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pro vyhledávání: '"Ayca Ersoy"'
Autor:
Ayca Ersoy, Bengi Altintel, Nurit Livnat Levanon, Nir Ben-Tal, Turkan Haliloglu, Oded Lewinson
Publikováno v:
eLife, Vol 12 (2023)
Malfunction of the CFTR protein results in cystic fibrosis, one of the most common hereditary diseases. CFTR functions as an anion channel, the gating of which is controlled by long-range allosteric communications. Allostery also has direct bearings
Externí odkaz:
https://doaj.org/article/28139476f459474b852567b971d3381c
