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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Lawrence E. Ostrowski

Department of Cell and Developmental Biology

Cystic Fibrosis/Pulmonary Research and Treatment Center

School of Medicine

The University of North Carolina

USA

[email]@med.unc.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Cell and Developmental Biology, Cystic Fibrosis/Pulmonary Research and Treatment Center, School of Medicine, The University of North Carolina, USA. 2012
  • The University of North Carolina at Chapel Hill School of Medicine, Cystic Fibrosis/Pulmonary Research and Treatment Center, CB# 7248, 6123A Thurston-Bowles Bldg., USA. 2010
  • Cystic Fibrosis/Pulmonary Research and Treatment Center, University of North Carolina, Chapel Hill, NC 27599, USA. 2002 - 2007

References

  1. Interferon γ Stimulates Accumulation of Gas Phase Nitric Oxide in Differentiated Cultures of Normal and Cystic Fibrosis Airway Epithelial Cells. Ostrowski, L.E., Stewart, D., Hazucha, M. Lung (2012) [Pubmed]
  2. Conditional deletion of dnaic1 in a murine model of primary ciliary dyskinesia causes chronic rhinosinusitis. Ostrowski, L.E., Yin, W., Rogers, T.D., Busalacchi, K.B., Chua, M., O'Neal, W.K., Grubb, B.R. Am. J. Respir. Cell Mol. Biol. (2010) [Pubmed]
  3. Expression of CFTR from a ciliated cell-specific promoter is ineffective at correcting nasal potential difference in CF mice. Ostrowski, L.E., Yin, W., Diggs, P.S., Rogers, T.D., O'Neal, W.K., Grubb, B.R. Gene Ther. (2007) [Pubmed]
  4. Targeting expression of a transgene to the airway surface epithelium using a ciliated cell-specific promoter. Ostrowski, L.E., Hutchins, J.R., Zakel, K., O'Neal, W.K. Mol. Ther. (2003) [Pubmed]
  5. A proteomic analysis of human cilia: identification of novel components. Ostrowski, L.E., Blackburn, K., Radde, K.M., Moyer, M.B., Schlatzer, D.M., Moseley, A., Boucher, R.C. Mol. Cell Proteomics (2002) [Pubmed]
 
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