T. Rokhlina

发表

Vaccinia Virus Entry, Exit, and Interaction with Differentiated Human Airway Epithelia

M. Welsh, J. Zabner, J. Mchugh, 2007, Journal of Virology.

Simplified and versatile method for isolation of high-quality RNA from pancreas.

Maisam Abu-El-Haija, A. Uc, Michelle A Griffin, 2012, BioTechniques.

Cystic Fibrosis Transmembrane Conductance Regulator Cl− Channels with R Domain Deletions and Translocations Show Phosphorylation-dependent and -independent Activity*

Joseph F. Cotten, M. Welsh, L. Ostedgaard, 2001, The Journal of Biological Chemistry.

Disruption of the CFTR Gene Produces a Model of Cystic Fibrosis in Newborn Pigs

David K. Meyerholz, Christopher S. Rogers, Joseph Zabner, 2008, Science.

Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs.

E. Hoffman, D. Meyerholz, M. Welsh, 2013, The Journal of clinical investigation.

Title Intestinal CFTR expression alleviates meconium ileus in cysticfibrosis pigs

E. Hoffman, D. Meyerholz, M. Welsh, 2013 .

Segregation of receptor and ligand regulates activation of epithelial growth factor receptor

M. Welsh, T. Moninger, J. Zabner, 2003, Nature.

A shortened adeno-associated virus expression cassette for CFTR gene transfer to cystic fibrosis airway epithelia.

M. Welsh, M. Stinski, J. Zabner, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Production of CFTR-null and CFTR-DeltaF508 heterozygous pigs by adeno-associated virus-mediated gene targeting and somatic cell nuclear transfer.

M. Welsh, L. Spate, C. Murphy, 2008, The Journal of clinical investigation.

CFTR with a partially deleted R domain corrects the cystic fibrosis chloride transport defect in human airway epithelia in vitro and in mouse nasal mucosa in vivo

M. Welsh, J. Zabner, A. Stecenko, 2002, Proceedings of the National Academy of Sciences of the United States of America.

A NOVEL GENE DELIVERY METHOD TRANSDUCES PORCINE PANCREATIC DUCT EPITHELIAL CELLS

B. Davidson, P. McCray, A. Uc, 2013, Gene Therapy.

The ΔF508 Mutation Causes CFTR Misprocessing and Cystic Fibrosis–Like Disease in Pigs

S. Richter, D. Meyerholz, M. Welsh, 2011, Science Translational Medicine.

Cystic Fibrosis Pigs Develop Lung Disease and Exhibit Defective Bacterial Eradication at Birth

S. Richter, D. Meyerholz, M. Welsh, 2010, Science Translational Medicine.

Processing and function of CFTR-ΔF508 are species-dependent

M. Welsh, L. Ostedgaard, C. Rogers, 2007, Proceedings of the National Academy of Sciences.

Processing and function of CFTR-DeltaF508 are species-dependent.

M. Welsh, L. Ostedgaard, C. Rogers, 2007, Proceedings of the National Academy of Sciences of the United States of America.

Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epithelia

M. Welsh, L. Ostedgaard, Philip H. Karp, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs.

E. Hoffman, D. Meyerholz, M. Welsh, 2013, The Journal of clinical investigation.

Disruption of the CFTR Gene Produces a Model of Cystic Fibrosis in Newborn Pigs

D. Meyerholz, M. Welsh, C. Murphy, 2008, Science.

Simplified and versatile method for isolation of high-quality RNA from pancreas.

A. Uc, Michelle A Griffin, T. Rokhlina, 2012, BioTechniques.