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首页> 外文期刊>Physiological Research >The pore architecture of the cystic fibrosis transmembrane conductance regulator channel revealed by co-mutation in pore-forming transmembrane regions.
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The pore architecture of the cystic fibrosis transmembrane conductance regulator channel revealed by co-mutation in pore-forming transmembrane regions.

机译:囊性纤维化跨膜电导调节通道的孔结构通过在成孔跨膜区域的共突变揭示。

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摘要

The cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel contains 12 transmembrane (TM) regions that are presumed to form the channel pore. However, there is no direct evidence clearly illustrating the involvement of these transmemb
机译:囊性纤维化跨膜电导调节剂(CFTR)氯化物通道包含12个跨膜(TM)区域,这些区域被认为会形成通道孔。但是,没有直接证据清楚地表明这些跨膜细胞的参与

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