Positional effects of premature termination codons on the biochemical and biophysical properties of CFTR

od Yeh, Jiunn-Tyng, Hwang, Tzyh-Chang
Izdano u J Physiol (2019)

Modulation of CFTR gating by permeant ions

od Yeh, Han-I, Yeh, Jiunn-Tyng, Hwang, Tzyh-Chang
Izdano u J Gen Physiol (2015)

Structural mechanisms for defective CFTR gating caused by the Q1412X mutation, a severe Class VI pathogenic mutation in cystic fibrosis

od Yeh, Jiunn‐Tyng, Yu, Ying‐Chun, Hwang, Tzyh‐Chang
Izdano u J Physiol (2018)

Functional characterization reveals that zebrafish CFTR prefers to occupy closed channel conformations

od Zhang, Jingyao, Yu, Ying-Chun, Yeh, Jiunn-Tyng, Hwang, Tzyh-Chang
Izdano u PLoS One (2018)

Structural mechanisms of CFTR function and dysfunction

od Hwang, Tzyh-Chang, Yeh, Jiunn-Tyng, Zhang, Jingyao, Yu, Ying-Chun, Yeh, Han-I, Destefano, Samantha
Izdano u J Gen Physiol (2018)

Organoids as a Personalized Medicine Tool for Ultra-Rare Mutations in Cystic Fibrosis: the Case of S955P and 1717–2A>G

od Silva, Iris AL, Doušová, Tereza, Ramalho, Sofia, Centeio, Raquel, Clarke, Luka A, Railean, Violeta, Botelho, Hugo M, Holubová, Andrea, Valášková, Iveta, Yeh, Jiunn-Tyng, Hwang, Tzyh-Chang, Farinha, Carlos M., Kunzelmann, Karl, Amaral, Margarida D
Izdano u Biochim Biophys Acta Mol Basis Dis (2020)