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COMBINATION TREATMENT OF SARCOGLYCANOPATHIES

机译:疯狂的组合治疗

摘要

Sarcoglycanopathies are autosomal recessive diseases caused by mutations in the one of the genes coding for any sarcoglycans (SG). The inventors previously showed that the application of small molecules developed to rescue ΔF508-CFTR trafficking, and known as CFTR correctors, improved the maturation of several α-sarcoglycan mutants that were consequently rescued at the plasma membrane (WO 014086687). Now, the inventors show that some specific CFTR correctors provide additive and even synergic effect when administered in combination.
机译:Sarcoglycanopathies是由编码任何Sarcoglycan(SG)的基因之一的突变引起的常染色剂隐性疾病。发明人之前表明,开发的小分子应用于拯救ΔF508-CFTR运输,并且称为CFTR校正,改善了几种α-生气蛋白突变体的成熟,这些突变体在质膜(WO 014086687)中拯救。现在,发明人表明,一些特定的CFTR校正在组合施用时提供添加剂甚至协同效果。

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