Ying Wang

发表

Single Channel Properties of Heterotetrameric Mutant RyR1 Ion Channels Linked to Core Myopathies*

G. Meissner, Le Xu, N. Yamaguchi, 2008, Journal of Biological Chemistry.

Characterization of recessive RYR1 mutations in core myopathies.

E. Bertini, F. Muntoni, Haiyan Zhou, 2006, Human molecular genetics.

Channel Gating Dependence on Pore Lining Helix Glycine Residues in Skeletal Muscle Ryanodine Receptor*

N. Dokholyan, D. Mowrey, G. Meissner, 2015, The Journal of Biological Chemistry.

Triadins Modulate Intracellular Ca2+ Homeostasis but Are Not Essential for Excitation-Contraction Coupling in Skeletal Muscle*

A. Caswell, J. Potter, Xiaohua Shen, 2007, Journal of Biological Chemistry.

Knocking Down Type 2 but Not Type 1 Calsequestrin Reduces Calcium Sequestration and Release in C2C12 Skeletal Muscle Myotubes*

J. Eu, G. Meissner, Le Xu, 2006, Journal of Biological Chemistry.

The chemical chaperone CFcor-325 repairs folding defects in the transmembrane domains of CFTR-processing mutants.

D. Clarke, T. W. Loo, M. Bartlett, 2006, The Biochemical journal.

Mild processing defect of porcine DeltaF508-CFTR suggests that DeltaF508 pigs may not develop cystic fibrosis disease.

T. Ma, Hong Yang, Xuechao Feng, 2008, Biochemical and Biophysical Research Communications - BBRC.

Two central core disease (CCD) deletions in the C‐terminal region of RYR1 alter muscle excitation–contraction (EC) coupling by distinct mechanisms

S. Ducreux, A. Ferreiro, S. Treves, 2007, Human mutation.

Cloning and characterization of porcine aquaporin 1 water channel expressed extensively in gastrointestinal system.

T. Ma, Hong Yang, Bao-xue Yang, 2006, World journal of gastroenterology.

Critical protein domains and amino acid residues for gating the KIR6.2 channel by intracellular ATP

Jianping Wu, Yunbo Shi, Fuxue Chen, 2004, Journal of cellular physiology.

Allosteric modulation of the mouse kir6.2 channel by intracellular H+ and ATP

Jianping Wu, N. Cui, Chun Jiang, 2002, The Journal of physiology.

G4941K substitution in the pore-lining S6 helix of the skeletal muscle ryanodine receptor increases RyR1 sensitivity to cytosolic and luminal Ca2+

N. Dokholyan, D. Mowrey, G. Meissner, 2017, The Journal of Biological Chemistry.

Two rings of negative charges in the cytosolic vestibule of type-1 ryanodine receptor modulate ion fluxes.

Dirk Gillespie, Ying Wang, Le Xu, 2006, Biophysical journal.

Additive effect of multiple pharmacological chaperones on maturation of CFTR processing mutants.

D. Clarke, M. Bartlett, Ying Wang, 2007, The Biochemical journal.

Correctors Promote Maturation of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)-processing Mutants by Binding to the Protein*

Ying Wang, D. Clarke, Tip W Loo, 2007, Journal of Biological Chemistry.

Modulating the Folding of P-Glycoprotein and Cystic Fibrosis Transmembrane Conductance Regulator Truncation Mutants with Pharmacological Chaperones

D. Clarke, M. Bartlett, Ying Wang, 2007, Molecular Pharmacology.

(De)constructing the ryanodine receptor: modeling ion permeation and selectivity of the calcium release channel.

Dirk Gillespie, Ying Wang, Le Xu, 2005, The journal of physical chemistry. B.

Specific Rescue of Cystic Fibrosis Transmembrane Conductance Regulator Processing Mutants Using Pharmacological Chaperones

Ying Wang, D. Clarke, Tip W Loo, 2006, Molecular Pharmacology.

Altered stored calcium release in skeletal myotubes deficient of triadin and junctin.

J. Eu, G. Meissner, Ying Wang, 2009, Cell calcium.

Mild processing defect of porcine DeltaF508-CFTR suggests that DeltaF508 pigs may not develop cystic fibrosis disease.

T. Ma, Hong Yang, Xuechao Feng, 2008, Biochemical and Biophysical Research Communications - BBRC.

Silencing genes of sarcoplasmic reticulum proteins clarifies their roles in excitation–contraction coupling

J. Eu, G. Meissner, Le Xu, 2009, Journal of Physiology.