The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Peadar G. Noone

Division of Pulmonary and Critical Care Medicine

Pulmonary/Cystic Fibrosis Research and Treatment Center

University of North Carolina at Chapel Hill

Chapel Hill

USA

[email]@med.unc.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Division of Pulmonary and Critical Care Medicine, Pulmonary/Cystic Fibrosis Research and Treatment Center, University of North Carolina at Chapel Hill, Chapel Hill, USA. 2002
  • Cystic Fibrosis/Pulmonary Research and Treatment Center, Department of Medicine, University of North Carolina at Chapel Hill, 27599-7248, USA. 1997 - 2001
  • Department of Medicine, University of North Carolina at Chapel Hill, 27599-7249, USA. 1999 - 2001

References

  1. Mutations in DNAI1 (IC78) cause primary ciliary dyskinesia. Noone, P.G., Zariwala, M., Sannuti, A., Minnix, S., Leigh, M.W., Carson, J., Knowles, M.R. Chest (2002) [Pubmed]
  2. Safety of aerosolized INS 365 in patients with mild to moderate cystic fibrosis: results of a phase I multi-center study. Noone, P.G., Hamblett, N., Accurso, F., Aitken, M.L., Boyle, M., Dovey, M., Gibson, R., Johnson, C., Kellerman, D., Konstan, M.W., Milgram, L., Mundahl, J., Retsch-Bogort, G., Rodman, D., Williams-Warren, J., Wilmott, R.W., Zeitlin, P., Ramsey, B. Pediatr. Pulmonol. (2001) [Pubmed]
  3. 'CFTR-opathies': disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations. Noone, P.G., Knowles, M.R. Respir. Res. (2001) [Pubmed]
  4. Safety and biological efficacy of a lipid-CFTR complex for gene transfer in the nasal epithelium of adult patients with cystic fibrosis. Noone, P.G., Hohneker, K.W., Zhou, Z., Johnson, L.G., Foy, C., Gipson, C., Jones, K., Noah, T.L., Leigh, M.W., Schwartzbach, C., Efthimiou, J., Pearlman, R., Boucher, R.C., Knowles, M.R. Mol. Ther. (2000) [Pubmed]
  5. Discordant organ laterality in monozygotic twins with primary ciliary dyskinesia. Noone, P.G., Bali, D., Carson, J.L., Sannuti, A., Gipson, C.L., Ostrowski, L.E., Bromberg, P.A., Boucher, R.C., Knowles, M.R. Am. J. Med. Genet. (1999) [Pubmed]
  6. Airway deposition and clearance and systemic pharmacokinetics of amiloride following aerosolization with an ultrasonic nebulizer to normal airways. Noone, P.G., Regnis, J.A., Liu, X., Brouwer, K.L., Robinson, M., Edwards, L., Knowles, M.R. Chest (1997) [Pubmed]
 
WikiGenes - Universities