Cystic fibrosis transmembrane conductance regulator: The purified NBF1 plus R protein interacts with the purified NBF2 domain to form a stable NBF1 plus R/NBF2 complex while inducing a conformational change transmitted to the C-terminal region (vol 3

Lu NT.; Pedersen PL.

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Cystic fibrosis transmembrane conductance regulator: The purified NBF1 plus R protein interacts with the purified NBF2 domain to form a stable NBF1 plus R/NBF2 complex while inducing a conformational change transmitted to the C-terminal region (vol 3

机译：囊性纤维化跨膜电导调节剂：纯化的NBF1加R蛋白与纯化的NBF2结构域相互作用，形成稳定的NBF1加R / NBF2复合物，同时诱导构象变化传递至C端区域（第3卷）

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《Archives of Biochemistry and Biophysics》 |2000年第1期|共1页
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Lu NT.; Pedersen PL.;
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1. Cystic fibrosis transmembrane conductance regulator: The purified NBF1 plus R protein interacts with the purified NBF2 domain to form a stable NBF1 plus R/NBF2 complex while inducing a conformational change transmitted to the C-terminal region (vol 3 [J] . Lu NT., Pedersen PL. Archives of Biochemistry and Biophysics . 2000,第1期

机译：囊性纤维化跨膜电导调节剂：纯化的NBF1加R蛋白与纯化的NBF2结构域相互作用，形成稳定的NBF1加R / NBF2复合物，同时诱导构象变化传递至C端区域（第3卷）
2. Cystic fibrosis transmembrane conductance regulator: The purified NBF1+R protein interacts with the purified NBF2 domain to form a stable NBF1+R/NBF2 complex while inducing a conformational change transmitted to the C-terminal region [J] . Lu NT., Pedersen PL. Archives of Biochemistry and Biophysics . 2000,第1期

机译：囊性纤维化跨膜电导调节剂：纯化的NBF1 + R蛋白与纯化的NBF2结构域相互作用，形成稳定的NBF1 + R / NBF2复合物，同时诱导构象变化传递至C端区域
3. Ystic fibrosis transmembrane conductance regulator: the purified NBF1+R protein interacts with the purified NBF2 domain to form a stable NBF1+R/NBF2 complex while inducing a conformational change transmitted to the c-terminal region~1 [J] . Natalie T. Lu, Peter L. Pedersen Archives of Biochemistry and Biophysics . 2000,第1期

机译：Ystic纤维化跨膜电导调节剂：纯化的NBF1 + R蛋白与纯化的NBF2结构域相互作用形成稳定的NBF1 + R / NBF2复合物，同时诱导构象变化传递至c端区域〜1
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. Molecular assembly of cystic fibrosis transmembrane conductance regulator and its interacting proteins. [D] . Li, Chunying. 2005

机译：囊性纤维化跨膜电导调节剂及其相互作用蛋白的分子组装。
6. Deletion of Phenylalanine 508 in the First Nucleotide-binding Domain of the Cystic Fibrosis Transmembrane Conductance Regulator Increases Conformational Exchange and Inhibits Dimerization [O] . P. Andrew Chong, Patrick J. Farber, Robert M. Vernon, 2015

机译：囊性纤维化跨膜电导调节剂的第一个核苷酸结合域中苯丙氨酸508的删除增加构象交换和抑制二聚。
7. Phosphorylation-induced conformational changes of cystic fibrosis transmembrane conductance regulator monitored by attenuated total reflection-Fourier transform IR spectroscopy and fluorescence spectroscopy. [O] . Grimard, Vinciane, Li, Canhui, Ramjeesingh, Mohabir, 2004

机译：衰减全反射-傅里叶变换红外光谱和荧光光谱监测的磷酸化诱导的囊性纤维化跨膜电导调节剂的构象变化。

Cystic fibrosis transmembrane conductance regulator: The purified NBF1 plus R protein interacts with the purified NBF2 domain to form a stable NBF1 plus R/NBF2 complex while inducing a conformational change transmitted to the C-terminal region (vol 3

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