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

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Scott H. Donaldson

Department of Medicine

University of North Carolina

Chapel Hill

North Carolina 27599

USA

[email]@med.unc.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Medicine, University of North Carolina, Chapel Hill, North Carolina 27599, USA. 2003 - 2007
  • Cystic Fibrosis Research and Treatment Center, Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, USA. 2002 - 2007
  • University of North Carolina at Chapel Hill Cystic Fibrosis Research and Treatment Center, Chapel Hill 27599, USA. 2006

References

  1. Mucociliary clearance as an outcome measure for cystic fibrosis clinical research. Donaldson, S.H., Corcoran, T.E., Laube, B.L., Bennett, W.D. Proc. Am. Thorac. Soc (2007) [Pubmed]
  2. Sodium channels and cystic fibrosis. Donaldson, S.H., Boucher, R.C. Chest (2007) [Pubmed]
  3. Mucus clearance and lung function in cystic fibrosis with hypertonic saline. Donaldson, S.H., Bennett, W.D., Zeman, K.L., Knowles, M.R., Tarran, R., Boucher, R.C. N. Engl. J. Med. (2006) [Pubmed]
  4. Update on pathogenesis of cystic fibrosis lung disease. Donaldson, S.H., Boucher, R.C. Curr. Opin. Pulm. Med (2003) [Pubmed]
  5. Regulation of the epithelial sodium channel by serine proteases in human airways. Donaldson, S.H., Hirsh, A., Li, D.C., Holloway, G., Chao, J., Boucher, R.C., Gabriel, S.E. J. Biol. Chem. (2002) [Pubmed]
  6. Secreted and cell-associated adenylate kinase and nucleoside diphosphokinase contribute to extracellular nucleotide metabolism on human airway surfaces. Donaldson, S.H., Picher, M., Boucher, R.C. Am. J. Respir. Cell Mol. Biol. (2002) [Pubmed]
 
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