Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne muscular dystrophy (DMD) gene mutation analysis

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Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne muscular dystrophy (DMD) gene mutation analysis

机译：多重连接依赖性探针扩增（MLPA）在杜氏肌营养不良症（DMD）基因突变分析中的应用

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《The Indian journal of medical research》 |2010年第2010期|共页
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1. Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne muscular dystrophy (DMD) gene mutation analysis [J] . Sakthivel Murugan S.M., Arthi Chandramohan, Bremadesam Raman Lakshmi The Indian journal of medical research. . 2010,第3期

机译：多重连接依赖性探针扩增（MLPA）在杜氏肌营养不良症（DMD）基因突变分析中的应用
2. Molecular analysis of the dystrophin gene in 407 Chinese patients with Duchenne/Becker muscular dystrophy by the combination of multiplex ligation-dependent probe amplification and Sanger sequencing [J] . ChenW.-J., LinQ.-F., ZhangQ.-J., Clinica chimica acta: International journal of clinical chemistry and applied molecular biology . 2013,第Null期

机译：多重连接依赖探针扩增和Sanger测序相结合对407例中国杜兴氏/贝克尔肌营养不良患者肌营养不良蛋白基因的分子分析
3. Identification of deletions and duplications in the Duchenne muscular dystrophy gene and female carrier status in western India using combined methods of multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification. [J] . Dastur RS, Kachwala MY, Khadilkar SV, Neurology India. . 2011,第6期

机译：使用多重聚合酶链反应和多重连接依赖探针扩增的组合方法，鉴定印度西部杜兴氏肌营养不良基因的缺失和重复以及女性携带者的状况。
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. AB032. Mutation spectrum in the dystrophin gene disclosed by multiplex ligation-dependent probe amplification in 181 Vietnamese Duchenne/Becker muscular dystrophy patients [O] . Van Khanh Tran, Ngoc Hai Do, Thinh Huy Tran, 2015

机译：AB032。多重结扎依赖性探针扩增揭示的肌营养不良蛋白基因的突变谱在181名越南Duchenne / Becker肌营养不良患者中
7. Cryptic intragenic deletion of the SHOX gene in a family with Léri-Weill dyschondrosteosis detected by Multiplex Ligation-Dependent Probe Amplification (MLPA) Deleção críptica intragênica do gene SHOX em uma família com discondrosteose de Léri-Weill detectada por Multiplex Ligation-Dependent Probe Amplification (MLPA) [O] . Mariana F. A. Funari, Alexander A. L. Jorge, Emilia M. Pinto, 2008

机译：通过多重连接依赖探针扩增（MLPA）检测到的莱里-威尔氏软骨异常的家庭中的SHOX基因的隐性基因内删除（MLPA） MLPA）

Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne muscular dystrophy (DMD) gene mutation analysis

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