derived from Duchenne Muscular Dystrophy specific induced pluripotent stem cells carrying the deletion of exon 46-55 in DMD gene [J] . D. Miyazaki, M. Sato, Y. Shiba, Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology . 2017,第期

机译：衍生自Dychenne肌营养不良特异性诱导多能干多能干多能干细胞的缺乏缺乏的心肌细胞，其在DMD基因中缺失外显子46-55
4. Identification of a gene expression core signature for Duchenne muscular dystrophy (DMD) via integrative analysis reveals novel potential compounds for treatment [C] . Ichim-Moreno Noru, Aranda Manuel, Voolstra Christian R. 2010 IEEE Symposium on Computational Intelligence in Bioinformatics and Computational Biology . 2010

机译：通过综合分析鉴定杜兴氏肌营养不良症（DMD）的基因表达核心标志揭示了治疗新的潜在化合物
5. Improving stem cell-based therapy and developing a novel gene therapy approach for treating Duchenne Muscular Dystrophy (DMD). [D] . Tabebordbar, Mohammadsharif. 2016

机译：改进基于干细胞的疗法，并开发一种新型的基因疗法来治疗杜兴氏肌营养不良症（DMD）。
6. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps meiotic and mitotic origin of the mutations. [O] . B T Darras, P Blattner, J F Harper, 1988

机译：用抗肌萎缩蛋白cDNA研究了21个杜兴氏肌营养不良症（DMD）/贝克尔肌营养不良症（BMD）家族的基因内缺失：HindIII和BglII外显子片段图谱上的断点位置突变的减数分裂和有丝分裂起源。
7. A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathy [O] . Tatianna Wai Ying Wong, Abdalla Ahmed, Grace Yang, 2020

机译：携带多封面DMD缺失的Duchenne肌营养不良小鼠模型表现出逐步肌营养不良和早期发作的心肌病

Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45–55 of the Duchenne muscular dystrophy (DMD) gene

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