Initial interrogation, confirmation and fine mapping of modifying genes: STAT3, IL1B and IFNGR1 determine cystic fibrosis disease manifestation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/ejhg2011129.pdf
Reference54 articles.
1. Strausbaugh SD, Davis PB : Cystic fibrosis: a review of epidemiology and pathobiology. Clin Chest Med 2007; 28: 279–288.
2. Rich DP, Anderson MP, Gregory RJ et al: Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells. Nature 1990; 347: 358–363.
3. Gregory RJ, Cheng SH, Rich DP et al: Expression and characterization of the cystic fibrosis transmembrane conductance regulator. Nature 1990; 347: 382–386.
4. Anderson MP, Gregory RJ, Thompson S et al: Demonstration that CFTR is a chloride channel by alteration of its anion selectivity. Science 1991; 253: 202–205.
5. Tang L, Fatehi M, Linsdell P : Mechanism of direct bicarbonate transport by the CFTR anion channel. J Cyst Fibros 2009; 8: 115–121.
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