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New Submission on 1st aug

Authors

  • zainab safi

    MUET
    Author

DOI:

https://doi.org/10.22581/muet1982.15

Keywords:

matata

Abstract

hi

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References

Boucher RC (2004) New concepts of the pathogenesis of cystic fibrosis lung disease. Eur Resp J 23: 146–158. DOI: https://doi.org/10.1183/09031936.03.00057003

Knowles MR, Boucher RC (2002) Mucus clearance as a primary innate defense mechanism for mammalian airways. J Clin Investig 109: 571–577. DOI: https://doi.org/10.1172/JCI0215217

Antunes MB, Cohen NA (2007) Mucociliary clearance - a critical upper airway host defence mechanism and methods of assessment. Curr Opin Allergy Clin Immunol 7: 5–10. DOI: https://doi.org/10.1097/ACI.0b013e3280114eef

Riordan JR, Rommens JM, Kerem BS, Alon N, Rozmahel R, et al. (1989) Identification of the Cystic-Fibrosis Gene - Cloning and Characterization of Complementary-Dna. Science 245: 1066–1072. DOI: https://doi.org/10.1126/science.2475911

Rommens JM, Iannuzzi MC, Kerem BS, Drumm ML, Melmer G, et al. (1989) Identification of the Cystic-Fibrosis Gene - Chromosome Walking and Jumping. Science 245: 1059–1065. DOI: https://doi.org/10.1126/science.2772657

Bobadilla JL, Macek M, Fine JP, Farrell PM (2002) Cystic fibrosis: A worldwide analysis of CFTR mutations - Correlation with incidence data and application to screening. Human Mutation 19: 575–606. DOI: https://doi.org/10.1002/humu.10041

Qu BH, Thomas PJ (1996) Alteration of the cystic fibrosis transmembrane conductance regulator folding pathway - Effects of the Delta F508 mutation on the thermodynamic stability and folding yield of NBD1. J Biol Chem 271: 7261–7264. DOI: https://doi.org/10.1074/jbc.271.13.7261

Published

2024-09-03 — Updated on 2024-09-03

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How to Cite

New Submission on 1st aug. (2024). Mehran University Research Journal of Engineering and Technology, 44(3). https://doi.org/10.22581/muet1982.15