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Rectification of cystic fibrosis transmembrane conductance regulator chloride channel mediated by extracellular divalent cations

机译：胞外二价阳离子介导的囊性纤维化跨膜电导调节剂氯离子通道的整流

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Zhao J.; Zerhusen B.; Xie J.; Drumm M.L.; Davis P.B.; Ma J.;
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年度 1996
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1. Interaction between 2 extracellular loops influences the activity of the cystic fibrosis transmembrane conductance regulator chloride channel [J] . BroadbentS.D., WangW., LinsdellP. Biochemistry and Cell Biology . 2014,第5期

机译：2个细胞外环之间的相互作用影响囊性纤维化跨膜电导调节剂氯离子通道的活性
2. Interaction between 2 extracellular loops influences the activity of the cystic fibrosis transmembrane conductance regulator chloride channel [J] . BroadbentS.D., WangW., LinsdellP. Biochemistry and Cell Biology . 2014,第5期

机译：2个细胞外环之间的相互作用影响囊性纤维化跨膜电导氯化物通道的活性
3. Cystic fibrosis transmembrane conductance regulator and the outwardly rectifying chloride channel: a relationship between two chloride channels expressed in epithelial cells. [J] . Hryciw DH, Guggino WB Clinical and experimental pharmacology & physiology . 2000,第11期

机译：囊性纤维化跨膜电导调节剂和向外整流的氯离子通道：在上皮细胞中表达的两个氯离子通道之间的关系。
4. Cystic fibrosis transmembrane conductance regulator gene mutations cause 'black' pigment gallstone formation: new insights from mouse models and implications for therapeutic interventions in cystic fibrosis [C] . A. L. BRODERICK, H. WITTENBURG, M. A. LYONS, Falk Symposium . 2004

机译：囊性纤维化跨膜电导调节剂基因突变引起'黑色'颜料胆结石形成：来自小鼠模型的新见解，以及对囊性纤维化治疗干预的影响
5. The cystic fibrosis transmembrane conductance regulator (CFTR) channel as a host determinant of influenza severity. [D] . Woods, Parker. 2016

机译：囊性纤维化跨膜电导调节器（CFTR）通道是流感严重程度的宿主决定因素。
6. Rectification of cystic fibrosis transmembrane conductance regulator chloride channel mediated by extracellular divalent cations. [O] . J Zhao, B Zerhusen, J Xie, 1996

机译：胞外二价阳离子介导的囊性纤维化跨膜电导调节剂氯离子通道的整流。
7. Rectification of cystic fibrosis transmembrane conductance regulator chloride channel mediated by extracellular divalent cations. [O] . Zhao, J, Zerhusen, B, Xie, J, 1996

机译：胞外二价阳离子介导的囊性纤维化跨膜电导调节剂氯离子通道的整流。

Rectification of cystic fibrosis transmembrane conductance regulator chloride channel mediated by extracellular divalent cations

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