T. Evans

发表

Lung phenotype of juvenile and adult cystic fibrosis transmembrane conductance regulator-knockout ferrets.

J. T. Fisher, D. Meyerholz, Z. A. Stewart, 2014, American journal of respiratory cell and molecular biology.

A glycopolymer improves vascoelasticity and mucociliary transport of abnormal cystic fibrosis mucus.

Gareth W. Hughes, K. Chu, G. Tearney, 2019, JCI insight.

In utero and postnatal VX-770 administration rescues multiorgan disease in a ferret model of cystic fibrosis

P. Negulescu, F. van Goor, K. Gibson-Corley, 2019, Science Translational Medicine.

Glandular Proteome Identifies Antiprotease Cystatin C as a Critical Modulator of Airway Hydration and Clearance.

N. Joo, J. Wine, S. Tyler, 2016, American journal of respiratory cell and molecular biology.

Abnormal endocrine pancreas function at birth in cystic fibrosis ferrets.

D. Meyerholz, Z. A. Stewart, Xingshen Sun, 2012, The Journal of clinical investigation.

Amendment history : Corrigendum ( May 2015 ) CGRP induction in cystic fibrosis airways alters the submucosal gland progenitor cell niche in mice

M. Goodheart, J. Engelhardt, Yulong Zhang, 2018 .

Ferret models of alpha-1 antitrypsin deficiency develop lung and liver disease

E. Hoffman, Junfeng Guo, C. Mueller, 2022, JCI insight.

CGRP induction in cystic fibrosis airways alters the submucosal gland progenitor cell niche in mice.

M. Goodheart, J. Engelhardt, Yulong Zhang, 2015, Journal of Clinical Investigation.

Submucosal Gland Myoepithelial Cells Are Reserve Stem Cells That Can Regenerate Mouse Tracheal Epithelium.

Daniel T. Montoro, Rui Zhao, S. Tyler, 2018, Cell stem cell.

Detargeting Lentiviral-Mediated CFTR Expression in Airway Basal Cells Using miR-106b

E. Devor, J. Engelhardt, D. Stoltz, 2020, Genes.