Area of research
Cell Biology · Pulmonary and Respiratory Medicine
Research interest
Research interests include Endoplasmic reticulum, Protein folding, Biology, Cell biology, Folding (DSP implementation), and Mutant.
The Folding Pathway of ABC Transporter CFTR: Effective and Robust
ABC-transporter CFTR folds with high fidelity through a modular, stepwise pathway
Redefining Hypo- and Hyper-Responding Phenotypes of CFTR Mutants for Understanding and Therapy
Co-Translational Folding of the First Transmembrane Domain of ABC-Transporter CFTR is Supported by Assembly with the First Cytosolic Domain
The CFTR P67L variant reveals a key role for N-terminal lasso helices in channel folding, maturation, and pharmacologic rescue
<scp>The importance of naturally attenuated SARS‐CoV</scp> ‐2 <scp>in the fight against COVID</scp> ‐19
Slowing ribosome velocity restores folding and function of mutant CFTR
Folding–function relationship of the most common cystic fibrosis–causing CFTR conductance mutants
Characterization of CNPY5 and its family members
CHAPTER 1.1. Disulfide Bonds in Protein Folding and Stability
Alteration of protein function by a silent polymorphism linked to tRNA abundance
Correcting CFTR folding defects by small-molecule correctors to cure cystic fibrosis
Structure and topology around the cleavage site regulate post-translational cleavage of the HIV-1 gp160 signal peptide
Co‐ and Post‐Translational Protein Folding in the <scp>ER</scp>
Protein quality control at the endoplasmic reticulum
TORC2 mediates the heat stress response in <i>Drosophila</i> by promoting the formation of stress granules
Deletion of the Highly Conserved N-Glycan at Asn260 of HIV-1 gp120 Affects Folding and Lysosomal Degradation of gp120, and Results in Loss of Viral Infectivity
Two phases of disulfide bond formation have differing requirements for oxygen
ERdj5 Is the ER Reductase that Catalyzes the Removal of Non-Native Disulfides and Correct Folding of the LDL Receptor
Quantifying Changes in the Cellular Thiol-Disulfide Status during Differentiation of B Cells into Antibody-Secreting Plasma Cells
Peroxisome Formation and Maintenance Are Dependent on the Endoplasmic Reticulum
Ero1–PDI interactions, the response to redox flux and the implications for disulfide bond formation in the mammalian endoplasmic reticulum
Biochemically Distinct Vesicles from the Endoplasmic Reticulum Fuse to Form Peroxisomes