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Cell Growth and Development

Maturation and Function of Cystic Fibrosis Transmembrane Conductance Regulator Variants Bearing Mutations in Putative Nucleotide-Binding Domains 1 and 2

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Pages 3886-3893 | Received 20 Mar 1991, Accepted 08 May 1991, Published online: 01 Apr 2023

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Xue Wang, Yao-Fang Zhang, Bo Yu, Shuang Yang, Jian Luan, Xin Liu & Hong Yang. (2013) Dehydrocostuslactone, a sesquiterpene lactone activates wild-type and ΔF508 mutant CFTR chloride channel. Journal of Asian Natural Products Research 15:8, pages 855-866.
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Isabel Carvalho-Oliveira, Bob J Scholte & Deborah Penque. (2007) What have we learned from mouse models for cystic fibrosis?. Expert Review of Molecular Diagnostics 7:4, pages 407-417.
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Articles from other publishers (3)

Xiaolong Gao & Tzyh-Chang Hwang. (2015) Localizing a gate in CFTR. Proceedings of the National Academy of Sciences 112:8, pages 2461-2466.
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Wei Wang, Jianping Wu, Karen Bernard, Ge Li, Guangyu Wang, Mark O. Bevensee & Kevin L. Kirk. (2010) ATP-independent CFTR channel gating and allosteric modulation by phosphorylation. Proceedings of the National Academy of Sciences 107:8, pages 3888-3893.
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Lynda S. Ostedgaard, Christopher S. Rogers, Qian DongChristoph O. Randak, Daniel W. Vermeer, Tatiana Rokhlina, Philip H. Karp & Michael J. Welsh. (2007) Processing and function of CFTR-ΔF508 are species-dependent. Proceedings of the National Academy of Sciences 104:39, pages 15370-15375.
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