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A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathy

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

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Tatianna Wai Ying Wong; Abdalla Ahmed; Grace Yang; Eleonora Maino; Sydney Steiman; Elzbieta Hyatt; Parry Chan; Kyle Lindsay; Nicole Wong; Diane Golebiowski; Joel Schneider; Paul Delgado-Olguín; Evgueni A. Ivakine; Ronald D. Cohn;
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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. Reprogramming of human Peripheral Blood Mononuclear Cell (PBMC) from a Chinese patient suffering Duchenne muscular dystrophy to iPSC line (SDQLCHi007-A) carrying deletion of 49–50 exons in the DMD gene [J] . Jingyun Guan, Xinnong Liu, Haiyan Zhang, Stem cell research . 2020,第2期

机译：来自中国患者的人外周血单个核细胞（PBMC）的重新编程来自DMCHENNE肌营养不良的中国患者（SDQLCHI007-A）在DMD基因中缺失49-50个外显子
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. Development of pharmacodynamic biomarkers for Duchenne muscular dystrophy using exon skipping treatment and mdx mouse model. [C] . Haeri Seol, Meng H Han, Aiping Zhang, ASMS Conference on Mass Spectrometry and Allied Topics . 2015

机译：外显子跳跃治疗和MDX小鼠模型的Duchenne肌营养不良药物动力学生物标志物的发展。
5. Modeling and Rescue of Duchenne Muscular Dystrophy Cardiomyopathy Using Human Induced Pluripotent-Derived Cardiomyocytes [D] . Kamdar, Forum Dipak Klaassen. 2021

机译：使用人诱导的多能衍生心肌细胞的Duchenne肌营养不良心肌病的建模与拯救
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. Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45–55 of the Duchenne muscular dystrophy (DMD) gene [O] . Daigo Miyazaki, Kunihiro Yoshida, Kazuhiro Fukushima, 2009

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

A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathy

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