Suchergebnisse - "Wang, Yiting"

PubPharm (10)

1

A small molecule CFTR potentiator restores ATP-dependent channel gating to the cystic fibrosis mutant G551D-CFTR

enthalten in: British journal of pharmacology | 2022

von Liu, J. | Berg, A. | Wang, Y. | +6

2

CFTR bearing variant p.Phe312del exhibits function inconsistent with phenotype and negligible response to ivacaftor

enthalten in: JCI insight | 2022

von Raraigh, K. | Paul, K. | Goralski, J. | +18

3

Extracellular phosphate enhances the function of F508del-CFTR rescued by CFTR correctors

enthalten in: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society | 2021

von Saint-Criq, V. | Wang, Y. | Delpiano, L. | +3

4

A topological switch in CFTR modulates channel activity and sensitivity to unfolding

enthalten in: Nature chemical biology | 2021

von Scholl, D. | Sigoillot, M. | Overtus, M. | +10

5

Differential thermostability and response to cystic fibrosis transmembrane conductance regulator potentiators of human and mouse F508del-CFTR

enthalten in: American journal of physiology. Lung cellular and molecular physiology | 2019

von Bose, S. | Bijvelds, M. | Wang, Y. | +5

6

Potentiation of the cystic fibrosis transmembrane conductance regulator Cl- channel by ivacaftor is temperature independent

enthalten in: American journal of physiology. Lung cellular and molecular physiology | 2018

von Wang, Y. | Cai, Z. | Gosling, M. | +1

7

Partial rescue of F508del-cystic fibrosis transmembrane conductance regulator channel gating with modest improvement of protein processing, but not stability, by a dual-acting small molecule

enthalten in: British journal of pharmacology | 2018

von Liu, J. | Bihler, H. | Farinha, C. | +11

8

Two Small Molecules Restore Stability to a Subpopulation of the Cystic Fibrosis Transmembrane Conductance Regulator with the Predominant Disease-causing Mutation

enthalten in: The Journal of biological chemistry | 2017

von Meng, X. | Wang, Y. | Wang, X. | +6

9

CFTR potentiators partially restore channel function to A561E-CFTR, a cystic fibrosis mutant with a similar mechanism of dysfunction as F508del-CFTR

enthalten in: British journal of pharmacology | 2014

von Wang, Y. | Liu, J. | Loizidou, A. | +7

10

Understanding how cystic fibrosis mutations disrupt CFTR function : from single molecules to animal models

enthalten in: The international journal of biochemistry & cell biology | 2014

von Wang, Y. | Wrennall, J. | Cai, Z. | +2

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